The Structure of Haplotype Blocks in the Human Genome
Gabriel, Stacey B., Schaffner, Stephen F., Nguyen, Huy, Moore, Jamie M., Roy, Jessica, Blumenstiel, Brendan, Higgins, John, DeFelice, Matthew +10 more·2002·Science
Cited by (1,035)
Items 601–700 of 1,035
- Genetic support for a quantitative trait nucleotide in the ABCG2 gene affecting milk composition of dairy cattleHanne Gro Olsen, Heidi Nilsen, Ben J. Hayes, Paul R. Berg, Morten Svendsen, Sigbjørn Lien, T.H.E. Meuwissen · 2007 · BMC Genetics
- Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndromeJuliane Winkelmann, Peter Lichtner, Barbara Schormair, Manfred Uhr, Stephanie Hauk, Karin Stiasny‐Kolster, Claudia Trenkwalder, Walter Paulus, Ines Peglau, Ilonka Eisensehr et al. · 2007 · Movement Disorders
- Genetic epidemiology of type 1 diabetesJoel N. Hirschhorn · 2003 · Pediatric Diabetes
- Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosisMairead L. Bermingham, Steve Bishop, J.A. Woolliams, Ricardo Pong‐Wong, A R Allen, Stewart H. McBride, Jon J Ryder, David M. Wright, R.A. Skuce, Stanley W. J. McDowell et al. · 2014 · Heredity
- Childhood maltreatment, the corticotropin‐releasing hormone receptor gene and adult depression in the general populationHans Jörgen Grabe, Christian Schwahn, Katja Appel, Jessie Mahler, Andrea Schulz, Carsten Spitzer, Kristin Fenske, Sven Barnow, Michael J. Lucht, Harald Jürgen Freyberger et al. · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of familiesIordanis Karagiannidis, Sandra Dehning, Paul Sandor, Zsanett Tárnok, Renata Rizzo, Tomasz Wolańczyk, Marcos Madruga-Garrido, Johannes Hebebrand, Markus Maria Nöthen, Gerd Lehmkuhl et al. · 2013 · Journal of Medical Genetics
- ANGPT2 Genetic Variant Is Associated with Trauma-associated Acute Lung Injury and Altered Plasma Angiopoietin-2 Isoform RatioNuala J. Meyer, Mingyao Li, Rui Feng, Jonathan P. Bradfield, Robert Gallop, Scarlett L. Bellamy, Barry D. Fuchs, Paul N. Lanken, Steven Μ. Albelda, Melanie Rushefski et al. · 2011 · American Journal of Respiratory and Critical Care Medicine
- Association of complement factor H polymorphisms with exudative age-related macular degeneration.Li Jia Chen, David T.L. Liu, Pancy O. S. Tam, Wai Man Chan, Ke Liu, Kelvin Kam Lung Chong, Dennis S.C. Lam, Chi Pui Pang · 2006 · PubMed
- Pharmacogenetics of the 5-lipoxygenase biosynthetic pathway and variable clinical response to montelukastMichael Klotsman, Timothy P. York, Sreekumar G Pillai, Cristina Vargas-Irwin, Sanjay Sharma, Edwin J. C. G. van den Oord, Wayne H. Anderson · 2007 · Pharmacogenetics and Genomics
- Identification of a Polycystic Ovary Syndrome Susceptibility Variant in Fibrillin-3 and Association with a Metabolic PhenotypeMargrit Urbanek, Susan Sam, Richard S. Legro, Andrea Elizabeth Dunaif · 2007 · The Journal of Clinical Endocrinology & Metabolism
- Genetic variability in the mitochondrial serine proteaseHTRA2contributes to risk for Parkinson diseaseVeerle Bogaerts, Karen Nuytemans, Joke Reumers, Philippe Pals, Sebastiaan Engelborghs, Barbara Anne Pickut, Ellen Corsmit, Karin Peeters, Joost W. H. Schymkowitz, Peter Paul De Deyn et al. · 2008 · Human Mutation
- Fine mapping association study and functional analysis implicate a SNP in MSMB at 10q11 as a causal variant for prostate cancer riskB. Chang, Scott D. Cramer, Fredrik E. Wiklund, Sarah D. Isaacs, Victoria L. Stevens, Jielin Sun, S. Smith, Kristen Pruett, L. M. Romero, Kathleen E. Wiley et al. · 2009 · Human Molecular Genetics
