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American Journal of Human Genetics|October 26, 2022
A founder event causing a dominant childhood epilepsy survives 800 years through weak selective pressureBronwyn E Grinton, Erandee Robertson, Liam G Fearnley, et al.
The Journal of Pathology|July 16, 2020
H3K27me3 expression and methylation status in histological variants of malignant peripheral nerve sheath tumoursIben Lyskjaer, Daniel Lindsay, Roberto Tirabosco, et al.
Nature Communications|December 4, 2021
Therapeutic vulnerability to PARP1,2 inhibition in RB1-mutant osteosarcomaGeorgia Zoumpoulidou, Carlos Alvarez-Mendoza, Caterina Mancusi, et al.
Thorax|March 12, 2014
Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health SurveyAndré F S Amaral, Adaikalavan Ramasamy, Francesc Castro-Giner, et al.
Endocrine-Related Cancer|July 19, 2021
Whole-genome sequencing of single circulating tumor cells from neuroendocrine neoplasmsAlexa Childs, Christopher D Steele, Clare Vesely, et al.
Human Molecular Genetics|January 3, 2012
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNPSimon Mead, James Uphill, John Beck, et al.
Forensic Science International|November 8, 2016
A comment on the PCAST report: Skip the "match"/"non-match" stageGeoffrey Stewart Morrison, David H Kaye, David J Balding, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Tobacco smoke carcinogens exacerbate APOBEC mutagenesis and carcinogenesisCameron Durfee, Erik N Bergstrom, Marcos Díaz-Gay, et al.
The New England Journal of Medicine|January 7, 2011
AIP mutation in pituitary adenomas in the 18th century and todayHarvinder S Chahal, Karen Stals, Martina Unterländer, et al.
Nature|February 13, 2007
A genome-wide association study identifies novel risk loci for type 2 diabetesRobert Sladek, Ghislain Rocheleau, Johan Rung, et al.
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