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 *

137 related articles for article (PubMed ID: 38031457)

  • 1.
    Jin Y; Li T; Wu S; Liu Z; Li Y
    Cardiol Young; 2024 Jan; 34(1):212-217. PubMed ID: 38031457
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing.
    Schubert JA; Landis BJ; Shikany AR; Hinton RB; Ware SM
    Am J Med Genet A; 2016 May; 170A(5):1288-94. PubMed ID: 26854089
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical Implications of Identifying Pathogenic Variants in Individuals With Thoracic Aortic Dissection.
    Wolford BN; Hornsby WE; Guo D; Zhou W; Lin M; Farhat L; McNamara J; Driscoll A; Wu X; Schmidt EM; Norton EL; Mathis MR; Ganesh SK; Douville NJ; Brummett CM; Kitzman J; Chen YE; Kim K; Deeb GM; Patel H; Eagle KA; Milewicz DM; J Willer C; Yang B
    Circ Genom Precis Med; 2019 Jun; 12(6):e002476. PubMed ID: 31211624
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD).
    Arnaud P; Hanna N; Benarroch L; Aubart M; Bal L; Bouvagnet P; Busa T; Dulac Y; Dupuis-Girod S; Edouard T; Faivre L; Gouya L; Lacombe D; Langeois M; Leheup B; Milleron O; Naudion S; Odent S; Tchitchinadze M; Ropers J; Jondeau G; Boileau C
    Genet Med; 2019 Sep; 21(9):2015-2024. PubMed ID: 30739908
    [TBL] [Abstract][Full Text] [Related]  

  • 5. MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.
    Barbier M; Gross MS; Aubart M; Hanna N; Kessler K; Guo DC; Tosolini L; Ho-Tin-Noe B; Regalado E; Varret M; Abifadel M; Milleron O; Odent S; Dupuis-Girod S; Faivre L; Edouard T; Dulac Y; Busa T; Gouya L; Milewicz DM; Jondeau G; Boileau C
    Am J Hum Genet; 2014 Dec; 95(6):736-43. PubMed ID: 25434006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. LTBP3 Pathogenic Variants Predispose Individuals to Thoracic Aortic Aneurysms and Dissections.
    Guo DC; Regalado ES; Pinard A; Chen J; Lee K; Rigelsky C; Zilberberg L; Hostetler EM; Aldred M; Wallace SE; Prakash SK; ; Leal SM; Bamshad MJ; Nickerson DA; Natowicz M; Rifkin DB; Milewicz DM
    Am J Hum Genet; 2018 Apr; 102(4):706-712. PubMed ID: 29625025
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel variants in the ACTA2 and MYH11 genes in a Cypriot family with thoracic aortic aneurysms: a case report.
    Keravnou A; Bashiardes E; Michailidou K; Soteriou M; Moushi A; Cariolou M
    BMC Med Genet; 2018 Dec; 19(1):208. PubMed ID: 30526509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Exome sequencing identifies SMAD3 mutations as a cause of familial thoracic aortic aneurysm and dissection with intracranial and other arterial aneurysms.
    Regalado ES; Guo DC; Villamizar C; Avidan N; Gilchrist D; McGillivray B; Clarke L; Bernier F; Santos-Cortez RL; Leal SM; Bertoli-Avella AM; Shendure J; Rieder MJ; Nickerson DA; ; Milewicz DM
    Circ Res; 2011 Sep; 109(6):680-6. PubMed ID: 21778426
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole-exome sequencing uncovers a novel EFEMP2 gene variant (c.C247T) associated with dominant nonsyndromic thoracic aortic aneurysm.
    Sadeghipour P; Valuian M; Ghasemi S; Rafiee F; Pourirahim M; Mahmoodian M; Maleki M; Kalayinia S
    Lab Med; 2024 Jul; 55(4):447-453. PubMed ID: 38113391
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MAT2A mutations predispose individuals to thoracic aortic aneurysms.
    Guo DC; Gong L; Regalado ES; Santos-Cortez RL; Zhao R; Cai B; Veeraraghavan S; Prakash SK; Johnson RJ; Muilenburg A; Willing M; Jondeau G; Boileau C; Pannu H; Moran R; Debacker J; ; ; Bamshad MJ; Shendure J; Nickerson DA; Leal SM; Raman CS; Swindell EC; Milewicz DM
    Am J Hum Genet; 2015 Jan; 96(1):170-7. PubMed ID: 25557781
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease.
    Gago-Díaz M; Blanco-Verea A; Teixidó-Turà G; Valenzuela I; Del Campo M; Borregan M; Sobrino B; Amigo J; García-Dorado D; Evangelista A; Carracedo A; Brion M
    Clin Chim Acta; 2014 Nov; 437():88-92. PubMed ID: 25046559
    [TBL] [Abstract][Full Text] [Related]  

