The Structure of Haplotype Blocks in the Human Genome

Cited by (1,035)

Items 401–500 of 1,035

1. Genetic and Haplotypic Structure in 14 European and African Cattle Breeds
   Gautier, Mathieu, Faraut, Thomas, Moazami-Goudarzi, Katayoun, Navratil, Vincent, Foglio, Mario, Grohs, Cécile, Boland, Anne, Garnier, Jean-Guillaume, Boichard, Didier, Lathrop, G Mark et al. · 2007 · Genetics
2. Linkage disequilibrium patterns vary substantially among populations
   S. Sawyer, Namita Mukherjee, A. Pakstis, L. Feuk, J. Kidd, A. Brookes, K. Kidd · 2005 · European Journal of Human Genetics
3. Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25
   Lubitz, Steven A., Sinner, Moritz F., Lunetta, Kathryn L., Makino, Seiko, Pfeufer, Arne, Rahman, Rosanna, Veltman, Caroline E., Barnard, John, Bis, Joshua C., Danik, Stephan P. et al. · 2010 · Circulation
4. Multifactorial Etiology of Gastric Cancer
   Jovanny Zabaleta · 2012 · Methods in molecular biology
5. A candidate gene approach to searching for low-penetrance breast and prostate cancer genes
   David Hunter · 2005 · Nature reviews. Cancer
6. Statistical Tests for Admixture Mapping with Case-Control and Cases-Only Data
   Giovanni Montana, Jonathan K. Pritchard · 2004 · The American Journal of Human Genetics
7. The molecular basis of quantitative fibrinogen disorders
   Rosanna Asselta, Stefano Duga, Ml Tenchini · 2006 · Journal of Thrombosis and Haemostasis
8. MHC Haplotype Matching for Unrelated Hematopoietic Cell Transplantation
   Effie Wang Petersdorf, Mari Malkki, Ted Alan Gooley, Paul J. Martin, Zhen Guo · 2007 · PLoS Medicine
9. CRY2 Is Associated with Depression
   Catharina Lavebratt, Louise K. Sjöholm, Pia Soronen, Tiina Paunio, Marquis P. Vawter, William E. Bunney, Rolf Adolfsson, Yvonne Forsell, Joseph C. Wu, John R. Kelsoe et al. · 2010 · PLoS ONE
10. Candidate Gene Region for Polycystic Ovary Syndrome on Chromosome 19p13.2
    Margrit Urbanek, Abigail Woodroffe, Kathryn G. Ewens, Evanthia Diamanti‐Kandarakis, Richard S. Legro, Jerome F. Strauss, Andrea Elizabeth Dunaif, Richard S. Spielman · 2005 · The Journal of Clinical Endocrinology & Metabolism
11. A linkage disequilibrium map of the 1‐Mb 15q12 GABAA receptor subunit cluster and association to autism
    Jacob L. McCauley, Lana M. Olson, Ryan Delahanty, Taneem Amin, Erika L. Nurmi, Edward L. Organ, Michelle M. Jacobs, Susan E. Folstein, Jonathan L. Haines, James S. Sutcliffe · 2004 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
12. Association analysis identifies TLR7 and TLR8 as novel risk genes in asthma and related disorders
    Moller-Larsen, S, Nyegaard, M, Haagerup, A, Vestbo, J, Kruse, T A, Borglum, A D · 2008 · Thorax
13. Familial Aggregation of Common Sequence Variants on 15q24-25.1 in Lung Cancer
    Liu, Pengyuan, Vikis, Haris G., Wang, Daolong, Lu, Yan, Wang, Yian, Schwartz, Ann G., Pinney, Susan M., Yang, Ping, de Andrade, Mariza, Petersen, Gloria M. et al. · 2008 · JNCI: Journal of the National Cancer Institute
14. Mutations in SGOL1 cause a novel cohesinopathy affecting heart and gut rhythm
    Philippe Chétaille, Christoph Preuß, Silja Barbara Burkhard, Jean-Marc Côté, Christine Houde, Julie Castilloux, Jessica Piché, Natacha Gosset, Séverine Leclerc, Florian Wünnemann et al. · 2014 · Nature Genetics
15. Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis
    Nicola Whiffin, Fay J. Hosking, Susan Mary Farrington, Claire Palles, Sara E. Dobbins, Lina Zgaga, Amy Lloyd, Ben Kinnersley, Maggie Gorman, Albert Tenesa et al. · 2014 · Human Molecular Genetics
16. Genetic Variation in the Catechol-O-Methyltransferase (COMT) Gene and Morphine Requirements in Cancer Patients with Pain
