253 related articles for article (PubMed ID: 36670631)
61. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
O'Roak BJ; Vives L; Girirajan S; Karakoc E; Krumm N; Coe BP; Levy R; Ko A; Lee C; Smith JD; Turner EH; Stanaway IB; Vernot B; Malig M; Baker C; Reilly B; Akey JM; Borenstein E; Rieder MJ; Nickerson DA; Bernier R; Shendure J; Eichler EE
Nature; 2012 Apr; 485(7397):246-50. PubMed ID: 22495309
[TBL] [Abstract][Full Text] [Related]
62. Cortactin-binding protein 2 increases microtubule stability and regulates dendritic arborization.
Shih PY; Lee SP; Chen YK; Hsueh YP
J Cell Sci; 2014 Aug; 127(Pt 16):3521-34. PubMed ID: 24928895
[TBL] [Abstract][Full Text] [Related]
63. Genetic landscape of autism spectrum disorder in Vietnamese children.
Tran KT; Le VS; Bui HTP; Do DH; Ly HTT; Nguyen HT; Dao LTM; Nguyen TH; Vu DM; Ha LT; Le HTT; Mukhopadhyay A; Nguyen LT
Sci Rep; 2020 Mar; 10(1):5034. PubMed ID: 32193494
[TBL] [Abstract][Full Text] [Related]
64. Analysis of a Sardinian Multiplex Family with Autism Spectrum Disorder Points to Post-Synaptic Density Gene Variants and Identifies
Bacchelli E; Loi E; Cameli C; Moi L; Vega-Benedetti AF; Blois S; Fadda A; Bonora E; Mattu S; Fadda R; Chessa R; Maestrini E; Doneddu G; Zavattari P
J Clin Med; 2019 Feb; 8(2):. PubMed ID: 30736458
[TBL] [Abstract][Full Text] [Related]
65. [Analysis of NSD1 gene variant in a child with autism spectrum disorder in conjunct with congenital heart disease].
Yin H; Qiu Z; Li T; Chen Y; Xia J; Huang G; Xu W; Xie J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun; 40(6):701-705. PubMed ID: 37212006
[TBL] [Abstract][Full Text] [Related]
66. Global developmental delay and intellectual disability associated with a de novo TOP2B mutation.
Lam CW; Yeung WL; Law CY
Clin Chim Acta; 2017 Jun; 469():63-68. PubMed ID: 28343847
[TBL] [Abstract][Full Text] [Related]
67. Patterns of de novo tandem repeat mutations and their role in autism.
Mitra I; Huang B; Mousavi N; Ma N; Lamkin M; Yanicky R; Shleizer-Burko S; Lohmueller KE; Gymrek M
Nature; 2021 Jan; 589(7841):246-250. PubMed ID: 33442040
[TBL] [Abstract][Full Text] [Related]
68. Molecular diagnostic yield of whole-exome sequencing in Saudi autistic children with epilepsy.
Alharbi AA; Al-Zahrani MH; Ebbi MM; Alqurashi MM; Baqays AA; Shami A; Alghamdi RA; Alzahrani AH
Int J Health Sci (Qassim); 2024; 18(3):15-22. PubMed ID: 38721139
[TBL] [Abstract][Full Text] [Related]
69. PLXNA2 and LRRC40 as candidate genes in autism spectrum disorder.
Pijuan J; Ortigoza-Escobar JD; Ortiz J; Alcalá A; Calvo MJ; Cubells M; Hernando-Davalillo C; Palau F; Hoenicka J
Autism Res; 2021 Jun; 14(6):1088-1100. PubMed ID: 33749153
[TBL] [Abstract][Full Text] [Related]
70. Calculating genetic risk for dysfunction in pleiotropic biological processes using whole exome sequencing data.
Veatch OJ; Mazzotti DR; Schultz RT; Abel T; Michaelson JJ; Brodkin ES; Tunc B; Assouline SG; Nickl-Jockschat T; Malow BA; Sutcliffe JS; Pack AI
J Neurodev Disord; 2022 Jun; 14(1):39. PubMed ID: 35751013
[TBL] [Abstract][Full Text] [Related]
71. Rare heterozygous truncating variations and risk of autism spectrum disorder: Whole-exome sequencing of a multiplex family and follow-up study in a Japanese population.
