Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes-Reference-Cited by-同舟云学术

Correlation of rare coding variants in the gene encoding human glucokinase regulatory protein with phenotypic, cellular, and kinetic outcomes

Published:2012-01-03 Issue:1 Volume:122 Page:205-217
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Rees Matthew G.,Ng David,Ruppert Sarah,Turner Clesson,Beer Nicola L.,Swift Amy J.,Morken Mario A.,Below Jennifer E.,Blech Ilana,Mullikin James C.,McCarthy Mark I.,Biesecker Leslie G.,Gloyn Anna L.,Collins Francis S.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference63 articles.

1. Genomewide Association Studies and Human Disease

2. Finding the missing heritability of complex diseases

3. Genome-wide association studies: potential next steps on a genetic journey

4. Genome-wide association studies for complex traits: consensus, uncertainty and challenges

5. Rare Variants of IFIH1 , a Gene Implicated in Antiviral Responses, Protect Against Type 1 Diabetes

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Current Insight on the Role of Glucokinase and Glucokinase Regulatory Protein in Diabetes;Mini-Reviews in Medicinal Chemistry;2024-04

2. Glucokinase regulatory protein: a balancing act between glucose and lipid metabolism in NAFLD;Frontiers in Endocrinology;2023-08-29

3. Frequencies of variants in genes associated with dyslipidemias identified in Costa Rican genomes;Frontiers in Genetics;2023-03-30

4. Genotype first: Clinical genomics research through a reverse phenotyping approach;The American Journal of Human Genetics;2023-01

5. A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction;Endocrinology, Diabetes & Metabolism Case Reports;2022-12-01