Analysis of shared heritability in common disorders of the brain
2018 · Science · 1,991 citations
https://doi.org/10.1126/science.aap8757
M
Mark McCormack
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Mark McCormack is an academic researcher from Agriculture and Agri-Food Canada. The author has contributed to research in topics: Genomics and Rare Diseases & Epilepsy research and treatment & Genetics and Neurodevelopmental Disorders. The author has an h-index of 24, co-authored 47 publications.
ORCID: 0000-0002-8213-6141Papers by this author
worksGenome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies
2018 · Nature Communications · 499 citations
https://doi.org/10.1038/s41467-018-07524-z
Tibetans living at sea level have a hyporesponsive hypoxia-inducible factor system and blunted physiological responses to hypoxia
2013 · Journal of Applied Physiology · 133 citations
https://doi.org/10.1152/japplphysiol.00535.2013
Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized Epilepsy
2012 · The American Journal of Human Genetics · 100 citations
https://doi.org/10.1016/j.ajhg.2012.06.016
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
2018 · The Lancet Neurology · 93 citations
https://doi.org/10.1016/s1474-4422(18)30215-1
Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study
2018 · The Lancet Neurology · 93 citations
https://doi.org/10.1016/s1474-4422(18)30215-1
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