Associated Papers
Whole Exome Sequencing Identifies Damaging Variants in Indonesians with Clefts.
Aladenika E et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2025
TULP4, a novel E3 ligase gene, participates in neuronal migration as a candidate in schizophrenia.
Bi Y et al.
Cns Neuroscience & Therapeutics, 2023
PROM1, CXCL8, RUNX1, NAV1 and TP73 genes as independent markers predictive of prognosis or response to treatment in two cohorts of high-grade serous ovarian cancer patients.
Dansonka-Mieszkowska A et al.
Plos One, 2022
35867729 (PubMed )
Supplement: pone.0271539.s007.xlsx › All.SNPs.49.genes_val.coh.
Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency.
Kinjo K et al.
Scientific Reports, 2020
32620854 (PubMed )
Supplement: 41598_2020_67715_MOESM2_ESM.xlsx › Supplementary_Table_1
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