Works by Chanock, Stephen

Results: 418

A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer.

Published in:

2010

By:

Jia, Yanbin;
Persson, Christina;
Hou, Lifang;
Zheng, Zongli;
Yeager, Meredith;
Lissowska, Jolanta;
Chanock, Stephen;
Chow, Wong-Ho;
Ye, Weimin;
Chanock, Stephen J

Publication type:

journal article

Relationship between interferon regulatory factor 4 genetic polymorphisms, measures of sun sensitivity and risk for non-Hodgkin lymphoma.

Published in:

2009

By:

Gathany, Allison;
Hartge, Patricia;
Davis, Scott;
Cerhan, James;
Severson, Richard;
Cozen, Wendy;
Rothman, Nathaniel;
Chanock, Stephen;
Wang, Sophia;
Gathany, Allison H;
Cerhan, James R;
Severson, Richard K;
Chanock, Stephen J;
Wang, Sophia S

Publication type:

journal article

Genetic variants in frizzled-related protein (FRZB) and the risk of colorectal neoplasia.

Published in:

2009

By:

Berndt, Sonja;
Huang, Wen-Yi;
Yeager, Meredith;
Weissfeld, Joel;
Chanock, Stephen;
Hayes, Richard;
Berndt, Sonja I;
Weissfeld, Joel L;
Chanock, Stephen J;
Hayes, Richard B

Publication type:

journal article

Identification of New Genetic Susceptibility Loci for Breast Cancer Through Consideration of Gene-Environment Interactions.

Published in:

Genetic Epidemiology, 2014, v. 38, n. 1, p. 84, doi. 10.1002/gepi.21771

By:

Schoeps, Anja;
Rudolph, Anja;
Seibold, Petra;
Dunning, Alison M.;
Milne, Roger L.;
Bojesen, Stig E.;
Swerdlow, Anthony;
Andrulis, Irene;
Brenner, Hermann;
Behrens, Sabine;
Orr, Nicholas;
Jones, Michael;
Ashworth, Alan;
Li, Jingmei;
Cramp, Helen;
Connley, Dan;
Czene, Kamila;
Darabi, Hatef;
Chanock, Stephen J.;
Lissowska, Jolanta

Publication type:

Article

Leveraging Family History in Population-Based Case-Control Association Studies.

Published in:

Genetic Epidemiology, 2014, v. 38, n. 2, p. 114, doi. 10.1002/gepi.21785

By:

Ghosh, Arpita;
Hartge, Patricia;
Kraft, Peter;
Joshi, Amit D.;
Ziegler, Regina G.;
Barrdahl, Myrto;
Chanock, Stephen J.;
Wacholder, Sholom;
Chatterjee, Nilanjan

Publication type:

Article

A Two-Platform Design for Next Generation Genome-Wide Association Studies.

Published in:

Genetic Epidemiology, 2012, v. 36, n. 4, p. 401, doi. 10.1002/gepi.21634

By:

Sampson, Joshua N.;
Jacobs, Kevin;
Wang, Zhaoming;
Yeager, Meredith;
Chanock, Stephen;
Chatterjee, Nilanjan

Publication type:

Article

Evaluation of polygenic risk scores for predicting breast and prostate cancer risk.

Published in:

Genetic Epidemiology, 2011, v. 35, n. 6, p. 506, doi. 10.1002/gepi.20600

By:

Machiela, Mitchell J.;
Chen, Chia-Yen;
Chen, Constance;
Chanock, Stephen J.;
Hunter, David J.;
Kraft, Peter

Publication type:

Article

Methods for detecting interactions between genetic polymorphisms and prenatal environment exposure with a mother-child design.

Published in:

Genetic Epidemiology, 2010, v. 34, n. 2, p. 125, doi. 10.1002/gepi.20441

By:

Wang, Shuang;
Zheng, Tian;
Chanock, Stephen;
Jedrychowski, Wieslaw;
Perera, Frederica P.

Publication type:

Article

Genetic background comparison using distance-based regression, with applications in population stratification evaluation and adjustment.

Published in:

Genetic Epidemiology, 2009, v. 33, n. 5, p. 432, doi. 10.1002/gepi.20396

By:

Li, Qizhai;
Wacholder, Sholom;
Hunter, David J.;
Hoover, Robert N.;
Chanock, Stephen;
Thomas, Gilles;
Yu, Kai

Publication type:

Article

HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research.

