1020 related articles for article (PubMed ID: 28263302)
1. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
C Yuen RK; Merico D; Bookman M; L Howe J; Thiruvahindrapuram B; Patel RV; Whitney J; Deflaux N; Bingham J; Wang Z; Pellecchia G; Buchanan JA; Walker S; Marshall CR; Uddin M; Zarrei M; Deneault E; D'Abate L; Chan AJ; Koyanagi S; Paton T; Pereira SL; Hoang N; Engchuan W; Higginbotham EJ; Ho K; Lamoureux S; Li W; MacDonald JR; Nalpathamkalam T; Sung WW; Tsoi FJ; Wei J; Xu L; Tasse AM; Kirby E; Van Etten W; Twigger S; Roberts W; Drmic I; Jilderda S; Modi BM; Kellam B; Szego M; Cytrynbaum C; Weksberg R; Zwaigenbaum L; Woodbury-Smith M; Brian J; Senman L; Iaboni A; Doyle-Thomas K; Thompson A; Chrysler C; Leef J; Savion-Lemieux T; Smith IM; Liu X; Nicolson R; Seifer V; Fedele A; Cook EH; Dager S; Estes A; Gallagher L; Malow BA; Parr JR; Spence SJ; Vorstman J; Frey BJ; Robinson JT; Strug LJ; Fernandez BA; Elsabbagh M; Carter MT; Hallmayer J; Knoppers BM; Anagnostou E; Szatmari P; Ring RH; Glazer D; Pletcher MT; Scherer SW
Nat Neurosci; 2017 Apr; 20(4):602-611. PubMed ID: 28263302
[TBL] [Abstract][Full Text] [Related]
2. Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations.
Toraman B; Bilginer SÇ; Hesapçıoğlu ST; Göker Z; Soykam HO; Ergüner B; Dinçer T; Yıldız G; Ünsal S; Kasap BK; Kandil S; Kalay E
J Gene Med; 2021 Apr; 23(4):e3322. PubMed ID: 33591602
[TBL] [Abstract][Full Text] [Related]
3. Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.
Leppa VM; Kravitz SN; Martin CL; Andrieux J; Le Caignec C; Martin-Coignard D; DyBuncio C; Sanders SJ; Lowe JK; Cantor RM; Geschwind DH
Am J Hum Genet; 2016 Sep; 99(3):540-554. PubMed ID: 27569545
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Whole Exome Sequencing Identifies Novel De Novo Variants Interacting with Six Gene Networks in Autism Spectrum Disorder.
Kim N; Kim KH; Lim WJ; Kim J; Kim SA; Yoo HJ
Genes (Basel); 2020 Dec; 12(1):. PubMed ID: 33374967
[TBL] [Abstract][Full Text] [Related]
6. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort.
da Silva Montenegro EM; Costa CS; Campos G; Scliar M; de Almeida TF; Zachi EC; Silva IMW; Chan AJS; Zarrei M; Lourenço NCV; Yamamoto GL; Scherer S; Passos-Bueno MR
Autism Res; 2020 Feb; 13(2):199-206. PubMed ID: 31696658
[TBL] [Abstract][Full Text] [Related]
7. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J
Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study.
