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

DOI 10.1126/science.1069424

Cited by (1,035)

Items 901–1,000 of 1,035

Fine mapping of the -T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees
Nilufer Ertekin-Taner · 2003 · Human Molecular Genetics
Genetics, Genomics, and Breeding of Grapes
2011 · CRC Press eBooks
Genetic Variation in the Sodium-dependent Vitamin C Transporters, SLC23A1, and SLC23A2 and Risk for Preterm Delivery
Erichsen, Hans Christian, Engel, Stephanie A. Mulherin, Eck, Peter K., Welch, Robert, Yeager, Meredith, Levine, Mark, Siega-Riz, Anna Maria, Olshan, Andrew F., Chanock, Stephen J. · 2006 · American Journal of Epidemiology
Importance of Including Non-European Populations in Large Human Genetic Studies to Enhance Precision Medicine
Dan Ju, Daniel Hui, Dorothy Araba Hammond, Ambroise Wonkam, Sarah A. Tishkoff · 2022 · Annual Review of Biomedical Data Science
HLA genomics in the third millennium
John Trowsdale · 2005 · Current Opinion in Immunology
Association of galanin haplotypes with alcoholism and anxiety in two ethnically distinct populations
Inna Belfer, Heather S. Hipp, Colin D. McKnight, Catherine Evans, Barnabás Buzás, Antonella F Bollettino, Bernard Albaugh, Matti E. Virkkunen, Qiaoping Yuan, Mitchell B. Max et al. · 2005 · Molecular Psychiatry
Association of Sirtuin 1 (SIRT1) Gene SNPs and Transcript Expression Levels With Severe Obesity
Stephen J. Clark, Mario Falchi, Bob Olsson, Peter Jacobson, Stéphane Cauchi, Beverley Balkau, Michel Marre, Olivier Lantieri, Johanna C. Andersson‐Assarsson, Margareta Jernås et al. · 2011 · Obesity
Single nucleotide polymorphisms and haplotypes associated with feed efficiency in beef cattle
Nick V. L. Serão, Dianelys González-Peña, Jonathan E. Beever, Dan B. Faulkner, Bruce R. Southey, Sandra L. Rodriguez‐Zas · 2013 · BMC Genetics
Genome-wide association studies of atrial fibrillation: past, present, and future
Moritz F. Sinner, Patrick T. Ellinor, Thomas Meitinger, Emelia J. Benjamin, Stefan Kääb · 2011 · Cardiovascular Research
Association study of tardive dyskinesia and twelve DRD2 polymorphisms in schizophrenia patients
Clement C.H. Zai, Rudi Hwang, Vincenzo De Luca, Daniel J. Müller, Nicole A. King, Gwyneth C. Zai, Gary J. Remington, Herbert Y. Meltzer, Jeffrey Alan Lieberman, Steven G. Potkin et al. · 2006 · The International Journal of Neuropsychopharmacology
Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy
Luis Javier Leandro-Garcia, Lucía Inglada‐Pérez, Guillermo Pita, Elisabet Hjerpe, Susanna Leskelä, Carlos Jara, Xabier Mielgo-Rubio, Anna González‐Neira, Mercedes Robledo, Elisabeth H. Åvall-Lundqvist et al. · 2013 · Journal of Medical Genetics
Usefulness of a Multiparent Advanced Generation Intercross Population With a Greatly Reduced Mating Design for Genetic Studies in Winter Wheat
Melanie Stadlmeier, Lorenz Hartl, Volker Mohler · 2018 · Frontiers in Plant Science
Genetics of psoriasis: the potential impact on new therapies
Anne M. Bowcock, Jonathan N Barker · 2003 · Journal of the American Academy of Dermatology
