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Page 1
Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease.
DeMichele-Sweet MAA, Klei L, Creese B, Harwood JC, Weamer EA, McClain L, Sims R, Hernandez I, Moreno-Grau S, Tárraga L, Boada M, Alarcón-Martín E, Valero S; NIA-LOAD Family Based Study Consortium, Alzheimer’s Disease Genetics Consortium (ADGC); Liu Y, Hooli B, Aarsland D, Selbaek G, Bergh S, Rongve A, Saltvedt I, Skjellegrind HK, Engdahl B, Stordal E, Andreassen OA, Djurovic S, Athanasiu L, Seripa D, Borroni B, Albani D, Forloni G, Mecocci P, Serretti A, De Ronchi D, Politis A, Williams J, Mayeux R, Foroud T, Ruiz A, Ballard C, Holmans P, Lopez OL, Kamboh MI, Devlin B, Sweet RA. DeMichele-Sweet MAA, et al. Among authors: mcclain l. Mol Psychiatry. 2021 Oct;26(10):5797-5811. doi: 10.1038/s41380-021-01152-8. Epub 2021 Jun 10. Mol Psychiatry. 2021. PMID: 34112972 Free PMC article.
Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk.
McKinney BC, McClain LL, Hensler CM, Wei Y, Klei L, Lewis DA, Devlin B, Wang J, Ding Y, Sweet RA. McKinney BC, et al. Among authors: mcclain ll. Transl Psychiatry. 2022 Aug 20;12(1):340. doi: 10.1038/s41398-022-02071-0. Transl Psychiatry. 2022. PMID: 35987687 Free PMC article.
How rare and common risk variation jointly affect liability for autism spectrum disorder.
Klei L, McClain LL, Mahjani B, Panayidou K, De Rubeis S, Grahnat AS, Karlsson G, Lu Y, Melhem N, Xu X, Reichenberg A, Sandin S, Hultman CM, Buxbaum JD, Roeder K, Devlin B. Klei L, et al. Among authors: mcclain ll. Mol Autism. 2021 Oct 6;12(1):66. doi: 10.1186/s13229-021-00466-2. Mol Autism. 2021. PMID: 34615521 Free PMC article.
Age dependent association of inbreeding with risk for schizophrenia in Egypt.
McClain L, Mansour H, Ibrahim I, Klei L, Fathi W, Wood J, Kodavali C, Maysterchuk A, Wood S, El-Chennawi F, Ibrahim N, Eissa A, El-Bahaei W, El Sayed H, Yassein A, Tobar S, El-Boraie H, El-Sheshtawy E, Salah H, Ali A, Erdin S, Devlin B, Talkowski M, Nimgaonkar V. McClain L, et al. Schizophr Res. 2020 Feb;216:450-459. doi: 10.1016/j.schres.2019.10.039. Epub 2020 Jan 9. Schizophr Res. 2020. PMID: 31928911 Free PMC article.
A network of dopaminergic gene variations implicated as risk factors for schizophrenia.
Talkowski ME, Kirov G, Bamne M, Georgieva L, Torres G, Mansour H, Chowdari KV, Milanova V, Wood J, McClain L, Prasad K, Shirts B, Zhang J, O'Donovan MC, Owen MJ, Devlin B, Nimgaonkar VL. Talkowski ME, et al. Among authors: mcclain l. Hum Mol Genet. 2008 Mar 1;17(5):747-58. doi: 10.1093/hmg/ddm347. Epub 2007 Nov 27. Hum Mol Genet. 2008. PMID: 18045777 Free PMC article.
Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples.
Talkowski ME, McClain L, Allen T, Bradford LD, Calkins M, Edwards N, Georgieva L, Go R, Gur R, Gur R, Kirov G, Chowdari K, Kwentus J, Lyons P, Mansour H, McEvoy J, O'Donovan MC, O'Jile J, Owen MJ, Santos A, Savage R, Toncheva D, Vockley G, Wood J, Devlin B, Nimgaonkar VL. Talkowski ME, et al. Among authors: mcclain l. Am J Med Genet B Neuropsychiatr Genet. 2009 Jun 5;150B(4):560-9. doi: 10.1002/ajmg.b.30862. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18937293 Free PMC article.
Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia.
Mansour HA, Talkowski ME, Wood J, Chowdari KV, McClain L, Prasad K, Montrose D, Fagiolini A, Friedman ES, Allen MH, Bowden CL, Calabrese J, El-Mallakh RS, Escamilla M, Faraone SV, Fossey MD, Gyulai L, Loftis JM, Hauser P, Ketter TA, Marangell LB, Miklowitz DJ, Nierenberg AA, Patel J, Sachs GS, Sklar P, Smoller JW, Laird N, Keshavan M, Thase ME, Axelson D, Birmaher B, Lewis D, Monk T, Frank E, Kupfer DJ, Devlin B, Nimgaonkar VL. Mansour HA, et al. Among authors: mcclain l. Bipolar Disord. 2009 Nov;11(7):701-10. doi: 10.1111/j.1399-5618.2009.00756.x. Bipolar Disord. 2009. PMID: 19839995 Free PMC article.
Fine-mapping reveals novel alternative splicing of the dopamine transporter.
Talkowski ME, McCann KL, Chen M, McClain L, Bamne M, Wood J, Chowdari KV, Watson A, Prasad KM, Kirov G, Georgieva L, Toncheva D, Mansour H, Lewis DA, Owen M, O'Donovan M, Papasaikas P, Sullivan P, Ruderfer D, Yao JK, Leonard S, Thomas P, Miyajima F, Quinn J, Lopez AJ, Nimgaonkar VL. Talkowski ME, et al. Among authors: mcclain l. Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1434-47. doi: 10.1002/ajmg.b.31125. Epub 2010 Oct 18. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20957647 Free PMC article.
Genetic associations of perinatal pain and depression.
McClain L, Farrell L, LaSorda K, Pan LA, Peters D, Lim G. McClain L, et al. Mol Pain. 2019 Jan-Dec;15:1744806919882139. doi: 10.1177/1744806919882139. Mol Pain. 2019. PMID: 31552780 Free PMC article.
109 results