Rungnapa Ittiwut

Mutations in Kinesin family member 6 reveal specific role in ependymal cell ciliogenesis and human neurological development

Mia J. Konjikusic, Patra Yeetong, Curtis W. Boswell et al. · PLoS Genetics · 2018 · 67 citations · Full text

Brain Development, Genetics, Reveal Specific Role +16

A germline STAT6 gain-of-function variant is associated with early-onset allergies

Narissara Suratannon, Chupong Ittiwut, Willem A. Dik et al. · Journal of Allergy and Clinical Immunology · 2022 · 53 citations

Asthma, Allergy, Allergy Medicine +10

Association between polymorphisms in catechol‐<i>O</i>‐methyltransferase (<i>COMT</i>) and cocaine‐induced paranoia in European‐American and African‐American populations

Rungnapa Ittiwut, Jennifer B. Listman, Chupong Ittiwut et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2011 · 33 citations · Full text

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

Trinucleotide repeat expansion in the transcription factor 4 (TCF4) gene in Thai patients with Fuchs endothelial corneal dystrophy

Naoki Okumura, Vilavun Puangsricharern, Raina Jindasak et al. · Eye · 2019 · 24 citations · Full text

Ocular Disease, Ophthalmology, Corneal Dystrophy +8