Mapping QTLs Regulating Morpho-physiological Traits and Yield: Case Studies, Shortcomings and Perspectives in Drought-stressed Maize

Introduction to Quantitative Genetics.

Edwards, A. W. F., & Falconer, D. S. (1982) · Biometrics · doi:10.2307/2529912 · Cited by 21,447 · see citing works

AFLP: a new technique for DNA fingerprinting

Vos, P., Hogers, R. C. J., Bleeker, M., Reijans, M., van de Lee, T., Hornes, M., Frijters, A., Pot, J., Paleman, J., Kuiper, M. T. R., et al. (1995) · Nucleic Acids Research · doi:10.1093/nar/23.21.4407 · Cited by 12,433 · see citing works

Analysis of the genome sequence of the flowering plant Arabidopsis thaliana

Initiative, T. A. G. (2000) · Nature · doi:10.1038/35048692 · Cited by 9,301 · see citing works

Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Botstein, D., White, R. L., Skolnick, M. H., & Davis, R. W. (1980) · Europe PMC (PubMed Central) · Cited by 8,327 · see citing works

Genetics and Analysis of Quantitative Traits

(2002) · Journal of Animal Breeding and Genetics · doi:10.1046/j.1439-0388.2002.00356.x · Cited by 6,172 · see citing works

Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

Lander, E. S., & Botstein, D. (1989) · Genetics · doi:10.1093/genetics/121.1.185 · Cited by 5,236 · see citing works

Differential Display of Eukaryotic Messenger RNA by Means of the Polymerase Chain Reaction

Liang, P., & Pardee, A. B. (1992) · Science · doi:10.1126/science.1354393 · Cited by 5,040 · see citing works

Empirical threshold values for quantitative trait mapping.

Churchill, G. A., & Doerge, R. W. (1994) · Genetics · doi:10.1093/genetics/138.3.963 · Cited by 4,950 · see citing works

Identification of markers linked to disease-resistance genes by bulked segregant analysis: a rapid method to detect markers in specific genomic regions by using segregating populations.

Michelmore, R. W., Paran, I., & Kesseli, R. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.21.9828 · Cited by 4,551 · see citing works

Serial Analysis of Gene Expression

Velculescu, V. E., Zhang, L., Vogelstein, B., & Kinzler, K. W. (1995) · Science · doi:10.1126/science.270.5235.484 · Cited by 3,713 · see citing works

Precision mapping of quantitative trait loci.

Zeng, Z. B. (1994) · Genetics · doi:10.1093/genetics/136.4.1457 · Cited by 3,182 · see citing works

THE MOLECULAR BASIS OF DEHYDRATION TOLERANCE IN PLANTS

Ingram, J., & Bartels, D. (1996) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.47.1.377 · Cited by 2,204 · see citing works

Large-Scale Identification, Mapping, and Genotyping of Single-Nucleotide Polymorphisms in the Human Genome

Wang, D. G., Fan, J., Siao, C.-J., Berno, A. J., Young, P. R., Sapolsky, R., Ghandour, G., Perkins, N., Winchester, E., Spencer, J. B., et al. (1998) · Science · doi:10.1126/science.280.5366.1077 · Cited by 2,162 · see citing works

Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor

Kasuga, M., Liu, Q., Miura, S., Yamaguchi‐Shinozaki, K., & Shinozaki, K. (1999) · Nature Biotechnology · doi:10.1038/7036 · Cited by 2,105 · see citing works

Genetics and analysis of quantitative traits

Ewens, W. J. (1999) · American Journal of Human Biology · doi:10.1002/(sici)1520-6300(199911/12)11:6 · Cited by 2,084 · see citing works

Genomics, gene expression and DNA arrays

Lockhart, D. J., & Winzeler, E. A. (2000) · Nature · doi:10.1038/35015701 · Cited by 2,055 · see citing works

Quantitative Genetics in Maize Breeding

Carena, M. J., Hallauer, A. R., & Filho, J. B. M. (2010) · Springer eBooks · doi:10.1007/978-1-4419-0766-0 · Cited by 1,962 · see citing works

Quantitative Genetics in Maize Breeding

Hallauer, A. R., Carena, M. J., & Filho, J. B. M. (1988) · Medical Entomology and Zoology · Cited by 1,701 · see citing works

Arabidopsis CBF1 Overexpression Induces COR Genes and Enhances Freezing Tolerance

Jaglo‐Ottosen, K. R., Gilmour, S. J., Zarka, D. G., Schabenberger, O., & Thomashow, M. F. (1998) · Science · doi:10.1126/science.280.5360.104 · Cited by 1,692 · see citing works

Plant responses to water deficit

Bray, E. A. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)82562-9 · Cited by 1,609 · see citing works

Hd1, a Major Photoperiod Sensitivity Quantitative Trait Locus in Rice, Is Closely Related to the Arabidopsis Flowering Time Gene CONSTANS

Yano, M., Katayose, Y., Ashikari, M., Yamanouchi, U., Monna, L., Fuse, T., Baba, T., Yamamoto, K., Umehara, Y., Nagamura, Y., et al. (2000) · The Plant Cell · doi:10.1105/tpc.12.12.2473 · Cited by 1,608 · see citing works

Metabolism and Physiology of Abscisic Acid

Zeevaart, J. A. D., & Creelman, R. A. (1988) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.39.060188.002255 · Cited by 1,427 · see citing works

fw2.2 : A Quantitative Trait Locus Key to the Evolution of Tomato Fruit Size

Frary, A., Nesbitt, T. C., Frary, A., Grandillo, S., van der Knaap, E., Cong, B., Liu, J., Meller, J., Elber, R., Alpert, K. B., et al. (2000) · Science · doi:10.1126/science.289.5476.85 · Cited by 1,416 · see citing works

Root Signals and the Regulation of Growth and Development of Plants in Drying Soil

Davies, W. J., & Zhang, J. (1991) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.pp.42.060191.000415 · Cited by 1,390 · see citing works

Association study designs for complex diseases

Cardon, L. R., & Bell, J. I. (2001) · Nature Reviews Genetics · doi:10.1038/35052543 · Cited by 1,380 · see citing works

A Critical Evaluation of Traits for Improving Crop Yields in Water-Limited Environments

Ludlow, M. M., & Muchow, R. C. (1990) · Advances in agronomy · doi:10.1016/s0065-2113(08)60477-0 · Cited by 1,331 · see citing works

Plant Breeding for Stress Environments

Blum, A. (2018) · doi:10.1201/9781351075718 · Cited by 1,309 · cited 4× · see citing works

Dwarf8 polymorphisms associate with variation in flowering time

Thornsberry, J. M., Goodman, M. M., Doebley, J., Kresovich, S., Nielsen, D. M., & Buckler, E. S. (2001) · Nature Genetics · doi:10.1038/90135 · Cited by 1,102 · see citing works

High resolution of quantitative traits into multiple loci via interval mapping.

Jansen, R. C., & Stam, P. (1994) · Genetics · doi:10.1093/genetics/136.4.1447 · Cited by 1,046 · see citing works

Advanced backcross QTL analysis: a method for the simultaneous discovery and transfer of valuable QTLs from unadapted germplasm into elite breeding lines

Tanksley, S. D., & Nelson, J. C. (1996) · Theoretical and Applied Genetics · doi:10.1007/bf00223376 · Cited by 1,029 · see citing works

MAPPING POLYGENES

Tanksley, S. D. (1993) · Annual Review of Genetics · doi:10.1146/annurev.ge.27.120193.001225 · Cited by 1,017 · see citing works

Abiotic stress signalling pathways: specificity and cross-talk

Knight, H., & Knight, M. R. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01946-x · Cited by 972 · see citing works

Diversity Arrays: a solid state technology for sequence information independent genotyping

Jaccoud, D. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.4.e25 · Cited by 968 · see citing works

ROOT SIGNALS AND THE REGULATION OF GROWTH AND DEVELOPMENT OF PLANTS IN DRYING SOIL

Zhang, L. (2002) · Cited by 966 · see citing works

Dehydrins: Emergence of a biochemical role of a family of plant dehydration proteins

Close, T. J. (1996) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1996.tb00546.x · Cited by 950 · see citing works

Multiple Interval Mapping for Quantitative Trait Loci

Kao, C.-H., Zeng, Z., & Teasdale, R. D. (1999) · Genetics · doi:10.1093/genetics/152.3.1203 · Cited by 949 · see citing works

Gene Expression Profiles during the Initial Phase of Salt Stress in Rice

Kawasaki, S., Borchert, C., Deyholos, M. K., Wang, H., Brazille, S. M., Kawai, K., Galbraith, D. W., & Bohnert, H. J. (2001) · The Plant Cell · doi:10.1105/tpc.13.4.889 · Cited by 934 · see citing works

Tansley Review No. 112

Foyer, C. H., & Noctor, G. (2000) · New Phytologist · doi:10.1046/j.1469-8137.2000.00667.x · Cited by 924 · see citing works

Specific Oxidative Cleavage of Carotenoids by VP14 of Maize

Schwartz, S. H., Tan, B. C., Gage, D. A., Zeevaart, J. A. D., & McCarty, D. R. (1997) · Science · doi:10.1126/science.276.5320.1872 · Cited by 909 · see citing works

Mendelian factors underlying quantitative traits in tomato: comparison across species, generations, and environments.

Paterson, A. H., Damon, S., Hewitt, J. D., Zamir, D., Rabinowitch, H. D., Lincoln, S. E., Lander, E. S., & Tanksley, S. D. (1991) · Genetics · doi:10.1093/genetics/127.1.181 · Cited by 899 · see citing works

Identifying differences in mRNA expression by representational difference analysis of cDNA

Hubank, M. J. F., & Schatz, D. G. (1994) · Nucleic Acids Research · doi:10.1093/nar/22.25.5640 · Cited by 873 · see citing works

Visualization of differential gene expression using a novel method of RNA fingerprinting based on AFLP: Analysis of gene expression during potato tuber development

Bachem, C., van der Hoeven, R. S., de Bruijn, S. M., Vreugdenhil, D., Zabeau, M., & Visser, R. G. F. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.9050745.x · Cited by 853 · see citing works

Dehydrins: A commonalty in the response of plants to dehydration and low temperature

Close, T. J. (1997) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1997.tb04785.x · Cited by 850 · see citing works

Interval mapping of multiple quantitative trait loci.

