Works matching DE "PARKINSON'S disease %26 genetics"

Results: 516

Kufor-Rakeb Syndrome/PARK9: One Novel and One Possible Recurring Ashkenazi ATP13A2 Mutation.

Published in:

Journal of Parkinson's Disease, 2018, v. 8, n. 3, p. 399, doi. 10.3233/JPD-181360

By:

Inzelberg, Rivka;
Estrada-Cuzcano, Alejandro;
Laitman, Yael;
De Vriendt, Els;
Friedman, Eitan;
Jordanova, Albena

Publication type:

Article

The Five Dimensions of Parkinson's Disease Genetic Risk.

Published in:

Journal of Parkinson's Disease, 2018, v. 8, n. 1, p. 13, doi. 10.3233/JPD-171256

By:

Coetzee, Gerhard A.;
Pierce, Steven

Publication type:

Article

The Changing Landscape of Parkinson Epidemiologic Research.

Published in:

Journal of Parkinson's Disease, 2018, v. 8, n. 1, p. 1, doi. 10.3233/JPD-171238

By:

Chen, Honglei

Publication type:

Article

What is Functional Mobility Applied to Parkinson's Disease?

Published in:

Journal of Parkinson's Disease, 2018, v. 8, n. 1, p. 121, doi. 10.3233/JPD-171233

By:

Bouça-Machado, Raquel;
Maetzler, Walter;
Ferreira, Joaquim J.

Publication type:

Article

Phenotypic Characteristics in GBA-Associated Parkinson's Disease: A Study in a Greek Population.

Published in:

Journal of Parkinson's Disease, 2018, v. 8, n. 1, p. 101, doi. 10.3233/JPD-171221

By:

Simitsi, Athina;
Koros, Christos;
Moraitou, Marina;
Papagiannakis, Nikos;
Antonellou, Roubina;
Bozi, Maria;
Angelopoulou, Efthalia;
Stamelou, Maria;
Michelakakis, Helen;
Stefanis, Leonidas

Publication type:

Article

c-Abl and Parkinson's Disease: Mechanisms and Therapeutic Potential.

Published in:

Journal of Parkinson's Disease, 2017, v. 7, n. 4, p. 589, doi. 10.3233/JPD-171191

By:

Brahmachari, Saurav;
Karuppagounder, Senthilkumar S.;
Ge, Preston;
Lee, Saebom;
Dawson, Valina L.;
Dawson, Ted M.;
Han Seok Ko

Publication type:

Article

VPS35, the Retromer Complex and Parkinson's Disease.

Published in:

Journal of Parkinson's Disease, 2017, v. 7, n. 2, p. 219, doi. 10.3233/JPD-161020

By:

Williams, Erin T.;
Xi Chen;
Moore, Darren J.

Publication type:

Article

The Identification of Alpha-Synuclein as the First Parkinson Disease Gene.

Published in:

Journal of Parkinson's Disease, 2017, v. 7, p. S45, doi. 10.3233/JPD-179003

By:

Nussbaum, Robert L.

Publication type:

Article

Personalized Medicine Approaches in Parkinson's Disease: The Genetic Perspective.

Published in:

Journal of Parkinson's Disease, 2016, v. 6, n. 4, p. 699, doi. 10.3233/JPD-160876

By:

Gasser, Thomas

Publication type:

Article

Investigation of Genetic Variants Associated with Alzheimer Disease in Parkinson Disease Cognition.

Published in:

Journal of Parkinson's Disease, 2016, v. 6, n. 1, p. 119, doi. 10.3233/JPD-150706

By:

Barrett, Matthew J.;
Koeppel, Alexander F.;
Flanigan, Joseph L.;
Turner, Stephen D.;
Worrall, Bradford B.

Publication type:

Article

The Synaptic Function of α-Synuclein.

Published in:

Journal of Parkinson's Disease, 2015, v. 5, n. 4, p. 699, doi. 10.3233/JPD-150642

By:

Burré, Jacqueline

Publication type:

Article

Parkinson's Disease Subtypes in the Oxford Parkinson Disease Centre (OPDC) Discovery Cohort.

