The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
Open accessAbstract
We present methods for imputing data for ungenotyped markers and for inferring haplotype phase in large data sets of unrelated individuals and parent-offspring trios. Our methods make use of known haplotype phase when it is available, and our methods are computationally efficient so that the full information in large reference panels with thousands of individuals is utilized. We demonstrate that substantial gains in imputation accuracy accrue with increasingly large reference panel sizes, particularly when imputing low-frequency variants, and that unphased reference panels can provide highly accurate genotype imputation. We place our methodology in a unified framework that enables the simultaneous use of unphased and phased data from trios and unrelated individuals in a single analysis. For unrelated individuals, our imputation methods produce well-calibrated posterior genotype probabilities and highly accurate allele-frequency estimates. For trios, our haplotype-inference method is four orders of magnitude faster than the gold-standard PHASE program and has excellent accuracy. Our methods enable genotype imputation to be performed with unphased trio or unrelated reference panels, thus accounting for haplotype-phase uncertainty in the reference panel. We present a useful measure of imputation accuracy, allelic R(2), and show that this measure can be estimated accurately from posterior genotype probabilities. Our methods are implemented in version 3.0 of the BEAGLE software package.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Each study was first subject to GWAS quality control filters (customized taking into account study specific features21 as detailed in Supplementary Table 2) and standardized to the HapMap reference panel and statistical genotype imputation22–25.”
From Seven new loci associated with age-related macular degeneration (2013) · cites this paper as [24]
Citations
Cites
A tutorial on hidden Markov models and selected applications in speech recognition
Rabiner, L. R. (1989) · Proceedings of the IEEE · doi:10.1109/5.18626 · Cited by 22,743
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
A New Statistical Method for Haplotype Reconstruction from Population Data
Stephens, M., Smith, N. J. C., & Donnelly, P. (2001) · The American Journal of Human Genetics · doi:10.1086/319501 · Cited by 7,512
A second generation human haplotype map of over 3.1 million SNPs
The International HapMap Consortium (2007) · Nature · doi:10.1038/nature06258 · Cited by 4,438
Browning, S. R., & Browning, B. L. (2007) · The American Journal of Human Genetics · doi:10.1086/521987 · Cited by 3,217
Self-citationA new multipoint method for genome-wide association studies by imputation of genotypes
Marchini, J., Howie, B., Myers, S., McVean, G., & Donnelly, P. (2007) · Nature Genetics · doi:10.1038/ng2088 · Cited by 2,609
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
the NIDDK IBD Genetics Consortium, Barrett, J. C., the Belgian-French IBD Consortium, the Wellcome Trust Case Control Consortium, Hansoul, S., Nicolae, D. L., Cho, J. H., Duerr, R. H., Rioux, J. D., Brant, S. R., et al. (2008) · Nature Genetics · doi:10.1038/ng.175 · Cited by 2,593
Scheet, P. A., & Stephens, M. (2006) · The American Journal of Human Genetics · doi:10.1086/502802 · Cited by 1,959