Sequence variation in the soluble epoxide hydrolase gene and subclinical coronary atherosclerosis: Interaction with cigarette smoking
Qi Wei, Peter A. Doris, Martin V. Pollizotto, Eric Boerwinkle, David R. Jacobs, David S. Siscovick, Myriam Fornage · 2006 · Atherosclerosis
Systematic Evaluation of Genetic Variation at the Androgen Receptor Locus and Risk of Prostate Cancer in a Multiethnic Cohort Study
Matthew L. Freedman, Celeste Leigh Pearce, Kathryn L. Penney, Joel N. Hirschhorn, Laurence N. Kolonel, Brian E. Henderson, David Altshuler · 2004 · The American Journal of Human Genetics
Linkage disequilibrium in human populations
Christine Lonjou, Weihua Zhang, Andrew R Collins, William Tapper, Eiram Elahi, Nikolas Maniatis, Newton E. Morton · 2003 · Proceedings of the National Academy of Sciences
Genetic Epidemiology of Tuberculosis Susceptibility: Impact of Study Design
Catherine M. Stein · 2011 · PLoS Pathogens
Challenges of SNP genotyping and genetic variation: its future role in diagnosis and treatment of cancer
Toralf Bernig, Stephen Jacob Chanock · 2006 · Expert Review of Molecular Diagnostics
RUNX2 Polymorphisms Associated with OPLL and OLF in the Han Population
Yang Liu, Yongfei Zhao, Yu Chen, Guodong Shi, Wen Yuan · 2010 · Clinical Orthopaedics and Related Research
Diversity and evolution of 11 innate immune genes in Bos taurus taurus and Bos taurus indicus cattle
Christopher M. Seabury, Paul M. Seabury, Jared E. Decker, Robert D. Schnabel, Jeremy F. Taylor, James E. Womack · 2009 · Proceedings of the National Academy of Sciences
Preterm Birth in Caucasians Is Associated with Coagulation and Inflammation Pathway Gene Variants
Digna Rosa Velez, Stephen J. Fortunato, Poul Thorsen, Salvatore J. Lombardi, Scott M. Williams, Ramkumar Menon · 2008 · PLoS ONE
Association of the calpain-10 gene with type 2 diabetes in Europeans: Results of pooled and meta-analyses
Takafumi Tsuchiya, Peter E. H. Schwarz, Laura del Bosque‐Plata, M. Geoffrey Hayes, Christian Dina C, Philippe Froguel, Gordon Wayne Towers, Sabine Fischer, Theodora S Temelkova-Kurktschiev, Hannes Rietzsch · 2006 · Molecular Genetics and Metabolism
Molekulartechnische DNA‐Modifizierung: Molecular Beacons
Kemin Wang, Zhiwen Tang, Chaoyong James Yang, Youngmi Kim, Xiaohong Fang, Wei Li, Yanrong Wu, Colin D. Medley, Zehui Charles Cao, Jun Li et al. · 2008 · Angewandte Chemie
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations
Sheng Gu, ANDREW J. PAKSTIS, Hui Li, William C. Speed, Judith R. Kidd, Kenneth K. Kídd · 2007 · European Journal of Human Genetics
Association of Common Variation in the HNF1α Gene Region With Risk of Type 2 Diabetes
Wendy Winckler, Noël P. Burtt, Johan Holmkvist, Camilla Cervin, Paul I. W. de Bakker, Maria W. Sun, Peter Almgren, Tiinamaija Tuomi, Daniel Gaudet, Thomas J. Hudson et al. · 2005 · Diabetes
Importance of Race/Ethnicity in Clinical Trials
Anne L. Taylor, Jackson T. Wright · 2005 · Circulation
Genetic susceptibility to malignant pleural mesothelioma and other asbestos-associated diseases
