Definition And Clinical Importance Of Haplotypes.

Haploview: analysis and visualization of LD and haplotype maps

Barrett, J. C., Fry, B., Maller, J., & Daly, M. J. (2004) · Bioinformatics · doi:10.1093/bioinformatics/bth457 · Cited by 14,563

The sequence of the human genome

Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., Sutton, G. G., Smith, H. O., Yandell, M., Evans, C. A., Holt, R. A., et al. (2001) · Science · doi:10.1126/science.1058040 · Cited by 13,909

Database resources of the National Center for Biotechnology Information: update

Wheeler, D. L. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh073 · Cited by 10,695

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

dbSNP: the NCBI database of genetic variation

Sherry, S. T. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.1.308 · Cited by 7,502

SIFT: predicting amino acid changes that affect protein function

Ng, P. C. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg509 · Cited by 6,601

The International HapMap Project

†The International HapMap Consortium, Genotyping centres: Baylor College of Medicine and ParAllele BioScience, Gibbs, R. A., Belmont, J. W., Hardenbol, P., Willis, T. D., Yu, F., Chinese HapMap Consortium, Yang, H., Ch'ang, L.-Y., et al. (2003) · Nature · doi:10.1038/nature02168 · Cited by 6,057

The Structure of Haplotype Blocks in the Human Genome

Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., et al. (2002) · Science · doi:10.1126/science.1069424 · Cited by 5,863

The Future of Genetic Studies of Complex Human Diseases

Risch, N., & Merikangas, K. (1996) · Science · doi:10.1126/science.273.5281.1516 · Cited by 5,355

A Comparison of Bayesian Methods for Haplotype Reconstruction from Population Genotype Data

Stephens, M., & Donnelly, P. (2003) · The American Journal of Human Genetics · doi:10.1086/379378 · Cited by 3,516

Renin-Angiotensin System Haplotypes and the Risk of Myocardial Infarction and Stroke in Pharmacologically Treated Hypertensive Patients

Marciante, K. D., Bis, J. C., Rieder, M. J., Reiner, A. P., Lumley, T., Monks, S. A., Kooperberg, C. L., Carlson, C. J., Heckbert, S. R., & Psaty, B. M. (2007) · American Journal of Epidemiology · doi:10.1093/aje/kwm059 · Cited by 26

Paediatric pharmacogenomics: an overview

Hawcutt, D. B., Thompson, B., Smyth, R. L., & Pirmohamed, M. (2012) · Archives of Disease in Childhood · doi:10.1136/archdischild-2012-302852 · Cited by 26

The interleukin-10 family cytokines gene polymorphisms in plaque psoriasis

Kingo, K. (2005) · DSpace repository (University of Tartu) · Cited by 26

Gene–environment interaction

Cicchetti, D. (2007) · Development and Psychopathology · doi:10.1017/s0954579407000466 · Cited by 28

A genetic polymorphism of matrix metalloproteinase 9 (MMP-9) affects the changes in circulating MMP-9 levels induced by highly active antiretroviral therapy in HIV patients

Demacq, C., Vasconcellos, V. B., Marcaccini, A. M., Gerlach, R. F., Machado, A. A., & Tanus-Santos, J. E. (2009) · The Pharmacogenomics Journal · doi:10.1038/tpj.2009.13 · Cited by 24

Genetic polymorphisms of interleukin 8 and risk of ulcerative colitis in the Chinese population

Li, K., Yao, S., Liu, S., Wang, B., & Mao, D. (2009) · Clinica Chimica Acta · doi:10.1016/j.cca.2009.03.053 · Cited by 24

Interleukin-10 family cytokines pathway: genetic variants and psoriasis

Galimova, E. S., Rätsep, R., Traks, T., Kingo, K., Escott‐Price, V., & Kõks, S. (2017) · British Journal of Dermatology · doi:10.1111/bjd.15363 · Cited by 24

Single nucleotide polymorphisms as prognostic and predictive biomarkers in renal cell carcinoma

Garrigós, C., Espinosa, M., Salinas, A. M., Osman, I., López, R. A. M., Tarón, M., Molina‐Pinelo, S., & Durán, I. (2017) · Oncotarget · doi:10.18632/oncotarget.22533 · Cited by 24

