Mark I. Rees

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

Yen‐Chen Anne Feng, Daniel P. Howrigan, Liam Abbott et al. · The American Journal of Human Genetics · 2019 · 303 citations · Full text

Medicine, Genetics, Molecular Genetics +14

The GDP-GTP Exchange Factor Collybistin: An Essential Determinant of Neuronal Gephyrin Clustering

Kirsten Harvey, Ian Duguid, Melissa J. Alldred et al. · Journal of Neuroscience · 2004 · 259 citations · Full text

Life Sciences, Neurobiology, Neuroscience +16

Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle disease

Mark I. Rees, Kirsten Harvey, Brian R. Pearce et al. · Nature Genetics · 2006 · 236 citations · Full text

Life Sciences, Genetics, Neuroscience +11

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

Andrew S. Allen, Susannah T. Bellows, Samuel F. Berkovic et al. · The Lancet Neurology · 2017 · 234 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Immunohistochemical staining of post-mortem adult human brain sections

Henry J. Waldvogel, Maurice A. Curtis, Kristin Baer et al. · Nature Protocols · 2006 · 221 citations

Medicine, Neuroscience, Pathology +14