271 related articles for article (PubMed ID: 23074333)
41. Cardiomyopathy and Preeclampsia.
Gammill HS; Chettier R; Brewer A; Roberts JM; Shree R; Tsigas E; Ward K
Circulation; 2018 Nov; 138(21):2359-2366. PubMed ID: 30021846
[TBL] [Abstract][Full Text] [Related]
42. Incident Atrial Fibrillation Is Associated With MYH7 Sarcomeric Gene Variation in Hypertrophic Cardiomyopathy.
Lee SP; Ashley EA; Homburger J; Caleshu C; Green EM; Jacoby D; Colan SD; Arteaga-Fernández E; Day SM; Girolami F; Olivotto I; Michels M; Ho CY; Perez MV;
Circ Heart Fail; 2018 Sep; 11(9):e005191. PubMed ID: 30354366
[TBL] [Abstract][Full Text] [Related]
43. Primary Myocardial Fibrosis as an Alternative Phenotype Pathway of Inherited Cardiac Structural Disorders.
Junttila MJ; Holmström L; Pylkäs K; Mantere T; Kaikkonen K; Porvari K; Kortelainen ML; Pakanen L; Kerkelä R; Myerburg RJ; Huikuri HV
Circulation; 2018 Jun; 137(25):2716-2726. PubMed ID: 29915098
[TBL] [Abstract][Full Text] [Related]
44. Semiconductor Whole Exome Sequencing for the Identification of Genetic Variants in Colombian Patients Clinically Diagnosed with Long QT Syndrome.
Burgos M; Arenas A; Cabrera R
Mol Diagn Ther; 2016 Aug; 20(4):353-62. PubMed ID: 27251404
[TBL] [Abstract][Full Text] [Related]
45. Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.
Probst S; Oechslin E; Schuler P; Greutmann M; Boyé P; Knirsch W; Berger F; Thierfelder L; Jenni R; Klaassen S
Circ Cardiovasc Genet; 2011 Aug; 4(4):367-74. PubMed ID: 21551322
[TBL] [Abstract][Full Text] [Related]
46. Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions.
Zhang X; Walsh R; Whiffin N; Buchan R; Midwinter W; Wilk A; Govind R; Li N; Ahmad M; Mazzarotto F; Roberts A; Theotokis PI; Mazaika E; Allouba M; de Marvao A; Pua CJ; Day SM; Ashley E; Colan SD; Michels M; Pereira AC; Jacoby D; Ho CY; Olivotto I; Gunnarsson GT; Jefferies JL; Semsarian C; Ingles J; O'Regan DP; Aguib Y; Yacoub MH; Cook SA; Barton PJR; Bottolo L; Ware JS
Genet Med; 2021 Jan; 23(1):69-79. PubMed ID: 33046849
[TBL] [Abstract][Full Text] [Related]
47. Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.
Bick AG; Flannick J; Ito K; Cheng S; Vasan RS; Parfenov MG; Herman DS; DePalma SR; Gupta N; Gabriel SB; Funke BH; Rehm HL; Benjamin EJ; Aragam J; Taylor HA; Fox ER; Newton-Cheh C; Kathiresan S; O'Donnell CJ; Wilson JG; Altshuler DM; Hirschhorn JN; Seidman JG; Seidman C
Am J Hum Genet; 2012 Sep; 91(3):513-9. PubMed ID: 22958901
[TBL] [Abstract][Full Text] [Related]
48. Characterizing genetic variation of adrenergic signalling pathways in Takotsubo (stress) cardiomyopathy exomes.
Goodloe AH; Evans JM; Middha S; Prasad A; Olson TM
Eur J Heart Fail; 2014 Sep; 16(9):942-9. PubMed ID: 25132214
[TBL] [Abstract][Full Text] [Related]
49. 267 Spanish Exomes Reveal Population-Specific Differences in Disease-Related Genetic Variation.