    Trude Teoline Nausthaug Rakvåg, Joy R. Ross, Hiroe Sato, Frank Skorpen, Stein Kaasa, Pål Klepstad · 2008 · Molecular Pain
17. A Novel Tiller Angle Gene, TAC3, together with TAC1 and D2 Largely Determine the Natural Variation of Tiller Angle in Rice Cultivars
    Haijiao Dong, Hu Zhao, Weibo Xie, Zhongmin Han, Guangwei Li, Wen Yao, Xufeng Bai, Yong Hu, Zilong Guo, Kai Lü et al. · 2016 · PLoS Genetics
18. Performance of Single Nucleotide Polymorphisms versus Haplotypes for Genome-Wide Association Analysis in Barley
    Aaron Joel Lorenz, Martha T. Hamblin, Jean‐Luc Jannink · 2010 · PLoS ONE
19. Association between two µ-opioid receptor gene (OPRM1) haplotype blocks and drug or alcohol dependence
    Huiping Zhang, Xingguang Luο, Henry R. Kranzler, Jaakko Lappalainen, Bao‐Zhu Yang, Evgeny M. Krupitsky, Edwin E. Zvartau, Joel E. Gelernter · 2006 · Human Molecular Genetics
20. Polygenic Type 2 Diabetes Prediction at the Limit of Common Variant Detection
    Jason L. Vassy, Marie‐France Hivert, Bianca Porneala, Marco Dauriz, José C. Florez, Josée Dupuis, David S. Siscovick, Myriam Fornage, Laura J. Rasmussen‐Torvik, Claude Bouchard et al. · 2014 · Diabetes
21. The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts
    Helen N. Lyon, Valur Emilsson, Anke Hinney, Iris M. Heid, Jessica Ann Lasky-Su, Xiaofeng Zhu, Guðmar Þorleifsson, Steinunn Gunnarsdottir, G. Bragi Walters, Unnur Þorsteinsdóttir et al. · 2007 · PLoS Genetics
22. Widespread balancing selection and pathogen-driven selection at blood group antigen genes
    Matteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, Stefania Riva, Giacomo P. Comi, Giorgia Menozzi, Nereo Bresolin, Manuela Sironi · 2008 · Genome Research
23. Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population
    Arne Pfeufer, Shapour Jalilzadeh, Siegfried Perz, Jakob C. Mueller, Martin Hinterseer, Thomas Illig, Mahmut Akyol, Cornelia Huth, Andreas Schöpfer-Wendels, Bernhard Kuch et al. · 2005 · Circulation Research
24. A model for the comprehensive investigation of a chronic autoimmune disease: The multiple sclerosis CLIMB study
    Susan A. Gauthier, Bonnie I. Glanz, Micha Mandel, Howard L. Weiner · 2006 · Autoimmunity Reviews
25. Genetical genomic determinants of alcohol consumption in rats and humans
    WHO/ISBRA Study on State and Trait Markers of Alcoholism, Boris Tabakoff, Laura M. Saba, Morton P. Printz, Pamela L. Flodman, Colin A. Hodgkinson, David A Goldman, George F. Koob, Heather N. Richardson, Katerina J. Kechris et al. · 2009 · BMC Biology
26. Digital genotyping and haplotyping with polymerase colonies
    Robi David Mitra, Vincent L. Butty, Jay Shendure, Benjamin R. Williams, David E. Housman, George McDonald Church · 2003 · Proceedings of the National Academy of Sciences
27. Novel Polymorphisms in the Myosin Light Chain Kinase Gene Confer Risk for Acute Lung Injury
    Li Gao, Audrey Virginia Grant, Indrani Halder, Roy G. Brower, Jonathan Sevransky, James P. Maloney, Marc M. Moss, Carl B. Shanholtz, Charles Ryan Yates, Gianfranco Umberto Meduri et al. · 2006 · American Journal of Respiratory Cell and Molecular Biology
28. Analysis of Association Between the Serotonin Transporter and Antidepressant Response in a Large Clinical Sample
    Jeffrey B. Kraft, Eric J Peters, Susan L. Slager, G. Douglas Jenkins, Megan S. Reinalda, Patrick J. McGrath, Steven P. Hamilton · 2006 · Biological Psychiatry
29. Association of AKT1 with schizophrenia confirmed in a Japanese population
    Masashi Ikeda, Nakao Iwata, Tatsuyo Suzuki, Tsuyoshi Kitajima, Yoshio Yamanouchi, Yoko Kinoshita, Toshiya Inada, Norio Ozaki · 2004 · Biological Psychiatry
