Orapan Sripichai

1.2k total citations
29 papers, 894 citations indexed

About

Orapan Sripichai is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Orapan Sripichai has authored 29 papers receiving a total of 894 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 15 papers in Hematology and 10 papers in Molecular Biology. Recurrent topics in Orapan Sripichai's work include Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (15 papers) and Erythrocyte Function and Pathophysiology (6 papers). Orapan Sripichai is often cited by papers focused on Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (15 papers) and Erythrocyte Function and Pathophysiology (6 papers). Orapan Sripichai collaborates with scholars based in Thailand, United States and Japan. Orapan Sripichai's co-authors include Suthat Fucharoen, Thongperm Munkongdee, Pranee Winichagoon, Colleen Byrnes, Toshihiko Tanno, Jeffery L. Miller, Wattanan Makarasara, Seung-Jae Noh, Julia B. Goodnough and Robert F. Paulson and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Orapan Sripichai

28 papers receiving 883 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Orapan Sripichai Thailand	16	687	598	215	145	140	29	894
D Stefanova United States	6	298 0.4×	397 0.7×	67 0.3×	50 0.3×	11 0.1×	12	518
Sanne M. Meinderts Netherlands	6	73 0.1×	95 0.2×	86 0.4×	134 0.9×	23 0.2×	8	353
Albert C. Sek United States	8	167 0.2×	216 0.4×	60 0.3×	59 0.4×	4 0.0×	11	399
Thassila Nogueira Pitanga Brazil	11	138 0.2×	99 0.2×	135 0.6×	40 0.3×	16 0.1×	24	338
Shenghe Cai United States	7	138 0.2×	116 0.2×	62 0.3×	29 0.2×	4 0.0×	9	373
J.M.C. Wessels Netherlands	12	47 0.1×	116 0.2×	202 0.9×	55 0.4×	19 0.1×	27	497
Diana Hanekamp Netherlands	11	88 0.1×	267 0.4×	283 1.3×	40 0.3×	8 0.1×	16	559
Ji Young Huh South Korea	11	48 0.1×	64 0.1×	232 1.1×	30 0.2×	30 0.2×	26	440
Rachel E. Brown United States	12	17 0.0×	97 0.2×	180 0.8×	38 0.3×	39 0.3×	33	474

Countries citing papers authored by Orapan Sripichai

Since Specialization

Citations

This map shows the geographic impact of Orapan Sripichai'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 Orapan Sripichai with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Orapan Sripichai more than expected).

Fields of papers citing papers by Orapan Sripichai

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Orapan Sripichai. 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 Orapan Sripichai. The network helps show where Orapan Sripichai may publish in the future.

Co-authorship network of co-authors of Orapan Sripichai

This figure shows the co-authorship network connecting the top 25 collaborators of Orapan Sripichai. A scholar is included among the top collaborators of Orapan Sripichai 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 Orapan Sripichai. Orapan Sripichai is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sripichai, Orapan, et al.. (2023). Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in β0-thalassemia/HbE erythroid cells. PLoS ONE. 18(3). e0281059–e0281059.

Sripichai, Orapan, et al.. (2022). Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β0-thalassemia/HbE. Scientific Reports. 12(1). 4952–4952. 5 indexed citations

Paiboonsukwong, Kittiphong, et al.. (2022). Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar. Hemoglobin. 46(1). 66–70. 1 indexed citations

Hongeng, Suradej, et al.. (2021). Association of the Degree of Erythroid Expansion and Maturation Arrest with the Clinical Severity of β<sup>0</sup>-Thalassemia/Hemoglobin E Patients. Acta Haematologica. 144(6). 660–671. 2 indexed citations

Munkongdee, Thongperm, Kanet Wongravee, Orapan Sripichai, et al.. (2020). Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation. Microchimica Acta. 187(4). 238–238. 18 indexed citations

Munkongdee, Thongperm, Kittiphong Paiboonsukwong, Orapan Sripichai, et al.. (2020). Development of DNA controls for detection of β‐thalassemia mutations commonly found in Asian. International Journal of Laboratory Hematology. 42(6). 727–733. 2 indexed citations

Wangroongsarb, Piyada, et al.. (2020). Prevalence and antimicrobial susceptibility of Campylobacter isolated from retail chickens in Thailand. International Journal of Food Microbiology. 339. 109017–109017. 22 indexed citations

Songdej, Duantida, Kittiphong Paiboonsukwong, Orapan Sripichai, et al.. (2020). UNC0638 induces high levels of fetal hemoglobin expression in β-thalassemia/HbE erythroid progenitor cells. Annals of Hematology. 99(9). 2027–2036. 18 indexed citations

Sripichai, Orapan, et al.. (2017). Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease. International Journal of Hematology. 107(3). 297–310. 15 indexed citations

10.

Sripichai, Orapan & Suthat Fucharoen. (2016). Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches. Expert Review of Hematology. 9(12). 1129–1137. 35 indexed citations

11.

Wangkumhang, Pongsakorn, Philip J. Shaw, Kridsadakorn Chaichoompu, et al.. (2013). Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure. PLoS ONE. 8(11). e79522–e79522. 25 indexed citations

12.

Sherva, Richard, Orapan Sripichai, Kenneth J. Abel, et al.. (2010). Genetic modifiers of Hb E/β0 thalassemia identified by a two-stage genome-wide association study. BMC Medical Genetics. 11(1). 51–51. 22 indexed citations

13.

Nuinoon, Manit, Wattanan Makarasara, Taisei Mushiroda, et al.. (2009). A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E. Human Genetics. 127(3). 303–314. 146 indexed citations

14.

Sripichai, Orapan, Christine Mione Kiefer, Natarajan V. Bhanu, et al.. (2009). Cytokine-mediated increases in fetal hemoglobin are associated with globin gene histone modification and transcription factor reprogramming. Blood. 114(11). 2299–2306. 51 indexed citations

15.

Sripichai, Orapan, Wattanan Makarasara, Thongperm Munkongdee, et al.. (2008). A scoring system for the classification of β‐thalassemia/Hb E disease severity. American Journal of Hematology. 83(6). 482–484. 106 indexed citations

16.

Svasti, Saovaros, Orapan Sripichai, Thongperm Munkongdee, et al.. (2008). Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E. International Journal of Hematology. 88(4). 357–361. 15 indexed citations

17.

Sripichai, Orapan, Thongperm Munkongdee, Chutima Kumkhaek, et al.. (2007). Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease. Annals of Hematology. 87(5). 375–379. 40 indexed citations

18.

Sripichai, Orapan & Suthat Fucharoen. (2007). Genetic polymorphisms and implications for human diseases.. PubMed. 90(2). 394–8. 20 indexed citations

19.

Ma, Qianli, Kenneth J. Abel, Orapan Sripichai, et al.. (2007). β‐Globin gene cluster polymorphisms are strongly associated with severity of HbE/β⁰‐thalassemia. Clinical Genetics. 72(6). 497–505. 25 indexed citations

20.

Sripichai, Orapan, Johanna L. Whitacre, Thongperm Munkongdee, et al.. (2005). Genetic Analysis of Candidate Modifier Polymorphisms in Hb E‐β⁰‐Thalassemia Patients. Annals of the New York Academy of Sciences. 1054(1). 433–438. 15 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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