Polymorphisms in the receptor for advanced glycation end-products (RAGE) gene and circulating RAGE levels as a susceptibility factor for non-alcoholic steatohepatitis (NASH)

Mehta, R., Shaw, G. A., Masschelin, P. M., Felix, S. C., Otgonsuren, M., Baranova, A. V., Goodman, Z. D., & Younossi, Z. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199294 · Cited by 25

Políticas públicas para la promoción de la alimentación saludable y la prevención de la obesidad

Lobo, F. (2007) · Revista Española de Salud Pública · doi:10.1590/s1135-57272007000500001 · Cited by 23

ADAM33′s Role in Asthma Pathogenesis: An Overview

Sleziak, J., Gawor, A., Błażejewska, M., Antosz, K., & Gomułka, K. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25042318 · Cited by 23

Polymorphisms

Sukhumsirichart, W. (2018) · InTech eBooks · doi:10.5772/intechopen.76728 · Cited by 31

Implicações farmacogenéticas de polimorfismos da eNOS para drogas de ação cardiovascular

Silva, P. S., Lacchini, R., Gomes, V. A., & Tanus-Santos, J. E. (2011) · Arquivos Brasileiros de Cardiologia · doi:10.1590/s0066-782x2011000200017 · Cited by 23

Association of TNF-α Genetic Polymorphisms with Hepatocellular Carcinoma Susceptibility: A Case-Control Study in a Han Chinese Population

Chen, X., Zhang, L., Chang, Y., Shen, T., Wang, L., Zhuang, H., & Lu, F. (2011) · The International Journal of Biological Markers · doi:10.5301/jbm.2011.8580 · Cited by 23

eNOS Tag SNP Haplotypes in Hypertensive Disorders of Pregnancy

Muniz, L. G., Luizon, M. R., Palei, A. C., Lacchini, R., Duarte, G. G., Cavalli, R. D. C., Tanus-Santos, J. E., & Sandrim, V. C. (2012) · DNA and Cell Biology · doi:10.1089/dna.2012.1768 · Cited by 23

The Maternal ITPK1 Gene Polymorphism Is Associated with Neural Tube Defects in a High-Risk Chinese Population

Guan, Z., Wang, J., Guo, J., Wang, F., Wang, X., Li, G., Xie, Q., Han, X., Niu, B., & Zhang, T. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086145 · Cited by 22

The Interaction between Coagulation Factor 2 Receptor and Interleukin 6 Haplotypes Increases the Risk of Myocardial Infarction in Men

Gigante, B., Bennet, A. M., Leander, K., Vikström, M., & Fairé, U. D. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011300 · Cited by 22

Lead and cognitive function in VDR genotypes in the third National Health and Nutrition Examination Survey

Krieg, E. F., Butler, M. A., Chang, M., Liu, T., Yesupriya, A., Dowling, N. F., & Lindegren, M. L. (2009) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2009.12.004 · Cited by 22

The long non‐coding RNA H19 rs217727 polymorphism is associated with PE susceptibility

Harati‐Sadegh, M., Kohan, L., Teimoori, B., & Salimi, S. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26708 · Cited by 21

BAX and BCL ‐2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: the R etina 4 project

Pastor‐Idoate, S., Rodríguez‐Hernández, I., Rojas, J., Fernández, I., García-Gutiérrez, M.-T., Ruiz‐Moreno, J. M., Rocha‐Sousa, A., Ramkissoon, Y., Harsum, S., MacLaren, R. E., et al. (2015) · Acta Ophthalmologica · doi:10.1111/aos.12718 · Cited by 21

The HMG‐CoA Reductase Gene and Lipid and Lipoprotein Levels: the Multi‐Ethnic Study of Atherosclerosis

Chen, Y., Chen, Y. I., Li, X., Post, W., Herrington, D., Polak, J. F., Rotter, J. I., & Taylor, K. D. (2009) · Lipids · doi:10.1007/s11745-009-3314-6 · Cited by 21

Vitamin D receptor haplotypes affect lead levels during pregnancy

Rezende, V. B., Amaral, J. H., Quintana, S. M., Gerlach, R. F., Barbosa, F., & Tanus-Santos, J. E. (2010) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2010.07.039 · Cited by 21

A greedier approach for finding tag SNPs

Chang, C.-J., Huang, Y., & Chao, K. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btk035 · Cited by 21