Jansen, R. C. (1993) · Genetics · doi:10.1093/genetics/135.1.205 · Cited by 850 · see citing works

From Proteins to Proteomes: Large Scale Protein Identification by Two-Dimensional Electrophoresis and Arnino Acid Analysis

Wilkins, M. R., Pasquali, C., Appel, R. D., Ou, K., Golaz, O., Sanchez, J., Yan, J. X., Gooley, A. A., Hughes, G. J., Humphery‐Smith, I., et al. (1996) · Nature Biotechnology · doi:10.1038/nbt0196-61 · Cited by 836 · see citing works

Statistical Genomics: Linkage, Mapping, and QTL Analysis

Liu, B. H. (1997) · Medical Entomology and Zoology · Cited by 795 · see citing works

teosinte branched1 and the origin of maize: evidence for epistasis and the evolution of dominance.

Doebley, J., Stec, A. O., & Gustus, C. D. (1995) · Genetics · doi:10.1093/genetics/141.1.333 · Cited by 768 · see citing works

Mass spectrometry and the age of the proteome

Yates, J. R. (1998) · Journal of Mass Spectrometry · doi:10.1002/(sici)1096-9888(199801)33:1 · Cited by 730 · see citing works

The Human Transcriptome Map: Clustering of Highly Expressed Genes in Chromosomal Domains

Caron, H. N., van Schaik, B. D. C., van der Mee, M., Baas, F., Riggins, G. J., Sluis, P. V., Hermus, M.-C., van Asperen, R., Boon, K., Voûte, P. A., et al. (2001) · Science · doi:10.1126/science.1056794 · Cited by 730 · see citing works

Genomic approaches to plant stress tolerance

Cushman, J. C., & Bohnert, H. J. (2000) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(99)00052-7 · Cited by 722 · see citing works

THE ASSOCIATION OF SIZE DIFFERENCES WITH SEED-COAT PATTERN AND PIGMENTATION IN PHASEOLUS VULGARIS

Sax, K. (1923) · Genetics · doi:10.1093/genetics/8.6.552 · Cited by 677 · see citing works

The importance of the anthesis-silking interval in breeding for drought tolerance in tropical maize

Bolaños, J., & Edmeades, G. O. (1996) · Field Crops Research · doi:10.1016/0378-4290(96)00036-6 · Cited by 652 · see citing works

Genetic control of abscisic acid biosynthesis in maize

Tan, B. C., Schwartz, S. H., Zeevaart, J. A. D., & McCarty, D. R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.22.12235 · Cited by 629 · see citing works

Reproductive Development in Grain Crops during Drought

Saini, H. S., & Westgate, M. E. (1999) · Advances in agronomy · doi:10.1016/s0065-2113(08)60843-3 · Cited by 623 · see citing works

A Statistical Framework for Quantitative Trait Mapping

Sen, Ś., & Churchill, G. A. (2001) · Genetics · doi:10.1093/genetics/159.1.371 · Cited by 611 · see citing works

Monitoring large-scale changes in transcript abundance in drought- and salt-stressed barley

Ozturk, Z. N., Talamé, V., Deyholos, M. K., Michalowski, C. B., Galbraith, D. W., Gözükırmızı, N., Tuberosa, R., & Bohnert, H. J. (2002) · Plant Molecular Biology · doi:10.1023/a:1014875215580 · Cited by 571 · see citing works

Identification of Trait-Improving Quantitative Trait Loci Alleles From a Wild Rice Relative, Oryza rufipogon

Xiao, J., Li, J., Grandillo, S., Ahn, S. N., Yuan, L., Tanksley, S. D., & McCouch, S. R. (1998) · Genetics · doi:10.1093/genetics/150.2.899 · Cited by 570 · see citing works

Molecular and physiological approaches to maize improvement for drought tolerance

Bruce, W. B., Edmeades, G. O., & Barker, T. C. (2002) · Journal of Experimental Botany · doi:10.1093/jexbot/53.366.13 · Cited by 562 · see citing works

Mapping QTLs with epistatic effects and QTL×environment interactions by mixed linear model approaches

Wang, D. L., Zhu, J., Li, Z. K. L., & Paterson, A. H. (1999) · Theoretical and Applied Genetics · doi:10.1007/s001220051331 · Cited by 559 · see citing works

A computational analysis of whole-genome expression data reveals chromosomal domains of gene expression

Cohen, B. A., Mitra, R. D., Hughes, J. D., & Church, G. M. (2000) · Nature Genetics · doi:10.1038/79896 · Cited by 533 · see citing works

Quantitative Trait Locus (QTL) Mapping Using Different Testers and Independent Population Samples in Maize Reveals Low Power of QTL Detection and Large Bias in Estimates of QTL Effects

Melchinger, A. E., Utz, H. F., & Schön, C. (1998) · Genetics · doi:10.1093/genetics/149.1.383 · Cited by 532 · see citing works

Towards a Better Understanding of the Genetic and Physiological Basis for Nitrogen Use Efficiency in Maize

Hirel, B. J., Bertin, P., Quilleré, I., Bourdoncle, W., Attagnant, C., Dellay, C., Gouy, A., Cadiou, S., Retailliau, C., Falque, M., et al. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.125.3.1258 · Cited by 532 · see citing works

Marker-assisted selection: new tools and strategies

Ribaut, J., & Hoisington, D. A. (1998) · Trends in Plant Science · doi:10.1016/s1360-1385(98)01240-0 · Cited by 516 · see citing works

A cDNA-based comparison of dehydration-induced proteins (dehydrins) in barley and corn

Close, T. J., Kortt, A. A., & Chandler, P. M. (1989) · Plant Molecular Biology · doi:10.1007/bf00027338 · Cited by 511 · see citing works

A genomic perspective on plant transcription factors

Riechmann, J. L., & Ratcliffe, O. J. (2000) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00107-2 · Cited by 504 · see citing works

QTL analysis in plants; where are we now?

Kearsey, M. J., & Farquhar, A. G. L. (1998) · Heredity · doi:10.1046/j.1365-2540.1998.00500.x · Cited by 492 · see citing works

Detecting marker-QTL linkage and estimating QTL gene effect and map location using a saturated genetic map.

Darvasi, A., Weinreb, A., Minke, V., Weller, J. I., & Soller, M. (1993) · Genetics · doi:10.1093/genetics/134.3.943 · Cited by 489 · see citing works

Hd6 , a rice quantitative trait locus involved in photoperiod sensitivity, encodes the α subunit of protein kinase CK2

Takahashi, Y., Shomura, A., Sasaki, T., & Yano, M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.111136798 · Cited by 483 · see citing works

The structure and reproduction of corn

Kiesselbach, T. A. (1980) · Lincoln (University of Nebraska) · Cited by 469 · see citing works

Naturally occurring variation in Arabidopsis: an underexploited resource for plant genetics

Alonso‐Blanco, C., & Koornneef, M. (2000) · Trends in Plant Science · doi:10.1016/s1360-1385(99)01510-1 · Cited by 461 · see citing works

Molecular Marker‐Facilitated Investigations of Quantitative Trait Loci in Maize. II. Factors Influencing Yield and its Component Traits1

Stuber, C. W., Edwards, M. D., & Wendel, J. F. (1987) · Crop Science · doi:10.2135/cropsci1987.0011183x002700040006x · Cited by 451 · see citing works

Regulation of Abscisic Acid-Induced Stomatal Closure and Anion Channels by Guard Cell AAPK Kinase

Li, J., Wang, Q., Watson, M. B., & Assmann, S. M. (2000) · Science · doi:10.1126/science.287.5451.300 · Cited by 444 · see citing works

Advanced backcross QTL analysis in a cross between an elite processing line of tomato and its wild relative L. pimpinellifolium

Tanksley, S. D., Grandillo, S., Fulton, T. M., Zamir, D., Eshed, Y., Pétiard, V., Lopez, J. W., & Beck-Bunn, T. (1996) · Theoretical and Applied Genetics · doi:10.1007/bf00223378 · Cited by 442 · see citing works

Identification of quantitative trait loci under drought conditions in tropical maize. 2. Yield components and marker-assisted selection strategies

Ribaut, J., Jiang, C., González-de-León, D., Edmeades, G. O., & Hoisington, D. A. (1997) · Theoretical and Applied Genetics · doi:10.1007/s001220050492 · Cited by 437 · see citing works

A recombination hotspot delimits a wild-species quantitative trait locus for tomato sugar content to 484 bp within an invertase gene

Fridman, E., Pleban, T., & Zamir, D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.9.4718 · Cited by 437 · see citing works

Molecular-marker-facilitated investigations of quantitative trait loci in maize

Edwards, M. D., Helentjaris, T., Wright, S., & Stuber, C. W. (1992) · Theoretical and Applied Genetics · doi:10.1007/bf00226696 · Cited by 437 · see citing works

A Whole-Plant Perspective on Carbon-Nitrogen Interactions.

Burke, M. K., Dickson, R. E., Roy, J., & Garnier, É. (1996) · Ecology · doi:10.2307/2265523 · Cited by 434 · see citing works

Linkage disequilibrium and the search for complex disease genes.Preprint

Jorde, L. (2000) · Genome Research · doi:10.1101/gr.144500 · Cited by 422 · see citing works

Locating genes associated with root morphology and drought avoidance in rice via linkage to molecular markers

Champoux, M. C., Wang, G., Sarkarung, S., Mackill, D. J., O'Toole, J. C., Huang, N., & McCouch, S. R. (1995) · Theoretical and Applied Genetics · doi:10.1007/bf00222910 · Cited by 421 · see citing works

Chromosome landing: a paradigm for map-based gene cloning in plants with large genomes

Tanksley, S. D., Ganal, M. W., & Martin, G. B. (1995) · Trends in Genetics · doi:10.1016/s0168-9525(00)88999-4 · Cited by 420 · see citing works

Construction of genetic linkage maps in maize and tomato using restriction fragment length polymorphisms

Helentjaris, T., Slocum, M. K., Wright, S., Schaefer, A., & Nienhuis, J. (1986) · Theoretical and Applied Genetics · doi:10.1007/bf00266542 · Cited by 420 · see citing works

Selective genotyping for determination of linkage between a marker locus and a quantitative trait locus

Darvasi, A., & Soller, M. (1992) · Theoretical and Applied Genetics · doi:10.1007/bf00222881 · Cited by 410 · see citing works

Osmotic adjustment and the inhibition of leaf, root, stem and silk growth at low water potentials in maize

Westgate, M. E., & Boyer, J. S. (1985) · Planta · doi:10.1007/bf00395973 · Cited by 406 · see citing works

ABA plays a central role in mediating the regulatory effects of nitrate on root branching in Arabidopsis

Signora, L., Smet, I. D., Foyer, C. H., & Zhang, H. (2001) · The Plant Journal · doi:10.1046/j.1365-313x.2001.01185.x · Cited by 403 · see citing works

Comparative analysis of QTLs affecting plant height and maturity across the Poaceae, in reference to an interspecific sorghum population.

