Genetic research in autism spectrum disorders

Por Robinson, Elise B., Neale, Benjamin M., Hyman, Steven E.
Publicado no Curr Opin Pediatr (2015)

Examining and interpreting the female protective effect against autistic behavior

Por Robinson, Elise B., Lichtenstein, Paul, Anckarsäter, Henrik, Happé, Francesca, Ronald, Angelica
Publicado em 2013

Bringing a developmental perspective to anxiety genetics

Por MCGRATH, LAUREN M., WEILL, SYDNEY, ROBINSON, ELISE B., MACRAE, REBECCA, SMOLLER, JORDAN W.
Publicado em 2012

A longitudinal twin study of the association between childhood autistic traits and psychotic experiences in adolescence

Por Taylor, Mark J., Robinson, Elise B., Happé, Francesca, Bolton, Patrick, Freeman, Daniel, Ronald, Angelica
Publicado no Mol Autism (2015)

Brief Report: No Association Between Parental Age and Extreme Social-Communicative Autistic Traits in the General Population

Por Robinson, Elise B., Munir, Kerim, McCormick, Marie C., Koenen, Karestan C., Santangelo, Susan L.
Publicado em 2011

Language and Traits of Autism Spectrum Conditions: Evidence of Limited Phenotypic and Etiological Overlap

Por Taylor, Mark J., Charman, Tony, Robinson, Elise B., Hayiou-Thomas, Marianna E., Happé, Francesca, Dale, Philip S., Ronald, Angelica
Publicado no Am J Med Genet B Neuropsychiatr Genet (2014)

A multivariate twin study of autistic traits in 12-year-olds: testing the fractionable autism triad hypothesis

Por Robinson, Elise B., Koenen, Karestan C., McCormick, Marie C., Munir, Kerim, Hallett, Victoria, Happé, Francesca, Plomin, Robert, Ronald, Angelica
Publicado em 2011

Autism spectrum disorder severity reflects the average contribution of de novo and familial influences

Por Robinson, Elise B., Samocha, Kaitlin E., Kosmicki, Jack A., McGrath, Lauren, Neale, Benjamin M., Perlis, Roy H., Daly, Mark J.
Publicado em 2014

Bipolar polygenic loading and bipolar spectrum features in major depressive disorder

Por Wiste, Anna, Robinson, Elise B, Milaneschi, Yuri, Meier, Sandra, Ripke, Stephan, Clements, Caitlin C, Fitzmaurice, Garrett M, Rietschel, Marcella, Penninx, Brenda W, Smoller, Jordan W, Perlis, Roy H
Publicado no Bipolar Disord (2014)

Genetic Predictors of Risk and Resilience in Psychiatric Disorders: A Cross-Disorder Genome-wide Association Study of Functional Impairment in Major Depressive Disorder, Bipolar Di...

Por McGrath, Lauren M., Cornelis, Marilyn C., Lee, Phil H., Robinson, Elise B., Duncan, Laramie E., Barnett, Jennifer H., Huang, Jie, Gerber, Gloria, Sklar, Pamela, Sullivan, Patrick, Perlis, Roy H., Smoller, Jordan W.
Publicado em 2013

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

Por Robinson, Elise B., Kirby, Andrew, Ruparel, Kosha, Yang, Jian, McGrath, Lauren, Anttila, Verneri, Neale, Benjamin M., Merikangas, Kathleen, Lehner, Thomas, Sleiman, Patrick M.A., Daly, Mark J., Gur, Ruben, Gur, Raquel, Hakonarson, Hakon
Publicado no Mol Psychiatry (2014)

An Atlas of Genetic Correlations across Human Diseases and Traits

Por Bulik-Sullivan, Brendan, Finucane, Hilary K, Anttila, Verneri, Gusev, Alexander, Day, Felix R., Loh, Po-Ru, Duncan, Laramie, Perry, John R.B., Patterson, Nick, Robinson, Elise B., Daly, Mark J., Price, Alkes L., Neale, Benjamin M.
Publicado no Nat Genet (2015)