16th IHIW: Global distribution of extended HLA haplotypes

Askar, M. Z., Daghstani, J., Thomas, D., Leahy, N., Dunn, P. P. J., Claas, F. H. J., Doran, S., Saji, H., Kanangat, S., Karoichane, M., et al. (2013) · International Journal of Immunogenetics · doi:10.1111/iji.12029 · Cited by 21

Genetic polymorphisms and haplotypes of the organic cation transporter 1 gene (SLC22A1) in the Xhosa population of South Africa

Jacobs, C., Pearce, B., Plessis, M. D., Hoosain, N., & Benjeddou, M. (2014) · Genetics and Molecular Biology · doi:10.1590/s1415-47572014005000002 · Cited by 21

The effects of NAMPT haplotypes and metabolic risk factors on circulating visfatin/NAMPT levels in childhood obesity

Belo, V. D. A., Luizon, M. R., Lacchini, R., de Miranda, J. A., Lanna, C. M. M., Souza-Costa, D. C., & Tanus-Santos, J. E. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.173 · Cited by 20

Haplotypes of Microsomal Epoxide Hydrolase and X-Ray Cross-Complementing Group 1 Genes in Indian Hepatocellular Carcinoma Patients

Kiran, M., Chawla, Y. K., Jain, M., & Kaur, J. (2009) · DNA and Cell Biology · doi:10.1089/dna.2009.0921 · Cited by 20

Genotype and Haplotype Analyses of TP53 Gene in Breast Cancer Patients: Association with Risk and Clinical Outcomes

Vymetalkova, V. P., Souček, P., Kunická, T., Jirásková, K., Brynychová, V., Pardini, B., Novosadová, V., Polívková, Z., Kubáčková, K., Koževnikovová, R., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0134463 · Cited by 20

Discovery of genetic profiles impacting response to chemotherapy: application to gemcitabine

Jarjanazi, H., Kiefer, J., Savas, S., Briollais, L., Tüzmen, Ş., Pabalan, N., Ibrahim-zada, I., Mousses, S., & Özçelik, H. (2008) · Human Mutation · doi:10.1002/humu.20732 · Cited by 21

Haplotype analysis of the endothelial nitric oxide synthase gene in asthma

Hollá, L. I., Jurajda, M., Pohunek, P., & Znojil, V. (2008) · Human Immunology · doi:10.1016/j.humimm.2008.03.003 · Cited by 20

Human Nutrition and Genetic Variation

Stover, P. J. (2007) · Food and Nutrition Bulletin · doi:10.1177/15648265070281s109 · Cited by 20

Efficacy, cost-utility and physiological effects of Acceptance and Commitment Therapy (ACT) and Behavioural Activation Treatment for Depression (BATD) in patients with chronic low back pain and depression: study protocol of a randomised, controlled trial including mobile-technology-based ecological momentary assessment (IMPACT study)

Sanabria-Mazo, J. P., Forero, C. G., Cristobal-Narváez, P., Suso-Ribera, C., García-Palacios, A., Colomer-Carbonell, A., Pérez-Aranda, A., Andrés-Rodríguez, L., McCracken, L. M., D'Amico, F., et al. (2020) · BMJ Open · doi:10.1136/bmjopen-2020-038107 · Cited by 16

Genetic Variants of DNA Repair Genes as Predictors of Radiation-Induced Subcutaneous Fibrosis in Oropharyngeal Carcinoma

Gupta, A., Mathew, D., Bhat, S. A., Ghoshal, S., & Pal, A. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.652049 · Cited by 19

Exercise training improves muscle vasodilatation in individuals with T786C polymorphism of endothelial nitric oxide synthase gene

Negrao, M. V., Alves, C. R., Alves, G. B., Pereira, A. C., Dias, R. G., Laterza, M. C., da Mota, G. D. F. A., de Oliveira, E. M., Bassaneze, V., Krieger, J. E., et al. (2010) · Physiological Genomics · doi:10.1152/physiolgenomics.00145.2009 · Cited by 19

The Expression of Human Microsomal Epoxide Hydrolase Is Predominantly Driven by a Genetically Polymorphic Far Upstream Promoter

Yang, X., Liang, S.-H., Coslo, D. M., Lazarus, P. J., Gallagher, C. J., & Omiecinski, C. J. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.150870 · Cited by 18

