Associated Papers
Quantitative thresholds for variant enrichment in 13,845 cases: improving pathogenicity classification in genetic hearing loss.
Liu S et al.
Genome Medicine, 2023
38111038 (PubMed )
Supplement: 13073_2023_1271_MOESM1_ESM.xlsx › Table_S7
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.
Bateman NW et al.
Iscience, 2022
35036865 (PubMed )
Supplement: mmc2.xlsx › SupplementalTable1A
Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis.
Cheung AC et al.
Journal of Hepatology, 2017
Reply to: "Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis".
Grammatikopoulos T et al.
Journal of Hepatology, 2017
Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.
Venkatesh SK et al.
Journal of Human Genetics, 2013
An examination of candidate gene SNPs for dyslexia in an Indian sample.
Venkatesh SK et al.
Behavior Genetics, 2011
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