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Bhakbhoom Panthan · SciRah

Researcher profile · Semantic Scholar

Bhakbhoom Panthan

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Bhakbhoom Panthan — researcher profile on SciRah

h-index: 6
Works: 19
Citations: 143

Most-cited papers

Genomic surveillance of SARS-CoV-2 in Thailand reveals mixed imported populations, a local lineage expansion and a virus with truncated ORF7a
Khajohn Joonlasak, E. Batty, T. Kochakarn, Bhakbhoom Panthan +17 more
2020medRxiv31 citations Open access
Semantic Scholar
Host genetic polymorphisms involved in long-term symptoms of COVID-19
W. Udomsinprasert, Nuttakant Nontawong, Wacharapol Saengsiwaritt, Bhakbhoom Panthan +8 more
2023Emerging Microbes and Infections25 citations Open access
Semantic Scholar
Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single center
C. Satirapod, Matchuporn Sukprasert, Bhakbhoom Panthan, A. Charoenyingwattana +5 more
2019PLoS ONE18 citations Open access
Semantic Scholar
DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients
Kinnaree Sorapipatcharoen, Thipwimol Tim-Aroon, P. Mahachoklertwattana, W. Chantratita +11 more
2020Endocrine Connections13 citations Open access
Semantic Scholar
First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration
Objoon Trachoo, C. Satirapod, Bhakbhoom Panthan, Matchuporn Sukprasert +4 more
2016Journal of Assisted Reproduction and Genetics11 citations Open access
Semantic Scholar
Cost-minimization analysis of sequential genetic testing versus targeted next-generation sequencing gene panels in patients with pheochromocytoma and paraganglioma
Weenita Pipitprapat, O. Pattanaprateep, N. Iemwimangsa, I. Sensorn +10 more
2021Annals medicus9 citations Open access
Semantic Scholar
Comparing library preparation methods for SARS-CoV-2 multiplex amplicon sequencing on the Illumina MiSeq platform
E. Batty, T. Kochakarn, Arporn Wangwiwatsin, K. Joonlasak +16 more
2020bioRxiv6 citations Open access
Semantic Scholar
Epileptic spasms related to neuronal differentiation factor 2 (NEUROD2) mutation respond to combined vigabatrin and high dose prednisolone therapy
Kullasate Sakpichaisakul, Rachata Boonkrongsak, Punjama Lertbutsayanukul, N. Iemwimangsa +3 more
2022BMC Neurology5 citations Open access
Semantic Scholar
Low oxygen saturation and severe anemia in compound heterozygous Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val]
Parin Kamseng, S. Trakulsrichai, Objoon Trachoo, Walaiporn Yimniam +6 more
2017Hematology5 citations Open access
Semantic Scholar
A Novel PRKAR1A Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease
Sira Korpaisarn, Objoon Trachoo, Bhakbhoom Panthan, R. Aroonroch +2 more
2017Case Reports in Oncology5 citations Open access
Semantic Scholar
FIRST IDENTIFICATION OF HEMOGLOBIN LANSINGRAMATHIBODI [α87(F8)His → Gln; CAC>CAG (HBA1: c.264C>G)] IN A THAI FAMILY WITH SPURIOUS HYPOXEMIA.
S. Trakulsrichai, Bhakbhoom Panthan, P. Jittorntam, P. Niparuck +4 more
2016Southeast Asian Journal of Tropical Medicine and Public Health5 citations
Semantic Scholar
Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration.
Kullasate Sakpichaisakul, V. E. Saengow, Papit Suwanpratheep, Kanokpan Rongnoparat +2 more
2019Journal of clinical neuroscience4 citations
Semantic Scholar
Nationwide carrier screening for congenital adrenal hyperplasia: integrated approach of CYP21A2 pathogenic variant genotyping and comprehensive large gene deletion analysis
Y. Suwanlikit, Bhakbhoom Panthan, Pawares Chitayanan, Sommon Klumsathian +3 more
2025BMC Medical Genomics3 citations
Semantic Scholar
Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service
Objoon Trachoo, T. Yingchoncharoen, T. Ngernsritrakul, N. Iemwimangsa +9 more
2022PLoS ONE3 citations Open access
Semantic Scholar
AB034. Carrier frequency of inherited genetic disorders in Thai population: implication for designing expanded carrier screening panel.
Sommon Klumsathian, Woramon Lorlipiwong, N. Iemwimangsa, I. Sensorn +4 more
20171 citations Open access
Semantic Scholar
Molecular alterations, tumor microenvironment and clinical correlations in Thai cholangiocarcinoma patients.
Panuchai Bamrungwong, S. Oranratnachai, P. Sornmayura, P. Incharoen +10 more
20210 citations
Semantic Scholar
P76.39 Acquired Resistance Mechanisms in T790M-Positive Advanced NSCLC Tested by Non-Invasive Molecular Testing (NIMT) and Their Clinical Relevance
P. Watcharenwong, N. Trachu, P. Incharoen, D. Munthum +6 more
20210 citations Open access
Semantic Scholar
AB138. Next-generation sequencing as a tool for molecular diagnosis of hypertrophic and dilated cardiomyopathies in Thai patients.
Objoon Trachoo, Bhakbhoom Panthan, P. Jittorntam, Sithakom Phusanti +8 more
20150 citations
Semantic Scholar
AB137. Preimplantation genetic diagnosis for rare monogenic disorder: a lesson from pantothenate kinase-associated neurodegeneration
Objoon Trachoo, C. Satirapod, Bhakbhoom Panthan, Matchuporn Sukprasert +4 more
20150 citations
Semantic Scholar

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