667 related articles for article (PubMed ID: 30392412)
1. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. A Protective Role of Low Polygenic Risk Score in Healthy Individuals Carrying Attention-Deficit/Hyperactivity Disorder-Associated Copy Number Variations.
Chang X; Qu H; Liu Y; Glessner J; Hakonarson H
Biol Psychiatry; 2024 May; 95(9):881-887. PubMed ID: 37865391
[TBL] [Abstract][Full Text] [Related]
4. Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
Charney AW; Stahl EA; Green EK; Chen CY; Moran JL; Chambert K; Belliveau RA; Forty L; Gordon-Smith K; Lee PH; Bromet EJ; Buckley PF; Escamilla MA; Fanous AH; Fochtmann LJ; Lehrer DS; Malaspina D; Marder SR; Morley CP; Nicolini H; Perkins DO; Rakofsky JJ; Rapaport MH; Medeiros H; Sobell JL; Backlund L; Bergen SE; Juréus A; Schalling M; Lichtenstein P; Knowles JA; Burdick KE; Jones I; Jones LA; Hultman CM; Perlis R; Purcell SM; McCarroll SA; Pato CN; Pato MT; Di Florio A; Craddock N; Landén M; Smoller JW; Ruderfer DM; Sklar P
Biol Psychiatry; 2019 Jul; 86(2):110-119. PubMed ID: 30686506
[TBL] [Abstract][Full Text] [Related]
5. A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
Rudd DS; Axelsen M; Epping EA; Andreasen NC; Wassink TH
Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):619-26. PubMed ID: 25228354
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genome-wide association study of multiplex schizophrenia pedigrees.
Levinson DF; Shi J; Wang K; Oh S; Riley B; Pulver AE; Wildenauer DB; Laurent C; Mowry BJ; Gejman PV; Owen MJ; Kendler KS; Nestadt G; Schwab SG; Mallet J; Nertney D; Sanders AR; Williams NM; Wormley B; Lasseter VK; Albus M; Godard-Bauché S; Alexander M; Duan J; O'Donovan MC; Walsh D; O'Neill A; Papadimitriou GN; Dikeos D; Maier W; Lerer B; Campion D; Cohen D; Jay M; Fanous A; Eichhammer P; Silverman JM; Norton N; Zhang N; Hakonarson H; Gao C; Citri A; Hansen M; Ripke S; ; Dudbridge F; Holmans PA
Am J Psychiatry; 2012 Sep; 169(9):963-73. PubMed ID: 22885689
[TBL] [Abstract][Full Text] [Related]
8. Polygenic risk scores in schizophrenia with clinically significant copy number variants.
Taniguchi S; Ninomiya K; Kushima I; Saito T; Shimasaki A; Sakusabe T; Momozawa Y; Kubo M; Kamatani Y; Ozaki N; Ikeda M; Iwata N
Psychiatry Clin Neurosci; 2020 Jan; 74(1):35-39. PubMed ID: 31461559
[TBL] [Abstract][Full Text] [Related]
9. A New Method for Detecting Associations with Rare Copy-Number Variants.
Tzeng JY; Magnusson PK; Sullivan PF; ; Szatkiewicz JP
PLoS Genet; 2015 Oct; 11(10):e1005403. PubMed ID: 26431523
[TBL] [Abstract][Full Text] [Related]
10. Common alleles contribute to schizophrenia in CNV carriers.
Tansey KE; Rees E; Linden DE; Ripke S; Chambert KD; Moran JL; McCarroll SA; Holmans P; Kirov G; Walters J; Owen MJ; O'Donovan MC
Mol Psychiatry; 2016 Aug; 21(8):1085-9. PubMed ID: 26390827
[TBL] [Abstract][Full Text] [Related]
11. A weighted burden test using logistic regression for integrated analysis of sequence variants, copy number variants and polygenic risk score.
Curtis D
Eur J Hum Genet; 2019 Jan; 27(1):114-124. PubMed ID: 30258123
[TBL] [Abstract][Full Text] [Related]
12. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Bassett AS; Lowther C; Merico D; Costain G; Chow EWC; van Amelsvoort T; McDonald-McGinn D; Gur RE; Swillen A; Van den Bree M; Murphy K; Gothelf D; Bearden CE; Eliez S; Kates W; Philip N; Sashi V; Campbell L; Vorstman J; Cubells J; Repetto GM; Simon T; Boot E; Heung T; Evers R; Vingerhoets C; van Duin E; Zackai E; Vergaelen E; Devriendt K; Vermeesch JR; Owen M; Murphy C; Michaelovosky E; Kushan L; Schneider M; Fremont W; Busa T; Hooper S; McCabe K; Duijff S; Isaev K; Pellecchia G; Wei J; Gazzellone MJ; Scherer SW; Emanuel BS; Guo T; Morrow BE; Marshall CR;
Am J Psychiatry; 2017 Nov; 174(11):1054-1063. PubMed ID: 28750581
[TBL] [Abstract][Full Text] [Related]
13. Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.
Martin AK; Robinson G; Reutens D; Mowry B
Am J Med Genet B Neuropsychiatr Genet; 2015 Jul; 168B(5):374-82. PubMed ID: 25943776
[TBL] [Abstract][Full Text] [Related]
14. The relative contribution of common and rare genetic variants to ADHD.
Martin J; O'Donovan MC; Thapar A; Langley K; Williams N
Transl Psychiatry; 2015 Feb; 5(2):e506. PubMed ID: 25668434
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Copy number variation in schizophrenia in Sweden.
Szatkiewicz JP; O'Dushlaine C; Chen G; Chambert K; Moran JL; Neale BM; Fromer M; Ruderfer D; Akterin S; Bergen SE; Kähler A; Magnusson PK; Kim Y; Crowley JJ; Rees E; Kirov G; O'Donovan MC; Owen MJ; Walters J; Scolnick E; Sklar P; Purcell S; Hultman CM; McCarroll SA; Sullivan PF
Mol Psychiatry; 2014 Jul; 19(7):762-73. PubMed ID: 24776740
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N
Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
[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]
