David J Cutler

David J Cutler

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David J Cutler

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Blood-Derived DNA Methylation Signatures of Crohn's Disease and Severity of Intestinal Inflammation.

Gastroenterology 2019 06 16;156(8):2254-2265.e3. Epub 2019 Feb 16.

Genetics and Molecular Biology Program, Emory University, Atlanta, Georgia; Division of Pediatric Gastroenterology, Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, Georgia; Department of Human Genetics, Emory University, Atlanta, Georgia. Electronic address:

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http://dx.doi.org/10.1053/j.gastro.2019.01.270DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6529254PMC
June 2019

Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale.

Genome Biol 2018 02 6;19(1):14. Epub 2018 Feb 6.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.

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http://dx.doi.org/10.1186/s13059-018-1387-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801807PMC
February 2018

Testing Two Evolutionary Theories of Human Aging with DNA Methylation Data.

Genetics 2017 12 30;207(4):1547-1560. Epub 2017 Aug 30.

Department of Human Genetics, Emory University School of Medicine, Emory University, Atlanta, Georgia 30322.

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http://dx.doi.org/10.1534/genetics.117.300217DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5714465PMC
December 2017

Rigor of non-dairy galactose restriction in early childhood, measured by retrospective survey, does not associate with severity of five long-term outcomes quantified in 231 children and adults with classic galactosemia.

J Inherit Metab Dis 2017 11 10;40(6):813-821. Epub 2017 Jul 10.

Department of Human Genetics, Emory University School of Medicine, 3rd Floor Whitehead Bldg., 615 Michael St, Atlanta, GA, 30322, USA.

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http://dx.doi.org/10.1007/s10545-017-0067-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656392PMC
November 2017

Reply to Plüss et al.: The strength of PEMapper/PECaller lies in unbiased calling using large sample sizes.

Proc Natl Acad Sci U S A 2017 10 15;114(40):E8323. Epub 2017 Sep 15.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322;

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http://dx.doi.org/10.1073/pnas.1714535114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5635938PMC
October 2017

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the Locus on 5q14.3.

Circ Cardiovasc Genet 2017 Oct;10(5)

From the Department of Genetics (T.G., J.H.C., H.N., C.L.C., T.W., B.E.M.) and Department of Epidemiology and Population Health (T.W.), Albert Einstein College of Medicine, Bronx, NY; Center for Human Genetics, Facultad de Medicina Clinica Alemana Universidad del Desarrollo, Santiago, Chile (G.M.R.); Division of Human Genetics (D.M.M.M., E.E.M., E.Z., B.S.E.), Division of Cardiology (E.G.), and Department of Pediatrics (E.G.), Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia; Department of Genetics, Wroclaw Medical University, Poland (A.B.); Clinical Genetics Research Program, Center for Addiction and Mental Health and Department of Psychiatry, University of Toronto (A.S.B., E.W.C.C.); Dalglish Family 22q Clinic, Department of Psychiatry and Toronto General Research Institute, University Health Network, Canada (A.S.B.); Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Canada (A.S.B.); Center for Human Genetics, University of Leuven (KU Leuven), Belgium (A.S., J.V., K.D.); The Child Psychiatry Division, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel (D.G.); Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Israel (D.G., M.C., E.M.); Felsenstein Medical Research Center, Sackler Faculty of Medicine, Tel Aviv University, Petah Tikva, Israel (M.C., E.M.); Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Switzerland (M.S., S.E.); Department of Genetic Medicine, UNIGE and iGE3 Institute of Genetics and Genomics of Geneva, University of Geneva Medical Center, Switzerland (S.E.A.); Marcus Autism Center, Children's Healthcare of Atlanta, GA (K.C.); Division of Pediatric Cardiovascular Surgery, Children's Hospital of Wisconsin, Milwaukee (A.T.-M., M.E.M.); Department of Surgery, Medical College of Wisconsin, Milwaukee (A.T.-M., M.E.M.); Department of Medical Genetics, Bambino Gesù Hospital, Rome, Italy (M.C.D., B.D.); Department of Pediatrics, La Sapienza University of Rome, Italy (B.M.); Department of Medical Genetics, Aix Marseille University, APHM, GMGF, Timone Hospital, France (N.P., T.B.); Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California at Los Angeles (L.K.-W., C.E.B.); Department of Genetics, Polish Mother's Memorial Hospital, Research Institute, Łódź, Poland (M.P., W.H.); Department of Cardiology and Division of Genetics, Boston Children's Hospital, MA (A.E.R.); M.I.N.D. Institute and Department of Psychiatry and Behavioral Sciences (F.T.) and M.I.N.D. Institute and Department of Biochemistry and Molecular Medicine (T.J.S.), University of California, Davis; Department of Psychiatry and Psychology, University of Maastricht, The Netherlands (E.D.A.V.D., T.A.v.A.); Department of Psychiatry and Behavioral Sciences, and Program in Neuroscience, SUNY Upstate Medical University, Syracuse, NY (T.A.v.A., W.R.K.); Department of Human Genetics, Emory University School of Medicine, Atlanta, GA (H.R.J., D.J.C.); Department of Biostatistics and Bioinformatics, Emory University Rollins School of Public Health, Atlanta, GA (H.R.J.); and Human Genetics Center and Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, TX (A.J.A., L.E.M.).

