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Items: 32

1.

Nordic OCD & Related Disorders Consortium: Rationale, design, and methods.

Mataix-Cols D, Hansen B, Mattheisen M, Karlsson EK, Addington AM, Boberg J, Djurfeldt DR, Halvorsen M, Lichtenstein P, Solem S, Lindblad-Toh K; Nordic OCD and Related Disorders Consortium (NORDiC), Haavik J, Kvale G, Rück C, Crowley JJ.

Am J Med Genet B Neuropsychiatr Genet. 2019 Aug 19. doi: 10.1002/ajmg.b.32756. [Epub ahead of print]

PMID:
31424634
2.

Introduction to special section on Leveraging Electronic Health Records for psychiatric genetic research.

Addington AM.

Am J Med Genet B Neuropsychiatr Genet. 2018 Oct;177(7):599-600. doi: 10.1002/ajmg.b.32686. Epub 2018 Oct 31. No abstract available.

PMID:
30381872
3.

The Open Translational Science in Schizophrenia (OPTICS) project: an open-science project bringing together Janssen clinical trial and NIMH data.

Wilcox MA, Savitz AJ, Addington AM, Gray GS, Guinan EC, Jackson JW, Lehner T, Normand SL, Ranu H, Senthil G, Spertus J, Valeri L, Ross JS.

NPJ Schizophr. 2018 Jun 27;4(1):14. doi: 10.1038/s41537-018-0055-7. Review.

4.

Publisher Correction: Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S, Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, Gur RE, Handsaker RE, McCarroll SA, Ophoff RA, Palotie A, Pato CN, Sabatti C, State MW, Willsey AJ, Hyman SE, Addington AM, Lehner T, Freimer NB; Whole Genome Sequencing for Psychiatric Disorders (WGSPD).

Nat Neurosci. 2018 Jul;21(7):1017. doi: 10.1038/s41593-018-0102-8.

5.

Whole genome sequencing in psychiatric disorders: the WGSPD consortium.

Sanders SJ, Neale BM, Huang H, Werling DM, An JY, Dong S; Whole Genome Sequencing for Psychiatric Disorders (WGSPD), Abecasis G, Arguello PA, Blangero J, Boehnke M, Daly MJ, Eggan K, Geschwind DH, Glahn DC, Goldstein DB, Gur RE, Handsaker RE, McCarroll SA, Ophoff RA, Palotie A, Pato CN, Sabatti C, State MW, Willsey AJ, Hyman SE, Addington AM, Lehner T, Freimer NB.

Nat Neurosci. 2017 Dec;20(12):1661-1668. doi: 10.1038/s41593-017-0017-9. Review. No abstract available. Erratum in: Nat Neurosci. 2018 Mar 16;:.

6.

Convergence of advances in genomics, team science, and repositories as drivers of progress in psychiatric genomics.

Lehner T, Senthil G, Addington AM.

Biol Psychiatry. 2015 Jan 1;77(1):6-14. doi: 10.1016/j.biopsych.2014.01.003. Epub 2014 Jan 15. Review.

PMID:
24503471
7.

Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia.

Lee Y, Mattai A, Long R, Rapoport JL, Gogtay N, Addington AM.

Psychiatr Genet. 2012 Aug;22(4):206-9. doi: 10.1097/YPG.0b013e328353ae3d.

8.

Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.

Nguyen LS, Jolly L, Shoubridge C, Chan WK, Huang L, Laumonnier F, Raynaud M, Hackett A, Field M, Rodriguez J, Srivastava AK, Lee Y, Long R, Addington AM, Rapoport JL, Suren S, Hahn CN, Gamble J, Wilkinson MF, Corbett MA, Gecz J.

Mol Psychiatry. 2012 Nov;17(11):1103-15. doi: 10.1038/mp.2011.163. Epub 2011 Dec 20.

9.

Annual research review: impact of advances in genetics in understanding developmental psychopathology.

Addington AM, Rapoport JL.

J Child Psychol Psychiatry. 2012 May;53(5):510-8. doi: 10.1111/j.1469-7610.2011.02478.x. Epub 2011 Nov 8. Review.

PMID:
22067053
10.

A Novel Microduplication in the Neurodevelopmental Gene SRGAP3 That Segregates with Psychotic Illness in the Family of a COS Proband.

Wilson NK, Lee Y, Long R, Hermetz K, Rudd MK, Miller R, Rapoport JL, Addington AM.

Case Rep Genet. 2011;2011:585893. doi: 10.1155/2011/585893. Epub 2011 Sep 12.

11.

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts.

Awadalla P, Gauthier J, Myers RA, Casals F, Hamdan FF, Griffing AR, Côté M, Henrion E, Spiegelman D, Tarabeux J, Piton A, Yang Y, Boyko A, Bustamante C, Xiong L, Rapoport JL, Addington AM, DeLisi JL, Krebs MO, Joober R, Millet B, Fombonne E, Mottron L, Zilversmit M, Keebler J, Daoud H, Marineau C, Roy-Gagnon MH, Dubé MP, Eyre-Walker A, Drapeau P, Stone EA, Lafrenière RG, Rouleau GA.

