About: Rhys H Thomas

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

British neuroscientist

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) araştırmacı (tr) эрдэмтэн (mn) 研究者 (zh) հետազոտող (hy) hulumtues (sq) onderzoeker (nl) British neuroscientist (en)
rdfs:label	Rhys H Thomas (en) Rhys H Thomas (es) Rhys H Thomas (nl) Rhys H Thomas (sl) Rhys H Thomas (ast) Rhys H. Thomas (it)
skos:prefLabel	Rhys H Thomas (en) Rhys H Thomas (es) Rhys H Thomas (nl) Rhys H Thomas (sl) Rhys H Thomas (ast) Rhys H. Thomas (it)
name	Rhys H Thomas (en) Rhys H Thomas (es) Rhys H Thomas (nl) Rhys H Thomas (sl) Rhys H Thomas (ast) Rhys H. Thomas (it)
Scopus author ID	wds:Q37831108-353EB8DD-53BE-48ED-AEC4-BEA4372E8802
Scopus author ID	14326449800
given name	wds:Q37831108-C1CC629A-3AB6-4304-8AFC-EE4B5193A325
given name	Rhys
instance of	wds:Q37831108-7C3B9EC6-A824-4C7D-81C7-6DD0CCACD33E
instance of	Homo sapiens
Loop ID	wds:Q37831108-9993AFBF-5544-45E9-A1CE-6D746406C6BF
Loop ID	6462
Google Scholar author ID	wds:Q37831108-A2BB7251-ACC0-4AE0-9121-63C1AF094E4B
Google Scholar author ID	Hd9NNoEAAAAJ
skos:altLabel	Rhys Thomas (en) Rhys Huw Thomas (en)
occupation	wds:Q37831108-BAF44172-AF1F-4995-A731-D1107F75AC2A
sex or gender	wds:Q37831108-143C2364-9AF5-4A5D-AD5F-EAE2283AD305
date of birth	wds:Q37831108-04E67898-C24D-4B7E-9A02-E1F8D5CD0EC8
family name	wds:Q37831108-9BE470EA-8CC8-4F15-A921-F84CCACEF5E9
official website	wds:Q37831108-E25BE381-8055-47DE-8F0F-920AEF252AC7
occupation	researcher
sex or gender	male
date of birth	2000-01-01 00:00:00Z (xsd:dateTime)
family name	Thomas
official website	https://www.ncl.ac.uk/medical-sciences/people/profile/rhysthomas.html
Springer Nature person ID	wds:Q37831108-E77A78DE-E875-4264-B91E-2CBFE2F09CCB
ORCID iD	wds:Q37831108-B91CAD03-D54A-4C66-86BF-BE1AF0002B42
Dimensions author ID	wds:Q37831108-98E2D623-8ADF-4FE0-B4AB-9B6309CC6B66
ORCID iD	https://orcid.org/0000-0003-2062-8623
Springer Nature person ID	0672076330.74
ORCID iD	0000-0003-2062-8623
Dimensions author ID	0672076330.74
ResearcherID	wds:Q37831108-164C41BC-DC01-42EA-960A-6ACA7600F0A9
Publons author ID	wds:Q37831108-8B07D3BF-7E98-4C4D-84BC-2A2A86EEBE95
ResearcherID	I-3840-2019
Publons author ID	1300345
Mendeley person ID	wds:Q37831108-3A167F7C-A35C-45CA-96CB-9586E38BE4C6
Mendeley person ID	rhys-thomas5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37831108
is author of	A comprehensive neuropsychological description of cognition in drug-refractory juvenile myoclonic epilepsy. A novel dominant hyperekplexia mutation Y705C alters trafficking and biochemical properties of the presynaptic glycine transporter GlyT2 Mutations in the GlyT2 gene (SLC6A5) are a second major cause of startle disease New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms. Pathophysiological mechanisms of dominant and recessive GLRA1 mutations in hyperekplexia Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay The hidden genetics of epilepsy-a clinically important new paradigm Encephalitis guidelines: a recipe for success? Epilepsy and deprivation, a data linkage study Juvenile myoclonic epilepsy The glycinergic system in human startle disease: a genetic screening approach Novel missense mutations in the glycine receptor β subunit gene (GLRB) in startle disease GLRB is the third major gene of effect in hyperekplexia. Epilepsy and bipolar disorder Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects Impulsive and episodic disorders of aggressive behaviour following traumatic brain injury Cluster of atypical adult Guillain-Barré syndrome temporally associated with neurological illness due to EV-D68 in children, South Wales, United Kingdom, October 2015 to January 2016. Hyperconnectivity in juvenile myoclonic epilepsy: a network analysis Translation of genetic findings to clinical practice in juvenile myoclonic epilepsy. Concepts and controversies of juvenile myoclonic epilepsy: still an enigmatic epilepsy Executive functions and psychiatric symptoms in drug-refractory juvenile myoclonic epilepsy. Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy Generalized Epilepsy and Myoclonic Seizures in 22q11.2 Deletion Syndrome CHD2 myoclonic encephalopathy is frequently associated with self-induced seizures Gamification of Medication Adherence in Epilepsy. High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies. Dental injury during seizures associated with juvenile myoclonic epilepsy Weight change associated with antiepileptic drugs Ethnicity can predict GLRA1 genotypes in hyperekplexia. Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study. Complement system biomarkers in epilepsy Educational attainment of children born to mothers with epilepsy Genetic chameleons: remember the relapsing disorders

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