Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Originally published in Science Express on 26 April 2007
Science 1 June 2007:
Vol. 316. no. 5829, pp. 1331 - 1336
DOI: 10.1126/science.1142358

Reports

Genome-Wide Association Analysis Identifies Loci for Type 2 Diabetes and Triglyceride Levels

Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research: *{dagger} Richa Saxena,1,2,3,4,5,6 Benjamin F. Voight,1,2,3,5 Valeriya Lyssenko,7 Noël P. Burtt,1 Paul I. W. de Bakker,1,2,3,4,5,6 Hong Chen,8 Jeffrey J. Roix,8 Sekar Kathiresan,1,3,5 Joel N. Hirschhorn,1,6,9,10,11 Mark J. Daly,1,2,3,5 Thomas E. Hughes,8 Leif Groop,7,12 David Altshuler,1,2,3,4,5,6 Peter Almgren,7 Jose C. Florez,1,2,3,4,5,6 Joanne Meyer,8 Kristin Ardlie,1 Kristina Bengtsson Boström,13 Bo Isomaa,14,15 Guillaume Lettre,1,6,9,10,11 Ulf Lindblad,16 Helen N. Lyon,1,6,9,10,11 Olle Melander,7 Christopher Newton-Cheh,1,2,3,5 Peter Nilsson,17 Marju Orho-Melander,7 Lennart Råstam,16 Elizabeth K. Speliotes,1,3,6,9,10,11 Marja-Riitta Taskinen,12 Tiinamaija Tuomi,12,15 Candace Guiducci,1 Anna Berglund,7 Joyce Carlson,18 Lauren Gianniny,1 Rachel Hackett,1 Liselotte Hall,18 Johan Holmkvist,7 Esa Laurila,7 Marketa Sjögren,7 Maria Sterner,18 Aarti Surti,1 Margareta Svensson,7 Malin Svensson,7 Ryan Tewhey,1 Brendan Blumenstiel,1 Melissa Parkin,1 Matthew DeFelice,1 Rachel Barry,1 Wendy Brodeur,1 Jody Camarata,1 Nancy Chia,1 Mary Fava,1 John Gibbons,1 Bob Handsaker,1 Claire Healy,1 Kieu Nguyen,1 Casey Gates,1 Carrie Sougnez,1 Diane Gage,1 Marcia Nizzari,1 Stacey B. Gabriel,1 Gung-Wei Chirn,8 Qicheng Ma,8 Hemang Parikh,7 Delwood Richardson,8 Darrell Ricke,8 Shaun Purcell1,2,19

New strategies for prevention and treatment of type 2 diabetes (T2D) require improved insight into disease etiology. We analyzed 386,731 common single-nucleotide polymorphisms (SNPs) in 1464 patients with T2D and 1467 matched controls, each characterized for measures of glucose metabolism, lipids, obesity, and blood pressure. With collaborators (FUSION and WTCCC/UKT2D), we identified and confirmed three loci associated with T2D—in a noncoding region near CDKN2A and CDKN2B, in an intron of IGF2BP2, and an intron of CDKAL1—and replicated associations near HHEX and in SLC30A8 found by a recent whole-genome association study. We identified and confirmed association of a SNP in an intron of glucokinase regulatory protein (GCKR) with serum triglycerides. The discovery of associated variants in unsuspected genes and outside coding regions illustrates the ability of genome-wide association studies to provide potentially important clues to the pathogenesis of common diseases.

1 Broad Institute of Harvard and Massachusetts Institute of Technology (MIT), Cambridge, MA 02142, USA.
2 Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA.
3 Department of Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.
4 Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA.
5 Department of Medicine, Harvard Medical School, Boston, MA 02115, USA.
6 Department of Genetics, Harvard Medical School, Boston, MA 02115, USA.
7 Department of Clinical Sciences, Diabetes and Endocrinology Research Unit, University Hospital Malmö, Lund University, Malmö, Sweden.
8 Diabetes and Metabolism Disease Area, Novartis Institutes for BioMedical Research, 100 Technology Square, Cambridge, MA 02139, USA.
9 Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.
10 Division of Endocrinology, Children’s Hospital, Boston, MA 02115, USA.
11 Division of Genetics, Children’s Hospital, Boston, MA 02115, USA.
12 Department of Medicine, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
13 Skaraborg Institute, Skövde, Sweden.
14 Malmska Municipal Health Center and Hospital, Jakobstad, Finland.
15 Folkhälsan Research Center, Helsinki, Finland.
16 Department of Clinical Sciences, Community Medicine Research Unit, University Hospital Malmö, Lund University, Malmö, Sweden.
