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Genome-wide study of gene-by-sex interactions identifies risks for cleft palate.
Published in:
Human Genetics, 2024, v. 143, n. 11, p. 1341, doi. 10.1007/s00439-024-02704-y
By:
- Robinson, Kelsey;
- Parrish, Randy;
- Adeyemo, Wasiu Lanre;
- Beaty, Terri H.;
- Butali, Azeez;
- Buxó, Carmen J.;
- Gowans, Lord J. J.;
- Hecht, Jacqueline T.;
- Moreno Uribe, Lina;
- Murray, Jeffrey C.;
- Shaw, Gary M.;
- Weinberg, Seth M.;
- Brand, Harrison;
- Marazita, Mary L.;
- Cutler, David J.;
- Epstein, Michael P.;
- Yang, Jingjing;
- Leslie, Elizabeth J.
Publication type:
Article
Rare variant modifier analysis identifies variants in SEC24D associated with orofacial cleft subtypes.
Published in:
Human Genetics, 2023, v. 142, n. 10, p. 1531, doi. 10.1007/s00439-023-02596-4
By:
- Curtis, Sarah W.;
- Carlson, Jenna C.;
- Beaty, Terri H.;
- Murray, Jeffrey C.;
- Weinberg, Seth M.;
- Marazita, Mary L.;
- Cotney, Justin L.;
- Cutler, David J.;
- Epstein, Michael P.;
- Leslie, Elizabeth J.
Publication type:
Article
Correcting systematic inflation in genetic association tests that consider interaction effects: application to a genome-wide association study of posttraumatic stress disorder.
Published in:
2014
By:
- Almli, Lynn M;
- Duncan, Richard;
- Feng, Hao;
- Ghosh, Debashis;
- Binder, Elisabeth B;
- Bradley, Bekh;
- Ressler, Kerry J;
- Conneely, Karen N;
- Epstein, Michael P
Publication type:
journal article
Correcting Systematic Inflation in Genetic Association Tests That Consider Interaction Effects.
Published in:
JAMA Psychiatry, 2014, v. 71, n. 12, p. 1392, doi. 10.1001/jamapsychiatry.2014.1339
By:
- Almli, Lynn M.;
- Duncan, Richard;
- Hao Feng;
- Ghosh, Debashis;
- Binder, Elisabeth B.;
- Bradley, Bekh;
- Ressler, Kerry J.;
- Conneely, Karen N.;
- Epstein, Michael P.
Publication type:
Article
Association between DNA methylation levels in brain tissue and late-life depression in community-based participants.
Published in:
Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00948-6
By:
- Hüls, Anke;
- Robins, Chloe;
- Conneely, Karen N.;
- De Jager, Philip L.;
- Bennett, David A.;
- Epstein, Michael P.;
- Wingo, Thomas S.;
- Wingo, Aliza P.
Publication type:
Article
Depression and Anxiety Symptoms Among Women Who Carry the FMR1 Premutation: Impact of Raising a Child With Fragile X Syndrome Is Moderated by CRHR1 Polymorphisms.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2012, v. 159B, n. 5, p. 549, doi. 10.1002/ajmg.b.32061
By:
- Hunter, Jessica Ezzell;
- Leslie, Mary;
- Novak, Gloria;
- Hamilton, Debra;
- Shubeck, Lisa;
- Charen, Krista;
- Abramowitz, Ann;
- Epstein, Michael P.;
- Lori, Adriana;
- Binder, Elisabeth;
- Cubells, Joseph F.;
- Sherman, Stephanie L.
Publication type:
Article
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Published in:
American Journal of Medical Genetics. Part A, 2023, v. 191, n. 10, p. 2558, doi. 10.1002/ajmg.a.63336
By:
- Diaz Perez, Kimberly K.;
- Chung, Sydney;
- Head, S. Taylor;
- Epstein, Michael P.;
- Hecht, Jacqueline T.;
- Wehby, George L.;
- Weinberg, Seth M.;
- Murray, Jeffrey C.;
- Marazita, Mary L.;
- Leslie, Elizabeth J.
Publication type:
Article
Modifiers of ovarian function in girls and women with classic galactosemia.
