| Title | Author | Year | SCOPUS | PUBMED | ISI | TCI | |
|---|---|---|---|---|---|---|---|
| 1. | Incidence of hepatocellular carcinoma in children in Khon Kaen before and after national hepatitis B vaccine program. | Wichajarn, K Kosalaraksa, P Wiangnon, S |
0 | ||||
| 2. | Incidence of Hepatocellular Carcinoma in Children in Khon Kaen before and after National Hepatitis B Vaccine Program | Wichajarn, K. Kosalaraksa, P. Wiangnon, S. |
2008 | ||||
| 3. | Difference of clinical phenotypes and immunological features of 22q11.2 deletion syndrome in north-eastern thai children compare to western countries | Wichajarn, K. Kampan, J. |
2014 | ||||
| 4. | Prevalence and type of associated syndromes in patients with cleft lip and cleft palate who received the treatment in Tawanchai center until 4-5 years of age | Wichajarn, K Panamonta, O Pradubwong, S Panamonta, M Weraarchakul, W Chowchuen, B |
2014 | ||||
| 5. | Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: A 5-year retrospective study | Khunton Wichajarn Somporn Liammongkolkul Nithiwat Vatanavicharn Duangrurdee Wattanasirichaigoon |
2017 | ||||
| 6. | Cardiovascular malformations in patients with treacher collins syndrome: A systematic review | Panamonta, M. Chaikitpinyo, A. Wongswadiwat, Y. Panamonta, O. Wichajarn, K. |
2018 | ||||
| 7. | Gastrointestinal malformations in patients with treacher collins syndrome: A systematic review | Panamonta, M. Panamonta, O. Wichajarn, K. |
2018 | ||||
| 8. | Urinary system malformations in patients with treacher collins syndrome: A systematic review | Wisanuyotin, S. Komvilaisak, P. Jirapradittha, J. Panamonta, M. Panamonta, O. Wichajarn, K. |
2018 | ||||
| 9. | Detection of the G1138A mutation in the FGFR3 gene for the diagnosis of achondroplasia by allele-specific polymerase chain reaction | Imtawil, K.J. Loilome, W. Tangrassameeprasert, R. Wichajarn, K. |
2019 | ||||
| 10. | PHACE syndrome: A review of clinical manifestation and management | Techasatian, L Uppala, R. Panombualert, S. Wichajarn, K. Winaikosol, K. |
2019 | ||||
| 11. | Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years | Nantiya Mongkollarp Thipwimol Tim-Aroon Chusak Okascharoen Khunton Wichajarn Jeeraparn Phosuwattanakul Nalinee Chongviriyaphan Duangrurdee Wattanasirichaigoon |
2020 | ||||
| 12. | Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years. | Mongkollarp, N Tim-Aroon, T Okascharoen, C Wichajarn, K Phosuwattanakul, J Chongviriyaphan, N Wattanasirichaigoon, D |
2020 | ||||
| 13. | The Effects of the Face Mask on the Skin Underneath: A Prospective Survey During the COVID-19 Pandemic | Techasatian, L. Uppala, R. Supakunpinyo, C. Panombualert, S. Wichajarn, K. Kiatchoosakun, P. Kosalaraksa, P. |
2020 | ||||
| 14. | Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients | Phetthong, T Tim-Aroon, T Khongkraparn, A Noojarern, S Kuptanon, C Wichajarn, K Sathienkijkanchai, A Suphapeetiporn, K Charoenkwan, P Tantiworawit, A Noentong, N Wattanasirichaigoon, D |
2021 | ||||
| 15. | Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients. | Thipwimol Tim-Aroon Khunton Wichajarn Kamornwan Katanyuwong Pranoot Tanpaiboon Nithiwat Vatanavicharn Kullasate Sakpichaisakul Arthaporn Kongkrapan Jakris Eu-ahsunthornwattana Supranee Thongpradit Kanya Moolsuwan Nusara Satproedprai Surakameth Mahasirimongkol Tassanee Lerksuthirat Bhoom Suktitipat Natini Jinawath Duangrurdee Wattanasirichaigoon |
2021 | ||||
| 16. | Application of the PCR and allele-specific PCR-nucleic acid lateral flow immunoassay for the detection of the SRY gene and the G1138A mutation in the FGFR3 gene for the human DNA | Sukjai, A. Puangmali, T. Wichajarn, K. Monthatong, M. |
