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 *

196 related articles for article (PubMed ID: 25044326)

  • 1. Missing genetic risk in neural tube defects: can exome sequencing yield an insight?
    Krupp DR; Soldano KL; Garrett ME; Cope H; Ashley-Koch AE; Gregory SG
    Birth Defects Res A Clin Mol Teratol; 2014 Aug; 100(8):642-6. PubMed ID: 25044326
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole exome sequencing identifies novel predisposing genes in neural tube defects.
    Lemay P; De Marco P; Traverso M; Merello E; Dionne-Laporte A; Spiegelman D; Henrion É; Diallo O; Audibert F; Michaud JL; Cama A; Rouleau GA; Kibar Z; Capra V
    Mol Genet Genomic Med; 2019 Jan; 7(1):e00467. PubMed ID: 30415495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic epidemiology of neural tube defects.
    Lupo PJ; Agopian AJ; Castillo H; Castillo J; Clayton GH; Dosa NP; Hopson B; Joseph DB; Rocque BG; Walker WO; Wiener JS; Mitchell LE
    J Pediatr Rehabil Med; 2017 Dec; 10(3-4):189-194. PubMed ID: 29125517
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of new candidate genes for spina bifida through exome sequencing.
    Azzarà A; Rendeli C; Crivello AM; Brugnoletti F; Rumore R; Ausili E; Sangiorgi E; Gurrieri F
    Childs Nerv Syst; 2021 Aug; 37(8):2589-2596. PubMed ID: 33855610
    [TBL] [Abstract][Full Text] [Related]  

  • 5. TRIM4 is associated with neural tube defects based on genome-wide DNA methylation analysis.
    Zhang H; Guo Y; Gu H; Wei X; Ma W; Liu D; Yu K; Luo W; Ma L; Liu Y; Xue J; Huang J; Wang Y; Jia S; Dong N; Wang H; Yuan Z
    Clin Epigenetics; 2019 Feb; 11(1):17. PubMed ID: 30709423
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Digenic variants of planar cell polarity genes in human neural tube defect patients.
    Wang L; Xiao Y; Tian T; Jin L; Lei Y; Finnell RH; Ren A
    Mol Genet Metab; 2018 May; 124(1):94-100. PubMed ID: 29573971
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exome versus transcriptome sequencing in identifying coding region variants.
    Ku CS; Wu M; Cooper DN; Naidoo N; Pawitan Y; Pang B; Iacopetta B; Soong R
    Expert Rev Mol Diagn; 2012 Apr; 12(3):241-51. PubMed ID: 22468815
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathway.
    Renard E; Chéry C; Oussalah A; Josse T; Perrin P; Tramoy D; Voirin J; Klein O; Leheup B; Feillet F; Guéant-Rodriguez RM; Guéant JL
    Hum Genet; 2019 Jul; 138(7):703-713. PubMed ID: 31139930
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Loss-of-function de novo mutations play an important role in severe human neural tube defects.
    Lemay P; Guyot MC; Tremblay É; Dionne-Laporte A; Spiegelman D; Henrion É; Diallo O; De Marco P; Merello E; Massicotte C; Désilets V; Michaud JL; Rouleau GA; Capra V; Kibar Z
    J Med Genet; 2015 Jul; 52(7):493-7. PubMed ID: 25805808
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans.
    Safra N; Bassuk AG; Ferguson PJ; Aguilar M; Coulson RL; Thomas N; Hitchens PL; Dickinson PJ; Vernau KM; Wolf ZT; Bannasch DL
    PLoS Genet; 2013; 9(7):e1003646. PubMed ID: 23874236
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder.
    Cruceanu C; Ambalavanan A; Spiegelman D; Gauthier J; Lafrenière RG; Dion PA; Alda M; Turecki G; Rouleau GA
    Genome; 2013 Oct; 56(10):634-40. PubMed ID: 24237345
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Exome analysis in an Estonian multiplex family with neural tube defects-a case report.
    Pappa L; Kals M; Kivistik PA; Metspalu A; Paal A; Nikopensius T
    Childs Nerv Syst; 2017 Sep; 33(9):1575-1581. PubMed ID: 28721594
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Evaluation of common genetic variants in 82 candidate genes as risk factors for neural tube defects.
    Pangilinan F; Molloy AM; Mills JL; Troendle JF; Parle-McDermott A; Signore C; O'Leary VB; Chines P; Seay JM; Geiler-Samerotte K; Mitchell A; VanderMeer JE; Krebs KM; Sanchez A; Cornman-Homonoff J; Stone N; Conley M; Kirke PN; Shane B; Scott JM; Brody LC
    BMC Med Genet; 2012 Aug; 13():62. PubMed ID: 22856873
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Exome Sequencing of Familial Bipolar Disorder.
    Goes FS; Pirooznia M; Parla JS; Kramer M; Ghiban E; Mavruk S; Chen YC; Monson ET; Willour VL; Karchin R; Flickinger M; Locke AE; Levy SE; Scott LJ; Boehnke M; Stahl E; Moran JL; Hultman CM; Landén M; Purcell SM; Sklar P; Zandi PP; McCombie WR; Potash JB
    JAMA Psychiatry; 2016 Jun; 73(6):590-7. PubMed ID: 27120077
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Epidemiologic and genetic aspects of spina bifida and other neural tube defects.
    Au KS; Ashley-Koch A; Northrup H
    Dev Disabil Res Rev; 2010; 16(1):6-15. PubMed ID: 20419766
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Diagnosing rare diseases after the exome.
    Frésard L; Montgomery SB
    Cold Spring Harb Mol Case Stud; 2018 Dec; 4(6):. PubMed ID: 30559314
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
    Francesca LC; Claudia R; Molinario C; Annamaria M; Chiara F; Natalia C; Emanuele A; Valentina P; Giovanni N; Costantino R; Eugenio S; Fiorella G
    Childs Nerv Syst; 2016 Jun; 32(6):1061-7. PubMed ID: 27125519
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects.
    Leduc RY; Singh P; McDermid HE
    Birth Defects Res; 2017 Jan; 109(2):140-152. PubMed ID: 27768235
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Approaches to studying the genomic architecture of complex birth defects.
    Taiwo TE; Cao X; Cabrera RM; Lei Y; Finnell RH
    Prenat Diagn; 2020 Aug; 40(9):1047-1055. PubMed ID: 32468575
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Developments in our understanding of the genetic basis of birth defects.
    Webber DM; MacLeod SL; Bamshad MJ; Shaw GM; Finnell RH; Shete SS; Witte JS; Erickson SW; Murphy LD; Hobbs C
    Birth Defects Res A Clin Mol Teratol; 2015 Aug; 103(8):680-91. PubMed ID: 26033863
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.