Oranud Praditsap

Association between Human Prothrombin Variant (T165M) and Kidney Stone Disease

P. Yenchitsomanus, Prapaporn Jungtrakoon, N. Rungroj, 2012, PloS one.

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome

Chumpol Ngamphiw, S. Tongsima, A. Tucker, 2022, Clinical genetics.

Molecular Genetics of Kidney Stone Disease

P. Yenchitsomanus, N. Rungroj, N. Sawasdee, 2014 .

A novel loss-of-function mutation of PBK associated with human kidney stone disease

N. Deejai, W. Chaowagul, P. Yenchitsomanus, 2020, Scientific Reports.

Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease

S. Dib-Hajj, S. Waxman, W. Chaowagul, 2018, Scientific Reports.

A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease

P. Yenchitsomanus, N. Rungroj, S. Sritippayawan, 2014, BMC Medical Genetics.

Meta-analysis of the plasminogen activator inhibitor-1 (PAI-1) gene with insertion/deletion 4G/5G polymorphism and its susceptibility to ischemic stroke in Thai population

N. Sriratanaviriyakul, A. Assawamakin, S. Tongsima, 2012 .