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http://dx.doi.org/10.1161/CIRCGENETICS.116.001690DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5647121PMC
October 2017

Integrating Next-Generation Genomic Sequencing and Mass Spectrometry To Estimate Allele-Specific Protein Abundance in Human Brain.

J Proteome Res 2017 09 9;16(9):3336-3347. Epub 2017 Aug 9.

Division of Neurology, Department of Veterans Affairs Medical Center , Decatur, Georgia 30033, United States.

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http://dx.doi.org/10.1021/acs.jproteome.7b00324DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5698003PMC
September 2017

PEMapper and PECaller provide a simplified approach to whole-genome sequencing.

Proc Natl Acad Sci U S A 2017 03 21;114(10):E1923-E1932. Epub 2017 Feb 21.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322;

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http://dx.doi.org/10.1073/pnas.1618065114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347547PMC
March 2017

Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.

Gastroenterology 2017 01 28;152(1):206-217.e2. Epub 2016 Sep 28.

Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia; Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia. Electronic address:

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http://dx.doi.org/10.1053/j.gastro.2016.09.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5164948PMC
January 2017

MPD: multiplex primer design for next-generation targeted sequencing.

BMC Bioinformatics 2017 Jan 5;18(1):14. Epub 2017 Jan 5.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street NE, Atlanta, GA, 30322, USA.

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http://dx.doi.org/10.1186/s12859-016-1453-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217220PMC
January 2017

Population genetics identifies challenges in analyzing rare variants.

Genet Epidemiol 2015 Mar 12;39(3):145-8. Epub 2015 Jan 12.

Department of Biostatistics and Bioinformatics, Emory University, Atlanta, Georgia, United States of America.

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http://doi.wiley.com/10.1002/gepi.21881
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http://dx.doi.org/10.1002/gepi.21881DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4366269PMC
March 2015

Synaptic, transcriptional and chromatin genes disrupted in autism.

Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease.

J Pediatr Gastroenterol Nutr 2014 May;58(5):561-8

*Department of Pediatrics †Department of Human Genetics, Emory University School of Medicine, Atlanta, GA ‡Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN §Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.

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http://dx.doi.org/10.1097/MPG.0000000000000302DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4277865PMC
May 2014

A comprehensive search for recombinogenic motifs in the human genome.

PLoS One 2013 23;8(4):e62920. Epub 2013 Apr 23.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0062920PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3633838PMC
November 2013

Common NOD2 risk variants in African Americans with Crohn's disease are due exclusively to recent Caucasian admixture.

Inflamm Bowel Dis 2012 Dec 22;18(12):2357-9. Epub 2012 Mar 22.

Division of Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1002/ibd.22944DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3392535PMC
December 2012

Identification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorder.

Mol Autism 2012 Sep 28;3(1). Epub 2012 Sep 28.

Department of Human Genetics, Emory University School of Medicine, Whitehead Biomedical Research Building, Suite 301, Atlanta, 30322, GA, USA.

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http://dx.doi.org/10.1186/2040-2392-3-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3492087PMC
September 2012

Population demographic history can cause the appearance of recombination hotspots.