Interaction between FKBP5 variability and recent life events in the anxiety spectrum: Evidence for the differential susceptibility model

Pérez, B. P., Cristóbal-Narváez, P., Sheinbaum, T., Kwapil, T. R., Ballespí, S., Peña, E., de Castro-Català, M., Riba, M. D., Rosa, A., & Neus Barrantes-vidal, A. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193044 · Cited by 18

Pharmacogenetic Relevance of Endothelial Nitric Oxide Synthase Polymorphisms and Gene Interactions

Luizon, M. R., Pereira, D. A., & Tanus-Santos, J. E. (2018) · Pharmacogenomics · doi:10.2217/pgs-2018-0098 · Cited by 18

GC Gene Polymorphisms and Vitamin D-Binding Protein Levels Are Related to the Risk of Generalized Aggressive Periodontitis

Song, W., Wang, X., Tian, Y., Zhang, X., Lu, R., & Meng, H. (2016) · International Journal of Endocrinology · doi:10.1155/2016/5141089 · Cited by 17

Genetic Association and Gene Expression Profiles of TGFB1 and the Contribution of TGFB1 to Otosclerosis Susceptibility

Priyadarshi, S., Ray, C. S., Panda, K. C., Desai, A., Nayak, S. R., Biswal, N. C., & Ramchander, P. V. (2013) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.1991 · Cited by 17

Endothelial nitric oxide synthase polymorphisms affect the changes in blood pressure and nitric oxide bioavailability induced by propofol

Oliveira‐Paula, G. H., Lacchini, R., Pinheiro, L. C., Ferreira, G. C., Luizon, M. R., Garcia, W. N. D. P., Garcia, L. V., & Tanus-Santos, J. E. (2018) · Nitric Oxide · doi:10.1016/j.niox.2018.02.007 · Cited by 17

Inteurleukin-8 gene variations and the susceptibility to schizophrenia

Afia, A. B., Aflouk, Y., Saoud, H., Zaafrane, F., Gaha, L., & Jrad, B. B. H. (2020) · Psychiatry Research · doi:10.1016/j.psychres.2020.113421 · Cited by 17

Sources of Interindividual Variability

Lin, Y. S., Thummel, K. E., Thompson, B. D., Totah, R. A., & Cho, C. W. (2021) · Methods in molecular biology · doi:10.1007/978-1-0716-1554-6_17 · Cited by 18

Endothelial Nitric Oxide Synthase Gene Polymorphisms Associated with Susceptibility to High Altitude Pulmonary Edema in Chinese Railway Construction Workers at Qinghai-Tibet over 4 500 Meters above Sea Level

Sun, Y., Fang, M.-W., Niu, W., Li, G., Liu, J.-L., Ding, S.-Q., Xu, Y., Yu, G.-S., Dong, J.-Q., Pan, Y.-J., et al. (2010) · Chinese Medical Sciences Journal · doi:10.1016/s1001-9294(11)60005-9 · Cited by 16

Polymorphisms in the TGFB1 signal peptide influence human papillomavirus infection and development of cervical lesions

Trugilo, K. P., Cebinelli, G. C. M., Berti, F. C. B., Okuyama, N. C. M., Cezar‐dos‐Santos, F., Sena, M. M., Mangieri, L. F. L., Watanabe, M. A. E., & de Oliveira, K. B. (2018) · Medical Microbiology and Immunology · doi:10.1007/s00430-018-0557-y · Cited by 19

Evaluation of two methods for computational HLA haplotypes inference using a real dataset

Bettencourt, B. F., Santos, M. R., Fialho, R. N., Couto, A. R., Peixoto, M. J., Pinheiro, J. P., Spínola, H., Mora, M. G., dos Santos, C. M. P., Brehm, A., et al. (2008) · BMC Bioinformatics · doi:10.1186/1471-2105-9-68 · Cited by 16

Association study between genetic polymorphisms in MTHFR and stroke susceptibility in Egyptian population: a case–control study

El-Khawaga, O. Y., Al-azzawy, M. F., El-Dawa, A. N., Elsaid, A. M. M., Mustafa, W., & Saad, M. (2024) · Scientific Reports · doi:10.1038/s41598-023-50277-z · Cited by 15