Wellcome Trust Case Control Consortium, Zeggini, E., Scott, L. J., Saxena, R., Voight, B. F., Marchini, J. L., Hu, T., de Bakker, P. I., Abecasis, G. R., Almgren, P., et al. (2008) · Nature Genetics · doi:10.1038/ng.120 · Cited by 1,864
A high-resolution recombination map of the human genome
Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S. L., Barnard, J., Hallbeck, B., Másson, G., et al. (2002) · Nature Genetics · doi:10.1038/ng917 · Cited by 1,750
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–200 of 1,000
Power, R. A., Tansey, K. E., Buttenschøn, H. N., Cohen‐Woods, S., Bigdeli, T. B., Hall, L. S., Kutalik, Z., Lee, S., Ripke, S., Steinberg, S., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.05.010 · Cited by 210
Detection of selection signatures in dairy and beef cattle using high-density genomic information
Zhao, F., McParland, S., Kearney, F. J., Du, L., & Berry, D. P. (2015) · Genetics Selection Evolution · doi:10.1186/s12711-015-0127-3 · Cited by 210
Brøndum, R. F., Su, G., Janss, L., Sahana, G., Guldbrandtsen, B., Boichard, D., & Lund, M. S. (2015) · Journal of Dairy Science · doi:10.3168/jds.2014-9005 · Cited by 202
Nebel, A., Kleindorp, R., Caliebe, A., Nothnagel, M., Blanché, H., Junge, O., Wittig, M., Ellinghaus, D., Flachsbart, F., Wichmann, H. ‐., et al. (2011) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2011.06.008 · Cited by 201
Tissue-Specific Effects of Genetic and Epigenetic Variation on Gene Regulation and Splicing
Gutiérrez‐Arcelus, M., Ongen, H., Lappalainen, T., Montgomery, S. B., Buil, A., Yurovsky, A., Bryois, J., Padioleau, I., Romano, L., Planchon, A., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1004958 · Cited by 198
Identity by Descent Between Distant Relatives: Detection and Applications
Browning, S. R., & Browning, B. L. (2012) · Annual Review of Genetics · doi:10.1146/annurev-genet-110711-155534 · Cited by 206
Self-citationMeta-analysis of gene-level tests for rare variant association
Liu, D. J., Peloso, G. M., Zhan, X., Holmen, O. L., Zawistowski, M., Feng, S., Nikpay, M., Auer, P. L., Goel, A., Zhang, H., et al. (2013) · Nature Genetics · doi:10.1038/ng.2852 · Cited by 200
Fast and accurate imputation of summary statistics enhances evidence of functional enrichment
Paşaniuc, B., Zaitlen, N., Shi, H., Bhatia, G., Gusev, A., Pickrell, J. K., Hirschhorn, J. N., Strachan, D. P., Patterson, N. J., & Price, A. L. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu416 · Cited by 189
Yang, J., Mezmouk, S., Baumgarten, A., Buckler, E. S., Guill, K. E., McMullen, M. D., Mumm, R. H., & Ross‐Ibarra, J. (2017) · PLoS Genetics · doi:10.1371/journal.pgen.1007019 · Cited by 183
Genomic Selection Improves Heat Tolerance in Dairy Cattle
Garner, J. B., Douglas, M. L., Williams, S. R. O., Wales, W. J., Marett, L. C., Nguyen, T. T. T., Reich, C. M., & Hayes, B. J. (2016) · Scientific Reports · doi:10.1038/srep34114 · Cited by 190
Properties of different selection signature statistics and a new strategy for combining them
Ma, Y., Ding, X., Qanbari, S., Weigend, S., Zhang, Q., & Simianer, H. (2015) · Heredity · doi:10.1038/hdy.2015.42 · Cited by 189
Protein-coding repeat polymorphisms strongly shape diverse human phenotypes
Mukamel, R. E., Handsaker, R. E., Sherman, M. A., Barton, A. R., Zheng, Y., McCarroll, S. A., & Loh, P.-R. (2021) · Science · doi:10.1126/science.abg8289 · Cited by 178
