| 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 |
| Akt is upstream and MAPKs are downstream of NF-κB in paclitaxel-induced survival signaling events, which are down-regulated by curcumin contributing to their synergism SV Bava, CN Sreekanth, AKT Thulasidasan, NP Anto, VT Cheriyan, ... The international journal of biochemistry & cell biology 43 (3), 331-341, 2011 | 100 | 2011 |
| Bone marrow failure and developmental delay caused by mutations in poly (A)-specific ribonuclease (PARN) S Dhanraj, SMR Gunja, AP Deveau, M Nissbeck, B Boonyawat, ... Journal of Medical Genetics 52 (11), 738-748, 2015 | 93 | 2015 |
| Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromes I Ghemlas, H Li, B Zlateska, R Klaassen, CV Fernandez, RA Yanofsky, ... Journal of medical genetics 52 (9), 575-584, 2015 | 82 | 2015 |
| Combined de-novo mutation and non-random X-chromosome inactivation causing Wiskott-Aldrich syndrome in a female with thrombocytopenia B Boonyawat, S Dhanraj, F Al Abbas, B Zlateska, E Grunenbaum, ... Journal of clinical immunology 33, 1150-1155, 2013 | 38 | 2013 |
| Proximal radio-ulnar synostosis with bone marrow failure syndrome in an infant without a HOXA11 mutation P Castillo-Caro, S Dhanraj, P Haut, K Robertson, Y Dror, ... Journal of pediatric hematology/oncology 32 (6), 479-485, 2010 | 33 | 2010 |
| Molecular characteristics of a pancreatic adenocarcinoma associated with Shwachman‐Diamond syndrome S Dhanraj, A Manji, D Pinto, SW Scherer, H Favre, ML Loh, R Chetty, ... Pediatric blood & cancer 60 (5), 754-760, 2013 | 26 | 2013 |
| The clinical impact of copy number variants in inherited bone marrow failure syndromes N Waespe, S Dhanraj, M Wahala, E Tsangaris, T Enbar, B Zlateska, H Li, ... NPJ genomic medicine 2 (1), 18, 2017 | 12 | 2017 |
| 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 |
| Cellular and molecular architecture of hematopoietic stem cells and progenitors in genetic models of bone marrow failure S Heidemann, B Bursic, S Zandi, H Li, S Abelson, RJ Klaassen, S Abish, ... JCI insight 5 (4), 2020 | 7 | 2020 |
| 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 |
| 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 |
| Characterizing Dyskeratosis Congenita Caused By Parn Mutations in the Zebrafish A Cordeiro, AP Deveau, S Dhanraj, Y Dror, J Berman Blood 134, 3744, 2019 | 1 | 2019 |
| Cellular and Molecular Architecture of Hematopoietic Stem Cells and Progenitors in Genetic Models of Bone Marrow Failure SC Heidemann, B Bursic, S Zandi, H Li, RJ Klaassen, S Abish, M Rayar, ... Blood, The Journal of the American Society of Hematology 134 (Supplement_1 …, 2019 | | 2019 |
| Curcumin: A Potent Candidate to be Evaluated as a Chemosensitizer in Paclitaxel Chemotherapy Against Cervical Cancer CN Sreekanth, SV Bava, AKT Thulasidasan, NP Anto, VT Cheriyan, ... Perspectives in Cancer Prevention-Translational Cancer Research, 21-43, 2014 | | 2014 |
| THE FIRST REPORT OF A SOLID TUMOR IN SHWACHMAN-DIAMOND SYNDROME (SDS): A CLINICAL AND GENETIC ANALYSIS A Manji, S Dhanraj, C Anath, SL Adams, S Scherer, R Chetty, A Wei, ... PEDIATRIC BLOOD & CANCER 54 (6), 801-801, 2010 | | 2010 |
| Letter to Blood S Dhanraj, A Matveev, H Li, S Lauhasurayotin, L Jardine, M Cada, ... | | |