Lin, Y., Schertz, K. F., & Paterson, A. H. (1995) · Genetics · doi:10.1093/genetics/141.1.391 · Cited by 399 · see citing works

Genotypic Variation in Crop Plant Root Systems

O'Toole, J. C., & Bland, W. L. (1987) · Advances in agronomy · doi:10.1016/s0065-2113(08)60803-2 · Cited by 398 · see citing works

Abscisic Acid Accumulation Maintains Maize Primary Root Elongation at Low Water Potentials by Restricting Ethylene Production

Spollen, W. G., LeNoble, M. E., Samuels, T. D., Bernstein, N., & Sharp, R. E. (2000) · PLANT PHYSIOLOGY · doi:10.1104/pp.122.3.967 · Cited by 395 · see citing works

Estimating the locations and the sizes of the effects of quantitative trait loci using flanking markers

Martínez, O., & Curnow, R. N. (1992) · Theoretical and Applied Genetics · doi:10.1007/bf00222330 · Cited by 355 · see citing works

Identification of QTLs for root characteristics in maize grown in hydroponics and analysis of their overlap with QTLs for grain yield in the field at two water regimes

Tuberosa, R., Sanguineti, M. C., Landi, P., Giuliani, M. M., Salvi, S., & Conti, S. (2002) · Plant Molecular Biology · doi:10.1023/a:1014897607670 · Cited by 354 · see citing works

DNA Markers and Plant Breeding Programs

Lee, M. (1995) · Advances in agronomy · doi:10.1016/s0065-2113(08)60542-8 · Cited by 346 · see citing works

Molecular Dissection of Complex Traits

Paterson, A. H. (2010) · CRC Press eBooks · doi:10.1201/9781420049381 · Cited by 345 · see citing works

PLABQTL: a program for composite interval mapping of QTL.

Utz, H. F., & Melchinger, A. E. (1996) · Cited by 338 · see citing works

Defining selection criteria to improve yield under drought

Richards, R. A. (1996) · Springer eBooks · doi:10.1007/978-94-017-1299-6_10 · Cited by 333 · see citing works

Abscisic acid : physiology and biochemistry

Davies, W. J., & Jones, H. G. (1991) · BIOS Scientific Publishers eBooks · Cited by 323 · see citing works

Identification of quantitative trait loci under drought conditions in tropical maize. 1. Flowering parameters and the anthesis-silking interval

Ribaut, J., Hoisington, D. A., Deutsch, J. A., Jiang, C., & González-de-León, D. (1996) · Theoretical and Applied Genetics · doi:10.1007/bf00221905 · Cited by 315 · see citing works

Development and mapping of SSR markers for maize

Sharopova, N., McMullen, M. D., Schultz, L., Schroeder, S., Sánchez‐Villeda, H., Gardiner, J. M., Bergstrom, D., Houchins, K. E., Melia-Hancock, S., Musket, T. A., et al. (2002) · Plant Molecular Biology · doi:10.1023/a:1014868625533 · Cited by 312 · see citing works

Plant Functional Genomics

Somerville, C. R., & Somerville, S. C. (1999) · Science · doi:10.1126/science.285.5426.380 · Cited by 312 · see citing works

Finding the molecular basis of quatitative traits: successes and pitfalls

Jonathan Flint, C., & Mott, R. (2001) · Nature Reviews Genetics · doi:10.1038/35076585 · Cited by 309 · see citing works

Developing drought- and low N-tolerant maize

Edmeades, G. O., Bänziger, M., Mickelson, H. R., & Peña-Valdivia, C. B. (1997) · Cited by 307 · see citing works

A cautiously optimistic vision for marker-assisted breeding

Young, N. D. (1999) · Molecular Breeding · doi:10.1023/a:1009684409326 · Cited by 303 · see citing works

Starch and the Control of Kernel Number in Maize at Low Water Potentials

Zinselmeier, C., Jeong, B., & Boyer, J. S. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.1.25 · Cited by 294 · see citing works

Advanced backcross QTL analysis in tomato. I. Identification of QTLs for traits of agronomic importance from Lycopersicon hirsutum

Bernacchi, D., Beck-Bunn, T., Eshed, Y., Lopez, J. W., Pétiard, V., Uhlig, J., Zamir, D., & Tanksley, S. D. (1998) · Theoretical and Applied Genetics · doi:10.1007/s001220050908 · Cited by 285 · see citing works

Abscisic acid and hydraulic conductivity of maize roots: a study using cell- and root-pressure probes

Hose, E., Steudle, E., & Hartung, W. (2000) · Planta · doi:10.1007/s004250000412 · Cited by 282 · see citing works

Drought and drought tolerance

Passioura, J. B. (1996) · Plant Growth Regulation · doi:10.1007/bf00024003 · Cited by 281 · see citing works

Eight cycles of selection for drought tolerance in lowland tropical maize. I. Responses in grain yield, biomass, and radiation utilization

Bolaños, J., & Edmeades, G. O. (1993) · Field Crops Research · doi:10.1016/0378-4290(93)90064-t · Cited by 279 · see citing works

Genome-wide mapping with biallelic markers in Arabidopsis thaliana

Cho, R. J., Mindrinos, M. N., Richards, D. R., Sapolsky, R. J., Anderson, M. A., Drenkard, E., Dewdney, J., Reuber, T. L., Stammers, M., Federspiel, N. A., et al. (1999) · Nature Genetics · doi:10.1038/13833 · Cited by 276 · see citing works

Mutants of Maize

Neuffer, M. G., Coe, E. H., & Wessler, S. R. (1997) · Medical Entomology and Zoology · Cited by 274 · see citing works

Identification of QTL for drought responses in maize and their use in testing causal relationships between traits

Lebreton, C. M., Lazić-Jančić, V., Steed, A., Pekic, S., & Quarrie, S. A. (1995) · Journal of Experimental Botany · doi:10.1093/jxb/46.7.853 · Cited by 274 · see citing works

Plant Responses to Cellular Dehydration During Environmental Stress

Close, T.-J., & Bray, E. A. (1993) · Cited by 273 · see citing works

Fine Mapping of Quantitative Trait Loci Using Linkage Disequilibria With Closely Linked Marker Loci

Meuwissen, T. H. E., & Goddard, M. E. (2000) · Genetics · doi:10.1093/genetics/155.1.421 · Cited by 271 · see citing works

Drought and drought tolerance

Passioura, J. B. (1996) · Springer eBooks · doi:10.1007/978-94-017-1299-6_1 · Cited by 267 · see citing works

Mapping quantitative trait loci in plants: uses and caveats for evolutionary biology

Mauricio, R. (2001) · Nature Reviews Genetics · doi:10.1038/35072085 · Cited by 264 · see citing works

Effects of Abscisic Acid and Water Stress on Development and Morphology of Wheat

Quarrie, S. A., & Jones, H. G. (1977) · Journal of Experimental Botany · doi:10.1093/jxb/28.1.192 · Cited by 263 · see citing works

Crop improvement in the 21st century

Miflin, B. J. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.342.1 · Cited by 253 · see citing works

The pathway of biosynthesis of abscisic acid in vascular plants: a review of the present state of knowledge of ABA biosynthesis

Milborrow, B. V. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.359.1145 · Cited by 252 · see citing works

The maize Dwarf3 gene encodes a cytochrome P450-mediated early step in Gibberellin biosynthesis.

Winkler, R. G., & Helentjaris, T. (1995) · The Plant Cell · doi:10.1105/tpc.7.8.1307 · Cited by 252 · see citing works

Two high-density AFLP® linkage maps of Zea mays L.: analysis of distribution of AFLP markers

Vuylsteke, M., Mank, R. A., Antonise, R., Bastiaans, E., Senior, M. L., Stuber, C. W., Melchinger, A. E., Lübberstedt, T., Xia, X. C., Stam, P., et al. (1999) · Theoretical and Applied Genetics · doi:10.1007/s001220051399 · Cited by 240 · see citing works

A Maize Map Standard With Sequenced Core Markers, Grass Genome Reference Points and 932 Expressed Sequence Tagged Sites (ESTs) in a 1736-Locus Map

Davis, G., McMullen, M. D., Baysdorfer, C., Musket, T. A., Grant, D., Staebell, M., Xu, G., Polacco, M. L., Koster, L., Melia-Hancock, S., et al. (1999) · Genetics · doi:10.1093/genetics/152.3.1137 · Cited by 238 · see citing works

Confirmation that abscisic acid accumulation is required for maize primary root elongation at low water potentials

Sharp, R. E., Wu, Y., Voetberg, G. S., Saab, I. N., & LeNoble, M. E. (1994) · Journal of Experimental Botany · doi:10.1093/jxb/45.special_issue.1743 · Cited by 236 · see citing works

Quantitative trait loci underlying gene product variation: a novel perspective for analyzing regulation of genome expression.

