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1 . Academic Journal
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
저자
by
Zhu, William
;
Huang, Xiaoping
;
Yoon, Esther
;
Bandres-Ciga, Sara
;
Blauwendraat, Cornelis
, et al.
소스
Brain: A Journal of Neurology
. Jun2022, Vol. 145 Issue 6, p2077-2091. 15p.
Full Text (OUP)
Scopus
Web of Science
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7 . Academic Journal
The Parkinson's Disease DNA Variant Browser.
저자
by
Kim, Jonggeol J.
;
Makarious, Mary B.
;
Bandres‐Ciga, Sara
;
Gibbs, Jesse Raphael
;
Ding, Jinhui
, et al.
소스
Movement Disorders
. May2021, Vol. 36 Issue 5, p1250-1258. 9p.
Full Text (Wiley)
Scopus
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7 . Academic Journal
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease
저자
by
Blauwendraat, Cornelis
;
Kia, Demis A.
;
Pihlstrøm, Lasse
;
Gan-Or, Ziv
;
Lesage, Suzanne
, et al.
소스
In
Neurobiology of Aging
April 2018 64:159-159
Full Text (Clinical Key)
Full Text (ScienceDirect)
Scopus
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7 . Academic Journal
A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study.
저자
by
Driscoll, Ira
;
Snively, Beverly M.
;
Espeland, Mark A.
;
Shumaker, Sally A.
;
Rapp, Stephen R.
, et al.
소스
International Journal of Geriatric Psychiatry
. May2019, Vol. 34 Issue 5, p692-699. 8p. 2 Charts, 1 Graph.
Full Text (Wiley)
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7 . Academic Journal
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.
저자
by
Blauwendraat, Cornelis
;
Reed, Xylena
;
Kia, Demis A.
;
Gan-Or, Ziv
;
Lesage, Suzanne
, et al.
소스
JAMA Neurology; Nov2018, Vol. 75 Issue 11, p1416-1422, 7p
Full Text (AMA)
Scopus
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7 . Academic Journal
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
저자
by
Nalls, Mike A.
;
Bras, Jose
;
Hernandez, Dena G.
;
Keller, Margaux F.
;
Majounie, Elisa
, et al.
소스
In
Neurobiology of Aging
March 2015 36(3):1605-1605
Full Text (Clinical Key)
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Scopus
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7 . Academic Journal
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease
저자
by
Robak, Laurie A
;
Jansen, Iris E
;
van Rooij, Jeroen
;
Uitterlinden, André G
;
Kraaij, Robert
, et al.
소스
Brain
. Dec 01, 2017 140(12):3191-3203
Full Text (OUP)
Full Text (OUP Near Archive)
Scopus
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7 . Academic Journal
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinsonʼs disease with a sexual dimorphism
저자
by
Klebe, Stephan
;
Golmard, Jean-Louis
;
Nalls, Michael A
;
Saad, Mohamad
;
Singleton, Andrew B
, et al.
소스
Journal of Neurology, Neurosurgery & Psychiatry
. Jun 01, 2013 84(6):666-673
Full Text (BMJ Journals)
Scopus
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7 . Academic Journal
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinsonʼs disease
저자
by
Holmans, Peter
;
Moskvina, Valentina
;
Jones, Lesley
;
Sharma, Manu
;
Vedernikov, Alexey
, et al.
소스
Human Molecular Genetics
. Mar 01, 2013 22(5):1039-1049
Full Text (OUP)
Full Text (OUP Near Archive)
Scopus
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7 . Academic Journal
No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson’s disease in nine ADHD candidate SNPs
저자
by
Geissler, Julia M.
;
Romanos, Marcel
;
Gerlach, Manfred
;
Berg, Daniela
;
Schulte, Claudia
, et al.
소스
ADHD Attention Deficit and Hyperactivity Disorders
. June 2017 9(2):121-127
Scopus
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