Am J Hum Genet. 2010 Sep 10;87(3):316-24. doi: 10.1016/j.ajhg.2010.07.019.

12.

A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

Addington AM, Gauthier J, Piton A, Hamdan FF, Raymond A, Gogtay N, Miller R, Tossell J, Bakalar J, Inoff-Germain G, Gochman P, Long R, Rapoport JL, Rouleau GA.

Mol Psychiatry. 2011 Mar;16(3):238-9. doi: 10.1038/mp.2010.59. Epub 2010 May 18. No abstract available. Erratum in: Mol Psychiatry. 2012 Apr;17(4):468. Germain, G [corrected to Inoff-Germain, G].

13.

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia.

Gauthier J, Champagne N, Lafrenière RG, Xiong L, Spiegelman D, Brustein E, Lapointe M, Peng H, Côté M, Noreau A, Hamdan FF, Addington AM, Rapoport JL, Delisi LE, Krebs MO, Joober R, Fathalli F, Mouaffak F, Haghighi AP, Néri C, Dubé MP, Samuels ME, Marineau C, Stone EA, Awadalla P, Barker PA, Carbonetto S, Drapeau P, Rouleau GA; S2D Team.

Proc Natl Acad Sci U S A. 2010 Apr 27;107(17):7863-8. doi: 10.1073/pnas.0906232107. Epub 2010 Apr 12.

14.

Microduplications of 16p11.2 are associated with schizophrenia.

McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, Zackai EH, Kaplan P, Ganesh J, Krantz ID, Spinner NB, Roccanova P, Bhandari A, Pavon K, Lakshmi B, Leotta A, Kendall J, Lee YH, Vacic V, Gary S, Iakoucheva LM, Crow TJ, Christian SL, Lieberman JA, Stroup TS, Lehtimäki T, Puura K, Haldeman-Englert C, Pearl J, Goodell M, Willour VL, Derosse P, Steele J, Kassem L, Wolff J, Chitkara N, McMahon FJ, Malhotra AK, Potash JB, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Leibenluft E, Kustanovich V, Lajonchere CM, Sutcliffe JS, Skuse D, Gill M, Gallagher L, Mendell NR; Wellcome Trust Case Control Consortium, Craddock N, Owen MJ, O'Donovan MC, Shaikh TH, Susser E, Delisi LE, Sullivan PF, Deutsch CK, Rapoport J, Levy DL, King MC, Sebat J.

Nat Genet. 2009 Nov;41(11):1223-7. doi: 10.1038/ng.474. Epub 2009 Oct 25.

15.

The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent.

Addington AM, Rapoport JL.

Curr Psychiatry Rep. 2009 Apr;11(2):156-61. Review.

16.

Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation.

Hamdan FF, Gauthier J, Spiegelman D, Noreau A, Yang Y, Pellerin S, Dobrzeniecka S, Côté M, Perreau-Linck E, Carmant L, D'Anjou G, Fombonne E, Addington AM, Rapoport JL, Delisi LE, Krebs MO, Mouaffak F, Joober R, Mottron L, Drapeau P, Marineau C, Lafrenière RG, Lacaille JC, Rouleau GA, Michaud JL; Synapse to Disease Group.

N Engl J Med. 2009 Feb 5;360(6):599-605. doi: 10.1056/NEJMoa0805392. Erratum in: N Engl J Med. 2009 Oct 29;361(18):1814. Perreault-Linck, Elizabeth [corrected to Perreau-Linck, Elizabeth].

17.

Sex chromosome anomalies in childhood onset schizophrenia: an update.

Eckstrand K, Addington AM, Stromberg T, Merriman B, Miller R, Gochman P, Long R, Dutra A, Chen Z, Meltzer P, Nelson SF, Rapoport JL.

Mol Psychiatry. 2008 Oct;13(10):910-1. doi: 10.1038/mp.2008.67. No abstract available.

18.

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.

Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM, Nord AS, Kusenda M, Malhotra D, Bhandari A, Stray SM, Rippey CF, Roccanova P, Makarov V, Lakshmi B, Findling RL, Sikich L, Stromberg T, Merriman B, Gogtay N, Butler P, Eckstrand K, Noory L, Gochman P, Long R, Chen Z, Davis S, Baker C, Eichler EE, Meltzer PS, Nelson SF, Singleton AB, Lee MK, Rapoport JL, King MC, Sebat J.

Science. 2008 Apr 25;320(5875):539-43. doi: 10.1126/science.1155174. Epub 2008 Mar 27.

19.

Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder.

Idol JR, Addington AM, Long RT, Rapoport JL, Green ED.

J Autism Dev Disord. 2008 Apr;38(4):668-77. Epub 2007 Sep 19.

PMID:
17879154
20.

