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 sncavariantassociatedwithparkinsondiseaseandplasma Alpha synucleinlevel‏ ‎‡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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