Published in:

Human Mutation, 2013, v. 34, n. 4, p. 657, doi. 10.1002/humu.22270

By:

Gonzaludo, Nina;
Zheng, Hong‐Xiang;
Wang, Jiucun;
Chanock, Stephen J.;
Jin, Li;
Scherer, Stephen;
Wijmenga, Cisca;
Kwok, Pui‐Yan;
Brookes, Anthony J.

Publication type:

Article

Human Variation 2.0: Using GWAS to Probe Intermediate Phenotypes.

Published in:

Human Mutation, 2013, v. 34, n. 3, p. iv, doi. 10.1002/humu.22181

By:

Chanock, Stephen J.

Publication type:

Article

HGV2011: Personalized genomic medicine meets the incidentalome.

Published in:

Human Mutation, 2012, v. 33, n. 3, p. 582, doi. 10.1002/humu.22008

By:

Wilson Sayres, Melissa A.;
Brookes, Anthony J.;
Chanock, Stephen J.;
Cheung, Vivian G.;
Goldstein, David B.;
Jin, Li;
Kwok, Pui-Yan

Publication type:

Article

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study.

Published in:

Human Mutation, 2011, v. 32, n. 2, p. 240, doi. 10.1002/humu.21398

By:

Marenne, Gaëlle;
Rodríguez-Santiago, Benjamín;
Closas, Montserrat García;
Pérez-Jurado, Luis;
Rothman, Nathaniel;
Rico, Daniel;
Pita, Guillermo;
Pisano, David G.;
Kogevinas, Manolis;
Silverman, Debra T.;
Valencia, Alfonso;
Real, Francisco X.;
Chanock, Stephen J.;
Génin, Emmanuelle;
Malats, Núria

Publication type:

Article

A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.

Published in:

Human Mutation, 2010, v. 31, n. 9, p. 1080, doi. 10.1002/humu.21322

By:

Wang, Hong-Ying;
Gopalan, Vivek;
Aksentijevich, Ivona;
Yeager, Meredith;
Ma, Chi Adrian;
Mohamoud, Yasmin Ali;
Quinones, Mariam;
Matthews, Casey;
Boland, Joseph;
Niemela, Julie E.;
Torgerson, Troy R.;
Giliani, Silvia;
Uzel, Gulbu;
Orange, Jordan S.;
Shapiro, Ralph;
Notarangelo, Luigi;
Ochs, Hans D.;
Fleisher, Thomas;
Kastner, Daniel;
Chanock, Stephen J.

Publication type:

Article

HGV2009 meeting: bigger and better studies provide more answers and more questions.

Published in:

Human Mutation, 2010, v. 31, n. 7, p. 886, doi. 10.1002/humu.21270

By:

Reekie, Katherine;
Metspalu, Andres;
Chanock, Stephen J.;
Liu, Edison T.;
Mardis, Elaine R.;
Scherer, Stephen W.;
Kwok, Pui-Yan;
Brookes, Anthony J.

Publication type:

Article

Genomic variation in a global village: Report of the 10th annual Human Genome Variation Meeting 2008.

Published in:

Human Mutation, 2009, v. 30, n. 7, p. 1134, doi. 10.1002/humu.21008

By:

Brookes, Anthony J.;
Chanock, Stephen J.;
Hudson, Thomas J.;
Peltonen, Leena;
Abecasis, Gonçalo;
Kwok, Pui-Yan;
Scherer, Stephen W.

Publication type:

Article

CYBB, an NADPH-oxidase gene: restricted diversity in humans and evidence for differential long-term purifying selection on transmembrane and cytosolic domains.

Published in:

Human Mutation, 2008, v. 29, n. 5, p. 623, doi. 10.1002/humu.20667

By:

Tarazona-Santos, Eduardo;
Bernig, Toralf;
Burdett, Laurie;
Magalhaes, Wagner C.S.;
Fabbri, Cristina;
Liao, Jason;
Redondo, Rodrigo A.F.;
Welch, Robert;
Yeager, Meredith;
Chanock, Stephen J.

