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.
194 related articles for article (PubMed ID: 38523305)
1. Clinical spectrum of Transthyretin amyloidogenic mutations among diverse population origins. De Lillo A; Pathak GA; Low A; De Angelis F; Abou Alaiwi S; Miller EJ; Fuciarelli M; Polimanti R Hum Genomics; 2024 Mar; 18(1):31. PubMed ID: 38523305 [TBL] [Abstract][Full Text] [Related]
2. Association of Transthyretin Val122Ile Variant With Incident Heart Failure Among Black Individuals. Parcha V; Malla G; Irvin MR; Armstrong ND; Judd SE; Lange LA; Maurer MS; Levitan EB; Goyal P; Arora G; Arora P JAMA; 2022 Apr; 327(14):1368-1378. PubMed ID: 35377943 [TBL] [Abstract][Full Text] [Related]
3. Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis. Iorio A; De Lillo A; De Angelis F; Di Girolamo M; Luigetti M; Sabatelli M; Pradotto L; Mauro A; Mazzeo A; Stancanelli C; Perfetto F; Frusconi S; My F; Manfellotto D; Fuciarelli M; Polimanti R Eur J Hum Genet; 2017 Sep; 25(9):1055-1060. PubMed ID: 28635949 [TBL] [Abstract][Full Text] [Related]
4. Phenome-wide association study of TTR and RBP4 genes in 361,194 individuals reveals novel insights in the genetics of hereditary and wildtype transthyretin amyloidoses. De Lillo A; De Angelis F; Di Girolamo M; Luigetti M; Frusconi S; Manfellotto D; Fuciarelli M; Polimanti R Hum Genet; 2019 Dec; 138(11-12):1331-1340. PubMed ID: 31659433 [TBL] [Abstract][Full Text] [Related]
5. Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes. Polimanti R; Di Girolamo M; Manfellotto D; Fuciarelli M Amyloid; 2013 Dec; 20(4):256-62. PubMed ID: 24111657 [TBL] [Abstract][Full Text] [Related]
7. Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis. Iorio A; De Angelis F; Di Girolamo M; Luigetti M; Pradotto LG; Mazzeo A; Frusconi S; My F; Manfellotto D; Fuciarelli M; Polimanti R BMC Genomics; 2017 Mar; 18(1):254. PubMed ID: 28335735 [TBL] [Abstract][Full Text] [Related]
8. Prevalence of the amyloidogenic transthyretin (TTR) V122I allele in 14 333 African-Americans. Jacobson DR; Alexander AA; Tagoe C; Buxbaum JN Amyloid; 2015; 22(3):171-4. PubMed ID: 26123279 [TBL] [Abstract][Full Text] [Related]
9. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis. Coelho T; Maurer MS; Suhr OB Curr Med Res Opin; 2013 Jan; 29(1):63-76. PubMed ID: 23193944 [TBL] [Abstract][Full Text] [Related]
10. Epigenomic Profiles of African-American Pathak GA; Wendt FR; De Lillo A; Nunez YZ; Goswami A; De Angelis F; Fuciarelli M; Kranzler HR; Gelernter J; Polimanti R Circ Genom Precis Med; 2021 Feb; 14(1):e003011. PubMed ID: 33428857 [TBL] [Abstract][Full Text] [Related]
11. Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino Ancestry. Damrauer SM; Chaudhary K; Cho JH; Liang LW; Argulian E; Chan L; Dobbyn A; Guerraty MA; Judy R; Kay J; Kember RL; Levin MG; Saha A; Van Vleck T; Verma SS; Weaver J; Abul-Husn NS; Baras A; Chirinos JA; Drachman B; Kenny EE; Loos RJF; Narula J; Overton J; Reid J; Ritchie M; Sirugo G; Nadkarni G; Rader DJ; Do R JAMA; 2019 Dec; 322(22):2191-2202. PubMed ID: 31821430 [TBL] [Abstract][Full Text] [Related]
12. A case of cardiac amyloidosis in an elderly Japanese patient with amyloidogenic transthyretin Val122Ile variant. Ono R; Takahashi H; Sato T; Yamazaki T; Hori Y; Fukushima K J Cardiol Cases; 2020 Nov; 22(5):221-225. PubMed ID: 33133314 [TBL] [Abstract][Full Text] [Related]
13. DISCOVERY: prevalence of transthyretin ( Akinboboye O; Shah K; Warner AL; Damy T; Taylor HA; Gollob J; Powell C; Karsten V; Vest J; Maurer MS Amyloid; 2020 Dec; 27(4):223-230. PubMed ID: 32456532 [TBL] [Abstract][Full Text] [Related]
14. Most recent common ancestor of TTR Val30Met mutation in Italian population and its potential role in genotype-phenotype correlation. Iorio A; De Angelis F; Di Girolamo M; Luigetti M; Pradotto L; Mauro A; Manfellotto D; Fuciarelli M; Polimanti R Amyloid; 2015; 22(2):73-8. PubMed ID: 25510352 [TBL] [Abstract][Full Text] [Related]
15. Transthyretin-related hereditary amyloidosis in a Chinese family with TTR Y114C mutation. Zhang Y; Deng YL; Ma JF; Zheng L; Hong Z; Wang ZQ; Sheng CY; Xiao Q; Cao L; Chen SD Neurodegener Dis; 2011; 8(4):187-93. PubMed ID: 21135536 [TBL] [Abstract][Full Text] [Related]
16. Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population. Kozlitina J; Garg S; Drazner MH; Matulevicius SA; Ayers C; Overton J; Reid J; Baras A; Rao K; Pandey A; Berry J; de Lemos JA; Grodin JL J Card Fail; 2022 Mar; 28(3):403-414. PubMed ID: 34634447 [TBL] [Abstract][Full Text] [Related]
19. Counseling Family Members and Monitoring for Evidence of Disease in Asymptomatic Carriers of Amyloid Transthyretin Cardiac Amyloidosis. Barker N; Judge DP Am J Cardiol; 2022 Dec; 185 Suppl 1():S43-S50. PubMed ID: 36216601 [TBL] [Abstract][Full Text] [Related]
20. Characterizing the polygenic architecture of complex traits in populations of East Asian and European descent. De Lillo A; Wendt FR; Pathak GA; Polimanti R Hum Genomics; 2023 Jul; 17(1):67. PubMed ID: 37475089 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]