Family-based approaches: design, imputation, analysis, and beyond

por Wijsman, Ellen M.
Publicado 2016

Contrasting identity-by-descent estimators, association studies, and linkage analyses using the Framingham Heart Study data

por Marchani, Elizabeth E, Di, Yanming, Choi, Yoonha, Cheung, Charles, Su, Ming, Boehm, Frederick, Thompson, Elizabeth A, Wijsman, Ellen M
Publicado 2009

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

por Peter, Beate, Raskind, Wendy H., Matsushita, Mark, Lisowski, Mark, Vu, Tiffany, Berninger, Virginia W., Wijsman, Ellen M., Brkanac, Zoran
Publicado 2010

Comparison and assessment of family- and population-based genotype imputation methods in large pedigrees

por Ullah, Ehsan, Mall, Raghvendra, Abbas, Mostafa M., Kunji, Khalid, Nato, Alejandro Q., Bensmail, Halima, Wijsman, Ellen M., Saad, Mohamad
Publicado 2019

Approaches to mapping genetically correlated complex traits

por George, Andrew W, Basu, Saonli, Li, Na, Rothstein, Joseph H, Sieberts, Solveig K, Stewart, William, Wijsman, Ellen M, Thompson, Elizabeth A
Publicado 2003

Comparison of multipoint linkage analyses for quantitative traits in the CEPH data: parametric LOD scores, variance components LOD scores, and Bayes factors

por Sung, Yun Ju, Di, Yanming, Fu, Audrey Q, Rothstein, Joseph H, Sieh, Weiva, Tong, Liping, Thompson, Elizabeth A, Wijsman, Ellen M
Publicado 2007

Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analyses

por Blue, Elizabeth Marchani, Cheung, Charles YK, Glazner, Christopher G, Conomos, Matthew P, Lewis, Steven M, Sverdlov, Serge, Thornton, Timothy, Wijsman, Ellen M
Publicado 2014

Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing

por Thornton, Timothy, Conomos, Matthew P, Sverdlov, Serge, Blue, Elizabeth M, Cheung, Charles YK, Glazner, Christopher G, Lewis, Steven M, Wijsman, Ellen M
Publicado 2014

Comparison of marker types and map assumptions using Markov chain Monte Carlo-based linkage analysis of COGA data

por Sieh, Weiva, Basu, Saonli, Fu, Audrey Q, Rothstein, Joseph H, Scheet, Paul A, Stewart, William CL, Sung, Yun J, Thompson, Elizabeth A, Wijsman, Ellen M
Publicado 2005

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data

por Saad, Mohamad, Nato, Alejandro Q., Grimson, Fiona L., Lewis, Steven M., Brown, Lisa A., Blue, Elizabeth M., Thornton, Timothy A., Thompson, Elizabeth A., Wijsman, Ellen M.
Publicado 2016

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

por Peter, Beate, Wijsman, Ellen M., Nato, Alejandro Q., Matsushita, Mark M., Chapman, Kathy L., Stanaway, Ian B., Wolff, John, Oda, Kaori, Gabo, Virginia B., Raskind, Wendy H.
Publicado 2016

Estimating relationships between phenotypes and subjects drawn from admixed families

por Blue, Elizabeth M., Brown, Lisa A., Conomos, Matthew P., Kirk, Jennifer L., Nato, Alejandro Q., Popejoy, Alice B., Raffa, Jesse, Ranola, John, Wijsman, Ellen M., Thornton, Timothy
Publicado 2016

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals

por Engelman, Corinne D., Greenwood, Celia M. T., Bailey, Julia N., Cantor, Rita M., Kent, Jack W., König, Inke R., Bermejo, Justo Lorenzo, Melton, Phillip E., Santorico, Stephanie A., Schillert, Arne, Wijsman, Ellen M., MacCluer, Jean W., Almasy, Laura
Publicado 2016

Genome-Wide Association of Familial Late-Onset Alzheimer's Disease Replicates BIN1 and CLU and Nominates CUGBP2 in Interaction with APOE

por Wijsman, Ellen M., Pankratz, Nathan D., Choi, Yoonha, Rothstein, Joseph H., Faber, Kelley M., Cheng, Rong, Lee, Joseph H., Bird, Thomas D., Bennett, David A., Diaz-Arrastia, Ramon, Goate, Alison M., Farlow, Martin, Ghetti, Bernardino, Sweet, Robert A., Foroud, Tatiana M., Mayeux, Richard
Publicado 2011

