Zobrazeno 1 - 10
of 23
pro vyhledávání: '"James M. Jaworski"'
Autor:
Susan Slifer, Sarada Fuzzell, Jeffery M. Vance, Renee Laux, Sharlene D. Herington, Paula Ogrocki, Jonathan L. Haines, Leighanne R. Main, Jairo Ramos, Alan J. Lerner, Jane L. Sewell, Michael L. Cuccaro, James M. Jaworski, Sherri D. Miller, Larry D. Adams, Yeunjoo E. Song, William K. Scott, Kristy Miskimen, Jason E. Clouse, M. Denise Fuzzell, Laura Caywood, Margaret A. Pericak-Vance, Michael Prough
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Daria Salyakina, Holly N Cukier, Joycelyn M Lee, Stephanie Sacharow, Laura D Nations, Deqiong Ma, James M Jaworski, Ioanna Konidari, Patrice L Whitehead, Harry H Wright, Ruth K Abramson, Scott M Williams, Ramkumar Menon, Jonathan L Haines, John R Gilbert, Michael L Cuccaro, Margaret A Pericak-Vance
Publikováno v:
PLoS ONE, Vol 6, Iss 10, p e26049 (2011)
Copy number variations (CNVs) are a major cause of genetic disruption in the human genome with far more nucleotides being altered by duplications and deletions than by single nucleotide polymorphisms (SNPs). In the multifaceted etiology of autism spe
Externí odkaz:
https://doaj.org/article/a763b4dff8ec48fdad221a499acb13ca
Autor:
Anita L. DeStefano, Badri N. Vardarajan, Timothy A. Thornton, Elizabeth Blue, James M. Jaworski, Rafael Lantigua, Cornelia M. van Duijn, Li-San Wang, Haines Jl, Martin Medrano, Gary W. Beecham, Ellen M. Wijsman, Giuseppe Tosto, Eric Boerwinkle, Gerard D. Schellenberg, William S. Bush, Richard Mayeux, Sandra Barral, Dolly Reyes-Dumeyer, Alison Goate, Margaret A. Pericak-Vance, Adam C. Naj, Lisa M. Brown, Lindsay A. Farrer, Eden R. Martin
Publikováno v:
Alzheimer's & Dementia. 14
Autor:
Elizabeth Blue, Margaret A. Pericak-Vance, Sandra Barral, Richard Mayeux, Brian W. Kunkle, Ellen M. Wijsman, Cornelia M. van Duijn, Christiane Reitz, Eden R. Martin, William S. Bush, Gary W. Beecham, Gerard D. Schellenberg, Jonathan L. Haines, James M. Jaworski, Badri N. Vardarajan
Publikováno v:
Alzheimer's & Dementia. 14
Autor:
Alison Goate, Farid Rajabli, Gary W. Beecham, Tatiana Foroud, Richard Mayeux, Margaret A. Pericak-Vance, James M. Jaworski, Brian W. Kunkle, Larry D. Adams, Christiane Reitz, Jeffery M. Vance, Michael L. Cuccaro, Eden R. Martin
Publikováno v:
Alzheimer's & Dementia. 14
Autor:
Farid Rajabli, Takiyah D. Starks, Brian W. Kunkle, James M. Jaworski, Jeffery M. Vance, Michael L. Cuccaro, Richard Mayeux, Alison Goate, Goldie S. Byrd, Eden R. Martin, Margaret A. Pericak-Vance, Larry D. Adams, Christiane Reitz, Gary W. Beecham, Tatiana Foroud
Publikováno v:
Alzheimer's & Dementia. 15:P919-P920
Autor:
Martin Medrano, Richard Mayeux, Lindsay A. Farrer, William S. Bush, Badri N. Vardarajan, Alzheimer’s Disease Sequencing, Dolly Reyes-Dumeyer, Gerard D. Schellenberg, Eden R. Martin, Adam C. Naj, Li-San Wang, Gary W. Beecham, Yuk Yee Leung, James M. Jaworski, Sandra Barral, Margaret A. Pericak-Vance, Jonathan L. Haines, Rafael Lantigua
Publikováno v:
Alzheimer's & Dementia. 15:P1312-P1312
Autor:
Badri N. Vardarajan, Gary W. Beecham, Anita L. DeStefano, James M. Jaworski, Timothy A. Thornton, Allison Goate, Farid Rajabli, Elizabeth Blue, Kara L. Hamilton-Nelson, Eric Boerwinkle, Lindsay A. Farrer, Eden R. Martin, Richard Mayeux, Margaret A. Pericak-Vance, J. Haines, Gerard D. Schellenberg, Ellen M. Wijsman, Brian W. Kunkle, Adam C. Naj, Cornelia M. van Duijn, Sandra Barral, Christiane Reitz, Sudha Seshadri, William S. Bush
Publikováno v:
Neurology: Genetics
Neurology. Genetics, 4(6):UNSP e286. Lippincott Williams & Wilkins
Neurology. Genetics, 4(6):UNSP e286. Lippincott Williams & Wilkins
ObjectiveTo identify genetic variation influencing late-onset Alzheimer disease (LOAD), we used a large data set of non-Hispanic white (NHW) extended families multiply-affected by LOAD by performing whole genome sequencing (WGS).MethodsAs part of the
Autor:
Ren-Hua Chung, Harry H. Wright, Laura D. Nations, Michael L. Cuccaro, Anthony J. Griswold, Ramkumar Menon, Patrice L. Whitehead, Ruth K. Abramson, Daria Salyakina, James M. Jaworski, Michael A. Schmidt, Holly N. Cukier, Ioanna Konidari, Eden R. Martin, Jonathan L. Haines, Margaret A. Pericak-Vance, Deqiong Ma, Scott M. Williams, John R. Gilbert
Publikováno v:
Human Molecular Genetics. 21:3513-3523
Autism spectrum disorders (ASDs) are highly heritable, yet relatively few associated genetic loci have been replicated. Copy number variations (CNVs) have been implicated in autism; however, the majority of loci contribute to
Autor:
Ioanna Konidari, Stephanie Sacharow, Harry H. Wright, R. Henson, Ruth K. Abramson, James M. Jaworski, Joycelyn L. Robinson, Margaret A. Pericak-Vance, J. R. Gilbert, Daria Salyakina, Patrice L. Whitehead, David Cuadra Martínez, Deqiong Ma, Michael L. Cuccaro
Publikováno v:
Autism Research. 3:303-310
Asperger disorder (ASP) is one of the autism spectrum disorders (ASD) and is differentiated from autism largely on the absence of clinically significant cognitive and language delays. Analysis of a homogenous subset of families with ASP may help to a