Technow, F., Riedelsheimer, C., Schrag, T. A., & Melchinger, A. E. (2012) · Theoretical and Applied Genetics · doi:10.1007/s00122-012-1905-8 · Cited by 182
Schrag, T. A., Westhues, M., Schipprack, W., Seifert, F., Thiemann, A., Scholten, S., & Melchinger, A. E. (2018) · Genetics · doi:10.1534/genetics.117.300374 · Cited by 186
Han, B., Diogo, D., Eyre, S., Källberg, H., Zhernakova, A., Bowes, J., Padyukov, L., Okada, Y., González-Gay, M. Á., Rantapää‐Dahlqvist, S., et al. (2014) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2014.02.013 · Cited by 176
Accuracy of imputation to whole-genome sequence data in Holstein Friesian cattle
van Binsbergen, R., Bink, M. C. A. M., Calus, M. P. L., van Eeuwijk, F. A., Hayes, B. J., Hulsegge, I., & Veerkamp, R. F. (2014) · Genetics Selection Evolution · doi:10.1186/1297-9686-46-41 · Cited by 183
Sequence diversity analyses of an improved rhesus macaque genome enhance its biomedical utility
Warren, W. C., Harris, R. A., Haukness, M., Fiddes, I. T., Murali, S. C., Fernandes, J. D., Dishuck, P. C., Storer, J. M., Raveendran, M., Hillier, L., et al. (2020) · Science · doi:10.1126/science.abc6617 · Cited by 174
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles
Goldstein, J. I., Jarskog, L. F., Hilliard, C., Alfirevic, A., Duncan, L. E., Fourches, D., Huang, H., Lek, M., Neale, B. M., Ripke, S., et al. (2014) · Nature Communications · doi:10.1038/ncomms5757 · Cited by 179
Carmona, F. D., Mackie, S. L., Martín, J., Taylor, J., Vaglio, A., Eyre, S., Bossini‐Castillo, L., Castañeda, S., Cid, M. C., Hernández‐Rodríguez, J., et al. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.02.009 · Cited by 180
Costa-Neto, G., Fritsche-Neto, R., & Crossa, J. (2021) · Heredity · doi:10.1038/s41437-020-00353-1 · Cited by 153
Karlsson, E. K., Sigurðsson, S., Ivansson, E. L., Thomas, R. J., Elvers, I., Wright, J. B., Howald, C., Tonomura, N., Perloski, M., Swofford, R., et al. (2013) · Genome biology · doi:10.1186/gb-2013-14-12-r132 · Cited by 178
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy
Zhang, F., Liu, H., Chen, S., Low, H.-Q., Sun, L., Cui, Y., Chu, T., Li, Y., Fu, X., Yu, Y., et al. (2011) · Nature Genetics · doi:10.1038/ng.973 · Cited by 173
Risk for myasthenia gravis maps to a 151 Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08
Gregersen, P. K., Kosoy, R., Lee, A. T., Lamb, J. A., Sussman, J. D., McKee, D., Simpfendorfer, K. R., Pirskanen, R., Piehl, F., Pan‐Hammarström, Q., et al. (2012) · Annals of Neurology · doi:10.1002/ana.23691 · Cited by 170
Genomic prediction using imputed whole-genome sequence data in Holstein Friesian cattle
van Binsbergen, R., Calus, M. P. L., Bink, M. C. A. M., van Eeuwijk, F. A., Schrooten, C., & Veerkamp, R. F. (2015) · Genetics Selection Evolution · doi:10.1186/s12711-015-0149-x · Cited by 166
Structural haplotypes and recent evolution of the human 17q21.31 region
Boettger, L. M., Handsaker, R. E., Zody, M. C., & McCarroll, S. A. (2012) · Nature Genetics · doi:10.1038/ng.2334 · Cited by 167
Current status of genome-wide association studies in cancer
Chung, C. C., & Chanock, S. J. (2011) · Human Genetics · doi:10.1007/s00439-011-1030-9 · Cited by 166
Genome-wide association study of coronary artery disease in the Japanese
Takeuchi, F., Yokota, M., Yamamoto, K., Nakashima, E., Katsuya, T., Asano, H., Isono, M., Nabika, T., Sugiyama, T., Fujioka, A., et al. (2011) · European Journal of Human Genetics · doi:10.1038/ejhg.2011.184 · Cited by 163
Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder
Neale, B. M., Medland, S. E., Ripke, S., Anney, R., Asherson, P. J., Buitelaar, J. K., Franke, B., Gill, M., Kent, L., Holmans, P., et al. (2010) · Journal of the American Academy of Child & Adolescent Psychiatry · doi:10.1016/j.jaac.2010.06.007 · Cited by 169
Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability
Lagou, V., Mägi, R., Hottenga, J., Grallert, H., Perry, J. R. B., Bouatia‐Naji, N., Marullo, L., Rybin, D. V., Jansen, R., Min, J. L., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-19366-9 · Cited by 157
A genome-wide association study of attempted suicide
Willour, V. L., Seifuddin, F., Mahon, P. B., Jancic, D., Pirooznia, M., Steele, J., Schweizer, B. W., Goes, F. S., Mondimore, F. M., MacKinnon, D. F., et al. (2011) · Molecular Psychiatry · doi:10.1038/mp.2011.4 · Cited by 162
Characterization of Gene–Environment Interactions for Colorectal Cancer Susceptibility Loci
Hutter, C. M., Chang-Claude, J. C., Slattery, M. L., Pflugeisen, B. M., Lin, Y., Duggan, D. J., Nan, H., Lemire, M., Rangrej, J., Figueiredo, J. C., et al. (2012) · Cancer Research · doi:10.1158/0008-5472.can-11-4067 · Cited by 162
Genetic Architecture of Skin and Eye Color in an African-European Admixed Population
Beleza, S., Johnson, N. A., Candille, S. I., Absher, D. M., Coram, M. A., Lopes, J., Campos, J., Araújo, I. I., Anderson, T. M., Vilhjálmsson, B. J., et al. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003372 · Cited by 161
Components of the accuracy of genomic prediction in a multi-breed sheep population1
Daetwyler, H. D., Kemper, K. E., van der Werf, J. H. J., & Hayes, B. J. (2012) · Journal of Animal Science · doi:10.2527/jas.2011-4557 · Cited by 164
Verma, S., Gupta, S., Bandhiwal, N., Kumar, T., Bharadwaj, C., & Bhatia, S. (2015) · Scientific Reports · doi:10.1038/srep17512 · Cited by 160
Littlejohn, M. D., Tiplady, K., Fink, T., Lehnert, K., Lopdell, T., Johnson, T., Couldrey, C., Keehan, M., Sherlock, R. G., Harland, C., et al. (2016) · Scientific Reports · doi:10.1038/srep25376 · Cited by 161
Minamikawa, M. F., Nonaka, K., Kaminuma, E., Kajiya‐Kanegae, H., Onogi, A., Goto, S., Yoshioka, T., Imai, A., Hamada, H., Hayashi, T., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-05100-x · Cited by 160
Genome re-sequencing reveals the evolutionary history of peach fruit edibility
Yu, Y., Fu, J., Xu, Y., Zhang, J., Ren, F., Zhao, H., Tian, S., Guo, W., Tu, X., Zhao, J., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07744-3 · Cited by 164
Structural diversity and African origin of the 17q21.31 inversion polymorphism
Steinberg, K. M., Antonacci, F., Sudmant, P. H., Kidd, J. M., Campbell, C. D., Vives, L., Malig, M., Scheinfeldt, L., Beggs, W. R., Ibrahim, M. E., et al. (2012) · Nature Genetics · doi:10.1038/ng.2335 · Cited by 156
Pryce, J. E., Arias, J., Bowman, P. J., Davis, S. R., Macdonald, K. A., Waghorn, G. C., Wales, W. J., Williams, Y. J., Spelman, R. J., & Hayes, B. J. (2012) · Journal of Dairy Science · doi:10.3168/jds.2011-4628 · Cited by 156
Aung, T., Ozaki, M., Lee, M., Schlötzer-Schrehardt, U. M., Þorleifsson, G., Mizoguchi, T., Igo, R. P., Haripriya, A., Williams, S. E. I., Astakhov, Y. S., et al. (2017) · Nature Genetics · doi:10.1038/ng.3875 · Cited by 153
Sang, Y., Long, Z., Dan, X., Feng, J., Shi, T., Jia, C., Zhang, X., Lai, Q., Yang, G., Zhang, H., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34206-8 · Cited by 176