Prenatal antidepressant exposure is associated with risk for attention deficit-hyperactivity disorder but not autism spectrum disorder in a large health system

Por Clements, Caitlin C., Castro, Victor M., Blumenthal, Sarah R., Rosenfield, Hannah R., Murphy, Shawn N., Fava, Maurizio, Erb, Jane L., Churchill, Susanne E., Kaimal, Anjali J., Doyle, Alysa E., Robinson, Elise B., Smoller, Jordan W., Kohane, Isaac S., Perlis, Roy H.
Publicado no Mol Psychiatry (2014)

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Por Robinson, Elise B., St. Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A., Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E., Sanders, Stephan J., Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V., Werge, Thomas, Hougaard, David M., Neale, Benjamin M., Evans, David M., Skuse, David, Mortensen, Preben Bo, Børglum, Anders D., Ronald, Angelica, Smith, George Davey, Daly, Mark J.
Publicado no Nat Genet (2016)

A framework for the interpretation of de novo mutation in human disease

Por Samocha, Kaitlin E., Robinson, Elise B., Sanders, Stephan J., Stevens, Christine, Sabo, Aniko, McGrath, Lauren M., Kosmicki, Jack A., Rehnström, Karola, Mallick, Swapan, Kirby, Andrew, Wall, Dennis P., MacArthur, Daniel G., Gabriel, Stacey B., dePristo, Mark, Purcell, Shaun M., Palotie, Aarno, Boerwinkle, Eric, Buxbaum, Joseph D., Cook, Edwin H., Gibbs, Richard A., Schellenberg, Gerard D., Sutcliffe, James S., Devlin, Bernie, Roeder, Kathryn, Neale, Benjamin M., Daly, Mark J.
Publicado no Nat Genet (2014)

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

Por Ganna, Andrea, Genovese, Giulio, Howrigan, Daniel P., Byrnes, Andrea, Kurki, Mitja, Zekavat, Seyedeh M., Whelan, Christopher W., Kals, Mart, Nivard, Michel G., Bloemendal, Alex, Bloom, Jonathan M., Goldstein, Jacqueline I., Poterba, Timothy, Seed, Cotton, Handsaker, Robert E., Natarajan, Pradeep, Mägi, Reedik, Gage, Diane, Robinson, Elise B., Metspalu, Andres, Salomaa, Veikko, Suvisaari, Jaana, Purcell, Shaun M., Sklar, Pamela, Kathiresan, Sekar, Daly, Mark J., McCarroll, Steven A., Sullivan, Patrick F., Palotie, Aarno, Esko, Tõnu, Hultman, Christina, Neale, Benjamin M.
Publicado no Nat Neurosci (2016)

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

Por Sanders, Stephan J., He, Xin, Willsey, A. Jeremy, Ercan-Sencicek, A. Gulhan, Samocha, Kaitlin E., Cicek, A. Ercument, Murtha, Michael T., Bal, Vanessa H., Bishop, Somer L., Dong, Shan, Goldberg, Arthur P., Jinlu, Cai, Keaney, John F., Klei, Lambertus, Mandell, Jeffrey D., Moreno-De-Luca, Daniel, Poultney, Christopher S., Robinson, Elise B., Smith, Louw, Solli-Nowlan, Tor, Su, Mack Y., Teran, Nicole A., Walker, Michael F., Werling, Donna M., Beaudet, Arthur L., Cantor, Rita M., Fombonne, Eric, Geschwind, Daniel H., Grice, Dorothy E., Lord, Catherine, Lowe, Jennifer K., Mane, Shrikant M., Martin, Donna M., Morrow, Eric M., Talkowski, Michael E., Sutcliffe, James S., Walsh, Christopher A., Yu, Timothy W., Ledbetter, David H., Martin, Christa Lese, Cook, Edwin H., Buxbaum, Joseph D., Daly, Mark J., Devlin, Bernie, Roeder, Kathryn, State, Matthew W.
Publicado no Neuron (2015)