17 Department of Clinical Sciences, Medicine Research Unit, University Hospital Malmö, Lund University, Malmö, Sweden.
18 Clinical Chemistry, University Hospital Malmö, Lund University, Malmö, Sweden.
19 Department of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02115, USA.

{dagger} All authors with their contributions and affiliations appear at the end of this paper.

* To whom correspondence should be addressed: David Altshuler, Leif Groop, Thomas E. Hughes. E-mail: altshuler{at}molbio.mgh.harvard.edu (D.A.); leif.groop{at}med.lu.se (L.G.); thomase.hughes{at}novartis.com (T.E.H.)

Read the Full Text


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
The search for genes contributing to endometriosis risk.
G. W. Montgomery, D. R. Nyholt, Z. Z. Zhao, S. A. Treloar, J. N. Painter, S. A. Missmer, S. H. Kennedy, and K. T. Zondervan (2008)
Hum. Reprod. Update 14, 447-457
   Abstract »    Full Text »    PDF »
Systematic biological prioritization after a genome-wide association study: an application to nicotine dependence.
S. F. Saccone, N. L. Saccone, G. E. Swan, P. A. F. Madden, A. M. Goate, J. P. Rice, and L. J. Bierut (2008)
Bioinformatics 24, 1805-1811
   Abstract »    PDF »
An apolipoprotein A-V gene SNP is associated with marked hypertriglyceridemia among Asian-American patients.
C. R. Pullinger, B. E. Aouizerat, I. Movsesyan, V. Durlach, E. J. Sijbrands, K. Nakajima, A. Poon, G. M. Dallinga-Thie, H. Hattori, L. L. Green, et al. (2008)
J. Lipid Res. 49, 1846-1854
   Abstract »    Full Text »    PDF »
Evidence that the gene encoding insulin degrading enzyme influences human lifespan.
M.-G. Hong, C. Reynolds, M. Gatz, B. Johansson, J. C. Palmer, H. F. Gu, K. Blennow, P. G. Kehoe, U. de Faire, N. L. Pedersen, et al. (2008)
Hum. Mol. Genet. 17, 2370-2378
   Abstract »    Full Text »    PDF »
Replication of Genome-Wide Association Studies of Type 2 Diabetes Susceptibility in Japan.
Y. Horikawa, K. Miyake, K. Yasuda, M. Enya, Y. Hirota, K. Yamagata, Y. Hinokio, Y. Oka, N. Iwasaki, Y. Iwamoto, et al. (2008)
J. Clin. Endocrinol. Metab. 93, 3136-3141
   Abstract »    Full Text »    PDF »
Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology.
P. R Burton, A. L Hansell, I. Fortier, T. A Manolio, M. J Khoury, J. Little, and P. Elliott (2008)
Int. J. Epidemiol.
   Abstract »    Full Text »    PDF »
Association Analysis in African Americans of European-Derived Type 2 Diabetes Single Nucleotide Polymorphisms From Whole-Genome Association Studies.
J. P. Lewis, N. D. Palmer, P. J. Hicks, M. M. Sale, C. D. Langefeld, B. I. Freedman, J. Divers, and D. W. Bowden (2008)
Diabetes 57, 2220-2225
   Abstract »    Full Text »    PDF »
Implication of Genetic Variants Near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in Type 2 Diabetes and Obesity in 6,719 Asians.
M. C.Y. Ng, K. S. Park, B. Oh, C. H.T. Tam, Y. M. Cho, H. D. Shin, V. K.L. Lam, R. C.W. Ma, W. Y. So, Y. S. Cho, et al. (2008)
Diabetes 57, 2226-2233
   Abstract »    Full Text »    PDF »
Common Variation in the Fat Mass and Obesity-Associated (FTO) Gene Confers Risk of Obesity and Modulates BMI in the Chinese Population.
Y.-C. Chang, P.-H. Liu, W.-J. Lee, T.-J. Chang, Y.-D. Jiang, H.-Y. Li, S.-S. Kuo, K.-C. Lee, and L.-M. Chuang (2008)
Diabetes 57, 2245-2252
   Abstract »    Full Text »    PDF »
The Common P446L Polymorphism in GCKR Inversely Modulates Fasting Glucose and Triglyceride Levels and Reduces Type 2 Diabetes Risk in the DESIR Prospective General French Population.
