Author

C. Wungu

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Open access Oct 2026

The impact of angiotensin II type 1 receptor A1166C gene polymorphism on blood pressure levels in patients with hypertension: A cross-sectional study

Background: Hypertension is a condition characterized by elevated blood pressure, posing a risk factor for various cardiovascular diseases (CVDs) with increasing prevalence worldwide. One risk factor for hypertension includes single nucleotide polymorphism (SNP) A1166C (rs5186) in angiotensin II type 1 receptor (AT1R)...

N. Tjipta, Hendri Susilo, C. Wungu et al. · Heart Science Journal · 0 citations

Aug 2026

Computational insights into the regulatory role and functional significance of NOTCH1 intronic SNP rs3124599 and its link to NPC.

BACKGROUND Nasopharyngeal carcinoma (NPC) is a multifactorial disease driven by both genetic and environmental factors. The neurogenic locus notch homolog 1 (NOTCH1) gene has dual oncogenic and tumor-suppressive effects that depend on the cellular context. An intronic single nucleotide polymorphism (SNP) in NOTCH1, rs3...

Mujeeb A. Sultan, A. Romdhoni, C. Wungu et al. · Computational biology and ch... · 0 citations

Open access Jul 2026

Rare VDR variant rs1338135647 and lower vitamin D levels in autism spectrum disorder: An exploratory case-control study in Indonesian children.

Lower vitamin D levels and the rare rs1338135647 variant may independently co-occur with ASD in Indonesian children; however, these hypothesis-generating findings require replication and functional validation in larger independent cohorts.

S. M. Samosir, C. Wungu, R. Noviandi et al. · Biomolecules & biomedicine · 0 citations