Jeerawan Klangjorhor

4PUBLICATIONS
30CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)NeonatologyPredictive and prognostic markers
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Publications (4)

|May 04, 2026
Prenatal Whole-Genome Sequencing for Fetal Anomalies: Diagnostic Performance, Challenges, and Clinical Implications.

|Oct 02, 2025
Compound Heterozygous Null Variants in ITGB4 Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.

Jeerawan Klangjorhor, Mallika Pomrop, Patcharawadee Thongkumkoon

|Mar 27, 2025
A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient.

Jeerawan Klangjorhor, Natrujee Wiwattanadittakul, Thanapak Jaimalai

|Feb 03, 2023
Characterization of Cell-Free DNA Size Distribution in Osteosarcoma Patients.

Sasimol Udomruk, Areerak Phanphaisarn, Thanat Kanthawang

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Frequent Collaborators

3 joint publications

Patcharawadee Thongkumkoon

3 joint publications

Arnat Pasena

2 joint publications

Parunya Chaiyawat

2 joint publications

Pathacha Suksakit