M. Vaxillaire, C. Cavalcanti-Proenca, A. Dechaume, J. Tichet, M. Marre, B. Balkau, P. Froguel, and for the DESIR Study Group (2008)
Diabetes 57, 2253-2257
   Abstract »    Full Text »    PDF »
Gaining Insights in Coronary Disease Genomics.
S. S. Murray and E. J. Topol (2008)
J. Am. Coll. Cardiol. 52, 385-386
   Full Text »    PDF »
Fetuin-A and Incident Diabetes Mellitus in Older Persons.
J. H. Ix, C. L. Wassel, A. M. Kanaya, E. Vittinghoff, K. C. Johnson, A. Koster, J. A. Cauley, T. B. Harris, S. R. Cummings, M. G. Shlipak, et al. (2008)
JAMA 300, 182-188
   Abstract »    Full Text »    PDF »
Approaches for Unraveling the Joint Genetic Determinants of Schizophrenia and Bipolar Disorder.
P.-I Lin and B. D. Mitchell (2008)
Schizophr Bull 34, 791-797
   Abstract »    Full Text »    PDF »
Haplotype Structure of the ENPP1 Gene and Nominal Association of the K121Q Missense Single Nucleotide Polymorphism With Glycemic Traits in the Framingham Heart Study.
E. S. Stolerman, A. K. Manning, J. B. McAteer, J. Dupuis, C. S. Fox, L. A. Cupples, J. B. Meigs, and J. C. Florez (2008)
Diabetes 57, 1971-1977
   Abstract »    Full Text »    PDF »
Association Analysis of Type 2 Diabetes Loci in Type 1 Diabetes.
H.-Q. Qu, S. F.A. Grant, J. P. Bradfield, C. Kim, E. Frackelton, H. Hakonarson, and C. Polychronakos (2008)
Diabetes 57, 1983-1986
   Abstract »    Full Text »    PDF »
Evaluation of the Association of IGF2BP2 Variants With Type 2 Diabetes in French Caucasians.
K. Duesing, G. Fatemifar, G. Charpentier, M. Marre, J. Tichet, S. Hercberg, B. Balkau, P. Froguel, and F. Gibson (2008)
Diabetes 57, 1992-1996
   Abstract »    Full Text »    PDF »
Microarray Technology and Applications in the Arena of Genome-Wide Association.
S. F. A. Grant and H. Hakonarson (2008)
Clin. Chem. 54, 1116-1124
   Abstract »    Full Text »    PDF »
The Genetic Architecture of Intracerebral Hemorrhage.
N. S. Rost, S. M. Greenberg, and J. Rosand (2008)
Stroke 39, 2166-2173
   Abstract »    Full Text »    PDF »
Genome-wide association scans identified CTNNBL1 as a novel gene for obesity.
Y.-J. Liu, X.-G. Liu, L. Wang, C. Dina, H. Yan, J.-F. Liu, S. Levy, C. J. Papasian, B. M. Drees, J. J. Hamilton, et al. (2008)
Hum. Mol. Genet. 17, 1803-1813
   Abstract »    Full Text »    PDF »
SNPing away at sickle cell pathophysiology.
M. H. Steinberg (2008)
Blood 111, 5420-5421
   Full Text »    PDF »
A meta-analysis of QTL for diabetes-related traits in rodents.
C. Schmidt, N. P. Gonzaludo, S. Strunk, S. Dahm, J. Schuchhardt, F. Kleinjung, S. Wuschke, H.-G. Joost, and H. Al-Hasani (2008)
Physiol Genomics 34, 42-53
   Abstract »    Full Text »    PDF »
Mitochondria as Chi.
D. C. Wallace (2008)
Genetics 179, 727-735
   Full Text »    PDF »
Common Variants in Maturity-Onset Diabetes of the Young Genes and Future Risk of Type 2 Diabetes.
J. Holmkvist, P. Almgren, V. Lyssenko, C. M. Lindgren, K.-F. Eriksson, B. Isomaa, T. Tuomi, P. Nilsson, and L. Groop (2008)
Diabetes 57, 1738-1744
   Abstract »    Full Text »    PDF »
Molecular correlates for maximal oxygen uptake and type 1 fibers.
