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 *

180 related articles for article (PubMed ID: 39240962)

  • 1. Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve.
    Carlisle SG; Albasha H; Michelena HI; Sabate-Rotes A; Bianco L; De Backer J; Mosquera LM; Yetman AT; Bissell MM; Andreassi MG; Foffa I; Hui DS; Caffarelli A; Kim YY; Guo D; Citro R; De Marco M; Tretter JT; McBride KL; Milewicz DM; Body SC; Prakash SK; ;
    PLoS One; 2024; 19(9):e0304514. PubMed ID: 39240962
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare Genomic Copy Number Variants Implicate New Candidate Genes for Bicuspid Aortic Valve.
    Carlisle SG; Albasha H; Michelena H; Sabate-Rotes A; Bianco L; De Backer J; Mosquera LM; Yetman AT; Bissell MM; Andreassi MG; Foffa I; Hui DS; Caffarelli A; Kim YY; Guo DC; Citro R; De Marco M; Tretter JT; McBride KL; ; ; Milewicz DM; Body SC; Prakash SK
    medRxiv; 2023 Oct; ():. PubMed ID: 37961530
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent Rare Genomic Copy Number Variants and Bicuspid Aortic Valve Are Enriched in Early Onset Thoracic Aortic Aneurysms and Dissections.
    Prakash S; Kuang SQ; ; Regalado E; Guo D; Milewicz D
    PLoS One; 2016; 11(4):e0153543. PubMed ID: 27092555
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare deleterious variants of NOTCH1, GATA4, SMAD6, and ROBO4 are enriched in BAV with early onset complications but not in BAV with heritable thoracic aortic disease.
    Musfee FI; Guo D; Pinard AC; Hostetler EM; Blue EE; Nickerson DA; ; Bamshad MJ; Milewicz DM; Prakash SK
    Mol Genet Genomic Med; 2020 Oct; 8(10):e1406. PubMed ID: 32748548
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene.
    Luyckx I; Kumar AA; Reyniers E; Dekeyser E; Vanderstraeten K; Vandeweyer G; Wünnemann F; Preuss C; Mazzella JM; Goudot G; Messas E; Albuisson J; Jeunemaitre X; Eriksson P; Mohamed SA; Kempers M; Salemink S; Duijnhouwer A; Andelfinger G; Dietz HC; Verstraeten A; Van Laer L; Loeys BL;
    Eur J Hum Genet; 2019 Jul; 27(7):1033-1043. PubMed ID: 30820038
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole-exome sequencing uncovers the genetic complexity of bicuspid aortic valve in families with early-onset complications.
    Mansoorshahi S; Yetman AT; Bissell MM; Kim YY; Michelena HI; De Backer J; Mosquera LM; Hui DS; Caffarelli A; Andreassi MG; Foffa I; Guo D; Citro R; De Marco M; Tretter JT; Morris SA; Body SC; Chong JX; Bamshad MJ; ; ; ; Milewicz DM; Prakash SK
    Am J Hum Genet; 2024 Oct; 111(10):2219-2231. PubMed ID: 39226896
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Variants in cardiac GATA genes associated with bicuspid aortic valve.
    Alonso-Montes C; Martín M; Martínez-Arias L; Coto E; Naves-Díaz M; Morís C; Cannata-Andía JB; Rodríguez I
    Eur J Clin Invest; 2018 Dec; 48(12):e13027. PubMed ID: 30229885
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis.
    Fulmer D; Toomer K; Guo L; Moore K; Glover J; Moore R; Stairley R; Lobo G; Zuo X; Dang Y; Su Y; Fogelgren B; Gerard P; Chung D; Heydarpour M; Mukherjee R; Body SC; Norris RA; Lipschutz JH
    Circulation; 2019 Oct; 140(16):1331-1341. PubMed ID: 31387361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.
    Li RG; Xu YJ; Wang J; Liu XY; Yuan F; Huang RT; Xue S; Li L; Liu H; Li YJ; Qu XK; Shi HY; Zhang M; Qiu XB; Yang YQ
    Am J Cardiol; 2018 Feb; 121(4):469-474. PubMed ID: 29325903
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic abnormalities in bicuspid aortic valve root phenotype: preliminary results.
    Girdauskas E; Geist L; Disha K; Kazakbaev I; Groß T; Schulz S; Ungelenk M; Kuntze T; Reichenspurner H; Kurth I
    Eur J Cardiothorac Surg; 2017 Jul; 52(1):156-162. PubMed ID: 28387797
    [TBL] [Abstract][Full Text] [Related]  