Soft Computing Methods in Bioinformatics: A Comprehensive Review

Karlık, B. (2013) · Mathematical and Computational Applications · doi:10.3390/mca18030176 · Cited by 15

Dual biomarkers long non-coding RNA GAS5 and its target, NR3C1, contribute to acute myeloid leukemia

Ketab, F. N. G., Gharesouran, J., Ghafouri‐Fard, S., Dastar, S., Mazraeh, S. A., Hosseinzadeh, H., Moradi, M., Javadlar, M., Hiradfar, A., Rezamand, A., et al. (2020) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2020.104399 · Cited by 15

The Genetic Diversity and Structure of Linkage Disequilibrium of the MTHFR Gene in Populations of Northern Eurasia

Trifonova, E. A., Робертовна, Е. Е., Urnov, F. D., & Степанов, В. А. (2012) · Acta Naturae · doi:10.32607/20758251-2012-4-1-53-69 · Cited by 15

Haplotype Diversity in Four Genes (CLCNKA, CLCNKB, BSND, NEDD4L) Involved in Renal Salt Reabsorption

Sile, S., Velez, D. R., Gillani, N. B., Alexander, C., George, A. L., & Williams, S. M. (2007) · Human Heredity · doi:10.1159/000106060 · Cited by 15

Association of Endothelial Nitric Oxide Synthase (eNOS) G894T Polymorphism With High Altitude Pulmonary Edema Susceptibility: A Meta-Analysis

Luo, Y., Chen, Y., Zhang, Y., Zhou, Q., & Gao, Y. (2012) · Wilderness and Environmental Medicine · doi:10.1016/j.wem.2012.03.007 · Cited by 14

Analysis of the MTHFR gene linkage disequilibrium structure and association of polymorphic gene variants with coronary atherosclerosis

Trifonova, E. A., Спиридонова, М. Г., Габидулина, Т. В., Urnov, F. D., Puzyrev, V. P., & Степанов, В. А. (2012) · Russian Journal of Genetics · doi:10.1134/s1022795412100122 · Cited by 14

Direct molecular haplotyping of multiple polymorphisms within exon 4 of the human catechol-O-methyltransferase gene by liquid chromatography–electrospray ionization time-of-flight mass spectrometry

Oberacher, H., Pitterl, F., Niederstätter, H., Weiss, E. M., Stadelmann, E., Marksteiner, J., & Parson, W. (2006) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-006-0589-9 · Cited by 14

Endothelial Nitric Oxide Synthase Gene Polymorphisms (G894T, 4b/a and T-786C) and Preeclampsia: Meta-Analysis of 18 Case–Control Studies

Chen, H., Zhao, G., Sun, M., Wang, H., Liu, J., Gao, W., & Meng, T. (2011) · DNA and Cell Biology · doi:10.1089/dna.2011.1406 · Cited by 14

IL4 gene polymorphisms and their relation to periodontal disease in a Macedonian population

Atanasovska-Stojanovska, A., Трајков, Д., Nares, S., Angelov, N., & Spiroski, M. Z. (2011) · Human Immunology · doi:10.1016/j.humimm.2011.02.005 · Cited by 14

Reconstruction of N-acetyltransferase 2 haplotypes using PHASE

Golka, K., Blaszkewicz, M., Samimi, M., Bolt, H. M., & Selinski, S. (2007) · Archives of Toxicology · doi:10.1007/s00204-007-0247-9 · Cited by 14

The Contribution of JAK2 46/1 Haplotype in the Predisposition to Myeloproliferative Neoplasms

Paes, J. F., Silva, G., Tarragô, A. M., & Mourão, L. P. D. S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232012582 · Cited by 13

Iron metabolism in autism spectrum disorder; inference through single nucleotide polymorphisms in key iron metabolism genes

Rabaya, S., Nairat, S., Bader, K. A., Herzallah, M. M., & Darwish, H. M. (2023) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2023.120817 · Cited by 13

A strategy for building and using a human reference pangenome

Llamas, B., Narzisi, G., Schneider, V. A., Audano, P., Biederstedt, E., Blauvelt, L. J., Bradbury, P., Chang, X., Chin, C., Fungtammasan, A., et al. (2019) · F1000Research · doi:10.12688/f1000research.19630.1 · Cited by 16

Vascular Endothelial Growth Factor Haplotypes Associated with Childhood Obesity

Belo, V. D. A., Souza-Costa, D. C., Luizon, M. R., Izidoro‐Toledo, T. C., Lanna, C. M. M., Pinheiro, L. C., & Tanus-Santos, J. E. (2011) · DNA and Cell Biology · doi:10.1089/dna.2011.1260 · Cited by 13

Mutations and Polymorphisms: What Is The Difference?