NERI, M, UGOLINI, D, DIANZANI, I, GEMIGNANI, F, LANDI, S, CESARIO, A, MAGNANI, C, MUTTI, L, PUNTONI, R, BONASSI, S · 2008 · Mutation Research/Reviews in Mutation Research
Genome-Wide Association Studies for Dynamic Plant Height and Number of Nodes on the Main Stem in Summer Sowing Soybeans
Fangguo Chang, Chengyu Guo, Fengluan Sun, Jishun Zhang, Zili Wang, Jiejie Kong, Qingyuan He, Ripa Akter Sharmin, Tuanjie Zhao · 2018 · Frontiers in Plant Science
Patterns of molecular genetic variation among cat breeds
Marilyn A. Menotti-Raymond, Victor A. David, Solveig Pflueger, Kerstin Lindblad‐Toh, Claire M. Wade, Stephen J. O’Brien, Warren E. Johnson · 2007 · Genomics
Common genetic variations in human brain-specific tryptophan hydroxylase-2 and response to antidepressant treatment
Mladen Vassilev Tzvetkov, Jürgen Brockmöller, Ivar Roots, Julia Kirchheiner · 2008 · Pharmacogenetics and Genomics
Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson’s disease – a multicenter study
Malin von Otter, Petra Bergström, Aldo Quattrone, Elvira Valeria De Marco, Grazia Annesi, Peter Söderkvist, Stephanie Bezzina Wettinger, Marek Droździk, Monika Anna Białecka, Hans Nissbrandt et al. · 2014 · BMC Medical Genetics
EFFICIENT INFERENCE OF HAPLOTYPES FROM GENOTYPES ON A PEDIGREE
Jing Li, Tao Jiang · 2003 · Journal of Bioinformatics and Computational Biology
Genetic progress towards the molecular basis of autoimmunity
Simon H. S. Pearce, Tony Raymond Merriman · 2006 · Trends in Molecular Medicine
Common Variants in the ENPP1 Gene Are Not Reproducibly Associated With Diabetes or Obesity
Helen N. Lyon, José C. Florez, Todd Bersaglieri, Richa Saxena, Wendy Winckler, Peter Almgren, Ulf Lindblad, Jaakko Tuomilehto, Daniel Gaudet, Xiaofeng Zhu et al. · 2006 · Diabetes
Genome-wide Diversity and Association Mapping for Capsaicinoids and Fruit Weight in Capsicum annuum L
Padma Nimmakayala, Venkata Lakshmi Abburi, Thangasamy Saminathan, Suresh Babu Alaparthi, Aldo Almeida, Brittany Davenport, Marjan Nadimi, Joshua Davidson, Krittika Tonapi, Lav Kumar Yadav et al. · 2016 · Scientific Reports
Genome-Wide SNP Markers Based on SLAF-Seq Uncover Breeding Traces in Rapeseed (Brassica napus L.)
Qinghong Zhou, Can Zhou, Wei Zheng, Annaliese S. Mason, Fan Shuying, Caijun Wu, Donghui Fu, Yingjin Huang · 2017 · Frontiers in Plant Science
Genetic diversity patterns and domestication origin of soybean
Soon‐Chun Jeong, Jung‐Kyung Moon, Soo-Kwon Park, Myung‐Shin Kim, Kwanghee Lee, Soo‐Rang Lee, Namhee Jeong, Man Soo Choi, Namshin Kim, Sung‐Taeg Kang et al. · 2018 · Theoretical and Applied Genetics
A single nucleotide polymorphism alters the sequence of SP1 binding site in the adiponectin promoter region and is associated with diabetic nephropathy among type 1 diabetic patients in the Genetics of Kidneys in Diabetes Study
Dongying Zhang, Jun Ma, Kerstin Brismar, Suad Efendić, Harvest F. Gu · 2008 · Journal of Diabetes and its Complications
Genome-wide association studies of chronic kidney disease: what have we learned?
