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Cell Genomics|February 13, 2023
The female protective effect against autism spectrum disorderEmilie M Wigdor, Daniel J Weiner, Jakob Grove, et al.Nature Genetics|September 18, 2025
Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effectsKonrad J Karczewski, Rahul Gupta, Masahiro Kanai, et al.Cell Genomics|February 13, 2023
Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomesKonrad J Karczewski, Matthew Solomonson, Katherine R Chao, et al.Nature Genetics|April 14, 2025
Genome-wide analyses identify 25 infertility loci and relationships with reproductive traits across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.Nature Genetics|April 12, 2022
Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophreniaDuncan S Palmer, Daniel P Howrigan, Sinéad B Chapman, et al.Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrumSamvida S Venkatesh, Laura B L Wittemans, Duncan S Palmer, et al.Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.Nature Genetics|March 28, 2026
Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosityHye In Kim, Christopher DeBoever, Klaudia Walter, et al.Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Systematic common and rare variant association testing in 392,030 whole genomes in <i>All of Us</i>Wenhan Lu, Robert J Carroll, Matthew Solomonson, et al.Nature Genetics|February 27, 2019
Identification of common genetic risk variants for autism spectrum disorderJakob Grove, Stephan Ripke, Thomas D Als, et al.Pageof 4