30. A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1
    Laura Fachal, Antonio Gómez‐Caamaño, Gillian C. Barnett, Paula Peleteiro, Ana M. Carballo, Patricia Calvo, Sarah L. Kerns, Manuel Sánchez-García, Ramón Lobato-Busto, Leila Dorling et al. · 2014 · Nature Genetics
31. Genetic Polymorphisms in Base-Excision Repair Pathway Genes and Risk of Breast Cancer
    Yawei Zhang, Polly A. Newcomb, Kathleen M. Egan, Linda T. Titus-Ernstoff, Stephen Jacob Chanock, Robert Alan Welch, Louise Annette Brinton, Jolanta Lissowska, Alicja Bardin‐Mikolajczak, Beata Pepłońska et al. · 2006 · Cancer Epidemiology Biomarkers & Prevention
32. A comprehensive haplotype analysis of CYP19 and breast cancer risk: the Multiethnic Cohort
    C.A. Haiman · 2003 · Human Molecular Genetics
33. Association Analysis in African Americans of European-Derived Type 2 Diabetes Single Nucleotide Polymorphisms From Whole-Genome Association Studies
    Joshua P. Lewis, Nicholette D. Palmer, Pamela J. Hicks, Michèle M. Sale, Carl D. Langefeld, Barry I. Freedman, Jasmin Divers, Donald W. Bowden · 2008 · Diabetes
34. Assessing the performance of the haplotype block model of linkage disequilibrium.
    J. Wall, J. Pritchard · 2003 · American Journal of Human Genetics
35. Darwinian and demographic forces affecting human protein coding genes
    Rasmus Nielsen, Melissa J. Hubisz, Ines Hellmann, Dara G. Torgerson, Aida M. Andrés, Anders Albrechtsen, Ryan N. Gutenkunst, Mark D. Adams, Michele Cargill, Adam R. Boyko et al. · 2009 · Genome Research
36. Genetic Variation at the CYP19A1 Locus Predicts Circulating Estrogen Levels but not Breast Cancer Risk in Postmenopausal Women
    Christopher A. Haiman, Laure Dossus, Veronica Wendy Setiawan, Daniel O. Stram, Alison M. Dunning, Gilles D. Thomas, Michael J. Thun, Demetrius Albanes, David Altshuler, Eva Ardanáz et al. · 2007 · Cancer Research
37. Variation at the DAOA/G30 Locus Influences Susceptibility to Major Mood Episodes but Not Psychosis in Schizophrenia and Bipolar Disorder
    Nigel M. Williams, Elaine Green, Stuart MacGregor, Sarah Dwyer, Nadine Norton, Hywel J. Williams, Rachel Raybould, Detelina Grozeva, Marian L. Hamshere, Stanley Zammit et al. · 2006 · Archives of General Psychiatry
38. Selection of Genetic Markers for Association Analyses, Using Linkage Disequilibrium and Haplotypes
    Zhaoling Meng, Dmitri V. Zaykin, Chun‐Fang Xu, Michael J. Wagner, Margaret G. Ehm · 2003 · The American Journal of Human Genetics
39. The genetics of SLE: an update in the light of genome-wide association studies
    Benjamin Rhodes, Timothy James Vyse · 2008 · Rheumatology
40. Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1
    Audrey Sabbagh, Éric Pasmant, Ingrid Laurendeau, Béatrice Parfait, S. Barbarot, Bernard Guillot, P. Combemale, Salah Ferkal, Michel Vidaud, Patrick R. Aubourg et al. · 2009 · Human Molecular Genetics
41. Investigation of Neuroanatomical Differences Between Autism and AspergerSyndrome
    Linda J. Lotspeich, Hower Kwon, Cynthia Mills Schumann, Susanna L. Fryer, Beth L. Goodlin‐Jones, Michael H. Buonocore, Cathy R. Lammers, David G. Amaral, Allan L. Reiss · 2004 · Archives of General Psychiatry
42. Pharmacogenetics of drug‐induced liver injury†
    Stefan Russmann, Alexander Jetter, Gerd Achim Kullak-Ublick · 2010 · Hepatology
43. Association of GABRG3 With Alcohol Dependence
    Danielle M. Dick, Howard J. Edenberg, Xiaoling Xuei, Alison Goate, Samuel Kuperman C, Marc Alan Schuckit, Raymond Crowe, Tom L. Smith, Bernice Porjesz A, Henri Begleiter et al. · 2004 · Alcoholism Clinical and Experimental Research
