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

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  1. Genetic support for a quantitative trait nucleotide in the ABCG2 gene affecting milk composition of dairy cattle
    Hanne Gro Olsen, Heidi Nilsen, Ben J. Hayes, Paul R. Berg, Morten Svendsen, Sigbjørn Lien, T.H.E. Meuwissen · 2007 · BMC Genetics
  2. Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome
    Juliane 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
  3. Genetic epidemiology of type 1 diabetes
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  4. Genome-wide association study identifies novel loci associated with resistance to bovine tuberculosis
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    Nuala 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
  8. 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
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  11. Genetic variability in the mitochondrial serine proteaseHTRA2contributes to risk for Parkinson disease
    Veerle 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
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    B. 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
  13. The Association of Interleukin 6 Haplotype Clades With Mortality in Critically Ill Adults
    Ainsley M. Sutherland, Keith R. Walley, Sanjay Manocha, James A. Russell · 2005 · Archives of Internal Medicine
  14. Understanding human DNA sequence variation.
    K. Kidd, A. Pakstis, W. C. Speed, J. Kidd · 2004 · Journal of Heredity
  15. Association of TRPV4 gene polymorphisms with chronic obstructive pulmonary disease
    Guohua 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
  16. Evolutionary‐based association analysis using haplotype data
    Howard J. Seltman, Kathryn Roeder, Bernie Devlin · 2003 · Genetic Epidemiology
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  18. The molecular signature of selection underlying human adaptations
    Eugene E. Harris, Diogo Meyer · 2006 · American Journal of Physical Anthropology
  19. Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
    Derek 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
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    Matthew R. Nelson, George Marnellos, Stefan Kammerer, Carolyn R. Hoyal, Michael M. Shi, Charles R. Cantor, Andreas Dominik Braun · 2004 · Genome Research
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    Niels 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
  22. A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region
    Evelyn Png, Anbupalam Thalamuthu, Rick TH Ong, Harm Snippe, Greet J. Boland, Mark T. Seielstad · 2011 · Human Molecular Genetics
  23. Identification of major loci and genomic regions controlling acid and volatile content in tomato fruit: implications for flavor improvement
    Guillaume 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
  24. Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association study
    Yan 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
  25. Principal component analysis for selection of optimal SNP‐sets that capture intragenic genetic variation
    Benjamin Davies Horne, Nicola J. Camp · 2003 · Genetic Epidemiology
  26. Multiple Genes for Essential-Hypertension Susceptibility on Chromosome 1q
    Yen-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
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    Daniel L. Dries, Mark H Strong, Richard Cooper, Mark H. Drazner · 2002 · Journal of the American College of Cardiology
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    Xingguang Luο, Henry R. Kranzler, Lingjun Zuo, Jaakko Lappalainen, Bao‐Zhu Yang, Joel E. Gelernter · 2005 · Neuropsychopharmacology
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    Marcus 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
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    Alessandro Rinaldo, Silviu‐Alin Bacanu, Bernie Devlin, Vibhor A. Sonpar, Larry Wasserman, Kathryn Roeder · 2005 · Genetic Epidemiology
  31. Unexpected complexity in the haplotypes of commonly used inbred strains of laboratory mice
    Binnaz 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
  32. 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 participants
    Hamidovic, Ajna, Dlugos, Andrea, Skol, Andrew, Palmer, Abraham A., de Wit, Harriet · 2009 · Experimental and Clinical Psychopharmacology
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    James 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
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    Takashi 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
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  41. Candidate Gene Studies of Human Pain Mechanisms
    Inna Belfer, Tianxia Wu, Albert Kingman, Raj K. Krishnaraju, David A Goldman, Mitchell B. Max, David C. Warltier · 2004 · Anesthesiology
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    Orna 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
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    Hojin 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
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    Ling‐Ling Chen, Shengying Qin, Jing Xie, Jimin Tang, Lun Yang, Wen Shen, Xinzhi Zhao, Jing Du, Guang He, Guoyin Feng et al. · 2008 · Pharmacogenomics
  45. Generation and annotation of the DNA sequences of human chromosomes 2 and 4
    LaDeana 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
  46. 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
  47. Choosing SNPs using feature selection
    Tu Minh Phuong, Zhen Lin, Russ Biagio Altman · 2005 · IEEE Computational Systems Bioinformatics Conference (CSB)
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    Branwen J. Hennig, Anthony J. C. Fulford, Giorgio Sirugo, Pura Rayco‐Solon, Andrew Tym Hattersley, Timothy M. Frayling, Andrew M. Prentice · 2009 · BMC Medical Genetics
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    Benjamin Fry, John Maeda · 2004 · DSpace@MIT (Massachusetts Institute of Technology)
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    Yun 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
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    M. 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
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