Publication type:

Article

Validation of the performance of a comprehensive genotyping assay panel of single nucleotide polymorphisms in drug metabolism enzyme genes.

Published in:

Human Mutation, 2008, v. 29, n. 5, p. 750, doi. 10.1002/humu.20703

By:

Welch, Robert A.;
Lazaruk, Katherine;
Haque, Kashif A.;
Hyland, Fiona;
Xiao, Nianqing;
Wronka, Loni;
Burdett, Laura;
Chanock, Stephen J.;
Ingber, Daniel;
De La Vega, Francisco M.;
Yeager, Meredith

Publication type:

Article

Functional profiling of uncommon VCAM1 promoter polymorphisms prevalent in African American populations.

Published in:

Human Mutation, 2007, v. 28, n. 8, p. 824, doi. 10.1002/humu.20523

By:

Idelman, Gila;
Taylor, James G.;
Tongbai, Ron;
Chen, Renee A.;
Haggerty, Cynthia M.;
Bilke, Sven;
Chanock, Stephen J.;
Gardner, Kevin

Publication type:

Article

The ATM missense mutation p.Ser49Cys (c.146C>G) and the risk of breast cancer.

Published in:

Human Mutation, 2006, v. 27, n. 6, p. 538, doi. 10.1002/humu.20323

By:

Stredrick, Denise L.;
Garcia-Closas, Montserrat;
Pineda, Marbin A.;
Bhatti, Parveen;
Alexander, Bruce H.;
Doody, Michele M.;
Lissowska, Jolanta;
Peplonska, Beata;
Brinton, Louise A.;
Chanock, Stephen J.;
Struewing, Jeffery P.;
Sigurdson, Alice J.

Publication type:

Article

Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection.

Published in:

Human Mutation, 2006, v. 27, n. 2, p. 173, doi. 10.1002/humu.20289

By:

Fredman, David;
Sawyer, Sarah L.;
Strömqvist, Linda;
Mottagui-Tabar, Salim;
Kidd, Kenneth K.;
Wahlestedt, Claes;
Chanock, Stephen J.;
Brookes, Anthony J.

Publication type:

Article

Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint.

Published in:

Human Mutation, 2005, v. 26, n. 4, p. 343, doi. 10.1002/humu.20226

By:

Savage, Sharon A.;
Stewart, Brian J.;
Eckert, Andrew;
Kiley, Maureen;
Liao, Jason S.;
Chanock, Stephen J.

Publication type:

Article

Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex™ whole genome amplified DNA generated from multiple DNA sources.

Published in:

Human Mutation, 2005, v. 26, n. 3, p. 262, doi. 10.1002/humu.20213

By:

Bergen, Andrew W.;
Haque, Kashif A.;
Qi, Ying;
Beerman, Michael B.;
Garcia-Closas, Montserrat;
Rothman, Nathaniel;
Chanock, Stephen J.

Publication type:

Article

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants.

Published in:

Bioinformatics, 2015, v. 31, n. 21, p. 3555, doi. 10.1093/bioinformatics/btv402

By:

Machiela, Mitchell J.;
Chanock, Stephen J.

Publication type:

Article

White Blood Cell Count and Risk of Incident Lung Cancer in the UK Biobank.

Published in:

JNCI Cancer Spectrum, 2020, v. 4, n. 2, p. 1, doi. 10.1093/jncics/pkz102

By:

Wong, Jason Y Y;
Bassig, Bryan A;
Loftfield, Erikka;
Hu, Wei;
Freedman, Neal D;
Ji, Bu-tian;
Elliott, Paul;
Silverman, Debra T;
Chanock, Stephen J;
Rothman, Nathaniel;
Lan, Qing

Publication type:

Article

Predictors of mosaic chromosome Y loss and associations with mortality in the UK Biobank.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-30759-1

By:

Loftfield, Erikka;
Zhou, Weiyin;
Graubard, Barry I.;
Yeager, Meredith;
Chanock, Stephen J.;
Freedman, Neal D.;
Machiela, Mitchell J.

Publication type:

Article

Genetic Variation in a4GnT in Relation to Helicobacter pylori Serology and Gastric Cancer Risk.

