BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

207 related articles for article (PubMed ID: 37914828)

  • 1. Comparison of three bioinformatics tools in the detection of ASD candidate variants from whole exome sequencing data.
    Shil A; Levin L; Golan H; Meiri G; Michaelovski A; Sadaka Y; Aran A; Dinstein I; Menashe I
    Sci Rep; 2023 Nov; 13(1):18853. PubMed ID: 37914828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test.
    Sheth F; Shah J; Jain D; Shah S; Patel H; Patel K; Solanki DI; Iyer AS; Menghani B; Mhatre P; Mehta S; Bajaj S; Patel V; Pandya M; Dhami D; Patel D; Sheth J; Sheth H
    BMC Neurol; 2023 Aug; 23(1):292. PubMed ID: 37543562
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Diagnostic Yield and Economic Implications of Whole-Exome Sequencing for ASD Diagnosis in Israel.
    Tal-Ben Ishay R; Shil A; Solomon S; Sadigurschi N; Abu-Kaf H; Meiri G; Flusser H; Michaelovski A; Dinstein I; Golan H; Davidovitch N; Menashe I
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052376
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Next Generation Sequencing-Based Protocol for Screening of Variants of Concern in Autism Spectrum Disorder.
    Huang J; Liu J; Tian R; Liu K; Zhuang P; Sherman HT; Budjan C; Fong M; Jeong MS; Kong XJ
    Cells; 2021 Dec; 11(1):. PubMed ID: 35011571
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder.
    Cameli C; Viggiano M; Rochat MJ; Maresca A; Caporali L; Fiorini C; Palombo F; Magini P; Duardo RC; Ceroni F; Scaduto MC; Posar A; Seri M; Carelli V; Visconti P; Bacchelli E; Maestrini E
    J Cell Mol Med; 2021 Mar; 25(5):2459-2470. PubMed ID: 33476483
    [TBL] [Abstract][Full Text] [Related]  

  • 10. An integrated analysis of rare CNV and exome variation in Autism Spectrum Disorder using the Infinium PsychArray.
    Bacchelli E; Cameli C; Viggiano M; Igliozzi R; Mancini A; Tancredi R; Battaglia A; Maestrini E
    Sci Rep; 2020 Feb; 10(1):3198. PubMed ID: 32081867
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Rare genetic susceptibility variants assessment in autism spectrum disorder: detection rate and practical use.
    Husson T; Lecoquierre F; Cassinari K; Charbonnier C; Quenez O; Goldenberg A; Guerrot AM; Richard AC; Drouin-Garraud V; Brehin AC; Soleimani M; Taton R; Rotharmel M; Rosier A; Chambon P; Le Meur N; Joly-Helas G; Saugier-Veber P; Boland A; Deleuze JF; Olaso R; Frebourg T; Nicolas G; Guillin O; Campion D
    Transl Psychiatry; 2020 Feb; 10(1):77. PubMed ID: 32094338
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional relationships between recessive inherited genes and genes with de novo variants in autism spectrum disorder.
    Wang L; Zhang Y; Li K; Wang Z; Wang X; Li B; Zhao G; Fang Z; Ling Z; Luo T; Xia L; Li Y; Guo H; Hu Z; Li J; Sun Z; Xia K
    Mol Autism; 2020 Oct; 11(1):75. PubMed ID: 33023636
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis.
    Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW
    Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [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]  

  • 17. Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.
    Al-Mubarak B; Abouelhoda M; Omar A; AlDhalaan H; Aldosari M; Nester M; Alshamrani HA; El-Kalioby M; Goljan E; Albar R; Subhani S; Tahir A; Asfahani S; Eskandrani A; Almusaiab A; Magrashi A; Shinwari J; Monies D; Al Tassan N
    Sci Rep; 2017 Jul; 7(1):5679. PubMed ID: 28720891
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-exome sequencing and neurite outgrowth analysis in autism spectrum disorder.
    Hashimoto R; Nakazawa T; Tsurusaki Y; Yasuda Y; Nagayasu K; Matsumura K; Kawashima H; Yamamori H; Fujimoto M; Ohi K; Umeda-Yano S; Fukunaga M; Fujino H; Kasai A; Hayata-Takano A; Shintani N; Takeda M; Matsumoto N; Hashimoto H
    J Hum Genet; 2016 Mar; 61(3):199-206. PubMed ID: 26582266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants.
    Han Q; Yang Y; Wu S; Liao Y; Zhang S; Liang H; Cram DS; Zhang Y
    BMC Genomics; 2021 Jun; 22(1):407. PubMed ID: 34082700
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.