Conall M. O’Seaghdha, Caroline S. Fox · 2011 · Nature Reviews Nephrology
Variation in PTX3 Is Associated with Primary Graft Dysfunction after Lung Transplantation
Joshua Matthew Diamond, Nuala J. Meyer, Rui Feng, Melanie Rushefski, David J. Lederer, Steven M. Kawut, James C. Lee, Edward Cantu, Rupal Shah, Vibha N. Lama et al. · 2012 · American Journal of Respiratory and Critical Care Medicine
Family-Based Association Analysis of Hepatocyte Growth Factor ( HGF ) Gene Polymorphisms in High Myopia
Wei Han, Maurice K. H. Yap, Jing Wang, Shea Ping Yip · 2006 · Investigative Ophthalmology & Visual Science
SNP Function Portal: a web database for exploring the function implication of SNP alleles
Pinglang Wang, Manhong Dai, Weijian Xuan, Richard C. McEachin, Anne Jackson, Laura J. Scott, Brian D. Athey, Stanley J. Watson, Fan Meng · 2006 · Bioinformatics
Information on ancestry from genetic markers
C. Pfaff, J. Barnholtz-Sloan, Jennifer K. Wagner, J. Long · 2004 · Genetic Epidemiology
Genetic Factors and Orofacial Clefting
Andrew Carl Lidral, Lina M. Moreno, Steven A. Bullard · 2008 · Seminars in Orthodontics
Association of toll-like receptors with susceptibility to tuberculosis suggests sex-specific effects of TLR8 polymorphisms
Muneeb Salie, Michelle Daya, Lance A. Lucas, Robin M. Warren, Gian D van der Spuy, Paul D. van Helden, Eileen Garner Hoal, Marlo Möller · 2015 · Infection Genetics and Evolution
Nucleotide excision repair genes and risk of lung cancer among San Francisco Bay Area Latinos and African Americans
Jeffrey Shu-Ming Chang, Margaret Wrensch, Helen M. Hansen, Jennette D. Sison, Melinda C. Aldrich, Charles P. Quesenberry, Michael F. Seldin, Karl T. Kelsey, Rick A. Kittles, GABRIEL HENRIQUE DE OLIVEIRA SILVA et al. · 2008 · International Journal of Cancer
Deficiency of immunoregulatory indoleamine 2,3-dioxygenase 1 in juvenile diabetes
Ciriana Orabona, Giada Mondanelli, Maria Teresa Pallotta, Agostinho Carvalho, Elisa Albini, Francesca Fallarino, Carmine Vacca, Claudia Volpi, Maria Laura Belladonna, Maria Giulia Berioli et al. · 2018 · JCI Insight
Association and linkage mapping to unravel genetic architecture of phenological traits and lateral bearing in Persian walnut (Juglans regia L.)
Anthony Bernard, Annarita Marrano, Armel S. L. Donkpegan, Patrick J. Brown, Charles A. Leslie, David B. Neale, Fabrice Lheureux, Elisabeth Dirlewanger · 2020 · BMC Genomics
Dissection of phenotype reveals possible association between schizophrenia and Glutamate Receptor Delta 1 (GRID1) gene promoter
Jens Treutlein, Thomas W. Mühleisen, Josef Frank, Manuel Mattheisen, Stefan Herms, Kerstin U. Ludwig, Tsendsesmee Lkhagvajav Treutlein, Christine Schmael, Jana Strohmaier, Katja V. Böhenz et al. · 2009 · Schizophrenia Research
Genetic and physical interaction of the B-cell systemic lupus erythematosus-associated genes BANK1 and BLK
Casimiro Castillejo-López, Angelica Maria Delgado-Vega, Jérôme Wojcik, Sergey V. Kozyrev, Elangovan Thavathiru, Ying-Yu Wu, Elena Sánchez, David Pöllmann, Juan R. Lopez-Egido, Serena Fineschi et al. · 2011 · Annals of the Rheumatic Diseases
Single Nucleotide Polymorphisms of DNA Repair Genes as Predictors of Radioresponse
