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Lauren M. McGrath, Ph.D. - Publications

Affiliations: 
American University, Washington, DC, United States 
Area:
learning disabilities, child neuropsychology
Website:
http://www.american.edu/cas/faculty/mcgrath.cfm
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40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 McGrath LM, Peterson RL, Pennington BF. The Multiple Deficit Model: Progress, Problems, and Prospects. Scientific Studies of Reading : the Official Journal of the Society For the Scientific Study of Reading. 24: 7-13. PMID 32440085 DOI: 10.1080/10888438.2019.1706180  0.757
2020 Anderson A, Sarlo GL, Pearlstein H, McGrath LM. A Review of Online Dyslexia Learning Modules Frontiers in Education. 5. DOI: 10.3389/Feduc.2020.00118  0.302
2019 McGrath LM, Stoodley CJ. Are there shared neural correlates between dyslexia and ADHD? A meta-analysis of voxel-based morphometry studies. Journal of Neurodevelopmental Disorders. 11: 31. PMID 31752659 DOI: 10.1186/S11689-019-9287-8  0.608
2019 Willcutt EG, McGrath LM, Pennington BF, Keenan JM, DeFries JC, Olson RK, Wadsworth SJ. Understanding Comorbidity Between Specific Learning Disabilities. New Directions For Child and Adolescent Development. PMID 31070302 DOI: 10.1002/Cad.20291  0.596
2018 Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, ... ... McGrath L, et al. Analysis of shared heritability in common disorders of the brain. Science (New York, N.Y.). 360. PMID 29930110 DOI: 10.1126/Science.Aap8757  0.471
2017 Doyle AE, Vuijk PJ, Doty ND, McGrath LM, Willoughby BL, O'Donnell EH, Wilson HK, Colvin MK, Toner DC, Hudson KE, Blais JE, Ditmars HL, Faraone SV, Seidman LJ, Braaten EB. Cross-Disorder Cognitive Impairments in Youth Referred for Neuropsychiatric Evaluation. Journal of the International Neuropsychological Society : Jins. 1-13. PMID 28774351 DOI: 10.1017/S1355617717000601  0.523
2017 Hirschtritt ME, Darrow SM, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King RA, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, McGrath LM, et al. Genetic and phenotypic overlap of specific obsessive-compulsive and attention-deficit/hyperactive subtypes with Tourette syndrome. Psychological Medicine. 1-15. PMID 28651666 DOI: 10.1017/S0033291717001672  0.49
2017 Huang AY, Yu D, Davis LK, Sul JH, Tsetsos F, Ramensky V, Zelaya I, Ramos EM, Osiecki L, Chen JA, McGrath LM, Illmann C, Sandor P, Barr CL, Grados M, et al. Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome. Neuron. 94: 1101-1111.e7. PMID 28641109 DOI: 10.1016/J.Neuron.2017.06.010  0.306
2017 Hirschtritt M, Darrow SM, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King RA, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, McGrath LM, et al. 896. Genetic and Phenotypic Overlap of Specific Obsessive-Compulsive Subtypes with Tourette Syndrome Biological Psychiatry. 81: S361-S362. DOI: 10.1016/J.Biopsych.2017.02.621  0.579
2016 Moore DM, D'Mello AM, McGrath LM, Stoodley CJ. The developmental relationship between specific cognitive domains and grey matter in the cerebellum. Developmental Cognitive Neuroscience. 24: 1-11. PMID 28088647 DOI: 10.1016/J.Dcn.2016.12.001  0.443
2016 Darrow SM, Hirschtritt ME, Davis LK, Illmann C, Osiecki L, Grados M, Sandor P, Dion Y, King R, Pauls D, Budman CL, Cath DC, Greenberg E, Lyon GJ, Yu D, ... McGrath LM, et al. Identification of Two Heritable Cross-Disorder Endophenotypes for Tourette Syndrome. The American Journal of Psychiatry. appiajp201616020240. PMID 27809572 DOI: 10.1176/Appi.Ajp.2016.16020240  0.45
2016 McGrath LM, Oates JM, Dai YG, Dodd HF, Waxler J, Clements CC, Weill S, Hoffnagle A, Anderson E, MacRae R, Mullett J, McDougle CJ, Pober BR, Smoller JW. Attention Bias to Emotional Faces Varies by IQ and Anxiety in Williams Syndrome. Journal of Autism and Developmental Disorders. PMID 26886469 DOI: 10.1007/S10803-016-2748-Y  0.378
2016 Peterson RL, Boada R, McGrath LM, Willcutt EG, Olson RK, Pennington BF. Cognitive Prediction of Reading, Math, and Attention: Shared and Unique Influences. Journal of Learning Disabilities. PMID 26825667 DOI: 10.1177/0022219415618500  0.813
