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Items: 1 to 20 of 523

1.

Identification of novel candidate disease genes from de novo exonic copy number variants.

Gambin T, Yuan B, Bi W, Liu P, Rosenfeld JA, Coban-Akdemir Z, Pursley AN, Nagamani SCS, Marom R, Golla S, Dengle L, Petrie HG, Matalon R, Emrick L, Proud MB, Treadwell-Deering D, Chao HT, Koillinen H, Brown C, Urraca N, Mostafavi R, Bernes S, Roeder ER, Nugent KM, Bader PI, Bellus G, Cummings M, Northrup H, Ashfaq M, Westman R, Wildin R, Beck AE, Immken L, Elton L, Varghese S, Buchanan E, Faivre L, Lefebvre M, Schaaf CP, Walkiewicz M, Yang Y, Kang SL, Lalani SR, Bacino CA, Beaudet AL, Breman AM, Smith JL, Cheung SW, Lupski JR, Patel A, Shaw CA, Stankiewicz P.

Genome Med. 2017 Sep 21;9(1):83. doi: 10.1186/s13073-017-0472-7.

2.

Progress in genome-wide association studies of schizophrenia in Han Chinese populations.

Yue W, Yu X, Zhang D.

NPJ Schizophr. 2017 Aug 10;3(1):24. doi: 10.1038/s41537-017-0029-1. Review.

3.

Genome-wide association analysis identifies common variants influencing infant brain volumes.

Xia K, Zhang J, Ahn M, Jha S, Crowley JJ, Szatkiewicz J, Li T, Zou F, Zhu H, Hibar D, Thompson P; ENIGMA Consortium, Sullivan PF, Styner M, Gilmore JH, Knickmeyer RC.

Transl Psychiatry. 2017 Aug 1;7(8):e1188. doi: 10.1038/tp.2017.159.

4.

Loss-of-function mutation in Mirta22/Emc10 rescues specific schizophrenia-related phenotypes in a mouse model of the 22q11.2 deletion.

Diamantopoulou A, Sun Z, Mukai J, Xu B, Fenelon K, Karayiorgou M, Gogos JA.

Proc Natl Acad Sci U S A. 2017 Jul 25;114(30):E6127-E6136. doi: 10.1073/pnas.1615719114. Epub 2017 Jul 10.

PMID:
28696314
5.

Genetics of Schizophrenia: Overview of Methods, Findings and Limitations.

Henriksen MG, Nordgaard J, Jansson LB.

Front Hum Neurosci. 2017 Jun 22;11:322. doi: 10.3389/fnhum.2017.00322. eCollection 2017. Review.

6.

Potential Value of Genomic Copy Number Variations in Schizophrenia.

Zhuo C, Hou W, Lin C, Hu L, Li J.

Front Mol Neurosci. 2017 Jun 21;10:204. doi: 10.3389/fnmol.2017.00204. eCollection 2017. Review.

7.

Translating advances in the molecular basis of schizophrenia into novel cognitive treatment strategies.

O'Tuathaigh CMP, Moran PM, Zhen XC, Waddington JL.

Br J Pharmacol. 2017 Oct;174(19):3173-3190. doi: 10.1111/bph.13938. Epub 2017 Aug 3. Review.

PMID:
28667666
8.

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability.

Singh T, Walters JTR, Johnstone M, Curtis D, Suvisaari J, Torniainen M, Rees E, Iyegbe C, Blackwood D, McIntosh AM, Kirov G, Geschwind D, Murray RM, Di Forti M, Bramon E, Gandal M, Hultman CM, Sklar P; INTERVAL Study; UK10K Consortium, Palotie A, Sullivan PF, O'Donovan MC, Owen MJ, Barrett JC.

Nat Genet. 2017 Aug;49(8):1167-1173. doi: 10.1038/ng.3903. Epub 2017 Jun 26.

PMID:
28650482
9.

Genetic tests in major psychiatric disorders-integrating molecular medicine with clinical psychiatry-why is it so difficult?

Demkow U, Wolańczyk T.

