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 *

112 related articles for article (PubMed ID: 31008308)

  • 1. Next generation sequencing analysis of patients with familial cervical artery dissection.
    Grond-Ginsbach C; Brandt T; Kloss M; Aksay SS; Lyrer P; Traenka C; Erhart P; Martin JJ; Altintas A; Siva A; de Freitas GR; Thie A; Machetanz J; Baumgartner RW; Dichgans M; Engelter ST
    Eur Stroke J; 2017 Jun; 2(2):137-143. PubMed ID: 31008308
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare genetic variants in patients with cervical artery dissection.
    Traenka C; Kloss M; Strom T; Lyrer P; Brandt T; Bonati LH; Grond-Ginsbach C; Engelter S
    Eur Stroke J; 2019 Dec; 4(4):355-362. PubMed ID: 31903434
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 99-Case Study of Sporadic Aortic Dissection by Whole Exome Sequencing Indicated Novel Disease-Associated Genes and Variants in Chinese Population.
    Wang Z; Zhuang X; Chen B; Wen J; Peng F; Liu X; Wei M
    Biomed Res Int; 2020; 2020():7857043. PubMed ID: 33083483
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Good performance of the criteria of American College of Medical Genetics and Genomics/Association for Molecular Pathology in prediction of pathogenicity of genetic variants causing thoracic aortic aneurysms and dissections.
    Ponińska JK; Bilińska ZT; Truszkowska G; Michalak E; Podgórska A; Stępień-Wojno M; Chmielewski P; Lutyńska A; Płoski R
    J Transl Med; 2022 Jan; 20(1):42. PubMed ID: 35078481
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Multiple Arterial Dissections and Connective Tissue Abnormalities.
    Erhart P; Körfer D; Dihlmann S; Qiao JL; Hausser I; Ringleb P; Männer J; Dikow N; Schaaf CP; Grond-Ginsbach C; Böckler D
    J Clin Med; 2022 Jun; 11(12):. PubMed ID: 35743335
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of TGFBR1 and TGFBR2 genetic variants in Marfan syndrome.
    De Cario R; Sticchi E; Lucarini L; Attanasio M; Nistri S; Marcucci R; Pepe G; Giusti B
    J Vasc Surg; 2018 Jul; 68(1):225-233.e5. PubMed ID: 28847661
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm.
    van de Luijtgaarden KM; Heijsman D; Maugeri A; Weiss MM; Verhagen HJ; IJpma A; Brüggenwirth HT; Majoor-Krakauer D
    Hum Genet; 2015 Aug; 134(8):881-93. PubMed ID: 26017485
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China.
    Li Y; Fang M; Yang J; Yu C; Kuang J; Sun T; Fan R
    Am J Transl Res; 2021; 13(5):4281-4295. PubMed ID: 34150014
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial occurrence of cervical artery dissection--coincidence or sign of familial predisposition?
    Grond-Ginsbach C; de Freitas GR; Campos CR; Thie A; Caso V; Machetanz J; Kloss M
    Cerebrovasc Dis; 2012; 33(5):466-70. PubMed ID: 22507869
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients.
    Renner S; Schüler H; Alawi M; Kolbe V; Rybczynski M; Woitschach R; Sheikhzadeh S; Stark VC; Olfe J; Roser E; Seggewies FS; Mahlmann A; Hempel M; Hartmann MJ; Hillebrand M; Wieczorek D; Volk AE; Kloth K; Koch-Hogrebe M; Abou Jamra R; Mitter D; Altmüller J; Wey-Fabrizius A; Petersen C; Rau I; Borck G; Kubisch C; Mir TS; von Kodolitsch Y; Kutsche K; Rosenberger G
    Genet Med; 2019 Aug; 21(8):1832-1841. PubMed ID: 30675029
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Performant Mutation Identification Using Targeted Next-Generation Sequencing of 14 Thoracic Aortic Aneurysm Genes.
    Proost D; Vandeweyer G; Meester JA; Salemink S; Kempers M; Ingram C; Peeters N; Saenen J; Vrints C; Lacro RV; Roden D; Wuyts W; Dietz HC; Mortier G; Loeys BL; Van Laer L
    Hum Mutat; 2015 Aug; 36(8):808-14. PubMed ID: 25907466
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the COL3A1 gene in patients with spontaneous cervical artery dissections.
    von Pein F; Välkkilä M; Schwarz R; Morcher M; Klima B; Grau A; Ala-Kokko L; Hausser I; Brandt T; Grond-Ginsbach C
    J Neurol; 2002 Jul; 249(7):862-6. PubMed ID: 12140670
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gene panel sequencing in heritable thoracic aortic disorders and related entities - results of comprehensive testing in a cohort of 264 patients.
    Campens L; Callewaert B; Muiño Mosquera L; Renard M; Symoens S; De Paepe A; Coucke P; De Backer J
    Orphanet J Rare Dis; 2015 Feb; 10():9. PubMed ID: 25644172
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial thoracic aortic aneurysm with dissection presenting as flash pulmonary edema in a 26-year-old man.
    Omar S; Moore T; Payne D; Momeni P; Mulkey Z; Paone R; Nugent K
    Case Rep Med; 2014; 2014():842872. PubMed ID: 25104961
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Exome sequencing in seven families and gene-based association studies indicate genetic heterogeneity and suggest possible candidates for fibromuscular dysplasia.
    Kiando SR; Barlassina C; Cusi D; Galan P; Lathrop M; Plouin PF; Jeunemaitre X; Bouatia-Naji N
    J Hypertens; 2015 Sep; 33(9):1802-10; discussion 1810. PubMed ID: 26147384
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Acute Stanford type B aortic dissection-who benefits from genetic testing?
    Erhart P; Gieldon L; Ante M; Körfer D; Strom T; Grond-Ginsbach C; Böckler D
    J Thorac Dis; 2020 Nov; 12(11):6806-6812. PubMed ID: 33282382
    [TBL] [Abstract][Full Text] [Related]  

  • 17. WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases.
    Pinard A; Salgado D; Desvignes JP; Rai G; Hanna N; Arnaud P; Guien C; Martinez M; Faivre L; Jondeau G; Boileau C; Zaffran S; Béroud C; Collod-Béroud G
    Hum Mutat; 2016 Dec; 37(12):1308-1317. PubMed ID: 27647783
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Optimising the mutation screening strategy in Marfan syndrome and identifying genotypes with more severe aortic involvement.
    Stengl R; Bors A; Ágg B; Pólos M; Matyas G; Molnár MJ; Fekete B; Csabán D; Andrikovics H; Merkely B; Radovits T; Szabolcs Z; Benke K
    Orphanet J Rare Dis; 2020 Oct; 15(1):290. PubMed ID: 33059708
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.
    Blue GM; Kirk EP; Giannoulatou E; Dunwoodie SL; Ho JW; Hilton DC; White SM; Sholler GF; Harvey RP; Winlaw DS
    J Am Coll Cardiol; 2014 Dec; 64(23):2498-506. PubMed ID: 25500235
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic Risk for Aortic Aneurysm in Adolescent Idiopathic Scoliosis.
    Haller G; Alvarado DM; Willing MC; Braverman AC; Bridwell KH; Kelly M; Lenke LG; Luhmann SJ; Gurnett CA; Dobbs MB
    J Bone Joint Surg Am; 2015 Sep; 97(17):1411-7. PubMed ID: 26333736
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.