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Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> 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.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.Nature Genetics|November 24, 2020
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individualsPraveen Surendran, Elena V Feofanova, Najim Lahrouchi, et al.Nature Genetics|February 20, 2019
Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distributionAnne E Justice, Tugce Karaderi, Heather M Highland, 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.Nature Genetics|May 13, 2022
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translationAnubha Mahajan, Cassandra N Spracklen, Weihua Zhang, et al.Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complicationsKen Suzuki, Konstantinos Hatzikotoulas, Lorraine Southam, et al.Nature|February 2, 2017
Rare and low-frequency coding variants alter human adult heightEirini Marouli, Mariaelisa Graff, Carolina Medina-Gomez, et al.Pageof 21