Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Irina Astrovskaya"'
Autor:
Alexandra Goler, Jessica Wright, Sarah Barns, Jacob Hall, Bing Han, Irina Astrovskaya, SPARK Consortium, Natalia Volfovsky, Aaron Wong, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101084- (2024)
Externí odkaz:
https://doaj.org/article/2408e6cb4de947f9b08ae00b95ab44bf
Autor:
Sarah Barns, Jessica Wright, Alexandra Goler, Jacob Hall, Irina Astrovskaya, Bing Han, SPARK Consortium, Natalia Volfovsky, Aaron Wong, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101096- (2024)
Externí odkaz:
https://doaj.org/article/5694561c406a420a8c974d0226c1a8f5
Autor:
Alexandra Goler, Jessica Wright, Sarah Barns, Jacob Hall, Bing Han, Irina Astrovskaya, Natalia Volfovsky, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100076- (2023)
Externí odkaz:
https://doaj.org/article/cf24b3acceaa42288a92579968480d34
Autor:
Sarah Barns, Chang Shu, Jessica Wright, Alexandra Goler, Jacob Hall, Bing Han, Irina Astrovskaya, Natalia Volfovsky, Yufeng Shen, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100140- (2023)
Externí odkaz:
https://doaj.org/article/09a2007415554ee283f42765878a8bd4
Autor:
Tianyun Wang, S Francis, Tychele Turner, Joseph Obiajulu, Chang Shu, Irina Astrovskaya, Michael Morrier
Publikováno v:
Nature Genetics. 54:1305-1319
To capture the full spectrum of genetic risk for autism, we performed a two-stage analysis of rare de novo and inherited coding variants in 42,607 autism cases, including 35,130 new cases recruited online by SPARK. We identified 60 genes with exome-w
Autor:
Tianyun Wang, Jessica Wright, Natalia Volfovsky, Simon Xuming Xu, Brian J. O'Roak, Christopher Fleisch, Leo Brueggeman, LeeAnne Green Snyder, Evan E. Eichler, Sarah D. Barns, Olena Marchenko, Wendy K. Chung, Shwetha C. Murali, Joseph U. Obiajulu, Xueya Zhou, Jacob B. Hall, William T. Harvey, Jacob J. Michaelson, Timothy S. Chang, Daniel H. Geschwind, Irina Astrovskaya, Pamela Feliciano, Bing Han, Andrew Nishida, Chang Shu, Taylor R. Thomas, Yufeng Shen, Tychele N. Turner
Despite the known heritable nature of autism spectrum disorder (ASD), studies have primarily identified risk genes with de novo variants (DNVs). To capture the full spectrum of ASD genetic risk, we performed a two-stage analysis of rare de novo and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::57bbda70b96aededbabea20ebf74af08
https://doi.org/10.1101/2021.10.08.21264256
https://doi.org/10.1101/2021.10.08.21264256
Autor:
Xueya, Zhou, Pamela, Feliciano, Chang, Shu, Tianyun, Wang, Irina, Astrovskaya, Jacob B, Hall, Joseph U, Obiajulu, Jessica R, Wright, Shwetha C, Murali, Simon Xuming, Xu, Leo, Brueggeman, Taylor R, Thomas, Olena, Marchenko, Christopher, Fleisch, Sarah D, Barns, LeeAnne Green, Snyder, Bing, Han, Timothy S, Chang, Tychele N, Turner, William T, Harvey, Andrew, Nishida, Brian J, O'Roak, Daniel H, Geschwind, Jacob J, Michaelson, Natalia, Volfovsky, Evan E, Eichler, Yufeng, Shen, Zachary E, Warren
Publikováno v:
Nature genetics. 54(9)
To capture the full spectrum of genetic risk for autism, we performed a two-stage analysis of rare de novo and inherited coding variants in 42,607 autism cases, including 35,130 new cases recruited online by SPARK. We identified 60 genes with exome-w
Autor:
Jessica Wright, Sarah Barns, Alexandra Goler, Jacob Hall, Bing Han, Irina Astrovskaya, Olena Marchenko, Swaminathan Ganesan, Natalia Volfovsky, Pamela Feliciano, Wendy Chung
Publikováno v:
Genetics in Medicine. 24:S181-S182
Autor:
Pamela Feliciano, Xueya Zhou, Tianyun Wang, Irina Astrovskaya, Chang Shu, Jacob Hall, Joseph Obiajulu, Jessica Wright, Schwetha Murali, Simon Xu, Leo Brueggeman, Taylor Thomas, Olena Marchenko, Christopher Fleisch, Sarah Barns, LeeAnne Green Snyder, Bing Han, Timothy Chang, Tychele Turner, William Harvey, Andrew Nishida, Brian O'Roak, Daniel Geschwind, The SPARK. Consortium, Jacob Michaelson, Natalia Volfovsky, Evan Eichler, Yufeng Shen, Wendy Chung