Published in:

Journal of Parkinson's Disease, 2015, v. 5, n. 2, p. 269, doi. 10.3233/JPD-140523

By:

Lawton, Michael;
Baig, Fahd;
Rolinski, Michal;
Ruffman, Claudio;
Nithi, Kannan;
May, Margaret T.;
Ben-Shlomo, Yoav;
Hu, Michele T. M.

Publication type:

Article

Usefulness of Genetic Testing in PD and PD Trials: A Balanced Review.

Published in:

Journal of Parkinson's Disease, 2015, v. 5, n. 2, p. 209, doi. 10.3233/JPD-140507

By:

Gasser, Thomas

Publication type:

Article

Behavioral Deficits and Striatal DA Signaling in LRRK2 p.G2019S Transgenic Rats: A Multimodal Investigation Including PET Neuroimaging.

Published in:

Journal of Parkinson's Disease, 2014, v. 4, n. 3, p. 483, doi. 10.3233/JPD-140344

By:

Walker, Matthew D.;
Volta, Mattia;
Cataldi, Stefano;
Dinelle, Katherine;
Beccano-Kelly, Dayne;
Munsie, Lise;
Kornelsen, Rick;
Mah, Chenoa;
Chou, Patrick;
Co, Kimberley;
Khinda, Jaskaran;
Mroczek, Marta;
Bergeron, Sabrina;
Yu, Katrina;
Cao, Li Ping;
Funk, Natalja;
Ott, Thomas;
Galter, Dagmar;
Riess, Olaf;
Biskup, Saskia

Publication type:

Article

Genetic Susceptibility Model of Parkinson's Disease Resulting from Exposure of DJ-1 Deficient Mice to MPTP: Evaluation of Neuroprotection by Ubisol-Q10.

Published in:

Journal of Parkinson's Disease, 2014, v. 4, n. 3, p. 523, doi. 10.3233/JPD-140368

By:

Muthukumaran, Krithika;
Smith, Jessica;
Jasra, Harshil;
Sikorska, Marianna;
Sandhu, Jagdeep K.;
Cohen, Jerome;
Lopatin, Daniel;
Pandey, Siyaram

Publication type:

Article

Investigating the causal and genetic relationship between migraine and Parkinson's disease.

Published in:

Headache: The Journal of Head & Face Pain, 2025, v. 65, n. 5, p. 835, doi. 10.1111/head.14881

By:

Deng, Ming‐Gang;
Zhou, Xiuxiu;
Liu, Fang;
Wang, Kai;
Luo, Lingli;
Zhang, Min‐Jie;
Feng, Qianqian;
Liu, Jiewei

Publication type:

Article

Mobile phone use characteristics, genetic predisposition and the risk of Parkinson's disease: a prospective cohort study.

Published in:

Age & Ageing, 2025, v. 54, n. 5, p. 1, doi. 10.1093/ageing/afaf143

By:

Zhang, Juanjuan;
Zou, Junjie;
He, Yuerong;
Shen, Jiale;
Jing, Kunjuan;
An, Ruiqi;
Wang, Zhen;
Yao, Xiaoyan;
Ren, Chao;
Xia, Yang

Publication type:

Article

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

Published in:

Neurogenetics, 2004, v. 5, n. 3, p. 147, doi. 10.1007/s10048-004-0180-5

By:

Oliveira, Sofia A.;
Scott, William K.;
Fengyu Zhang;
Stajich, Jeffrey M.;
Fujiwara, Kenichiro;
Hauser, Michael;
Scott, Burton L.;
Pericak-Vance, Margaret A.;
Vance, Jeffrey M.;
Martin, Eden R.

Publication type:

Article

Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer disease.

Published in:

Neurogenetics, 2004, v. 5, n. 2, p. 115, doi. 10.1007/s10048-004-0173-4

By:

Blomqvist, Mia E.-L.;
Silburn, Peter A.;
Buchanan, Daniel D.;
Andreasen, Niels;
Blennow, Kaj;
Pedersen, Nancy L.;
Brookes, Anthony J.;
Mellick, George D.;
Prince, Jonathan A.