H. Parikh, E. Nilsson, C. Ling, P. Poulsen, P. Almgren, H. Nittby, K.-F. Eriksson, A. Vaag, and L. C. Groop (2008)
Am J Physiol Endocrinol Metab 294, E1152-E1159
   Abstract »    Full Text »    PDF »
A Polymorphism Within the G6PC2 Gene Is Associated with Fasting Plasma Glucose Levels.
N. Bouatia-Naji, G. Rocheleau, L. Van Lommel, K. Lemaire, F. Schuit, C. Cavalcanti-Proenca, M. Marchand, A.-L. Hartikainen, U. Sovio, F. De Graeve, et al. (2008)
Science 320, 1085-1088
   Abstract »    Full Text »    PDF »
The complex genetics of multiple sclerosis: pitfalls and prospects.
S. Sawcer (2008)
Brain
   Abstract »    Full Text »    PDF »
Glucolipotoxicity: Fuel Excess and {beta}-Cell Dysfunction.
V. Poitout and R. P. Robertson (2008)
Endocr. Rev. 29, 351-366
   Abstract »    Full Text »    PDF »
Cytokines and {beta}-Cell Biology: from Concept to Clinical Translation.
M. Y. Donath, J. Storling, L. A. Berchtold, N. Billestrup, and T. Mandrup-Poulsen (2008)
Endocr. Rev. 29, 334-350
   Abstract »    Full Text »    PDF »
Monogenic Diabetes in the Young, Pharmacogenetics and Relevance to Multifactorial Forms of Type 2 Diabetes.
M. Vaxillaire and P. Froguel (2008)
Endocr. Rev. 29, 254-264
   Abstract »    Full Text »    PDF »
Single-Nucleotide Polymorphism rs7754840 of CDKAL1 Is Associated with Impaired Insulin Secretion in Nondiabetic Offspring of Type 2 Diabetic Subjects and in a Large Sample of Men with Normal Glucose Tolerance.
A. Stancakova, J. Pihlajamaki, J. Kuusisto, N. Stefan, A. Fritsche, H. Haring, F. Andreozzi, E. Succurro, G. Sesti, T. W. Boesgaard, et al. (2008)
J. Clin. Endocrinol. Metab. 93, 1924-1930
   Abstract »    Full Text »    PDF »
Insulin Stimulates Primary {beta}-Cell Proliferation via Raf-1 Kinase.
J. L. Beith, E. U. Alejandro, and J. D. Johnson (2008)
Endocrinology 149, 2251-2260
   Abstract »    Full Text »    PDF »
A gene expression network model of type 2 diabetes links cell cycle regulation in islets with diabetes susceptibility.
M. P. Keller, Y. Choi, P. Wang, D. Belt Davis, M. E. Rabaglia, A. T. Oler, D. S. Stapleton, C. Argmann, K. L. Schueler, S. Edwards, et al. (2008)
Genome Res. 18, 706-716
   Abstract »    Full Text »    PDF »
Common Variation in the FTO Gene Alters Diabetes-Related Metabolic Traits to the Extent Expected Given Its Effect on BMI.
R. M. Freathy, N. J. Timpson, D. A. Lawlor, A. Pouta, Y. Ben-Shlomo, A. Ruokonen, S. Ebrahim, B. Shields, E. Zeggini, M. N. Weedon, et al. (2008)
Diabetes 57, 1419-1426
   Abstract »    Full Text »    PDF »
Genetic Similarities Between Latent Autoimmune Diabetes in Adults, Type 1 Diabetes, and Type 2 Diabetes.
C. Cervin, V. Lyssenko, E. Bakhtadze, E. Lindholm, P. Nilsson, T. Tuomi, C. M. Cilio, and L. Groop (2008)
Diabetes 57, 1433-1437
   Abstract »    Full Text »    PDF »
Whole Genome Analyses Suggest Ischemic Stroke and Heart Disease Share an Association With Polymorphisms on Chromosome 9p21.
M. Matarin, W. M. Brown, A. Singleton, J. A. Hardy, J. F. Meschia, and for the ISGS investigators (2008)
Stroke 39, 1586-1589
   Abstract »    Full Text »    PDF »
Schizophrenia Candidate Genes: Are We Really Coming Up Blank?.
S. P. Hamilton (2008)
Am J Psychiatry 165, 420-423
   Full Text »    PDF »
No Significant Association of 14 Candidate Genes With Schizophrenia in a Large European Ancestry Sample: Implications for Psychiatric Genetics.