Transl Psychiatry. 2017 Jun 13;7(6):e1151. doi: 10.1038/tp.2017.106. Review.

10.

Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred.

Melhem NM, Hamdan S, Klei L, Wood S, Zelazny J, Frisch A, Weizman A, Carmel M, Michaelovsky E, Farbstein I, Wasserman D, El-Heib M, Ferrell R, Apter A, Devlin B, Brent D.

Psychiatr Genet. 2017 Oct;27(5):169-177. doi: 10.1097/YPG.0000000000000177.

PMID:
28570395
11.

Schizophrenia-Related Microdeletion Impairs Emotional Memory through MicroRNA-Dependent Disruption of Thalamic Inputs to the Amygdala.

Eom TY, Bayazitov IT, Anderson K, Yu J, Zakharenko SS.

Cell Rep. 2017 May 23;19(8):1532-1544. doi: 10.1016/j.celrep.2017.05.002.

12.

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.

Yilmaz Z, Szatkiewicz JP, Crowley JJ, Ancalade N, Brandys MK, van Elburg A, de Kovel CGF, Adan RAH, Hinney A, Hebebrand J, Gratacos M, Fernandez-Aranda F, Escaramis G, Gonzalez JR, Estivill X; Genetic Consortium for Anorexia Nervosa, Wellcome Trust Case Control Consortium 3, Zeggini E, Sullivan PF, Bulik CM.

Psychiatr Genet. 2017 Aug;27(4):152-158. doi: 10.1097/YPG.0000000000000172.

PMID:
28368970
13.

Positive Traits in the Bipolar Spectrum: The Space between Madness and Genius.

Greenwood TA.

Mol Neuropsychiatry. 2017 Feb;2(4):198-212. doi: 10.1159/000452416. Epub 2016 Dec 9. Review.

14.

Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31.

Bodea CA, Middleton FA, Melhem NM, Klei L, Song Y, Tiobech J, Marumoto P, Yano V, Faraone SV, Roeder K, Myles-Worsley M, Devlin B, Byerley W.

Mol Neuropsychiatry. 2017 Feb;2(4):173-184. doi: 10.1159/000450726. Epub 2016 Oct 12.

15.

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.

Rosenfeld JA, Patel A.

J Pediatr Genet. 2017 Mar;6(1):42-50. doi: 10.1055/s-0036-1584306. Epub 2016 May 30. Review.

PMID:
28180026
16.

A replication study of schizophrenia-related rare copy number variations in a Han Southern Chinese population.

Yuan J, Hu J, Li Z, Zhang F, Zhou D, Jin C.

Hereditas. 2017 Jan 14;154:2. doi: 10.1186/s41065-016-0025-x. eCollection 2017.

17.

Common developmental genome deprogramming in schizophrenia - Role of Integrative Nuclear FGFR1 Signaling (INFS).

Narla ST, Lee YW, Benson CA, Sarder P, Brennand KJ, Stachowiak EK, Stachowiak MK.

Schizophr Res. 2017 Jul;185:17-32. doi: 10.1016/j.schres.2016.12.012. Epub 2017 Jan 13.

18.

Chrna7 deficient mice manifest no consistent neuropsychiatric and behavioral phenotypes.

Yin J, Chen W, Yang H, Xue M, Schaaf CP.

Sci Rep. 2017 Jan 3;7:39941. doi: 10.1038/srep39941.

19.

Schizophrenia copy number variants and associative learning.

Clifton NE, Pocklington AJ, Scholz B, Rees E, Walters JT, Kirov G, O'Donovan MC, Owen MJ, Wilkinson LS, Thomas KL, Hall J.

Mol Psychiatry. 2017 Feb;22(2):178-182. doi: 10.1038/mp.2016.227. Epub 2016 Dec 13.

20.

Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome.

Vangkilde A, Jepsen JR, Schmock H, Olesen C, Arnarsdóttir S, Baaré WF, Plessen KJ, Didriksen M, Siebner HR, Werge T, Olsen L.

J Neurodev Disord. 2016 Nov 16;8:42. eCollection 2016.

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