Matthew B. Parliament, David L. Murray · 2010 · Seminars in Radiation Oncology
A Visfatin Promoter Polymorphism Is Associated with Low‐Grade Inflammation and Type 2 Diabetes
Yuan‐Yuan Zhang, Lucia Gottardo, Ryan Thompson, Christine M. Powers, David A Nolan, Jill E. Duffy, Maria Cristina Marescotti, Angelo Avogaro, Alessandro Doria · 2006 · Obesity
BDNF Polymorphism Predicts General Intelligence after Penetrating Traumatic Brain Injury
Elham Rostami, Frank Krüeger, Serguei Zoubak, Olga Dal Monte, Vanessa Raymont, Matteo Pardini, Colin A. Hodgkinson, David A Goldman, Mårten Risling, Jordan Henry Grafman · 2011 · PLoS ONE
Association of Genetic Polymorphisms of Interleukins With New-Onset Diabetes After Transplantation in Renal Transplantation
Yang‐Gyun Kim, Chun‐Gyoo Ihm, Tae Won Lee, Sang Ho Lee, Kyung Hwan Jeong, Ju-Young Moon, Joo‐Ho Chung, Su Kang Kim, Yeong Hoon Kim · 2012 · Transplantation
Gain-of-function of P2X7 receptor gene variants in multiple sclerosis
Olatz Oyanguren-Desez, Alfredo Rodríguez Antigüedad, Pablo Villoslada, Marı́a Domercq, Elena M Alberdi, Carlos Matute · 2011 · Cell Calcium
Neanderthal Introgression at Chromosome 3p21.31 Was Under Positive Natural Selection in East Asians
Qiliang Ding, Ya Hu, Shuhua Xu, Jiucun Wang, Jin Li · 2013 · Molecular Biology and Evolution
Linkage disequilibrium and inbreeding estimation in Spanish Churra sheep
Elsa García-Gámez, Goutam Sahana, Beatriz Gutiérrez‐Gil, J. J. Arranz · 2012 · BMC Genetics
Linkage Analysis of a Complex Disease through Use of Admixed Populations
Xiaofeng Zhu, Richard Cooper, Robert C. Elston · 2004 · The American Journal of Human Genetics
Common Genetic Variation in Five Thrombosis Genes and Relations to Plasma Hemostatic Protein Level and Cardiovascular Disease Risk
Sekar Kathiresan, Qiong Yang, Martin G. Larson, Amy L. Camargo, Geoffrey H. Tofler, Joel N. Hirschhorn, Stacey Gabriel, Christopher J. O’Donnell · 2006 · Arteriosclerosis Thrombosis and Vascular Biology
Association Testing of Variants in the Hepatocyte Nuclear Factor 4α Gene With Risk of Type 2 Diabetes in 7,883 People
Wendy Winckler, Robert Graham, Paul I. W. de Bakker, Maria W. Sun, Peter Almgren, Tiinamaija Tuomi, Daniel Gaudet, Thomas J. Hudson, Kristin Ardlie, Mark J. Daly et al. · 2005 · Diabetes
Haplotypic analysis of the TNF locus by association efficiency and entropy
Hans Christian Ackerman, Stanley Usen, Richard Mott, Anna E. Jeffreys, Fatoumatta Sisay-Joof, Pauline Katundu, Terrie Ellen Taylor, Ryk H. Ward, Malcolm Edward Molyneux, Margaret Pinder et al. · 2003 · Genome biology
Haplotype block structures show significant variation among populations
Nianjun Liu, Sarah L. Sawyer, Namita Mukherjee, ANDREW J. PAKSTIS, Judith R. Kidd, Kenneth K. Kídd, Anthony J. Brookes, Hongyu Zhao · 2004 · Genetic Epidemiology
Finding genes underlying risk of complex disease by linkage disequilibrium mapping
Andrew G. Clark · 2003 · Current Opinion in Genetics & Development
Genetic variation in <i><scp>DNMT3B</scp></i> and increased global <scp>DNA</scp> methylation is associated with suicide attempts in psychiatric patients
