266 related articles for article (PubMed ID: 35893043)
1. Frequency of Parkinson's Disease Genes and Role of
Vacchiano V; Bartoletti-Stella A; Rizzo G; Avoni P; Parchi P; Salvi F; Liguori R; Capellari S
Genes (Basel); 2022 Jul; 13(8):. PubMed ID: 35893043
[TBL] [Abstract][Full Text] [Related]
2. Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis.
Wainberg M; Andrews SJ; Tripathy SJ
Alzheimers Res Ther; 2023 Jun; 15(1):113. PubMed ID: 37328865
[TBL] [Abstract][Full Text] [Related]
3. Pathway analysis of two amyotrophic lateral sclerosis GWAS highlights shared genetic signals with Alzheimer's disease and Parkinson's disease.
Shang H; Liu G; Jiang Y; Fu J; Zhang B; Song R; Wang W
Mol Neurobiol; 2015 Feb; 51(1):361-9. PubMed ID: 24647822
[TBL] [Abstract][Full Text] [Related]
4. The genetic landscape of Parkinson's disease.
Lunati A; Lesage S; Brice A
Rev Neurol (Paris); 2018 Nov; 174(9):628-643. PubMed ID: 30245141
[TBL] [Abstract][Full Text] [Related]
5. The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy.
Chen Y; Cao B; Chen X; Ou R; Wei Q; Zhao B; Wu Y; Yuan L; Shang HF
Neurosci Lett; 2018 Nov; 686():205-210. PubMed ID: 30144538
[TBL] [Abstract][Full Text] [Related]
6. Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
Chen Y; Wei QQ; Ou R; Cao B; Chen X; Zhao B; Guo X; Yang Y; Chen K; Wu Y; Song W; Shang HF
PLoS One; 2015; 10(7):e0133776. PubMed ID: 26208350
[TBL] [Abstract][Full Text] [Related]
7. SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF
Neurobiol Aging; 2014 Dec; 35(12):2882.e1-2882.e6. PubMed ID: 25129240
[TBL] [Abstract][Full Text] [Related]
8. Alzheimer's, Parkinson's Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement.
Garofalo M; Pandini C; Bordoni M; Pansarasa O; Rey F; Costa A; Minafra B; Diamanti L; Zucca S; Carelli S; Cereda C; Gagliardi S
Int J Mol Sci; 2020 Dec; 21(24):. PubMed ID: 33327559
[TBL] [Abstract][Full Text] [Related]
9. Mutation Analysis of the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia.
Luukkainen L; Huttula S; Väyrynen H; Helisalmi S; Kytövuori L; Haapasalo A; Hiltunen M; Remes AM; Krüger J
J Alzheimers Dis; 2020; 76(3):955-965. PubMed ID: 32568194
[TBL] [Abstract][Full Text] [Related]
10. No association of GPNMB rs156429 polymorphism with Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in Chinese population.
Xu Y; Chen Y; Ou R; Wei QQ; Cao B; Chen K; Shang HF
Neurosci Lett; 2016 May; 622():113-7. PubMed ID: 27132081
[TBL] [Abstract][Full Text] [Related]
11. A genetic analysis of a Spanish population with early onset Parkinson's disease.
Cristina TP; Pablo M; Teresa PM; Lydia VD; Irene AR; Araceli AC; Inmaculada BB; Marta BT; Dolores BR; José CM; Rocío GR; José GP; Ismael HF; Silvia J; Labrador MA; Lydia LM; Carlos MJ; Posada IJ; Ana RS; Cristina RH; Javier DV; Gómez-Garre P
PLoS One; 2020; 15(9):e0238098. PubMed ID: 32870915
[TBL] [Abstract][Full Text] [Related]
12. PINK1/PARKIN signalling in neurodegeneration and neuroinflammation.
Quinn PMJ; Moreira PI; Ambrósio AF; Alves CH
Acta Neuropathol Commun; 2020 Nov; 8(1):189. PubMed ID: 33168089
[TBL] [Abstract][Full Text] [Related]
13. The genetics and neuropathology of Parkinson's disease.
Houlden H; Singleton AB
Acta Neuropathol; 2012 Sep; 124(3):325-38. PubMed ID: 22806825
[TBL] [Abstract][Full Text] [Related]
14. SLC1A2 rs3794087 are associated with susceptibility to Parkinson's disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population.
Xu Y; Cao B; Chen Y; Ou R; Wei Q; Yang J; Zhao B; Song W; Shang HF
J Neurol Sci; 2016 Jun; 365():96-100. PubMed ID: 27206883
[TBL] [Abstract][Full Text] [Related]
15. Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.
Xi J; Yang X; Zhao Q; Zheng J; An R; Tian S; Huang H; Hu F; Ning P; Xu Y
Neurosci Lett; 2018 Jan; 662():181-184. PubMed ID: 28917980
[TBL] [Abstract][Full Text] [Related]
16. Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.
Gorostidi A; Martí-Massó JF; Bergareche A; Rodríguez-Oroz MC; López de Munain A; Ruiz-Martínez J
Mol Diagn Ther; 2016 Oct; 20(5):481-91. PubMed ID: 27294386
[TBL] [Abstract][Full Text] [Related]
17. [Gene diagnosis of Alzheimer's disease and Parkinson's disease].
Tanaka S
Rinsho Byori; 2002 Oct; 50(10):965-9. PubMed ID: 12451676
[TBL] [Abstract][Full Text] [Related]
18. [Pathology of familial Parkinson's disease].
Wakabayashi K; Takahashi H
Brain Nerve; 2007 Aug; 59(8):851-64. PubMed ID: 17713121
[TBL] [Abstract][Full Text] [Related]
19. Mutational analysis of TARDBP in neurodegenerative diseases.
Ticozzi N; LeClerc AL; van Blitterswijk M; Keagle P; McKenna-Yasek DM; Sapp PC; Silani V; Wills AM; Brown RH; Landers JE
Neurobiol Aging; 2011 Nov; 32(11):2096-9. PubMed ID: 20031275
[TBL] [Abstract][Full Text] [Related]
20. Monogenic Parkinson's disease and parkinsonism: clinical phenotypes and frequencies of known mutations.
Puschmann A
Parkinsonism Relat Disord; 2013 Apr; 19(4):407-15. PubMed ID: 23462481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]