Am J Hum Genet 2012 May;90(5):774-83

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1016/j.ajhg.2012.03.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3376637PMC
May 2012

Paraoxonase-1 polymorphisms in Alzheimer's disease, Parkinson's disease, and AD-PD spectrum diseases.

Neurobiol Aging 2012 Jan 13;33(1):204.e13-5. Epub 2010 Oct 13.

Department of Neurology, Emory University, Atlanta, GA 30322-1047, USA.

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http://dx.doi.org/10.1016/j.neurobiolaging.2010.08.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3021799PMC
January 2012

Autosomal recessive causes likely in early-onset Alzheimer disease.

Arch Neurol 2012 Jan 12;69(1):59-64. Epub 2011 Sep 12.

Veterans Affairs Medical Center, Emory University School of Medicine, Atlanta, Georgia.

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http://dx.doi.org/10.1001/archneurol.2011.221DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332307PMC
January 2012

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

G3 (Bethesda) 2012 Jan 1;2(1):143-50. Epub 2012 Jan 1.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322.

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http://dx.doi.org/10.1534/g3.111.001669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276189PMC
January 2012

Multiplex Chromosomal Exome Sequencing Accelerates Identification of ENU-Induced Mutations in the Mouse.

G3 (Bethesda) 2012 Jan 1;2(1):143-50. Epub 2012 Jan 1.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia 30322.

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http://dx.doi.org/10.1534/g3.111.001669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276189PMC
January 2012

Targeted sequencing of the human X chromosome exome.

Genomics 2011 Oct 16;98(4):260-5. Epub 2011 Apr 16.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30322, USA

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http://dx.doi.org/10.1016/j.ygeno.2011.04.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154473PMC
October 2011

SeqAnt: a web service to rapidly identify and annotate DNA sequence variations.

BMC Bioinformatics 2010 Sep 20;11:471. Epub 2010 Sep 20.

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA.

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http://dx.doi.org/10.1186/1471-2105-11-471DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955049PMC
September 2010

To pool, or not to pool?

Genetics 2010 Sep;186(1):41-3

Department of Human Genetics, Emory University School of Medicine, Atlanta, GA 30222, USA.

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http://dx.doi.org/10.1534/genetics.110.121012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2940305PMC
September 2010

Empirical evaluation of oligonucleotide probe selection for DNA microarrays.

PLoS One 2010 Mar 29;5(3):e9921. Epub 2010 Mar 29.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0009921PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2847945PMC
March 2010

Variation in the lymphotoxin-alpha/tumor necrosis factor locus modifies risk of erythema nodosum in sarcoidosis.

J Invest Dermatol 2009 Aug 19;129(8):1921-6. Epub 2009 Feb 19.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1038/jid.2008.456DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877485PMC
August 2009

Simultaneous neutron scattering and Raman scattering.

Appl Spectrosc 2009 Jul;63(7):727-32

STFC, ISIS Pulsed Neutron Facility, Chilton, Didcot, Oxon, OX11 0QX.

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http://journals.sagepub.com/doi/10.1366/000370209788701107
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http://dx.doi.org/10.1366/000370209788701107DOI Listing
July 2009

What is a suitable dissolution method for drug nanoparticles?

Pharm Res 2008 Jul 5;25(7):1696-701. Epub 2008 Mar 5.

Advanced Drug Delivery Group, Faculty of Pharmacy, The University of Sydney, Sydney, NSW 2006, Australia.

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http://dx.doi.org/10.1007/s11095-008-9560-0DOI Listing
July 2008

Interaction between a novel TGFB1 haplotype and CFTR genotype is associated with improved lung function in cystic fibrosis.

Hum Mol Genet 2008 Jul 17;17(14):2228-37. Epub 2008 Apr 17.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1093/hmg/ddn123DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2902288PMC
July 2008

Dissolution kinetic behavior of drug nanoparticles and their conformity to the diffusion model.

Langmuir 2008 Jul 18;24(14):7538-44. Epub 2008 Jun 18.

Advanced Drug Delivery Group, Faculty of Pharmacy, A15, The University of Sydney, NSW 2006, Australia.