- The Association of Interleukin 6 Haplotype Clades With Mortality in Critically Ill AdultsAinsley M. Sutherland, Keith R. Walley, Sanjay Manocha, James A. Russell · 2005 · Archives of Internal Medicine
- Understanding human DNA sequence variation.K. Kidd, A. Pakstis, W. C. Speed, J. Kidd · 2004 · Journal of Heredity
- Association of TRPV4 gene polymorphisms with chronic obstructive pulmonary diseaseGuohua Zhu, ICGN Investigators, Amund Gulsvik, Per S. Bakke, Srinivas Ghatta, Wayne H. Anderson, David A. Lomas, Edwin K. Silverman, Sreekumar G Pillai · 2009 · Human Molecular Genetics
- Evolutionary‐based association analysis using haplotype dataHoward J. Seltman, Kathryn Roeder, Bernie Devlin · 2003 · Genetic Epidemiology
- Genome-wide association and pathway analysis of feed efficiency in pigs reveal candidate genes and pathways for residual feed intakeDuy N. Do, Anders Bjerring Strathe, Tage Ostersen, Sameer D. Pant, Haja N. Kadarmideen · 2014 · Frontiers in Genetics
- The molecular signature of selection underlying human adaptationsEugene E. Harris, Diogo Meyer · 2006 · American Journal of Physical Anthropology
- Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalonDerek Spieler, Maria Kaffe, Franziska Knauf, José Bessa, Juan J. Tena, Florian Giesert, Barbara Schormair, Erik Tilch, Heekyoung Lee, Marion Horsch et al. · 2014 · Genome Research
- Large-Scale Validation of Single Nucleotide Polymorphisms in Gene RegionsMatthew R. Nelson, George Marnellos, Stefan Kammerer, Carolyn R. Hoyal, Michael M. Shi, Charles R. Cantor, Andreas Dominik Braun · 2004 · Genome Research
- The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myelomaNiels Weinhold, David C. Johnson, Daniel Chubb, Bowang Chen, Asta Försti, Fay J. Hosking, Peter Broderick, Yussanne P. Ma, Sara E. Dobbins, Dirk Hose et al. · 2013 · Nature Genetics
- A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA regionEvelyn Png, Anbupalam Thalamuthu, Rick TH Ong, Harm Snippe, Greet J. Boland, Mark T. Seielstad · 2011 · Human Molecular Genetics
- Identification of major loci and genomic regions controlling acid and volatile content in tomato fruit: implications for flavor improvementGuillaume Jean Bauchet, Stéphane Grenier, Nicolas Samson, Vincent Segura, Anikó Kende, Jules Beekwilder, Katarina Cankar, Jean‐Luc Gallois, Justine Gricourt, Julien Bonnet et al. · 2017 · New Phytologist
- Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association studyYan Guo, Dong-hai Xiong, Hui Shen, Lan‐Juan Zhao, Peng Xiao, Yan Guo, Wei Wang, Tie‐Lin Yang, Robert R. Recker, Hong‐Wen Deng · 2006 · Journal of Medical Genetics
- Principal component analysis for selection of optimal SNP‐sets that capture intragenic genetic variationBenjamin Davies Horne, Nicola J. Camp · 2003 · Genetic Epidemiology
- Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1qYen-Pei C. Chang, Xin Liu, James Dae Ok Kim, Morna A. Ikeda, Marnie R. Layton, Alan B. Weder, Richard Cooper, Sharon L.R. Kardia, D. C. Rao, Steve C. Hunt et al. · 2007 · The American Journal of Human Genetics
- Efficacy of angiotensin-converting enzyme inhibition in reducing progression from asymptomatic left ventricular dysfunction to symptomatic heart failure in black and white patientsDaniel L. Dries, Mark H Strong, Richard Cooper, Mark H. Drazner · 2002 · Journal of the American College of Cardiology
- ADH4 Gene Variation is Associated with Alcohol Dependence and Drug Dependence in European Americans: Results from HWD Tests and Case–Control Association StudiesXingguang Luο, Henry R. Kranzler, Lingjun Zuo, Jaakko Lappalainen, Bao‐Zhu Yang, Joel E. Gelernter · 2005 · Neuropsychopharmacology
- Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic NephropathyMarcus G. Pezzolesi, Pisut Katavetin, Masahiko Kure, G. David Poznik, JAN K. SKUPIEN, Josyf C. Mychaleckyj, Stephen S. Rich, James H. Warram, Andrzej S. Królewski · 2009 · Diabetes
- Characterization of multilocus linkage disequilibriumAlessandro Rinaldo, Silviu‐Alin Bacanu, Bernie Devlin, Vibhor A. Sonpar, Larry Wasserman, Kathryn Roeder · 2005 · Genetic Epidemiology
- Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory miceBinnaz Yalcin, Janice M. Fullerton, S J Miller, David A. Keays, S. Brady, Amarjit Bhomra, Andrew Jefferson, Emanuela Valeria Volpi, Richard R. Copley, Jonathan Flint C et al. · 2004 · Proceedings of the National Academy of Sciences
- Evaluation of genetic variability in the dopamine receptor D2 in relation to behavioral inhibition and impulsivity/sensation seeking: an exploratory study with d-amphetamine in healthy participantsHamidovic, Ajna, Dlugos, Andrea, Skol, Andrew, Palmer, Abraham A., de Wit, Harriet · 2009 · Experimental and Clinical Psychopharmacology
- The Missing Association: Sequencing-Based Discovery of Novel SNPs in VKORC1 and CYP2C9 That Affect Warfarin Dose in African AmericansMinoli A. Perera, Eric R. Gamazon, Larisa H. Cavallari, Shitalben Patel, Shenika V. Poindexter, R. A. Kittles, Dan L. Nicolae, Nancy Jean Cox · 2011 · Clinical Pharmacology & Therapeutics
- Linkage disequilibrium and haplotype block structure in a composite beef cattle breedFabiana Barichello Mokry, Marcos Eli Buzanskas, Maurício A. Mudadu, Daniela do Amaral Grossi, Roberto Hiroshi Higa, Ricardo Vieira Ventura, Andressa Oliveira de Lima, Mehdi Sargolzaei, Sarah Laguna Conceição Meirelles, Flávio Schramm Schenkel et al. · 2014 · BMC Genomics
- Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell diseaseJames G. Taylor, Delia C. Tang, Sharon A. Savage, Susan F. Leitman, Seth I. Heller, Graham Roger Serjeant, Griffin P. Rodgers, Stephen Jacob Chanock · 2002 · Blood
- Progress in defining the molecular basis of type 2 diabetes mellitus through susceptibility-gene identificationMark I. McCarthy · 2004 · Human Molecular Genetics
- Rapid Evolution of Major Histocompatibility Complex Class I Genes in Primates Generates New Disease Alleles in Humans via Hitchhiking DiversityTakashi Shiina, Masao Ôta, Sayoko Shimizu, Yoshihiko Katsuyama, Nami Hashimoto, Miwa Takasu, Tatsuya Anzai, Jerzy K. Kulski, Eri F. Kikkawa, Taeko K. Naruse et al. · 2006 · Genetics
- Wanted: regulatory SNPsThomas J. Hudson · 2003 · Nature Genetics
- Patterns of linkage disequilibrium in the MHC region on human chromosome 6pAnnette Stenzel, Timothy T. Lu, W. Andreas Koch, Jochen Hampe, Simone M. Guenther, Francisco M. De La Vega, Michael Krawczak, Stefan Schreiber · 2004 · Human Genetics
- Common Genetic Variation in IGF1 and Prostate Cancer Risk in the Multiethnic CohortIona C. Cheng, Daniel O. Stram, Kathryn L. Penney, Malcolm C. Pike, Loı̈c Le Marchand, Laurence N. Kolonel, Joel N. Hirschhorn, David Altshuler, Brian E. Henderson, Matthew L. Freedman · 2006 · JNCI Journal of the National Cancer Institute
- Candidate Gene Studies of Human Pain MechanismsInna Belfer, Tianxia Wu, Albert Kingman, Raj K. Krishnaraju, David A Goldman, Mitchell B. Max, David C. Warltier · 2004 · Anesthesiology
- Heroin addiction in African Americans: a hypothesis‐driven association studyOrna Levran, Douglas Londoño, K. O’Hara, Matthew Randesi, John Rotrosen, Paul P. Casadonte, Shirley Linzy, Jürg Ott, Miriam Adelson, Mary Jeanne Kreek · 2009 · Genes Brain & Behavior
