MR. SITTIDETH SANGNUAL

Molecular Genetics Senior Scientist

” Bridging the gap between people and Reproductive Technology “

WORK EXPERIENCE

CONTACT

EDUCATION

HONORS, PRESENTATIONS, AND WORKSHOPS

1. 1. Gold Medalist of Microbiology Major (the highest-ranking undergraduate), 2010

2. Excellent Science Student Award, Professor Dr. Tab Nilanidhi Foundation for graduates in science nationwide, 2010

3. Sangnual S, Rungroj N, Nettuwakul C, Sawasdee N, Sritippayawan S, Chuawattana D, Yenchitsomanus P. High Resolution Melting Analysis for Detection of SCN10A Gene Mutation in Northeastern Thai Patients with Nephrolithiasis. International Conference in Medicine and Public Health (ICMPH2013), 24-28th June 2013, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok. (3rd prize of oral presentation)

4. Sangnual S, Rungroj N, Nettuwakul C, Sawasdee N, Sritippayawan S, Chuawattana D, Yenchitsomanus P. Analysis of SCN10A gene mutation in Northeastern Thai patients with nephrolithiasis by high resolution melting method. 18th National Genetics Conference 2013
(NGC2013) “Genetics towards ASEAN”, 17-19th July 2013, Ambassador Hotel, Bangkok. (Best prize of oral presentation)

5. Attended “Reproductive and Genetic Health Workshop” held at Mandarin Oriental, Bangkok (2015) organized by illumina

6. Attended “Reproductive and Genetic Health Symposium” held at Le Meridian Hotel, Bangkok (2016) organized by illumina

7. Attended training program “NGS and SNP array for PGT testing” held at Shanghai, China (2017) organized by Unimed Biotech (Shanghai) Co., Ltd.

PUBLICATIONS

1. Sangnual S, Rungroj N, Nettuwakul C, Sawasdee N, Sritippayawan S, Chuawattana D, Yenchitsomanus P. Analysis of SCN10A gene mutation in Northeastern Thai patients with nephrolithiasis by high resolution melting method. Thai J Genet 2013; S(1):87-90.

2. Nettuwakul C, Praditsap O, Sawasdee N, Rungroj N, Ruamyod K, Watanapa WB, Junking M, Sangnual S, Sritippayawan S, Cheunsuchon B, Chuawattana D, Rojsatapong S,Chaowagul W, Dib-Hajj SD, Waxman SG, Yenchitsomanus PT. Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease. Sci Rep. 2018 Jul 11;8(1):10453.

3. Rungroj N, Nettuwakul C, Sawasdee N, Sangnual S, Deejai N, Misgar RA, Pasena A, Khositseth S, Kirdpon S, Sritippayawan S, Vasuvattakul S, Yenchitsomanus PT. Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations. Clin
Genet. 2018 Nov;94(5):409-418.