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http://pubs.acs.org/doi/abs/10.1021/la800694j
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http://dx.doi.org/10.1021/la800694jDOI Listing
July 2008

Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays.

Genome Biol 2008 Apr 3;9(4):R63. Epub 2008 Apr 3.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, N. Broadway, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1186/gb-2008-9-4-r63DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2643934PMC
April 2008

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Am J Hum Genet 2008 Jan;82(1):160-4

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://dx.doi.org/10.1016/j.ajhg.2007.09.015DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253968PMC
January 2008

Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression.

Am J Med Genet B Neuropsychiatr Genet 2007 Dec;144B(8):1079-82

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

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http://dx.doi.org/10.1002/ajmg.b.30514DOI Listing
December 2007

Microarray-based genomic selection for high-throughput resequencing.

Nat Methods 2007 Nov 14;4(11):907-9. Epub 2007 Oct 14.

Department of Human Genetics, Emory University School of Medicine, 615 Michael Street, Suite 301, Atlanta, Georgia 30322, USA.

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http://dx.doi.org/10.1038/nmeth1109DOI Listing
November 2007

Simultaneous discovery and testing of deletions for disease association in SNP genotyping studies.

Am J Hum Genet 2007 Oct 14;81(4):684-99. Epub 2007 Aug 14.

McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S000292970763046
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http://dx.doi.org/10.1086/520823DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2227920PMC
October 2007

A second generation human haplotype map of over 3.1 million SNPs.

Authors:
Kelly A Frazer Dennis G Ballinger David R Cox David A Hinds Laura L Stuve Richard A Gibbs John W Belmont Andrew Boudreau Paul Hardenbol Suzanne M Leal Shiran Pasternak David A Wheeler Thomas D Willis Fuli Yu Huanming Yang Changqing Zeng Yang Gao Haoran Hu Weitao Hu Chaohua Li Wei Lin Siqi Liu Hao Pan Xiaoli Tang Jian Wang Wei Wang Jun Yu Bo Zhang Qingrun Zhang Hongbin Zhao Hui Zhao Jun Zhou Stacey B Gabriel Rachel Barry Brendan Blumenstiel Amy Camargo Matthew Defelice Maura Faggart Mary Goyette Supriya Gupta Jamie Moore Huy Nguyen Robert C Onofrio Melissa Parkin Jessica Roy Erich Stahl Ellen Winchester Liuda Ziaugra David Altshuler Yan Shen Zhijian Yao Wei Huang Xun Chu Yungang He Li Jin Yangfan Liu Yayun Shen Weiwei Sun Haifeng Wang Yi Wang Ying Wang Xiaoyan Xiong Liang Xu Mary M Y Waye Stephen K W Tsui Hong Xue J Tze-Fei