Sirisak Chanprasert

1.1k total citations
13 papers, 228 citations indexed

About

Sirisak Chanprasert is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Sirisak Chanprasert has authored 13 papers receiving a total of 228 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 4 papers in Genetics. Recurrent topics in Sirisak Chanprasert's work include Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Sirisak Chanprasert is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Sirisak Chanprasert collaborates with scholars based in United States, United Arab Emirates and Thailand. Sirisak Chanprasert's co-authors include Fernando Scaglia, William J. Craigen, Ayman W. El‐Hattab, Lisa Emrick, Jean W. Hsu, Farook Jahoor, Mohammed Almannai, Jerry R. Mendell, Zarife Sahenk and Gregory M. Enns and has published in prestigious journals such as Anesthesiology, The International Journal of Biochemistry & Cell Biology and Breast Cancer Research and Treatment.

In The Last Decade

Sirisak Chanprasert

13 papers receiving 224 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Sirisak Chanprasert United States	8	158	96	33	33	17	13	228
Makiko Tajika Japan	8	217 1.4×	144 1.5×	39 1.2×	19 0.6×	10 0.6×	15	283
Paulina Halat Poland	6	173 1.1×	98 1.0×	11 0.3×	58 1.8×	11 0.6×	8	259
Colleen Muraresku United States	10	263 1.7×	175 1.8×	30 0.9×	41 1.2×	13 0.8×	19	313
Magdalena Pajdowska Poland	11	316 2.0×	209 2.2×	27 0.8×	76 2.3×	12 0.7×	22	422
Joyeeta Rahman United Kingdom	6	389 2.5×	226 2.4×	38 1.2×	57 1.7×	19 1.1×	7	458
Magalie Barth France	12	274 1.7×	171 1.8×	92 2.8×	35 1.1×	7 0.4×	32	378
Pablo Serrano‐Lorenzo Spain	9	152 1.0×	42 0.4×	37 1.1×	29 0.9×	9 0.5×	20	250
H. Serap Kalkanoğlu Türkiye	10	93 0.6×	121 1.3×	46 1.4×	20 0.6×	39 2.3×	17	216
Kate Craig United Kingdom	10	233 1.5×	124 1.3×	13 0.4×	29 0.9×	22 1.3×	16	312
Mary Anne D. Chiong Philippines	10	168 1.1×	142 1.5×	54 1.6×	36 1.1×	12 0.7×	31	295

Countries citing papers authored by Sirisak Chanprasert

Since Specialization

Citations

This map shows the geographic impact of Sirisak Chanprasert's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sirisak Chanprasert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sirisak Chanprasert more than expected).

Fields of papers citing papers by Sirisak Chanprasert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sirisak Chanprasert. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sirisak Chanprasert. The network helps show where Sirisak Chanprasert may publish in the future.

Co-authorship network of co-authors of Sirisak Chanprasert

This figure shows the co-authorship network connecting the top 25 collaborators of Sirisak Chanprasert. A scholar is included among the top collaborators of Sirisak Chanprasert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sirisak Chanprasert. Sirisak Chanprasert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Chung, Wendy K., Kyle B. Brothers, Angela R. Bradbury, et al.. (2021). Genomic medicine implementation protocols in the PhenX Toolkit: tools for standardized data collection. Genetics in Medicine. 23(9). 1783–1788. 2 indexed citations

Thongnoppakhun, Wanna, et al.. (2021). Thai patients who fulfilled NCCN criteria for breast/ovarian cancer genetic assessment demonstrated high prevalence of germline mutations in cancer susceptibility genes: implication to Asian population testing. Breast Cancer Research and Treatment. 188(1). 237–248. 11 indexed citations

Songsaeng, Dittapong, et al.. (2019). A large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: a case report. BMC Neurology. 19(1). 106–106. 6 indexed citations

Thomas, Elizabeth R., Andrea M. Lewis, Yaping Yang, et al.. (2019). Novel Missense Variants in ADAT3 as a Cause of Syndromic Intellectual Disability. Journal of Pediatric Genetics. 8(4). 244–251. 12 indexed citations

Maleszewski, Joseph J., et al.. (2019). Glycogen storage disease type IV: dilated cardiomyopathy as the isolated initial presentation in an adult patient. BMJ Case Reports. 12(9). e230068–e230068. 6 indexed citations

Shurtleff, Hillary A., et al.. (2018). Cognitive characteristics of mitochondrial diseases in children. Epilepsy & Behavior. 88. 235–243. 11 indexed citations

Chanprasert, Sirisak, et al.. (2018). Anesthetics Have Different Effects on the Electrocorticographic Spectra of Wild-type and Mitochondrial Mutant Mice. Anesthesiology. 129(4). 744–755. 7 indexed citations

El‐Hattab, Ayman W., Lisa Emrick, Jean W. Hsu, et al.. (2016). Impaired nitric oxide production in children with MELAS syndrome and the effect of arginine and citrulline supplementation. Molecular Genetics and Metabolism. 117(4). 407–412. 65 indexed citations

Chanprasert, Sirisak & Fernando Scaglia. (2014). Adult liver disorders caused by inborn errors of metabolism: Review and update. Molecular Genetics and Metabolism. 114(1). 1–10. 17 indexed citations

10.

El‐Hattab, Ayman W., Lisa Emrick, Jean W. Hsu, et al.. (2014). Glucose metabolism derangements in adults with the MELAS m.3243A>G mutation. Mitochondrion. 18. 63–69. 31 indexed citations

11.

El‐Hattab, Ayman W., Lisa Emrick, Sirisak Chanprasert, William J. Craigen, & Fernando Scaglia. (2014). Mitochondria: Role of citrulline and arginine supplementation in MELAS syndrome. The International Journal of Biochemistry & Cell Biology. 48. 85–91. 32 indexed citations

12.

Chanprasert, Sirisak, Janice Smith, Patricia Hixson, Ankita Patel, & Seema R. Lalani. (2014). Heterozygous deletion of exons 18 and 19 of IGF1R in an individual with short stature. Clinical Dysmorphology. 23(3). 98–100. 1 indexed citations

13.

Chanprasert, Sirisak, Jing Wang, Gregory M. Enns, et al.. (2013). Molecular and clinical characterization of the myopathic form of mitochondrial DNA depletion syndrome caused by mutations in the thymidine kinase (TK2) gene. Molecular Genetics and Metabolism. 110(1-2). 153–161. 27 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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