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Kitiwan Rojnueangnit

Observed names: K Rojnueangnit, Kitiwan Rojnueangit, Rojnueangnit K, Rojnueangnit, Kitiwan
ORCID: 0000-0002-9488-4470
Observed ORCID: 0000-0002-9488-4470
OpenAlex ID: A5036200726
High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype–Phenotype Correlation
2015 · Kitiwan Rojnueangnit, Jing Xie, et al. · Human Mutation · 188
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Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder
2017 · Areerat Hnoonual, Weerin Thammachote, et al. · Scientific Reports · 51
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Oxygen saturation trends in preterm infants during the first 15 min after birth
2009 · P Nuntnarumit, K Rojnueangnit, et al. · Journal of Perinatology · 40
Studying Down syndrome recognition probabilities in Thai children with de‐identified computer‐aided facial analysis
2018 · Nattariya Vorravanpreecha, Thanayoot Lertboonnum, et al. · American Journal of Medical Genetics Part A · 30
Hajdu–Cheney syndrome
2014 · Maria Descartes, Kitiwan Rojnueangnit, et al. · Clinical Dysmorphology · 30
Sex‐discordant monochorionic twins with blood and tissue chimerism
2015 · David Rodriguez‐Buritica, Kitiwan Rojnueangnit, et al. · American Journal of Medical Genetics Part A · 27
Quality of life and comprehensive health supervision for children with Down syndrome in Thailand
2020 · Kitiwan Rojnueangnit, Penrawee Khaosamlee, et al. · Journal of Community Genetics · 25
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Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand
2021 · Wuttichart Kamolvisit, Prasit Phowthongkum, et al. · Clinical Genetics · 20
Novel SOX10 Mutations in Waardenburg Syndrome: Functional Characterization and Genotype-Phenotype Analysis
2020 · Supranee Thongpradit, Natini Jinawath, et al. · Frontiers in Genetics · 20
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Expanding phenotypic and mutational spectra of mitochondrial HMG-CoA synthase deficiency
2020 · Kitiwan Rojnueangnit, Parisa Maneechai, et al. · European Journal of Medical Genetics · 18
Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing
2019 · Kitiwan Rojnueangnit, Boonchu Sirichongkolthong, et al. · Pediatric Cardiology · 15
Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand
2019 · Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, et al. · BMC Medical Genetics · 15
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Facial recognition accuracy in photographs of Thai neonates with Down syndrome among physicians and the Face2Gene application
2021 · Wewika Srisraluang, Kitiwan Rojnueangnit · American Journal of Medical Genetics Part A · 14
Craniosynostosis and radial ray defect: A rare presentation of 22q11.2 deletion syndrome
2013 · Kitiwan Rojnueangnit, Nathaniel H. Robin · American Journal of Medical Genetics Part A · 11
Perinatal lethal osteogenesis imperfecta in a Thai newborn: the autopsy and histopathogical findings.
2012 · Wanwisa Himakhun, Kitiwan Rojnueangnit, et al. · PubMed · 11
Classic phenotype of Coffin–lowry syndrome in a female with stimulus‐induced drop episodes and a genotype with preserved N‐terminal kinase domain
2013 · Kitiwan Rojnueangnit, Julie R. Jones, et al. · American Journal of Medical Genetics Part A · 9
Clinical delineation of 18q11‐q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects
2019 · Kitiwan Rojnueangnit, Chariyawan Charalsawadi, et al. · Molecular Genetics & Genomic Medicine · 8
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Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients with Cleft Lip and/or Palate
2014 · Kitiwan Rojnueangnit, Fady M. Mikhail, et al. · The Cleft Palate-Craniofacial Journal · 7
Genetic diagnosis for adult patients at a genetic clinic
2022 · Kitiwan Rojnueangnit, Pimjai Anthanont, et al. · Molecular Case Studies · 6
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A novel DLL4 mutation in Adams–Oliver syndrome with absence of the right pulmonary artery in newborn
2021 · Kitiwan Rojnueangnit, Thanyalak Phawan, et al. · American Journal of Medical Genetics Part A · 6
Bleeding solitary SEGA in non-tuberous sclerosis complex adolescent: a case illustration and review of literature
2024 · Vich Yindeedej, Kitiwan Rojnueangnit, et al. · Child s Nervous System · 4
LACHT syndrome ( Mardini–Nyhan association) with tracheal stenosis in a Thai newborn
2020 · Kitiwan Rojnueangnit, Sudatip Kositamongkol, et al. · American Journal of Medical Genetics Part A · 4
Growth Patterns of Thai Children with Down Syndrome from Birth to 5 Years
2020 · Naiyana Boontan, Kitiwan Rojnueangnit · Journal of Pediatric Genetics · 4
Microspherophakic Angle Closure Glaucoma in a Patient with Coffin-Siris Syndrome: Case Report
2023 · Kulawan Rojananuangnit, Kitiwan Rojnueangnit · The Application of Clinical Genetics · 3
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Acute Intermittent Porphyria: Complete Phenotype in a Patient with p.Arg173Trp Variant in Thailand
2022 · Vachiravit Sriprakoon, Chalisa Ittagornpunth, et al. · American Journal of Case Reports · 3
Works count: 51
Citation count: 582
H-index: 13
I10-index: 15
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