Wong Luana M Galver Jian-Bing Fan Kevin Gunderson Sarah S Murray Arnold R Oliphant Mark S Chee Alexandre Montpetit Fanny Chagnon Vincent Ferretti Martin Leboeuf Jean-François Olivier Michael S Phillips Stéphanie Roumy Clémentine Sallée Andrei Verner Thomas J Hudson Pui-Yan Kwok Dongmei Cai Daniel C Koboldt Raymond D Miller Ludmila Pawlikowska Patricia Taillon-Miller Ming Xiao Lap-Chee Tsui William Mak You Qiang Song Paul K H Tam Yusuke Nakamura Takahisa Kawaguchi Takuya Kitamoto Takashi Morizono Atsushi Nagashima Yozo Ohnishi Akihiro Sekine Toshihiro Tanaka Tatsuhiko Tsunoda Panos Deloukas Christine P Bird Marcos Delgado Emmanouil T Dermitzakis Rhian Gwilliam Sarah Hunt Jonathan Morrison Don Powell Barbara E Stranger Pamela Whittaker David R Bentley Mark J Daly Paul I W de Bakker Jeff Barrett Yves R Chretien Julian Maller Steve McCarroll Nick Patterson Itsik Pe'er Alkes Price Shaun Purcell Daniel J Richter Pardis Sabeti Richa Saxena Stephen F Schaffner Pak C Sham Patrick Varilly David Altshuler Lincoln D Stein Lalitha Krishnan Albert Vernon Smith Marcela K Tello-Ruiz Gudmundur A Thorisson Aravinda Chakravarti Peter E Chen David J Cutler Carl S Kashuk Shin Lin Gonçalo R Abecasis Weihua Guan Yun Li Heather M Munro Zhaohui Steve Qin Daryl J Thomas Gilean McVean Adam Auton Leonardo Bottolo Niall Cardin Susana Eyheramendy Colin Freeman Jonathan Marchini Simon Myers Chris Spencer Matthew Stephens Peter Donnelly Lon R Cardon Geraldine Clarke David M Evans Andrew P Morris Bruce S Weir Tatsuhiko Tsunoda James C Mullikin Stephen T Sherry Michael Feolo Andrew Skol Houcan Zhang Changqing Zeng Hui Zhao Ichiro Matsuda Yoshimitsu Fukushima Darryl R Macer Eiko Suda Charles N Rotimi Clement A Adebamowo Ike Ajayi Toyin Aniagwu Patricia A Marshall Chibuzor Nkwodimmah Charmaine D M Royal Mark F Leppert Missy Dixon Andy Peiffer Renzong Qiu Alastair Kent Kazuto Kato Norio Niikawa Isaac F Adewole Bartha M Knoppers Morris W Foster Ellen Wright Clayton Jessica Watkin Richard A Gibbs John W Belmont Donna Muzny Lynne Nazareth Erica Sodergren George M Weinstock David A Wheeler Imtaz Yakub Stacey B Gabriel Robert C Onofrio Daniel J Richter Liuda Ziaugra Bruce W Birren Mark J Daly David Altshuler Richard K Wilson Lucinda L Fulton Jane Rogers John Burton Nigel P Carter Christopher M Clee Mark Griffiths Matthew C Jones Kirsten McLay Robert W Plumb Mark T Ross Sarah K Sims David L Willey Zhu Chen Hua Han Le Kang Martin Godbout John C Wallenburg Paul L'Archevêque Guy Bellemare Koji Saeki Hongguang Wang Daochang An Hongbo Fu Qing Li Zhen Wang Renwu Wang Arthur L Holden Lisa D Brooks Jean E McEwen Mark S Guyer Vivian Ota Wang Jane L Peterson Michael Shi Jack Spiegel Lawrence M Sung Lynn F Zacharia Francis S Collins Karen Kennedy Ruth Jamieson John Stewart