Damerval, C., Maurice, A. I., Josse, J.-M., & de Vienne, D. (1994) · Genetics · doi:10.1093/genetics/137.1.289 · Cited by 234 · see citing works

Fine mapping of quantitative trait loci Hd-1, Hd-2 and Hd-3, controlling heading date of rice, as single Mendelian factors

Yamamoto, T., Kuboki, Y., Lin, S., Sasaki, T., & Yano, M. (1998) · Theoretical and Applied Genetics · doi:10.1007/s001220050864 · Cited by 234 · see citing works

Simple sequence repeats for germplasm analysis and mapping in maize

Taramino, G., & Tingey, S. V. (1996) · Genome · doi:10.1139/g96-038 · Cited by 233 · see citing works

The barley (Hordeum vulgare L.) dehydrin multigene family: sequences, allele types, chromosome assignments, and expression characteristics of 11 Dhn genes of cv Dicktoo

Choi, D., Zhu, B., & Close, T. J. (1999) · Theoretical and Applied Genetics · doi:10.1007/s001220051189 · Cited by 233 · see citing works

In vitro cloning of complex mixtures of DNA on microbeads: Physical separation of differentially expressed cDNAs

Brenner, S., Williams, S. R., Vermaas, E. H., Storck, T., Moon, K. W., McCollum, C., Mao, J.-I., Luo, S. J., Kirchner, J. J., Eletr, S., et al. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.4.1665 · Cited by 232 · see citing works

Synergy of Empirical Breeding, Marker‐Assisted Selection, and Genomics to Increase Crop Yield Potential

Stuber, C. W., Polacco, M. L., & Senior, M. L. (1999) · Crop Science · doi:10.2135/cropsci1999.3961571x · Cited by 227 · see citing works

Genotype-by-environment interaction in genetic mapping of multiple quantitative trait loci

Jansen, R. C., van Ooijen, J. W., Stam, P., Lister, C., & Dean, C. (1995) · Theoretical and Applied Genetics · doi:10.1007/bf00220855 · Cited by 226 · see citing works

A combined RFLP and AFLP linkage map of upland rice (Oryza sativa L.) used to identify QTLs for root-penetration ability

Price, A. H., Steele, K. A., Moore, B. J., Barraclough, P. B., & Clark, L. J. (2000) · Theoretical and Applied Genetics · doi:10.1007/s001220050007 · Cited by 217 · see citing works

Growth Maintenance of the Maize Primary Root at Low Water Potentials Involves Increases in Cell-Wall Extension Properties, Expansin Activity, and Wall Susceptibility to Expansins

Wu, Y., Sharp, R. E., Durachko, D. M., & Cosgrove, D. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.3.765 · Cited by 216 · see citing works

Expression Profiling of the Maize Flavonoid Pathway Genes Controlled by Estradiol-Inducible Transcription Factors CRC and P

Bruce, W., Folkerts, O., Garnaat, C., Crasta, O. R., Roth, B., & Bowen, B. (2000) · The Plant Cell · doi:10.1105/tpc.12.1.65 · Cited by 214 · see citing works

Comparative mapping in F2∶3 and F6∶7 generations of quantitative trait loci for grain yield and yield components in maize

Austin, D. F., & Lee, M. (1996) · Theoretical and Applied Genetics · doi:10.1007/bf00221893 · Cited by 212 · see citing works

Drought tolerance in winter cereals:

Mayer, A. M. (1988) · Phytochemistry · doi:10.1016/0031-9422(88)80070-0 · Cited by 212 · see citing works

Targeting detoxification pathways: an efficient approach to obtain plants with multiple stress tolerance?

Bartels, D. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01983-5 · Cited by 208 · see citing works

Eight cycles of selection for drought tolerance in lowland tropical maize. III. Responses in drought-adaptive physiological and morphological traits

Bolaños, J., Edmeades, G. O., & Martinez, L. (1993) · Field Crops Research · doi:10.1016/0378-4290(93)90066-v · Cited by 206 · see citing works

Does ABA in the Xylem Control the Rate of Leaf Growth in Soil-Dried Maize and Sunflower Plants?

Zhang, J., & Davies, W. J. (1990) · Journal of Experimental Botany · doi:10.1093/jxb/41.9.1125 · Cited by 205 · see citing works

Xylem ABA controls the stomatal conductance of field‐grown maize subjected to soil compaction or soil drying

Tardieu, F., Zhang, J., Katerji, N., Bethenod, O., PALMER, S., & Davies, W. J. (1992) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1992.tb01473.x · Cited by 203 · see citing works

Low Water Potential Disrupts Carbohydrate Metabolism in Maize (Zea mays L.) Ovaries

Zinselmeier, C., Westgate, M. E., Schussler, J. R., & Jones, R. J. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.107.2.385 · Cited by 203 · see citing works

Selection Improves Drought Tolerance in Tropical Maize Populations: II. Direct and Correlated Responses among Secondary Traits

Chapman, S. C., & Edmeades, G. O. (1999) · Crop Science · doi:10.2135/cropsci1999.3951315x · Cited by 201 · see citing works

Genetic analysis of drought tolerance in maize by molecular markers I. Yield components

Frova, C., Krajewski, P., di Fonzo, N., Villa, M., & Sari-Gorla, M. (1999) · Theoretical and Applied Genetics · doi:10.1007/s001220051233 · Cited by 187 · see citing works

Proteomics for genetic and physiological studies in plants

Thiellement, H., Bahrman, N., Damerval, C., Plomion, C., Rossignol, M., Santoni, V., de Vienne, D., & Zivy, M. (1999) · doi:10.1002/9783527613489.ch4 · Cited by 183 · see citing works

Toward a unified genetic map of higher plants, transcending the monocot–dicot divergence

Paterson, A. H., Lan, T., Reischmann, K. P., Chang, C., Lin, Y., Liu, S., Burow, M. D., Kowalski, S. P., Katsar, C. S., DelMonte, T. A., et al. (1996) · Nature Genetics · doi:10.1038/ng1296-380 · Cited by 182 · see citing works

TowardsArabidopsisgenome analysis: monitoring expression profiles of 1400 genes using cDNA microarrays

Ruan, Y., Gilmore, J., & Conner, T. W. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00254.x · Cited by 177 · see citing works

Regions of the Genome That Affect Grain and Malt Quality in a North American Two‐Row Barley Cross

Mather, D. E., Tinker, N. A., LaBerge, D. E., Edney, M. J., Jones, B. L., Rossnagel, B. G., Legge, W. G., Briggs, K. G., Irvine, R. G., Falk, D. E., et al. (1997) · Crop Science · doi:10.2135/cropsci1997.0011183x003700020039x · Cited by 175 · see citing works

Bulk segregant analysis with molecular markers and its use for improving drought resistance in maize

Quarrie, S. A., Lazić-Jančić, V., Kovačević, D., Steed, A., & Pekic, S. (1999) · Journal of Experimental Botany · doi:10.1093/jxb/50.337.1299 · Cited by 174 · see citing works

Identification of quantitative trait loci for nitrogen use efficiency in maize

Agrama, H. A., Zakaria, A. G., Said, F. B., & Tuinstra, M. R. (1999) · Molecular Breeding · doi:10.1023/a:1009669507144 · Cited by 172 · see citing works

Gene expression analysis by transcript profiling coupled to a gene database query

Shimkets, R. A., Lowe, D. G., Tai, J., Sehl, P. D., Jin, H., Yang, R., Predki, P. F., Rothberg, B. E. G., Murtha, M. T., Roth, M. E., et al. (1999) · Nature Biotechnology · doi:10.1038/11743 · Cited by 168 · see citing works

Transcript profiling in rice (Oryza sativa L.) seedlings using serial analysis of gene expression (SAGE)

Matsumura, H., Nirasawa, S., & Terauchi, R. (1999) · The Plant Journal · doi:10.1046/j.1365-313x.1999.00640.x · Cited by 168 · see citing works

Inferences on the Genome Structure of Progenitor Maize Through Comparative Analysis of Rice, Maize and the Domesticated Panicoids

Wilson, W. A., Harrington, S. E., Woodman, W. L., Lee, M., Sorrells, M. E., & McCouch, S. R. (1999) · Genetics · doi:10.1093/genetics/153.1.453 · Cited by 167 · see citing works

Insertion-deletion polymorphisms in 3′ regions of maize genes occur frequently and can be used as highly informative genetic markers

Bhattramakki, D., Dolan, M., Hanafey, M., Wineland, R., Vaske, D. A., Register, J. C., Tingey, S. V., & Rafalski, A. J. (2002) · Plant Molecular Biology · doi:10.1023/a:1014841612043 · Cited by 163 · see citing works

The development and application of molecular markers for abiotic stress tolerance in barley

Forster, B. P., Ellis, R. P., Thomas, W. T. B., Newton, A. C., Tuberosa, R., This, D., El‐Enein, R. A., Bahri, M., & Salem, M. B. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.342.19 · Cited by 162 · see citing works

Transgenic approaches to increase dehydration-stress tolerance in plants

Bajaj, S., Targolli, J., Liu, L., Ho, T. D., & Wu, R. (1999) · Molecular Breeding · doi:10.1023/a:1009660413133 · Cited by 161 · see citing works

Characterization of a Yield Quantitative Trait Locus on Chromosome Five of Maize by Fine Mapping

Graham, G. I., Wolff, D. W., & Stuber, C. W. (1997) · Crop Science · doi:10.2135/cropsci1997.0011183x003700050033x · Cited by 161 · see citing works

Root Signals And The Regulation Of Growth And Development Of Plants In Drying Soil

Davies, W. J. (1991) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.42.1.55 · Cited by 159 · see citing works

Mapping QTLs for root traits in a recombinant inbred population from two indica ecotypes in rice

Ali, M. L., Pathan, M. S., Zhang, J., Bai, G., Sarkarung, S., & Nguyen, H. T. (2000) · Theoretical and Applied Genetics · doi:10.1007/s001220051541 · Cited by 158 · see citing works

Molecular approaches for the genetic improvement of cereals for stable production in water-limited environments

Ribaut, J., & Poland, D. (2000) · Cited by 157 · see citing works

Detecting the Undetected: Estimating the Total Number of Loci Underlying a Quantitative Trait

Otto, S. P., & Jones, C. D. (2000) · Genetics · doi:10.1093/genetics/156.4.2093 · Cited by 157 · see citing works

QTL Analysis in Plants

Xu, S. (2003) · Humana Press eBooks · doi:10.1385/1-59259-176-0:283 · Cited by 154 · see citing works

Keeping in Touch: Responses of the Whole Plant to Deficits in Water and Nitrogen Supply

McDonald, A. J. S., & Davies, W. J. (1996) · Advances in botanical research · doi:10.1016/s0065-2296(08)60059-2 · Cited by 151 · see citing works

Mapping QTLs in breeding for drought tolerance in maize (Zea mays L.)