Published in:
2013
By:
- Spencer, Jessica B;
- Badik, Jennifer R;
- Ryan, Emily L;
- Gleason, Tyler J;
- Broadaway, K Alaine;
- Epstein, Michael P;
- Fridovich-Keil, Judith L
Publication type:
journal article
Identifying latent genetic interactions in genome-wide association studies using multiple traits.
Published in:
Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01329-0
By:
- Bass, Andrew J.;
- Bian, Shijia;
- Wingo, Aliza P.;
- Wingo, Thomas S.;
- Cutler, David J.;
- Epstein, Michael P.
Publication type:
Article
Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer's dementia.
Published in:
PLoS Genetics, 2021, v. 17, n. 4, p. 1, doi. 10.1371/journal.pgen.1009482
By:
- Tang, Shizhen;
- Buchman, Aron S.;
- De Jager, Philip L.;
- Bennett, David A.;
- Epstein, Michael P.;
- Yang, Jingjing
Publication type:
Article
Metabolic effects of the schizophrenia-associated 3q29 deletion.
Published in:
Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01824-1
By:
- Pollak, Rebecca M.;
- Purcell, Ryan H.;
- Rutkowski, Timothy P.;
- Malone, Tamika;
- Pachura, Kimberly J.;
- Bassell, Gary J.;
- Epstein, Michael P.;
- Dawson, Paul A.;
- Smith, Matthew R.;
- Jones, Dean P.;
- Zwick, Michael E.;
- Warren, Stephen T.;
- Caspary, Tamara;
- Weinshenker, David;
- Mulle, Jennifer G.
Publication type:
Article
Association between maternal depression during pregnancy and newborn DNA methylation.
Published in:
Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01697-w
By:
- Drzymalla, Emily;
- Gladish, Nicole;
- Koen, Nastassja;
- Epstein, Michael P.;
- Kobor, Michael S.;
- Zar, Heather J.;
- Stein, Dan J.;
- Hüls, Anke
Publication type:
Article
Genotypic and haplotypic associations of the DBH gene with plasma dopamine β-hydroxylase activity in African Americans.
Published in:
European Journal of Human Genetics, 2007, v. 15, n. 8, p. 878, doi. 10.1038/sj.ejhg.5201838
By:
- Yi-lang Tang;
- Epstein, Michael P.;
- Anderson, George M.;
- Zabetian, Cyrus P.;
- Cubells, Joseph F.
Publication type:
Article
Powerful and Efficient Strategies for Genetic Association Testing of Symptom and Questionnaire Data in Psychiatric Genetic Studies.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-44046-0
By:
- Holleman, Aaron M.;
- Broadaway, K. Alaine;
- Duncan, Richard;
- Todor, Andrei;
- Almli, Lynn M.;
- Bradley, Bekh;
- Ressler, Kerry J.;
- Ghosh, Debashis;
- Mulle, Jennifer G.;
- Epstein, Michael P.
Publication type:
Article
Association of FKBP5 Polymorphisms and Childhood Abuse With Risk of Posttraumatic Stress Disorder Symptoms in Adults.
Published in:
JAMA: Journal of the American Medical Association, 2008, v. 299, n. 11, p. 1291, doi. 10.1001/jama.299.11.1291
By:
- Binder, Elisabeth B.;
- Bradley, Rebekah G.;
- Wei Liu;
- Epstein, Michael P.;
- Deveau, Todd C.;
- Mercer, Kristina B.;
- Yilang Tang;
- Gillespie, Charles F.;
- Heim, Christine M.;
- Nemeroff, Charles B.;
- Schwartz, Ann C.;
- Cubells, Joseph F.;
- Ressler, Kerry J.
Publication type:
Article
Phenotypic Characterization of Juvenile Idiopathic Arthritis in African American Children.
Published in:
2016
By:
- Fitzpatrick, Lauren;
- Alaine Broadaway, K.;
- Ponder, Lori;
- Angeles-Han, Sheila T.;
- Jenkins, Kirsten;
- Rouster-Stevens, Kelly;
- Pelajo, Christina F.;
- Conneely, Karen;
- Epstein, Michael P.;
- Lopez-Benitez, Jorge;
- Vogler, Larry B.;
- Prahalad, Sampath;
- Broadaway, K Alaine;
- CARRA Registry Investigators
Publication type:
journal article
Familial aggregation of seizure outcomes in four familial epilepsy cohorts.
