Matthew Solomonson
Genetics · 2016–2023
A researcher in the Science corpus: 14 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 322 citations into it
- Computational Biology & Bioinformatics — 39 citations into it
Whom Matthew Solomonson trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- James Y. Zou (in Genetics)
Papers from Matthew Solomonson's perspective
Ordered by how strongly the researchers Matthew Solomonson trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- dbSNP: the NCBI database of genetic variation
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor
- Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
- dbNSFP: A Lightweight Database of Human Non-synonymous SNPs and Their Functional Predictions (Human Mutation)
- Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
- dbNSFP v2.0: A Database of Human Non-synonymous SNVs and Their Functional Predictions and Annotations (Human Mutation)
- ClinVar: public archive of relationships among sequence variation and human phenotype
- The human genome browser at UCSC.
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
Their papers
- The mutational constraint spectrum quantified from variation in 141,456 humans (2020) — 8,441 citations
- The ExAC browser: displaying reference data information from over 60 000 exomes (2016) — 700 citations
- Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes (2019) — 1,088 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- A genomic mutational constraint map using variation in 76,156 human genomes (2023) — 1,228 citations
- A genome-wide mutational constraint map quantified from variation in 76,156 human genomes (2022) — 258 citations
- Rare coding variants in 10 genes confer substantial risk for schizophrenia (2022) — 659 citations
- Variant interpretation using population databases: lessons from gnomAD (2021) — 533 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) — 126 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Transcript expression-aware annotation improves rare variant discovery and interpretation (2019) — 26 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- An open resource of structural variation for medical and population genetics (2019) — 76 citations