Inoue E; Watanabe Y; Egawa J; Sugimoto A; Nunokawa A; Shibuya M; Igeta H; Someya T
Psychiatry Clin Neurosci; 2015 Aug; 69(8):472-6. PubMed ID: 25601189
[TBL] [Abstract][Full Text] [Related]
72. Genetics of autism spectrum disorder.
Ramaswami G; Geschwind DH
Handb Clin Neurol; 2018; 147():321-329. PubMed ID: 29325621
[TBL] [Abstract][Full Text] [Related]
73. Sex bias in social deficits, neural circuits and nutrient demand in Cttnbp2 autism models.
Yen TL; Huang TN; Lin MH; Hsu TT; Lu MH; Shih PY; Ellegood J; Lerch J; Hsueh YP
Brain; 2023 Jun; 146(6):2612-2626. PubMed ID: 36385662
[TBL] [Abstract][Full Text] [Related]
74. Autism Spectrum Disorder/Intellectual Disability-Associated Mutations in Trio Disrupt Neuroligin 1-Mediated Synaptogenesis.
Tian C; Paskus JD; Fingleton E; Roche KW; Herring BE
J Neurosci; 2021 Sep; 41(37):7768-7778. PubMed ID: 34353896
[TBL] [Abstract][Full Text] [Related]
75. Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case.
Bradshaw G; Lualhati RR; Albury CL; Maksemous N; Roos-Araujo D; Smith RA; Benton MC; Eccles DA; Lea RA; Sutherland HG; Haupt LM; Griffiths LR
Front Immunol; 2018; 9():420. PubMed ID: 29556235
[TBL] [Abstract][Full Text] [Related]
76. The genetic landscape of autism spectrum disorder in the Middle Eastern population.
Al-Sarraj Y; Taha RZ; Al-Dous E; Ahram D; Abbasi S; Abuazab E; Shaath H; Habbab W; Errafii K; Bejaoui Y; AlMotawa M; Khattab N; Aqel YA; Shalaby KE; Al-Ansari A; Kambouris M; Abouzohri A; Ghazal I; Tolfat M; Alshaban F; El-Shanti H; Albagha OME
Front Genet; 2024; 15():1363849. PubMed ID: 38572415
[No Abstract] [Full Text] [Related]
77. [A study on KIF1A gene missense variant analysis and its protein expression and structure profiles of an autism spectrum disorder family trio].
Huang Y; Jiao J; Zhang M; Situ M; Yuan D; Lyu P; Li S; Wang Z; Yang Y; Huang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Jul; 38(7):620-625. PubMed ID: 34247363
[TBL] [Abstract][Full Text] [Related]
78. Next Generation Sequencing Mitochondrial DNA Analysis in Autism Spectrum Disorder.
Patowary A; Nesbitt R; Archer M; Bernier R; Brkanac Z
Autism Res; 2017 Aug; 10(8):1338-1343. PubMed ID: 28419775
[TBL] [Abstract][Full Text] [Related]
79. Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.
Amiri-Yekta A; Coutton C; Kherraf ZE; Karaouzène T; Le Tanno P; Sanati MH; Sabbaghian M; Almadani N; Sadighi Gilani MA; Hosseini SH; Bahrami S; Daneshipour A; Bini M; Arnoult C; Colombo R; Gourabi H; Ray PF
Hum Reprod; 2016 Dec; 31(12):2872-2880. PubMed ID: 27798045
[TBL] [Abstract][Full Text] [Related]
80.
Zhang S; Yang J; Ji D; Meng X; Zhu C; Zheng G; Glessner J; Qu HQ; Cui Y; Liu Y; Wang W; Li X; Zhang H; Xiu Z; Sun Y; Sun L; Li J; Hakonarson H; Li J; Xia Q
J Med Genet; 2024 Jun; 61(7):677-688. PubMed ID: 38443156
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]