Two GWASs are better than one: Enhancing genetic discovery for developmental phenotypes

Por McGrath, Lauren M.
Publicado no J Am Acad Child Adolesc Psychiatry (2018)

Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies

Por McGrath, Lauren M., Stoodley, Catherine J.
Publicado no J Neurodev Disord (2019)

Executive Dysfunction and Its Relation to Language Ability in Verbal School-Age Children With Autism

Por Joseph, Robert M., McGrath, Lauren M., Tager-Flusberg, Helen
Publicado em 2005

The Multiple Deficit Model: Progress, Problems, and Prospects

Por McGrath, Lauren M., Peterson, Robin L., Pennington, Bruce F.
Publicado no Sci Stud Read (2019)

Dispelling the Myth: Training in Education or Neuroscience Decreases but Does Not Eliminate Beliefs in Neuromyths

Por Macdonald, Kelly, Germine, Laura, Anderson, Alida, Christodoulou, Joanna, McGrath, Lauren M.
Publicado no Front Psychol (2017)

The developmental relationship between specific cognitive domains and grey matter in the cerebellum

Por Moore, Dorothea M., D’Mello, Anila M., McGrath, Lauren M., Stoodley, Catherine J.
Publicado no Dev Cogn Neurosci (2016)

Cognitive Prediction of Reading, Math, and Attention: Shared and Unique Influences

Por Peterson, Robin L., Boada, Richard, McGrath, Lauren M., Willcutt, Erik G., Olson, Richard K., Pennington, Bruce F.
Publicado no J Learn Disabil (2016)

Housing Mobility and Cognitive Development: Change in Verbal and Nonverbal Abilities

Por Fowler, Patrick J., McGrath, Lauren M., Henry, David B., Schoeny, Michael, Chavira, Dina, Taylor, Jeremy J., Day, Orin
Publicado no Child Abuse Negl (2015)

Etiology And Neuropsychology Of Comorbidity Between RD And ADHD: The Case For Multiple-Deficit Models

Por Willcutt, Erik G., Betjemann, Rebecca S., McGrath, Lauren M., Chhabildas, Nomita A., Olson, Richard K., DeFries, John C., Pennington, Bruce F.
Publicado em 2010

A multiple deficit model of Reading Disability and Attention-Deficit/Hyperactivity Disorder: Searching for shared cognitive deficits

Por McGrath, Lauren M., Pennington, Bruce F., Shanahan, Michelle A., Santerre-Lemmon, Laura E., Barnard, Holly D., Willcutt, Erik G., DeFries, John C., Olson, Richard K.
Publicado em 2010

Gene × Environment Interactions in Reading Disability and Attention-Deficit/Hyperactivity Disorder

Por Pennington, Bruce F., McGrath, Lauren M., Rosenberg, Jenni, Barnard, Holly, Smith, Shelley D., Munroe, Hattie B., Willcutt, Erik G., Friend, Angela, DeFries, John C., Olson, Richard K.
Publicado em 2009

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

Attention bias to emotional faces varies by IQ and anxiety in Williams syndrome

Por McGrath, Lauren M., Oates, Joyce M., Dai, Yael G., Dodd, Helen F., Waxler, Jessica, Clements, Caitlin C., Weill, Sydney, Hoffnagle, Alison, Anderson, Erin, MacRae, Rebecca, Mullett, Jennifer, McDougle, Christopher J., Pober, Barbara R., Smoller, Jordan W.
Publicado no J Autism Dev Disord (2016)

Cross-Disorder Cognitive Impairments in Youth Referred for Neuropsychiatric Evaluation

Por Doyle, Alysa E., Vuijk, Pieter J., Doty, Nathan D., McGrath, Lauren M., Willoughby, Brian L., O’Donnell, Ellen H., Wilson, H. Kent, Colvin, Mary K., Toner, Deanna C., Hudson, Kelsey E., Blais, Jessica E., Ditmars, Hillary L., Faraone, Stephen V., Seidman, Larry J., Braaten, Ellen B.
Publicado no J Int Neuropsychol Soc (2017)

Extending the ‘cross-disorder’ relevance of executive functions to dimensional neuropsychiatric traits in youth

Por McGrath, Lauren M., Braaten, Ellen B., Doty, Nathan D., Willoughby, Brian L., Wilson, H. Kent, O’Donnell, Ellen H., Colvin, Mary K., Ditmars, Hillary L., Blais, Jessica E., Hill, Erin N., Metzger, Aaron, Perlis, Roy H., Willcutt, Erik G., Smoller, Jordan W., Waldman, Irwin D., Faraone, Stephen V., Seidman, Larry J., Doyle, Alysa E.
Publicado no J Child Psychol Psychiatry (2015)

Social disinhibition is a heritable subphenotype of tics in Tourette syndrome

Por Hirschtritt, Matthew E., Darrow, Sabrina M., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert A., Pauls, David L., Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A.
Publicado no Neurology (2016)

Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome

Por Hirschtritt, Matthew E., Darrow, Sabrina M., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert A., Pauls, David, Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A.
Publicado no Psychol Med (2017)

Identification of two heritable cross-disorder endophenotypes for Tourette Syndrome

Por Darrow, Sabrina M., Hirschtritt, Matthew E., Davis, Lea K., Illmann, Cornelia, Osiecki, Lisa, Grados, Marco, Sandor, Paul, Dion, Yves, King, Robert, Pauls, David, Budman, Cathy L., Cath, Danielle C., Greenberg, Erica, Lyon, Gholson J., Yu, Dongmei, McGrath, Lauren M., McMahon, William M., Lee, Paul C., Delucchi, Kevin L., Scharf, Jeremiah M., Mathews, Carol A.
Publicado no Am J Psychiatry (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)

CNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1

Por Nag, Abhishek, Bochukova, Elena G., Kremeyer, Barbara, Campbell, Desmond D., Muller, Heike, Valencia-Duarte, Ana V., Cardona, Julio, Rivas, Isabel C., Mesa, Sandra C., Cuartas, Mauricio, Garcia, Jharley, Bedoya, Gabriel, Cornejo, William, Herrera, Luis D., Romero, Roxana, Fournier, Eduardo, Reus, Victor I., Lowe, Thomas L., Farooqi, I. Sadaf, Mathews, Carol A., McGrath, Lauren M., Yu, Dongmei, Cook, Ed, Wang, Kai, Scharf, Jeremiah M., Pauls, David L., Freimer, Nelson B., Plagnol, Vincent, Ruiz-Linares, Andrés
Publicado em 2013