A. R. Sanders, J. Duan, D. F. Levinson, J. Shi, D. He, C. Hou, G. J. Burrell, J. P. Rice, D. A. Nertney, A. Olincy, et al. (2008)
Am J Psychiatry 165, 497-506
   Abstract »    Full Text »    PDF »
A survey of allelic imbalance in F1 mice.
C. D. Campbell, A. Kirby, J. Nemesh, M. J. Daly, and J. N. Hirschhorn (2008)
Genome Res. 18, 555-563
   Abstract »    Full Text »    PDF »
The ENPP1 K121Q Polymorphism Is Associated With Type 2 Diabetes in European Populations: Evidence From an Updated Meta-Analysis in 42,042 Subjects.
J. B. McAteer, S. Prudente, S. Bacci, H. N. Lyon, J. N. Hirschhorn, V. Trischitta, J. C. Florez, and for the ENPP1 Consortium (2008)
Diabetes 57, 1125-1130
   Abstract »    Full Text »    PDF »
Association of Variants in the Sterol Regulatory Element-Binding Factor 1 (SREBF1) Gene With Type 2 Diabetes, Glycemia, and Insulin Resistance: A Study of 15,734 Danish Subjects.
N. Grarup, K. L. Stender-Petersen, E. A. Andersson, T. Jorgensen, K. Borch-Johnsen, A. Sandbaek, T. Lauritzen, O. Schmitz, T. Hansen, and O. Pedersen (2008)
Diabetes 57, 1136-1142
   Abstract »    Full Text »    PDF »
A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study.
H. Hakonarson, H.-Q. Qu, J. P. Bradfield, L. Marchand, C. E. Kim, J. T. Glessner, R. Grabs, T. Casalunovo, S. P. Taback, E. C. Frackelton, et al. (2008)
Diabetes 57, 1143-1146
   Abstract »    Full Text »    PDF »
Quantitative Trait Analysis of Type 2 Diabetes Susceptibility Loci Identified From Whole Genome Association Studies in the Insulin Resistance Atherosclerosis Family Study.
N. D. Palmer, M. O. Goodarzi, C. D. Langefeld, J. Ziegler, J. M. Norris, S. M. Haffner, M. Bryer-Ash, R. N. Bergman, L. E. Wagenknecht, K. D. Taylor, et al. (2008)
Diabetes 57, 1093-1100
   Abstract »    Full Text »    PDF »
Genetic Variants of FTO Influence Adiposity, Insulin Sensitivity, Leptin Levels, and Resting Metabolic Rate in the Quebec Family Study.
R. Do, S. D. Bailey, K. Desbiens, A. Belisle, A. Montpetit, C. Bouchard, L. Perusse, M.-C. Vohl, and J. C. Engert (2008)
Diabetes 57, 1147-1150
   Abstract »    Full Text »    PDF »
Polymorphisms Associated with Cholesterol and Risk of Cardiovascular Events.
S. Kathiresan, O. Melander, D. Anevski, C. Guiducci, N. P. Burtt, C. Roos, J. N. Hirschhorn, G. Berglund, B. Hedblad, L. Groop, et al. (2008)
N. Engl. J. Med. 358, 1240-1249
   Abstract »    Full Text »    PDF »
How to Interpret a Genome-wide Association Study.
T. A. Pearson and T. A. Manolio (2008)
JAMA 299, 1335-1344
   Abstract »    Full Text »    PDF »
Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
H. M. Broadbent, J. F. Peden, S. Lorkowski, A. Goel, H. Ongen, F. Green, R. Clarke, R. Collins, M. G. Franzosi, G. Tognoni, et al. (2008)
Hum. Mol. Genet. 17, 806-814
   Abstract »    Full Text »    PDF »
The HapMap: Charting a Course for Genetic Discovery in Neurological Diseases.
J. Hardy and A. Singleton (2008)
Arch Neurol 65, 319-321
   Abstract »    Full Text »    PDF »
Defining Pancreatic Endocrine Precursors and Their Descendants.
P. White, C. Lee May, R. N. Lamounier, J. E. Brestelli, and K. H. Kaestner (2008)
Diabetes 57, 654-668
   Abstract »    Full Text »    PDF »
Association of CDKAL1, IGF2BP2, CDKN2A/B, HHEX, SLC30A8, and KCNJ11 With Susceptibility to Type 2 Diabetes in a Japanese Population.