Key variants via Alzheimer’s Disease Sequencing Project whole genome sequence data

por Wang, Yanbing, Sarnowski, Chloé, Lin, Honghuang, Pitsillides, Achilleas N, Heard-Costa, Nancy L, Choi, Seung Hoan, Wang, Dongyu, Bis, Joshua C, Blue, Elizabeth E, Boerwinkle, Eric, De Jager, Philip L, Fornage, Myriam, Wijsman, Ellen M, Seshadri, Sudha, Dupuis, Josée, Peloso, Gina M, DeStefano, Anita L
Publicado 2023

Evidence for Involvement of GNB1L in Autism

por Chen, Ying-Zhang, Matsushita, Mark, Girirajan, Santhosh, Lisowski, Mark, Sun, Elizabeth, Sul, Youngmee, Bernier, Raphael, Estes, Annette, Dawson, Geraldine, Minshew, Nancy, Shellenberg, Gerard D, Eichler, Evan E, Rieder, Mark J, Nickerson, Deborah A, Tsuang, Debby W, Tsuang, Ming T, Wijsman, Ellen M, Raskind, Wendy H, Brkanac, Zoran
Publicado 2012

Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations

por Horimoto, Andrea R.V.R., Boyken, Lisa A., Blue, Elizabeth E., Grinde, Kelsey E., Nafikov, Rafael A., Sohi, Harkirat K., Nato, Alejandro Q., Bis, Joshua C., Brusco, Luis I., Morelli, Laura, Ramirez, Alfredo, Dalmasso, Maria Carolina, Temple, Seth, Satizabal, Claudia, Browning, Sharon R., Seshadri, Sudha, Wijsman, Ellen M., Thornton, Timothy A.
Publicado 2023

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci

por Cordell, Heather J, de Andrade, Mariza, Babron, Marie-Claude, Bartlett, Christopher W, Beyene, Joseph, Bickeböller, Heike, Culverhouse, Robert, Cupples, L Adrienne, Daw, E Warwick, Dupuis, Josée, Falk, Catherine T, Ghosh, Saurabh, Goddard, Katrina A, Goode, Ellen L, Hauser, Elizabeth R, Martin, Lisa J, Martinez, Maria, North, Kari E, Saccone, Nancy L, Schmidt, Silke, Tapper, William, Thomas, Duncan, Tritchler, David, Vieland, Veronica J, Wijsman, Ellen M, Wilcox, Marsha A, Witte, John S, Yang, Qiong, Ziegler, Andreas, Almasy, Laura, MacCluer, Jean W
Publicado 2007

Alternative splicing in a presenilin 2 variant associated with Alzheimer disease

por Braggin, Jacquelyn E., Bucks, Stephanie A., Course, Meredith M., Smith, Carole L., Sopher, Bryce, Osnis, Leah, Shuey, Kiel D., Domoto‐Reilly, Kimiko, Caso, Christina, Kinoshita, Chizuru, Scherpelz, Kathryn P., Cross, Chloe, Grabowski, Thomas, Nik, Seyyed H. M., Newman, Morgan, Garden, Gwenn A., Leverenz, James B., Tsuang, Debby, Latimer, Caitlin, Gonzalez‐Cuyar, Luis F., Keene, Christopher Dirk, Morrison, Richard S., Rhoads, Kristoffer, Wijsman, Ellen M., Dorschner, Michael O., Lardelli, Michael, Young, Jessica E., Valdmanis, Paul N., Bird, Thomas D., Jayadev, Suman
Publicado 2019

The Advisory Group on Risk Evidence Education for Dementia: Multidisciplinary and Open to All

por Rosen, Allyson C., Arias, Jalayne J., Ashford, J. Wesson, Blacker, Deborah, Chhatwal, Jasmeer P., Chin, Nathan A., Clark, Lindsay, Denny, Sharon S., Goldman, Jill S., Gleason, Carey E., Grill, Joshua D., Heidebrink, Judith L., Henderson, Victor W., Lavacot, James A., Lingler, Jennifer H., Menon, Malavika, Nosheny, Rachel L., Oliveira, Fabricio F., Parker, Monica W., Rahman-Filipiak, Annalise, Revoori, Anwita, Rumbaugh, Malia C., Sanchez, Danurys L., Schindler, Suzanne E., Schwarz, Christopher G., Toy, Leslie, Tyrone, Jamie, Walter, Sarah, Wang, Li-san, Wijsman, Ellen M., Zallen, Doris T., Aggarwal, Neelum T.
Publicado 2022