Wang, Y., Wang, X., Sun, S., Jin, C., Su, J., Wei, J., Luo, X., Wen, J., Wei, T., Sahu, S. K., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33238-4 · Cited by 157
Functionally reciprocal mutations of the prolactin signalling pathway define hairy and slick cattle
Littlejohn, M. D., Henty, K., Tiplady, K., Johnson, T., Harland, C., Lopdell, T., Sherlock, R. G., Li, W., Lukefahr, S. D., Shanks, B. C., et al. (2014) · Nature Communications · doi:10.1038/ncomms6861 · Cited by 151
McLaren, P. J., Coulonges, C., Ripke, S., van den Berg, L. H., Buchbinder, S., Carrington, M. N., Cossarizza, A., Dalmau, J., Deeks, S. G., Delaneau, O., et al. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003515 · Cited by 155
Genomics of Divergence along a Continuum of Parapatric Population Differentiation
Feulner, P. G. D., Chain, F. J. J., Panchal, M., Huang, Y., Eizaguirre, C., Kalbe, M., Lenz, T. L., Samonte, I. E., Stoll, M., Bornberg‐Bauer, E., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1004966 · Cited by 151
Designing dairy cattle breeding schemes under genomic selection: a review of international research
Pryce, J. E., & Daetwyler, H. D. (2011) · Animal Production Science · doi:10.1071/an11098 · Cited by 150
Estimation of linkage disequilibrium in four US pig breeds
Badke, Y. M., Bates, R. O., Ernst, C. W., Schwab, C. R., & Steibel, J. P. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-24 · Cited by 148
Spracklen, C. N., Chen, P., Kim, Y. J., Wang, X., Cai, H., Li, S., Long, J., Wu, Y., Wang, Y. X., Takeuchi, F., et al. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx062 · Cited by 149
Prospects for Genomic Selection in Cassava Breeding
Wolfe, M. D., Carpio, D. P. D., Alabi, O., Ezenwaka, L., Ikeogu, U. N., Kayondo, S. I., Lozano, R. D., Okeke, U. G., Ozimati, A., Esuma, W., et al. (2017) · The Plant Genome · doi:10.3835/plantgenome2017.03.0015 · Cited by 147
Biernacka, J. M., Sangkuhl, K., Jenkins, G., Whaley, R. M., Barman, P., Batzler, A., Altman, R. B., Arolt, V, Brockmöller, J., Chen, C. H., et al. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.47 · Cited by 140
Justice, C. M., Yagnik, G., Kim, Y., Peter, I., Jabs, E. W., Erazo, M., Ye, X., Ainehsazan, E., Shi, L., Cunningham, M. L., et al. (2012) · Nature Genetics · doi:10.1038/ng.2463 · Cited by 140
Hayes, M. G., Urbanek, M., Hivert, M., Armstrong, L. L., Morrison, J., Guo, C., Lowe, L. P., Scheftner, D. A., Pluzhnikov, A., Levine, D., et al. (2013) · Diabetes · doi:10.2337/db12-1692 · Cited by 141
Su, G., Brøndum, R. F., Ma, P., Guldbrandtsen, B., Aamand, G. P., & Lund, M. S. (2012) · Journal of Dairy Science · doi:10.3168/jds.2012-5379 · Cited by 142
Genomic insights into divergence and dual domestication of cultivated allotetraploid cottons
Fang, L., Gong, H., Hu, Y., Liu, C., Zhou, B., Huang, T., Wang, Y., Chen, S., Fang, D. D., Du, X., et al. (2017) · Genome biology · doi:10.1186/s13059-017-1167-5 · Cited by 145
Dittberner, H., Korte, A., Mettler‐Altmann, T., Weber, A. P. M., Monroe, J. G., & de Meaux, J. (2018) · Molecular Ecology · doi:10.1111/mec.14838 · Cited by 138
Cell Specific eQTL Analysis without Sorting Cells
Westra, H.-J., Arends, D., Esko, T., Peters, M. J., Schurmann, C., Schramm, K., Kettunen, J., Yaghootkar, H., Fairfax, B. P., Andiappan, A. K., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005223 · Cited by 138