- Identification and Functional Characterization of Genetic Variants of Human Organic Cation Transporters in a Korean PopulationHojin Kang, Im‐Sook Song, Ho Jung Shin, Woo‐Young Kim, Choong‐Hee Lee, Joo-Cheol Shim, Hong‐Hao Zhou, Sang Seop Lee, Jae‐Gook Shin · 2007 · Drug Metabolism and Disposition
- Genetic Polymorphism Analysis ofCYP2C19in Chinese Han Populations from Different Geographic Areas of Mainland ChinaLing‐Ling Chen, Shengying Qin, Jing Xie, Jimin Tang, Lun Yang, Wen Shen, Xinzhi Zhao, Jing Du, Guang He, Guoyin Feng et al. · 2008 · Pharmacogenomics
- Generation and annotation of the DNA sequences of human chromosomes 2 and 4LaDeana W. Hillier, Tina Graves, Robert S. Fulton, Lucinda A. Fulton, Kymberlie Pepin, Patrick J. Minx, Caryn Wagner-McPherson, Dan Layman, Kristine M. Wylie, Mandeep Sekhon et al. · 2005 · Nature
- The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)Moritz F. Sinner, Arne Pfeufer, Mahmut Akyol, Britt-Maria Beckmann, Martin Hinterseer, Annette Wacker, Siegfried Perz, Wiebke Sauter, Thomas Illig, Michael Näbauer et al. · 2008 · European Heart Journal
- Choosing SNPs using feature selectionTu Minh Phuong, Zhen Lin, Russ Biagio Altman · 2005 · IEEE Computational Systems Bioinformatics Conference (CSB)
- FTOgene variation and measures of body mass in an African populationBranwen J. Hennig, Anthony J. C. Fulford, Giorgio Sirugo, Pura Rayco‐Solon, Andrew Tym Hattersley, Timothy M. Frayling, Andrew M. Prentice · 2009 · BMC Medical Genetics
- Computational information designBenjamin Fry, John Maeda · 2004 · DSpace@MIT (Massachusetts Institute of Technology)
- Genome‐wide association studies for discovery of genes involved in asthmaLoubna Akhabir, Andrew J. Sandford · 2011 · Respirology
- GeMes, Clusters of DNA Methylation under Genetic Control, Can Inform Genetic and Epigenetic Analysis of DiseaseYun Liu, Xin Li, Martin J. Aryee, Tomas J. Ekström, Leonid Padyukov, Lars Klareskog, Amy R. Vandiver, Ann Zenobia Moore, Toshiko Tanaka, Luigi Ferrucci et al. · 2014 · The American Journal of Human Genetics
- Effect of 5‐HT1A gene polymorphisms on antidepressant response in major depressive disorderMasaki Kato, Tsuyoshi Fukuda, Masataka Wakeno, Gaku Okugawa, Yoshiteru Takekita, Syunsuke Watanabe, Megumi Yamashita, Yuka Hosoi, Junichi Azuma, Toshihiko Kinoshita et al. · 2008 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Association of Genetic Variants in the Neurotrophic Receptor–Encoding Gene NTRK2 and a Lifetime History of Suicide Attempts in Depressed PatientsM. Kohli, D. Salyakina, A. Pfennig, S. Lucae, S. Horstmann, A. Menke, S. Kloiber, J. Hennings, B. Bradley, K. Ressler et al. · 2010 · Archives of General Psychiatry
- Genome-Wide Association Study Reveals Genetic Architecture of Eating Behavior in Pigs and Its Implications for Humans Obesity by Comparative MappingDuy Ngoc Do, Anders Bjerring Strathe, Tage Ostersen, Just Jensen, Thomas Mark, Haja N. Kadarmideen · 2013 · PLoS ONE
- Population genomics reveals the origin and asexual evolution of human infective trypanosomesWilliam Weir, Paul Capewell, Bernardo Javier Foth, Caroline Clucas, Andrew W. Pountain, Pieter C. Steketee, Nicola Veitch, Mathurin Koffi, Thierry De Meeûs, Jacques Kaboré et al. · 2016 · eLife