Publication type:

Article

MicroRNAs in Parkinson's disease.

Published in:

Experimental Brain Research, 2017, v. 235, n. 8, p. 2359, doi. 10.1007/s00221-017-4989-1

By:

Singh, Abhishek;
Sen, Dwaipayan

Publication type:

Article

Context-sensitive network-based disease genetics prediction and its implications in drug discovery.

Published in:

Bioinformatics, 2017, v. 33, n. 7, p. 1031, doi. 10.1093/bioinformatics/btw737

By:

Yang Chen;
Rong Xu

Publication type:

Article

Influence of Consanguinity and Medication on the Development of Parkinson's Disease.

Published in:

Dementia & Geriatric Cognitive Disorders, 2020, v. 49, n. 4, p. 390, doi. 10.1159/000509586

By:

Tufail, Muhammad;
Hassan, Ishtiaq

Publication type:

Article

LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi Jews.

Published in:

Dementia & Geriatric Cognitive Disorders, 2016, v. 42, n. 1/2, p. 1, doi. 10.1159/000447450

By:

Dagan, Efrat;
Schlesinger, Ilana;
Kurolap, alina;
ayoub, Mareemar;
Nassar, Maria;
Peretz-aharon, Judith;
Gershoni-Baruch, Ruth

Publication type:

Article

Early-onset Parkinson's disease with PARK2 gene mutation: one case report.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 6, p. 482, doi. 10.3969/j.issn.1672-6731.2021.06.010

By:

LI Mao-lin;
ZENG Tao;
FENG Qin;
WANG Chun

Publication type:

Article

Clinical characteristics and therapeutic evaluation of autosomal recessive juvenil - onset Parkinson's disease.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 6, p. 454, doi. 10.3969/j.issn.1672-6731.2021.06.005

By:

ZHANG Yue;
ZHANG Cheng;
LI Juan;
WU Jing-jing;
LIN Dong

Publication type:

Article

A childhood-onset rapid-onset dystonia Parkinsonism patient with ATP1A3 gene mutation and literature review.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 4, p. 304, doi. 10.3969/j.issn.1672-6731.2021.04.012

By:

KANG Qing-yun;
LIAO Cai-shi;
LIAO Hong-mei;
CHEN Bo;
YANG Li-ming

Publication type:

Article

Progress of translational research on the pathogenesis, diagnosis and treatment of Parkinson's disease.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2018, v. 18, n. 1, p. 19, doi. 10.3969/j.issn.1672-6731.2018.01.003

By:

WANG Gang;
CUI Hai-lun;
LIU Jun;
DING Jian-qing;
XIAO Qin;
MA Jian-fang;
CHEN Sheng-di

Publication type:

Article

Expression profiles of genes in wild-type DJ-1 and L10P mutant DJ-1 in monoclonal cell strains.

Published in:

Chinese Journal of Contemporary Neurology & Neurosurgery, 2013, v. 13, n. 7, p. 587, doi. 10.3969/j.issn.1672-6731.2013.07.007

By:

Zhen-hua LIU;
Bei-sha TANG;
Xin-xiang YAN;
Ji-feng GUO

Publication type:

Article

α-Synuclein lipoprotein nanoparticles.

Published in:

Nanotechnology Reviews, 2017, v. 6, n. 1, p. 105, doi. 10.1515/ntrev-2016-0062

By:

Eichmann, Cédric;
Bibow, Stefan;
Riek, Roland

Publication type:

Article

Mitochondrial Protein PINK1 Positively Regulates RLR Signaling.

Published in:

Frontiers in Immunology, 2019, p. N.PAG, doi. 10.3389/fimmu.2019.01069

By:

Zhou, Jun;
Yang, Rui;
Zhang, Zhaoru;
Liu, Qianru;
Zhang, Yuanyuan;
Wang, Qingqing;
Yuan, Hongbin

Publication type:

Article

The Parkinson's gene PINK1 regulates cell cycle progression and promotes cancer-associated phenotypes.