2023 | ||||
| 17. | Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians | Khongthon, N. Theeraviwatwong, M. Wichajarn, K. Rojnueangnit, K. |
2024 | ||||
| 18. | Exploring molecular spectrum in thai patients with maple syrup urine disease: unveiling a common variant | Lakkhana, P. Tim-Aroon, T. Khongkraparn, A. Noojarern, S. Wongkittichote, P. Wichajarn, K. Kuptanon, C. Boonyawat, B. Suphapeetiporn, K. Wejaphikul, K. Seo, G.H. Wattanasirichaigoon, D. |
2024 | ||||
| 19. | Assessing the Value for Money of Enzyme Replacement Therapy in Gaucher Disease Types 1 and 3b: Can Expanded Coverage Be Justified? | Rattanavipapong, W Anothaisintawee, T Isaranuwatchai, W Wattanasirichaigoon, D Tim-Aroon, T Wichajarn, K Sathienkijkanchai, A Charoenkwan, P Suphapeetiporn, K Traivaree, C Kuptanon, C Teerawattananon, Y |
2025 | Count | 16 | 7 | 6 | 0 |
| Title | Authors | Year | Publication name | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | Total | ||||||
| 1. | Incidence of hepatocellular carcinoma in children in Khon Kaen before and after national hepatitis B vaccine program | Wichajarn, K. Kosalaraksa, P. Wiangnon, S. |
2008 |
Asian Pacific Journal of Cancer Prevention 3 (9), pp. 507-510 |
||||||||
| 2. | Difference of clinical phenotypes and immunological features of 22q11.2 deletion syndrome in north-eastern thai children compare to western countries | Wichajarn, K. Kampan, J. |
2014 |
Journal of the Medical Association of Thailand (97), pp. S59-S66 |
||||||||
| 3. | Prevalence and type of associated syndromes in patients with cleft lip and cleft palate who received the treatment in Tawanchai center until 4-5 years of age | Wichajarn, K. Panamonta, O. Pradubwong, S. Panamonta, M. Weraarchakul, W. Chowchuen, B. |
2014 |
Journal of the Medical Association of Thailand (97), pp. S105-S109 |
||||||||
| 4. | Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: A 5-year retrospective study | Wichajarn, K. | 2017 |
Asian Biomedicine 1 (11), pp. 41-47 |
||||||||
| 5. | Cardiovascular malformations in patients with treacher collins syndrome: A systematic review | Panamonta, M. Chaikitpinyo, A. Wongswadiwat, Y. Panamonta, O. Wichajarn, K. |
2018 |
Journal of the Medical Association of Thailand 5 (101), pp. S221-S226 |
||||||||
| 6. | Gastrointestinal malformations in patients with treacher collins syndrome: A systematic review | Panamonta, M. Panamonta, O. Wichajarn, K. |
2018 |
Journal of the Medical Association of Thailand 5 (101), pp. S227-S232 |
||||||||
| 7. | Urinary system malformations in patients with treacher collins syndrome: A systematic review | Wisanuyotin, S. Komvilaisak, P. Jirapradittha, J. Panamonta, M. Panamonta, O. Wichajarn, K. |
2018 |
Journal of the Medical Association of Thailand 5 (101), pp. S233-S237 |
||||||||
| 8. | Detection of the G1138A mutation in the FGFR3 gene for the diagnosis of achondroplasia by allele-specific polymerase chain reaction | Imtawil, K.J. Loilome, W. Tangrassameeprasert, R. Wichajarn, K. |
2019 |
Journal of the Medical Association of Thailand 6 (102), pp. 118-121 |
||||||||
| 9. | PHACE syndrome: A review of clinical manifestation and management | Techasatian, L Uppala, R. Panombualert, S. Wichajarn, K. Winaikosol, K. |
2019 |
Journal of the Medical Association of Thailand 6 (102), pp. 132-138 |
||||||||
| 10. | Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years | Wichajarn, K. | 2020 |
Orphanet Journal of Rare Diseases 1 (15), pp. |
||||||||
