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

by McGrath, Lauren M.
Published in J Am Acad Child Adolesc Psychiatry (2018)

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

by McGrath, Lauren M., Stoodley, Catherine J.
Published in J Neurodev Disord (2019)

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

by Joseph, Robert M., McGrath, Lauren M., Tager-Flusberg, Helen
Published 2005

The Multiple Deficit Model: Progress, Problems, and Prospects

by McGrath, Lauren M., Peterson, Robin L., Pennington, Bruce F.
Published in Sci Stud Read (2019)

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

by Macdonald, Kelly, Germine, Laura, Anderson, Alida, Christodoulou, Joanna, McGrath, Lauren M.
Published in Front Psychol (2017)

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

by Moore, Dorothea M., D’Mello, Anila M., McGrath, Lauren M., Stoodley, Catherine J.
Published in Dev Cogn Neurosci (2016)

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

by Peterson, Robin L., Boada, Richard, McGrath, Lauren M., Willcutt, Erik G., Olson, Richard K., Pennington, Bruce F.
Published in J Learn Disabil (2016)

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

by Fowler, Patrick J., McGrath, Lauren M., Henry, David B., Schoeny, Michael, Chavira, Dina, Taylor, Jeremy J., Day, Orin
Published in Child Abuse Negl (2015)

How Specific Are Learning Disabilities?

by Peterson, Robin L., McGrath, Lauren M., Willcutt, Erik G., Keenan, Janice M., Olson, Richard K., Pennington, Bruce F.
Published in J Learn Disabil (2021)

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

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

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

by 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.
Published 2010

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

by 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.
Published 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...

by 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.
Published 2013

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

by 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.
Published in J Autism Dev Disord (2016)

Cross-Disorder Cognitive Impairments in Youth Referred for Neuropsychiatric Evaluation

by 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.
Published in J Int Neuropsychol Soc (2017)

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

by 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.
Published in J Child Psychol Psychiatry (2015)

Social disinhibition is a heritable subphenotype of tics in Tourette syndrome

by 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.
Published in Neurology (2016)

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

by 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.
Published in Psychol Med (2017)

Identification of two heritable cross-disorder endophenotypes for Tourette Syndrome

by 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.
Published in Am J Psychiatry (2016)

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

by 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.
Published in Nat Genet (2014)