384 related articles for article (PubMed ID: 29187259)
1. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
[TBL] [Abstract][Full Text] [Related]
2. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR
Am J Med Genet B Neuropsychiatr Genet; 2018 Jul; 177(5):489-502. PubMed ID: 29687944
[TBL] [Abstract][Full Text] [Related]
3. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
[TBL] [Abstract][Full Text] [Related]
4. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
Costain G; Lionel AC; Merico D; Forsythe P; Russell K; Lowther C; Yuen T; Husted J; Stavropoulos DJ; Speevak M; Chow EW; Marshall CR; Scherer SW; Bassett AS
Hum Mol Genet; 2013 Nov; 22(22):4485-501. PubMed ID: 23813976
[TBL] [Abstract][Full Text] [Related]
5. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
[TBL] [Abstract][Full Text] [Related]
6. Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Huguet G; Schramm C; Douard E; Jiang L; Labbe A; Tihy F; Mathonnet G; Nizard S; Lemyre E; Mathieu A; Poline JB; Loth E; Toro R; Schumann G; Conrod P; Pausova Z; Greenwood C; Paus T; Bourgeron T; Jacquemont S;
JAMA Psychiatry; 2018 May; 75(5):447-457. PubMed ID: 29562078
[TBL] [Abstract][Full Text] [Related]
7. Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Rees E; Kendall K; Pardiñas AF; Legge SE; Pocklington A; Escott-Price V; MacCabe JH; Collier DA; Holmans P; O'Donovan MC; Owen MJ; Walters JTR; Kirov G
JAMA Psychiatry; 2016 Sep; 73(9):963-969. PubMed ID: 27602560
[TBL] [Abstract][Full Text] [Related]
8. Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Chawner SJRA; Owen MJ; Holmans P; Raymond FL; Skuse D; Hall J; van den Bree MBM
Lancet Psychiatry; 2019 Jun; 6(6):493-505. PubMed ID: 31056457
[TBL] [Abstract][Full Text] [Related]
9. Copy number variations and cognitive phenotypes in unselected populations.
Männik K; Mägi R; Macé A; Cole B; Guyatt AL; Shihab HA; Maillard AM; Alavere H; Kolk A; Reigo A; Mihailov E; Leitsalu L; Ferreira AM; Nõukas M; Teumer A; Salvi E; Cusi D; McGue M; Iacono WG; Gaunt TR; Beckmann JS; Jacquemont S; Kutalik Z; Pankratz N; Timpson N; Metspalu A; Reymond A
JAMA; 2015 May; 313(20):2044-54. PubMed ID: 26010633
[TBL] [Abstract][Full Text] [Related]
10. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
Roberts JL; Hovanes K; Dasouki M; Manzardo AM; Butler MG
Gene; 2014 Feb; 535(1):70-8. PubMed ID: 24188901
[TBL] [Abstract][Full Text] [Related]
11. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
Sokolowski M; Wasserman J; Wasserman D
PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
[TBL] [Abstract][Full Text] [Related]
12. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Derks EM; Ayub M; Chambert K; Del Favero J; Johnstone M; MacGregor S; Maclean A; McKechanie AG; McRae AF; Moran JL; Pickard BS; Purcell S; Sklar P; StClair DM; Wray NR; Visscher PM; Blackwood DH
Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):847-54. PubMed ID: 24115684
[TBL] [Abstract][Full Text] [Related]
13. Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.
Kendall KM; Bracher-Smith M; Fitzpatrick H; Lynham A; Rees E; Escott-Price V; Owen MJ; O'Donovan MC; Walters JTR; Kirov G
Br J Psychiatry; 2019 May; 214(5):297-304. PubMed ID: 30767844
[TBL] [Abstract][Full Text] [Related]
14. Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders.
Thygesen JH; Wolfe K; McQuillin A; Viñas-Jornet M; Baena N; Brison N; D'Haenens G; Esteba-Castillo S; Gabau E; Ribas-Vidal N; Ruiz A; Vermeesch J; Weyts E; Novell R; Buggenhout GV; Strydom A; Bass N; Guitart M; Vogels A
Br J Psychiatry; 2018 May; 212(5):287-294. PubMed ID: 29693535
[TBL] [Abstract][Full Text] [Related]
15. Association of Rare Copy Number Variants With Risk of Depression.
Kendall KM; Rees E; Bracher-Smith M; Legge S; Riglin L; Zammit S; O'Donovan MC; Owen MJ; Jones I; Kirov G; Walters JTR
JAMA Psychiatry; 2019 Aug; 76(8):818-825. PubMed ID: 30994872
[TBL] [Abstract][Full Text] [Related]
16. Reduced burden of very large and rare CNVs in bipolar affective disorder.
Grozeva D; Kirov G; Conrad DF; Barnes CP; Hurles M; Owen MJ; O'Donovan MC; Craddock N
Bipolar Disord; 2013 Dec; 15(8):893-8. PubMed ID: 24127788
[TBL] [Abstract][Full Text] [Related]
17. Clinical relevance of small copy-number variants in chromosomal microarray clinical testing.
Hollenbeck D; Williams CL; Drazba K; Descartes M; Korf BR; Rutledge SL; Lose EJ; Robin NH; Carroll AJ; Mikhail FM
Genet Med; 2017 Apr; 19(4):377-385. PubMed ID: 27632688
[TBL] [Abstract][Full Text] [Related]
18. Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Saarentaus EC; Havulinna AS; Mars N; Ahola-Olli A; Kiiskinen TTJ; Partanen J; Ruotsalainen S; Kurki M; Urpa LM; Chen L; Perola M; Salomaa V; Veijola J; Männikkö M; Hall IM; Pietiläinen O; Kaprio J; Ripatti S; Daly M; Palotie A
Mol Psychiatry; 2021 Sep; 26(9):4884-4895. PubMed ID: 33526825
[TBL] [Abstract][Full Text] [Related]
19. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
Grozeva D; Kirov G; Ivanov D; Jones IR; Jones L; Green EK; St Clair DM; Young AH; Ferrier N; Farmer AE; McGuffin P; Holmans PA; Owen MJ; O'Donovan MC; Craddock N;
Arch Gen Psychiatry; 2010 Apr; 67(4):318-27. PubMed ID: 20368508
[TBL] [Abstract][Full Text] [Related]
20. Schizophrenia genetic variants are not associated with intelligence.
van Scheltinga AF; Bakker SC; van Haren NE; Derks EM; Buizer-Voskamp JE; Cahn W; Ripke S; ; Ophoff RA; Kahn RS
Psychol Med; 2013 Dec; 43(12):2563-70. PubMed ID: 23410598
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