Published in:

Oncogene, 2015, v. 34, n. 11, p. 1363, doi. 10.1038/onc.2014.81

By:

O'Flanagan, C H;
Morais, V A;
Wurst, W;
De Strooper, B;
O'Neill, C

Publication type:

Article

Recent Developments in LRRK2-Targeted Therapy for Parkinson's Disease.

Published in:

Drugs, 2019, v. 79, n. 10, p. 1037, doi. 10.1007/s40265-019-01139-4

By:

Zhao, Ye;
Dzamko, Nicolas

Publication type:

Article

Psychosis in Parkinson's Disease: Epidemiology, Pathophysiology, and Management.

Published in:

Drugs, 2016, v. 76, n. 11, p. 1093, doi. 10.1007/s40265-016-0600-5

By:

Chang, Anna;
Fox, Susan

Publication type:

Article

Plasma Epidermal Growth Factor Decreased in the Early Stage of Parkinson's Disease.

Published in:

Aging & Disease, 2015, v. 6, n. 3, p. 168, doi. 10.14336/AD.2014.0925

By:

Qian-Wen Jiang;
Cheng Wang;
Yi Zhou;
Miao-Miao Hou;
Xi Wang;
Hui-Dong Tang;
Yi-Wen Wu;
Jian-Fang Ma;
Sheng-Di Chen

Publication type:

Article

PARTIAL LINEAR VARYING MULTI-INDEX COEFFICIENT MODEL FOR INTEGRATIVE GENE-ENVIRONMENT INTERACTIONS.

Published in:

Statistica Sinica, 2016, v. 26, n. 3, p. 1037, doi. 10.5705/ss.202015.0114

By:

Xu Liu;
Yuehua Cui;
Runze Li

Publication type:

Article

Brain Mitochondria, Aging, and Parkinson’s Disease.

Published in:

Genes, 2018, v. 9, n. 5, p. 250, doi. 10.3390/genes9050250

By:

Rango, Mario;
Bresolin, Nereo

Publication type:

Article

SNCA Is a Functionally Low-Expressed Gene in Lung Adenocarcinoma.

Published in:

Genes, 2018, v. 9, n. 1, p. 16, doi. 10.3390/genes9010016

By:

Yan, Yuanliang;
Xu, Zhijie;
Hu, Xiaofang;
Qian, Long;
Li, Zhi;
Zhou, Yangying;
Dai, Shuang;
Zeng, Shuangshuang;
Gong, Zhicheng

Publication type:

Article

Dopamine D4 receptor polymorphism and idiopathic Parkinson's disease.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 3, p. 397, doi. 10.1038/sj.ejhg.5200297

By:

Kronenberg, Martina F;
Menzel, Hans-Jürgen;
Ebersbach, Georg;
Wenning, Gregor K;
Luginger, Elisabeth;
Gollner, Martin;
Ransmayr, Gerhard;
Utermann, Gerd;
Poewe, Werner;
Kronenberg, Florian

Publication type:

Article

PSMC1 Gene in Parkinson's Disease.

Published in:

European Neurology, 2012, v. 68, n. 4, p. 193, doi. 10.1159/000339003

By:

Gómez-Garre, Pilar;
Jesús, Silvia;
Carrillo, Fátima;
Cáceres-Redondo, Maria Teresa;
Bernal-Bernal, Inmaculada;
Carballo, Manuel;
Gao, Lin;
Mir, Pablo

Publication type:

Article

Regulation of LRRK2 promoter activity and gene expression by Sp1.

Published in:

Molecular Brain, 2016, v. 9, p. 1, doi. 10.1186/s13041-016-0215-5

By:

Juelu Wang;
Weihong Song

Publication type:

Article

Mutations in EIF4G1 are not a common cause of Parkinson's disease.

Published in:

European Journal of Neurology, 2013, v. 20, n. 4, p. e59, doi. 10.1111/ene.12051

By:

Siitonen, A.;
Majounie, E.;
Federoff, M.;
Ding, J.;
Majamaa, K.;
Singleton, A. B.