Published in:

Helicobacter, 2009, v. 14, n. 5, p. 120, doi. 10.1111/j.1523-5378.2009.00708.x

By:

Zongli Zheng;
Yanbin Jia;
Lifang Hou;
Persson, Christina;
Yeager, Meredith;
Lissowska, Jolanta;
Chanock, Stephen J.;
Blaser, Martin;
Wong-Ho Chow;
Weimin Ye

Publication type:

Article

Genotypes and haplotypes in the insulin-like growth factors, their receptors and binding proteins in relation to plasma metabolic levels and mammographic density.

Published in:

BMC Medical Genomics, 2010, v. 3, p. 9, doi. 10.1186/1755-8794-3-9

By:

Biong, Margarethe;
Gram, Inger T.;
Brill, Ilene;
Johansen, Fredrik;
Solvang, Hiroko K.;
Alnaes, Grethe I. G.;
Fagerheim, Toril;
Bremnes, Yngve;
Chanock, Stephen J.;
Burdett, Laurie;
Yeager, Meredith;
Ursin, Giske;
Kristensen, Vessela N.

Publication type:

Article

A step toward slaying the hydra of second cancers.

Published in:

2011

By:

Morton, Lindsay M.;
Chanock, Stephen J.

Publication type:

Opinion

Effects of Macrophage Colony-Stimulating Factor on Antifungal Activity of Mononuclear Phagocytes against Aspergillus fumigatus.

Published in:

Journal of Infectious Diseases, 1995, v. 172, n. 4, p. 1028

By:

Roilides, Emmanuel;
Sein, Tin;
Holmes, Andrew;
Chanock, Stephen;
Blake, Cassann;
Pizzo, Philip A.;
Walsh, Thomas J.

Publication type:

Article

Human Rotaviruses and Genome RNA.

Published in:

Journal of Infectious Diseases, 1983, v. 148, n. 1, p. 49

By:

Chanock, Stephen J.;
Wenske, Elizabeth A.;
Fields, Bernard N.

Publication type:

Article

Chimeric EWSR1-FLI1 regulates the Ewing sarcoma susceptibility gene EGR2 via a GGAA microsatellite.

Published in:

Nature Genetics, 2015, v. 47, n. 9, p. 1073, doi. 10.1038/ng.3363

By:

Raynal, Virginie;
Surdez, Didier;
Delattre, Olivier;
Frio, Thomas Rio;
Perot, Gaëlle;
Lapouble, Eve;
Oberlin, Odile;
Reynaud, Stephanie;
Grünewald, Thomas G P;
Mirabeau, Olivier;
Jonker, Anneliene H;
Machiela, Mitchell J;
Chanock, Stephen J;
Alonso, Javier;
Le Deley, Marie-Cécile;
Véron, Amélie S;
Pierron, Gaëlle;
Aynaud, Marie-Ming;
Gilardi-Hebenstreit, Pascale;
Cidre-Aranaz, Florencia

Publication type:

Article

Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.

Published in:

Nature Genetics, 2015, v. 47, n. 8, p. 911, doi. 10.1038/ng.3341

By:

Childs, Erica J;
Scelo, Ghislaine;
Brennan, Paul;
Amundadottir, Laufey T;
Chanock, Stephen J;
Hoover, Robert N;
Bamlet, William R;
Chaffee, Kari G;
Oberg, Ann L;
Petersen, Gloria M;
Bijlsma, Maarten F;
Brenner, Hermann;
Bueno-de-Mesquita, H Bas;
Canzian, Federico;
Rizzato, Cosmeri;
Capurso, Gabriele;
Cavestro, Giulia M;
Cleary, Sean P;
Mocci, Evelina;
Blackford, Amanda

Publication type:

Article

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.

Published in:

Nature Genetics, 2013, v. 45, n. 4, p. 385, doi. 10.1038/ng.2560

By:

Eeles, Rosalind A;
Haiman, Christopher A;
Schumacher, Fredrick;
Henderson, Brian E;
Ingles, Sue A;
Le Marchand, Loic;
Lindstrom, Sara;
Kraft, Peter;
Hunter, David J;
Gapstur, Susan;
Chanock, Stephen J;
Berndt, Sonja I;
Albanes, Demetrius;
Andriole, Gerald;
Schleutker, Johanna;
Weischer, Maren;
Canzian, Federico;
Campa, Daniele;
Olama, Ali Amin Al;
Benlloch, Sara

Publication type:

Article

Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies.

