Wuttichart Kamolvisit

Severe craniofrontonasal syndrome in a male patient mosaic for a novel nonsense mutation in EFNB1.

T. Porntaveetus, K. Suphapeetiporn, V. Shotelersuk, 2020, European journal of medical genetics.

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

K. Suphapeetiporn, V. Shotelersuk, T. Desudchit, 2022, European Journal of Human Genetics.

A LILRB1 variant with a decreased ability to phosphorylate SHP-1 leads to autoimmune diseases

T. Palaga, C. Srichomthong, K. Suphapeetiporn, 2022, Scientific Reports.

Factors and Outcomes of Persistent Pulmonary Hypertension of the Newborn Associated with Acute Kidney Injury in Thai Neonates

N. Nakwan, Wuttichart Kamolvisit, Sutthikiat Jaroensri, 2017, American Journal of Perinatology.

Fatal Vernix Caseosa Aspiration Associated With Persistent Pulmonary Hypertension of the Newborn

N. Nakwan, P. Chaiwiriyawong, Wuttichart Kamolvisit, 2016, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

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

T. Porntaveetus, T. Theerapanon, V. Shotelersuk, 2022, Journal of applied oral science : revista FOB.

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

K. Rojnueangnit, C. Srichomthong, K. Suphapeetiporn, 2021, Clinical genetics.

Widespread and debilitating hemangiomas in a patient with enchondromatosis and D-2-hydroxyglutaric aciduria

K. Suphapeetiporn, V. Shotelersuk, Wuttichart Kamolvisit, 2018, Skeletal Radiology.

Using an experiment among clinical experts to determine the cost and clinical impact of rapid whole exome sequencing in acute pediatric settings

V. Shotelersuk, Y. Teerawattananon, N. Sribundit, 2023, Frontiers in pediatrics.

Nine patients with KCNQ2-related neonatal seizures and functional studies of two missense variants

V. Shotelersuk, S. Tongkobpetch, S. Bongsebandhu-Phubhakdi, 2023, Scientific Reports.

AI-based diagnosis in mandibulofacial dysostosis with microcephaly using external ear shapes

F. Denoyelle, D. Milea, N. Garcelon, 2023, Frontiers in pediatrics.

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

K. Rojnueangnit, T. Porntaveetus, T. Theerapanon, 2020, European journal of medical genetics.

Case report: Severe nonketotic hyperglycinemia in a neonate without apparent seizures but concomitant cleft palate and cerebral sinovenous thrombosis

D. Wattanasirichaigoon, Wuttichart Kamolvisit, Chaiyos Khongkhatithum, 2023, Frontiers in Pediatrics.

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

N. Nakwan, Wuttichart Kamolvisit, Sutthikiat Jaroensri, 2020, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.