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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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997 | ‡a 0 0 lived 0 0 ‡9 1 |