Published in:
Epilepsia (Series 4), 2024, v. 65, n. 7, p. 2030, doi. 10.1111/epi.18004
By:
- Ellis, Colin A.;
- Tu, Danni;
- Oliver, Karen L.;
- Mefford, Heather C.;
- Hauser, W. Allen;
- Buchhalter, Jeffrey;
- Epstein, Michael P.;
- Cao, Quy;
- Berkovic, Samuel F.;
- Ottman, Ruth
Publication type:
Article
Diverse genetic causes of polymicrogyria with epilepsy.
Published in:
Epilepsia (Series 4), 2021, v. 62, n. 4, p. 973, doi. 10.1111/epi.16854
By:
- Allen, Andrew S;
- Aggarwal, Vimla;
- Berkovic, Samuel F;
- Cossette, Patrick;
- Delanty, Norman;
- Dlugos, Dennis;
- Eichler, Evan E;
- Epstein, Michael P;
- Freyer, Catharine;
- Goldstein, David B;
- Guerrini, Renzo;
- Glauser, Tracy;
- Heinzen, Erin L;
- Johnson, Michael R;
- Kuzniecky, Ruben;
- Lowenstein, Daniel H;
- Marson, Anthony G;
- Mefford, Heather C;
- O'Brien, Terence J;
- Ottman, Ruth
Publication type:
Article
Generalized, focal, and combined epilepsies in families: New evidence for distinct genetic factors.
Published in:
Epilepsia (Series 4), 2020, v. 61, n. 12, p. 2667, doi. 10.1111/epi.16732
By:
- Ellis, Colin A.;
- Ottman, Ruth;
- Epstein, Michael P.;
- Berkovic, Samuel F.
Publication type:
Article
Quantitative analysis of phenotypic elements augments traditional electroclinical classification of common familial epilepsies.
Published in:
Epilepsia (Series 4), 2019, v. 60, n. 11, p. 2194, doi. 10.1111/epi.16354
By:
- Abou‐Khalil, Bassel;
- Afawi, Zaid;
- Allen, Andrew S.;
- Bautista, Jocelyn F.;
- Bellows, Susannah T.;
- Berkovic, Samuel F.;
- Bluvstein, Judith;
- Burgess, Rosemary;
- Cascino, Gregory;
- Cossette, Patrick;
- Cristofaro, Sabrina;
- Crompton, Douglas E.;
- Delanty, Norman;
- Devinsky, Orrin;
- Dlugos, Dennis;
- Ellis, Colin A.;
- Epstein, Michael P.;
- Fountain, Nathan B.;
- Freyer, Catharine;
- Geller, Eric B.
Publication type:
Article
Genetic effects on sleep/wake variation of seizures.
Published in:
Epilepsia (Series 4), 2016, v. 57, n. 4, p. 557, doi. 10.1111/epi.13330
By:
- Winawer, Melodie R.;
- Shih, Jerry;
- Beck, Erin S.;
- Hunter, Jessica E.;
- Epstein, Michael P.
Publication type:
Article
The "maternal effect" on epilepsy risk: Analysis of familial epilepsies and reassessment of prior evidence.
Published in:
2020
By:
- Ellis, Colin A.;
- Berkovic, Samuel F.;
- Epstein, Michael P.;
- Ottman, Ruth;
- Epi4K Consortium
Publication type:
journal article
Epilepsy in families: Age at onset is a familial trait, independent of syndrome.
Published in:
2019
By:
- Ellis, Colin A.;
- Churilov, Leonid;
- Epstein, Michael P.;
- Xie, Sharon X.;
- Bellows, Susannah T.;
- Ottman, Ruth;
- Berkovic, Samuel F.;
- Epi4K Consortium
Publication type:
journal article
Copy number variant analysis from exome data in 349 patients with epileptic encephalopathy.
