Orapan Sripichai

1.2k citations

29 papers · 894 indexed · h-index 16

Genetics top 1%
- Hemoglobinopathies and Related Disorders 25
- Genetic Associations and Epidemiology 5
- Nutrition, Genetics, and Disease 1
Hematology top 2%
- Iron Metabolism and Disorders 15
- Blood groups and transfusion 4
Pediatrics, Perinatology and Child Health top 10%
- Prenatal Screening and Diagnostics 6
Nutrition and Dietetics top 10%
Physiology
- Erythrocyte Function and Pathophysiology 6
Molecular Biology
- Epigenetics and DNA Methylation 6

Co-authors: Suthat Fucharoen Thongperm Munkongdee Pranee Winichagoon Jeffery L. Miller Toshihiko Tanno Colleen Byrnes Wattanan Makarasara Y. Terry Lee
Cited by: Genetics Hematology Pediatrics, Perinatology and Child Health
Journals: Blood (5 papers)Journal of Clinical Medicine (2 papers)International Journal of Hematology (2 papers)
Partner nations: Thailand United States Sri Lanka

In The Last Decade

Orapan Sripichai

28 papers receiving 883 citations

Peers

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

The 25 scholars most cited alongside Orapan Sripichai, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Orapan Sripichai Line = papers co-authored together Orapan Sripichai links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Induction of fetal hemoglobin: Lentiviral shRNA knockdown of HBS1L in β0-thalassemia/HbE erythroid cells PLoS ONE ·Atanaskovic-Markovic Marina,Orapan Sripichai,Natee Jearawiriyapaisarn,Suthat Fucharoen,Chayanon Peerapittayamongkol	2023	0
2	Down-regulation of the transcriptional repressor ZNF802 (JAZF1) reactivates fetal hemoglobin in β0-thalassemia/HbE Scientific Reports ·Filip Vercruysse,Atanaskovic-Markovic Marina,Orapan Sripichai,J.-R. Samoano,Nuankanya Sathirapongsasuti,Duantida Songdej,Amornrat Tangprasittipap,Suradej Hongeng	2022	5
3	Clinical Severity of β-Thalassemia Pediatric Patients in Myanmar Hemoglobin ·I Buendía-Roldán,Caroline Bouteiller-Reuter,Kittiphong Paiboonsukwong,Khin Maung Win,Suthat Fucharoen,Orapan Sripichai	2022	1
4	Impaired Terminal Erythroid Maturation in β0-Thalassemia/HbE Patients with Different Clinical Severity Journal of Clinical Medicine ·Abdul-Hafeed Ali Fakih,Pranee Winichagoon,Suthat Fucharoen,Orapan Sripichai	2022	6
5	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 ·Abdul-Hafeed Ali Fakih,雅志藤井,S. Mukherjee,Atanaskovic-Markovic Marina,Suradej Hongeng,Suthat Fucharoen,Orapan Sripichai	2021	2
6	Visual genotyping of thalassemia by using pyrrolidinyl peptide nucleic acid probes immobilized on carboxymethylcellulose-modified paper and enzyme-induced pigmentation Microchimica Acta ·Silvia Araneo,Thongperm Munkongdee,Kanet Wongravee,Orapan Sripichai,Suthat Fucharoen,Thanit Praneenararat,Tirayut Vilaivan	2020	18
7	UNC0638 induces high levels of fetal hemoglobin expression in β-thalassemia/HbE erythroid progenitor cells Annals of Hematology ·Manolo Cleiton,S. Mukherjee,Cen Zhexin,雅志藤井,Duantida Songdej,Kittiphong Paiboonsukwong,Orapan Sripichai,James Douglas Engel,Suradej Hongeng,Suthat Fucharoen,Natee Jearawiriyapaisarn	2020	18
8	Prevalence and antimicrobial susceptibility of Campylobacter isolated from retail chickens in Thailand International Journal of Food Microbiology ·Piyada Wangroongsarb,喜成山寺,Brad Wilk,Alison Kirby Record,Marcus Gil Barbosa Dias,Kayla Watabu,Chaiwat Pulsrikarn,Sittiporn Parnmen,Orapan Sripichai	2020	22
9	Development of DNA controls for detection of β‐thalassemia mutations commonly found in Asian International Journal of Laboratory Hematology ·Thongperm Munkongdee,Manolo Cleiton,Alexander Netreba,Almira Rizki Pontania,Kittiphong Paiboonsukwong,Orapan Sripichai,Saovaros Svasti,Pranee Winichagoon,Suthat Fucharoen,Natee Jearawiriyapaisarn	2020	2
10	Genetic variation of Krüppel-like factor 1 (KLF1) and fetal hemoglobin (HbF) levels in β0-thalassemia/HbE disease International Journal of Hematology ·S. Mukherjee,Orapan Sripichai,Thongperm Munkongdee,Suthat Fucharoen,Sissades Tongsima,Duncan R. Smith	2017	15
