The Fundamentals of Modern Statistical Genetics

por Laird, Nan M
Publicado 2011

Identifying rare variants using a Bayesian regression approach

por Yan, Aimin, Laird, Nan M, Li, Cheng
Publicado 2011

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set

por Yip, Wai-Ki, De, Gourab, Raby, Benjamin A, Laird, Nan
Publicado 2011

Rare Variant Analysis for Family-Based Design

por De, Gourab, Yip, Wai-Ki, Ionita-Laza, Iuliana, Laird, Nan
Publicado 2013

EFBAT: exact family-based association tests

por Schneiter, Kady, Degnan, James H, Corcoran, Christopher, Xu, Xin, Laird, Nan
Publicado 2007

Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measures

por Moreno-Macias, Hortensia, Romieu, Isabelle, London, Stephanie J, Laird, Nan M
Publicado 2010

A New Testing Strategy to Identify Rare Variants with Either Risk or Protective Effect on Disease

por Ionita-Laza, Iuliana, Buxbaum, Joseph D., Laird, Nan M., Lange, Christoph
Publicado 2011

A general semi-parametric approach to the analysis of genetic association studies in population-based designs

por Lutz, Sharon, Yip, Wai-Ki, Hokanson, John, Laird, Nan, Lange, Christoph
Publicado 2013

A comparative analysis of family-based and population-based association tests using whole genome sequence data

por Zhou, Jin J, Yip, Wai-Ki, Cho, Michael H, Qiao, Dandi, McDonald, Merry-Lynn N, Laird, Nan M
Publicado 2014

Comparison of linkage and association strategies for quantitative traits using the COGA dataset

por McQueen, Matthew B, Murphy, Amy, Kraft, Peter, Su, Jessica, Lazarus, Ross, Laird, Nan M, Lange, Christoph, Van Steen, Kristel
Publicado 2005

Genomic screening in family-based association testing

por Murphy, Amy, McQueen, Matthew B, Su, Jessica, Kraft, Peter, Lazarus, Ross, Laird, Nan M, Lange, Christoph, Van Steen, Kristel
Publicado 2005

Obesity and Weight Gain in Relation to Depression: Findings from the Stirling County Study

por Murphy, Jane M., Horton, Nicholas J., Burke, Jack D., Monson, Richard R., Laird, Nan M., Lesage, Alain, Sobol, Arthur M.
Publicado 2009

Cluster analysis in severe emphysema subjects using phenotype and genotype data: an exploratory investigation

por Cho, Michael H, Washko, George R, Hoffmann, Thomas J, Criner, Gerard J, Hoffman, Eric A, Martinez, Fernando J, Laird, Nan, Reilly, John J, Silverman, Edwin K
Publicado 2010

Analyzing networks of phenotypes in complex diseases: methodology and applications in COPD

por Chu, Jen-hwa, Hersh, Craig P, Castaldi, Peter J, Cho, Michael H, Raby, Benjamin A, Laird, Nan, Bowler, Russell, Rennard, Stephen, Loscalzo, Joseph, Quackenbush, John, Silverman, Edwin K
Publicado 2014

Identification of Novel Alzheimer’s Disease Loci Using Sex-Specific Family-Based Association Analysis of Whole-Genome Sequence Data

por Prokopenko, Dmitry, Hecker, Julian, Kirchner, Rory, Chapman, Brad A., Hoffman, Oliver, Mullin, Kristina, Hide, Winston, Bertram, Lars, Laird, Nan, DeMeo, Dawn L., Lange, Christoph, Tanzi, Rudolph E.
Publicado 2020

Region-based analysis of rare genomic variants in whole-genome sequencing datasets reveal two novel Alzheimer’s disease-associated genes: DTNB and DLG2

por Prokopenko, Dmitry, Lee, Sanghun, Hecker, Julian, Mullin, Kristina, Morgan, Sarah, Katsumata, Yuriko, Weiner, Michael W., Fardo, David W., Laird, Nan, Bertram, Lars, Hide, Winston, Lange, Christoph, Tanzi, Rudolph E.
Publicado 2022

Ozone exposure, vitamin C intake, and genetic susceptibility of asthmatic children in Mexico City: a cohort study

por Moreno-Macías, Hortensia, Dockery, Douglas W, Schwartz, Joel, Gold, Diane R, Laird, Nan M, Sienra-Monge, Juan J, Del Río-Navarro, Blanca E, Ramírez-Aguilar, Matiana, Barraza-Villarreal, Albino, Li, Huiling, London, Stephanie J, Romieu, Isabelle
Publicado 2013

X chromosome associations with chronic obstructive pulmonary disease and related phenotypes: an X chromosome-wide association study

por Hayden, Lystra P., Hobbs, Brian D., Busch, Robert, Cho, Michael H., Liu, Ming, Lopes-Ramos, Camila M., Lomas, David A., Bakke, Per, Gulsvik, Amund, Silverman, Edwin K., Crapo, James D., Beaty, Terri H., Laird, Nan M., Lange, Christoph, DeMeo, Dawn L.
Publicado 2023

Identifying rare variants from exome scans: the GAW17 experience

por Ghosh, Saurabh, Bickeböller, Heike, Bailey, Julia, Bailey-Wilson, Joan E, Cantor, Rita, Culverhouse, Robert, Daw, Warwick, DeStefano, Anita L, Engelman, Corinne D, Hinrichs, Anthony, Houwing-Duistermaat, Jeanine, König, Inke R, Kent, Jack, Laird, Nan, Pankratz, Nathan, Paterson, Andrew, Pugh, Elizabeth, Suarez, Brian, Sun, Yan, Thomas, Alun, Tintle, Nathan, Zhu, Xiaofeng, Ziegler, Andreas, MacCluer, Jean W, Almasy, Laura
Publicado 2011

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations

por Howrigan, Daniel P., Rose, Samuel A., Samocha, Kaitlin E., Fromer, Menachem, Cerrato, Felecia, Chen, Wei J., Churchhouse, Claire, Chambert, Kimberly, Chandler, Sharon D., Daly, Mark J., Dumont, Ashley, Genovese, Giulio, Hwu, Hai-Gwo, Laird, Nan, Kosmicki, Jack A., Moran, Jennifer L., Roe, Cheryl, Singh, Tarjinder, Wang, Shi-Heng, Faraone, Stephen V., Glatt, Stephen J., McCarroll, Steven A., Tsuang, Ming, Neale, Benjamin M.
Publicado 2020