BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 37025335)

  • 1. Applying whole exome sequencing in a consanguineous population with autism spectrum disorder.
    Al-Mamari W; Idris AB; Al-Thihli K; Abdulrahim R; Jalees S; Al-Jabri M; Gabr A; Al Murshedi F; Al Kindy A; Al-Hadabi I; Bruwer Z; Islam MM; Alsayegh A
    Int J Dev Disabil; 2023; 69(2):190-200. PubMed ID: 37025335
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
    Tammimies K; Marshall CR; Walker S; Kaur G; Thiruvahindrapuram B; Lionel AC; Yuen RK; Uddin M; Roberts W; Weksberg R; Woodbury-Smith M; Zwaigenbaum L; Anagnostou E; Wang Z; Wei J; Howe JL; Gazzellone MJ; Lau L; Sung WW; Whitten K; Vardy C; Crosbie V; Tsang B; D'Abate L; Tong WW; Luscombe S; Doyle T; Carter MT; Szatmari P; Stuckless S; Merico D; Stavropoulos DJ; Scherer SW; Fernandez BA
    JAMA; 2015 Sep; 314(9):895-903. PubMed ID: 26325558
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Diagnostic Evaluation of Trio-Based Whole Exome Sequencing Among Children With Diagnosed or Suspected Autism Spectrum Disorder.
    Du X; Gao X; Liu X; Shen L; Wang K; Fan Y; Sun Y; Luo X; Liu H; Wang L; Wang Y; Gong Z; Wang J; Yu Y; Li F
    Front Genet; 2018; 9():594. PubMed ID: 30555518
    [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. Towards a Change in the Diagnostic Algorithm of Autism Spectrum Disorders: Evidence Supporting Whole Exome Sequencing as a First-Tier Test.
    Arteche-López A; Gómez Rodríguez MJ; Sánchez Calvin MT; Quesada-Espinosa JF; Lezana Rosales JM; Palma Milla C; Gómez-Manjón I; Hidalgo Mayoral I; Pérez de la Fuente R; Díaz de Bustamante A; Darnaude MT; Gil-Fournier B; Ramiro León S; Ramos Gómez P; Sierra Tomillo O; Juárez Rufián A; Arranz Cano MI; Villares Alonso R; Morales-Pérez P; Segura-Tudela A; Camacho A; Nuñez N; Simón R; Moreno-García M; Alvarez-Mora MI
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33921431
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The Results of Whole Exome Sequencing Performed On Previously Undiagnosed Pediatric Neurology Patients.
    Ahmadnia N; Beiraghi Toosi M; Ghayour Karimiani E; Ashrafzadeh F; Faraji Rad M
    Iran J Child Neurol; 2021; 15(2):17-31. PubMed ID: 36213152
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders.
    Rossi M; El-Khechen D; Black MH; Farwell Hagman KD; Tang S; Powis Z
    Pediatr Neurol; 2017 May; 70():34-43.e2. PubMed ID: 28330790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dendritic Spine in Autism Genetics: Whole-Exome Sequencing Identifying De Novo Variant of
    Xie Y; Wang H; Hu B; Zhang X; Liu A; Cai C; Li S; Chen C; Wang Z; Yin Z; Wang M
    Children (Basel); 2022 Dec; 10(1):. PubMed ID: 36670631
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recent Advances in Autism Spectrum Disorders: Applications of Whole Exome Sequencing Technology.
    Sener EF; Canatan H; Ozkul Y
    Psychiatry Investig; 2016 May; 13(3):255-64. PubMed ID: 27247591
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Combining Metagenomic Sequencing With Whole Exome Sequencing to Optimize Clinical Strategies in Neonates With a Suspected Central Nervous System Infection.
    Ge M; Gan M; Yan K; Xiao F; Yang L; Wu B; Xiao M; Ba Y; Zhang R; Wang J; Cheng G; Wang L; Cao Y; Zhou W; Hu L
    Front Cell Infect Microbiol; 2021; 11():671109. PubMed ID: 34222042
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
    Ghieh F; Barbotin AL; Swierkowski-Blanchard N; Leroy C; Fortemps J; Gerault C; Hue C; Mambu Mambueni H; Jaillard S; Albert M; Bailly M; Izard V; Molina-Gomes D; Marcelli F; Prasivoravong J; Serazin V; Dieudonne MN; Delcroix M; Garchon HJ; Louboutin A; Mandon-Pepin B; Ferlicot S; Vialard F
    Hum Reprod; 2022 May; 37(6):1334-1350. PubMed ID: 35413094
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. The Utility of Whole Exome Sequencing in Diagnosing Pediatric Neurological Disorders.
    Muthaffar OY
    Balkan J Med Genet; 2020 Nov; 23(2):17-24. PubMed ID: 33816068
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comprehensive Genetic Analysis of Non-syndromic Autism Spectrum Disorder in Clinical Settings.
    Ohashi K; Fukuhara S; Miyachi T; Asai T; Imaeda M; Goto M; Kurokawa Y; Anzai T; Tsurusaki Y; Miyake N; Matsumoto N; Yamagata T; Saitoh S
    J Autism Dev Disord; 2021 Dec; 51(12):4655-4662. PubMed ID: 33590427
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Impaired Neurodevelopmental Genes in Slovenian Autistic Children Elucidate the Comorbidity of Autism With Other Developmental Disorders.
    Krgovic D; Gorenjak M; Rihar N; Opalic I; Stangler Herodez S; Gregoric Kumperscak H; Dovc P; Kokalj Vokac N
    Front Mol Neurosci; 2022; 15():912671. PubMed ID: 35813072
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A semiautomated whole-exome sequencing workflow leads to increased diagnostic yield and identification of novel candidate variants.
    Ji J; Shen L; Bootwalla M; Quindipan C; Tatarinova T; Maglinte DT; Buckley J; Raca G; Saitta SC; Biegel JA; Gai X
    Cold Spring Harb Mol Case Stud; 2019 Apr; 5(2):. PubMed ID: 30755392
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.