Low load for disruptive mutations in autism genes and their biased transmission

Por Iossifov, Ivan, Levy, Dan, Allen, Jeremy, Ye, Kenny, Ronemus, Michael, Lee, Yoon-ha, Yamrom, Boris, Wigler, Michael
Publicado no Proc Natl Acad Sci U S A (2015)

Reducing system noise in copy number data using principal components of self-self hybridizations

Por Lee, Yoon-ha, Ronemus, Michael, Kendall, Jude, Lakshmi, B., Leotta, Anthony, Levy, Dan, Esposito, Diane, Grubor, Vladimir, Ye, Kenny, Wigler, Michael, Yamrom, Boris
Publicado em 2012

Accurate detection of de novo and transmitted indels within exome-capture data using micro-assembly

Por Narzisi, Giuseppe, O'Rawe, Jason A., Iossifov, Ivan, Fang, Han, Lee, Yoon-ha, Wang, Zihua, Wu, Yiyang, Lyon, Gholson J., Wigler, Michael, Schatz, Michael C.
Publicado em 2014

The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left hear...

Por Warburton, Dorothy, Ronemus, Michael, Kline, Jennie, Jobanputra, Vaidehi, Williams, Ismee, Anyane-Yeboa, Kwame, Chung, Wendy, Yu, Lan, Wong, Nancy, Awad, Danielle, Yu, Chih-yu, Leotta, Anthony, Kendall, Jude, Yamrom, Boris, Lee, Yoon-ha, Wigler, Michael, Levy, Dan
Publicado em 2013

Indel variant analysis of short-read sequencing data with Scalpel

Por Fang, Han, Bergmann, Ewa A, Arora, Kanika, Vacic, Vladimir, Zody, Michael C, Iossifov, Ivan, O’Rawe, Jason A, Wu, Yiyang, Barron, Laura T Jimenez, Rosenbaum, Julie, Ronemus, Michael, Lee, Yoon-ha, Wang, Zihua, Dikoglu, Esra, Jobanputra, Vaidehi, Lyon, Gholson J, Wigler, Michael, Schatz, Michael C, Narzisi, Giuseppe
Publicado no Nat Protoc (2016)

Rare De Novo Germline Copy-Number Variation in Testicular Cancer

Por Stadler, Zsofia K., Esposito, Diane, Shah, Sohela, Vijai, Joseph, Yamrom, Boris, Levy, Dan, Lee, Yoon-ha, Kendall, Jude, Leotta, Anthony, Ronemus, Michael, Hansen, Nichole, Sarrel, Kara, Rau-Murthy, Rohini, Schrader, Kasmintan, Kauff, Noah, Klein, Robert J., Lipkin, Steven M., Murali, Rajmohan, Robson, Mark, Sheinfeld, Joel, Feldman, Darren, Bosl, George, Norton, Larry, Wigler, Michael, Offit, Kenneth
Publicado em 2012

Strong Association of De Novo Copy Number Mutations with Autism

Por Sebat, Jonathan, Lakshmi, B., Malhotra, Dheeraj, Troge, Jennifer, Lese-Martin, Christa, Walsh, Tom, Yamrom, Boris, Yoon, Seungtai, Krasnitz, Alex, Kendall, Jude, Leotta, Anthony, Pai, Deepa, Zhang, Ray, Lee, Yoon-Ha, Hicks, James, Spence, Sarah J., Lee, Annette T., Puura, Kaija, Lehtimäki, Terho, Ledbetter, David, Gregersen, Peter K., Bregman, Joel, Sutcliffe, James S., Jobanputra, Vaidehi, Chung, Wendy, Warburton, Dorothy, King, Mary-Claire, Skuse, David, Geschwind, Daniel H., Gilliam, T. Conrad, Ye, Kenny, Wigler, Michael
Publicado em 2007

De Novo Gene Disruptions in Children on the Autistic Spectrum

Por Iossifov, Ivan, Ronemus, Michael, Levy, Dan, Wang, Zihua, Hakker, Inessa, Rosenbaum, Julie, Yamrom, Boris, Lee, Yoon-ha, Narzisi, Giuseppe, Leotta, Anthony, Kendall, Jude, Grabowska, Ewa, Ma, Beicong, Marks, Steven, Rodgers, Linda, Stepansky, Asya, Troge, Jennifer, Andrews, Peter, Bekritsky, Mitchell, Pradhan, Kith, Ghiban, Elena, Kramer, Melissa, Parla, Jennifer, Demeter, Ryan, Fulton, Lucinda L., Fulton, Robert S., Magrini, Vincent J., Ye, Kenny, Darnell, Jennifer C., Darnell, Robert B., Mardis, Elaine R., Wilson, Richard K., Schatz, Michael C., McCombie, W. Richard, Wigler, Michael
Publicado em 2012

The contribution of de novo coding mutations to autism spectrum disorder

Por Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali, Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jefferey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael
Publicado no Nature (2014)

Microduplications of 16p11.2 are Associated with Schizophrenia

Por McCarthy, Shane, Makarov, Vladimir, Kirov, George, Addington, Anjene, McClellan, Jon, Yoon, Seungtai, Perkins, Dianna, Dickel, Diane E., Kusenda, Mary, Krastoshevsky, Olga, Krause, Verena, Kumar, Ravinesh A., Grozeva, Detelina, Malhotra, Dheeraj, Walsh, Tom, Zackai, Elaine H., Kaplan, Paige, Ganesh, Jaya, Krantz, Ian D., Spinner, Nancy B., Roccanova, Patricia, Bhandari, Abhishek, Pavon, Kevin, Lakshmi, B., Leotta, Anthony, Kendall, Jude, Lee, Yoon-ha, Vacic, Vladimir, Gary, Sydney, Iakoucheva, Lilia, Crow, Timothy J., Christian, Susan L., Lieberman, Jeffrey, Stroup, Scott, Lehtimäki, Terho, Puura, Kaija, Haldeman-Englert, Chad, Pearl, Justin, Goodell, Meredith, Willour, Virginia L., DeRosse, Pamela, Steele, Jo, Kassem, Layla, Wolff, Jessica, Chitkara, Nisha, McMahon, Francis J., Malhotra, Anil K., Potash, James B., Schulze, Thomas G., Nöthen, Markus M., Cichon, Sven, Rietschel, Marcella, Leibenluft, Ellen, Kustanovich, Vlad, Lajonchere, Clara M., Sutcliffe, James S., Skuse, David, Gill, Michael, Gallagher, Louise, Mendell, Nancy R., Craddock, Nick, Owen, Michael J., O’Donovan, Michael C., Shaikh, Tamim H., Susser, Ezra, DeLisi, Lynn E., Sullivan, Patrick F., Deutsch, Curtis K., Rapoport, Judith, Levy, Deborah L., King, Mary-Claire, Sebat, Jonathan
Publicado em 2009