Murphy, T. M., Mullins, N., Ryan, M., Foster, T., Kelly, C., McClelland, R., O'Grady, J., Corcoran, E., Brady, J., Reilly, M. et al. · 2013 · Genes, Brain and Behavior
Tackling Salinity in Sustainable Agriculture—What Developing Countries May Learn from Approaches of the Developed World
Sajid Shokat, Dominik K. Großkinsky · 2019 · Sustainability
Discovery of beneficial haplotypes for complex traits in maize landraces
Manfred Mayer, Armin C. Hölker, Eric Gerardo González Segovia, Eva Bauer, Thomas Presterl, Milena Ouzunova, Albrecht E. Melchinger, Chris‐Carolin Schön · 2020 · Nature Communications
A comprehensive study of polymorphisms inABCB1, ABCC2andABCG2and lung cancer chemotherapy response and prognosis
Daniele Campa, Phillip Müller, Lutz Edler, Lena Franziska Knoefel, Roberto Barale, Claus Peter Heußel, Michael Thomas, Federico Canzian, Angela Risch · 2012 · International Journal of Cancer
eNOS haplotypes affect the responsiveness to antihypertensive therapy in preeclampsia but not in gestational hypertension
Valéria C. Sandrim, Ana Carolina Palei, Marcelo R. Luizon, Tatiane C. Izidoro‐Toledo, Ricardo de Carvalho Cavalli, José Eduardo Tanus-Santos · 2009 · The Pharmacogenomics Journal
Genetic variation in APOE cluster region and Alzheimer's disease risk
Sebastián Cervantes, Lluı́s Samaranch, Jose Manuel Vidal-Taboada, Isabel Lamet, Maria Jesus Bullido, Ana Frank, Francisco Coria, Albert Lleó, Jordi Clarimón, Elena Lorenzo et al. · 2011 · Neurobiology of Aging
A Functional Haplotype Implicated in Vulnerability to Develop Cocaine Dependence is Associated with Reduced PDYN Expression in Human Brain
Vadim P. Yuferov, Fei Ji, David A. Nielsen, Orna Levran, Ann Ho, Susan Morgello, Ruijin Shi, Jürg Ott, Mary Jeanne Kreek · 2008 · Neuropsychopharmacology
Natural selection at genomic regions associated with obesity and type-2 diabetes: East Asians and sub-Saharan Africans exhibit high levels of differentiation at type-2 diabetes regions
Yann C. Klimentidis, Marshall Abrams, Jelai Wang, José R. Fernández, David B. Allison · 2010 · Human Genetics
High-Resolution Recombination Patterns in a Region of Human Chromosome 21 Measured by Sperm Typing
Irene Tiemann‐Boege, Peter P. Calabrese, David Michael Cochran, Rebecca Z. Sokol, Norman Arnheim · 2006 · PLoS Genetics
Polymorphisms in Angiogenesis-Related Genes and Prostate Cancer
Eric J. Jacobs, Ann W. Hsing, Elizabeth B. Bain, Victoria L. Stevens, Yiting Wang, Jinbo Chen, Stephen Jacob Chanock, Shusen Zheng, Jianfeng Xu, Michael J. Thun et al. · 2008 · Cancer Epidemiology Biomarkers & Prevention
Molecular analysis of HLA allele frequencies and haplotypes in Baloch of Iran compared with related populations of Pakistan
Shirin Farjadian, Taeko K. Naruse, Hisako Kawata, Abbas Ali Ghaderi, Seiamak Bahram, Hidetoshi Inoko · 2004 · Tissue Antigens
Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms
Ynte Marije Ruigrok, Gabriël J.E. Rinkel, Ruben van ‘t Slot, Marcel G. M. Wolfs, Tang Song, Cisca Wijmenga · 2006 · Human Molecular Genetics
Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia
Ellen A. Tsai, Christopher M. Grochowski, Kathleen M. Loomes, Kazuhiko Bessho, Hakon H. Hakonarson, Jorge A. Bezerra, Pierre Russo, Barbara Anne Haber, Nancy Bettina Spinner, Marcella Devoto · 2013 · Human Genetics
