Ma J - Search Results

1

Convolutional neural network optimizes the application of diffusion kurtosis imaging in Parkinson's disease.

Sun J, Chen R, Tong Q, Ma J, Gao L, Fang J, Zhang D, Chan P, He H, Wu T. Sun J, et al. Among authors: ma j. Brain Inform. 2021 Sep 28;8(1):18. doi: 10.1186/s40708-021-00139-z. Brain Inform. 2021. PMID: 34585306 Free PMC article.

2

Impulse control disorders in Parkinson's disease in a Chinese population.

Fan W, Ding H, Ma J, Chan P. Fan W, et al. Among authors: ma j. Neurosci Lett. 2009 Nov 6;465(1):6-9. doi: 10.1016/j.neulet.2009.06.074. Epub 2009 Jun 26. Neurosci Lett. 2009. PMID: 19560522

3

Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population.

Cai Y, Ding H, Gu Z, Ma J, Chan P. Cai Y, et al. Among authors: ma j. Neurosci Lett. 2011 Jul 8;498(2):124-6. doi: 10.1016/j.neulet.2011.04.073. Epub 2011 May 5. Neurosci Lett. 2011. PMID: 21565251

4

PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population.

Cai Y, Ding H, Gu Z, Baskys A, Ma J, Chan P. Cai Y, et al. Among authors: ma j. Neurosci Lett. 2011 Nov 21;505(3):260-2. doi: 10.1016/j.neulet.2011.10.034. Epub 2011 Oct 21. Neurosci Lett. 2011. PMID: 22037506

5

Promoter methylation analysis of seven clock genes in Parkinson's disease.

Lin Q, Ding H, Zheng Z, Gu Z, Ma J, Chen L, Chan P, Cai Y. Lin Q, et al. Among authors: ma j. Neurosci Lett. 2012 Jan 24;507(2):147-50. doi: 10.1016/j.neulet.2011.12.007. Epub 2011 Dec 14. Neurosci Lett. 2012. PMID: 22193177

6

Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.

Wang C, Cai Y, Zheng Z, Tang BS, Xu Y, Wang T, Ma J, Chen SD, Langston JW, Tanner CM, Chan P; Chinese Parkinson Study Group (CPSG). Wang C, et al. Among authors: ma j. Parkinsonism Relat Disord. 2012 Sep;18(8):958-63. doi: 10.1016/j.parkreldis.2012.05.003. Epub 2012 Jun 2. Parkinsonism Relat Disord. 2012. PMID: 22658533

7

Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individuals.

Wang C, Cai Y, Gu Z, Ma J, Zheng Z, Tang BS, Xu Y, Zhou Y, Feng T, Wang T, Chen SD, Chan P; Chinese Parkinson Study Group. Wang C, et al. Among authors: ma j. Neurobiol Aging. 2014 Mar;35(3):725.e1-6. doi: 10.1016/j.neurobiolaging.2013.08.012. Epub 2013 Oct 3. Neurobiol Aging. 2014. PMID: 24095219

8

MAPT IVS1+124 C>G modifies risk of LRRK2 G2385R for Parkinson's disease in Chinese individuals.

Dan X, Wang C, Ma J, Feng X, Wang T, Zheng Z, Chan P. Dan X, et al. Among authors: ma j. Neurobiol Aging. 2014 Jul;35(7):1780.e7-1780.e10. doi: 10.1016/j.neurobiolaging.2014.01.025. Epub 2014 Jan 25. Neurobiol Aging. 2014. PMID: 24559644

9

Non-motor symptoms in Chinese Parkinson's disease patients with and without LRRK2 G2385R and R1628P variants.

Li DW, Gu Z, Wang C, Ma J, Tang BS, Chen SD, Chan P. Li DW, et al. Among authors: ma j. J Neural Transm (Vienna). 2015 May;122(5):661-7. doi: 10.1007/s00702-014-1281-4. Epub 2014 Jul 26. J Neural Transm (Vienna). 2015. PMID: 25062988

10

Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2.

Wang C, Xu Y, Feng X, Ma J, Xie S, Zhang Y, Tang BS, Chan P. Wang C, et al. Among authors: ma j. Neurobiol Aging. 2015 Jan;36(1):545.e1-7. doi: 10.1016/j.neurobiolaging.2014.07.039. Epub 2014 Aug 2. Neurobiol Aging. 2015. PMID: 25189117

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