  • 11. GATA6 Regulates Aortic Valve Remodeling, and Its Haploinsufficiency Leads to Right-Left Type Bicuspid Aortic Valve.
    Gharibeh L; Komati H; Bossé Y; Boodhwani M; Heydarpour M; Fortier M; Hassanzadeh R; Ngu J; Mathieu P; Body S; Nemer M;
    Circulation; 2018 Sep; 138(10):1025-1038. PubMed ID: 29567669
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Focus on the unique mechanisms involved in thoracic aortic aneurysm formation in bicuspid aortic valve versus tricuspid aortic valve patients: clinical implications of a pilot study.
    Balistreri CR; Pisano C; Candore G; Maresi E; Codispoti M; Ruvolo G
    Eur J Cardiothorac Surg; 2013 Jun; 43(6):e180-6. PubMed ID: 23248206
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Protein-altering and regulatory genetic variants near GATA4 implicated in bicuspid aortic valve.
    Yang B; Zhou W; Jiao J; Nielsen JB; Mathis MR; Heydarpour M; Lettre G; Folkersen L; Prakash S; Schurmann C; Fritsche L; Farnum GA; Lin M; Othman M; Hornsby W; Driscoll A; Levasseur A; Thomas M; Farhat L; Dubé MP; Isselbacher EM; Franco-Cereceda A; Guo DC; Bottinger EP; Deeb GM; Booher A; Kheterpal S; Chen YE; Kang HM; Kitzman J; Cordell HJ; Keavney BD; Goodship JA; Ganesh SK; Abecasis G; Eagle KA; Boyle AP; Loos RJF; Eriksson P; Tardif JC; Brummett CM; Milewicz DM; Body SC; Willer CJ
    Nat Commun; 2017 May; 8():15481. PubMed ID: 28541271
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Search for genetic factors in bicuspid aortic valve disease: ACTA2 mutations do not play a major role.
    Tortora G; Wischmeijer A; Berretta P; Alfonsi J; Di Marco L; Barbieri A; Marconi C; Isidori F; Rossi C; Leone O; Di Bartolomeo R; Seri M; Pacini D
    Interact Cardiovasc Thorac Surg; 2017 Nov; 25(5):813-817. PubMed ID: 29049801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted next-generation sequencing identified ADAMTS5 as novel genetic substrate in patients with bicuspid aortic valve.
    Lin X; Liu X; Wang L; Jiang J; Sun Y; Zhu Q; Chen Z; He Y; Hu P; Xu Q; Gao F; Lin Y; Jaiswal S; Xiang M; Wang J
    Int J Cardiol; 2018 Feb; 252():150-155. PubMed ID: 29162281
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing.
    Chen S; Jin Q; Hou S; Li M; Zhang Y; Guan L; Pan W; Ge J; Zhou D
    Hum Genomics; 2022 Sep; 16(1):36. PubMed ID: 36071494
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Bicuspid Aortic Valve-Associated Regulatory Regions Reveal
    Huang T; Cheng J; Feng H; Zhou W; Qiu P; Zhou D; Yang D; Zhang J; Willer C; Chen YE; Mizrak D; Yang B
    Arterioscler Thromb Vasc Biol; 2023 Feb; 43(2):312-322. PubMed ID: 36519469
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of Gender-Specific Genetic Variants in Patients With Bicuspid Aortic Valve.
    Dargis N; Lamontagne M; Gaudreault N; Sbarra L; Henry C; Pibarot P; Mathieu P; Bossé Y
    Am J Cardiol; 2016 Feb; 117(3):420-6. PubMed ID: 26708639
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.
    Xu YJ; Di RM; Qiao Q; Li XM; Huang RT; Xue S; Liu XY; Wang J; Yang YQ
    Gene; 2018 Jul; 663():115-120. PubMed ID: 29653232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Low transcriptional activity haplotype of matrix metalloproteinase 1 is less frequent in bicuspid aortic valve patients.
    Martín M; Pichel IA; Flórez Muñoz JP; Naves-Díaz M; Palacín M; Cannata-Andía JB; Morís C; Rodríguez I
    Gene; 2013 Jul; 524(2):304-8. PubMed ID: 23603351
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.