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Nature Communications|July 11, 2019
Mapping the drivers of within-host pathogen evolution using massive data setsDuncan S Palmer, Isaac Turner, Sarah Fidler, et al.Biorxiv : the Preprint Server for Biology|November 24, 2025
Disruption of Cell-Type-Specific Molecular Programs of Medium Spiny Neurons in AutismGuohua Yuan, Varun Suresh, Emilie Wigdor, et al.Nature Communications|September 23, 2018
A naturally protective epitope of limited variability as an influenza vaccine targetCraig P Thompson, José Lourenço, Adam A Walters, et al.Nature Communications|July 10, 2024
Characterising the genetic architecture of changes in adiposity during adulthood using electronic health recordsSamvida S Venkatesh, Habib Ganjgahi, Duncan S Palmer, et al.Biorxiv : the Preprint Server for Biology|April 10, 2026
Molecular dynamics of Brodmann Area 22 in development and autismVarun Suresh, Emilie M Wigdor, Yuhan Hao, et al.American Journal of Human Genetics|May 2, 2026
Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseasesFrederik H Lassen, Georgios Kalantzis, Andrea Eoli, et al.Science Translational Medicine|August 18, 2020
Predicting functional effects of missense variants in voltage-gated sodium and calcium channelsHenrike O Heyne, David Baez-Nieto, Sumaiya Iqbal, et al.Nature Human Behaviour|July 4, 2024
Principled distillation of UK Biobank phenotype data reveals underlying structure in human variationCaitlin E Carey, Rebecca Shafee, Robbee Wedow, et al.Nature Communications|April 24, 2021
The impact of non-additive genetic associations on age-related complex diseasesMarta Guindo-Martínez, Ramon Amela, Silvia Bonàs-Guarch, et al.Nature Neuroscience|November 27, 2019
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variantsF Kyle Satterstrom, Raymond K Walters, Tarjinder Singh, et al.Pageof 4