BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

248 related articles for article (PubMed ID: 36670631)

  • 81. 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]  

  • 82. 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]  

  • 83.
    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]  

  • 84. Identification of a
    Tang Y; Liu Y; Tong L; Feng S; Du D; Chen F
    Biomed Res Int; 2020; 2020():8872577. PubMed ID: 33204724
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Molecular Dysregulation in Autism Spectrum Disorder.
    Gill PS; Clothier JL; Veerapandiyan A; Dweep H; Porter-Gill PA; Schaefer GB
    J Pers Med; 2021 Aug; 11(9):. PubMed ID: 34575625
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Neuron-specific regulation on F-actin cytoskeletons: The role of CTTNBP2 in dendritic spinogenesis and maintenance.
    Hsueh YP
    Commun Integr Biol; 2012 Jul; 5(4):334-6. PubMed ID: 23060955
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Whole-genome sequencing of quartet families with autism spectrum disorder.
    Yuen RK; Thiruvahindrapuram B; Merico D; Walker S; Tammimies K; Hoang N; Chrysler C; Nalpathamkalam T; Pellecchia G; Liu Y; Gazzellone MJ; D'Abate L; Deneault E; Howe JL; Liu RS; Thompson A; Zarrei M; Uddin M; Marshall CR; Ring RH; Zwaigenbaum L; Ray PN; Weksberg R; Carter MT; Fernandez BA; Roberts W; Szatmari P; Scherer SW
    Nat Med; 2015 Feb; 21(2):185-91. PubMed ID: 25621899
    [TBL] [Abstract][Full Text] [Related]  

  • 88. 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]  

  • 89. Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half.
    Bar O; Vahey E; Mintz M; Frye RE; Boles RG
    Int J Mol Sci; 2024 Jan; 25(2):. PubMed ID: 38256266
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems.
    Farajzadeh Valilou S; Alavi A; Pashaei M; Ghasemi Firouzabadi S; Shafeghati Y; Nozari A; Hadipour F; Hadipour Z; Maghsoodlou Estrabadi B; Gholamreza Noorazar S; Banihashemi S; Karimian J; Fattahi M; Behjati F
    Mol Syndromol; 2020 Jun; 11(2):62-72. PubMed ID: 32655337
    [TBL] [Abstract][Full Text] [Related]  

  • 91. 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]  

  • 92. Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
    Roberts JL; Hovanes K; Dasouki M; Manzardo AM; Butler MG
    Gene; 2014 Feb; 535(1):70-8. PubMed ID: 24188901
    [TBL] [Abstract][Full Text] [Related]  

  • 93. De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
    Babbs C; Lloyd D; Pagnamenta AT; Twigg SR; Green J; McGowan SJ; Mirza G; Naples R; Sharma VP; Volpi EV; Buckle VJ; Wall SA; Knight SJ; ; Parr JR; Wilkie AO
    J Med Genet; 2014 Nov; 51(11):737-47. PubMed ID: 25228304
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Whole exome sequencing for a patient with Rubinstein-Taybi syndrome reveals de novo variants besides an overt CREBBP mutation.
    Yoo HJ; Kim K; Kim IH; Rho SH; Park JE; Lee KY; Kim SA; Choi BY; Kim N
    Int J Mol Sci; 2015 Mar; 16(3):5697-713. PubMed ID: 25768348
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.
    Chapman NH; Nato AQ; Bernier R; Ankenman K; Sohi H; Munson J; Patowary A; Archer M; Blue EM; Webb SJ; Coon H; Raskind WH; Brkanac Z; Wijsman EM
    Hum Genet; 2015 Oct; 134(10):1055-68. PubMed ID: 26204995
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
    Wang C; Horigane SI; Wakamori M; Ueda S; Kawabata T; Fujii H; Kushima I; Kimura H; Ishizuka K; Nakamura Y; Iwayama Y; Ikeda M; Iwata N; Okada T; Aleksic B; Mori D; Yoshida T; Bito H; Yoshikawa T; Takemoto-Kimura S; Ozaki N
    Transl Psychiatry; 2022 Feb; 12(1):84. PubMed ID: 35220405
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Identification of two novel autism genes,
    Gupta V; Ben-Mahmoud A; Ku B; Velayutham D; Jan Z; Yousef Aden A; Kubbar A; Alshaban F; Stanton LW; Jithesh PV; Layman LC; Kim HG
    Front Psychiatry; 2023; 14():1251884. PubMed ID: 38025430
    [TBL] [Abstract][Full Text] [Related]  

  • 98. Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals ascertained for diagnosis of autism spectrum disorder.
    Fernandez BA; Roberts W; Chung B; Weksberg R; Meyn S; Szatmari P; Joseph-George AM; Mackay S; Whitten K; Noble B; Vardy C; Crosbie V; Luscombe S; Tucker E; Turner L; Marshall CR; Scherer SW
    J Med Genet; 2010 Mar; 47(3):195-203. PubMed ID: 19755429
    [TBL] [Abstract][Full Text] [Related]  

  • 99. A de novo convergence of autism genetics and molecular neuroscience.
    Krumm N; O'Roak BJ; Shendure J; Eichler EE
    Trends Neurosci; 2014 Feb; 37(2):95-105. PubMed ID: 24387789
    [TBL] [Abstract][Full Text] [Related]  

  • 100. Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism.
    Sjaarda CP; Wood S; McNaughton AJM; Taylor S; Hudson ML; Liu X; Guerin A; Ayub M
    J Hum Genet; 2020 Mar; 65(3):287-296. PubMed ID: 31827253
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.