| Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome S Dhanraj, A Matveev, H Li, S Lauhasurayotin, L Jardine, M Cada, ... Blood, The Journal of the American Society of Hematology 129 (11), 1557-1562, 2017 | 138 | 2017 |
| Androgen therapy in inherited bone marrow failure syndromes: analysis from the Canadian Inherited Marrow Failure Registry A Català, SS Ali, GDE Cuvelier, MG Steele, RJ Klaassen, CV Fernandez, ... British journal of haematology 189 (5), 976-981, 2020 | 10 | 2020 |
| The pattern of microorganisms and drug susceptibility in pediatric oncologic patients with febrile neutropenia T Jungrungrueng, S Anugulruengkitt, S Lauhasurayotin, K Chiengthong, ... Journal of Pathogens 2021, 2021 | 9 | 2021 |
| Biallelic mutations in EXOC3L2 cause a novel syndrome that affects the brain, kidney and blood A Shalata, S Lauhasurayotin, Z Leibovitz, H Li, D Hebert, S Dhanraj, ... Journal of medical genetics 56 (5), 340-346, 2019 | 9 | 2019 |
| Immune response after 2 doses of BNT162b2 mRNA COVID-19 vaccinations in children and adolescents with cancer and hematologic diseases H Poparn, C Srichumpuang, D Sosothikul, W Jantarabenjakul, ... Asian Pacific Journal of Cancer Prevention 23 (6), 2049-2055, 2022 | 8 | 2022 |
| Clinical and molecular characteristics of Thai patients with ELANE-related neutropaenia R Ittiwut, K Sengpanich, S Lauhasurayotin, C Ittiwut, V Shotelersuk, ... Journal of clinical pathology 75 (2), 99-103, 2022 | 7 | 2022 |
| A study to assess and improve adherence to Iron Chelation Therapy in Transfusion-Dependent Thalassemia patients K Theppornpitak, B Trakarnsanga, S Lauhasurayotin, H Poparn, ... Hemoglobin 45 (3), 171-174, 2021 | 5 | 2021 |
| Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels S Lauhasurayotin, GD Cuvelier, RJ Klaassen, CV Fernandez, YD Pastore, ... NPJ Genomic Medicine 4 (1), 30, 2019 | 4 | 2019 |
| Red blood cell alloimmunization and other transfusion‐related complications in patients with transfusion‐dependent thalassemia: a multi‐center study in Thailand N Teawtrakul, D Songdej, C Hantaweepant, A Tantiworawit, ... Transfusion 62 (10), 2039-2047, 2022 | 3 | 2022 |
| KRAS mutation in pediatric intracranial germ cell tumors C Khaiman, P Techavichit, H Poparn, K Chiengthong, S Lauhasurayotin, ... Asian Pacific Journal of Cancer Prevention: APJCP 23 (9), 3179, 2022 | 2 | 2022 |
| A study of the TP53 Germline Mutation and Clinicopathologic Features in Thai Children with Adrenocortical Carcinoma N Aungkawattanapong, P Techavichit, S Lauhasurayotin, K Chiengthong, ... Journal of Health Science and Medical Research 39 (6), 491-502, 2021 | 2 | 2021 |
| Predictive factors of severe adverse events in pediatric oncologic patients with febrile neutropenia J Thangthong, S Anugulruengkitt, S Lauhasurayotin, K Chiengthong, ... Asian Pacific Journal of Cancer Prevention: APJCP 21 (12), 3487, 2020 | 2 | 2020 |
| Thalassemia‐related complications in pediatric, adolescent, and young adult patients with transfusion‐dependent thalassemia: A multicenter study in Thailand P Surapolchai, D Songdej, C Hantaweepant, A Tantiworawit, ... Pediatric Blood & Cancer 70 (10), e30599, 2023 | 1 | 2023 |
| Complicated bleeding challenge and intraoperative safety strategies in a case of hemophilia a with rhabdomyosarcoma P Chaweephisal, H Poparn, K Chiengthong, P Seksarn, P Techavichit, ... Pediatric Hematology and Oncology 39 (7), 672-677, 2022 | 1 | 2022 |
| Germline PTPN13 mutations in patients with bone marrow failure and acute lymphoblastic leukemia H Moshiri, DA Cabrera Riofrío, YJ Lim, S Lauhasurayotin, M Manisterski, ... Leukemia 36 (8), 2132-2135, 2022 | 1 | 2022 |
| Prenatal Diagnosis Leads to Early Diagnosis of Transfusion-Dependent Thalassemia and Better Growth Outcomes N Asawasudsakorn, S Lauhasurayotin, H Poparn, K Chiengthong, ... Global Pediatric Health 8, 2333794X211046104, 2021 | 1 | 2021 |
| Correction to: Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi‑center registry (Annals of Hematology,(2024), 103, 2,(385-393), 10 … D Songdej, P Surapolchai, P Komwilaisak, P Sripornsawan, ... Annals of Hematology 103 (2), 395, 2024 | | 2024 |
| Molecular characteristics of hereditary red blood cell membrane disorders in Thailand: a multi-center registry D Songdej, P Surapolchai, P Komwilaisak, P Sripornsawan, ... Annals of Hematology 103 (2), 385-393, 2024 | | 2024 |
| A pharmacokinetic study of native E. coli asparaginase for acute lymphoblastic leukemia treated with ThaiPOG protocol T Thranpanich, A Suroengrit, P Aungbamnet, P Seksarn, D Sosothikul, ... | | 2024 |
| Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand S Lauhasurayotin, C Moonla, R Ittiwut, C Ittiwut, N Songthawee, ... Journal of Clinical Pathology, 2023 | | 2023 |