Published in:
Annals of Neurology, 2015, v. 78, n. 2, p. 323, doi. 10.1002/ana.24457
By:
- Allen, Andrew S.;
- Berkovic, Samuel F.;
- Coe, Bradley P.;
- Cook, Joseph;
- Cossette, Patrick;
- Delanty, Norman;
- Dlugos, Dennis;
- Eichler, Evan E.;
- Epstein, Michael P.;
- Glauser, Tracy;
- Goldstein, David B.;
- Heinzen, Erin L.;
- Johnson, Michael R.;
- Krumm, Nik;
- Kuzniecky, Ruben;
- Lowenstein, Daniel H.;
- Marson, Anthony G.;
- Mefford, Heather C.;
- Nelson, Ben;
- Esmaeeli Nieh, Sahar
Publication type:
Article
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 14, p. 2309, doi. 10.1093/hmg/ddz063
By:
- Kim, Hyerim;
- Lim, Junghwa;
- Bao, Han;
- Jiao, Bin;
- Canon, Se Min;
- Epstein, Michael P;
- Xu, Keqin;
- Jiang, Jie;
- Parameswaran, Janani;
- Li, Yingjie;
- Moberg, Kenneth H;
- Landers, John E;
- Fournier, Christina;
- Allen, Emily G;
- Glass, Jonathan D;
- Wingo, Thomas S;
- Jin, Peng
Publication type:
Article
Association of inflammation-related exposures and ovarian cancer survival in a multi-site cohort study of Black women.
Published in:
British Journal of Cancer, 2023, v. 129, n. 7, p. 1119, doi. 10.1038/s41416-023-02385-w
By:
- Johnson, Courtney E.;
- Alberg, Anthony J.;
- Bandera, Elisa V.;
- Peres, Lauren C.;
- Akonde, Maxwell;
- Collin, Lindsay J.;
- Cote, Michele L.;
- Hastert, Theresa A.;
- Hébert, James R.;
- Peters, Edward S.;
- Qin, Bonnie;
- Terry, Paul;
- Schwartz, Ann G.;
- Bondy, Melissa;
- Epstein, Michael P.;
- Mandle, Hannah B.;
- Marks, Jeffrey R.;
- Lawson, Andrew B.;
- Schildkraut, Joellen M.
Publication type:
Article
De novo mutations in epileptic encephalopathies.
Published in:
Nature, 2013, v. 501, n. 7466, p. 217, doi. 10.1038/nature12439
By:
- Allen, Andrew S.;
- Berkovic, Samuel F.;
- Cossette, Patrick;
- Delanty, Norman;
- Dlugos, Dennis;
- Eichler, Evan E.;
- Epstein, Michael P.;
- Glauser, Tracy;
- Goldstein, David B.;
- Han, Yujun;
- Heinzen, Erin L.;
- Hitomi, Yuki;
- Howell, Katherine B.;
- Johnson, Michael R.;
- Kuzniecky, Ruben;
- Lowenstein, Daniel H.;
- Lu, Yi-Fan;
- Madou, Maura R. Z.;
- Marson, Anthony G.;
- Mefford, Heather C.
Publication type:
Article
Leveraging Family History in Case-Control Analyses of Rare Variation.
Published in:
Genetics, 2020, v. 214, n. 2, p. 295, doi. 10.1534/genetics.119.302846
By:
- Solis-Lemus, Claudia R.;
- Fischer, S. Taylor;
- Todor, Andrei;
- Cuining Liu;
- Leslie, Elizabeth J.;
- Cutler, David J.;
- Ghosh, Debashis;
- Epstein, Michael P.
Publication type:
Article
Powerful Genetic Association Analysis for Common or Rare Variants with High-Dimensional Structured Traits.
Published in:
Genetics, 2017, v. 206, n. 4, p. 1779, doi. 10.1534/genetics.116.199646
By:
- Xiang Zhan;
- Ni Zhao;
- Plantinga, Anna;
- Thornton, Timothy A.;
- Conneely, Karen N.;
- Epstein, Michael P.;
- Wu, Michael C.
Publication type:
Article
Meta-analysis confirms association between TNFAG238A variant and JIA, and between PTPN22- C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA.