2015 McGrath LM, Braaten EB, Doty ND, Willoughby BL, Wilson HK, O'Donnell EH, Colvin MK, Ditmars HL, Blais JE, Hill EN, Metzger A, Perlis RH, Willcutt EG, Smoller JW, Waldman ID, et al. Extending the 'cross-disorder' relevance of executive functions to dimensional neuropsychiatric traits in youth. Journal of Child Psychology and Psychiatry, and Allied Disciplines. PMID 26411927 DOI: 10.1111/Jcpp.12463  0.499
2015 Fowler PJ, McGrath LM, Henry DB, Schoeny M, Chavira D, Taylor JJ, Day O. Housing mobility and cognitive development: Change in verbal and nonverbal abilities. Child Abuse & Neglect. 48: 104-18. PMID 26184055 DOI: 10.1016/J.Chiabu.2015.06.002  0.387
2015 Yu D, Mathews CA, Scharf JM, Neale BM, Davis LK, Gamazon ER, Derks EM, Evans P, Edlund CK, Crane J, Fagerness JA, Osiecki L, Gallagher P, Gerber G, Haddad S, ... ... McGrath LM, et al. Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. The American Journal of Psychiatry. 172: 82-93. PMID 25158072 DOI: 10.1176/Appi.Ajp.2014.13101306  0.421
2015 Robinson EB, Kirby A, Ruparel K, Yang J, McGrath L, Anttila V, Neale BM, Merikangas K, Lehner T, Sleiman PM, Daly MJ, Gur R, Gur R, Hakonarson H. The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort. Molecular Psychiatry. 20: 454-8. PMID 25023143 DOI: 10.1038/Mp.2014.65  0.38
2014 Robinson EB, Samocha KE, Kosmicki JA, McGrath L, Neale BM, Perlis RH, Daly MJ. Autism spectrum disorder severity reflects the average contribution of de novo and familial influences. Proceedings of the National Academy of Sciences of the United States of America. 111: 15161-5. PMID 25288738 DOI: 10.1073/Pnas.1409204111  0.429
2014 McGrath LM, Yu D, Marshall C, Davis LK, Thiruvahindrapuram B, Li B, Cappi C, Gerber G, Wolf A, Schroeder FA, Osiecki L, O'Dushlaine C, Kirby A, Illmann C, Haddad S, et al. Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study. Journal of the American Academy of Child and Adolescent Psychiatry. 53: 910-9. PMID 25062598 DOI: 10.1016/J.Jaac.2014.04.022  0.423
2013 Davis LK, Yu D, Keenan CL, Gamazon ER, Konkashbaev AI, Derks EM, Neale BM, Yang J, Lee SH, Evans P, Barr CL, Bellodi L, Benarroch F, Berrio GB, Bienvenu OJ, ... ... McGrath LM, et al. Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture. Plos Genetics. 9: e1003864. PMID 24204291 DOI: 10.1371/Journal.Pgen.1003864  0.401
2013 McGrath LM, Cornelis MC, Lee PH, Robinson EB, Duncan LE, Barnett JH, Huang J, Gerber G, Sklar P, Sullivan P, Perlis RH, Smoller JW. Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 779-88. PMID 24039173 DOI: 10.1002/Ajmg.B.32190  0.459
2013 Nag A, Bochukova EG, Kremeyer B, Campbell DD, Muller H, Valencia-Duarte AV, Cardona J, Rivas IC, Mesa SC, Cuartas M, Garcia J, Bedoya G, Cornejo W, Herrera LD, Romero R, ... ... McGrath LM, et al. CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1. Plos One. 8: e59061. PMID 23533600 DOI: 10.1371/Journal.Pone.0059061  0.327
2013 Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Davis LK, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, et al. Genome-wide association study of obsessive-compulsive disorder. Molecular Psychiatry. 18: 788-98. PMID 22889921 DOI: 10.1038/Mp.2012.85  0.323
2013 Stewart SE, Yu D, Scharf JM, Neale BM, Fagerness JA, Mathews CA, Arnold PD, Evans PD, Gamazon ER, Osiecki L, McGrath L, Haddad S, Crane J, Hezel D, Illman C, et al. Erratum: Genome-wide association study of obsessive-compulsive disorder Molecular Psychiatry. 18: 843-843. DOI: 10.1038/Mp.2013.15  0.305
2012 McGrath LM, Weill S, Robinson EB, Macrae R, Smoller JW. Bringing a developmental perspective to anxiety genetics Development and Psychopathology. 24: 1179-1193. PMID 23062290 DOI: 10.1017/S0954579412000636  0.379
2011 Middeldorp CM, de Moor MH, McGrath LM, Gordon SD, Blackwood DH, Costa PT, Terracciano A, Krueger RF, de Geus EJ, Nyholt DR, Tanaka T, Esko T, Madden PA, Derringer J, Amin N, et al. The genetic association between personality and major depression or bipolar disorder. A polygenic score analysis using genome-wide association data. Translational Psychiatry. 1: e50. PMID 22833196 DOI: 10.1038/Tp.2011.45  0.394