Risk- and non-risk-associated variants at the 10q26 AMD locus influence ARMS2 mRNA expression but exclude pathogenic effects due to protein deficiency
Ulrike Friedrich, Connie A. Myers, Lars G. Fritsche, Andrea Milenkovic, Armin Wolf, Joseph C. Corbo, Bernhard H. F. Weber · 2011 · Human Molecular Genetics
Promoter variants of the cannabinoid receptor 1 gene (CNR1) in interaction with 5‐HTTLPR affect the anxious phenotype
Judit Lazáry, Áron Lazáry, Xénia Gonda, Anita Benkő, Eszter Molnár, László Hunyady, Gabriella Juhász, György Bagdy · 2009 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
Applications of Linkage Disequilibrium and Association Mapping in Maize
Elhan S. Ersoz, Jianming Yu, Edward S. Buckler · 2008 · Biotechnology in agriculture and forestry
Genetic variation in the IL-10 pathway modulates severity of acute graft-versus-host disease following hematopoietic cell transplantation: synergism between IL-10 genotype of patient and IL-10 receptor β genotype of donor
Ming‐Tseh Lin, Barry E. Storer, Paul J. Martin, Li‐Hui Tseng, Bryan M. Grogan, Pei‐Jer Chen, Lue Ping Zhao, John A. Hansen · 2005 · Blood
Toward understanding MHC disease associations: Partial resequencing of 46 distinct HLA haplotypes
Wade P. Smith, Quyen Vu, Shuying Sue Li, John A. Hansen, Lue Ping Zhao, Daniel E. Geraghty · 2006 · Genomics
Understanding the accuracy of statistical haplotype inference with sequence data of known phase
Andrés, Aida M., Clark, Andrew G., Shimmin, Lawrence, Boerwinkle, Eric, Sing, Charles F., Hixson, James E. · 2007 · Genetic Epidemiology
Genome‐wide association study of theta band event‐related oscillations identifies serotonin receptor geneHTR7influencing risk of alcohol dependence
Mark Zlojutro, Niklas Manz, Madhavi Rangaswamy, Xiaoling Xuei, Leah Flury Wetherill, Daniel L. Koller, Laura Jean Bierut, Alison Goate, VICTOR M. HESSELBROCK, Samuel Kuperman C et al. · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
Vincristine Pharmacokinetics Pathway And Neurotoxicity During Early Phases Of Treatment in Pediatric Acute Lymphoblastic Leukemia
Elixabet López-López, Ángela Gutiérrez-Camino, Itziar Astigarraga, Aurora Navajas, Aizpea Echebarria-Barona, Purificación García‐Miguel, Nagore García de Andoín, Carmen Lobo, Isabel Guerra‐Merino, Idoia Martín‐Guerrero et al. · 2016 · Pharmacogenomics
The evolution and expression of virulence
Dieter Ebert, James J. Bull · 2007 · Oxford University Press eBooks
A Genome-Wide Association Study Reveals Candidate Genes Related to Salt Tolerance in Rice (Oryza sativa) at the Germination Stage
Jie Yu, Weiguo Zhao, Wei Tong, Qiang He, Min-Young Yoon, Feng-Peng Li, Buung Choi, Eun-Beom Heo, Kyu‐Won Kim, Yong‐Jin Park · 2018 · International Journal of Molecular Sciences
Computing the Minimum Recombinant Haplotype Configuration from Incomplete Genotype Data on a Pedigree by Integer Linear Programming
Jing Li, Tao Jiang · 2005 · Journal of Computational Biology
Family‐based genetic association study of DLGAP3 in Tourette Syndrome
Jacquelyn N. Crane, Jesen A. Fagerness, Lisa Osiecki, Boyd Gunnell, S. Evelyn Stewart, David L. Pauls, Jeremiah M. Scharf · 2010 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