Jenkins, R. B., Xiao, Y., Sicotte, H., Decker, P. A., Kollmeyer, T. M., Hansen, H. M., Kosel, M., Zheng, S., Walsh, K. M., Rice, T., et al. (2012) · Nature Genetics · doi:10.1038/ng.2388 · Cited by 140
Genome-wide association analysis identifies six new loci associated with forced vital capacity
Loth, D. W., Artigas, M. S., Gharib, S. A., Wain, L. V., Franceschini, N., Koch, B., Pottinger, T. D., Smith, A. V., Duan, Q., Oldmeadow, C. J., et al. (2014) · Nature Genetics · doi:10.1038/ng.3011 · Cited by 137
Carson, A. R., Smith, E. N., Matsui, H., Brækkan, S. K., Jepsen, K., Hansen, J., & Frazer, K. A. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-125 · Cited by 141
The contribution of rare variation to prostate cancer heritability
Mancuso, N., Rohland, N., Rand, K. A., Tandon, A., Allen, A., Quinque, D., Mallick, S., Li, H., Stram, A. H., Sheng, X., et al. (2015) · Nature Genetics · doi:10.1038/ng.3446 · Cited by 136
Hussain, W., Baenziger, P. S., Belamkar, V., Guttieri, M. J., Venegas, J. P., Easterly, A. C., Sallam, A., & Poland, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-16006-z · Cited by 136
Daetwyler, H. D., Swan, A. A., van der Werf, J. H. J., & Hayes, B. J. (2012) · Genetics Selection Evolution · doi:10.1186/1297-9686-44-33 · Cited by 135
Sabuncu, M. R., Buckner, R. L., Smoller, J. W., Lee, P. H., Fischl, B. R., & Sperling, R. A. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr348 · Cited by 134
MaCH‐Admix: Genotype Imputation for Admixed Populations
Liu, E. Y., Li, M., Wang, W. W., & Li, Y. (2012) · Genetic Epidemiology · doi:10.1002/gepi.21690 · Cited by 130
Advances in genome-wide association studies of complex traits in rice
Wang, Q., Jiali, T., Han, B., & Huang, X. (2019) · Theoretical and Applied Genetics · doi:10.1007/s00122-019-03473-3 · Cited by 138
Huang, J., Ellinghaus, D., Franke, A., Howie, B., & Li, Y. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.3 · Cited by 134
Imputation and quality control steps for combining multiple genome-wide datasets
Verma, S. S., de Andrade, M., Tromp, G., Kuivaniemi, H., Pugh, E., Namjou‐Khales, B., Mukherjee, S., Jarvik, G. P., Kottyan, L. C., Burt, A., et al. (2014) · Frontiers in Genetics · doi:10.3389/fgene.2014.00370 · Cited by 130
Accuracy of genotype imputation in sheep breeds
Hayes, B. J., Bowman, P. J., Daetwyler, H. D., Kijas, J., & van der Werf, J. H. J. (2011) · Animal Genetics · doi:10.1111/j.1365-2052.2011.02208.x · Cited by 129
Usefulness of Multiparental Populations of Maize ( Zea mays L.) for Genome-Based Prediction
Lehermeier, C., Krämer, N., Bauer, E., Bauland, C., Camisan, C., Campo, L., Flament, P., Melchinger, A. E., Menz, M. A., Meyer, N., et al. (2014) · Genetics · doi:10.1534/genetics.114.161943 · Cited by 126
Sahana, G., Guldbrandtsen, B., Thomsen, B., Holm, L., Panitz, F., Brøndum, R. F., Bendixen, C., & Lund, M. S. (2014) · Journal of Dairy Science · doi:10.3168/jds.2014-8141 · Cited by 129
Technow, F., Bürger, A., & Melchinger, A. E. (2013) · G3 Genes|Genomes|Genetics · doi:10.1534/g3.112.004630 · Cited by 147
Genome-wide analysis correlates Ayurveda Prakriti
Govindaraj, P., Nizamuddin, S., Sharath, A., Jyothi, V., Rotti, H., Raval, R., Nayak, J., Bhat, B. K., Prasanna, B. V., Shintre, P., et al. (2015) · Scientific Reports · doi:10.1038/srep15786 · Cited by 172