Published in:

Nature Genetics, 2013, v. 45, n. 4, p. 400, doi. 10.1038/ng.2579

By:

Chatterjee, Nilanjan;
Sampson, Joshua;
Hartge, Patricia;
Chanock, Stephen J;
Wheeler, Bill;
Park, Ju-Hyun

Publication type:

Article

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.

Published in:

Nature Genetics, 2011, v. 43, n. 8, p. 785, doi. 10.1038/ng.882

By:

Zsofia^Kote-Jarai;
Ali Amin^Al Olama;
Graham G.^Giles;
Gianluca^Severi;
Johanna^Schleutker;
Maren^Weischer;
Daniele^Campa;
Elio^Riboli;
Tim^Key;
Henrik^Gronberg;
David J.^Hunter;
Peter^Kraft;
Michael J.^Thun;
Sue^Ingles;
Stephen^Chanock;
Demetrius^Albanes;
Richard B.^Hayes;
David E.^Neal;
Freddie C.^Hamdy;
Jenny L.^Donovan

Publication type:

Article

A twist on admixture mapping.

Published in:

Nature Genetics, 2011, v. 43, n. 3, p. 178, doi. 10.1038/ng0311-178

By:

Chanock, Stephen J.

Publication type:

Article

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries.

Published in:

Nature Genetics, 2010, v. 42, n. 7, p. 570, doi. 10.1038/ng.610

By:

Park, Ju-Hyun;
Wacholder, Sholom;
Gail, Mitchell H;
Peters, Ulrike;
Jacobs, Kevin B;
Chanock, Stephen J;
Chatterjee, Nilanjan

Publication type:

Article

A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies.

Published in:

Nature Genetics, 2009, v. 41, n. 11, p. 1253, doi. 10.1038/ng.455

By:

Jacobs, Kevin B.;
Yeager, Meredith;
Wacholder, Sholom;
Craig, David;
Kraft, Peter;
Hunter, David J.;
Paschal, Justin;
Manolio, Teri A.;
Tucker, Margaret;
Hoover, Robert N.;
Thomas, Gilles D.;
Chanock, Stephen J.;
Chatterjee, Nilanjan

Publication type:

Article

High marks for GWAS.

Published in:

Nature Genetics, 2009, v. 41, n. 7, p. 765, doi. 10.1038/ng0709-765

By:

Chanock, Stephen

Publication type:

Article

Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.

Published in:

Nature Genetics, 2009, v. 41, n. 6, p. 724, doi. 10.1038/ng.385

By:

Chunyan He;
Kraft, Peter;
Chen, Constance;
Buring, Julie E.;
Paré, Guillaume;
Hankinson, Susan E.;
Chanock, Stephen J.;
Ridker, Paul M.;
Hunter, David J.;
Chasman, Daniel I.

Publication type:

Article

Common variants of FUT2 are associated with plasma vitamin B<sub>12</sub> levels.

Published in:

Nature Genetics, 2008, v. 40, n. 10, p. 1160, doi. 10.1038/ng.210

By:

Hazra, Aditi;
Kraft, Peter;
Selhub, Jacob;
Giovannucci, Edward L.;
Thomas, Gilles;
Hoover, Robert N.;
Chanock, Stephen J.;
Hunter, David J.

Publication type:

Article

Variation in KLK genes, prostate-specific antigen and risk of prostate cancer.

Published in:

2008

By:

Ahn, Jiyoung;
Berndt, Sonja I.;
Wacholder, Sholom;
Kraft, Peter;
Kibel, Adam S.;
Yeager, Meredith;
Albanes, Demetrius;
Giovannucci, Edward;
Stampfer, Meir J.;
Virtamo, Jarmo;
Thun, Michael J.;
Feigelson, Heather Spencer;
Cancel-Tassin, Geraldine;
Cussenot, Olivier;
Thomas, Gilles;
Hunter, David J.;
Fraumeni Jr., Joseph F.;
Hoover, Robert N.;
Chanock, Stephen J.;
Hayes, Richard B.

