Kitiwan Rojnueangnit (Kitiwan Rojnueangit)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Topics

Pulmonary Artery

Obstructive Sleep Apnea

Top Venues

American journal of medical genetics. Part A

The application of clinical genetics

Journal of pediatric genetics

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Nop Khongthon, Midi Theeraviwatwong, Khunton Wichajarn, Kitiwan Rojnueangnit
Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians. The application of clinical genetics 17 (2024)
Nop Khongthon, Midi Theeraviwatwong, Khunton Wichajarn, Kitiwan Rojnueangnit
Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians. The application of clinical genetics 17 (2024)
Kulawan Rojananuangnit, Kitiwan Rojnueangnit
Microspherophakic Angle Closure Glaucoma in a Patient with Coffin-Siris Syndrome: Case Report. The application of clinical genetics 16 (2023)
Kitiwan Rojnueangnit, Pimjai Anthanont, Thanitchet Khetkham, Sukita Puttamanee, Chupong Ittiwut
Genetic diagnosis for adult patients at a genetic clinic. Cold Spring Harbor molecular case studies (2022)
Kanokwan Sriwattanapong, Kitiwan Rojnueangnit, Thanakorn Theerapanon, Chalurmpon Srichomthong, Thantrira Porntaveetus, Vorasuk Shotelersuk
Compound Heterozygosity for a Novel Frameshift Variant Causing Fatal Infantile Liver Failure and Genotype-Phenotype Correlation of POLG c.3286C>T Variant. International journal of neonatal screening 7 (1) (2021)
Kitiwan Rojnueangnit, Thanyalak Phawan, Thanitchet Khetkham, Wilaiporn Techasatid, Boonchu Sirichongkolthong
A novel DLL4 mutation in Adams-Oliver syndrome with absence of the right pulmonary artery in newborn. American journal of medical genetics. Part A (2021)
Wewika Srisraluang, Kitiwan Rojnueangnit
Facial recognition accuracy in photographs of Thai neonates with Down syndrome among physicians and the Face2Gene application. American journal of medical genetics. Part A 185 (12) (2021)
Kitiwan Rojnueangnit, Sudatip Kositamongkol, Wanida Paoin, Araya Satdhabudha, Onsuthi Pharadornuwat, Ratthapon Wongwandee, Weerin Thammachote, Natini Jinawath
LACHT syndrome (Mardini-Nyhan association) with tracheal stenosis in a Thai newborn. American journal of medical genetics. Part A 182 (9) (2020)
Kitiwan Rojnueangnit, Penrawee Khaosamlee, Issarapa Chunsuwan, Nattariya Vorravanpreecha, Tanayoot Lertboonnum, Rungrote Rodjanadit, Pak Sriplienchan
Quality of life and comprehensive health supervision for children with Down syndrome in Thailand. Journal of community genetics 11 (3) (2020)
Naiyana Boontan, Kitiwan Rojnueangnit
Growth Patterns of Thai Children with Down Syndrome from Birth to 5 Years. Journal of pediatric genetics 10 (1) (2020)
Kitiwan Rojnueangnit, Thanitchet Khetkham, Preyaporn Onsod, Takol Chareonsirisuthigul
Clinical Features to Predict 22q11.2 Deletion Syndrome Proven by Molecular Genetic Testing. Journal of pediatric genetics 11 (1) (2020)
Kitiwan Rojnueangnit, Chariyawan Charalsawadi, Weerin Thammachote, Ariya Pradabmuksiri, Thipwimol Tim-Aroon, Antonio Novelli, Sara Loddo, Silvana Briuglia, Cutrupi M Concetta, Duangrurdee Wattanasirichaigoon, Natini Jinawath
Clinical delineation of 18q11-q12 microdeletion: Intellectual disability, speech and behavioral disorders, and conotruncal heart defects. Molecular genetics & genomic medicine 7 (9) (2019)
Kitiwan Rojnueangnit, Boonchu Sirichongkolthong, Ratthapon Wongwandee, Thanitchet Khetkham, Saisuda Noojarern, Arthaporn Khongkraparn, Duangrurdee Wattanasirichaigoon
Identification of Gene Mutations in Primary Pediatric Cardiomyopathy by Whole Exome Sequencing. Pediatric cardiology 41 (1) (2019)
Kitiwan Rojnueangnit, Maria Descartes
Congenital central hypoventilation syndrome mimicking mitochondrial disease. Clinical case reports 6 (3) (2018)
Nattariya Vorravanpreecha, Thanayoot Lertboonnum, Rungrote Rodjanadit, Pak Sriplienchan, Kitiwan Rojnueangnit
Studying Down syndrome recognition probabilities in Thai children with de-identified computer-aided facial analysis. American journal of medical genetics. Part A 176 (9) (2018)