Agrama, H. A., & Moussa, M. (1996) · Euphytica · doi:10.1007/bf00035278 · Cited by 151 · see citing works

Drought as a challenge for the plant breeder

Ceccarelli, S., & Grando, S. (1996) · Plant Growth Regulation · doi:10.1007/bf00024011 · Cited by 151 · see citing works

Proline Accumulation in Maize (Zea mays L.) Primary Roots at Low Water Potentials (I. Requirement for Increased Levels of Abscisic Acid)

Ober, E. S., & Sharp, R. E. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.105.3.981 · Cited by 150 · see citing works

Enhanced Efficiency of Quantitative Trait Loci Mapping Analysis Based on Multivariate Complexes of Quantitative Traits

Korol, A. B., Ronin, Y. I., Itskovich, A. M., Peng, J. H., & Nevo, E. (2001) · Genetics · doi:10.1093/genetics/157.4.1789 · Cited by 149 · see citing works

Stomatal control by both [ABA] in the xylem sap and leaf water status: a test of a model for draughted or ABA‐fed field‐grown maize

Tardieu, F., Zhang, J., & GOWING, D. J. G. (1993) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1993.tb00887.x · Cited by 149 · see citing works

Drought as a challenge for the plant breeder

Ceccarelli, S., & Grando, S. (1996) · Springer eBooks · doi:10.1007/978-94-017-1299-6_9 · Cited by 143 · see citing works

RFLP mapping of quantitative trait loci controlling abscisic acid concentration in leaves of drought-stressed maize (Zea mays L.)

Tuberosa, R., Sanguineti, M. C., Landi, P., Salvi, S., Casarini, E., & Conti, S. (1998) · Theoretical and Applied Genetics · doi:10.1007/s001220050951 · Cited by 142 · see citing works

Dissecting complex physiological functions through the use of molecular quantitative genetics

Prioul, J., Quarrie, S. A., Causse, M., & de Vienne, D. (1997) · Journal of Experimental Botany · doi:10.1093/jxb/48.6.1151 · Cited by 141 · see citing works

A possible technique for isolating genic DNA for quantitative traits in plants

Robertson, D. S. (1985) · Journal of Theoretical Biology · doi:10.1016/s0022-5193(85)80161-2 · Cited by 141 · see citing works

Analyses of mutants of three genes that influence root hair development in Zea mays (Gramineae) suggest that root hairs are dispensable

Wen, T., & Schnable, P. S. (1994) · American Journal of Botany · doi:10.1002/j.1537-2197.1994.tb15564.x · Cited by 137 · see citing works

Toward positional cloning of Vgt1, a QTL controlling the transition from the vegetative to the reproductive phase in maize

Salvi, S., Tuberosa, R., Chiapparino, E., Maccaferri, M., Veillet, S., van Beuningen, L., Isaac, P. G., Edwards, K., & Phillips, R. L. (2002) · Plant Molecular Biology · doi:10.1023/a:1014838024509 · Cited by 134 · see citing works

Genetic analysis of drought tolerance in maize by molecular markers. II. Plant height and flowering

Sari-Gorla, M., Krajewski, P., di Fonzo, N., Villa, M., & Frova, C. (1999) · Theoretical and Applied Genetics · doi:10.1007/s001220051234 · Cited by 133 · see citing works

Proteomics: a link between genomics, genetics and physiology

Zivy, M., & de Vienne, D. (2000) · Plant Molecular Biology · doi:10.1023/a:1026525406953 · Cited by 132 · see citing works

What is yield

Duvick, D. N. (1997) · Cited by 130 · see citing works

Maize stomatal conductance in the field: its relationship with soil and plant water potentials, mechanical constraints and ABA concentration in the xylem sap

Tardieu, F., Katerji, N., Bethenod, O., Zhang, J., & Davies, W. J. (1991) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1991.tb01378.x · Cited by 129 · see citing works

Quantitative trait loci and metabolic pathways

McMullen, M. D., Byrne, P. F., Snook, M. E., Wiseman, B. R., Lee, E. A., Widstrom, N. W., & Coe, E. H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.5.1996 · Cited by 129 · see citing works

Arabidopsis–Rice: Will Colinearity Allow Gene Prediction Across the Eudicot–Monocot Divide?Preprint

Devos, K. M., Beales, J., Nagamura, Y., & Sasaki, T. (1999) · Genome Research · doi:10.1101/gr.9.9.825 · Cited by 126 · see citing works

A major effect QTL determined by multiple genes in epileptic EL mice.

Legare, M. E., Bartlett, F. S., & Frankel, W. N. (2000) · PubMed · Cited by 122 · see citing works

Advanced backcross QTL analysis: a method for the simultaneous discovery and transfer of valuable QTLs from unadapted germplasm into elite breeding lines

Tanksley, S. D., & Nelson, J. C. (1996) · Theoretical and Applied Genetics · doi:10.1007/s001220050114 · Cited by 116 · see citing works

Toward elucidating the global gene expression patternsof developing Arabidopsis: Parallel analysis of 8 300 genesby a high-density oligonucleotide probe array

Zhu, T., Budworth, P. R., Han, B., Brown, D., Chang, H., Zou, G., & Wang, X. (2001) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(00)01234-1 · Cited by 114 · see citing works

pH, abscisic acid and the integration of metabolism in plants under stressed and non‐stressed conditions: cellular responses to stress and their implication for plant water relations

Netting, A. G. (2000) · Journal of Experimental Botany · doi:10.1093/jexbot/51.343.147 · Cited by 113 · see citing works

Metabolism And Physiology Of Abscisic Acid

Zeevaart, J. (1988) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.39.1.439 · Cited by 113 · see citing works

Crop Science: Progress and Prospects

Nösberger, J., Geiger, H. H., & Struik, P. C. (2001) · Socio-Environmental Systems Modeling · Cited by 109 · see citing works

QTL analysis of drought-related traits and grain yield in relation to genetic variation for leaf abscisic acid concentration in field-grown maize

Sanguineti, M. C., Tuberosa, R., Landi, P., Salvi, S., Maccaferri, M., Casarini, E., & Conti, S. (1999) · Journal of Experimental Botany · doi:10.1093/jxb/50.337.1289 · Cited by 109 · see citing works

How Do Stomata Read Abscisic Acid Signals?

Trejo, C. L., Clephan, A. L., & Davies, W. J. (1995) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.3.803 · Cited by 107 · see citing works

From QTLs for enzyme activity to candidate genes in maize

Prioul, J., Pelleschi, S., Séne, M., Thévenot, C., Causse, M., de Vienne, D., & Leonardi, A. (1999) · Journal of Experimental Botany · doi:10.1093/jxb/50.337.1281 · Cited by 105 · see citing works

Early post‐embryonic root formation is specifically affected in the maize mutantlrt1

Hochholdinger, F., & Feix, G. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00280.x · Cited by 104 · see citing works

Genetics of proteome variation for QTL characterization: application to drought-stress responses in maize

de Vienne, D., Leonardi, A., Damerval, C., & Zivy, M. (1999) · Journal of Experimental Botany · doi:10.1093/jxb/50.332.303 · Cited by 102 · see citing works

What If We Knew All the Genes for a Quantitative Trait in Hybrid Crops?

Bernardo, R. (2001) · Crop Science · doi:10.2135/cropsci2001.4111 · Cited by 97 · see citing works

Effects of water stress on growth, osmotic potential and abscisic acid content of maize roots

Ribaut, J., & Pilet, P. (1991) · Physiologia Plantarum · doi:10.1111/j.1399-3054.1991.tb02123.x · Cited by 93 · see citing works

A composite map of expressed sequences in maize

Causse, M., Santoni, S., Damerval, C., Maurice, A., Charcosset, A., Deatrick, J., & de Vienne, D. (1996) · Genome · doi:10.1139/g96-053 · Cited by 93 · see citing works

Genetic dissection of the relationship between carbon metabolism and early growth in maize, with emphasis on key-enzyme loci

Causse, M., Rocher, J., Henry, A., Charcosset, A., Prioul, J., & de Vienne, D. (1995) · Molecular Breeding · doi:10.1007/bf02277426 · Cited by 91 · see citing works

Genetic engineering for abiotic stress resistance in crop plants

Zhang, J., Klueva, N. Y., Wang, Z., Wu, R., Ho, T. D., & Nguyen, H. T. (2000) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-000-0022-6 · Cited by 89 · see citing works

Mapped genomic locations for developmental functions and QTLs reflect concerted groups in maize (Zea mays L.)

Ефимович, Х. Э., & Coe, E. H. (1997) · Theoretical and Applied Genetics · doi:10.1007/s001220050569 · Cited by 85 · see citing works

Water deficit in developing endosperm of maize: cell division and nuclear DMA endoreduplication

Artlip, T. S., Madison, J. T., & Setter, T. L. (1995) · Plant Cell & Environment · doi:10.1111/j.1365-3040.1995.tb00614.x · Cited by 83 · see citing works

Assessment of DNA pooling strategies for mapping of QTLs

Wang, G.-L., & Paterson, A. H. (1994) · Theoretical and Applied Genetics · doi:10.1007/bf00223645 · Cited by 81 · see citing works

From linked marker to gene

Wicking, C., & Williamson, B. (1991) · Trends in Genetics · doi:10.1016/0168-9525(91)90310-m · Cited by 80 · see citing works

Monitoring genome-wide expression in plants

Schaffer, R. J., Landgraf, J., Perez-Amador, M. A., & Wisman, E. (2000) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(00)00084-7 · Cited by 77 · see citing works

Ivr2, a candidate gene for a QTL of vacuolar invertase activity in maize leaves. Gene-specific expression under water stress

Pelleschi, S., Guy, S., Kim, J., Pointe, C., Mahé, A., Barthes, L., Leonardi, A., & Prioul, J. (1999) · Plant Molecular Biology · doi:10.1023/a:1006116310463 · Cited by 76 · see citing works

Genetic analysis of root traits in maize

Guingo, E., Hébert, Y., & Charcosset, A. (1998) · Agronomie · doi:10.1051/agro:19980305 · Cited by 75 · see citing works

The elongation rate at the base of a maize leaf shows an invariant pattern during both the steady‐state elongation and the establishment of the elongation zone

Muller, B., Reymond, M., & Tardieu, F. (2001) · Journal of Experimental Botany · doi:10.1093/jexbot/52.359.1259 · Cited by 75 · see citing works

Statistical methods for QTL mapping in cereals

Hackett, C. A. (2002) · Plant Molecular Biology · doi:10.1023/a:1014896712447 · Cited by 73 · see citing works

Some effects of genetic variation in drought-induced abscisic acid accumulation on the yield and water use of spring wheat

Innes, P., Blackwell, R. D., & Quarrie, S. A. (1984) · The Journal of Agricultural Science · doi:10.1017/s0021859600042660 · Cited by 71 · see citing works

Mechanisms underlying plant resilience to water deficits: prospects for water-saving agriculture

Chaves, M. M. (2004) · Journal of Experimental Botany · doi:10.1093/jxb/erh269 · Cited by 1,363 · see citing works

Roots of the Second Green Revolution

Lynch, J. P. (2007) · Australian Journal of Botany · doi:10.1071/bt06118 · Cited by 1,285 · see citing works

Plant breeding and drought in C3 cereals: What should we breed for?