Published in:
Pediatric Rheumatology, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1546-0096-11-40
By:
- Kaalla, Merlyn J.;
- Broadaway, K. Alaine;
- Rohani-Pichavant, Mina;
- Conneely, Karen N.;
- Whiting, April;
- Ponder, Lori;
- Okou, David T.;
- Angeles-Han, Sheila;
- Rouster-Stevens, Kelly;
- Brown, Milton R.;
- Vogler, Larry B.;
- Jorde, Lynn B.;
- Bohnsack, John F.;
- Epstein, Michael P.;
- Prahalad, Sampath
Publication type:
Article
SR-TWAS: leveraging multiple reference panels to improve transcriptome-wide association study power by ensemble machine learning.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50983-w
By:
- Parrish, Randy L.;
- Buchman, Aron S.;
- Tasaki, Shinya;
- Wang, Yanling;
- Avey, Denis;
- Xu, Jishu;
- De Jager, Philip L.;
- Bennett, David A.;
- Epstein, Michael P.;
- Yang, Jingjing
Publication type:
Article
Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Published in:
Molecular Autism, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13229-019-0281-5
By:
- Pollak, Rebecca M.;
- Murphy, Melissa M.;
- Epstein, Michael P.;
- Zwick, Michael E.;
- Klaiman, Cheryl;
- Saulnier, Celine A.;
- Mulle, Jennifer G.
Publication type:
Article
Efficient estimation of indirect effects in case‐control studies using a unified likelihood framework.
Published in:
Statistics in Medicine, 2022, v. 41, n. 15, p. 2879, doi. 10.1002/sim.9390
By:
- Satten, Glen A.;
- Curtis, Sarah W.;
- Solis‐Lemus, Claudia;
- Leslie, Elizabeth J.;
- Epstein, Michael P.
Publication type:
Article
FAT4 identified as a potential modifier of orofacial cleft laterality.
Published in:
Genetic Epidemiology, 2021, v. 45, n. 7, p. 721, doi. 10.1002/gepi.22420
By:
- Curtis, Sarah W.;
- Chang, Daniel;
- Sun, Miranda R.;
- Epstein, Michael P.;
- Murray, Jeffrey C.;
- Feingold, Eleanor;
- Beaty, Terri H.;
- Weinberg, Seth M.;
- Marazita, Mary L.;
- Lipinski, Robert J.;
- Carlson, Jenna C.;
- Leslie, Elizabeth J.
Publication type:
Article
Powerful and robust cross‐phenotype association test for case‐parent trios.
Published in:
Genetic Epidemiology, 2018, v. 42, n. 5, p. 447, doi. 10.1002/gepi.22116
By:
- Fischer, S. Taylor;
- Jiang, Yunxuan;
- Broadaway, K. Alaine;
- Conneely, Karen N.;
- Epstein, Michael P.
Publication type:
Article
Testing cross-phenotype effects of rare variants in longitudinal studies of complex traits.
Published in:
Genetic Epidemiology, 2018, v. 42, n. 4, p. 320, doi. 10.1002/gepi.22121
By:
- Rudra, Pratyaydipta;
- Broadaway, K. Alaine;
- Ware, Erin B.;
- Jhun, Min A.;
- Bielak, Lawrence F.;
- Zhao, Wei;
- Smith, Jennifer A.;
- Peyser, Patricia A.;
- Kardia, Sharon L.R.;
- Epstein, Michael P.;
- Ghosh, Debashis
Publication type:
Article
Kernel machine methods for integrative analysis of genome-wide methylation and genotyping studies.
Published in:
Genetic Epidemiology, 2018, v. 42, n. 2, p. 156, doi. 10.1002/gepi.22100
By:
- Ni Zhao;
- Xiang Zhan;
- Yen-Tsung Huang;
- Almli, Lynn M;
- Smith, Alicia;
- Epstein, Michael P.;
- Conneely, Karen;
- Wu, Michael C.
Publication type:
Article
Kernel Approach for Modeling Interaction Effects in Genetic Association Studies of Complex Quantitative Traits.
Published in:
Genetic Epidemiology, 2015, v. 39, n. 5, p. 366, doi. 10.1002/gepi.21901
By:
- Broadaway, K. Alaine;
- Duncan, Richard;
- Conneely, Karen N.;
- Almli, Lynn M.;
- Bradley, Bekh;
- Ressler, Kerry J.;
- Epstein, Michael P.
Publication type:
Article
Flexible and Robust Methods for Rare-Variant Testing of Quantitative Traits in Trios and Nuclear Families.
Published in:
Genetic Epidemiology, 2014, v. 38, n. 6, p. 542, doi. 10.1002/gepi.21839
By:
- Jiang, Yunxuan;
- Conneely, Karen N.;
- Epstein, Michael P.
Publication type:
Article
Accounting for Population Stratification in DNA Methylation Studies.
