About: William McKenna

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) araştırmacı (tr) chercheur (fr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
rdfs:label	William McKenna (en) William McKenna (es) William McKenna (nl) William McKenna (sl) William McKenna (ast)
skos:prefLabel	William McKenna (en) William McKenna (es) William McKenna (nl) William McKenna (sl) William McKenna (ast)
name	William McKenna (en) William McKenna (es) William McKenna (nl) William McKenna (sl) William McKenna (ast)
given name	wds:Q37375368-FFA14A72-79A0-477A-9D54-D8A4848C88B0
given name	William
instance of	wds:Q37375368-D936FF9E-41DA-4BB7-887D-59B237070546
instance of	Homo sapiens
Nationale Thesaurus voor Auteursnamen ID	wds:Q37375368-4f2dffe8-c286-4245-9005-19e1526490f7
occupation	wds:Q37375368-D89C57C7-0202-4404-BDC7-37D1B4CDDCB8
employer	wds:Q37375368-B91E32AE-33FE-49AD-BDE2-5C6BE511079F
sex or gender	wds:Q37375368-FEBE58FA-EE5A-42C7-A3B3-74E74C6A1B5C
ISNI	wds:Q37375368-E283E784-0BCC-4313-8EA0-DF96B19AA6AF
VIAF ID	wds:Q37375368-1D9DA207-E3F6-4719-9F14-55FD3A15DDE2
IdRef ID	wds:Q37375368-6AF81124-BFF2-4100-BCB7-BFA1B17F8168
family name	wds:Q37375368-CBF51572-18DE-4573-A3CF-71BAA79384CB
official website	wds:Q37375368-2EE93E84-FB02-4C75-8651-3104443C2CF8
Nationale Thesaurus voor Auteursnamen ID	http://data.bibliotheken.nl/id/thes/p126714967
VIAF ID	http://viaf.org/viaf/316013332
IdRef ID	http://www.idref.fr/163544816/id
Nationale Thesaurus voor Auteursnamen ID	126714967
occupation	researcher
employer	University College London
sex or gender	male
ISNI	0000000394478437
VIAF ID	316013332
IdRef ID	163544816
family name	McKenna
official website	http://iris.ucl.ac.uk/iris/browse/profile?upi=WMCKE30
ORCID iD	wds:Q37375368-33CDFBDF-9578-478D-8A1F-FE271B797E92
Dimensions author ID	wds:Q37375368-F9991EB9-EADA-4A82-91F4-20F36C4C0B49
ORCID iD	https://orcid.org/0000-0001-7994-2460
ORCID iD	0000-0001-7994-2460
Dimensions author ID	011155252553.05
ResearcherID	wds:Q37375368-19F6673D-B784-40C4-AF84-3D25744836F2
Publons author ID	wds:Q37375368-123390d1-fc1c-48a4-a95a-272aac87d1a5
ResearcherID	C-3243-2008
Publons author ID	2881824
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37375368
is author of	Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy. Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype Cardiomyopathy mutations reveal variable region of myosin converter as major element of cross-bridge compliance. Metabolic modulator perhexiline corrects energy deficiency and improves exercise capacity in symptomatic hypertrophic cardiomyopathy. Cardiovascular magnetic resonance measurement of myocardial extracellular volume in health and disease Comparison of electrocardiographic criteria for the detection of cardiac abnormalities in elite black and white athletes. Current electrocardiographic criteria for diagnosis of Brugada pattern: a consensus report Disease pathways and novel therapeutic targets in hypertrophic cardiomyopathy A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM risk-SCD). Mutations in PDLIM3 and MYOZ1 encoding myocyte Z line proteins are infrequently found in idiopathic dilated cardiomyopathy Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria Genetic variation in SCN10A influences cardiac conduction Prevalence of Desmosomal Protein Gene Mutations in Patients With Dilated Cardiomyopathy HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Rare nonconservative LRP6 mutations are associated with metabolic syndrome. Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy. Homozygous mutation of desmocollin-2 in arrhythmogenic right ventricular cardiomyopathy with mild palmoplantar keratoderma and woolly hair. Family History of Premature Death and Risk of Early Onset Cardiovascular Disease Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the task force criteria. Role of late gadolinium enhancement cardiovascular magnetic resonance in the risk stratification of hypertrophic cardiomyopathy Role of genetic analysis in the management of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2

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