44. A principal components regression approach to multilocus genetic association studies
    Kai Wang, Diana Abbott · 2007 · Genetic Epidemiology
45. Demography, Recombination Hotspot Intensity, and the Block Structure of Linkage Disequilibrium
    Michael P. H. Stumpf, David B. Goldstein · 2003 · Current Biology
46. Factors influencing recombination frequency and distribution in a human meiotic crossover hotspot
    Alec J. Jeffreys, Rita Neumann · 2005 · Human Molecular Genetics
47. Diabetes Mellitus, Glycemic Traits, and Cerebrovascular Disease
    Marios K. Georgakis, Eric L. Harshfield, Rainer Malik, Nora Franceschini, Claudia Langenberg, Nicholas J. Wareham, Hugh Stephen Markus, Martin Dichgans · 2021 · Neurology
48. Genotypes and haplotypes predisposing to myocardial infarction: a multilocus case-control study
    Martin D. Tobin · 2004 · European Heart Journal
49. Promoter Polymorphisms in the Plasma Glutathione Peroxidase ( GPx-3 ) Gene
    Barbara Voetsch, Richard C. Jin, Charlene Bierl, Kelly Suzanne Benke, Gili Kenet, Paolo Simioni, Filomena G. Ottaviano, Benito P. Damasceno, Joyce M. Annichino-Bizacchi, Diane E. Handy et al. · 2006 · Stroke
50. Dementia Risk in Parkinson Disease
    Núria Setó‐Salvia, Jordi Clarimón, Javier Pagonabarraga, Berta Pascual‐Sedano, Antònia Campolongo, Onofre Combarros, Jose Ignacio Mateo, Daniel Regaña, Merce Martínez-Corral, Marta Marquié et al. · 2011 · Archives of Neurology
51. Genetic Variants on Chromosome 15q25 Associated with Lung Cancer Risk in Chinese Populations
    Chen Hsuan Wu, Zhibin Hu, Dianke Yu, Liming Huang, Guangfu Jin, Jie Liang, Huan Guo, Wen Tan, Mingfeng Zhang, Ji Qian et al. · 2009 · Cancer Research
52. Evolutionary Selection and Constraint on Human Knee Chondrocyte Regulation Impacts Osteoarthritis Risk
    Daniel J. Richard, Zun Liu, Jiaxue Cao, Ata M. Kiapour, Jessica Willen, Siddharth Yarlagadda, Evelyn Jagoda, Vijaya B. Kolachalama, Jakob T. Sieker, Gary H. Chang et al. · 2020 · Cell
53. A single-nucleotide polymorphism tagging set for human drug metabolism and transport
    Kourosh R. Ahmadi, Mike E Weale, Zhengyu Xue, Nicole Soranzo, David P. Yarnall, J. D. Briley, Yuka Maruyama, Mikiro Kobayashi, Nicholas William Wood, Nigel K. Spurr et al. · 2004 · Nature Genetics
54. Genetic–epigenetic interactions in cis: a major focus in the post-GWAS era
    Catherine Do, Alyssa Shearer, Masako Suzuki, Mary Beth Terry, Joel E. Gelernter, John M. Greally, Benjamin Tycko · 2017 · Genome biology
55. Candidate Gene Analyses of Skeletal Variation in Malocclusion
    Clarissa Souza Gomes da Fontoura, Steven F. Miller, George L. Wehby, Brad A. Amendt, Nathan E. Holton, Thomas E. Southard, Veerajalandhar Allareddy, Lina M. Moreno Uribe · 2015 · Journal of Dental Research
56. Toll-like Receptor 1 Polymorphisms Increase Susceptibility to Candidemia
    Theo S. Plantinga, Melissa D. Johnson, William K. Scott, Esther van de Vosse, Digna R. Velez Edwards, P. Brian Smith, Barbara Dudley Alexander, John C. Yang, Dennis Kremer, Gregory M. Laird et al. · 2012 · The Journal of Infectious Diseases
57. A genetic linkage map for Arctic char (Salvelinus alpinus): evidence for higher recombination rates and segregation distortion in hybrid versus pure strain mapping parents
    Rachael A. Woram, Colin McGowan, J A Stout, Karim Gharbi, Moira M. Ferguson, Bjørn Høyheim, Evelyn A Davidson, W. S. Davidson, Caird E. Rexroad, Roy G. Danzmann · 2004 · Genome
58. Comprehensive identification and characterization of diallelic insertion-deletion polymorphisms in 330 human candidate genes.