Aga, S. S., Banday, M. Z., & Nissar, S. (2021) · Springer eBooks · doi:10.1007/978-981-33-6699-2_1 · Cited by 15

Exploring genetic polymorphism in innate immune genes in Indian cattle (Bos indicus) and buffalo (Bubalus bubalis) using next generation sequencing technology

Patel, S. M., KORINGA, P. G., Nathani, N. M., Patel, N. V., Shah, T. M., & Joshi, C. G. (2015) · Meta Gene · doi:10.1016/j.mgene.2015.01.002 · Cited by 14

Functional VEGF haplotypes affect the susceptibility to hypertension

Sandrim, V. C., Luizon, M. R., Izidoro‐Toledo, T. C., Coelho, E. B., Moreno, H., & Tanus-Santos, J. E. (2011) · Journal of Human Hypertension · doi:10.1038/jhh.2011.110 · Cited by 12

Adrenergic receptors gene polymorphisms and autonomic nervous control of heart and vascular tone

Matuskova, L., & Javorka, M. (2022) · Physiological Research · doi:10.33549/physiolres.934799 · Cited by 12

Association between -786TC polymorphism in the endothelial nitric oxide synthase gene and hypertension in the Tunisian population

Jemaa, R., Kallel, A., Sédiri, Y., Omar, S., Feki, M., Elasmi, M., Haj-Taïeb, S., Sanhaji, H., & Kaabachi, N. (2010) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2010.12.006 · Cited by 12

Haplotype analysis of the CYP2J2 gene associated with myocardial infarction in a Chinese Han population

Jie, Z., Hong, K., Tao, J., Biao, C., Yongmei, Z., & Jingchuan, L. (2010) · Cell Biochemistry and Function · doi:10.1002/cbf.1661 · Cited by 12

Phenotype Data: A Neglected Resource in Biomedical Research?

Groth, P., & Weiss, B. (2006) · Current Bioinformatics · doi:10.2174/157489306777828008 · Cited by 12

An Investigation of the Relationship Between the Enos Gene Polymorphism and Diagnosed Migraine

Güler, S., Gürkan, H., Tozkır, H., Turan, N., & Çelik, Y. (2014) · Balkan Journal of Medical Genetics · doi:10.2478/bjmg-2014-0074 · Cited by 12

The Value of Molecular Haplotypes in a Family-Based Linkage Study

Gillanders, E. M., Pearson, J. V., Sorant, A. J. M., Trent, J. M., O’Connell, J. R., & Wilson, J. (2006) · The American Journal of Human Genetics · doi:10.1086/506626 · Cited by 12

Lack of association between G‐protein coupled receptor kinase 5 gene and Parkinson's disease

Tarantino, P., Marco, E. V. D., Annesi, G., Rocca, F. E., Annesi, F., Civitelli, D., Provenzano, G., Scornaienchi, V., Greco, V., Colica, C., et al. (2010) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.31129 · Cited by 11

Genetic polymorphisms of the organic cation transporter 1 gene (SLC22A1) within the Cape Admixed population of South Africa

Plessis, M. D., Pearce, B., Jacobs, C., Hoosain, N., & Benjeddou, M. (2014) · Molecular Biology Reports · doi:10.1007/s11033-014-3813-2 · Cited by 11

Platelet Polymorphisms

Afshar‐Kharghan, V., Vijayan, K. V., & Bray, P. F. (2007) · Elsevier eBooks · doi:10.1016/b978-012369367-9/50776-x · Cited by 11

Haplotype analysis can provide improved clinical information than single genotype analysis

Sandrim, V. C., & Tanus-Santos, J. E. (2006) · Thrombosis Research · doi:10.1016/j.thromres.2006.08.013 · Cited by 11

Vaspin in atherosclerotic disease and cardiovascular risk in axial spondyloarthritis: a genetic and serological study

