Choice of population structure informative principal components for adjustment in a case-control study

Por Lunetta Kathryn L, Peloso Gina M
Publicado em 2011-07-01

Choice of population structure informative principal components for adjustment in a case-control study

Por Peloso, Gina M, Lunetta, Kathryn L
Publicado em 2011

Principal-component-based population structure adjustment in the North American Rheumatoid Arthritis Consortium data: impact of single-nucleotide polymorphism set and analysis meth...

Por Peloso, Gina M, Timofeev, Nadia, Lunetta, Kathryn L
Publicado em 2009

What can we learn about lipoprotein metabolism and coronary heart disease from studying rare variants?

Por Jeff, Janina M., Peloso, Gina M., Do, Ron
Publicado no Curr Opin Lipidol (2016)

Genomic Medicine for Improved Prediction and Primordial Prevention of Cardiovascular Disease

Por Thanassoulis, George, Peloso, Gina M., O'Donnell, Christopher J
Publicado em 2013

Structured mating: Patterns and implications

Por Sebro, Ronnie, Peloso, Gina M., Dupuis, Josée, Risch, Neil J.
Publicado no PLoS Genet (2017)

Multiple associated variants increase the heritability explained for plasma lipids and coronary artery disease

Por Tada, Hayato, Won, Hong-Hee, Melander, Olle, Yang, Jian, Peloso, Gina M, Kathiresan, Sekar
Publicado no Circ Cardiovasc Genet (2014)

Phenotypic extremes in rare variant study designs

Por Peloso, Gina M, Rader, Daniel J, Gabriel, Stacey, Kathiresan, Sekar, Daly, Mark J, Neale, Benjamin M
Publicado no Eur J Hum Genet (2016)

QT Interval and Long‐Term Mortality Risk in the Framingham Heart Study

Por Noseworthy, Peter A., Peloso, Gina M., Hwang, Shih‐Jen, Larson, Martin G., Levy, Daniel, O’Donnell, Christopher J., Newton‐Cheh, Christopher
Publicado em 2012

A three-stage approach for genome-wide association studies with family data for quantitative traits

Por Guo Chao-Yu, Peloso Gina M, Hsu Yi-Hsiang, Larson Martin G, Chen Ming-Huei, Fox Caroline S, Atwood Larry D, Yang Qiong
Publicado em 2010-05-01

A three-stage approach for genome-wide association studies with family data for quantitative traits

Por Chen, Ming-Huei, Larson, Martin G, Hsu, Yi-Hsiang, Peloso, Gina M, Guo, Chao-Yu, Fox, Caroline S, Atwood, Larry D, Yang, Qiong
Publicado em 2010

Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease

Por Peloso, Gina M., Demissie, Serkalem, Collins, Dorothea, Mirel, Daniel B., Gabriel, Stacey B., Cupples, L. Adrienne, Robins, Sander J., Schaefer, Ernst J., Brousseau, Margaret E.
Publicado em 2010

Relations of Long-Term and Contemporary Lipid Levels and Lipid Genetic Risk Scores with Coronary Artery Calcium in the Framingham Heart Study

Por Tsao, Connie W., Preis, Sarah Rosner, Peloso, Gina M., Hwang, Shih-Jen, Kathiresan, Sekar, Fox, Caroline S., Cupples, L. Adrienne, Hoffmann, Udo, O’Donnell, Christopher J.
Publicado em 2012

A Genetic Risk Score is Associated with Incident Cardiovascular Disease and Coronary Artery Calcium - The Framingham Heart Study

Por Thanassoulis, George, Peloso, Gina M., Pencina, Michael J., Hoffmann, Udo, Fox, Caroline S., Cupples, L. Adrienne, Levy, Daniel, D'Agostino, Ralph B., Hwang, Shih-Jen, O'Donnell, Christopher J.
Publicado em 2012

A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

Por Kathiresan, Sekar, Manning, Alisa K, Demissie, Serkalem, D'Agostino, Ralph B, Surti, Aarti, Guiducci, Candace, Gianniny, Lauren, Burtt, Nöel P, Melander, Olle, Orho-Melander, Marju, Arnett, Donna K, Peloso, Gina M, Ordovas, Jose M, Cupples, L Adrienne
Publicado em 2007

The early repolarization pattern in the general population: clinical correlates and heritability

Por Noseworthy, Peter A., Tikkanen, Jani T., Porthan, Kimmo, Oikarinen, Lasse, Pietila, Arto, Harald, Kennet, Peloso, Gina M., Merchant, Faisal M., Jula, Antti, Väänänen, Heikki, Hwang, Shih-Jen, O'Donnell, Christopher J., Salomaa, Veikko, Newton-Cheh, Christopher, Huikuri, Heikki V.
Publicado em 2011

Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction

Por Thormaehlen, Aenne S., Schuberth, Christian, Won, Hong-Hee, Blattmann, Peter, Joggerst-Thomalla, Brigitte, Theiss, Susanne, Asselta, Rosanna, Duga, Stefano, Merlini, Pier Angelica, Ardissino, Diego, Lander, Eric S., Gabriel, Stacey, Rader, Daniel J., Peloso, Gina M., Pepperkok, Rainer, Kathiresan, Sekar, Runz, Heiko
Publicado no PLoS Genet (2015)

Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham Heart Study

Por Johnson, Andrew D., Hwang, Shih-Jen, Voorman, Arend, Morrison, Alanna, Peloso, Gina M., Hsu, Yi-Hsiang, Thanassoulis, George, Newton-Cheh, Christopher, Rogers, Ian S., Hoffmann, Udo, Freedman, Jane E., Fox, Caroline S., Psaty, Bruce M., Boerwinkle, Eric, Cupples, L. Adrienne, O’Donnell, Christopher J.
Publicado em 2013

A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans

Por Clapham, Katharine R., Chu, Audrey Y., Wessel, Jennifer, Natarajan, Pradeep, Flannick, Jason, Rivas, Manuel A., Sartori, Samantha, Mehran, Roxana, Baber, Usman, Fuster, Valentin, Scott, Robert A., Rader, Daniel J., Boehnke, Michael, McCarthy, Mark I., Altshuler, David M., Kathiresan, Sekar, Peloso, Gina M.
Publicado no BMC Endocr Disord (2016)

Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution

Por Patel, Aniruddh P., Peloso, Gina M., Pirruccello, James P., Johansen, Christopher T., Dubé, Joseph B., Larach, Daniel B., Ban, Matthew R., Dallinge-Thie, Geesje M., Gupta, Namrata, Boehnke, Michael, Abecasis, Gonçalo R., Kastelein, John J.P., Kees Hovingh, G., Hegele, Robert A., Rader, Daniel J., Kathiresan, Sekar
Publicado no Atherosclerosis (2016)