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European Journal of Human Genetics : EJHG|January 15, 2021
Extension of SKAT to multi-category phenotypes through a geometrical interpretationOzvan Bocher, Gaelle Marenne, Elisabeth Tournier-Lasserve, et al.Annals of Neurology|October 4, 2021
End-Truncated LAMB1 Causes a Hippocampal Memory Defect and a LeukoencephalopathyChaker Aloui, Dominique Hervé, Gaelle Marenne, et al.JCO Precision Oncology|September 17, 2025
Rare Variants Associated With Pediatric Cancer Treatment-Related Second Malignant Neoplasm RiskClaire Ducos, Brice Fresneau, Filippo Rosselli, et al.Nature Genetics|April 12, 2016
Mosaic loss of chromosome Y is associated with common variation near TCL1AWeiyin Zhou, Mitchell J Machiela, Neal D Freedman, et al.The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.Nature Genetics|May 8, 2012
Detectable clonal mosaicism and its relationship to aging and cancerKevin B Jacobs, Meredith Yeager, Weiyin Zhou, et al.Wellcome Open Research|September 16, 2024
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritizationSara M Willems, Natasha H J Ng, Juan Fernandez, et al.Pageof 1