ARAUS, J. L. (2002) · Annals of Botany · doi:10.1093/aob/mcf049 · Cited by 1,243 · see citing works

The Contribution of Breeding to Yield Advances in maize (Zea mays L.)

Duvick, D. N. (2005) · Advances in Agronomy · doi:10.1016/s0065-2113(05)86002-x · Cited by 1,214 · see citing works

Traits and selection strategies to improve root systems and water uptake in water-limited wheat crops

Wasson, A., Richards, R. A., Chatrath, R., Misra, S. C., Prasad, S. V. S., Rebetzke, G. J., Kirkegaard, J. A., Christopher, J., & Watt, M. (2012) · Journal of Experimental Botany · doi:10.1093/jxb/ers111 · Cited by 893 · see citing works

Breeding for Yield Potential and Stress Adaptation in Cereals

Araus, J., Slafer, G., Royo, C., & Serret, M. (2008) · Critical Reviews in Plant Sciences · doi:10.1080/07352680802467736 · Cited by 804 · see citing works

Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres

Nelson, D. E., Repetti, P. P., Adams, T. R., Creelman, R. A., Wu, J., Warner, D. C., Anstrom, D. C., Bensen, R. J., Castiglioni, P., Donnarummo, M. G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0707193104 · Cited by 743 · see citing works

The evolutionary dynamics of eukaryotic gene order

Hurst, L. D., Pál, C., & Lercher, M. J. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1319 · Cited by 719 · see citing works

Improving drought tolerance in maize: a view from industry

Campos, H., Cooper, M., Habben, J. E., Edmeades, G. O., & Schussler, J. R. (2004) · Field Crops Research · doi:10.1016/j.fcr.2004.07.003 · Cited by 646 · see citing works

Raising yield potential of wheat. III. Optimizing partitioning to grain while maintaining lodging resistance

Foulkes, J. M., Slafer, G. A., Davies, W. J., Berry, P., Sylvester-Bradley, R., Martre, P., Calderini, D. F., Griffiths, S., & Reynolds, M. P. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq300 · Cited by 633 · see citing works

Genomics-based approaches to improve drought tolerance of crops

Tuberosa, R., & Salvi, S. (2006) · Trends in Plant Science · doi:10.1016/j.tplants.2006.06.003 · Cited by 581 · see citing works

Quantitative Trait Loci and Crop Performance under Abiotic Stress: Where Do We Stand?: Table I.

Collins, N. C., Tardieu, F., & Tuberosa, R. (2008) · PLANT PHYSIOLOGY · doi:10.1104/pp.108.118117 · Cited by 559 · see citing works

Phenotyping for drought tolerance of crops in the genomics era

Tuberosa, R. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00347 · Cited by 555 · see citing works

Any trait or trait-related allele can confer drought tolerance: just design the right drought scenario

Tardieu, F. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/err269 · Cited by 549 · see citing works

To clone or not to clone plant QTLs: present and future challenges

Salvi, S., & Tuberosa, R. (2005) · Trends in Plant Science · doi:10.1016/j.tplants.2005.04.008 · Cited by 542 · see citing works

Drought Tolerance in Wheat

Nezhadahmadi, A., Prodhan, Z. H., & Faruq, G. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/610721 · Cited by 474 · see citing works

Breeding crop plants with deep roots: their role in sustainable carbon, nutrient and water sequestration

Kell, D. B. (2011) · Annals of Botany · doi:10.1093/aob/mcr175 · Cited by 439 · see citing works

Improving Salinity Tolerance in Cereals

Shahbaz, M., & Ashraf, M. (2013) · Critical Reviews in Plant Sciences · doi:10.1080/07352689.2013.758544 · Cited by 438 · see citing works

Breeding and Domesticating Crops Adapted to Drought and Salinity: A New Paradigm for Increasing Food Production

Ana Maria, F. I. T. A., Rodríguez‐Burruezo, A., Boşcaiu, M., Prohens, J., & Vicente, Ó. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00978 · Cited by 413 · see citing works

Quantitative Trait Loci for Grain Yield and Adaptation of Durum Wheat ( Triticum durum Desf.) Across a Wide Range of Water Availability

Maccaferri, M., Sanguineti, M. C., Corneti, S., Ortega, J. L. A., Salem, M. B., Bort, J., Deambrogio, E., del Moral, L. F. G., Demontis, A., El-Ahmed, A., et al. (2008) · Genetics · doi:10.1534/genetics.107.077297 · Cited by 378 · see citing works

Marker-assisted selection to improve drought adaptation in maize: the backcross approach, perspectives, limitations, and alternatives

Ribaut, J. M., & Ragot, M. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl214 · Cited by 365 · see citing works

Imaging and Analysis Platform for Automatic Phenotyping and Trait Ranking of Plant Root Systems

Iyer‐Pascuzzi, A. S., Symonova, O., Mileyko, Y., Hao, Y., Belcher, H., Harer, J., Weitz, J. S., & Benfey, P. N. (2010) · PLANT PHYSIOLOGY · doi:10.1104/pp.109.150748 · Cited by 364 · see citing works

From weeds to crops: genetic analysis of root development in cereals

Hochholdinger, F., Park, W. J., Sauer, M., & Woll, K. (2003) · Trends in Plant Science · doi:10.1016/j.tplants.2003.11.003 · Cited by 356 · see citing works

Reduced Lateral Root Branching Density Improves Drought Tolerance in Maize

Zhan, A., Schneider, H., & Lynch, J. P. (2015) · PLANT PHYSIOLOGY · doi:10.1104/pp.15.00187 · Cited by 336 · see citing works

Breeding upland rice for drought resistance

Bernier, J., Atlin, G. N., Serraj, R., Kumar, A., & Spaner, D. (2008) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.3153 · Cited by 334 · see citing works

Dissection and modelling of abiotic stress tolerance in plants

Tardieu, F., & Tuberosa, R. (2010) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2009.12.012 · Cited by 321 · see citing works

Bulked sample analysis in genetics, genomics and crop improvement

Zou, C., Wang, P., & Xu, Y. (2016) · Plant Biotechnology Journal · doi:10.1111/pbi.12559 · Cited by 323 · see citing works

Drought stress and tropical maize: QTL-by-environment interactions and stability of QTLs across environments for yield components and secondary traits

Messmer, R., Fracheboud, Y., Bänziger, M., Vargas, M., Stamp, P., & Ribaut, J. (2009) · Theoretical and Applied Genetics · doi:10.1007/s00122-009-1099-x · Cited by 309 · see citing works

Sorghum bicolor’s Transcriptome Response to Dehydration, High Salinity and ABA

Buchanan, C. D., Lim, S., Salzman, R. A., Kagiampakis, I., Morishige, D. T., Weers, B. D., Klein, R. R., Pratt, L. H., Cordonnier‐Pratt, M., Klein, P. G., et al. (2005) · Plant Molecular Biology · doi:10.1007/s11103-005-7876-2 · Cited by 308 · see citing works

Breeding for abiotic stresses for sustainable agriculture

Witcombe, J. R., Hollington, P. A., Howarth, C. J., Reader, S., & Steele, K. A. (2007) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2007.2179 · Cited by 287 · see citing works

Adaptation of potato to high temperatures and salinity-a review

Levy, D., & Veilleux, R. E. (2007) · American Journal of Potato Research · doi:10.1007/bf02987885 · Cited by 284 · see citing works

Genetic Dissection of Root Formation in Maize (Zea mays) Reveals Root-type Specific Developmental Programmes

Hochholdinger, F. (2004) · Annals of Botany · doi:10.1093/aob/mch056 · Cited by 267 · see citing works

Prospects for utilising plant-adaptive mechanisms to improve wheat and other crops in drought- and salinity-prone environments

Reynolds, M. P., Mujeeb‐Kazi, A., & Sawkins, M. C. (2005) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2005.040058.x · Cited by 257 · see citing works

Mapping of QTLs for lateral root branching and length in maize (Zea mays L.) under differential phosphorus supply

Zhu, J., Kaeppler, S. M., & Lynch, J. P. (2005) · Theoretical and Applied Genetics · doi:10.1007/s00122-005-2051-3 · Cited by 238 · see citing works

Yield–trait performance landscapes: from theory to application in breeding maize for drought tolerance

Messina, C. D., Podlich, D., Dong, Z., Samples, M., & Cooper, M. (2011) · Journal of Experimental Botany · doi:10.1093/jxb/erq329 · Cited by 233 · see citing works

Root phenotyping: from component trait in the lab to breeding: Table 1.

