Associated Papers
ONECUT1 variants beyond type 1 and type 2 diabetes: exploring clinical diversity and epigenetic associations in Arab cohorts.
Dashti M et al.
Frontiers in Genetics, 2023
Contribution of ONECUT1 variants to different forms of non-autoimmune diabetes mellitus in Italian patients.
Prudente S et al.
Acta Diabetologica, 2022
Mutations and variants of ONECUT1 in diabetes.
Philippi A et al.
Nature Medicine, 2021
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_S2.xlsx › Somatic_TSG_allVariants_
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
29449575 (PubMed )
Supplement: 41467_2017_2688_MOESM20_ESM.xlsx › b__Freq_TP096
Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.
Kaartokallio T et al.
Scientific Reports, 2016
27384325 (PubMed )
Supplement: srep29085-s2.xls › Sheet1
Hepatocyte nuclear factor-6: associations between genetic variability and type II diabetes and between genetic variability and estimates of insulin secretion.
Møller AM et al.
Diabetologia, 1999
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