Publikováno v:
Genetics in Medicine. 24:S76
Autor:
Ahmad S. Chatha, Amanda D. Shocklee, Xinwei Han, Hana Zaydens, Karen Pierce, Hai Li, Andrew Mason, Dalia Istephanous, Colleen M. Stock, Martin Butler, Amy Nicholson, Zachary Warren, Jason Neely, William Jensen, Amy M. Daniels, Eirene O’Connor, Lauren Kasparson, Nicole Bardett, Dzung Cong Nugyen, Mary Hannah Currin, Sara Eldred, Amy Esler, Lindsey A. Cartner, Elizabeth Berry-Kravis, Beverly E. Robertson, Jaclyn Gunderson, Suma Jacob, Melissa N. Hale, Soo J. Lee, Angela J. Gruber, Leonard J Abbeduto, Vincent Myers, Amanda G. Gulsrud, Jermel Wallace, John Acampado, Sunday M. Francis, Joseph Lillard, Barbara Rodriguez, Bonnie Van Metre, Julie Manoharan, Emily Palen, Shanping Qiu, Cora Taylor, Alexander P. McKenzie, Laurie Raymond, Craig A. Erickson, McLeod F. Gwynette, Malcolm D. Mallardi, David G. Amaral, Natalia Volfovsky, Nathan Hanna, Joseph Piven, Amy Stedman, Andrea R Simon, J. Kiely Law, Danielle Schmidt, Renee D. Clark, Jennifer A. Gerdts, Angela L. Rachubinski, Gail Stein, Ivette Arriaga, Aniko Sabo, Mary Verdi, Juhi Pandey, Christa Lese Martin, Stephen M. Kanne, Catherine Rice, Nicole M. Russo-Ponsaran, Lynette M. Herbert, Lucy Wasserburg, Mark Jones, Christine M. Eng, Stephanie Booker, Jennifer Tjernagel, Luke P. Grosvenor, Ben Negron, Meredith Yinger, Kaela O’Brien, Nicholas Carriero, Kaitlin Smith, Lisa Cordeiro, LeeAnne Green Snyder, Robin P. Goin-Kochel, Caitlin Hayes, Swapnil Shah, Kathryn A. Schweers, Kevin Layman, Matt Kent, Robert T. Schultz, Lark Huang-Storms, Meaghan V. Parladé, Jessica Scherr, Sarah Mastel, Andrei Salomatov, James S. Sutcliffe, Lillian D. Pacheco, Daniel L. Coury, Melissa Brown, Rick Remington, Kathryn Lowe, Jessica Orobio, Landon Hosmer-Quint, Louis F. Reichardt, Eugenia Hofammann, Amy L. Beaumont, Patricia Manning, Andrea J. Ace, Swami Ganesan, Richard A. Gibbs, Alexandra N. Stephens, Lorrin Higgins, James T. McCracken, Holly Lechniak, Anibal Gutierrez, Brianna M. Vernoia, Jacob J. Michaelson, Jay A. Nestle, Brooke G. McKenna, Corrie H. Walston, Wubin Chin, Michael Alessandri, A. Pablo Juárez, Deana Li, Michael J. Morrier, Nina Harris, Stephanie J. Brewster, Brittani A. Hilscher, Hannah E. Kaplan, Ericka L. Wodka, Christine Peura, Joseph F. Cubells, Donna M. Muzny, Leigh A. Coppola, Jeanette M. Cordova, Loran Casey White, Hoa Lam Schneider, Eric Butter, Samantha Plate, Alexies Camba, Christopher J. Smith, Noah Lawson, Eric Fombonne, Susan Hepburn, Kira E. Hamer, Michelle Heyman, Ron Edgar, Hanna Hutter, Katherine Dent, Katherine Roeder, Samantha Thompson, Sabrina White, Latha Soorya, Michelle Jordy, Emily T. Matthews, Rishiraj Rana, Sandra L. Friedman, Mustafa Sahin, Yufeng Shen, Lisa M. Prock, Richard Marini, Susannah Horner, Cesar Ochoa-Lubinoff, Dustin E. Sarver, Carrie Thomas, Opal Y. Ousley, Rebecca Landa, Anna Marie Paolicelli, Lindsey DeMarco, Alex E. Lash, Tyler Ramsey, Sophia Sandhu, Irina Astrovskaya, Anthony D. Krentz, Gabriela Marzano, Brian J. O'Roak, Natalie Pottschmidt, Leandra N. Berry, Crissy Ortiz, Alpha Amatya, Christina Harkins, Ian Fisk, Sarah Carpenter, Robert D. Annett, Amy Swanson, Catherine Lord, Gabriel S. Dichter, Catherine C. Bradley, Katherine G. Pawlowski, Laura A. Carpenter, Curtis Ridenour, Chris Rigby, Pamela Feliciano, Wha S. Yang, Cordelia Robinson Rosenberg, Raphael Bernier, Fiona Miller, Elena Lamarche, Cheryl Cohen, Nicole Takahashi, Laura Simon, Vini Singh, Maya Lazar, Brenda Hauf, Brenda Finucane, Matthew S. Siegel, Kristen Callahan, Jay L. Nestle, Wendy K. Chung, Eric Courchesne, Emily A. Fox
Publikováno v:
Neuron
The Simons Foundation Autism Research Initiative (SFARI) has launched SPARKForAutism.org, a dynamic platform that is engaging thousands of individuals with autism spectrum disorder (ASD) and connecting them to researchers. By making all data accessib