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Kin Mok

Showing results (11-20 of 23) with videos related to

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European Journal of Human Genetics : EJHG|April 25, 2013
Homozygosity analysis in amyotrophic lateral sclerosisKin Mok, Hannu Laaksovirta, Pentti J Tienari, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72Johnathan Cooper-Knock, Christopher Hewitt, J Robin Highley, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association studyWilliam J Scotton, Rebecca R Valentino, Alejandro Martinez-Carrasco, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Molecular Autism|July 4, 2017
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving <i>DPP10</i>Annisa Shui Lam Mak, Annie Ting Gee Chiu, Gordon Ka Chun Leung, et al.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
European Journal of Human Genetics : EJHG|April 25, 2013
Homozygosity analysis in amyotrophic lateral sclerosisKin Mok, Hannu Laaksovirta, Pentti J Tienari, et al.
Brain : a Journal of Neurology|February 28, 2012
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72Johnathan Cooper-Knock, Christopher Hewitt, J Robin Highley, et al.
Medrxiv : the Preprint Server for Health Sciences|January 2, 2026
Identification of common variants influencing risk of the three-repeat tauopathy Pick's disease: a genome wide association studyWilliam J Scotton, Rebecca R Valentino, Alejandro Martinez-Carrasco, et al.
Neurobiology of Aging|September 3, 2014
Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansionPietro Fratta, James M Polke, Jia Newcombe, et al.
Molecular Autism|July 4, 2017
Use of clinical chromosomal microarray in Chinese patients with autism spectrum disorder-implications of a copy number variation involving <i>DPP10</i>Annisa Shui Lam Mak, Annie Ting Gee Chiu, Gordon Ka Chun Leung, et al.
Neurobiology of Aging|September 20, 2011
Chromosome 9 ALS and FTD locus is probably derived from a single founderKin Mok, Bryan J Traynor, Jennifer Schymick, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Neurology|September 16, 2016
A genome-wide association study in multiple system atrophyAnna Sailer, Sonja W Scholz, Michael A Nalls, et al.
The Lancet. Neurology|April 17, 2024
MAPT H2 haplotype and risk of Pick's disease in the Pick's disease International Consortium: a genetic association studyRebecca R Valentino, William J Scotton, Shanu F Roemer, et al.
The Lancet. Neurology|March 13, 2012
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyElisa Majounie, Alan E Renton, Kin Mok, et al.
Pageof 3