Paşaniuc, B., Zaitlen, N., Lettre, G., Chen, G. K., Tandon, A., Kao, W. H. L., Ruczinski, I., Fornage, M., Siscovick, D. S., Zhu, X., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001371 · Cited by 124
Veerkamp, R. F., Bouwman, A. C., Schrooten, C., & Calus, M. P. L. (2016) · Genetics Selection Evolution · doi:10.1186/s12711-016-0274-1 · Cited by 127
Liu, Z., Yang, N., Yan, Y., Li, G., Liu, A., Wu, G., & Sun, C. (2019) · BMC Genetics · doi:10.1186/s12863-019-0771-7 · Cited by 127
Wimmer, V., Lehermeier, C., Albrecht, T., Auinger, H.-J., Wang, Y., & Schön, C. (2013) · Genetics · doi:10.1534/genetics.113.150078 · Cited by 132
Rowan, B. A., Patel, V., Weigel, D., & Schneeberger, K. (2015) · G3 Genes Genomes Genetics · doi:10.1534/g3.114.016501 · Cited by 126
Malomane, D. K., Simianer, H., Weigend, A., Reimer, C., Schmitt, A. O., & Weigend, S. (2019) · BMC Genomics · doi:10.1186/s12864-019-5727-9 · Cited by 126
Ellinghaus, E., Stanulla, M., Richter, G., Ellinghaus, D., Kronnie, G. T., Cario, G., Cazzaniga, G., Horstmann, M. A., Grümayer, R. P., Cavé, H., et al. (2011) · Leukemia · doi:10.1038/leu.2011.302 · Cited by 124
The genetic architecture of gene expression levels in wild baboons
Tung, J., Zhou, X., Alberts, S. C., Stephens, M., & Gilad, Y. (2015) · eLife · doi:10.7554/elife.04729 · Cited by 127
Chang, H., Lipka, A. E., Domier, L. L., & Hartman, G. L. (2016) · Phytopathology · doi:10.1094/phyto-01-16-0042-fi · Cited by 124
Pausch, H., MacLeod, I. M., Fries, R., Emmerling, R., Bowman, P. J., Daetwyler, H. D., & Goddard, M. E. (2017) · Genetics Selection Evolution · doi:10.1186/s12711-017-0301-x · Cited by 124
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia
Gockel, I., Becker, J., Wouters, M. M., Niebisch, S., Gockel, H. R., Hess, T., Ramonet, D., Zimmermann, J., Vigo, A., Trynka, G., et al. (2014) · Nature Genetics · doi:10.1038/ng.3029 · Cited by 123
Hayes, B. J., Panozzo, J., Walker, C. K., Choy, A.-L., Kant, S., Wong, D., Tibbits, J. F. G., Daetwyler, H. D., Rochfort, S. J., Hayden, M., et al. (2017) · Theoretical and Applied Genetics · doi:10.1007/s00122-017-2972-7 · Cited by 123
Genome-Wide Meta-Analysis of Psoriatic Arthritis Identifies Susceptibility Locus at REL
Ellinghaus, E., Stuart, P. E., Ellinghaus, D., Nair, R. P., Debrus, S., Raelson, J., Belouchi, M., Tejasvi, T., Li, Y., Tsoi, L. C., et al. (2011) · Journal of Investigative Dermatology · doi:10.1038/jid.2011.415 · Cited by 120
Brøndum, R. F., Guldbrandtsen, B., Sahana, G., Lund, M. S., & Su, G. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-728 · Cited by 121
Accuracy of genotype imputation in Nelore cattle
Carvalheiro, R., Boison, S. A., Neves, H. H. D. R., Sargolzaei, M., Schenkel, F. S., Utsunomiya, Y. T., O’Brien, A. M. P., Sölkner, J., McEwan, J. C., Tassell, C. P. V., et al. (2014) · Genetics Selection Evolution · doi:10.1186/s12711-014-0069-1 · Cited by 119
Runs of Homozygosity Implicate Autozygosity as a Schizophrenia Risk Factor
Keller, M. C., Simonson, M. A., Ripke, S., Neale, B. M., Gejman, P. V., Howrigan, D. P., Lee, S., Lencz, T., Levinson, D. F., & Sullivan, P. F. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002656 · Cited by 119
Al-Mamun, H. A., Clark, S., Kwan, P., & Gondro, C. (2015) · Genetics Selection Evolution · doi:10.1186/s12711-015-0169-6 · Cited by 129
Non-coding variability at the APOE locus contributes to the Alzheimer’s risk
