Mohsan Alvi

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes et al. · The American Journal of Human Genetics · 2019 · 97 citations · Full text

Neurodevelopmental Disorders, Developmental Biology, Heterozygous Variants +8

Clinical and molecular consequences of disease-associated de novo mutations in SATB2

Hemant Bengani, Mark T. Handley, Mohsan Alvi et al. · Genetics in Medicine · 2017 · 61 citations · Full text

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder

Margot R.F. Reijnders, Kerry A. Miller, Mohsan Alvi et al. · The American Journal of Human Genetics · 2018 · 48 citations · Full text

Prevalence, phenotype and architecture of developmental disorders caused by <i>de novo</i> mutation: The Deciphering Developmental Disorders Study

Jeremy F. McRae, Stephen Clayton, Tomas Fitzgerald et al. · 2016 · 36 citations · Full text

Exome Sequencing, Genetics, Genetic Epidemiology +23

Turning a Blind Eye: Explicit Removal of Biases and Variation from Deep Neural Network Embeddings

Mohsan Alvi, Andrew Zisserman, Christoffer Nellåker · arXiv (Cornell University) · 2018 · 13 citations · Full text

Artificial Intelligence, Convolutional Neural Network, Engineering +20