Author
Listed:
- Anubha Mahajan
- Xueling Sim
- Hui Jin Ng
- Alisa Manning
- Manuel A Rivas
- Heather M Highland
- Adam E Locke
- Niels Grarup
- Hae Kyung Im
- Pablo Cingolani
- Jason Flannick
- Pierre Fontanillas
- Christian Fuchsberger
- Kyle J Gaulton
- Tanya M Teslovich
- N William Rayner
- Neil R Robertson
- Nicola L Beer
- Jana K Rundle
- Jette Bork-Jensen
- Claes Ladenvall
- Christine Blancher
- David Buck
- Gemma Buck
- Noël P Burtt
- Stacey Gabriel
- Anette P Gjesing
- Christopher J Groves
- Mette Hollensted
- Jeroen R Huyghe
- Anne U Jackson
- Goo Jun
- Johanne Marie Justesen
- Massimo Mangino
- Jacquelyn Murphy
- Matt Neville
- Robert Onofrio
- Kerrin S Small
- Heather M Stringham
- Ann-Christine Syvänen
- Joseph Trakalo
- Goncalo Abecasis
- Graeme I Bell
- John Blangero
- Nancy J Cox
- Ravindranath Duggirala
- Craig L Hanis
- Mark Seielstad
- James G Wilson
- Cramer Christensen
- Ivan Brandslund
- Rainer Rauramaa
- Gabriela L Surdulescu
- Alex S F Doney
- Lars Lannfelt
- Allan Linneberg
- Bo Isomaa
- Tiinamaija Tuomi
- Marit E Jørgensen
- Torben Jørgensen
- Johanna Kuusisto
- Matti Uusitupa
- Veikko Salomaa
- Timothy D Spector
- Andrew D Morris
- Colin N A Palmer
- Francis S Collins
- Karen L Mohlke
- Richard N Bergman
- Erik Ingelsson
- Lars Lind
- Jaakko Tuomilehto
- Torben Hansen
- Richard M Watanabe
- Inga Prokopenko
- Josee Dupuis
- Fredrik Karpe
- Leif Groop
- Markku Laakso
- Oluf Pedersen
- Jose C Florez
- Andrew P Morris
- David Altshuler
- James B Meigs
- Michael Boehnke
- Mark I McCarthy
- Cecilia M Lindgren
- Anna L Gloyn
- On Behalf of the T2D-GENES consortium and GoT2D consortium
Abstract
Genome wide association studies (GWAS) for fasting glucose (FG) and insulin (FI) have identified common variant signals which explain 4.8% and 1.2% of trait variance, respectively. It is hypothesized that low-frequency and rare variants could contribute substantially to unexplained genetic variance. To test this, we analyzed exome-array data from up to 33,231 non-diabetic individuals of European ancestry. We found exome-wide significant (P
Suggested Citation
Anubha Mahajan & Xueling Sim & Hui Jin Ng & Alisa Manning & Manuel A Rivas & Heather M Highland & Adam E Locke & Niels Grarup & Hae Kyung Im & Pablo Cingolani & Jason Flannick & Pierre Fontanillas & C, 2015.
"Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus,"
PLOS Genetics, Public Library of Science, vol. 11(1), pages 1-25, January.
Handle:
RePEc:plo:pgen00:1004876
DOI: 10.1371/journal.pgen.1004876
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