Prostate stem‐cell antigen gene is associated with diffuse and intestinal gastric cancer in Caucasians: Results from the EPIC‐EURGAST study
Núria Sala, Xavier Muñoz, Noémie Travier, Antonio Agudo, Eric J. Duell, Victor Rau Moreno, Kim Overvad, Anne Marie Tjønneland, Marie‐Christine Boutron‐Ruault, Françoise Clavel‐Chapelon et al. · 2011 · International Journal of Cancer
Racial Differences in the Association Between SNPs on 15q25.1, Smoking Behavior, and Risk of Non-small Cell Lung Cancer
Ann G. Schwartz, Michele L. Coté, Angela S. Wenzlaff, Susan J. Land, Christopher Ian Amos · 2009 · Journal of Thoracic Oncology
Polymorphisms in fatty acid metabolism-related genes are associated with colorectal cancer risk
Birgit Hoeft, Jakob Linseisen, Lars Beckmann, Karin Müller‐Decker, Federico Canzian, Anika Hüsing, Rudolf Kaaks, Ulla Birgitte Vogel, Marianne Uhre Jakobsen, Kim Overvad et al. · 2009 · Carcinogenesis
Regulatory Polymorphisms in the Cyclophilin A Gene, PPIA, Accelerate Progression to AIDS
Ping An, Li Hua Wang, Holli Hutcheson-Dilks, George W. Nelson, Sharyne M Donfield, James J. Goedert, Charles R. Rinaldo, Susan Buchbinder, Gregory Dale Kirk, Stephen J. O’Brien et al. · 2007 · PLoS Pathogens
Linkage Disequilibrium Testing When Linkage Phase Is Unknown
Daniel J. Schaid · 2004 · Genetics
Potential of marker selection to increase prediction accuracy of genomic selection in soybean (Glycine max L.)
Yansong Ma, Jochen Christoph Reif, Yong Jiang, Zixiang Wen, Dechun Wang, Zhangxiong Liu, Yong Guo, Shuhong Wei, Shuming Wang, Chunming Yang et al. · 2016 · Molecular Breeding
Single Marker and Haplotype-Based Association Analysis of Semolina and Pasta Colour in Elite Durum Wheat Breeding Lines Using a High-Density Consensus Map
Amidou N’Diaye, Jemanesh K. Haile, Aron T. Cory, F. R. Clarke, J. M. Clarke, R. E. Knox, Curtis Jerry Pozniak · 2017 · PLoS ONE
Loci, genes, and mechanisms associated with tolerance to ferrous iron toxicity in rice (Oryza sativa L.)
Elsa Matthus, Lin‐Bo Wu, Yoshiaki Ueda, Stefanie Höller, M. Becker, Michael Frei · 2015 · Theoretical and Applied Genetics
Common genetic variation in IGF1, IGFBP-1, and IGFBP-3 in relation to mammographic density: a cross-sectional study
Rulla M. Tamimi, David G. Cox, Peter L. Kraft, Michaël Pollak, Christopher A. Haiman, Iona C. Cheng, Matthew L. Freedman, Susan E. Hankinson, David J Hunter, Graham A. Colditz · 2007 · Breast Cancer Research
AN MDL METHOD FOR FINDING HAPLOTYPE BLOCKS AND FOR ESTIMATING THE STRENGTH OF HAPLOTYPE BLOCK BOUNDARIES
Mikko Koivisto, Markus Perola, Teppo Varilo, William Hennah, Jesper Ekelund, Margus Lukk, Leena Peltonen, Esko Ukkonen, Heikki Mannila · 2002 · Pacific Symposium on Biocomputing (PSB)
Nonreplication in Genetic Studies of Complex Diseases—Lessons Learned From Studies of Osteoporosis and Tentative Remedies
Hui Shen, Yongjun Liu, Pengyuan Liu, Robert R. Recker, Hong‐Wen Deng · 2005 · Journal of Bone and Mineral Research
Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population
Yun Freudenberg‐Hua, Jan Freudenberg, Nadine Kluck, Sven Cichon, Peter Propping, Markus Maria Nöthen · 2003 · Genome Research