Neuregulin 1 (8p12) and childhood-onset schizophrenia: susceptibility haplotypes for diagnosis and brain developmental trajectories.

Addington AM, Gornick MC, Shaw P, Seal J, Gogtay N, Greenstein D, Clasen L, Coffey M, Gochman P, Long R, Rapoport JL.

Mol Psychiatry. 2007 Feb;12(2):195-205. Epub 2006 Oct 10.

PMID:
17033632
21.

Segmental uniparental isodisomy on 5q32-qter in a patient with childhood-onset schizophrenia.

Seal JL, Gornick MC, Gogtay N, Shaw P, Greenstein DK, Coffey M, Gochman PA, Stromberg T, Chen Z, Merriman B, Nelson SF, Brooks J, Arepalli S, Wavrant-De Vrièze F, Hardy J, Rapoport JL, Addington AM.

J Med Genet. 2006 Nov;43(11):887-92. Epub 2006 Jun 8.

22.

Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS).

Gornick MC, Addington AM, Sporn A, Gogtay N, Greenstein D, Lenane M, Gochman P, Ordonez A, Balkissoon R, Vakkalanka R, Weinberger DR, Rapoport JL, Straub RE.

J Autism Dev Disord. 2005 Dec;35(6):831-8.

PMID:
16283082
23.

Support for association between ADHD and two candidate genes: NET1 and DRD1.

Bobb AJ, Addington AM, Sidransky E, Gornick MC, Lerch JP, Greenstein DK, Clasen LS, Sharp WS, Inoff-Germain G, Wavrant-De Vrièze F, Arcos-Burgos M, Straub RE, Hardy JA, Castellanos FX, Rapoport JL.

Am J Med Genet B Neuropsychiatr Genet. 2005 Apr 5;134B(1):67-72.

PMID:
15717291
24.

Molecular genetic studies of ADHD: 1991 to 2004.

Bobb AJ, Castellanos FX, Addington AM, Rapoport JL.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):109-25. Review.

PMID:
15700344
25.

The neurodevelopmental model of schizophrenia: update 2005.

Rapoport JL, Addington AM, Frangou S, Psych MR.

Mol Psychiatry. 2005 May;10(5):434-49. Review.

PMID:
15700048
26.

GAD1 (2q31.1), which encodes glutamic acid decarboxylase (GAD67), is associated with childhood-onset schizophrenia and cortical gray matter volume loss.

Addington AM, Gornick M, Duckworth J, Sporn A, Gogtay N, Bobb A, Greenstein D, Lenane M, Gochman P, Baker N, Balkissoon R, Vakkalanka RK, Weinberger DR, Rapoport JL, Straub RE.

Mol Psychiatry. 2005 Jun;10(6):581-8.

PMID:
15505639
27.

Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?

Sporn AL, Addington AM, Gogtay N, Ordoñez AE, Gornick M, Clasen L, Greenstein D, Tossell JW, Gochman P, Lenane M, Sharp WS, Straub RE, Rapoport JL.

Biol Psychiatry. 2004 May 15;55(10):989-94.

PMID:
15121482
28.

Polymorphisms in the 13q33.2 gene G72/G30 are associated with childhood-onset schizophrenia and psychosis not otherwise specified.

Addington AM, Gornick M, Sporn AL, Gogtay N, Greenstein D, Lenane M, Gochman P, Baker N, Balkissoon R, Vakkalanka RK, Weinberger DR, Straub RE, Rapoport JL.

Biol Psychiatry. 2004 May 15;55(10):976-80.

PMID:
15121480
29.

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12.

McInnis MG, Lan TH, Willour VL, McMahon FJ, Simpson SG, Addington AM, MacKinnon DF, Potash JB, Mahoney AT, Chellis J, Huo Y, Swift-Scanlan T, Chen H, Koskela R, Stine OC, Jamison KR, Holmans P, Folstein SE, Ranade K, Friddle C, Botstein D, Marr T, Beaty TH, Zandi P, DePaulo JR.

Mol Psychiatry. 2003 Mar;8(3):288-98.

PMID:
12660801
30.

Multipoint linkage analysis under heterogeneity: incorporation of parametric and nonparametric approaches.

Chiu YF, Addington AM, Beaty TH, Klein AP, Liang KY.

Genet Epidemiol. 2001;21 Suppl 1:S55-60.

PMID:
11793735
31.

Multilocus linkage analysis of the German asthma data.

Zandi PP, Klein AP, Addington AM, Hetmanski JB, Roberts L, Peila R, Shrestha S, Shaw CK, Kiat HC, Langefeld CD, Beaty TH.

Genet Epidemiol. 2001;21 Suppl 1:S210-5.

PMID:
11793671
32.

Epidemiology of unexplained fatigue and major depression in the community: the Baltimore ECA follow-up, 1981-1994.

Addington AM, Gallo JJ, Ford DE, Eaton WW.

Psychol Med. 2001 Aug;31(6):1037-44.

PMID:
11513371

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