| 11. | The Effects of the Face Mask on the Skin Underneath: A Prospective Survey During the COVID-19 Pandemic | Techasatian, L. Uppala, R. Supakunpinyo, C. Panombualert, S. Wichajarn, K. Kiatchoosakun, P. Kosalaraksa, P. |
2020 |
Journal of Primary Care and Community Health (11), pp. |
||||||||
| 12. | Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients | Wichajarn, K. Suphapeetiporn, K. |
2021 |
Orphanet Journal of Rare Diseases 1 (16), pp. |
||||||||
| 13. | Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients | Wichajarn, K. Mahasirimongkol, S. |
2021 |
BMC Pediatrics 1 (21), pp. |
||||||||
| 14. | Application of the PCR and allele-specific PCR-nucleic acid lateral flow immunoassay for the detection of the SRY gene and the G1138A mutation in the FGFR3 gene for the human DNA | Sukjai, A. Puangmali, T. Wichajarn, K. Monthatong, M. |
2023 |
Journal of Applied Biology and Biotechnology 5 (11), pp. 165-173 |
||||||||
| 15. | Comparison of the Accuracy in Provisional Diagnosis of 22q11.2 Deletion and Williams Syndromes by Facial Photos in Thai Population Between De-Identified Facial Program and Clinicians | Khongthon, N. Theeraviwatwong, M. Wichajarn, K. Rojnueangnit, K. |
2024 |
Application of Clinical Genetics (17), pp. 107-115 |
||||||||
| 16. | Exploring molecular spectrum in thai patients with maple syrup urine disease: unveiling a common variant | Lakkhana, P. Tim-Aroon, T. Khongkraparn, A. Noojarern, S. Wongkittichote, P. Wichajarn, K. Kuptanon, C. Boonyawat, B. Suphapeetiporn, K. Wejaphikul, K. Seo, G.H. Wattanasirichaigoon, D. |
2024 |
Orphanet Journal of Rare Diseases 1 (19), pp. |
||||||||
| Title | Authors | Year | Journal title | ||
|---|---|---|---|---|---|
| 1. | Prevalence and type of associated syndromes in patients with cleft lip and cleft palate who received the treatment in Tawanchai Center until 4-5 years of age. | Wichajarn, K Panamonta, O Pradubwong, S Panamonta, M Weraarchakul, W Chowchuen, B |
2014 |
Journal of the Medical Association of Thailand = Chotmaihet thangphaet (97), pp. S105-9 |
|
| 2. | Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years. | Mongkollarp, N Tim-Aroon, T Okascharoen, C Wichajarn, K Phosuwattanakul, J Chongviriyaphan, N Wattanasirichaigoon, D |
2020 |
Orphanet journal of rare diseases 1 (15), pp. 111 |
|
| 3. | The Effects of the Face Mask on the Skin Underneath: A Prospective Survey During the COVID-19 Pandemic. | Techasatian, L Lebsing, S Uppala, R Thaowandee, W Chaiyarit, J Supakunpinyo, C Panombualert, S Mairiang, D Saengnipanthkul, S Wichajarn, K Kiatchoosakun, P Kosalaraksa, P |
2020 |
Journal of primary care & community health (11), pp. 2150132720966167 |
|
| 4. | Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients. | Phetthong, T Tim-Aroon, T Khongkraparn, A Noojarern, S Kuptanon, C Wichajarn, K Sathienkijkanchai, A Suphapeetiporn, K Charoenkwan, P Tantiworawit, A Noentong, N Wattanasirichaigoon, D |
2021 |
Orphanet journal of rare diseases 1 (16), pp. 519 |
|
| 5. | Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients. | Tim-Aroon, T Wichajarn, K Katanyuwong, K Tanpaiboon, P Vatanavicharn, N Sakpichaisakul, K Kongkrapan, A Eu-Ahsunthornwattana, J Thongpradit, S Moolsuwan, K Satproedprai, N Mahasirimongkol, S Lerksuthirat, T Suktitipat, B Jinawath, N Wattanasirichaigoon, D |
2021 |
BMC pediatrics 1 (21), pp. 22 |
|
| 6. | Assessing the Value for Money of Enzyme Replacement Therapy in Gaucher Disease Types 1 and 3b: Can Expanded Coverage Be Justified? | Rattanavipapong, W Anothaisintawee, T Isaranuwatchai, W Wattanasirichaigoon, D Tim-Aroon, T Wichajarn, K Sathienkijkanchai, A Charoenkwan, P Suphapeetiporn, K Traivaree, C Kuptanon, C Teerawattananon, Y |
