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Nature Genetics|November 30, 2023
A mutation rate model at the basepair resolution identifies the mutagenic effect of polymerase III transcriptionVladimir Seplyarskiy, Evan M Koch, Daniel J Lee, et al.Proteins|January 30, 2004
From analysis of protein structural alignments toward a novel approach to align protein sequencesShamil R Sunyaev, Gennady A Bogopolsky, Natalia V Oleynikova, et al.Molecular Biology and Evolution|April 21, 2019
Applicability of the Mutation-Selection Balance Model to Population Genetics of Heterozygous Protein-Truncating Variants in HumansDonate Weghorn, Daniel J Balick, Christopher Cassa, et al.Cell Reports|November 4, 2015
APOBEC-Induced Cancer Mutations Are Uniquely Enriched in Early-Replicating, Gene-Dense, and Active Chromatin RegionsMarat D Kazanov, Steven A Roberts, Paz Polak, et al.American Journal of Human Genetics|May 30, 2020
Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary StatisticsSung Chun, Maxim Imakaev, Daniel Hui, et al.Genes|January 25, 2025
Missing Regulation Between Genetic Association and Transcriptional Abundance for Hypercholesterolemia GenesAaron Hakim, Noah J Connally, Gavin R Schnitzler, et al.Nature|July 1, 2015
Identification of cis-suppression of human disease mutations by comparative genomicsDaniel M Jordan, Stephan G Frangakis, Christelle Golzio, et al.Elife|December 14, 2022
The missing link between genetic association and regulatory functionNoah J Connally, Sumaiya Nazeen, Daniel Lee, et al.Bioinformatics (Oxford, England)|October 13, 2012
Network-based inference from complex proteomic mixtures using SNIPEDavid P Nusinow, Adam Kiezun, Daniel J O'Connell, et al.Nature Genetics|December 5, 2018
Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutationsVladimir B Seplyarskiy, Evgeny E Akkuratov, Natalia Akkuratova, et al.Pageof 11