Kuijken, R. C. P., van Eeuwijk, F. A., Marcelis, L. F. M., & Bouwmeester, H. J. (2015) · Journal of Experimental Botany · doi:10.1093/jxb/erv239 · Cited by 217 · see citing works

Heat stress in crop plants: its nature, impacts and integrated breeding strategies to improve heat tolerance

Jha, U., Bohra, A., & Singh, N. (2014) · Plant Breeding · doi:10.1111/pbr.12217 · Cited by 197 · see citing works

Prioritizing quantitative trait loci for root system architecture in tetraploid wheat

Maccaferri, M., El‐Feki, W. M., Nazemi, G., Salvi, S., Cané, M. A., Colalongo, M. C., Stefanelli, S., & Tuberosa, R. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw039 · Cited by 215 · see citing works

Genetic diversity and genomic strategies for improving drought and waterlogging tolerance in soybeans

Valliyodan, B., Ye, H., Song, L., Murphy, M., Shannon, J. G., & Nguyen, H. T. (2016) · Journal of Experimental Botany · doi:10.1093/jxb/erw433 · Cited by 214 · see citing works

QTL for root angle and number in a population developed from bread wheats (Triticum aestivum) with contrasting adaptation to water-limited environments

Christopher, J., Christopher, M., Jennings, R., Jones, S., Fletcher, S., Borrell, A. K., Manschadi, A. M., Jordan, D. R., Mace, E., & Hammer, G. (2013) · Theoretical and Applied Genetics · doi:10.1007/s00122-013-2074-0 · Cited by 210 · see citing works

Model-assisted integration of physiological and environmental constraints affecting the dynamic and spatial patterns of root water uptake from soils

Draye, X., Kim, Y., Lobet, G., & Javaux, M. (2010) · Journal of Experimental Botany · doi:10.1093/jxb/erq077 · Cited by 204 · see citing works

Genetic diversity of root system architecture in response to drought stress in grain legumes

Ye, H., Roorkiwal, M., Valliyodan, B., Zhou, L., Chen, P., Varshney, R. K., & Nguyen, H. T. (2018) · Journal of Experimental Botany · doi:10.1093/jxb/ery082 · Cited by 203 · see citing works

Stay-Green Trait: A Prospective Approach for Yield Potential, and Drought and Heat Stress Adaptation in Globally Important Cereals

Kamal, N. M., Gorafi, Y. S. A., Abdelrahman, M., Abdellatef, E., & Tsujimoto, H. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20235837 · Cited by 204 · see citing works

Drought Tolerance in Maize

Ribaut, J., Betrán, J., Monneveux, P., & Setter, T. L. (2009) · Springer eBooks · doi:10.1007/978-0-387-79418-1_16 · Cited by 182 · see citing works

Adaptation to high temperature mitigates the impact of water deficit during combined heat and drought stress in C3 sunflower and C4 maize varieties with contrasting drought tolerance

Killi, D., Bussotti, F., Raschi, A., & Haworth, M. (2016) · Physiologia Plantarum · doi:10.1111/ppl.12490 · Cited by 182 · see citing works

Root-ABA1, a major constitutive QTL, affects maize root architecture and leaf ABA concentration at different water regimes

Giuliani, S., Sanguineti, M. C., Tuberosa, R., Bellotti, M., Salvi, S., & Landi, P. (2005) · Journal of Experimental Botany · doi:10.1093/jxb/eri303 · Cited by 181 · see citing works

Biotechnology and Drought Tolerance

Gosal, S. S., Wani, S. H., & Kang, M. S. (2009) · Journal of Crop Improvement · doi:10.1080/15427520802418251 · Cited by 179 · see citing works

Are source and sink strengths genetically linked in maize plants subjected to water deficit? A QTL study of the responses of leaf growth and of Anthesis-Silking Interval to water deficit

Welcker, C., Boussuge, B., Bencivenni, C., Ribaut, J.-M., & Tardieu, F. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl227 · Cited by 174 · see citing works

Genetic analysis of plant water status and osmotic adjustment in recombinant inbred lines of sunflower under two water treatments

Kiani, S. P., Talia, P. M., Maury, P., Grieu, P., Heinz, R., Perrault, A., Nishinakamasu, V., Hopp, H. E., Gentzbittel, L., Paniego, N. B., et al. (2006) · Plant Science · doi:10.1016/j.plantsci.2006.12.007 · Cited by 174 · see citing works

Effects of Climate Change and Drought Tolerance on Maize Growth

Kim, K., & Lee, B. (2023) · Plants · doi:10.3390/plants12203548 · Cited by 172 · see citing works

QTL controlling root and shoot traits of maize seedlings under cold stress

Hund, A., Fracheboud, Y., Soldati, A., Frascaroli, E., Salvi, S., & Stamp, P. (2004) · Theoretical and Applied Genetics · doi:10.1007/s00122-004-1665-1 · Cited by 171 · see citing works

Mapping As You Go: An Effective Approach for Marker‐Assisted Selection of Complex Traits

Podlich, D. W., Winkler, C. R., & Cooper, M. (2004) · Crop Science · doi:10.2135/cropsci2004.1560 · Cited by 169 · see citing works

Evaluation of physiological traits as indirect selection criteria for drought tolerance in sugar beet

Ober, E. S., Bloa, M. L., Clark, C. J. A., Royal, A., Jaggard, K. W., & Pidgeon, J. D. (2004) · Field Crops Research · doi:10.1016/j.fcr.2004.07.012 · Cited by 169 · see citing works

Breeding cereals for Mediterranean conditions: ecophysiological clues for biotechnology application

Araus, J., Bort, J., Steduto, P., Villegas, D., & Royo, C. (2003) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2003.tb00238.x · Cited by 171 · see citing works

Recent Advances for Drought Stress Tolerance in Maize (Zea mays L.): Present Status and Future Prospects

Sheoran, S., Kaur, Y., Kumar, S., Shukla, S., Rakshit, S., & Kumar, R. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.872566 · Cited by 164 · see citing works

Maize drought tolerance: Potential improvements through arbuscular mycorrhizal symbiosis?

Boomsma, C. R., & Vyn, T. J. (2008) · Field Crops Research · doi:10.1016/j.fcr.2008.03.002 · Cited by 158 · see citing works

Meta-analyses of QTL for grain yield and anthesis silking interval in 18 maize populations evaluated under water-stressed and well-watered environments

Semagn, K., Beyene, Y., Warburton, M. L., Tarekegne, A., Mugo, S., Meisel, B., Sehabiague, P., & Prasanna, B. M. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-313 · Cited by 150 · see citing works

Association mapping for root architectural traits in durum wheat seedlings as related to agronomic performance

Cané, M. A., Maccaferri, M., Nazemi, G., Salvi, S., Francia, R., Colalongo, C., & Tuberosa, R. (2014) · Molecular Breeding · doi:10.1007/s11032-014-0177-1 · Cited by 146 · see citing works

A Major Root Architecture QTL Responding to Water Limitation in Durum Wheat

Alahmad, S., Hassouni, K. E., Bassi, F. M., Dinglasan, E. G., Youssef, C., Quarry, G., Aksoy, A., Mazzucotelli, E., Juhász, A., Able, J. A., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00436 · Cited by 146 · see citing works

Genetic dissection of seminal root architecture in elite durum wheat germplasm

Sanguineti, M. C., Li, S., Maccaferri, M., Corneti, S., Rotondo, F., Chiari, T., & Tuberosa, R. (2007) · Annals of Applied Biology · doi:10.1111/j.1744-7348.2007.00198.x · Cited by 146 · see citing works

Mapping of QTL Associated with Waterlogging Tolerance during the Seedling Stage in Maize

Qiu, F., Zheng, Y., Zhang, Z., & Xu, S. (2007) · Annals of Botany · doi:10.1093/aob/mcm055 · Cited by 144 · see citing works

The genetic dissection of quantitative traits in crops

Semagn, K., Bjørnstad, Å., & Xu, Y. (2010) · Electronic Journal of Biotechnology · doi:10.2225/vol13-issue5-fulltext-14 · Cited by 138 · see citing works

Functional reversion to identify controlling genes in multigenic responses: analysis of floral abortion

Boyer, J. S., & McLaughlin, J. E. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl177 · Cited by 143 · see citing works

Genomic regions involved in response to grain yield selection at high and low nitrogen fertilization in maize

Coque, M., & Gallais, A. (2006) · Theoretical and Applied Genetics · doi:10.1007/s00122-006-0222-5 · Cited by 134 · see citing works

Maize leaf temperature responses to drought: Thermal imaging and quantitative trait loci (QTL) mapping

Liu, Y., Chander, S., Yan, J., Song, C., Zhao, J., & Li, J. (2010) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2010.11.010 · Cited by 130 · see citing works

Genome-wide association analysis for nine agronomic traits in maize under well-watered and water-stressed conditions

Xue, Y., Warburton, M. L., Sawkins, M. C., Zhang, X., Setter, T. L., Xu, Y., Grudloyma, P., Gethi, J., Ribaut, J., Li, W., et al. (2013) · Theoretical and Applied Genetics · doi:10.1007/s00122-013-2158-x · Cited by 129 · see citing works

Discovery, Biosynthesis and Stress-Related Accumulation of Dolabradiene-Derived Defenses in Maize

Mafu, S., Ding, Y., Murphy, K. M., Yaacoobi, O., Addison, B., Wang, Q., Shen, Z., Briggs, S. P., Bohlmann, J., Castro‐Falcón, G., et al. (2018) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.01351 · Cited by 123 · see citing works

Genetic variation for N-remobilization and postsilking N-uptake in a set of maize recombinant inbred lines. 3. QTL detection and coincidences

Coque, M., Martin, A., Veyrieras, J., Hirel, B. J., & Gallais, A. (2008) · Theoretical and Applied Genetics · doi:10.1007/s00122-008-0815-2 · Cited by 127 · see citing works

Drought Tolerance in Maize: Indirect Selection through Secondary Traits versus Genomewide Selection

Ziyomo, C., & Bernardo, R. (2013) · Crop Science · doi:10.2135/cropsci2012.11.0651 · Cited by 124 · see citing works

Plant Responses to Water Stress

Griffiths, H. (2002) · Annals of Botany · doi:10.1093/aob/mcf159 · Cited by 122 · see citing works

Modelling Crop Improvement in a G×E×M Framework via Gene–Trait–Phenotype Relationships

Messina, C., Hammer, G., Dong, Z., Podlich, D., & Cooper, M. (2009) · Crop Physiology · doi:10.1016/b978-0-12-374431-9.00010-4 · Cited by 121 · see citing works

Root System Architecture and Its Association with Yield under Different Water Regimes in Durum Wheat

Hassouni, K. E., Alahmad, S., Belkadi, B., Filali‐Maltouf, A., Hickey, L. T., & Bassi, F. M. (2018) · Crop Science · doi:10.2135/cropsci2018.01.0076 · Cited by 120 · see citing works

A consensus map of QTLs controlling the root length of maize

Hund, A., Reimer, R., & Messmer, R. (2011) · Plant and Soil · doi:10.1007/s11104-011-0735-9 · Cited by 117 · see citing works

Genomics and the physiologist: bridging the gap between genes and crop response

Edmeades, G. O., McMaster, G. S., White, J. W., & Campos, H. (2004) · Field Crops Research · doi:10.1016/j.fcr.2004.07.002 · Cited by 111 · see citing works

Genomic Selection Outperforms Marker Assisted Selection for Grain Yield and Physiological Traits in a Maize Doubled Haploid Population Across Water Treatments

