296 related articles for article (PubMed ID: 36835010)
41. Neuroimaging Findings in Neurodevelopmental Copy Number Variants: Identifying Molecular Pathways to Convergent Phenotypes.
Silva AI; Ehrhart F; Ulfarsson MO; Stefansson H; Stefansson K; Wilkinson LS; Hall J; Linden DEJ
Biol Psychiatry; 2022 Sep; 92(5):341-361. PubMed ID: 35659384
[TBL] [Abstract][Full Text] [Related]
42. Molecular diversity and phenotypic pleiotropy of ancient genomic regulatory loci derived from human endogenous retrovirus type H (HERVH) promoter LTR7 and HERVK promoter LTR5_Hs and their contemporary impacts on pathophysiology of Modern Humans.
Glinsky GV
Mol Genet Genomics; 2022 Nov; 297(6):1711-1740. PubMed ID: 36121513
[TBL] [Abstract][Full Text] [Related]
43. Neurodevelopmental Plasticity in Pre- and Postnatal Environmental Interactions: Implications for Psychiatric Disorders from an Evolutionary Perspective.
Lee YA; Yamaguchi Y; Goto Y
Neural Plast; 2015; 2015():291476. PubMed ID: 26060583
[TBL] [Abstract][Full Text] [Related]
44. Schizophrenia susceptibility genes and their neurodevelopmental implications: focus on neuregulin 1.
Harrison PJ
Novartis Found Symp; 2007; 288():246-55; discussion 255-9, 276-81. PubMed ID: 18494263
[TBL] [Abstract][Full Text] [Related]
45. 14-3-3 proteins at the crossroads of neurodevelopment and schizophrenia.
Antunes ASLM; Saia-Cereda VM; Crunfli F; Martins-de-Souza D
World J Biol Psychiatry; 2022 Jan; 23(1):14-32. PubMed ID: 33952049
[TBL] [Abstract][Full Text] [Related]
46. Species-conserved SYNGAP1 phenotypes associated with neurodevelopmental disorders.
Kilinc M; Creson T; Rojas C; Aceti M; Ellegood J; Vaissiere T; Lerch JP; Rumbaugh G
Mol Cell Neurosci; 2018 Sep; 91():140-150. PubMed ID: 29580901
[TBL] [Abstract][Full Text] [Related]
47. Human accelerated genome regions with value in medical genetics and drug discovery.
Chu XY; Quan Y; Zhang HY
Drug Discov Today; 2020 May; 25(5):821-827. PubMed ID: 32156545
[TBL] [Abstract][Full Text] [Related]
48. Chromosome conformation elucidates regulatory relationships in developing human brain.
Won H; de la Torre-Ubieta L; Stein JL; Parikshak NN; Huang J; Opland CK; Gandal MJ; Sutton GJ; Hormozdiari F; Lu D; Lee C; Eskin E; Voineagu I; Ernst J; Geschwind DH
Nature; 2016 Oct; 538(7626):523-527. PubMed ID: 27760116
[TBL] [Abstract][Full Text] [Related]
49. Decreased nuclear distribution nudE-like 1 enzyme activity in an animal model with dysfunctional disrupted-in-schizophrenia 1 signaling featuring aberrant neurodevelopment and amphetamine-supersensitivity.
Nani JV; Fonseca MC; Engi SA; Perillo MG; Dias CS; Gazarini ML; Korth C; Cruz FC; Hayashi MA
J Psychopharmacol; 2020 Apr; 34(4):467-477. PubMed ID: 31916893
[TBL] [Abstract][Full Text] [Related]
50. Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia.
Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium
Mol Autism; 2017; 8():21. PubMed ID: 28540026
[TBL] [Abstract][Full Text] [Related]
51. A functional missense variant in ITIH3 affects protein expression and neurodevelopment and confers schizophrenia risk in the Han Chinese population.
Li K; Li Y; Wang J; Huo Y; Huang D; Li S; Liu J; Li X; Liu R; Chen X; Yao YG; Chen C; Xiao X; Li M; Luo XJ
J Genet Genomics; 2020 May; 47(5):233-248. PubMed ID: 32712163
[TBL] [Abstract][Full Text] [Related]
52. Genetic insights into the neurodevelopmental origins of schizophrenia.
Birnbaum R; Weinberger DR
Nat Rev Neurosci; 2017 Dec; 18(12):727-740. PubMed ID: 29070826
[TBL] [Abstract][Full Text] [Related]
53. New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders.
Moyses-Oliveira M; Yadav R; Erdin S; Talkowski ME
Curr Opin Genet Dev; 2020 Dec; 65():195-206. PubMed ID: 32846283
[TBL] [Abstract][Full Text] [Related]
54. Cumulative role of rare and common putative functional genetic variants at NPAS3 in schizophrenia susceptibility.
González-Peñas J; Arrojo M; Paz E; Brenlla J; Páramo M; Costas J
Am J Med Genet B Neuropsychiatr Genet; 2015 Oct; 168(7):528-35. PubMed ID: 25982957
[TBL] [Abstract][Full Text] [Related]
55. Neurodevelopmental synaptopathies: Insights from behaviour in rodent models of synapse gene mutations.
Luo J; Norris RH; Gordon SL; Nithianantharajah J
Prog Neuropsychopharmacol Biol Psychiatry; 2018 Jun; 84(Pt B):424-439. PubMed ID: 29217145
[TBL] [Abstract][Full Text] [Related]
56. Copy number variant syndromes are frequent in schizophrenia: Progressing towards a CNV-schizophrenia model.
Sriretnakumar V; Zai CC; Wasim S; Barsanti-Innes B; Kennedy JL; So J
Schizophr Res; 2019 Jul; 209():171-178. PubMed ID: 31080157
[TBL] [Abstract][Full Text] [Related]
57. Evolutionary Perspectives on Genetic and Environmental Risk Factors for Psychiatric Disorders.
Keller MC
Annu Rev Clin Psychol; 2018 May; 14():471-493. PubMed ID: 29401047
[TBL] [Abstract][Full Text] [Related]
58. Neurodevelopmental hypothesis of schizophrenia.
Owen MJ; O'Donovan MC; Thapar A; Craddock N
Br J Psychiatry; 2011 Mar; 198(3):173-5. PubMed ID: 21357874
[TBL] [Abstract][Full Text] [Related]
59. A current view on contactin-4, -5, and -6: Implications in neurodevelopmental disorders.
Oguro-Ando A; Zuko A; Kleijer KTE; Burbach JPH
Mol Cell Neurosci; 2017 Jun; 81():72-83. PubMed ID: 28064060
[TBL] [Abstract][Full Text] [Related]
60. Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.
Torres F; Barbosa M; Maciel P
J Med Genet; 2016 Feb; 53(2):73-90. PubMed ID: 26502893
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]