  • 12. LOX Mutations Predispose to Thoracic Aortic Aneurysms and Dissections.
    Guo DC; Regalado ES; Gong L; Duan X; Santos-Cortez RL; Arnaud P; Ren Z; Cai B; Hostetler EM; Moran R; Liang D; Estrera A; Safi HJ; ; Leal SM; Bamshad MJ; Shendure J; Nickerson DA; Jondeau G; Boileau C; Milewicz DM
    Circ Res; 2016 Mar; 118(6):928-34. PubMed ID: 26838787
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing reveals a de novo PRKG1 mutation in a sporadic patient with aortic dissection.
    Zhang W; Han Q; Liu Z; Zhou W; Cao Q; Zhou W
    BMC Med Genet; 2018 Dec; 19(1):218. PubMed ID: 30577811
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Successes and challenges of using whole exome sequencing to identify novel genes underlying an inherited predisposition for thoracic aortic aneurysms and acute aortic dissections.
    Milewicz DM; Regalado ES; Shendure J; Nickerson DA; Guo DC
    Trends Cardiovasc Med; 2014 Feb; 24(2):53-60. PubMed ID: 23953976
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recurrent gain-of-function mutation in PRKG1 causes thoracic aortic aneurysms and acute aortic dissections.
    Guo DC; Regalado E; Casteel DE; Santos-Cortez RL; Gong L; Kim JJ; Dyack S; Horne SG; Chang G; Jondeau G; Boileau C; Coselli JS; Li Z; Leal SM; Shendure J; Rieder MJ; Bamshad MJ; Nickerson DA; ; ; Kim C; Milewicz DM
    Am J Hum Genet; 2013 Aug; 93(2):398-404. PubMed ID: 23910461
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.
    Poninska JK; Bilinska ZT; Franaszczyk M; Michalak E; Rydzanicz M; Szpakowski E; Pollak A; Milanowska B; Truszkowska G; Chmielewski P; Sioma A; Janaszek-Sitkowska H; Klisiewicz A; Michalowska I; Makowiecka-Ciesla M; Kolsut P; Stawinski P; Foss-Nieradko B; Szperl M; Grzybowski J; Hoffman P; Januszewicz A; Kusmierczyk M; Ploski R
    J Transl Med; 2016 May; 14(1):115. PubMed ID: 27146836
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel
    Vecoli C; Foffa I; Vittorini S; Botto N; Esposito A; Costa S; Piagneri V; Festa P; Ait-Ali L
    Per Med; 2024; 21(3):139-144. PubMed ID: 38634413
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta.
    Weerakkody R; Ross D; Parry DA; Ziganshin B; Vandrovcova J; Gampawar P; Abdullah A; Biggs J; Dumfarth J; Ibrahim Y; ; Bicknell C; Field M; Elefteriades J; Cheshire N; Aitman TJ
    Genet Med; 2018 Nov; 20(11):1414-1422. PubMed ID: 29543232
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel SMAD3 p.Arg386Thr genetic variant co-segregating with thoracic aortic aneurysm and dissection.
    Engström K; Vánky F; Rehnberg M; Trinks C; Jonasson J; Green A; Gunnarsson C
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1089. PubMed ID: 32022471
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Isolated aortic dilation without osteoarthritis: a case of SMAD3 mutation.
    Arroyave J; Carretero JM; Gruosso D
    Cardiol Young; 2018 May; 28(5):765-767. PubMed ID: 29444731
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.