S. Omori, Y. Tanaka, A. Takahashi, H. Hirose, A. Kashiwagi, K. Kaku, R. Kawamori, Y. Nakamura, and S. Maeda (2008)
Diabetes 57, 791-795
   Abstract »    Full Text »    PDF »
High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.
N. Kato, T. Miyata, Y. Tabara, T. Katsuya, K. Yanai, H. Hanada, K. Kamide, J. Nakura, K. Kohara, F. Takeuchi, et al. (2008)
Hum. Mol. Genet. 17, 617-627
   Abstract »    Full Text »    PDF »
The Role for Endoplasmic Reticulum Stress in Diabetes Mellitus.
D. L. Eizirik, A. K. Cardozo, and M. Cnop (2008)
Endocr. Rev. 29, 42-61
   Abstract »    Full Text »    PDF »
Four SNPs on Chromosome 9p21 in a South Korean Population Implicate a Genetic Locus That Confers High Cross-Race Risk for Development of Coronary Artery Disease.
G.-Q. Shen, L. Li, S. Rao, K. G. Abdullah, J. M. Ban, B.-S. Lee, J. E. Park, and Q. K. Wang (2008)
Arterioscler. Thromb. Vasc. Biol. 28, 360-365
   Abstract »    Full Text »    PDF »
Assessment of cumulative evidence on genetic associations: interim guidelines.
J. P. Ioannidis, P. Boffetta, J. Little, T. R O'Brien, A. G Uitterlinden, P. Vineis, D. J Balding, A. Chokkalingam, S. M Dolan, W D. Flanders, et al. (2008)
Int. J. Epidemiol. 37, 120-132
   Abstract »    Full Text »    PDF »
Commentary: Genetic association studies see light at the end of the tunnel.
T. M Frayling (2008)
Int. J. Epidemiol. 37, 133-135
   Full Text »    PDF »
A Candidate Type 2 Diabetes Polymorphism Near the HHEX Locus Affects Acute Glucose-Stimulated Insulin Release in European Populations: Results from the EUGENE2 study.
H. Staiger, A. Stancakova, J. Zilinskaite, M. Vanttinen, T. Hansen, M. A. Marini, A. Hammarstedt, P.-A. Jansson, G. Sesti, U. Smith, et al. (2008)
Diabetes 57, 514-517
   Abstract »    Full Text »    PDF »
Rationale, Design, and Methodology of the Women's Genome Health Study: A Genome-Wide Association Study of More Than 25 000 Initially Healthy American Women.
P. M Ridker, D. I. Chasman, R. Y.L. Zee, A. Parker, L. Rose, N. R. Cook, J. E Buring, and for the Women's Genome Health Study Working Group (2008)
Clin. Chem. 54, 249-255
   Abstract »    Full Text »    PDF »
Update on the Genetics of Stroke and Cerebrovascular Disease 2007.
R. A. Hegele and M. Dichgans (2008)
Stroke 39, 252-254
   Full Text »    PDF »
Required sample size and nonreplicability thresholds for heterogeneous genetic associations.
R. Moonesinghe, M. J. Khoury, T. Liu, and J. P. A. Ioannidis (2008)
PNAS 105, 617-622
   Abstract »    Full Text »    PDF »
Polymorphisms in the IDE-KIF11-HHEX Gene Locus Are Reproducibly Associated with Type 2 Diabetes in a Japanese Population.
Y. Furukawa, T. Shimada, H. Furuta, S. Matsuno, A. Kusuyama, A. Doi, M. Nishi, H. Sasaki, T. Sanke, and K. Nanjo (2008)
J. Clin. Endocrinol. Metab. 93, 310-314
   Abstract »    Full Text »    PDF »
Long-Range Enhancers Are Required to Maintain Expression of the Autoantigen Islet-Specific Glucose-6-Phosphatase Catalytic Subunit Related Protein in Adult Mouse Islets In Vivo.
Y. Wang, B. P. Flemming, C. C. Martin, S. R. Allen, J. Walters, J. K. Oeser, J. C. Hutton, and R. M. O'Brien (2008)
Diabetes 57, 133-141
   Abstract »    Full Text »    PDF »
Impact of Common Type 2 Diabetes Risk Polymorphisms in the DESIR Prospective Study.
M. Vaxillaire, J. Veslot, C. Dina, C. Proenca, S. Cauchi, G. Charpentier, J. Tichet, F. Fumeron, M. Marre, D. Meyre, et al. (2008)
Diabetes 57, 244-254
   Abstract »