Parith Wongkittichote

Author

St. Louis Children's Hospital ORCID

Also Known As

Parith Wongkittichote

Publications

447

Citations

H-Index

Concepts

All Affiliations

St. Louis Children's Hospital Mahidol University Washington University in St. Louis Children's Hospital of Philadelphia Ramathibodi Hospital

About

Parith Wongkittichote is an author at St. Louis Children's Hospital specializing in medicine, metabolic syndrome, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	28
2	Molecular Genetics	1	1	16
3	Genetics	1	1	16
4	Inherited Metabolic Disease	1	1	16
5	Metabolic Disease	1	1	12

Parith Wongkittichote

Publications

139

Citations

H-Index

Page 1

	Year	Citations
Tricarboxylic acid cycle enzyme activities in a mouse model of methylmalonic aciduria Parith Wongkittichote, Gary Cunningham, Marshall Summar, Molecular Genetics and Metabolism	2019	41
Prediction of the functional effect of novel <i>SLC25A13</i> variants using a <i>S. cerevisiae</i> model of AGC2 deficiency Parith Wongkittichote, Sumalee Tungpradabkul, Duangrurdee Wattanasirichaigoon, Journal of Inherited Metabolic Disease	2012	20
Screening of<i>SLC25A13</i>mutation in the Thai population Parith Wongkittichote World Journal of Gastroenterology	2013	18
Novel exon-skipping variant disrupting the basic domain of HCFC1 causes intellectual disability without metabolic abnormalities in both male and female patients Parith Wongkittichote, Daniel Wegner, Marwan Shinawi Journal of Human Genetics Metabolic SyndromeMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2021	16
Fatal <scp>COVID</scp>‐19 infection in a patient with long‐chain <scp>3‐hydroxyacyl‐CoA</scp> dehydrogenase deficiency: A case report Parith Wongkittichote, James R. Watson, Jennifer Leonard, JIMD Reports Metabolic SyndromePeripheral NeuropathyHeart FailureCardiomyopathyLong Covid	2020	12
Expanding allelic and phenotypic spectrum of ZC4H2‐related disorder: A novel hypomorphic variant and high prevalence of tethered cord Parith Wongkittichote, Tae‐Ik Choi, Oc‐Hee Kim, Clinical Genetics	2022	11
Biochemical characterization of patients with dihydrolipoamide dehydrogenase deficiency Parith Wongkittichote, Sanmati Cuddapah, Stephen R. Master, JIMD Reports	2023	11
Phenotypic, molecular, and functional characterization of COQ7-related primary CoQ10 deficiency: Hypomorphic variants and two distinct disease entities Parith Wongkittichote, Maria Laura Duque Lasio, Martina Magistrati, Molecular Genetics and Metabolism	2023	10

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