These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

299 related articles for article (PubMed ID: 31288856)

  • 41. Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
    Wang T; Hoekzema K; Vecchio D; Wu H; Sulovari A; Coe BP; Gillentine MA; Wilfert AB; Perez-Jurado LA; Kvarnung M; Sleyp Y; Earl RK; Rosenfeld JA; Geisheker MR; Han L; Du B; Barnett C; Thompson E; Shaw M; Carroll R; Friend K; Catford R; Palmer EE; Zou X; Ou J; Li H; Guo H; Gerdts J; Avola E; Calabrese G; Elia M; Greco D; Lindstrand A; Nordgren A; Anderlid BM; Vandeweyer G; Van Dijck A; Van der Aa N; McKenna B; Hancarova M; Bendova S; Havlovicova M; Malerba G; Bernardina BD; Muglia P; van Haeringen A; Hoffer MJV; Franke B; Cappuccio G; Delatycki M; Lockhart PJ; Manning MA; Liu P; Scheffer IE; Brunetti-Pierri N; Rommelse N; Amaral DG; Santen GWE; Trabetti E; Sedláček Z; Michaelson JJ; Pierce K; Courchesne E; Kooy RF; ; Nordenskjöld M; Romano C; Peeters H; Bernier RA; Gecz J; Xia K; Eichler EE
    Nat Commun; 2020 Oct; 11(1):4932. PubMed ID: 33004838
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Genetic subtypes, allelic effects, and convergent neurodevelopmental mechanisms.
    Das M; Girirajan S
    Genome Med; 2021 Jun; 13(1):99. PubMed ID: 34099044
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Zebrafish Models of Neurodevelopmental Disorders: Limitations and Benefits of Current Tools and Techniques.
    Vaz R; Hofmeister W; Lindstrand A
    Int J Mol Sci; 2019 Mar; 20(6):. PubMed ID: 30875831
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
    Reuter MS; Tawamie H; Buchert R; Hosny Gebril O; Froukh T; Thiel C; Uebe S; Ekici AB; Krumbiegel M; Zweier C; Hoyer J; Eberlein K; Bauer J; Scheller U; Strom TM; Hoffjan S; Abdelraouf ER; Meguid NA; Abboud A; Al Khateeb MA; Fakher M; Hamdan S; Ismael A; Muhammad S; Abdallah E; Sticht H; Wieczorek D; Reis A; Abou Jamra R
    JAMA Psychiatry; 2017 Mar; 74(3):293-299. PubMed ID: 28097321
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and Phenotypes.
    de Kovel CGF; Syrbe S; Brilstra EH; Verbeek N; Kerr B; Dubbs H; Bayat A; Desai S; Naidu S; Srivastava S; Cagaylan H; Yis U; Saunders C; Rook M; Plugge S; Muhle H; Afawi Z; Klein KM; Jayaraman V; Rajagopalan R; Goldberg E; Marsh E; Kessler S; Bergqvist C; Conlin LK; Krok BL; Thiffault I; Pendziwiat M; Helbig I; Polster T; Borggraefe I; Lemke JR; van den Boogaardt MJ; Møller RS; Koeleman BPC
    JAMA Neurol; 2017 Oct; 74(10):1228-1236. PubMed ID: 28806457
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Phenotypic features of patients with schizophrenia carrying de novo gene mutations: a pilot study.
    Malherbe PJ; Roos JL; Ehlers R; Karayiorgou M; Roos JL
    Psychiatry Res; 2015 Jan; 225(1-2):108-114. PubMed ID: 25467704
    [TBL] [Abstract][Full Text] [Related]  

  • 47. IDGenetics: a comprehensive database for genes and mutations of intellectual disability related disorders.
    Chen C; Chen D; Xue H; Liu X; Zhang T; Tang S; Li W; Xu X
    Neurosci Lett; 2018 Oct; 685():96-101. PubMed ID: 30144540
    [TBL] [Abstract][Full Text] [Related]  

  • 48. What a finding of gene copy number variation can add to the diagnosis of developmental neuropsychiatric disorders.
    Vorstman J; Scherer SW
    Curr Opin Genet Dev; 2021 Jun; 68():18-25. PubMed ID: 33454514
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genetic and environmental modulation of neurodevelopmental disorders: Translational insights from labs to beds.
    Homberg JR; Kyzar EJ; Scattoni ML; Norton WH; Pittman J; Gaikwad S; Nguyen M; Poudel MK; Ullmann JF; Diamond DM; Kaluyeva AA; Parker MO; Brown RE; Song C; Gainetdinov RR; Gottesman II; Kalueff AV
    Brain Res Bull; 2016 Jul; 125():79-91. PubMed ID: 27113433
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Case reports: novel TUBG1 mutations with milder neurodevelopmental presentations.
    Yuen YTK; Guella I; Roland E; Sargent M; Boelman C
    BMC Med Genet; 2019 May; 20(1):95. PubMed ID: 31151415
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The genetic landscapes of autism spectrum disorders.
    Huguet G; Ey E; Bourgeron T
    Annu Rev Genomics Hum Genet; 2013; 14():191-213. PubMed ID: 23875794
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.
    Krgovic D; Kokalj Vokac N; Zagorac A; Gregoric Kumperscak H
    Sci Rep; 2018 Jun; 8(1):9449. PubMed ID: 29930340
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Phenotype-loci associations in networks of patients with rare disorders: application to assist in the diagnosis of novel clinical cases.
    Bueno A; Rodríguez-López R; Reyes-Palomares A; Rojano E; Corpas M; Nevado J; Lapunzina P; Sánchez-Jiménez F; Ranea JAG
    Eur J Hum Genet; 2018 Oct; 26(10):1451-1461. PubMed ID: 29946186
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.
    Nagy D; Verheyen S; Wigby KM; Borovikov A; Sharkov A; Slegesky V; Larson A; Fagerberg C; Brasch-Andersen C; Kibæk M; Bader I; Hernan R; High FA; Chung WK; Schieving JH; Behunova J; Smogavec M; Laccone F; Witsch-Baumgartner M; Zobel J; Duba HC; Weis D
    Genes (Basel); 2022 Jan; 13(1):. PubMed ID: 35052493
    [No Abstract]   [Full Text] [Related]  

  • 55. Distinct selective forces and Neanderthal introgression shaped genetic diversity at genes involved in neurodevelopmental disorders.
    Mozzi A; Forni D; Cagliani R; Pozzoli U; Clerici M; Sironi M
    Sci Rep; 2017 Jul; 7(1):6116. PubMed ID: 28733602
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.
    Glessner JT; Li J; Wang D; March M; Lima L; Desai A; Hadley D; Kao C; Gur RE; Cohen N; Sleiman PMA; Li Q; Hakonarson H;
    Genome Med; 2017 Nov; 9(1):106. PubMed ID: 29191242
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. 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]  

  • 59. Somatic mutations in the human brain: implications for psychiatric research.
    Nishioka M; Bundo M; Iwamoto K; Kato T
    Mol Psychiatry; 2019 Jun; 24(6):839-856. PubMed ID: 30087451
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Prediction of Neurodevelopmental Disorders Based on De Novo Coding Variation.
    Chow JC; Hormozdiari F
    J Autism Dev Disord; 2023 Mar; 53(3):963-976. PubMed ID: 35596027
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.