Dopazo J; Amadoz A; Bleda M; Garcia-Alonso L; Alemán A; García-García F; Rodriguez JA; Daub JT; Muntané G; Rueda A; Vela-Boza A; López-Domingo FJ; Florido JP; Arce P; Ruiz-Ferrer M; Méndez-Vidal C; Arnold TE; Spleiss O; Alvarez-Tejado M; Navarro A; Bhattacharya SS; Borrego S; Santoyo-López J; Antiñolo G
Mol Biol Evol; 2016 May; 33(5):1205-18. PubMed ID: 26764160
[TBL] [Abstract][Full Text] [Related]
50. Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar.
Rodriguez-Flores JL; Fakhro K; Hackett NR; Salit J; Fuller J; Agosto-Perez F; Gharbiah M; Malek JA; Zirie M; Jayyousi A; Badii R; Al-Nabet Al-Marri A; Chouchane L; Stadler DJ; Mezey JG; Crystal RG
Hum Mutat; 2014 Jan; 35(1):105-16. PubMed ID: 24123366
[TBL] [Abstract][Full Text] [Related]
51. Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations.
Girolami F; Ho CY; Semsarian C; Baldi M; Will ML; Baldini K; Torricelli F; Yeates L; Cecchi F; Ackerman MJ; Olivotto I
J Am Coll Cardiol; 2010 Apr; 55(14):1444-53. PubMed ID: 20359594
[TBL] [Abstract][Full Text] [Related]
52. First identification of homozygous truncating CSRP3 variants in two unrelated cases with hypertrophic cardiomyopathy.
Janin A; Bessière F; Chauveau S; Chevalier P; Millat G
Gene; 2018 Nov; 676():110-116. PubMed ID: 30012424
[TBL] [Abstract][Full Text] [Related]
53. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
[TBL] [Abstract][Full Text] [Related]
54. Genetic variants in Chinese patients with sporadic dilated cardiomyopathy: a cross-sectional study.
Shen C; Xu L; Sun X; Sun A; Ge J
Ann Transl Med; 2022 Feb; 10(3):129. PubMed ID: 35284542
[TBL] [Abstract][Full Text] [Related]
55. Comparison and optimization of in silico algorithms for predicting the pathogenicity of sodium channel variants in epilepsy.
Holland KD; Bouley TM; Horn PS
Epilepsia; 2017 Jul; 58(7):1190-1198. PubMed ID: 28518218
[TBL] [Abstract][Full Text] [Related]
56. Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K; Wiskin AE; Gibson J; Tapper W; Willis C; Afzal NA; Upstill-Goddard R; Holloway JW; Simpson MA; Beattie RM; Collins A; Ennis S
Gut; 2013 Jul; 62(7):977-84. PubMed ID: 22543157
[TBL] [Abstract][Full Text] [Related]
57. Genetics of feline hypertrophic cardiomyopathy.
Gil-Ortuño C; Sebastián-Marcos P; Sabater-Molina M; Nicolas-Rocamora E; Gimeno-Blanes JR; Fernández Del Palacio MJ
Clin Genet; 2020 Sep; 98(3):203-214. PubMed ID: 32215921
[TBL] [Abstract][Full Text] [Related]
58. Genetic variant pathogenicity prediction trained using disease-specific clinical sequencing data sets.
Evans P; Wu C; Lindy A; McKnight DA; Lebo M; Sarmady M; Abou Tayoun AN
Genome Res; 2019 Jul; 29(7):1144-1151. PubMed ID: 31235655
[TBL] [Abstract][Full Text] [Related]
59. FLAGS, frequently mutated genes in public exomes.
Shyr C; Tarailo-Graovac M; Gottlieb M; Lee JJ; van Karnebeek C; Wasserman WW
BMC Med Genomics; 2014 Dec; 7():64. PubMed ID: 25466818
[TBL] [Abstract][Full Text] [Related]
60. Evaluating Mendelian nephrotic syndrome genes for evidence for risk alleles or oligogenicity that explain heritability.
Crawford BD; Gillies CE; Robertson CC; Kretzler M; Otto EA; Vega-Warner V; Sampson MG
Pediatr Nephrol; 2017 Mar; 32(3):467-476. PubMed ID: 27766458
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]