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Nature Genetics|August 29, 2022
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibilityAleksejs Sazonovs, Christine R Stevens, Guhan R Venkataraman, et al.Nature Communications|June 10, 2021
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomesJulia K Goodrich, Moriel Singer-Berk, Rachel Son, et al.Nature|May 24, 2019
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controlsJason Flannick, Josep M Mercader, Christian Fuchsberger, et al.American Journal of Human Genetics|December 21, 2021
Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomesGeorge Hindy, Peter Dornbos, Mark D Chaffin, et al.Diabetes|March 26, 2017
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.Scientific Data|January 24, 2018
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.Nature|July 12, 2016
The genetic architecture of type 2 diabetesChristian Fuchsberger, Jason Flannick, Tanya M Teslovich, et al.Scientific Data|December 20, 2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.Pageof 24