Genetic research in autism spectrum disorders

por Robinson, Elise B., Neale, Benjamin M., Hyman, Steven E.
Publicado 2015

A scoping review on the methods of assessment and role of resilience on function and movement-evoked pain when experiencing a musculoskeletal injury

por Robinson, Elise M., Clothier, Peter J., Slater, Helen, Gupta, Amitabh
Publicado 2022

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 2015

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 2014

Developmental Variability in Autism Across 17 000 Autistic Individuals and 4000 Siblings Without an Autism Diagnosis: Comparisons by Cohort, Intellectual Disability, Genetic Etiolo...

por Kuo, Susan S., van der Merwe, Celia, Fu, Jack M., Carey, Caitlin E., Talkowski, Michael E., Bishop, Somer L., Robinson, Elise B.
Publicado 2022

Validity of the SNAP-IV For ADHD Assessment in South African Children With Neurodevelopmental Disorders

por Zieff, Michal R., Hoogenhout, Michelle, Eastman, Emma, Christ, Björn U., Galvin, Alice, de Menil, Victoria, Abubakar, Amina, Newton, Charles R., Robinson, Elise, Donald, Kirsten A.
Publicado 2022

WebEase: Development of a Web-Based Epilepsy Self-Management Intervention

por DiIorio, Colleen, Escoffery, Cam, Yeager, Katherine A., Koganti, Archana, Reisinger, Elizabeth, Koganti, Archana, McCarty, Frances, Henry, Thomas R., Robinson, Elise, Kobau, Rosemarie, Price, Patricia
Publicado 2008

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 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 2015

Genetic influences on externalizing psychopathology overlap with cognitive functioning and show developmental variation

por Mollon, Josephine, Knowles, Emma E. M., Mathias, Samuel R., Rodrigue, Amanda, Moore, Tyler M., Calkins, Monica E., Gur, Ruben C., Peralta, Juan Manuel, Weiner, Daniel J., Robinson, Elise B., Gur, Raquel E., Blangero, John, Almasy, Laura, Glahn, David C.
Publicado 2021

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 2014

Assessing the utility of electronic measures as a proxy for cognitive ability

por Levy, Tess, Britvan, Bari, Grosman, Hannah, Giserman‐Kiss, Ivy, Meyering, Kristin, Weissman, Jordana, Halpern, Danielle, Zweifach, Jessica, Trelles, M. Pilar, Foss‐Feig, Jennifer H., Kolevzon, Alexander, Sanders, Stephan J., Robinson, Elise B., Buxbaum, Joseph D., Bishop, Somer, Siper, Paige M.
Publicado 2022

In vivo visualization and molecular targeting of the cardiac conduction system

por Goodyer, William R., Beyersdorf, Benjamin M., Duan, Lauren, van den Berg, Nynke S., Mantri, Sruthi, Galdos, Francisco X., Puluca, Nazan, Buikema, Jan W., Lee, Soah, Salmi, Darren, Robinson, Elise R., Rogalla, Stephan, Cogan, Dillon P., Khosla, Chaitan, Rosenthal, Eben L., Wu, Sean M.
Publicado 2022

Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples

por Kosmicki, Jack A., Samocha, Kaitlin E., Howrigan, Daniel P., Sanders, Stephan J., Slowikowski, Kamil, Lek, Monkol, Karczewski, Konrad J., Cutler, David J., Devlin, Bernie, Roeder, Kathryn, Buxbaum, Joseph D., Neale, Benjamin M., MacArthur, Daniel G., Wall, Dennis P., Robinson, Elise B., Daly, Mark J.
Publicado 2017

Genetic correlates of phenotypic heterogeneity in autism

por Warrier, Varun, Zhang, Xinhe, Reed, Patrick, Havdahl, Alexandra, Moore, Tyler M., Cliquet, Freddy, Leblond, Claire S., Rolland, Thomas, Rosengren, Anders, Rowitch, David H., Hurles, Matthew E., Geschwind, Daniel H., Børglum, Anders D., Robinson, Elise B., Grove, Jakob, Martin, Hilary C., Bourgeron, Thomas, Baron-Cohen, Simon
Publicado 2022

Immune modulation resulting from MR-guided high intensity focused ultrasound in a model of murine breast cancer

por Fite, Brett Z., Wang, James, Kare, Aris J., Ilovitsh, Asaf, Chavez, Michael, Ilovitsh, Tali, Zhang, Nisi, Chen, Weiyu, Robinson, Elise, Zhang, Hua, Kheirolomoom, Azadeh, Silvestrini, Matthew T., Ingham, Elizabeth S., Mahakian, Lisa M., Tam, Sarah M., Davis, Ryan R., Tepper, Clifford G., Borowsky, Alexander D., Ferrara, Katherine W.
Publicado 2021

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

por Antaki, Danny, Guevara, James, Maihofer, Adam X., Klein, Marieke, Gujral, Madhusudan, Grove, Jakob, Carey, Caitlin E., Hong, Oanh, Arranz, Maria J., Hervas, Amaia, Corsello, Christina, Vaux, Keith K., Muotri, Alysson R., Iakoucheva, Lilia M., Courchesne, Eric, Pierce, Karen, Gleeson, Joseph G., Robinson, Elise, Nievergelt, Caroline M., Sebat, Jonathan
Publicado 2022

Polygenic risk for schizophrenia and measured domains of cognition in individuals with psychosis and controls

por Shafee, Rebecca, Nanda, Pranav, Padmanabhan, Jaya L., Tandon, Neeraj, Alliey-Rodriguez, Ney, Kalapurakkel, Sreeja, Weiner, Daniel J., Gur, Raquel E., Keefe, Richard S. E., Hill, Scot K., Bishop, Jeffrey R., Clementz, Brett A., Tamminga, Carol A., Gershon, Elliot S., Pearlson, Godfrey D., Keshavan, Matcheri S., Sweeney, John A., McCarroll, Steven A., Robinson, Elise B.
Publicado 2018

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

por Weiner, Daniel J., Ling, Emi, Erdin, Serkan, Tai, Derek J. C., Yadav, Rachita, Grove, Jakob, Fu, Jack M., Nadig, Ajay, Carey, Caitlin E., Baya, Nikolas, Bybjerg-Grauholm, Jonas, Berretta, Sabina, Macosko, Evan Z., Sebat, Jonathan, O’Connor, Luke J., Hougaard, David M., Børglum, Anders D., Talkowski, Michael E., McCarroll, Steven A., Robinson, Elise B.
Publicado 2022

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 2016