2011 McGrath LM, Pennington BF, Shanahan MA, Santerre-Lemmon LE, Barnard HD, Willcutt EG, Defries JC, Olson RK. A multiple deficit model of reading disability and attention-deficit/hyperactivity disorder: searching for shared cognitive deficits. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 52: 547-57. PMID 21126246 DOI: 10.1111/J.1469-7610.2010.02346.X  0.601
2010 Willcutt EG, Betjemann RS, McGrath LM, Chhabildas NA, Olson RK, DeFries JC, Pennington BF. Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit models. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 46: 1345-61. PMID 20828676 DOI: 10.1016/J.Cortex.2010.06.009  0.805
2010 Hodge SM, Makris N, Kennedy DN, Caviness VS, Howard J, McGrath L, Steele S, Frazier JA, Tager-Flusberg H, Harris GJ. Cerebellum, language, and cognition in autism and specific language impairment. Journal of Autism and Developmental Disorders. 40: 300-16. PMID 19924522 DOI: 10.1007/S10803-009-0872-7  0.371
2009 Pennington BF, McGrath LM, Rosenberg J, Barnard H, Smith SD, Willcutt EG, Friend A, Defries JC, Olson RK. Gene X environment interactions in reading disability and attention-deficit/hyperactivity disorder. Developmental Psychology. 45: 77-89. PMID 19209992 DOI: 10.1037/A0014549  0.762
2008 McGrath LM, Hutaff-Lee C, Scott A, Boada R, Shriberg LD, Pennington BF. Children with comorbid speech sound disorder and specific language impairment are at increased risk for attention-deficit/hyperactivity disorder. Journal of Abnormal Child Psychology. 36: 151-63. PMID 17882543 DOI: 10.1007/S10802-007-9166-8  0.768
2007 McGrath LM, Pennington BF, Willcutt EG, Boada R, Shriberg LD, Smith SD. Gene x Environment interactions in speech sound disorder predict language and preliteracy outcomes. Development and Psychopathology. 19: 1047-72. PMID 17931434 DOI: 10.1017/S0954579407000533  0.706
2007 Peterson RL, McGrath LM, Smith SD, Pennington BF. Neuropsychology and genetics of speech, language, and literacy disorders. Pediatric Clinics of North America. 54: 543-61, vii. PMID 17543909 DOI: 10.1016/J.Pcl.2007.02.009  0.733
2006 McGrath LM, Smith SD, Pennington BF. Breakthroughs in the search for dyslexia candidate genes. Trends in Molecular Medicine. 12: 333-41. PMID 16781891 DOI: 10.1016/J.Molmed.2006.05.007  0.505
2006 Harris GJ, Chabris CF, Clark J, Urban T, Aharon I, Steele S, McGrath L, Condouris K, Tager-Flusberg H. Brain activation during semantic processing in autism spectrum disorders via functional magnetic resonance imaging. Brain and Cognition. 61: 54-68. PMID 16473449 DOI: 10.1016/J.Bandc.2005.12.015  0.377
2005 Joseph RM, McGrath LM, Tager-Flusberg H. Executive dysfunction and its relation to language ability in verbal school-age children with autism Developmental Neuropsychology. 27: 361-378. PMID 15843102 DOI: 10.1207/S15326942Dn2703_4  0.376
2004 De Fossé L, Hodge SM, Makris N, Kennedy DN, Caviness VS, McGrath L, Steele S, Ziegler DA, Herbert MR, Frazier JA, Tager-Flusberg H, Harris GJ. Language-association cortex asymmetry in autism and specific language impairment. Annals of Neurology. 56: 757-66. PMID 15478219 DOI: 10.1002/Ana.20275  0.343
2004 Hadjikhani N, Joseph RM, Snyder J, Chabris CF, Clark J, Steele S, McGrath L, Vangel M, Aharon I, Feczko E, Harris GJ, Tager-Flusberg H. Activation of the fusiform gyrus when individuals with autism spectrum disorder view faces. Neuroimage. 22: 1141-50. PMID 15219586 DOI: 10.1016/J.Neuroimage.2004.03.025  0.361
2004 Hadjikhani N, Chabris CF, Joseph RM, Clark J, McGrath L, Aharon I, Feczko E, Tager-Flusberg H, Harris GJ. Early visual cortex organization in autism: an fMRI study. Neuroreport. 15: 267-70. PMID 15076750 DOI: 10.1097/00001756-200402090-00011  0.351
2003 Tadevosyan-Leyfer O, Dowd M, Mankoski R, Winklosky B, Putnam S, McGrath L, Tager-Flusberg H, Folstein SE. A principal components analysis of the autism diagnostic interview-revised Journal of the American Academy of Child and Adolescent Psychiatry. 42: 864-872. PMID 12819447 DOI: 10.1097/01.Chi.0000046870.56865.90  0.319
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