    T. Bhangale, M. Rieder, Robert J. Livingston, D. Nickerson · 2005 · Human Molecular Genetics
59. <i>APOE</i> ε4 is not associated with Alzheimer's disease in elderly Nigerians
    Gureje, Oye, Ogunniyi, Adesola, Baiyewu, Olusegun, Price, Brandon, Unverzagt, Frederick W., Evans, Rebecca M., Smith‐Gamble, Valerie, Lane, Kathleen A., Gao, Sujuan, Hall, Kathleen S. et al. · 2006 · Annals of Neurology
60. Dectin-1 and DC-SIGN Polymorphisms Associated with Invasive Pulmonary Aspergillosis Infection
    Juan Sáinz, Carmen B. Lupiañez, Juana Segura-Catena, Lourdes Vázquez, Rafael Ríos, Salvador Oyonarte, Kari Hemminki, Asta Försti, Manuel Jurado · 2012 · PLoS ONE
61. Molecular pathogenesis of inflammatory bowel disease: Genotypes, phenotypes and personalized medicine
    Philippe Goyette, Catherine Labbé, Truc T. Trinh, Ramnik J. Xavier, John David Rioux · 2007 · Annals of Medicine
62. CTLA-4 gene polymorphisms in systemic lupus erythematosus: a highly significant association with a determinant in the promoter region
    Lori L. Hudson, Keith M. Rocca, Yeong Wook Song, Janardan P. Pandey · 2002 · Human Genetics
63. A comparison of linkage disequilibrium patterns and estimated population recombination rates across multiple populations.
    D. Evans, L. Cardon · 2005 · American Journal of Human Genetics
64. Extended linkage disequilibrium surrounding the hemoglobin E variant due to malarial selection
    Ohashi, Jun, Naka, Izumi, Patarapotikul, Jintana, Hananantachai, Hathairad, Brittenham, Gary, Looareesuwan, Sornchai, Clark, Andrew G., Tokunaga, Katsushi · 2004 · The American Journal of Human Genetics
65. Association screening of common and rare genetic variants by penalized regression
    Zhou, Hua, Sehl, Mary E., Sinsheimer, Janet S., Lange, Kenneth · 2010 · Bioinformatics
66. Genetic susceptibility for breast cancer: How many more genes to be found?
    R.A. Oldenburg, Hanne E.J. Meijers-Heijboer, Cees J. Cornelisse, Peter Devilee · 2007 · Critical Reviews in Oncology/Hematology
67. Importance of hedgehog interacting protein and other lung function genes in asthma
    Xingnan Li, Timothy D. Howard, Wendy C. Moore, Elizabeth J. Ampleford, Huashi Li, William W. Busse, William J. Calhoun, Mario Castro, Kian Fan Chung, SERPIL CEM ERZURUM et al. · 2011 · Journal of Allergy and Clinical Immunology
68. Identification of single nucleotide polymorphisms and haplotypes associated with yield and yield components in soybean (Glycine max) landraces across multiple environments
    Derong Hao, Hao Cheng, Zhitong Yin, Shiyou Cui, Dan Zhang, Hui Wang, Deyue Yu · 2011 · Theoretical and Applied Genetics
69. Association of the thyroid stimulating hormone receptor gene (TSHR) with Graves' disease
    Oliver J. Brand, Jeffrey C. Barrett, Matthew J. Simmonds, Paul Newby, Christopher J. McCabe, Christopher K Bruce, Boris P. Kysela, Jackie Carr‐Smith, Thomas Heiberg Brix, Penny J. Hunt et al. · 2009 · Human Molecular Genetics
70. Genetic Susceptibility Loci for Breast Cancer by Estrogen Receptor Status
    Montserrat García‐Closas, Stephen Jacob Chanock · 2008 · Clinical Cancer Research
71. The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans
    Rasika A. Mathias, Susan Sergeant, Ingo Ruczinski, Dara G. Torgerson, Christina E. Hugenschmidt, Meghan Kubala, Dhananjay M. Vaidya, Bhoom Suktitipat, Julie T. Ziegler, Priscilla Ivester et al. · 2011 · BMC Genetics
72. Significant Association of Catechol-O-Methyltransferase (COMT) Haplotypes with Nicotine Dependence in Male and Female Smokers of Two Ethnic Populations
