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Effect of Two- and Three-Locus Linkage Disequilibrium on the Power to Detect Marker/Phenotype Associations.
Published in:
Genetics, 2004, v. 168, n. 2, p. 1029, doi. 10.1534/genetics.103.022335
By:
- Nielsen, Dahlia M.;
- Ehm, Margaret G.;
- Zaykin, Dmitri V.;
- Weir, Bruce S.
Publication type:
Article
Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families.
Published in:
PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0031039
By:
- Cruchaga, Carlos;
- Chakraverty, Sumitra;
- Mayo, Kevin;
- Vallania, Francesco L. M.;
- Mitra, Robi D.;
- Faber, Kelley;
- Williamson, Jennifer;
- Bird, Tom;
- Diaz-Arrastia, Ramon;
- Foroud, Tatiana M.;
- Boeve, Bradley F.;
- Graff-Radford, Neill R.;
- Jean, Pamela St.;
- Lawson, Michael;
- Ehm, Margaret G.;
- Mayeux, Richard;
- Goate, Alison M.
Publication type:
Article
Genome-Wide Scan of Obesity in the Old Order Amish.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 3, p. 1199, doi. 10.1210/jcem.86.3.7358
By:
- WEN-CHI HSUEH;
- MITCHELL, BRAXTON D.;
- SCHNEIDER, JENNIFER L.;
- JEAN, PAMELA L. ST.;
- POLLIN, TONI I.;
- EHM, MARGARET G.;
- WAGNER, MICHAEL J.;
- BURNS, DANIEL K.;
- SAKUL, HAKAN;
- BELL, CALLUM J.;
- SHULDINER, ALAN R.
Publication type:
Article
On the utility of data from the International HapMap Project for Australian association studies.
Published in:
Human Genetics, 2006, v. 119, n. 1/2, p. 220, doi. 10.1007/s00439-005-0120-y
By:
- Stankovich, Jim;
- Cox, Charles J.;
- Tan, Rachel B.;
- Montgomery, Douglas S.;
- Huxtable, Stewart J.;
- Rubio, Justin P.;
- Ehm, Margaret G.;
- Johnson, Laura;
- Butzkueven, Helmut;
- Kilpatrick, Trevor J.;
- Speed, Terence P.;
- Roses, Allen D.;
- Bahlo, Melanie;
- Foote, Simon J.
Publication type:
Article
Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests.
Published in:
European Journal of Human Genetics, 2014, v. 22, n. 9, p. 1137, doi. 10.1038/ejhg.2013.297
By:
- Zawistowski, Matthew;
- Reppell, Mark;
- Wegmann, Daniel;
- St Jean, Pamela L;
- Ehm, Margaret G;
- Nelson, Matthew R;
- Novembre, John;
- Zöllner, Sebastian
Publication type:
Article
Comparing variant calling algorithms for target-exon sequencing in a large sample.
Published in:
BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0489-0
By:
- Yancy Lo;
- Kang, Hyun M.;
- Nelson, Matthew R.;
- Othman, Mohammad I.;
- Chissoe, Stephanie L.;
- Ehm, Margaret G.;
- Abecasis, Gonçalo R.;
- Zöllner, Sebastian
Publication type:
Article
Comparing variant calling algorithms for target-exon sequencing in a large sample.
Published in:
BMC Bioinformatics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12859-015-0489-0
By:
- Yancy Lo;
- Kang, Hyun M.;
- Nelson, Matthew R.;
- Othman, Mohammad I.;
- Chissoe, Stephanie L.;
- Ehm, Margaret G.;
- Abecasis, Gonçalo R.;
- Zöllner, Sebastian
Publication type:
Article
Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.
Published in:
Nature Communications, 2015, v. 6, n. 1, p. 5897, doi. 10.1038/ncomms6897
By:
- Wessel, Jennifer;
- Chu, Audrey Y;
- Willems, Sara M;
- Wang, Shuai;
- Yaghootkar, Hanieh;
- Brody, Jennifer A;
- Dauriz, Marco;
- Hivert, Marie-France;
- Raghavan, Sridharan;
- Lipovich, Leonard;
- Hidalgo, Bertha;
- Fox, Keolu;
- Huffman, Jennifer E;
- An, Ping;
- Lu, Yingchang;
- Rasmussen-Torvik, Laura J;
- Grarup, Niels;
- Ehm, Margaret G;
- Li, Li;
- Baldridge, Abigail S
Publication type:
Article
Integration of Real‐World Data and Genetics to Support Target Identification and Validation.
Published in:
Clinical Pharmacology & Therapeutics, 2022, v. 111, n. 1, p. 63, doi. 10.1002/cpt.2477
By:
- Davitte, Jonathan M.;
- Stott‐Miller, Marni;
- Ehm, Margaret G.;
- Cunnington, Marianne C.;
- Reynolds, Robert F.
Publication type:
Article
A low-frequency variant in MAPK14 provides mechanistic evidence of a link with myeloperoxidase: a prognostic cardiovascular risk marker.
Published in:
2014
By:
- Waterworth, Dawn M.;
- Li, Li;
- Scott, Robert;
- Warren, Liling;
- Gillson, Christopher;
- Aponte, Jennifer;
- Sarov‐Blat, Lea;
- Sprecher, Dennis;
- Dupuis, Josée;
- Reiner, Alex;
- Psaty, Bruce M.;
- Tracy, Russell P.;
- Lin, Honghuang;
- McPherson, Ruth;
- Chissoe, Stephanie;
- Wareham, Nick;
- Ehm, Margaret G.;
- Sarov-Blat, Lea;
- Dupuis, Josée
Publication type:
journal article
Genome-wide and fine-mapping linkage studies of type 2 diabetes and glucose traits in the Old Order Amish: evidence for a new diabetes locus on chromosome 14q11 and confirmation of a locus on chromosome 1q21-q24.
