Associated Papers
Rare Tumor-Normal Matched Whole Exome Sequencing Identifies Novel Genomic Pathogenic Germline and Somatic Aberrations.
Sprissler R et al.
Cancers, 2020
32570879 (PubMed )
Supplement: cancers-12-01618-s001.zip › cancers-817200-Supplementary_Materials3 › Supplementary_table_S1.xlsx › TSG
Recent advances in understanding the genetic architecture of type 2 diabetes.
Mohlke KL et al.
Human Molecular Genetics, 2015
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.
Hwang JY et al.
Diabetes, 2015
Rare and low-frequency variants in human common diseases and other complex traits.
Lettre G
Journal of Medical Genetics, 2014
Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.
Huyghe JR et al.
Nature Genetics, 2013
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