    Joke Beuten, Thomas J. Payne, Jennie Z. Ma, Ming D. Li · 2005 · Neuropsychopharmacology
73. The Impact of Genomics on the Study of Natural Variation in Arabidopsis
    Justin Borevitz, Magnus Nordborg · 2003 · PLANT PHYSIOLOGY
74. The SERPINE2 Gene is Associated with Chronic Obstructive Pulmonary Disease in Two Large Populations
    Guohua Zhu, Liling L. Warren, Jennifer L. Aponte, Amund Gulsvik, Per Sigvald Bakke, Wayne H. Anderson, David A. Lomas, Edwin K. Silverman, Sreekumar G. Pillai · 2007 · American Journal of Respiratory and Critical Care Medicine
75. Optimal Haplotype Block-Free Selection of Tagging SNPs for Genome-Wide Association Studies
    Bjarni V. Halldórsson, Vineet Bafna, Ross Lippert, Russell S. Schwartz, Francisco M. De La Vega, Andrew G. Clark, Sorin Istrail · 2004 · Genome Research
76. Genetic approaches to stature, pubertal timing, and other complex traits
    Palmert, Mark R, Hirschhorn, Joel N · 2003 · Molecular Genetics and Metabolism
77. A Genome-Wide Association Study Identifies 2 Susceptibility Loci for Crohn's Disease in a Japanese Population
    Keiko Yamazaki, Junji Umeno, Atsushi Takahashi, Atsushi Hirano, Todd A. Johnson, Natsuhiko Kumasaka, Takashi Morizono, Naoya Hosono, Takaaki Kawaguchi, Masakazu Takazoe et al. · 2012 · Gastroenterology
78. Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease
    Sumantra Chatterjee, Ashish Kapoor, Jennifer A. Akiyama, Dallas R. Auer, Dongwon Lee, Stacey Gabriel, Courtney Berrios, Len A. Pennacchio, Aravinda Chakravarti · 2016 · Cell
79. An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus
    Gabriele Carmine DeLuca, S. V. Ramagopalan, Blanca M. Herrera, David Alexandre Dyment, Matthew R. Lincoln, Alexandre Montpetit, Maura Pugliatti, Martin Barnardo, NEIL J. RISCH, Adele Dessa Sadovnick et al. · 2007 · Proceedings of the National Academy of Sciences
80. On the Identification of Disease Mutations by the Analysis of Haplotype Similarity and Goodness of Fit
    Jung‐Ying Tzeng, Bernie Devlin, Larry Wasserman, Kathryn Roeder · 2003 · The American Journal of Human Genetics
81. Direct molecular haplotyping of long-range genomic DNA with M1-PCR
    Chunming Ding, Charles R. Cantor · 2003 · Proceedings of the National Academy of Sciences
82. Commercially Available Outbred Mice for Genome-Wide Association Studies
    Binnaz Yalcin, Jérôme Nicod, Amarjit Bhomra, Stuart I. Davidson, James Cleak, Laurent Farinelli, Magne Østerås, Adam Whitley, Yuan Wei, Xiangchao Gan et al. · 2010 · PLoS Genetics
83. Detecting rare variants for complex traits using family and unrelated data
    Xiaofeng Zhu, Tao Feng, Yali Li, Qing Ling Lu, Robert C. Elston · 2009 · Genetic Epidemiology
84. A Functional Single Nucleotide Polymorphism in Mucin 1, at Chromosome 1q22, Determines Susceptibility to Diffuse-Type Gastric Cancer
    Norihisa Saeki, Akira Saito, Il Ju Choi, Keitaro Matsuo, Sumiko Ohnami, Hirohiko Totsuka, Suenori Chiku, Aya Kuchiba, Yeon-Su Lee, Kyong‐Ah Yoon et al. · 2010 · Gastroenterology
85. Asthma and genes encoding components of the vitamin D pathway
    Yohan Bossé, Mathieu Lemire, Audrey H. Poon, Denise Daley, Jian‐Qing He, Andrew J. Sandford, John H. White, Alan L James, W. Musk, Lyle John Palmer et al. · 2009 · Respiratory Research
86. Genomics refutes an exclusively African origin of humans
    Vinayak Eswaran, Henry C Harpending, Alan R. Rogers · 2005 · Journal of Human Evolution
87. Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families.