Cerrudo, D., Cao, S., Yuan, Y., Martinez, C., Suarez, E. A., Babu, R., Zhang, X., & Trachsel, S. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00366 · Cited by 107 · see citing works

Root-ABA1 QTL affects root lodging, grain yield, and other agronomic traits in maize grown under well-watered and water-stressed conditions

Landi, P., Sanguineti, M. C., Liu, C., Li, Y., Wang, T., Giuliani, S., Bellotti, M., Salvi, S., & Tuberosa, R. (2006) · Journal of Experimental Botany · doi:10.1093/jxb/erl161 · Cited by 106 · see citing works

Genetic dissection of maize drought tolerance for trait improvement

Liu, S., & Qin, F. (2021) · Molecular Breeding · doi:10.1007/s11032-020-01194-w · Cited by 105 · see citing works

Meta-analysis of constitutive and adaptive QTL for drought tolerance in maize

Hao, Z., Li, X., Liu, X., Xie, C., Li, M., Zhang, D., & Zhang, S. (2009) · Euphytica · doi:10.1007/s10681-009-0091-5 · Cited by 105 · see citing works

Mapping of QTLs for lateral and axile root growth of tropical maize

Trachsel, S., Messmer, R., Stamp, P., & Hund, A. (2009) · Theoretical and Applied Genetics · doi:10.1007/s00122-009-1144-9 · Cited by 104 · see citing works

Quantitative trait loci for yield and correlated traits under high and low soil nitrogen conditions in tropical maize

Ribaut, J., Fracheboud, Y., Monneveux, P., Bänziger, M., Vargas, M., & Jiang, C. (2007) · Molecular Breeding · doi:10.1007/s11032-006-9041-2 · Cited by 104 · see citing works

Productivity, water-use efficiency and tolerance to moderate water deficit correlate in 33 poplar genotypes from a Populus deltoides x Populus trichocarpa F1 progeny

Monclus, R., Villar, M., Barbaroux, C., Bastien, C., Fichot, R., Delmotte, F. M., Delay, D., Petit, J.-M., Bréchet, C., Dreyer, E., et al. (2009) · Tree Physiology · doi:10.1093/treephys/tpp075 · Cited by 104 · see citing works

Molecular mapping across three populations reveals a QTL hotspot region on chromosome 3 for secondary traits associated with drought tolerance in tropical maize

de Almeida, G. D., Nair, S. K., Borém, A., Cairns, J. E., Trachsel, S., Ribaut, J., Bänziger, M., Prasanna, B. M., Crossa, J. L., & Babu, R. (2014) · Molecular Breeding · doi:10.1007/s11032-014-0068-5 · Cited by 100 · see citing works

The inheritance of anther extrusion in hexaploid wheat and its relationship to Fusarium head blight resistance and deoxynivalenol content

Skinnes, H., Semagn, K., Tarkegne, Y., Marøy, A. G., & Bjørnstad, Å. (2010) · Plant Breeding · doi:10.1111/j.1439-0523.2009.01731.x · Cited by 97 · see citing works

Genome-wide analysis of yield in Europe: allelic effects as functions of drought and heat scenarios

Millet, E., Welcker, C., Kruijer, W., Negro, S., Nicolas, S., Praud, S., Ranc, N., Presterl, T., Tuberosa, R., Bedo, Z., et al. (2016) · Plant Physiology · doi:10.1104/pp.16.00621 · Cited by 160 · see citing works

Wild barley introgression lines revealed novel QTL alleles for root and related shoot traits in the cultivated barley (Hordeum vulgareL.)

Naz, A. A., Arifuzzaman, M., Muzammil, S., Pillen, K., & Léon, J. (2014) · BMC Genetics · doi:10.1186/s12863-014-0107-6 · Cited by 94 · see citing works

Genomics Approaches for Crop Improvement against Abiotic Stress

Akpınar, B. A., Lucas, S. J., & Budak, H. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/361921 · Cited by 92 · see citing works

A Common Genetic Determinism for Sensitivities to Soil Water Deficit and Evaporative Demand: Meta-Analysis of Quantitative Trait Loci and Introgression Lines of Maize

Welcker, C., Sadok, W., Dignat, G., Renault, M., Salvi, S., Charcosset, A., & Tardieu, F. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.176479 · Cited by 86 · see citing works

Quantitative Trait Loci Mapping for Chlorophyll Fluorescence and Associated Traits in Wheat (Triticum aestivum)

Yang, D., Jing, R., CHANG, X.-P., & Li, W. (2007) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2007.00443.x · Cited by 89 · see citing works

Genetic Variation of Stomatal Traits and Carbon Isotope Discrimination in Two Hybrid Poplar Families (Populus deltoides ‘S9-2’ × P. nigra ‘Ghoy’ and P. deltoides ‘S9-2’ × P. trichocarpa ‘V24’)

Dillen, S. Y., Marron, N., Koch, B., & Ceulemans, R. (2008) · Annals of Botany · doi:10.1093/aob/mcn107 · Cited by 86 · see citing works

Evaluation of leaf traits for indirect selection of high yielding poplar hybrids

Marron, N., Dillen, S. Y., & Ceulemans, R. (2007) · Environmental and Experimental Botany · doi:10.1016/j.envexpbot.2007.04.002 · Cited by 84 · see citing works

Root Water Uptake and Ideotypes of the Root System: Whole‐Plant Controls Matter

Tardieu, F., Draye, X., & Javaux, M. (2017) · Vadose Zone Journal · doi:10.2136/vzj2017.05.0107 · Cited by 82 · see citing works

Genome-Wide Association Study Reveals Natural Variations Contributing to Drought Resistance in Crops

Wang, H., & Qin, F. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2017.01110 · Cited by 78 · see citing works

Functional repair of embolized vessels in maize roots after temporal drought stress, as demonstrated by magnetic resonance imaging

Kaufmann, I., Schulze‐Till, T., Schneider, H. U., Zimmermann, U., Jakob, P. M., & Wegner, L. H. (2009) · New Phytologist · doi:10.1111/j.1469-8137.2009.02919.x · Cited by 77 · see citing works

Analysis of the Relationships between Growth, Photosynthesis and Carbohydrate Metabolism Using Quantitative Trait Loci (QTLs) in Young Maize Plants Subjected to Water Deprivation

Pelleschi, S., Leonardi, A., Rocher, J., Cornic, G., de Vienne, D., Thévenot, C., & Prioul, J.-L. (2006) · Molecular Breeding · doi:10.1007/s11032-005-1031-2 · Cited by 77 · see citing works

Addressing drought tolerance in maize by transcriptional profiling and mapping

Marino, R., Ponnaiah, M., Krajewski, P., Frova, C., Gianfranceschi, L., Pè, M. E., & Sari-Gorla, M. (2008) · Molecular Genetics and Genomics · doi:10.1007/s00438-008-0401-y · Cited by 77 · see citing works

Root architectural traits and yield: exploring the relationship in barley breeding trials

Robinson, H. M., Kelly, A. M., Fox, G. P., Franckowiak, J. D., Borrell, A. K., & Hickey, L. T. (2018) · Euphytica · doi:10.1007/s10681-018-2219-y · Cited by 75 · see citing works

Genetic architecture of maize chlorotic mottle virus and maize lethal necrosis through GWAS, linkage analysis and genomic prediction in tropical maize germplasm

Sitonik, C., Suresh, L. M., Beyene, Y., Olsen, M. S., Makumbi, D., Oliver, K., Das, B., Bright, J. M., Mugo, S., Crossa, J. L., et al. (2019) · Theoretical and Applied Genetics · doi:10.1007/s00122-019-03360-x · Cited by 75 · see citing works

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Zhang, R.-P., Wu, J., Li, X.-G., Khan, M. A., Chen, H., Korban, S. S., & Zhang, S.-L. (2012) · Plant Molecular Biology Reporter · doi:10.1007/s11105-012-0544-1 · Cited by 73 · see citing works

QTL Mapping of Agronomic Waterlogging Tolerance Using Recombinant Inbred Lines Derived from Tropical Maize (Zea mays L) Germplasm

Zaidi, P. H., Rashid, Z., Vinayan, M. T., de Almeida, G. D., Phagna, R. K., & Babu, R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124350 · Cited by 73 · see citing works

Bulk segregant analysis: “An effective approach for mapping consistent-effect drought grain yield QTLs in rice”

Vikram, P., Swamy, B. P. M., Dixit, S., Ahmed, H., Cruz, M. T. S., Singh, A., Ye, G., & Kumar, A. (2012) · Field Crops Research · doi:10.1016/j.fcr.2012.05.012 · Cited by 73 · see citing works

Comparative QTL analysis for yield components and morphological traits in maize (Zea mays L.) under water-stressed and well-watered conditions

Zhao, X., Zhang, J., Fang, P., & Peng, Y. (2019) · Ikushugaku zasshi · doi:10.1270/jsbbs.18021 · Cited by 22 · see citing works

Quantitative trait loci for yield and morphological traits in maize under drought stress

Nikolic, A., Andjelković, V., Dodig, D., & Ignjatović‐Micić, D. (2011) · Genetika · doi:10.2298/gensr1102263n · Cited by 21 · see citing works

QTL mapping in three tropical maize populations reveals a set of constitutive and adaptive genomic regions for drought tolerance

de Almeida, G. D., Makumbi, D., Magorokosho, C., Nair, S. K., Borém, A., Ribaut, J., Bänziger, M., Prasanna, B. M., Crossa, J. L., & Babu, R. (2012) · Theoretical and Applied Genetics · doi:10.1007/s00122-012-2003-7 · Cited by 152 · see citing works

Comprehensive Meta-Analysis of Maize QTLs Associated With Grain Yield, Flowering Date and Plant Height Under Drought Conditions

Liu, S., Zenda, T., Wang, X., Guo, L., Jin, H., Yang, Y., Dong, A., & Duan, H. (2019) · Journal of Agricultural Science · doi:10.5539/jas.v11n8p1 · Cited by 12 · see citing works

Quantitative trait locus analysis of drought tolerance and yield in Maize in China

Xiao, Y., Li, X. H., George, M. L. C., Li, M. S., ZHANG, S.-H., & Zheng, Y. L. (2005) · Plant Molecular Biology Reporter · doi:10.1007/bf02772706 · Cited by 69 · see citing works