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Nutsuchar Wangtiraumnuay

Observed name: N., Wangtiraumnuay
ORCID: 0000-0003-4835-1785
Observed ORCID: 0000-0003-4835-1785
OpenAlex ID: A5036771573
The Global Retinoblastoma Outcome Study: a prospective, cluster-based analysis of 4064 patients from 149 countries
2022 · Ido Didi Fabian, Elhassan Abdallah, et al. · The Lancet Global Health · 195
Retinoblastoma in Asia
2023 · Swathi Kaliki, Vijitha S. Vempuluru, et al. · Ophthalmology · 31
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Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations
2018 · Nutsuchar Wangtiraumnuay, Waleed Abed Alnabi, et al. · Ophthalmic Genetics · 20
Evaluation of a Free Public Smartphone Application to Detect Leukocoria in High-Risk Children Aged 1 to 6 Years
2019 · Aldo Vagge, Nutsuchar Wangtiraumnuay, et al. · Journal of Pediatric Ophthalmology & Strabismus · 11
Cryptophthalmos, dental anomalies, oral vestibule defect, and a novel FREM2 mutation
2021 · Piranit Nik Kantaputra, Nutsuchar Wangtiraumnuay, et al. · Journal of Human Genetics · 10
Correlation between clinical presentations, radiological findings and high risk histopathological features of primary enucleated eyes with advanced retinoblastoma at Queen Sirikit National Institute of Child Health: 5 years result
2022 · Supawan Surukrattanaskul, Bungornrat Keyurapan, et al. · PLoS ONE · 8
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Optical Coherence Tomography in Knobloch Syndrome
2019 · Avrey Thau, Mai Tsukikawa, et al. · Ophthalmic surgery, lasers & imaging retina · 7
Prevalence of Prescription Glasses in the First-Grade Thai Students (7–8 Years Old)
2021 · Nutsuchar Wangtiraumnuay, Sumalin Trichaiyaporn, et al. · Clinical Optometry · 6
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Novel ABCA4 mutation leads to loss of a conserved C-terminal motif: implications for predicting pathogenicity based on genetic testing
2017 · Nutsuchar Wangtiraumnuay, Jenina Capasso, et al. · European Journal of Ophthalmology · 5
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Protein modeling and in silico analysis to assess pathogenicity of ABCA4 variants in patients with inherited retinal disease.
2023 · Senem Cevik, Nutsuchar Wangtiraumnuay, et al. · PubMed Central · 4
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Ophthalmic manifestations associated with RARB mutations
2018 · Nutsuchar Wangtiraumnuay, Sarina Kopinsky, et al. · Clinical Dysmorphology · 4
Outcomes of pediatric accommodative esotropia with botulinum toxin A treatment in Thailand
2021 · Nutsuchar Wangtiraumnuay, Supawan Surukrattanaskul, et al. · Strabismus · 3
Sensory outcome of exotropia surgery in Thailand: a retrospective multicenter study
2025 · Narisa Rattanalert, Supawan Surukrattanaskul, et al. · International Journal of Ophthalmology · 1
Digital Gangrene and Antiphospholipid Syndrome in a Retinoblastoma Patient with Chromosome 13q Deletion: A Case Report
2023 · Nutsuchar Wangtiraumnuay, Supawan Surukrattanaskul, et al. · Case Reports in Oncology · 1
Periocular ecthyma gangrenosum with Pseudomonas septicemia in an infant: A case report
2023 · Supawan Surukrattanaskul, Rosana Pittayapongpat, et al. · IDCases · 1
RARB mutations presenting with variable clinical features in patients with microphthalmia, anophthalmia, and/or coloboma (MAC): A Case Series.
2016 · P A Narayana Iyer, Nutsuchar Wangtiraumnuay, et al. · Investigative Ophthalmology & Visual Science · 1
Rare WDR19 Variants in Patients With Dental and Retinal Anomalies
2026 · Kedkanya Mesil, Kathawut Tachasuttirut, et al. · International Dental Journal
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Genetic findings and clinical features of extreme refractive errors in Thai children using whole genome sequencing
2026 · Nutsuchar Wangtiraumnuay, Supawan Surukrattanaskul, et al. · Ophthalmic Genetics
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Global Patterns of Cross-Border Travel for Retinoblastoma Care
2026 · The Global Retinoblastoma Study Group, Eran Levanon, et al. · JAMA Ophthalmology
Increasing Familial Retinoblastoma in High-Income Countries despite Stable Overall Incidence, 2017 to 2024
2026 · Yael Lustig-Barzelay, Dupe S. Ademola-Popoola, et al. · Ophthalmology Retina
Supplementary Material for: Digital Gangrene and Antiphospholipid Syndrome in a Retinoblastoma Patient with Chromosome 13q Deletion: A Case Report
2023 · N., Wangtiraumnuay, S., Surukrattanaskul, et al. · Figshare
Orbital intramuscular lipoma with bone erosion: A case report and review of literature
2022 · Sirin Lueangaram, Rosana Pittayapongpat, et al. · Indian Journal of Ophthalmology - Case Reports
Chromosomal Microarray in Isolated Congenital and Developmental Cataract
2021 · Thales A. C. De Guimarães, Jenina E. Capasso, et al. · The Pan-American Journal of Ophthalmology
Optical coherence tomography in Knobloch syndrome
2018 · Avrey Thau, Mai Tsukikawa, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus
Chromosomal microarray analysis in congenital and developmental cataracts
2017 · Nutsuchar Wangtiraumnuay, Jenina Capasso, et al. · Journal of American Association for Pediatric Ophthalmology and Strabismus
Works count: 27
Citation count: 308
H-index: 7
I10-index: 5
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