Zhou, X., Chen, Y., Mok, K. Y., Kwok, T. C. Y., Mok, V. C. T., Guo, Q., Ip, F. C., Chen, Y., Mullapudi, N., Initiative, A. D. N., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10945-z · Cited by 120
Human Epistatic Interaction Controls IL7R Splicing and Increases Multiple Sclerosis Risk
Galarza-Muñoz, G., Briggs, F. B. S., Evsyukova, I. Y., Schott, G., Kennedy, E. M., Nyanhete, T. E., Wang, L., Bergamaschi, L., Widen, S. G., Tomaras, G. D., et al. (2017) · Cell · doi:10.1016/j.cell.2017.03.007 · Cited by 124
Signatures of founder effects, admixture, and selection in the Ashkenazi Jewish population
Bray, S. M., Mullé, J. G., Dodd, A., Pulver, A. E., Wooding, S., & Warren, S. T. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004381107 · Cited by 124
Ibeagha-Awemu, E. M., PETERS, S. O., Akwanji, K. A., Imumorin, I. G., & Zhao, X. (2016) · Scientific Reports · doi:10.1038/srep31109 · Cited by 128
Grenier, C., Cao, T., Ospina, Y., Quintero, C., Châtel, M. H., Tohme, J. M., Courtois, B., & Ahmadi, N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0136594 · Cited by 114
Su, G., Christensen, O. F., Janss, L., & Lund, M. S. (2014) · Journal of Dairy Science · doi:10.3168/jds.2014-8210 · Cited by 117
Ancestral components of admixed genomes in a Mexican cohort
Johnson, N. A., Coram, M. A., Shriver, M. D., Romieu, I., Barsh, G. S., London, S. J., & Tang, H. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002410 · Cited by 114
Xu, W., Cohen‐Woods, S., Chen, Q., Noor, A., Knight, J., Hosang, G. M., Parikh, S. V., Luca, V. D., Tozzi, F., Muglia, P., et al. (2014) · BMC Medical Genetics · doi:10.1186/1471-2350-15-2 · Cited by 117
Rahimi, Y., Bihamta, M. R., Taleei, A., Alipour, H., & Ingvarsson, P. K. (2019) · BMC Plant Biology · doi:10.1186/s12870-019-2165-4 · Cited by 114
Wu, J. H. Y., Lemaître, R. N., Manichaikul, A. W., Guan, W., Tanaka, T., Foy, M., Kabagambe, E. K., Djoussé, L., Siscovick, D. S., Fretts, A. M., et al. (2013) · Circulation Cardiovascular Genetics · doi:10.1161/circgenetics.112.964619 · Cited by 113
Self-citationHe, M., Xu, M., Zhang, B., Liang, J., Chen, P., Lee, J.-Y., Johnson, T. A., Li, H., Yang, X., Dai, J., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddu583 · Cited by 106
Metadata
- Authors
- Browning, B. L., & Browning, S. R.
- Affiliations
- University of Auckland (NZ)
- Corresponding author
- Browning, Brian L.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2009-02
- Volume
- 84
- Issue
- 2
- Pages
- 210-223
- ISSN
- 0002-9297 (ISSN-L)
- PMC
- PMC2668004
- OpenAlex
- W2059542829
- Cited by
- 1,640
- References
- 29
- Citations by year
- 2026: 35 · 2025: 44 · 2024: 62 · 2023: 50 · 2022: 86 · 2021: 99 · 2020: 94 · 2019: 102 · 2018: 98 · 2017: 121 · 2016: 123 · 2015: 161 · 2014: 172 · 2013: 132 · 2012: 120
- FWCI
- 50.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- The American Journal of Human Genetics (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust (076113)
- National Institutes of Health
- National Institute of General Medical Sciences (R01GM075091)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- genotype imputation, parent-offspring trios, low-frequency variants, allele frequency estimation, imputation accuracy, beagle dogs, phase comparison
- MeSH terms
- Computer Simulation, Female, Gene Frequency, Genotype, Haplotypes, Humans, Male, Markov Chains, Models, Genetic, Nuclear Family, Reproducibility of Results
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review