Associated Papers
Structural insights into tRNA recognition of the human FTSJ1-THADA complex.
Ishiguro K et al.
Communications Biology, 2025
Examining patient-specific responses to PARP inhibitors in a novel, human induced pluripotent stem cell-based model of breast cancer.
Weddle CJ et al.
Npj Precision Oncology, 2025
Type 2 Diabetes-Related Variants Influence the Risk of Developing Prostate Cancer: A Population-Based Case-Control Study and Meta-Analysis.
Sánchez-Maldonado JM et al.
Cancers, 2022
Replication study of THADA rs13429458 variant with PCOS susceptibility and its related traits in Indian women.
Dadachanji R et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2021
Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis.
Vujkovic M et al.
Nature Genetics, 2020
Progress in defining the genetic contribution to type 2 diabetes susceptibility.
Morris AP
Current Opinion in Genetics & Development, 2018
Functional annotation of sixty-five type-2 diabetes risk SNPs and its application in risk prediction.
Wu Y et al.
Scientific Reports, 2017
Uniparental disomy causes deficiencies of vitamin K-dependent proteins.
Dasi MA et al.
Journal of Thrombosis and Haemostasis : Jth, 2016
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
A common variant within the HNF1B gene is associated with overall survival of multiple myeloma patients: results from the IMMEnSE consortium and meta-analysis.
Ríos-Tamayo R et al.
Oncotarget, 2016
Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Samorodnitsky E et al.
Human Mutation, 2015
Type 2 diabetes-related variants influence the risk of developing multiple myeloma: results from the IMMEnSE consortium.
Ríos R et al.
Endocrine-related Cancer, 2015
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
Vascular associated gene variants in patients with preeclampsia: results from the Danish National Birth Cohort.
Lykke JA et al.
Acta Obstetricia Et Gynecologica Scandinavica, 2012
Is genetic testing useful to predict type 2 diabetes?
Vassy JL et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2012
Association analysis of 31 common polymorphisms with type 2 diabetes and its related traits in Indian sib pairs.
Gupta V et al.
Diabetologia, 2012
Type 2 diabetes risk variants and colorectal cancer risk: the Multiethnic Cohort and PAGE studies.
Cheng I et al.
Gut, 2011
Genetics of type 2 diabetes: the GWAS era and future perspectives [Review].
Imamura M et al.
Endocrine Journal, 2011
Physiologic characterization of type 2 diabetes-related loci.
Grarup N et al.
Current Diabetes Reports, 2010
Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study.
Morgan AR et al.
Bmc Medical Genetics, 2010
Gene variants in the novel type 2 diabetes loci CDC123/CAMK1D, THADA, ADAMTS9, BCL11A, and MTNR1B affect different aspects of pancreatic beta-cell function.
Simonis-Bik AM et al.
Diabetes, 2010
Genomics of type 2 diabetes mellitus: implications for the clinician.
Stolerman ES et al.
Nature Reviews. Endocrinology, 2009
Genetics of diabetic nephropathy: are there clues to the understanding of common kidney diseases?
Conway BR et al.
Nephron. Clinical Practice, 2009
Clinical review: the genetics of type 2 diabetes: a realistic appraisal in 2008.
Florez JC
The Journal of Clinical Endocrinology and Metabolism, 2008
Novel meta-analysis-derived type 2 diabetes risk loci do not determine prediabetic phenotypes.
Staiger H et al.
Plos One, 2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.
Zeggini E et al.
Nature Genetics, 2008