11	Fetal hemoglobin regulation in β-thalassemia: heterogeneity, modifiers and therapeutic approaches Expert Review of Hematology ·Orapan Sripichai,Suthat Fucharoen	2016	35
12	Insight into the Peopling of Mainland Southeast Asia from Thai Population Genetic Structure PLoS ONE ·Pongsakorn Wangkumhang,Philip J. Shaw,Kridsadakorn Chaichoompu,Chumpol Ngamphiw,Anunchai Assawamakin,Manit Nuinoon,Orapan Sripichai,Saovaros Svasti,Suthat Fucharoen,Verayuth Praphanphoj,Sissades Tongsima	2013	25
13	Genetic modifiers of Hb E/β0 thalassemia identified by a two-stage genome-wide association study BMC Medical Genetics ·Richard Sherva,Orapan Sripichai,Kenneth J. Abel,Qianli Ma,Johanna L. Whitacre,Vach Angkachatchai,Wattanan Makarasara,Pranee Winichagoon,Saovaros Svasti,Suthat Fucharoen,Andreas Braun,Lindsay A. Farrer	2010	22
14	A genome-wide association identified the common genetic variants influence disease severity in β0-thalassemia/hemoglobin E Human Genetics ·Manit Nuinoon,Wattanan Makarasara,Taisei Mushiroda,Iswari Setianingsih,Pustika Amalia Wahidiyat,Orapan Sripichai,Natsuhiko Kumasaka,Atsushi Takahashi,Saovaros Svasti,Thongperm Munkongdee,Surakameth Mahasirimongkol,Chayanon Peerapittayamongkol,Vip Viprakasit,Naoyuki Kamatani,Pranee Winichagoon,Michiaki Kubo,Yusuke Nakamura,Suthat Fucharoen	2009	146
15	Association of SNP in exon 1 of HBS1L with hemoglobin F level in β0-thalassemia/hemoglobin E International Journal of Hematology ·Homas Brighton Bhebhe,Saovaros Svasti,Orapan Sripichai,Thongperm Munkongdee,Kanokporn Triwitayakorn,Pranee Winichagoon,Suthat Fucharoen,Chayanon Peerapittayamongkol	2008	15
16	A scoring system for the classification of β‐thalassemia/Hb E disease severity American Journal of Hematology ·Orapan Sripichai,Wattanan Makarasara,Thongperm Munkongdee,Chutima Kumkhaek,Issarang Nuchprayoon,Ampaiwan Chuansumrit,Suporn Chuncharunee,His-Lin Hsiao,عبد الملك مرتــاض,Pranee Winichagoon,Suthat Fucharoen	2008	106
17	Coinheritance of the different copy numbers of α-globin gene modifies severity of β-thalassemia/Hb E disease Annals of Hematology ·Orapan Sripichai,Thongperm Munkongdee,Chutima Kumkhaek,Saovaros Svasti,Pranee Winichagoon,Suthat Fucharoen	2007	40
18	β‐Globin gene cluster polymorphisms are strongly associated with severity of HbE/β⁰‐thalassemia Clinical Genetics ·Qianli Ma,Kenneth J. Abel,Orapan Sripichai,Johanna L. Whitacre,Vach Angkachatchai,Wattanan Makarasara,Pattanee Winichagoon,Supan Fucharoen,Andreas Braun,Lindsay A. Farrer	2007	25
19	Genetic polymorphisms and implications for human diseases. PubMed ·Orapan Sripichai,Suthat Fucharoen	2007	20
20	Genetic Analysis of Candidate Modifier Polymorphisms in Hb E‐β⁰‐Thalassemia Patients Annals of the New York Academy of Sciences ·Orapan Sripichai,Johanna L. Whitacre,Thongperm Munkongdee,Chutima Kumkhaek,Wattanan Makarasara,Pranee Winichagoon,Ken Abel,Andreas Braun,Suthat Fucharoen	2005	15

About Orapan Sripichai

Orapan Sripichai is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 29 papers that have together received 894 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (25 papers), Iron Metabolism and Disorders (15 papers), Erythrocyte Function and Pathophysiology (6 papers), Epigenetics and DNA Methylation (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Associations and Epidemiology (5 papers), Blood groups and transfusion (4 papers) and Nutrition, Genetics, and Disease (1 paper). The work is most often cited by research in Genetics (687 citations), Hematology (598 citations) and Pediatrics, Perinatology and Child Health (140 citations). Orapan Sripichai has collaborated with scholars based in Thailand, United States and Sri Lanka. Frequent co-authors include Suthat Fucharoen, Thongperm Munkongdee, Pranee Winichagoon, Jeffery L. Miller, Toshihiko Tanno, Colleen Byrnes, Wattanan Makarasara, Y. Terry Lee, Ajoy Bhupatiraju and Omid F. Harandi. Their work appears in journals such as Blood, Journal of Clinical Medicine, International Journal of Hematology, Annals of Hematology and PLoS ONE.

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