Rueda‐Gotor, J., López‐Mejías, R., Remuzgo‐Martínez, S., Pulito‐Cueto, V., Corrales, A., Lera‐Gómez, L., Portilla, V., Gonzalez-Mazón, I., Blanco, R., Expósito, R., et al. (2021) · Arthritis Research & Therapy · doi:10.1186/s13075-021-02499-7 · Cited by 10

HapTree-X: An Integrative Bayesian Framework for Haplotype Reconstruction from Transcriptome and Genome Sequencing Data

Berger, E., Yörükoğlu, D., & Berger, B. (2015) · Lecture notes in computer science · doi:10.1007/978-3-319-16706-0_4 · Cited by 10

Antihypertensive therapy in preeclampsia is not modulated by VEGF polymorphisms

Sandrim, V. C., Palei, A. C., Eleuterio, N. M., Tanus-Santos, J. E., & Cavalli, R. D. C. (2014) · Archives of Gynecology and Obstetrics · doi:10.1007/s00404-014-3475-2 · Cited by 10

Response to chemotherapy and tandem autologous transplantation of multiple myeloma patients and GSTP1 and TYMS polymorphisms

Maggini, V., Buda, G., Galimberti, S., Conidi, E., Giuliani, N., Morabito, F., Genestreti, G., Iacopino, P., Rizzoli, V., Barale, R., et al. (2007) · Leukemia Research · doi:10.1016/j.leukres.2007.03.029 · Cited by 10

Matrix metalloproteinase (MMP)-2 and MMP-9 polymorphisms and haplotypes as disease biomarkers

Luizon, M. R., & Belo, V. D. A. (2012) · Biomarkers · doi:10.3109/1354750x.2012.657685 · Cited by 10

Single Nucleotide Polymorphisms of Caudal Type Homeobox 1 and 2 Are Associated with Barrett’s Esophagus

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Keijser, R., Olofsdotter, S., Nilsson, K. W., & Åslund, C. (2021) · Journal of Neural Transmission · doi:10.1007/s00702-021-02405-0 · Cited by 9

Positive Association of CC2D1A and CC2D2A Gene Haplotypes with Mental Retardation in a Han Chinese Population

Shi, Z., Li, Y., Zhang, K.-J., Gao, X.-C., Zheng, Z.-J., Han, N., & Zhang, F.-C. (2012) · DNA and Cell Biology · doi:10.1089/dna.2011.1253 · Cited by 10

Brain-derived Neurotrophic Factor Genetic Variants are Associated with Major Depression Susceptibility and Serotonin Reuptake Inhibitor Antidepressant Treatment Response in Taiwanese

Liou, Y., Chen, T., Cheng, C., Yu, Y. W., Hong, C., & Tsai, S. (2014) · Current pharmacogenomics and personalized medicine (Online)/Current pharmacogenomics and personalized medicine · doi:10.2174/1875692111666131211235804 · Cited by 8

Precision Nutrition for Cardiovascular Disease Prevention

Desjardins, L.-C., & Vohl, M. (2023) · Lifestyle Genomics · doi:10.1159/000529054 · Cited by 8

Identification and analysis of biomarkers for mismatch repair proteins: A bioinformatic approach

Singh, T., & Sehgal, M. (2012) · Journal of Natural Science Biology and Medicine · doi:10.4103/0976-9668.101887 · Cited by 8

How to Select Tag SNPs in Genetic Association Studies? The CLONTagger Method with Parameter Optimization

Ilhan, I., & Tezel, G. (2013) · Omics · doi:10.1089/omi.2012.0100 · Cited by 8

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Oliver, P., Lubomirov, R., & Carcas, A. J. (2010) · Clinical Chemistry and Laboratory Medicine (CCLM) · doi:10.1515/cclm.2010.130 · Cited by 8

Identification and functional significance of SNPs underlying conserved haplotype frameworks across ethnic populations

Ouyang, C., & Krontiris, T. (2006) · Pharmacogenetics & Genomics · doi:10.1097/01.fpc.0000220569.82842.9b · Cited by 9

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Rodríguez, M. B. S., Muñoz, L. M.-P., & Casieri, R. C. (2007) · Revista Española de Salud Pública · doi:10.1590/s1135-57272007000500005 · Cited by 8

Difference in Angiotensinogen Haplotype Frequencies Between Chronic Heart Failure and Advanced Atherosclerosis Patients – New Prognostic Factor?

