Kin Y. Mok - Concepedia

Author

Kin Y. Mok

University College London ORCID

Also Known As

Donald Grosset, Ip, Nancy Y., John Hardy, K Y Mok, K. Mok, K. Y. Mok, K.Y. Mok, KY Mok, Kin Mok, Kin Y Mok

148

Publications

16.7K

Citations

H-Index

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery Hong Kong University of Science and Technology King's College London University of Hong Kong

About

Kin Y. Mok is an author at University College London specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	8.5K
2	Health Sciences	2	2	55
3	Public Health	2	2	2K
4	Social Sciences	2	2	40
5	Education	1	1	33

Kin Y. Mok

Publications

13.2K

Citations

H-Index

Page 1

	Year	Citations
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD Alan E. Renton, Elisa Majounie, Adrian J. Waite, Neuron ChromatinNeurodegenerative DiseasesAmyotrophic Lateral SclerosisGenetic DisorderGenetics	2011	4.4K
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Elisa Majounie, Alan E. Renton, Kin Y. Mok, The Lancet Neurology Neurodegenerative DiseasesAmyotrophic Lateral SclerosisDementiaFrontotemporal DementiaNeuroscience	2012	1.2K
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling Vincent Plagnol, James Curtis, Michael P. Epstein, Bioinformatics	2012	727
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features Colin Mahoney, Jon Beck, Jonathan D. Rohrer, Brain	2012	434
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72 Johnathan Cooper‐Knock, Christopher Hewitt, J. Robin Highley, Brain Amyotrophic Lateral SclerosisNeurological DisorderIntronic ExpansionGeneticsMedicine	2012	334
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study Aleksey Shatunov, Kin Y. Mok, Stephen Newhouse, The Lancet Neurology	2010	225
Finding genetically-supported drug targets for Parkinson’s disease using Mendelian randomization of the druggable genome Catherine S. Storm, Demis A. Kia, Mona Mohammad Almramhi, Nature Communications	2021	204
The importance of understanding individual differences in Down syndrome Annette Karmiloff‐Smith, Tamara Al‐Janabi, Hana D’Souza, F1000Research	2016	203
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets Demis A. Kia, David Zhang, Sebastian Guelfi, JAMA Neurology	2021	195

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