Publication type:

Letter

Common variants near MC4R are associated with fat mass, weight and risk of obesity.

Published in:

Nature Genetics, 2008, v. 40, n. 6, p. 768, doi. 10.1038/ng.140

By:

Loos, Ruth J. F.;
Lindgren, Cecilia M.;
Li, Shengxu;
Wheeler, Eleanor;
Zhao, Jing Hua;
Prokopenko, Inga;
Inouye, Michael;
Freathy, Rachel M.;
Attwood, Antony P.;
Beckmann, Jacques S.;
Berndt, Sonja I.;
Jacobs, Kevin B.;
Chanock, Stephen J.;
Hayes, Richard B.;
Bergmann, Sven;
Bennett, Amanda J.;
Bingham, Sheila A.;
Bochud, Murielle;
Brown, Morris;
Cauchi, Stéphane

Publication type:

Article

Identification of ten loci associated with height highlights new biological pathways in human growth.

Published in:

Nature Genetics, 2008, v. 40, n. 5, p. 584, doi. 10.1038/ng.125

By:

Lettre, Guillaume;
Jackson, Anne U.;
Gieger, Christian;
Schumacher, Fredrick R.;
Berndt, Sonja I.;
Sanna, Serena;
Eyheramendy, Susana;
Voight, Benjamin F.;
Butler, Johannah L.;
Guiducci, Candace;
Illig, Thomas;
Hackett, Rachel;
Heid, Iris M.;
Jacobs, Kevin B.;
Lyssenko, Valeriya;
Uda, Manuela;
Boehnke, Michael;
Chanock, Stephen J.;
Groop, Leif C.;
Hu, Frank B.

Publication type:

Article

Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk.

Published in:

2007

By:

Cox, Angela;
Dunning, Alison M;
Garcia-Closas, Montserrat;
Balasubramanian, Sabapathy;
Reed, Malcolm W R;
Pooley, Karen A;
Scollen, Serena;
Baynes, Caroline;
Ponder, Bruce A J;
Chanock, Stephen;
Lissowska, Jolanta;
Brinton, Louise;
Peplonska, Beata;
Southey, Melissa C;
Hopper, John L;
McCredie, Margaret R E;
Giles, Graham G;
Fletcher, Olivia;
Johnson, Nichola;
dos Santos Silva, Isabel

Publication type:

Correction Notice

The devil is in the DNA.

Published in:

Nature Genetics, 2007, v. 39, n. 3, p. 283, doi. 10.1038/ng0307-283

By:

Chanock, Stephen J.;
Thomas, Gilles

Publication type:

Article

A common coding variant in CASP8 is associated with breast cancer risk.

Published in:

Nature Genetics, 2007, v. 39, n. 3, p. 352, doi. 10.1038/ng1981

By:

Cox, Angela;
Dunning, Alison M.;
Garcia-Closas, Montserrat;
Balasubramanian, Sabapathy;
Reed, Malcolm W. R.;
Pooley, Karen A.;
Scollen, Serena;
Baynes, Caroline;
Ponder, Bruce A. J.;
Chanock, Stephen;
Lissowska, Jolanta;
Brinton, Louise;
Peplonska, Beata;
Southey, Melissa C.;
Hopper, John L.;
McCredie, Margaret R. E.;
Giles, Graham G.;
Fletcher, Olivia;
Johnson, Nichola;
dos Santos Silva, Isabel

Publication type:

Article

Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis.

Published in:

Nature Genetics, 2007, v. 39, n. 2, p. 153, doi. 10.1038/ng0207-153

By:

Abecasis, Gonçalo;
Kwong-Hang Tam, Paul;
Bustamante, Carlos D.;
Ostrander, Elaine A.;
Scherer, Stephen W.;
Chanock, Stephen J.;
Pui-Yan Kwok;
Brookes, Anthony J.

Publication type:

Article

Genewindow: an interactive tool for visualization of genomic variation.

Published in:

Nature Genetics, 2005, v. 37, n. 2, p. 109, doi. 10.1038/ng0205-109

By:

Staats, Brian;
Qi, Liqun;
Beerman, Michael;
Sicotte, Hugues;
Burdett, Laura A;
Packer, Bernice;
Chanock, Stephen J;
Yeager, Meredith

Publication type:

Article