Published in:
2003
By:
- Hsueh, Wen-Chi;
- St. Jean, Pamela L.;
- Mitchell, Braxton D.;
- Pollin, Toni I.;
- Knowler, William C.;
- Ehm, Margaret G.;
- Bell, Callum J.;
- Sakul, Hakan;
- Wagner, Michael J.;
- Burns, Daniel K.;
- Shuldiner, Alan R.
Publication type:
journal article
Deep sequencing of the LRRK2 gene in 14,002 individuals reveals evidence of purifying selection and independent origin of the p.Arg1628Pro mutation in Europe.
Published in:
Human Mutation, 2012, v. 33, n. 7, p. 1087, doi. 10.1002/humu.22075
By:
- Rubio, Justin P.;
- Topp, Simon;
- Warren, Liling;
- St. Jean, Pamela L.;
- Wegmann, Daniel;
- Kessner, Darren;
- Novembre, John;
- Shen, Judong;
- Fraser, Dana;
- Aponte, Jennifer;
- Nangle, Keith;
- Cardon, Lon R.;
- Ehm, Margaret G.;
- Chissoe, Stephanie L.;
- Whittaker, John C.;
- Nelson, Matthew R.;
- Mooser, Vincent E.
Publication type:
Article
Guidelines for conducting and reporting whole genome/large-scale association studies.
Published in:
Human Molecular Genetics, 2005, v. 14, n. 17, p. 2485, doi. 10.1093/hmg/ddi252
By:
- Ehm, Margaret G.;
- Nelson, Matthew R.;
- Spurr, Nigel K.
Publication type:
Article
Effect of case and control definitions on genome‐wide association study (GWAS) findings.
Published in:
Genetic Epidemiology, 2023, v. 47, n. 5, p. 394, doi. 10.1002/gepi.22523
By:
- Isgut, Monica;
- Song, Kijoung;
- Ehm, Margaret G.;
- Wang, May Dongmei;
- Davitte, Jonathan
Publication type:
Article
Comparison of association methods for dense marker data.
Published in:
Genetic Epidemiology, 2008, v. 32, n. 8, p. 791, doi. 10.1002/gepi.20347
By:
- Bacanu, Silviu-Alin;
- Nelson, Matthew R.;
- Ehm, Margaret G.
Publication type:
Article
Case-control single-marker and haplotypic association analysis of pedigree data.
Published in:
Genetic Epidemiology, 2005, v. 28, n. 2, p. 110, doi. 10.1002/gepi.20051
By:
- Browning, Sharon R.;
- Briley, J. David;
- Briley, Linda P.;
- Chandra, Gyan;
- Charnecki, Jonathan H.;
- Ehm, Margaret G.;
- Johansson, Kelley A.;
- Jones, Brendan J.;
- Karter, Andrew J.;
- Yarnall, David P.;
- Wagner, Michael J.
Publication type:
Article
Identifying Susceptibility Genes Using Linkage and Linkage Disequilibrium Analysis in Large Pedigrees.
Published in:
Genetic Epidemiology, 2001, v. 21, p. S453, doi. 10.1002/gepi.2001.21.s1.s453
By:
- Meng, Zhaoling;
- Zaykin, Dmitri V.;
- Karnoub, Maha C.;
- Sreekumar, G.P.;
- St. Jean, Pamela L.;
- Ehm, Margaret G.
Publication type:
Article
Testing Association of Statistically Inferred Haplotypes with Discrete and Continuous Traits in Samples of Unrelated Individuals.
Published in:
Human Heredity, 2002, v. 53, n. 2, p. 79, doi. 10.1159/000057986
By:
- Zaykin, Dmitri V.;
- Westfall, Peter H.;
- Young, S. Stanley;
- Karnoub, Maha A.;
- Wagner, Michael J.;
- Ehm, Margaret G.
Publication type:
Article
Phenome-wide association study using research participants’ self-reported data provides insight into the Th17 and IL-17 pathway.
Published in:
PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0186405
By:
- Ehm, Margaret G.;
- Aponte, Jennifer L.;
- Chiano, Mathias N.;
- Yerges-Armstrong, Laura M.;
- Johnson, Toby;
- Barker, Jonathan N.;
- Cook, Suzanne F.;
- Gupta, Akanksha;
- Hinds, David A.;
- Li, Li;
- Nelson, Matthew R.;
- Simpson, Michael A.;
- Tian, Chao;
- McCarthy, Linda C.;
- Rajpal, Deepak K.;
- Waterworth, Dawn M.
Publication type:
Article
Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation.
Published in:
Diabetes, 2012, v. 61, n. 5, p. 1297, doi. 10.2337/db11-0985
By:
- Warren, Liling L.;
- Li Li;
- Nelson, Matthew R.;
- Ehm, Margaret G.;
- Shen, Judong;
- Fraser, Dana J.;
- Aponte, Jennifer L.;
- Nangle, Keith L.;
- Slater, Andrew J.;
- Woollard, Peter M.;
- Hall, Matt D.;
- Topp, Simon D.;
- Xin Yuan;
- Cardon, Lon R.;
- Chissoe, Stephanie L.;
- Mooser, Vincent;
- Morris, Andrew D.;
- Palmer, Colin N. A.;
- Perry, John R.;
- Frayling, Timothy M.
Publication type:
Article

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