Matthew Solomonson
Brigham and Women's Hospital(US)Harvard University(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, Genomics and Phylogenetic Studies, Genetics and Neurodevelopmental Disorders
Most-Cited Works
- → The mutational constraint spectrum quantified from variation in 141,456 humans(2020)9,855 cited
- → A structural variation reference for medical and population genetics(2020)1,132 cited
- → Mapping the human genetic architecture of COVID-19(2021)1,104 cited
- → Rare coding variants in ten genes confer substantial risk for schizophrenia(2022)839 cited
- → The ExAC browser: displaying reference data information from over 60 000 exomes(2016)819 cited
- → A genome-wide mutational constraint map quantified from variation in 76,156 human genomes(2022)324 cited
- → Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals(2019)299 cited
- → Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes(2022)283 cited
- → Transcript expression-aware annotation improves rare variant interpretation(2020)200 cited