- Macrophage migration inhibitory factor in acute lung injury: expression, biomarker, and associationsLi Gao, Carlos Flores, Shwu Fan Ma, Edmund J. Miller, Jaideep Moitra, L. Gutierrez Garcia Moreno, Raj Wadgaonkar, Brett A. Simon, Roy G. Brower, Jonathan Sevransky et al. · 2007 · Translational research
- Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II regionLiisa Kauppi · 2003 · Human Molecular Genetics
- SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese populationYukiko Sakamoto, Hiroshi Inoue, Parvaneh Keshavarz, Katsuyuki Miyawaki, Yuka Yamaguchi, Maki Moritani, Kiyoshi Kunika, Naoto Nakamura, Toshikazu Yoshikawa, Natsuo Yasui et al. · 2007 · Journal of Human Genetics
- A high-density single-nucleotide polymorphism screen of 23 candidate genes in attention deficit hyperactivity disorder: suggesting multiple susceptibility genes among Chinese Han populationLili Guan, B Wang, Y Chen, Li Yang, Jiexin Li, Qiujin Qian, Z Wang, Stephen V. Faraone, Ya-Ting Wang · 2008 · Molecular Psychiatry
- Genetic polymorphisms in Na+-taurocholate co-transporting polypeptide (NTCP) and ileal apical sodium-dependent bile acid transporter (ASBT) and ethnic comparisons of functional variants of NTCP among Asian populationsWei Dong Pan, Im‐Sook Song, Ho Jung Shin, Min-Hye Kim, Yeong-Lim Choi, Su-Jeong Lim, Woo‐Young Kim, Sang‐Seop Lee, Jae‐Gook Shin · 2011 · Xenobiotica
- The Haplotype Structure of the Human Major Histocompatibility ComplexChester A. Alper, Charles E. Larsen, Devendra P. Dubey, Z Awdeh, Dolores A. Fici, Edmond J. Yunis · 2006 · Human Immunology
- Variants of the Transcription Factor 7-Like 2 (TCF7L2) Gene Are Associated With Type 2 Diabetes in an African-American Population Enriched for NephropathyMichèle M. Sale, Shelly G. Smith, Josyf C. Mychaleckyj, Keith L. Keene, Carl D. Langefeld, Tennille S. Leak, Pamela J. Hicks, Donald W. Bowden, Stephen S. Rich, Barry I. Freedman · 2007 · Diabetes
- Genome amplification of single sperm using multiple displacement amplificationZhuang Jiang · 2005 · Nucleic Acids Research
- Gametic phase estimation over large genomic regions using an adaptive window approachLaurent Excoffier, Guillaume Laval, David J. Balding · 2003 · Human Genomics
- The Extent of Linkage Disequilibrium Caused by Selection on G6PD in HumansM. A. Saunders, M. Slatkin, C. Garner, M. Hammer, M. Nachman · 2005 · Genetics
- Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degenerationDeAngelis, Margaret M., Ji, Fei, Adams, Scott, Morrison, Margaux A., Harring, Amanda J., Sweeney, Meredith O., Capone, Antonio, Miller, Joan W., Dryja, Thaddeus P., Ott, Jurg et al. · 2008 · Ophthalmology
- Polymorphisms in the methotrexate transport pathwayElixabet López-López, Javier Ballesteros, M.A. Piñán, José Sanchez de Toledo, Nagore García de Andoín, Purificación García‐Miguel, Aurora Navajas, África García‐Orad · 2012 · Pharmacogenetics and Genomics
- Genomic and functional approaches reveal a case of adaptive introgression fromPopulus balsamifera(balsam poplar) inP. trichocarpa(black cottonwood)Adriana Suarez‐Gonzalez, Charles A. Hefer, Camille Christe, Oliver R.A. Corea, Christian Lexer, Quentin Cronk, Carl J. Douglas · 2016 · Molecular Ecology
- C5a-licensed phagocytes drive sterilizing immunity during systemic fungal infectionJigar V. Desai, Dhaneshwar Kumar, Tilo Freiwald, Daniel Chauss, Melissa D. Johnson, Michael S. Abers, Julie M. Steinbrink, John R. Perfect, Barbara Dudley Alexander, Vasiliki Matzaraki et al. · 2023 · Cell
- Why do young women smoke? I. Direct and interactive effects of environment, psychological characteristics and nicotinic cholinergic receptor genesLior Greenbaum, Kyra Kanyas, Osnat Karni, Yifat Merbl, Tsviya Olender, Anat Horowitz, Avi Yakir, Doron Lancet, Edna Ben‐Asher, Bernard Lerer · 2005 · Molecular Psychiatry
