Concepedia

Author

Chulaluck Kuptanon

Queen Sirikit National Institute of Child HealthORCID

Also Known As

C. Kuptanon, Chulaluck Kuptanon, Luhe Mian

30

Publications

342

Citations

13

H-Index

20

Concepts

All Affiliations

Queen Sirikit National Institute of Child HealthMahidol UniversityChulalongkorn UniversitySiriraj HospitalThai Red Cross Society
CK

About

Chulaluck Kuptanon is an author at Queen Sirikit National Institute of Child Health specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

5

5

109

2

Molecular Genetics

2

2

32

3

Molecular Biology

1

1

13

4

Nephrology

1

1

20

5

Pathology

1

1

19

Chulaluck Kuptanon

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12

Publications

242

Citations

12

H-Index

YearCitations

Mutation spectrum of and founder effects affecting the PTS gene in East Asian populations

Yen-Hui Chiu, Ying-Chen Chang, Yu-Hsin Chang,

Journal of Human Genetics

2012

37

An Economic Evaluation of Neonatal Screening for Inborn Errors of Metabolism Using Tandem Mass Spectrometry in Thailand

Kittiphong Thiboonboon, Pattara Leelahavarong, Duangrurdee Wattanasirichaigoon,

PLoS ONE

2015

32

Organic acid disorders detected by urine organic acid analysis: Twelve cases in Thailand over three-year experience

Pornswan Wasant, Somporn Liammongkolkul, Chulaluck Kuptanon,

Clinica Chimica Acta

2008

20

Glutaric Aciduria Type 2, Late Onset Type in Thai Siblings With Myopathy

Pornswan Wasant, Chulaluck Kuptanon, Nithiwat Vattanavicharn,

Pediatric Neurology

2010

20

Two novel compound heterozygous BMP1 mutations in a patient with osteogenesis imperfecta: a case report

Apiruk Sangsin, Chulaluck Kuptanon, Chalurmpon Srichomthong,

BMC Medical Genetics

2017

19

Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities

Chulaluck Kuptanon, Chalurmpon Srichomthong, Chupong Ittiwut,

Gene

2019

19

Clinical course, mutations and its functional characteristics of infantile-onset Pompe disease in Thailand

Lukana Ngiwsara, Duangrurdee Wattanasirichaigoon, Thipwimol Tim‐Aroon,

BMC Medical Genetics

2019

19

Rapid exome sequencing as the first‐tier investigation for diagnosis of acutely and severely ill children and adults in Thailand

Wuttichart Kamolvisit, Prasit Phowthongkum, Ponghatai Boonsimma,

Clinical Genetics

2021

18

Establishing of National Birth Defects Registry in Thailand.

Suthipong Pangkanon, Siraporn Sawasdivorn, Chulaluck Kuptanon,

PubMed

2014

16

Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients

Tim Phetthong, Thipwimol Tim‐Aroon, Arthaporn Khongkraparn,

Orphanet Journal of Rare Diseases

2021

15

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