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 *

152 related articles for article (PubMed ID: 37215497)

  • 1. Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing.
    Xing J; Wang H; Xie Y; Fan T; Cui C; Li Y; Wang S; Gu W; Wang C; Tang H; Liu L
    Open Life Sci; 2023; 18(1):20220593. PubMed ID: 37215497
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.
    Shi X; Zhang L; Bai K; Xie H; Shi T; Zhang R; Fu Q; Chen S; Lu Y; Yu Y; Sun K
    Comput Struct Biotechnol J; 2020; 18():381-392. PubMed ID: 32128068
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing.
    Zhou Y; Bai K; Wang Y; Meng Z; Zhou S; Jiang S; Wang H; Wang J; Yang M; Wang Q; Sun K; Chen S
    Front Cardiovasc Med; 2021; 8():811156. PubMed ID: 35141295
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect.
    Xie H; Hong N; Zhang E; Li F; Sun K; Yu Y
    Front Genet; 2019; 10():15. PubMed ID: 30745907
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare de novo copy number variants in patients with congenital pulmonary atresia.
    Xie L; Chen JL; Zhang WZ; Wang SZ; Zhao TL; Huang C; Wang J; Yang JF; Yang YF; Tan ZP
    PLoS One; 2014; 9(5):e96471. PubMed ID: 24826987
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data.
    Glessner JT; Bick AG; Ito K; Homsy J; Rodriguez-Murillo L; Fromer M; Mazaika E; Vardarajan B; Italia M; Leipzig J; DePalma SR; Golhar R; Sanders SJ; Yamrom B; Ronemus M; Iossifov I; Willsey AJ; State MW; Kaltman JR; White PS; Shen Y; Warburton D; Brueckner M; Seidman C; Goldmuntz E; Gelb BD; Lifton R; Seidman J; Hakonarson H; Chung WK
    Circ Res; 2014 Oct; 115(10):884-896. PubMed ID: 25205790
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH.
    Zhu N; Swietlik EM; Welch CL; Pauciulo MW; Hagen JJ; Zhou X; Guo Y; Karten J; Pandya D; Tilly T; Lutz KA; Martin JM; Treacy CM; Rosenzweig EB; Krishnan U; Coleman AW; Gonzaga-Jauregui C; Lawrie A; Trembath RC; Wilkins MR; ; ; ; ; Morrell NW; Shen Y; Gräf S; Nichols WC; Chung WK
    Genome Med; 2021 May; 13(1):80. PubMed ID: 33971972
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis.
    Haisma SM; Weersma RK; Joosse ME; de Koning BAE; de Meij T; Koot BGP; Wolters V; Norbruis O; Daly MJ; Stevens C; Xavier RJ; Koskela J; Rivas MA; Visschedijk MC; Verkade HJ; Barbieri R; Jansen DBH; Festen EAM; van Rheenen PF; van Diemen CC
    Liver Int; 2021 May; 41(5):1044-1057. PubMed ID: 33590606
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
    LaHaye S; Corsmeier D; Basu M; Bowman JL; Fitzgerald-Butt S; Zender G; Bosse K; McBride KL; White P; Garg V
    Circ Cardiovasc Genet; 2016 Aug; 9(4):320-9. PubMed ID: 27418595
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole-exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants.
    Olfson E; Lebowitz ER; Hommel G; Pashankar N; Silverman WK; Fernandez TV
    Depress Anxiety; 2022 Jun; 39(6):474-484. PubMed ID: 35312124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noise.
    Landstrom AP; Fernandez E; Rosenfeld JA; Yang Y; Dailey-Schwartz AL; Miyake CY; Allen HD; Penny DJ; Kim JJ
    Heart Rhythm; 2018 Jul; 15(7):1042-1050. PubMed ID: 29501670
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare Variants in Novel Candidate Genes Associated With Nonsyndromic Patent Ductus Arteriosus Identified With Whole-Exome Sequencing.
    Gao Y; Wu D; Chen B; Chen Y; Zhang Q; Zhao P
    Front Genet; 2022; 13():921925. PubMed ID: 35734438
    [No Abstract]   [Full Text] [Related]  

  • 14. Whole exome sequencing in 342 congenital cardiac left sided lesion cases reveals extensive genetic heterogeneity and complex inheritance patterns.
    Li AH; Hanchard NA; Furthner D; Fernbach S; Azamian M; Nicosia A; Rosenfeld J; Muzny D; D'Alessandro LCA; Morris S; Jhangiani S; Parekh DR; Franklin WJ; Lewin M; Towbin JA; Penny DJ; Fraser CD; Martin JF; Eng C; Lupski JR; Gibbs RA; Boerwinkle E; Belmont JW
    Genome Med; 2017 Oct; 9(1):95. PubMed ID: 29089047
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exome sequencing reveals new causal mutations in children with epileptic encephalopathies.
    Veeramah KR; Johnstone L; Karafet TM; Wolf D; Sprissler R; Salogiannis J; Barth-Maron A; Greenberg ME; Stuhlmann T; Weinert S; Jentsch TJ; Pazzi M; Restifo LL; Talwar D; Erickson RP; Hammer MF
    Epilepsia; 2013 Jul; 54(7):1270-81. PubMed ID: 23647072
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
    Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
    Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome-wide Analysis of De Novo and Rare Genetic Variants in Patients With Brain Arteriovenous Malformation.
    Wang K; Zhao S; Xie Z; Zhang M; Zhao H; Cheng X; Zhang Y; Niu Y; Liu J; Zhang TJ; Zhang Y; Wu Z; Chu J; Yang X; Wu N
    Neurology; 2022 Apr; 98(16):e1670-e1678. PubMed ID: 35228337
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Using whole-exome sequencing to identify variants inherited from mosaic parents.
    Rios JJ; Delgado MR
    Eur J Hum Genet; 2015 Apr; 23(4):547-50. PubMed ID: 24986828
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES).
    Liu Y; Cao Y; Li Y; Lei D; Li L; Hou ZL; Han S; Meng M; Shi J; Zhang Y; Wang Y; Niu Z; Xie Y; Xiao B; Wang Y; Li X; Yang L; Wang W; Jiang L
    Med Sci Monit; 2018 Mar; 24():1340-1358. PubMed ID: 29505555
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole-Exome Sequencing of Discordant Monozygotic Twin Families for Identification of Candidate Genes for Microtia-Atresia.
    Fan X; Ping L; Sun H; Chen Y; Wang P; Liu T; Jiang R; Zhang X; Chen X
    Front Genet; 2020; 11():568052. PubMed ID: 33193662
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.