Abdi M; Aliyev E; Trost B; Kohailan M; Aamer W; Syed N; Shaath R; Gandhi GD; Engchuan W; Howe J; Thiruvahindrapuram B; Geng M; Whitney J; Syed A; Lakshmi J; Hussein S; Albashir N; Hussein A; Poggiolini I; Elhag SF; Palaniswamy S; Kambouris M; de Fatima Janjua M; Tahir MOE; Nazeer A; Shahwar D; Azeem MW; Mokrab Y; Aati NA; Akil A; Scherer SW; Kamal M; Fakhro KA
Genome Med; 2023 Oct; 15(1):81. PubMed ID: 37805537
[TBL] [Abstract][Full Text] [Related]
10. Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Trost B; Thiruvahindrapuram B; Chan AJS; Engchuan W; Higginbotham EJ; Howe JL; Loureiro LO; Reuter MS; Roshandel D; Whitney J; Zarrei M; Bookman M; Somerville C; Shaath R; Abdi M; Aliyev E; Patel RV; Nalpathamkalam T; Pellecchia G; Hamdan O; Kaur G; Wang Z; MacDonald JR; Wei J; Sung WWL; Lamoureux S; Hoang N; Selvanayagam T; Deflaux N; Geng M; Ghaffari S; Bates J; Young EJ; Ding Q; Shum C; D'Abate L; Bradley CA; Rutherford A; Aguda V; Apresto B; Chen N; Desai S; Du X; Fong MLY; Pullenayegum S; Samler K; Wang T; Ho K; Paton T; Pereira SL; Herbrick JA; Wintle RF; Fuerth J; Noppornpitak J; Ward H; Magee P; Al Baz A; Kajendirarajah U; Kapadia S; Vlasblom J; Valluri M; Green J; Seifer V; Quirbach M; Rennie O; Kelley E; Masjedi N; Lord C; Szego MJ; Zawati MH; Lang M; Strug LJ; Marshall CR; Costain G; Calli K; Iaboni A; Yusuf A; Ambrozewicz P; Gallagher L; Amaral DG; Brian J; Elsabbagh M; Georgiades S; Messinger DS; Ozonoff S; Sebat J; Sjaarda C; Smith IM; Szatmari P; Zwaigenbaum L; Kushki A; Frazier TW; Vorstman JAS; Fakhro KA; Fernandez BA; Lewis MES; Weksberg R; Fiume M; Yuen RKC; Anagnostou E; Sondheimer N; Glazer D; Hartley DM; Scherer SW
Cell; 2022 Nov; 185(23):4409-4427.e18. PubMed ID: 36368308
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
Krishnan A; Zhang R; Yao V; Theesfeld CL; Wong AK; Tadych A; Volfovsky N; Packer A; Lash A; Troyanskaya OG
Nat Neurosci; 2016 Nov; 19(11):1454-1462. PubMed ID: 27479844
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Genomic selection signatures in autism spectrum disorder identifies cognitive genomic tradeoff and its relevance in paradoxical phenotypes of deficits versus potentialities.
Prakash A; Banerjee M
Sci Rep; 2021 May; 11(1):10245. PubMed ID: 33986442
[TBL] [Abstract][Full Text] [Related]
15. Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Liu X; Shimada T; Otowa T; Wu YY; Kawamura Y; Tochigi M; Iwata Y; Umekage T; Toyota T; Maekawa M; Iwayama Y; Suzuki K; Kakiuchi C; Kuwabara H; Kano Y; Nishida H; Sugiyama T; Kato N; Chen CH; Mori N; Yamada K; Yoshikawa T; Kasai K; Tokunaga K; Sasaki T; Gau SS
Autism Res; 2016 Mar; 9(3):340-9. PubMed ID: 26314684
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal microarray and whole-exome sequence analysis in Taiwanese patients with autism spectrum disorder.
Chang YS; Lin CY; Huang HY; Chang JG; Kuo HT
Mol Genet Genomic Med; 2019 Dec; 7(12):e996. PubMed ID: 31595719
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants.
Siu MT; Butcher DT; Turinsky AL; Cytrynbaum C; Stavropoulos DJ; Walker S; Caluseriu O; Carter M; Lou Y; Nicolson R; Georgiades S; Szatmari P; Anagnostou E; Scherer SW; Choufani S; Brudno M; Weksberg R
Clin Epigenetics; 2019 Jul; 11(1):103. PubMed ID: 31311581
[TBL] [Abstract][Full Text] [Related]
19. An integrative analysis of non-coding regulatory DNA variations associated with autism spectrum disorder.
Williams SM; An JY; Edson J; Watts M; Murigneux V; Whitehouse AJO; Jackson CJ; Bellgrove MA; Cristino AS; Claudianos C
Mol Psychiatry; 2019 Nov; 24(11):1707-1719. PubMed ID: 29703944
[TBL] [Abstract][Full Text] [Related]
20. Identification of de novo Mutations in the Chinese Autism Spectrum Disorder Cohort via Whole-Exome Sequencing Unveils Brain Regions Implicated in Autism.
Yuan B; Wang M; Wu X; Cheng P; Zhang R; Zhang R; Yu S; Zhang J; Du Y; Wang X; Qiu Z
Neurosci Bull; 2023 Oct; 39(10):1469-1480. PubMed ID: 36881370
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