Nature 2007 Oct;449(7164):851-61

The Scripps Research Institute, 10550 North Torrey Pines Road MEM275, La Jolla, California 92037, USA.

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https://www.genome.gov/Pages/Newsroom/CurrentNewsReleases/In
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http://www.nature.com/doifinder/10.1038/nature06258
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http://dx.doi.org/10.1038/nature06258DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2689609PMC
October 2007

Genome-wide detection and characterization of positive selection in human populations.

Authors:
Pardis C Sabeti Patrick Varilly Ben Fry Jason Lohmueller Elizabeth Hostetter Chris Cotsapas Xiaohui Xie Elizabeth H Byrne Steven A McCarroll Rachelle Gaudet Stephen F Schaffner Eric S Lander Kelly A Frazer Dennis G Ballinger David R Cox David A Hinds Laura L Stuve Richard A Gibbs John W Belmont Andrew Boudreau Paul Hardenbol Suzanne M Leal Shiran Pasternak David A Wheeler Thomas D Willis Fuli Yu Huanming Yang Changqing Zeng Yang Gao Haoran Hu Weitao Hu Chaohua Li Wei Lin Siqi Liu Hao Pan Xiaoli Tang Jian Wang Wei Wang Jun Yu Bo Zhang Qingrun Zhang Hongbin Zhao Hui Zhao Jun Zhou Stacey B Gabriel Rachel Barry Brendan Blumenstiel Amy Camargo Matthew Defelice Maura Faggart Mary Goyette Supriya Gupta Jamie Moore Huy Nguyen Robert C Onofrio Melissa Parkin Jessica Roy Erich Stahl Ellen Winchester Liuda Ziaugra David Altshuler Yan Shen Zhijian Yao Wei Huang Xun Chu Yungang He Li Jin Yangfan Liu Yayun Shen Weiwei Sun Haifeng Wang Yi Wang Ying Wang Xiaoyan Xiong Liang Xu Mary M Y Waye Stephen K W Tsui Hong Xue J Tze-Fei Wong Luana M Galver Jian-Bing Fan Kevin Gunderson Sarah S Murray Arnold R Oliphant Mark S Chee Alexandre Montpetit Fanny Chagnon Vincent Ferretti Martin Leboeuf Jean-François Olivier Michael S Phillips Stéphanie Roumy Clémentine Sallée Andrei Verner Thomas J Hudson Pui-Yan Kwok Dongmei Cai Daniel C Koboldt Raymond D Miller Ludmila Pawlikowska Patricia Taillon-Miller Ming Xiao Lap-Chee Tsui William Mak You Qiang Song Paul K H Tam Yusuke Nakamura Takahisa Kawaguchi Takuya Kitamoto Takashi Morizono Atsushi Nagashima Yozo Ohnishi Akihiro Sekine Toshihiro Tanaka Tatsuhiko Tsunoda Panos Deloukas Christine P Bird Marcos Delgado Emmanouil T Dermitzakis Rhian Gwilliam Sarah Hunt Jonathan Morrison Don Powell Barbara E Stranger Pamela Whittaker David R Bentley Mark J Daly Paul I W de Bakker Jeff Barrett Yves R Chretien Julian Maller Steve McCarroll Nick Patterson Itsik Pe'er Alkes Price Shaun Purcell Daniel J Richter Pardis Sabeti Richa Saxena Stephen F Schaffner Pak C Sham Patrick Varilly David Altshuler Lincoln D Stein Lalitha Krishnan Albert Vernon Smith Marcela K Tello-Ruiz Gudmundur A Thorisson Aravinda Chakravarti Peter E Chen David J Cutler Carl S Kashuk Shin Lin Gonçalo R Abecasis Weihua Guan Yun Li Heather M Munro Zhaohui Steve Qin Daryl J Thomas Gilean McVean Adam Auton Leonardo Bottolo Niall Cardin Susana Eyheramendy Colin Freeman Jonathan Marchini Simon Myers Chris Spencer Matthew Stephens Peter Donnelly Lon R Cardon Geraldine Clarke David M Evans Andrew P Morris Bruce S Weir Tatsuhiko Tsunoda Todd A Johnson James C Mullikin Stephen T Sherry Michael Feolo Andrew Skol Houcan Zhang Changqing Zeng Hui Zhao Ichiro Matsuda Yoshimitsu Fukushima Darryl R Macer Eiko Suda Charles N Rotimi Clement A Adebamowo Ike Ajayi Toyin Aniagwu Patricia A Marshall Chibuzor Nkwodimmah Charmaine D M Royal Mark F Leppert Missy Dixon Andy Peiffer Renzong Qiu Alastair Kent Kazuto Kato Norio Niikawa Isaac F Adewole Bartha M Knoppers Morris W Foster Ellen Wright Clayton Jessica Watkin Richard A Gibbs John W Belmont Donna Muzny Lynne Nazareth Erica Sodergren George M Weinstock David A Wheeler Imtaz Yakub Stacey B Gabriel Robert C Onofrio Daniel J Richter Liuda Ziaugra Bruce W Birren Mark J Daly David Altshuler Richard K Wilson Lucinda L Fulton Jane Rogers John Burton Nigel P Carter Christopher M Clee Mark Griffiths Matthew C Jones Kirsten McLay Robert W Plumb Mark T Ross Sarah K Sims David L Willey Zhu Chen Hua Han Le Kang Martin Godbout John C Wallenburg Paul L'Archevêque Guy Bellemare Koji Saeki Hongguang Wang Daochang An Hongbo Fu Qing Li Zhen Wang Renwu Wang Arthur L Holden Lisa D Brooks Jean E McEwen Mark S Guyer Vivian Ota Wang Jane L Peterson Michael Shi Jack Spiegel Lawrence M Sung Lynn F Zacharia Francis S Collins Karen Kennedy Ruth Jamieson John Stewart

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