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 · 298 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Whole-exome Sequencing Study +10

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

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 · 232 citations · Full text

Developmental Biology, Mendelian Disorder, Human Startle Disease +8

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 · 232 citations · Full text

Allelic Variant, Ultra-rare Genetic Variation, Medicine +8

Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men

Gwendolyn Behrendt, Kristin Baer, Annalisa Buffo et al. · Glia · 2012 · 215 citations · Full text