Goldbergová, M. P., Špinarová, L., Špinar, J., Pařenica, J., Šišková, L., Groch, L., Máchal, J., & Vašků, A. (2011) · Physiological Research · doi:10.33549/physiolres.931976 · Cited by 8

Random Projection for Fast and Efficient Multivariate Correlation Analysis of High-Dimensional Data: A New Approach

Grellmann, C., Neumann, J., Bitzer, S., Kovacs, P. L., Tönjes, A., Westlye, L. T., Andreassen, O. A., Stümvoll, M., Villringer, A., & Horstmann, A. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00102 · Cited by 8

A strategy for building and using a human reference pangenome

Llamas, B., Narzisi, G., Schneider, V., Audano, P. A., Biederstedt, E., Blauvelt, L., Bradbury, P. J., Chang, X. H., Chin, C.-S., Fungtammasan, A., et al. (2019) · F1000Research · doi:10.12688/f1000research.19630.2 · Cited by 17

Endothelial Nitric Oxide Genotypes and Haplotypes Are Not Associated with End-Stage Renal Disease

Marson, B. P., Dickel, S., Ishizawa, M. H., Metzger, I. F., Izidoro‐Toledo, T. C., da Costa, B. E. P., Poli‐de‐Figueiredo, C. E., & Tanus-Santos, J. E. (2010) · DNA and Cell Biology · doi:10.1089/dna.2010.1106 · Cited by 8

Association of folate transporter SLC19A1 polymorphisms with the outcome of multiple myeloma after chemotherapy and tandem autologous transplantation

Maggini, V., Buda, G., Galimberti, S., Conidi, E., Giuliani, N., Morabito, F., Genestreti, G., Iacopino, P., Rizzoli, V., Barale, R., et al. (2006) · Leukemia · doi:10.1038/sj.leu.2404455 · Cited by 8

Rheumatoid Arthritis: Genetics

Steel, K. J. A., & Barton, A. C. (2011) · Wiley eBooks · doi:10.1002/9780470015902.a0005566.pub2 · Cited by 8

Endothelial nitric oxide synthase polymorphisms and hypertension: Improved clinical evidence derived from haplotype analysis

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Associations between cytotoxic T lymphocyte-associated antigen-4 polymorphisms and serum tumor necrosis factor-α and interferon-γ levels in patients with chronic hepatitis B virus infection

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Interaction of both positive and negative daily-life experiences with FKBP5 haplotype on psychosis risk

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The Protective Effects of the VEGF −2578C>A and −1154G>A Polymorphisms Against Hypertension Susceptibility

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Haplotyping the human leukocyte antigen system from single chromosomes

Murphy, N. M., Burton, M., Powell, D., Rossello, F. J., Cooper, D., Chopra, A., Hsieh, M. J., Sayer, D. C., Gordon, L., Pertile, M. D., et al. (2016) · Scientific Reports · doi:10.1038/srep30381 · Cited by 7

HLA Haplotype Frequency Estimation from Real-Life Data with the Hapl-o-Mat Software

Sauter, J., Schäfer, C., & Schmidt, A. H. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8546-3_19 · Cited by 7

Summer Term

Satya, R. V., Professor, M., Mukherjee, A., & Satya, C. R. V. (2015)

Latest HapMap Update Aims to Direct Researchers to Genetic Basis of Disease

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Genotype and Epigenotype by Single Nucleotide Polymorphism (SNP) Analysis

Gunderson, K. L., Barker, D. L. A., Bibikova, M. V., & Fan, J. (2007) · Elsevier eBooks · doi:10.1016/b978-012370465-8/50012-0 · Cited by 2

Am. J. Hum. Genet. 77:988–998, 2005 The Effect of Single-Nucleotide Polymorphism Marker Selection on Patterns of Haplotype Blocks and Haplotype Frequency Estimates

Nothnagel, M., & Rohde, K. (2013)

The Structure of Haplotype Blocks in the Human Genome

Gabriel, S. B., Schaffner, S. F., Nguyen, H., Moore, J. M., Roy, J., Blumenstiel, B., Higgins, J., DeFelice, M., Lochner, A., Faggart, M., et al. (2002) · Science · doi:10.1126/science.1069424 · Cited by 5,863