Publication type:

Article

The PRIPS study: screening battery for subjects at risk for Parkinson's disease.

Published in:

European Journal of Neurology, 2013, v. 20, n. 1, p. 102, doi. 10.1111/j.1468-1331.2012.03798.x

By:

Berg, D.;
Godau, J.;
Seppi, K.;
Behnke, S.;
Liepelt‐Scarfone, I.;
Lerche, S.;
Stockner, H.;
Gaenslen, A.;
Mahlknecht, P.;
Huber, H.;
Srulijes, K.;
Klenk, J.;
Fassbender, K.;
Maetzler, W.;
Poewe, W.

Publication type:

Article

LRRK2 mutations are uncommon in Turkey.

Published in:

2011

By:

Hanagasi, H. A.;
Lohmann, E.;
Dursun, B.;
Honoré, A.;
Lesage, S.;
Dogu, O.;
Kaleagasi, H.;
Aydın, O.;
Gürvit, H.;
Erginel-Unaltuna, N.;
Brice, A.;
Emre, M.

Publication type:

Letter

The transcription factor Pitx3 is a risk modifier for Parkinson's disease in a Chinese Han population.

Published in:

European Journal of Neurology, 2011, v. 18, n. 5, p. 778, doi. 10.1111/j.1468-1331.2010.03281.x

By:

Yu, L.-H.;
Lin, Z.-F.;
Liu, Y.;
Hu, F.-Y.;
He, X.-H.;
Liu, Z.-L.;
Xu, Y.-M.

Publication type:

Article

Association of the glucocerebrosidase N370S allele with Parkinson's disease in two separate Chinese Han populations of mainland China.

Published in:

European Journal of Neurology, 2010, v. 17, n. 12, p. 1476, doi. 10.1111/j.1468-1331.2010.03097.x

By:

Hu, F.-Y.;
Xi, J.;
Guo, J.;
Yu, L.-H.;
Liu, L.;
He, X.-H.;
Liu, Z.-L.;
Zou, X.-Y.;
Xu, Y.-M.

Publication type:

Article

Summary of GIGYF2 studies in Parkinson’s disease: the burden of proof.

Published in:

2010

By:

Tan, E. K.;
Schapira, A. H.

Publication type:

Editorial

Molecular imaging in hereditary forms of parkinsonism.

Published in:

European Journal of Neurology, 2007, v. 14, n. 4, p. 359, doi. 10.1111/j.1468-1331.2007.01691.x

By:

Shih, M. C.;
Felicio, A. C.;
de Oliveira Godeiro-Junior, C.;
de Carvalho Aguiar, P.;
de Andrade, L. A. F.;
Ferraz, H. B.;
Bressan, R. A.

Publication type:

Article

Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants.

Published in:

European Journal of Neurology, 2007, v. 14, n. 1, p. 7, doi. 10.1111/j.1468-1331.2006.01551.x

By:

Xiromerisiou, G.;
Hadjigeorgiou, G. M.;
Gourbali, V.;
Johnson, J.;
Papakonstantinou, I.;
Papadimitriou, A.;
Singleton, A. B.

Publication type:

Article

Parkinson's disease: the genetics of a heterogeneous disorder.

Published in:

European Journal of Neurology, 2006, v. 13, n. 6, p. 616, doi. 10.1111/j.1468-1331.2006.01336.x

By:

Gosal, D.;
Ross, O. A.;
Toft, M.

Publication type:

Article

Distribution of VGF peptides in the human cortex and their selective changes in Parkinson's and Alzheimer's diseases C. Cocco et al. VGF peptides in the human cortex.

Published in:

Journal of Anatomy, 2010, v. 217, n. 6, p. 683, doi. 10.1111/j.1469-7580.2010.01309.x

By:

Cocco, Cristina;
D'Amato, Filomena;
Noli, Barbara;
Ledda, Antonella;
Brancia, Carla;
Bongioanni, Paolo;
Ferri, Gian-Luca

Publication type:

Article