Published in:
Genetic Epidemiology, 2014, v. 38, n. 3, p. 231, doi. 10.1002/gepi.21789
By:
- Barfield, Richard T.;
- Almli, Lynn M.;
- Kilaru, Varun;
- Smith, Alicia K.;
- Mercer, Kristina B.;
- Duncan, Richard;
- Klengel, Torsten;
- Mehta, Divya;
- Binder, Elisabeth B.;
- Epstein, Michael P.;
- Ressler, Kerry J.;
- Conneely, Karen N.
Publication type:
Article
SNP Set Association Analysis for Familial Data.
Published in:
Genetic Epidemiology, 2012, v. 36, n. 8, p. 797, doi. 10.1002/gepi.21676
By:
- Schifano, Elizabeth D.;
- Epstein, Michael P.;
- Bielak, Lawrence F.;
- Jhun, Min A.;
- Kardia, Sharon L. R.;
- Peyser, Patricia A.;
- Lin, Xihong
Publication type:
Article
Sparse Principal Component Analysis for Identifying Ancestry-Informative Markers in Genome-Wide Association Studies.
Published in:
Genetic Epidemiology, 2012, v. 36, n. 4, p. 293, doi. 10.1002/gepi.21621
By:
- Lee, Seokho;
- Epstein, Michael P.;
- Duncan, Richard;
- Lin, Xihong
Publication type:
Article
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.
Published in:
Genetic Epidemiology, 2010, v. 34, n. 6, p. 613, doi. 10.1002/gepi.20518
By:
- Locke, Adam E.;
- Dooley, Kenneth J.;
- Tinker, Stuart W.;
- Cheong, Soo Yeon;
- Feingold, Eleanor;
- Allen, Emily G.;
- Freeman, Sallie B.;
- Torfs, Claudine P.;
- Cua, Clifford L.;
- Epstein, Michael P.;
- Wu, Michael C.;
- Lin, Xihong;
- Capone, George;
- Sherman, Stephanie L.;
- Bean, Lora J.H.
Publication type:
Article
Score-based adjustment for confounding by population stratification in genetic association studies.
Published in:
Genetic Epidemiology, 2010, v. 34, n. 5, p. 383, doi. 10.1002/gepi.20487
By:
- Allen, Andrew;
- Epstein, Michael P.;
- Satten, Glen A.
Publication type:
Article
Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.
Published in:
Genetic Epidemiology, 2008, v. 32, n. 6, p. 553, doi. 10.1002/gepi.20329
By:
- Hunter, Jessica Ezzell;
- Epstein, Michael P.;
- Tinker, Stuart W.;
- Charen, Krista H.;
- Sherman, Stephanie L.
Publication type:
Article
Improved association analyses of disease subtypes in case‐parent triads.
Published in:
Genetic Epidemiology, 2006, v. 30, n. 3, p. 209, doi. 10.1002/gepi.20138
By:
- Michael P. Epstein;
- Irwin D. Waldman;
- Glen A. Satten
Publication type:
Article
Comparison of prospective and retrospective methods for haplotype inference in case‐control studiesThis article is a US Government work and, as such, is in the public domain in the United States of America.
Published in:
Genetic Epidemiology, 2004, v. 27, n. 3, p. 192, doi. 10.1002/gepi.20020
By:
- Glen A. Satten;
- Michael P. Epstein
Publication type:
Article
Comment on 'Ascertainment adjustment in complex diseases'.
Published in:
Genetic Epidemiology, 2002, v. 23, n. 3, p. 209, doi. 10.1002/gepi.10197
By:
- Epstein, Michael P.
Publication type:
Article
Analysis of Gene-Gene Interactions Using Gene-Trait Similarity Regression.
Published in:
Human Heredity, 2014, v. 78, n. 1, p. 17, doi. 10.1159/000360161
By:
- Wang, Xin;
- Epstein, Michael P.;
- Tzeng, Jung-Ying
Publication type:
Article
Assessing the Impact of Population Stratification on Association Studies of Rare Variation.
Published in:
Human Heredity, 2013, v. 76, n. 1, p. 28, doi. 10.1159/000353270
By:
- Jiang, Yunxuan;
- Epstein, Michael P.;
- Conneely, Karen N.
Publication type:
Article

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