Wuttichart Kamolvisit

Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impact

Ponghatai Boonsimma, Chupong Ittiwut, Wuttichart Kamolvisit et al. · European Journal of Human Genetics · 2022 · 30 citations · Full text

First-tier Genetic Testing, Exome Sequencing, Genetics +9

Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations

Sermporn Thaweesapphithak, Jirawat Saengsin, Wuttichart Kamolvisit et al. · Journal of Applied Oral Science · 2022 · 19 citations · Full text

Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency

Kitiwan Rojnueangnit, Parisa Maneechai, Patcharapa Thaweekul et al. · European Journal of Medical Genetics · 2020 · 18 citations

Mitochondrial Function, Biochemistry, Natural Sciences +8

Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand

Wuttichart Kamolvisit, Prasit Phowthongkum, Ponghatai Boonsimma et al. · Clinical Genetics · 2021 · 18 citations

Risk factor analysis of pneumothorax associated with persistent pulmonary hypertension of the newborn in Thai neonates

Sutthikiat Jaroensri, Wuttichart Kamolvisit, Narongsak Nakwan · The Journal of Maternal-Fetal & Neonatal Medicine · 2019 · 12 citations