440 related articles for article (PubMed ID: 29574884)
1. Progress in the genetics of autism spectrum disorder.
Woodbury-Smith M; Scherer SW
Dev Med Child Neurol; 2018 May; 60(5):445-451. PubMed ID: 29574884
[TBL] [Abstract][Full Text] [Related]
2. Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees.
Woodbury-Smith M; Zarrei M; Wei J; Thiruvahindrapuram B; O'Connor I; Paterson AD; Yuen RKC; Dastan J; Stavropoulos DJ; Howe JL; Thompson A; Parlier M; Fernandez B; Piven J; Anagnostou E; Scherer SW; Vieland VJ; Szatmari P
Am J Med Genet B Neuropsychiatr Genet; 2020 Jul; 183(5):268-276. PubMed ID: 32372567
[TBL] [Abstract][Full Text] [Related]
3. Genetics of autism spectrum disorder.
Ramaswami G; Geschwind DH
Handb Clin Neurol; 2018; 147():321-329. PubMed ID: 29325621
[TBL] [Abstract][Full Text] [Related]
4. Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.
Li SJ; Yu SS; Luo HY; Li X; Rao B; Wang Y; Li ZZ; Liu G; Zou LP; Zhang JS; Feng C; Liu J; Liu JW; Hu N; Chen XQ; Yu SY; Li K; He MW; Yu XG; Wang J; Guo SL; Chen ZY; Zhang L; Ma L
Clin Chim Acta; 2018 Apr; 479():144-147. PubMed ID: 29366832
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genetic testing including targeted gene panel in a diverse clinical population of children with autism spectrum disorder: Findings and implications.
Kalsner L; Twachtman-Bassett J; Tokarski K; Stanley C; Dumont-Mathieu T; Cotney J; Chamberlain S
Mol Genet Genomic Med; 2018 Mar; 6(2):171-185. PubMed ID: 29271092
[TBL] [Abstract][Full Text] [Related]
7. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
8. Recent advances in the genetics of autism spectrum disorder.
De Rubeis S; Buxbaum JD
Curr Neurol Neurosci Rep; 2015 Jun; 15(6):36. PubMed ID: 25946996
[TBL] [Abstract][Full Text] [Related]
9. The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability.
Chaste P; Roeder K; Devlin B
Annu Rev Genomics Hum Genet; 2017 Aug; 18():167-187. PubMed ID: 28426285
[TBL] [Abstract][Full Text] [Related]
10. [Genetic findings in autism spectrum disorders].
Freitag CM
Nervenarzt; 2017 Jul; 88(7):760-764. PubMed ID: 28536874
[TBL] [Abstract][Full Text] [Related]
11. Recent genetic and functional insights in autism spectrum disorder.
Nakanishi M; Anderson MP; Takumi T
Curr Opin Neurol; 2019 Aug; 32(4):627-634. PubMed ID: 31135459
[TBL] [Abstract][Full Text] [Related]
12. Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort.
Callaghan DB; Rogic S; Tan PPC; Calli K; Qiao Y; Baldwin R; Jacobson M; Belmadani M; Holmes N; Yu C; Li Y; Li Y; Kurtzke FE; Kuzeljevic B; Yu AY; Hudson M; Mcaughton AJM; Xu Y; Dionne-Laporte A; Girard S; Liang P; Separovic ER; Liu X; Rouleau G; Pavlidis P; Lewis MES
Clin Genet; 2019 Sep; 96(3):199-206. PubMed ID: 31038196
[TBL] [Abstract][Full Text] [Related]
13. Imaging genetics in autism spectrum disorders: Linking genetics and brain imaging in the pursuit of the underlying neurobiological mechanisms.
Fakhoury M
Prog Neuropsychopharmacol Biol Psychiatry; 2018 Jan; 80(Pt B):101-114. PubMed ID: 28322981
[TBL] [Abstract][Full Text] [Related]
14. Copy number variants in autism spectrum disorders.
Vicari S; Napoli E; Cordeddu V; Menghini D; Alesi V; Loddo S; Novelli A; Tartaglia M
Prog Neuropsychopharmacol Biol Psychiatry; 2019 Jun; 92():421-427. PubMed ID: 30797015
[TBL] [Abstract][Full Text] [Related]
15. Burden of de novo mutations and inherited rare single nucleotide variants in children with sensory processing dysfunction.
Marco EJ; Aitken AB; Nair VP; da Gente G; Gerdes MR; Bologlu L; Thomas S; Sherr EH
BMC Med Genomics; 2018 May; 11(1):50. PubMed ID: 29801487
[TBL] [Abstract][Full Text] [Related]
16. Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach.
Fernandez BA; Scherer SW
Dialogues Clin Neurosci; 2017 Dec; 19(4):353-371. PubMed ID: 29398931
[TBL] [Abstract][Full Text] [Related]
17. Genetics and epigenetics of autism spectrum disorder-current evidence in the field.
Wiśniowiecka-Kowalnik B; Nowakowska BA
J Appl Genet; 2019 Feb; 60(1):37-47. PubMed ID: 30627967
[TBL] [Abstract][Full Text] [Related]
18. Delineating the Common Biological Pathways Perturbed by ASD's Genetic Etiology: Lessons from Network-Based Studies.
Oron O; Elliott E
Int J Mol Sci; 2017 Apr; 18(4):. PubMed ID: 28420080
[TBL] [Abstract][Full Text] [Related]
19. Clinical Genetic Aspects of ASD Spectrum Disorders.
Schaefer GB
Int J Mol Sci; 2016 Jan; 17(2):. PubMed ID: 26840296
[TBL] [Abstract][Full Text] [Related]
20. Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders.
D'Abate L; Walker S; Yuen RKC; Tammimies K; Buchanan JA; Davies RW; Thiruvahindrapuram B; Wei J; Brian J; Bryson SE; Dobkins K; Howe J; Landa R; Leef J; Messinger D; Ozonoff S; Smith IM; Stone WL; Warren ZE; Young G; Zwaigenbaum L; Scherer SW
Nat Commun; 2019 Dec; 10(1):5519. PubMed ID: 31801954
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
