303 related articles for article (PubMed ID: 31921276)
1. Childhood-Onset Schizophrenia: A Systematic Overview of Its Genetic Heterogeneity From Classical Studies to the Genomic Era.
Fernandez A; Drozd MM; Thümmler S; Dor E; Capovilla M; Askenazy F; Bardoni B
Front Genet; 2019; 10():1137. PubMed ID: 31921276
[TBL] [Abstract][Full Text] [Related]
2. High rate of disease-related copy number variations in childhood onset schizophrenia.
Ahn K; Gotay N; Andersen TM; Anvari AA; Gochman P; Lee Y; Sanders S; Guha S; Darvasi A; Glessner JT; Hakonarson H; Lencz T; State MW; Shugart YY; Rapoport JL
Mol Psychiatry; 2014 May; 19(5):568-72. PubMed ID: 23689535
[TBL] [Abstract][Full Text] [Related]
3. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Gudmundsson OO; Walters GB; Ingason A; Johansson S; Zayats T; Athanasiu L; Sonderby IE; Gustafsson O; Nawaz MS; Jonsson GF; Jonsson L; Knappskog PM; Ingvarsdottir E; Davidsdottir K; Djurovic S; Knudsen GPS; Askeland RB; Haraldsdottir GS; Baldursson G; Magnusson P; Sigurdsson E; Gudbjartsson DF; Stefansson H; Andreassen OA; Haavik J; Reichborn-Kjennerud T; Stefansson K
Transl Psychiatry; 2019 Oct; 9(1):258. PubMed ID: 31624239
[TBL] [Abstract][Full Text] [Related]
4. 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; 9(1):83. PubMed ID: 28934986
[TBL] [Abstract][Full Text] [Related]
5. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
Hosak L; Silhan P; Hosakova J
Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
[TBL] [Abstract][Full Text] [Related]
6. The genetics of autism.
Muhle R; Trentacoste SV; Rapin I
Pediatrics; 2004 May; 113(5):e472-86. PubMed ID: 15121991
[TBL] [Abstract][Full Text] [Related]
7. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Levinson DF; Duan J; Oh S; Wang K; Sanders AR; Shi J; Zhang N; Mowry BJ; Olincy A; Amin F; Cloninger CR; Silverman JM; Buccola NG; Byerley WF; Black DW; Kendler KS; Freedman R; Dudbridge F; Pe'er I; Hakonarson H; Bergen SE; Fanous AH; Holmans PA; Gejman PV
Am J Psychiatry; 2011 Mar; 168(3):302-16. PubMed ID: 21285140
[TBL] [Abstract][Full Text] [Related]
8. Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.
Sagar A; Bishop JR; Tessman DC; Guter S; Martin CL; Cook EH
Am J Med Genet A; 2013 Apr; 161A(4):845-9. PubMed ID: 23443968
[TBL] [Abstract][Full Text] [Related]
9. Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Lionel AC; Crosbie J; Barbosa N; Goodale T; Thiruvahindrapuram B; Rickaby J; Gazzellone M; Carson AR; Howe JL; Wang Z; Wei J; Stewart AF; Roberts R; McPherson R; Fiebig A; Franke A; Schreiber S; Zwaigenbaum L; Fernandez BA; Roberts W; Arnold PD; Szatmari P; Marshall CR; Schachar R; Scherer SW
Sci Transl Med; 2011 Aug; 3(95):95ra75. PubMed ID: 21832240
[TBL] [Abstract][Full Text] [Related]
10. The landscape of copy number variations in Finnish families with autism spectrum disorders.
Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.