- Susceptible and protective eNOS haplotypes in hypertensive black and white subjectsValéria C. Sandrim, Eduardo Barbosa Coelho, Fernando Dantas Nobre, Gustavo Marin Arado, Vera Lúcia Lanchote, José Eduardo Tanus-Santos · 2005 · Atherosclerosis
- Reductions in claudin-1 may enhance susceptibility to herpes simplex virus 1 infections in atopic dermatitisAnna De Benedetto, Mark K. Slifka, Nicholas M. Rafaels, I‐Hsin Kuo, Steve N. Georas, Mark Boguniewicz, Tissa R. Hata, Lynda C. Schneider, Jon M. Hanifin, Richard L. Gallo et al. · 2011 · Journal of Allergy and Clinical Immunology
- Assessing the Reproducibility of Asthma Candidate Gene Associations, Using Genome-wide DataAngela J. Rogers, Benjamin A. Raby, Jessica Ann Lasky-Su, Amy Murphy, Ross M Lazarus, Barbara J. Klanderman, Jody Senter Sylvia, John P. Ziniti, Christoph Lange, Juan Carlos Celedon et al. · 2009 · American Journal of Respiratory and Critical Care Medicine
- Catechol-O-Methyltransferase Contributes to Genetic Susceptibility Shared Among Anxiety Spectrum PhenotypesJohn M. Hettema, Seon‐Sook An, József Bukszár, Edwin J. C. G. van den Oord, Michael Churton Neale, Kenneth S. Kendler, Xiangning Chen · 2008 · Biological Psychiatry
- Detection of ApoE E2, E3 and E4 alleles using MALDI-TOF mass spectrometry and the homogeneous mass-extend technologyNader Ghebranious · 2005 · Nucleic Acids Research
- The allelic structure of common diseaseDesmond Smith · 2002 · Human Molecular Genetics
- Oxytocin receptor (OXTR) does not play a major role in the aetiology of autism: Genetic and molecular studiesKatherine E. Tansey, Keeley J. Brookes, Matthew Hill, Lynne E. Cochrane, Michael Gill, David Skuse, Catarina Correia, Astrid Moura Vicente, Lindsey Kent, Louise Gallagher et al. · 2010 · Neuroscience Letters
- Lymphatic and Angiogenic Candidate Genes Predict the Development of Secondary Lymphedema following Breast Cancer SurgeryChristine A. Miaskowski, Marylin J. Dodd, S M Paul, Claudia M. West, Deborah Hamolsky, Gary Abrams, Bruce A. Cooper, Charles Elboim, John M Neuhaus, Brian L. Schmidt et al. · 2013 · PLoS ONE
- Identification of fetal and maternal single nucleotide polymorphisms in candidate genes that predispose to spontaneous preterm labor with intact membranesRoberto J. Romero, Digna R. Velez Edwards, Juan Pedro Kusanovic, Sonia S. Hassan, Shali Mazaki‐Tovi, Edi Vaisbuch, Chong Jai Kim, Tinnakorn Chaiworapongsa, Brad D. Pearce, Lara A. Friel et al. · 2010 · American Journal of Obstetrics and Gynecology
- Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsyKjell Heuser, Erlend Arnulf Nagelhus, Erik Taubøll, Ulf Geir Indahl, Paul R. Berg, Sigbjørn Lien, Sigve Nakken, Leif Gjerstad, Ole Petter Ottersen · 2009 · Epilepsy Research
- Genetic studies of stuttering in a founder populationJacqueline K. Wittke‐Thompson, Nicoline Grinager Ambrose, Ehud Yairi, Cheryl A. Roe, Edwin H. Cook, Carole Ober, Nancy Jean Cox · 2006 · Journal of Fluency Disorders
- Allelic Variation at Alcohol Metabolism Genes (ADH1B, ADH1C, ALDH2) and Alcohol Dependence in an American Indian PopulationMulligan, Connie J., Robin, Robert W., Osier, Michael V., Sambuughin, Nyamkhishig, Goldfarb, Lev G., Kittles, Rick A., Hesselbrock, Diane, Goldman, David, Long, Jeffrey C. · 2003 · Human Genetics
- Perspectives on Human Genetic Variation from the HapMap ProjectGil McVean, Chris C. A. Spencer, Raphaëlle Chaix · 2005 · PLoS Genetics