2025 |
PharmacoEconomics - open 4 (9), pp. 611-626 |
|
| 7. | Incidence of hepatocellular carcinoma in children in Khon Kaen before and after national hepatitis B vaccine program. | Wichajarn, K Kosalaraksa, P Wiangnon, S |
Asian Pacific journal of cancer prevention : APJCP 3 (9), pp. 507-9 |
| Title | Authors | Year | Journal title | Cited count | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| < 2020 | 2021 | 2022 | 2023 | 2024 | 2025 | Total | ||||||
| 1. | Incidence of Hepatocellular Carcinoma in Children in Khon Kaen before and after National Hepatitis B Vaccine Program | Khunton Wichajarn Pope Kosalaraksa Surapon Wiangnon |
2008 |
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION 3.0 (9.0), pp. 507.0-509.0 |
76 | 0 | 0 | 0 | 0 | 0 | 76 | |
| 2. | Clinical and laboratory findings and outcomes of classic organic acidurias in children from north-eastern Thailand: a 5-year retrospective study | Khunton Wichajarn Somporn Liammongkolkul Nithiwat Vatanavicharn Duangrurdee Wattanasirichaigoon |
2017 |
ASIAN BIOMEDICINE 1.0 (11.0), pp. 41.0-47.0 |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 3. | Growth charts for Thai children with Prader-Willi syndrome aged 0-18 years | Nantiya Mongkollarp Thipwimol Tim-Aroon Chusak Okascharoen Khunton Wichajarn Jeeraparn Phosuwattanakul Nalinee Chongviriyaphan Duangrurdee Wattanasirichaigoon |
2020 |
ORPHANET JOURNAL OF RARE DISEASES 1.0 (15.0), pp. |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 4. | The Effects of the Face Mask on the Skin Underneath: A Prospective Survey During the COVID-19 Pandemic | Leelawadee Techasatian Sirirus Lebsing Rattapon Uppala Wilairat Thaowandee Jitjira Chaiyarit Chanyut Supakunpinyo Sunee Panombualert Dara Mairiang Suchaorn Saengnipanthkul Khunton Wichajarn Pakaphan Kiatchoosakun Pope Kosalaraksa |
2020 |
JOURNAL OF PRIMARY CARE AND COMMUNITY HEALTH (11.0), pp. |
10 | 0 | 0 | 0 | 0 | 0 | 10 | |
| 5. | Gaucher disease: clinical phenotypes and refining GBA mutational spectrum in Thai patients | Tim Phetthong Thipwimol Tim-Aroon Arthaporn Khongkraparn Saisuda Noojarern Chulaluck Kuptanon Khunton Wichajarn Achara Sathienkijkanchai Kanya Suphapeetiporn Pimlak Charoenkwan Adisak Tantiworawit Naruwan Noentong Duangrurdee Wattanasirichaigoon |
2021 |
ORPHANET JOURNAL OF RARE DISEASES 1.0 (16.0), pp. |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| 6. | Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients | Thipwimol Tim-Aroon Khunton Wichajarn Kamornwan Katanyuwong Pranoot Tanpaiboon Nithiwat Vatanavicharn Kullasate Sakpichaisakul Arthaporn Kongkrapan Jakris Eu-ahsunthornwattana Supranee Thongpradit Kanya Moolsuwan Nusara Satproedprai Surakameth Mahasirimongkol Tassanee Lerksuthirat Bhoom Suktitipat Natini Jinawath Duangrurdee Wattanasirichaigoon |
2021 |
BMC PEDIATRICS 1.0 (21.0), pp. |
0 | 0 | 0 | 0 | 0 | 0 | 0 | |
| Title | Authors | Year | Journal title |
|---|
| Title | Authors | NRIIS type | Year | NRIIS Scholarship | ||
|---|---|---|---|---|---|---|
| 1. | รูปแบบการดูแลที่สมบูรณ์แบบในผู้ป่วยปากแหว่งเพดานโหว่ของศูนย์ตะวันฉาย |
ศ.นพ. บวรศิลป์ เชาวน์ชื่น นางเบญจมาศ พระธานี รศ.ดร.พญ. นิรมล พัจนสุนทร รศ.ดร.พญ. ผกาพรรณ เกียรติชูสกุล รศ.ดร.พญ. อมรรัตน์ รัตนสิริ ผศ.ดร.ทพ. ดร พูนศักดิ์ ผศ.ดร. ขนิษฐา วรธงชัย ผศ.ดร.นพ. พลากร สุรกุลประภา ผศ.ดร.นพ. กุณฑล วิชาจารย์ ผศ.ดร.พญ. รสวันต์ อารีมิตร อ.ดร.ทพญ. ปฏิมาพร พึ่งชาญชัยกุล อ.ดร. อภิศักดิ์ พัฒนจักร อ. จินตนา สิงขรอาจ นางสาวธารินี เพชรรัตน์ นางสุธีรา ประดับวงษ์ นางจำรัส วงศ์คำ นางสมจิตร์ หร่องบุตรศรี นางสมจิตร์ มณีกานนท์ |
โครงการ | 2562 | ทุนงบประมาณแผ่นดินประจำปี 2562 (งบบูรณาการวิจัยและนวัตกรรม) |