Ramos-Quiroga JA; Sánchez-Mora C; Casas M; Garcia-Martínez I; Bosch R; Nogueira M; Corrales M; Palomar G; Vidal R; Coll-Tané M; Bayés M; Cormand B; Ribasés M
J Psychiatr Res; 2014 Feb; 49():60-7. PubMed ID: 24269040
[TBL] [Abstract][Full Text] [Related]
12. Association testing of copy number variants in schizophrenia and autism spectrum disorders.
Crespi BJ; Crofts HJ
J Neurodev Disord; 2012 May; 4(1):15. PubMed ID: 22958593
[TBL] [Abstract][Full Text] [Related]
13. Subcortical Brain Alterations in Carriers of Genomic Copy Number Variants.
Kumar K; Modenato C; Moreau C; Ching CRK; Harvey A; Martin-Brevet S; Huguet G; Jean-Louis M; Douard E; Martin CO; Younis N; Tamer P; Maillard AM; Rodriguez-Herreros B; Pain A; ; Kushan L; Isaev D; Alpert K; Ragothaman A; Turner JA; Wang L; Ho TC; Schmaal L; Silva AI; van den Bree MBM; Linden DEJ; Owen MJ; Hall J; Lippé S; Dumas G; Draganski B; Gutman BA; Sønderby IE; Andreassen OA; Schultz LM; Almasy L; Glahn DC; Bearden CE; Thompson PM; Jacquemont S
Am J Psychiatry; 2023 Sep; 180(9):685-698. PubMed ID: 37434504
[TBL] [Abstract][Full Text] [Related]
14. Detection of Disease-Causing SNVs/Indels and CNVs in Single Test Based on Whole Exome Sequencing: A Retrospective Case Study in Epileptic Encephalopathies.
Sun D; Liu Y; Cai W; Ma J; Ni K; Chen M; Wang C; Liu Y; Zhu Y; Liu Z; Zhu F
Front Pediatr; 2021; 9():635703. PubMed ID: 34055682
[No Abstract] [Full Text] [Related]
15. Exploration and characterisation of the phenotypic and genetic profiles of patients with early onset schizophrenia associated with autism spectrum disorder and their first-degree relatives: a French multicentre case series study protocol (GenAuDiss).
Fernandez A; Dor E; Maurin T; Laure G; Menard ML; Drozd M; Poinso F; Bardoni B; Askenazy F; Thümmler S
BMJ Open; 2018 Jul; 8(7):e023330. PubMed ID: 29980548
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing of sporadic childhood-onset schizophrenia suggests the contribution of X-linked genes in males.
Ambalavanan A; Chaumette B; Zhou S; Xie P; He Q; Spiegelman D; Dionne-Laporte A; Bourassa CV; Therrien M; Rochefort D; Xiong L; Dion PA; Joober R; Rapoport JL; Girard SL; Rouleau GA
Am J Med Genet B Neuropsychiatr Genet; 2019 Sep; 180(6):335-340. PubMed ID: 30378261
[TBL] [Abstract][Full Text] [Related]
17. 15q13.3 duplication in two patients with childhood-onset schizophrenia.
Zhou D; Gochman P; Broadnax DD; Rapoport JL; Ahn K
Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):777-83. PubMed ID: 26968334
[TBL] [Abstract][Full Text] [Related]
18. Integrated Functional Analysis Implicates Syndromic and Rare Copy Number Variation Genes as Prominent Molecular Players in Pathogenesis of Autism Spectrum Disorders.
Ashitha SNM; Ramachandra NB
Neuroscience; 2020 Jul; 438():25-40. PubMed ID: 32407977
[TBL] [Abstract][Full Text] [Related]
19. The genetics of childhood-onset schizophrenia: when madness strikes the prepubescent.
Addington AM; Rapoport JL
Curr Psychiatry Rep; 2009 Apr; 11(2):156-61. PubMed ID: 19302770
[TBL] [Abstract][Full Text] [Related]
20. Identification of De Novo JAK2 and MAPK7 Mutations Related to Autism Spectrum Disorder Using Whole-Exome Sequencing in a Chinese Child and Adolescent Trio-Based Sample.
Jiao J; Zhang M; Yang P; Huang Y; Hu X; Cai J; Yang C; Situ M; Zhang H; Fu L; Guo K; Huang Y
J Mol Neurosci; 2020 Feb; 70(2):219-229. PubMed ID: 31838722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