- SNPAnalyzer 2.0: A web-based integrated workbench for linkage disequilibrium analysis and association analysisJinho Yoo, Young Bok Lee, Yujung Kim, Sun Young Rha, Yangseok Kim · 2008 · BMC Bioinformatics
- Refashioning Race: dna and the Politics of Health CareAnne Fausto‐Sterling · 2004 · differences
- Genome-Wide Association Studies: Results from the First Few Years and Potential Implications for Clinical MedicineJoel N. Hirschhorn, Zofia K. Z. Gajdos · 2010 · Annual Review of Medicine
- Extension of Type 2 Diabetes Genome-Wide Association Scan Results in the Diabetes Prevention ProgramAllan F. Moore, Kathleen A. Jablonski, Jarred B. McAteer, Richa Saxena, Toni I. Pollin, Paul W. Franks, Robert L. Hanson, Alan R. Shuldiner, William C. Knowler, David Altshuler et al. · 2008 · Diabetes
- Textual data compression in computational biology: a synopsisRaffaele Giancarlo, Davide Scaturro, Filippo Utro · 2009 · Bioinformatics
- Soybean BARCSoySNP6K: An assay for soybean genetics and breeding researchQijian Song, Long Yan, Charles Quigley, Edward Fickus, Wei He, Linfeng Chen, Faming Dong, Susan Araya, Jinyi Liu, David L. Hyten et al. · 2020 · The Plant Journal
- Haplotypic Variants in DRD2, ANKK1, TTC12, and NCAM1 are Associated With Comorbid Alcohol and Drug DependenceBao‐Zhu Yang, Henry R. Kranzler, Hongyu Zhao, Jeffrey R. Gruen, Xingguang Luο, Joel E. Gelernter · 2008 · Alcoholism Clinical and Experimental Research
- A Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in West AfricansCharles N. Rotimi, Guanjie Chen, Adebowale Adeyemo, Paulette M Furbert-Harris, Debra Guass, Jie Zhou, Kate A. Berg, Olufemi J. Adegoke, Albert G. B. Amoah, Samuel Owusu et al. · 2004 · Diabetes
- Genome‐wide analysis identifies 16q deletion associated with survival, molecular subtypes, mRNA expression, and germline haplotypes in breast cancer patientsSilje Nord, Fredrik Johansen, Grethe I.G. Alnæs, Elmar Bucher, Ann‐Christine Syvänen, Bjørn Naume, Anne‐Lise Børresen‐Dale, Vessela Nedelcheva Kristensen · 2008 · Genes Chromosomes and Cancer
- Genetics of Cardiovascular DiseasesFrançois Cambien, Laurence Tiret · 2007 · Circulation
- Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterolHans Knoblauch · 2004 · Human Molecular Genetics
- Recombination and Migration of Cryphonectria hypovirus 1 as Inferred From Gene Genealogies and the CoalescentIgnazio Carbone, Yir-Chung Liu, Bradley I Hillman, Michael G Milgroom · 2004 · Genetics
- Association between Common Variation in Genes Encoding Sweet Taste Signaling Components and Human Sucrose PerceptionAlexey A. Fushan, Christopher T. Simons, Jay P. Slack, Dennis T. Drayna · 2010 · Chemical Senses
- Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.J. Smoller, J. Biederman, L. Arbeitman, A. Doyle, J. Fagerness, R. Perlis, P. Sklar, S. Faraone · 2006 · Biological Psychiatry
- Pharmacogenetics in the Laboratory and the ClinicDavid B. Goldstein · 2003 · New England Journal of Medicine
- Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: A preliminary studyBiederman, Joseph, Kim, Jang Woo, Doyle, Alysa E., Mick, Eric, Fagerness, Jesen, Smoller, Jordan W., Faraone, Stephen V. · 2008 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- A genome-wide association study on androstenone levels in pigs reveals a cluster of candidate genes on chromosome 6Naomi Duijvesteijn, E.F. Knol, Jan W.M. Merks, Richard P. M. A. Crooijmans, Martien A. M. Groenen, Henk Bovenhuis, B. Harlizius · 2010 · BMC Genetics