VIAF

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Leader     00000nz a2200037n 45 0
001     WKP|Q110687691  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241120235713.0
008     241120nneanz||abbn n and d
035 ‎‡a  (WKP)Q110687691‏
035 ‎‡a  (OCoLC)Q110687691‏
100 0 ‎‡a  John W. Roberts‏ ‎‡c  neurology researcher and specialist in Parkinson's disease at Virginia Mason Medical Center, Seattle‏ ‎‡9  en‏
670 ‎‡a  Author's Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease‏
670 ‎‡a  Author's Association mapping of the PARK10 region for Parkinson's disease susceptibility genes‏
670 ‎‡a  Author's Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk‏
670 ‎‡a  Author's Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease‏
670 ‎‡a  Author's Common variation in the LRRK2 gene is a risk factor for Parkinson's disease‏
670 ‎‡a  Author's DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.‏
670 ‎‡a  Author's Exploring gene-environment interactions in Parkinson’s disease‏
670 ‎‡a  Author's Genetic association between α-synuclein and idiopathic parkinson's disease‏
670 ‎‡a  Author's Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee‏
670 ‎‡a  Author's Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders‏
670 ‎‡a  Author's Haptoglobin phenotype modifies serum iron levels and the effect of smoking on Parkinson disease risk‏
670 ‎‡a  Author's Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease‏
670 ‎‡a  Author's Lower plasma apolipoprotein A1 levels are found in Parkinson's disease and associate with apolipoprotein A1 genotype‏
670 ‎‡a  Author's LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.‏
670 ‎‡a  Author's Recognition memory for hand positions and spatial locations in patients with Huntington's disease: differential visuospatial memory impairment?‏
670 ‎‡a  Author's Response to the letter "Haptoglobin phenotype and Parkinson disease risk" by Delanghe et al.‏
670 ‎‡a  Author's Risk prediction for complex diseases: application to Parkinson disease.‏
670 ‎‡a  Author's SNCA variant associated with Parkinson disease and plasma alpha-synuclein level‏
670 ‎‡a  Author's Study of istradefylline in patients with Parkinson's disease on levodopa with motor fluctuations‏
670 ‎‡a  Author's The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease‏
670 ‎‡a  Author's Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease‏
919 ‎‡a  associationanalysisofmapth1haplotypeandsubhaplotypesinparkinsonsdisease‏ ‎‡A  Association analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  associationmappingofthepark10regionforparkinsonsdiseasesusceptibilitygenes‏ ‎‡A  Association mapping of the PARK10 region for Parkinson's disease susceptibility genes‏ ‎‡9  1‏
919 ‎‡a  dbh1021ctdoesnotmodifyriskorageatonsetinparkinsonsdisease‏ ‎‡A  DBH -1021C-->T does not modify risk or age at onset in Parkinson's disease.‏ ‎‡9  1‏
919 ‎‡a  sncavariantassociatedwithparkinsondiseaseandplasmaalphasynucleinlevel‏ ‎‡A  SNCA variant associated with Parkinson disease and plasma alpha-synuclein level‏ ‎‡9  1‏
919 ‎‡a  glucocerebrosidasegenemutationsariskfactorforlewybodydisorders‏ ‎‡A  Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders‏ ‎‡9  1‏
919 ‎‡a  commonvariationinthelrrk2geneisariskfactorforparkinsonsdisease‏ ‎‡A  Common variation in the LRRK2 gene is a risk factor for Parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  commongeneticvariationinthehlaregionisassociatedwithlateonsetsporadicparkinsonsdisease‏ ‎‡A  Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  riskpredictionforcomplexdiseasesapplicationtoparkinsondisease‏ ‎‡A  Risk prediction for complex diseases: application to Parkinson disease.‏ ‎‡9  1‏
919 ‎‡a  haptoglobinphenotypemodifiesserumironlevelsandtheeffectofsmokingonparkinsondiseaserisk‏ ‎‡A  Haptoglobin phenotype modifies serum iron levels and the effect of smoking on Parkinson disease risk‏ ‎‡9  1‏
919 ‎‡a  responsetotheletterhaptoglobinphenotypeandparkinsondiseaseriskbydelangheetal‏ ‎‡A  Response to the letter "Haptoglobin phenotype and Parkinson disease risk" by Delanghe et al.‏ ‎‡9  1‏
919 ‎‡a  combinedeffectsofsmokingcoffeeandnsaidsonparkinsonsdiseaserisk‏ ‎‡A  Combined effects of smoking, coffee, and NSAIDs on Parkinson's disease risk‏ ‎‡9  1‏
919 ‎‡a  exploringgeneenvironmentinteractionsinparkinsonsdisease‏ ‎‡A  Exploring gene-environment interactions in Parkinson’s disease‏ ‎‡9  1‏
919 ‎‡a  geneticassociationbetweenαsynucleinandidiopathicparkinsonsdisease‏ ‎‡A  Genetic association between α-synuclein and idiopathic parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  lackofevidenceforanassociationbetweenuchl1s18yandparkinsonsdisease‏ ‎‡A  Lack of evidence for an association between UCHL1 S18Y and Parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  validityandutilityofalrrk2g2019smutationtestforthediagnosisofparkinsonsdisease‏ ‎‡A  Validity and Utility of a LRRK2 G2019S Mutation Test for the Diagnosis of Parkinson's Disease‏ ‎‡9  1‏
919 ‎‡a  lowerplasmaapolipoproteina1levelsarefoundinparkinsonsdiseaseandassociatewithapolipoproteina1genotype‏ ‎‡A  Lower plasma apolipoprotein A1 levels are found in Parkinson's disease and associate with apolipoprotein A1 genotype‏ ‎‡9  1‏
919 ‎‡a  lrrk2g2019sinfamilieswithparkinsondiseasewhooriginatedfromeuropeandthemiddleeastevidenceof2distinctfoundingeventsbeginning2millenniaago‏ ‎‡A  LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.‏ ‎‡9  1‏
919 ‎‡a  rab39bpg192rmutationcauses10linkeddominantparkinsonsdisease‏ ‎‡A  The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease‏ ‎‡9  1‏
919 ‎‡a  genomewidegeneenvironmentstudyidentifiesglutamatereceptorgenegrin2aasaparkinsonsdiseasemodifiergeneviainteractionwithcoffee‏ ‎‡A  Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee‏ ‎‡9  1‏
919 ‎‡a  recognitionmemoryforhandpositionsandspatiallocationsinpatientswithhuntingtonsdiseasedifferentialvisuospatialmemoryimpairment‏ ‎‡A  Recognition memory for hand positions and spatial locations in patients with Huntington's disease: differential visuospatial memory impairment?‏ ‎‡9  1‏
919 ‎‡a  studyofistradefyllineinpatientswithparkinsonsdiseaseonlevodopawithmotorfluctuations‏ ‎‡A  Study of istradefylline in patients with Parkinson's disease on levodopa with motor fluctuations‏ ‎‡9  1‏
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