238 related articles for article (PubMed ID: 32855533)
1. Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Elbitar S; Renard M; Arnaud P; Hanna N; Jacob MP; Guo DC; Tsutsui K; Gross MS; Kessler K; Tosolini L; Dattilo V; Dupont S; Jonquet J; Langeois M; Benarroch L; Aubart M; Ghaleb Y; Abou Khalil Y; Varret M; El Khoury P; Ho-Tin-Noé B; Alembik Y; Gaertner S; Isidor B; Gouya L; Milleron O; Sekiguchi K; Milewicz D; De Backer J; Le Goff C; Michel JB; Jondeau G; Sakai LY; Boileau C; Abifadel M
Genet Med; 2021 Jan; 23(1):111-122. PubMed ID: 32855533
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections.
Regalado ES; Guo DC; Santos-Cortez RL; Hostetler E; Bensend TA; Pannu H; Estrera A; Safi H; Mitchell AL; Evans JP; Leal SM; Bamshad M; Shendure J; Nickerson DA; ; Milewicz DM
Clin Genet; 2016 Jun; 89(6):719-23. PubMed ID: 26621581
[TBL] [Abstract][Full Text] [Related]
4. Identification of Novel Clinically Relevant Variants in 70 Southern Chinese patients with Thoracic Aortic Aneurysm and Dissection by Next-generation Sequencing.
Fang M; Yu C; Chen S; Xiong W; Li X; Zeng R; Zhuang J; Fan R
Sci Rep; 2017 Aug; 7(1):10035. PubMed ID: 28855619
[TBL] [Abstract][Full Text] [Related]
5. Genetic testing and clinical relevance of patients with thoracic aortic aneurysm and dissection in northwestern China.
Li J; Yang L; Diao Y; Zhou L; Xin Y; Jiang L; Li R; Wang J; Duan W; Liu J
Mol Genet Genomic Med; 2021 Oct; 9(10):e1800. PubMed ID: 34498425
[TBL] [Abstract][Full Text] [Related]
6. Analysis of the genetic contribution to thoracic aortic aneurysm or dissection in a prospective cohort of patients with familial and sporadic cases in East China.
Duan Y; Xiong J; Lai Z; Zhong Y; Tian C; Du Z; Luo Z; Yu J; Li W; Xu W; Wang Y; Ding T; Zhong X; Pan M; Qiu Y; Lan X; Chen T; Li P; Liu K; Gao M; Hu Y; Liu Z
Orphanet J Rare Dis; 2023 Aug; 18(1):251. PubMed ID: 37644562
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Identification of clinically relevant variants by whole exome sequencing in Chinese patients with sporadic non-syndromic type A aortic dissection.
Zhao H; Yang Y; Pan X; Li W; Sun L; Guo J
Clin Chim Acta; 2020 Jul; 506():160-165. PubMed ID: 32209317
[TBL] [Abstract][Full Text] [Related]
9. ADAMTS-7 deficiency attenuates thoracic aortic aneurysm and dissection in mice.
Gong Z; Huang J; Wang D; Yang S; Ma Z; Fu Y; Ma Q; Kong W
J Mol Med (Berl); 2023 Mar; 101(3):237-248. PubMed ID: 36662289
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Urate-Lowering Therapy Inhibits Thoracic Aortic Aneurysm and Dissection Formation in Mice.
Yang L; Wu H; Luo C; Zhao Y; Dai R; Li Z; Zhang X; Gong Z; Cai Z; Shen Y; Yu F; Li W; Zhao H; Zhang T; Zhu J; Fu Y; Wang J; Kong W
Arterioscler Thromb Vasc Biol; 2023 Jun; 43(6):e172-e189. PubMed ID: 37128913
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. Genetic variants in FBN-1 and risk for thoracic aortic aneurysm and dissection.
Iakoubova OA; Tong CH; Rowland CM; Luke MM; Garcia VE; Catanese JJ; Moomiaie RM; Sotonyi P; Ascady G; Nikas D; Dedelias P; Tranquilli M; Elefteriades JA
PLoS One; 2014; 9(4):e91437. PubMed ID: 24743685
[TBL] [Abstract][Full Text] [Related]
16. Whole exome sequencing identifies FBN1 mutations in two patients with early‑onset type B aortic dissection.
Han Q; Zhang W; Liu C; Zhou M; Ran F; Yi L; Sun X; Liu Z
Mol Med Rep; 2017 Nov; 16(5):6620-6625. PubMed ID: 28901506
[TBL] [Abstract][Full Text] [Related]
17. Novel
Van Gucht I; Krebsova A; Diness BR; Laga S; Adlam D; Kempers M; Samani NJ; Webb TR; Baranowska AA; Van Den Heuvel L; Perik M; Luyckx I; Peeters N; Votypka P; Macek M; Meester J; Van Laer L; Verstraeten A; Loeys BL
Int J Mol Sci; 2021 Jul; 22(13):. PubMed ID: 34281165
[TBL] [Abstract][Full Text] [Related]
18. Nitric oxide mediates aortic disease in mice deficient in the metalloprotease Adamts1 and in a mouse model of Marfan syndrome.
Oller J; Méndez-Barbero N; Ruiz EJ; Villahoz S; Renard M; Canelas LI; Briones AM; Alberca R; Lozano-Vidal N; Hurlé MA; Milewicz D; Evangelista A; Salaices M; Nistal JF; Jiménez-Borreguero LJ; De Backer J; Campanero MR; Redondo JM
Nat Med; 2017 Feb; 23(2):200-212. PubMed ID: 28067899
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Genetic of thoracic aorta aneurysm].
Cadenet M; Hanna N; Arnaud P
Ann Biol Clin (Paris); 2022 Jul; 80(4):344-354. PubMed ID: 36099351
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