    Edwin J. C. G. van den Oord, Patrick F. Sullivan, Y Jiang, Dermot Walsh, F. Anthony O’Neill, Kenneth S. Kendler, Brien P. Riley · 2003 · Molecular Psychiatry
88. Untitled work
    Turner · 2004 · 10.1002/(issn)1099-0968
89. Identification and functional analysis ofCITED2 mutations in patients with congenital heart defects
    Silke Sperling, Christina Grimm, Ilona Dunkel, Siegrun Mebus, Hans-Peter Sperling, Arno Ebner, Raffaello Galli, Hans Rudolf Lehrach, Christoph Fusch, Felix F. Berger et al. · 2005 · Human Mutation
90. Cholangiocarcinoma in primary sclerosing cholangitis is associated with NKG2D polymorphisms
    Espen Melum, Tom H. Karlsen, Erik Schrumpf, Annika M Bergquist, Erik Thorsby, Kirsten Muri Boberg, Benedicte A. Lie · 2007 · Hepatology
91. Significant Association of ANKK1 and Detection of a Functional Polymorphism with Nicotine Dependence in an African-American Sample
    Weihua Huang, Thomas J. Payne, Jennie Z. Ma, Joke Beuten, Randolph T. Dupont, Naohiro Inohara, Ming D. Li · 2008 · Neuropsychopharmacology
92. Quantitative Analysis of Nucleic Acids - the Last Few Years of Progress
    Chunming Ding, Charles R. Cantor · 2004 · BMB Reports
93. High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33
    Christopher I. Amos, W. V. Chen, A. Lee, Wentian Li, Marlena Kern, Robert Lundsten, Franak Batliwalla, Mark H. Wener, Elaine F. Remmers, Daniel L. Kastner et al. · 2006 · Genes and Immunity
94. Sub-genomic selection patterns as a signature of breeding in the allopolyploid Brassica napus genome
    Lunwen Qian, Wei Qian, Rod John Snowdon · 2014 · BMC Genomics
95. The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene
    Julie S. Snowden, Quan Hu, Sara J. Rollinson, Nicola A. Halliwell, Andrew Robinson, Yvonne S. Davidson, Parastoo Momeni, Atik Baborie, Timothy David Griffiths, Evelyn Jaros et al. · 2011 · Acta Neuropathologica
96. Genetic investigation of chromosome 5q GABAA receptor subunit genes in schizophrenia
    Tracey L. Petryshen, Frank A. Middleton, A R Tahl, Graham N. Rockwell, Shaun Purcell, Kimberly A. Aldinger, Andrew W. Kirby, Christopher P. Morley, Lindsay McGann, Karen L. Gentile et al. · 2005 · Molecular Psychiatry
97. Association of IRF5 in UK SLE families identifies a variant involved in polyadenylation
    Deborah S. Cunninghame Graham, Harinder Manku, Susanne Wagner, Julia Reid, Kirsten M. Timms, Alexander Gutin, Jerry S. S. Lanchbury, Tim J. Vyse · 2006 · Human Molecular Genetics
98. Deciphering the Ancient and Complex Evolutionary History of Human Arylamine N-Acetyltransferase Genes
    Étienne Patin, Luis Bruno Barreiro, Pardis Christine Sabeti, Frédéric Austerlitz, Francesca Luca, Antti Sajantila, Doron M. Behar, Ornella Semino, Anavaj Sakuntabhai, Nicole Guiso et al. · 2006 · The American Journal of Human Genetics
99. Transcription Factor 7-Like 2 ( TCF7L2 ) Is Associated With Gestational Diabetes Mellitus and Interacts With Adiposity to Alter Insulin Secretion in Mexican Americans
    Richard M. Watanabe, Hooman Allayee, Anny H. Xiang, Enrique Trigo, Jaana Hartiala, Jean M. Lawrence, Thomas A. Buchanan · 2007 · Diabetes
100. PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease
     Taherzadeh-Fard, Elahe, Saft, Carsten, Akkad, Denis A, Wieczorek, Stefan, Haghikia, Aiden, Chan, Andrew, Epplen, Jörg T, Arning, Larissa · 2011 · Molecular Neurodegeneration