| Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 VB Pastor, SS Sahoo, J Boklan, GC Schwabe, E Saribeyoglu, B Strahm, ... haematologica 103 (3), 427, 2018 | 108 | 2018 |
| Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes SS Sahoo, VB Pastor, C Goodings, RK Voss, EJ Kozyra, A Szvetnik, ... Nature medicine 27 (10), 1806-1817, 2021 | 101 | 2021 |
| Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes SS Sahoo, EJ Kozyra, MW Wlodarski Best Practice & Research Clinical Haematology 33 (3), 101197, 2020 | 80 | 2020 |
| Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency EJ Kozyra, VB Pastor, S Lefkopoulos, SS Sahoo, H Busch, RK Voss, ... Leukemia 34 (10), 2673-2687, 2020 | 44 | 2020 |
| Clinical and molecular heterogeneity of RTEL1 deficiency C Speckmann, SS Sahoo, M Rizzi, S Hirabayashi, A Karow, NK Serwas, ... Frontiers in immunology 8, 449, 2017 | 42 | 2017 |
| Monosomy 7 in pediatric myelodysplastic syndromes MW Wlodarski, SS Sahoo, CM Niemeyer Hematology/Oncology Clinics 32 (4), 729-743, 2018 | 40 | 2018 |
| Evaluation of Salmonella enterica serovar Typhimurium TTSS-2 deficient fur mutant as safe live-attenuated vaccine candidate for immunocompromised mice V Vishwakarma, NB Pati, HS Chandel, SS Sahoo, B Saha, M Suar PLoS One 7 (12), e52043, 2012 | 40 | 2012 |
| Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue R Sharma, SS Sahoo, M Honda, SL Granger, C Goodings, L Sanchez, ... Blood, The Journal of the American Society of Hematology 139 (7), 1039-1051, 2022 | 35 | 2022 |
| Azacitidine is effective for targeting leukemia-initiating cells in juvenile myelomonocytic leukemia CF Krombholz, L Gallego-Villar, SS Sahoo, PK Panda, MW Wlodarski, ... Leukemia 33 (7), 1805-1810, 2019 | 13 | 2019 |
| Somatic mosaicism in inherited bone marrow failure syndromes F Gutierrez-Rodrigues, SS Sahoo, MW Wlodarski, NS Young Best Practice & Research Clinical Haematology 34 (2), 101279, 2021 | 11 | 2021 |
| Germline gain-of-function JAK3 mutation in familial chronic lymphoproliferative disorder of NK cells H Lesmana, M Popescu, S Lewis, SS Sahoo, C Goodings-Harris, M Onciu, ... Blood 136, 9-10, 2020 | 11 | 2020 |
| Germline GATA1 exon 2 mutation associated with chronic cytopenia and a non-down syndrome transient abnormal myelopoiesis with clonal trisomy 21 R Camargo, SS Sahoo, JC Córdoba, IQ Magalhães Leukemia 36 (9), 2347-2350, 2022 | 10 | 2022 |
| SAMD9 and SAMD9L germline disorders in patients Enrolled in studies of the European working group of MDS in childhood (EWOG-MDS): prevalence, outcome, phenotype and functional … SS Sahoo, VP Loyola, PK Panda, EA Szvetnik, EJ Kozyra, RK Voss, ... Blood 132, 643, 2018 | 10 | 2018 |
| Cholera toxin-B (ctxB) antigen expressing Salmonella Typhimurium polyvalent vaccine exerts protective immune response against Vibrio cholerae infection V Vishwakarma, SS Sahoo, S Das, S Ray, WD Hardt, M Suar Vaccine 33 (15), 1880-1889, 2015 | 10 | 2015 |
| European Working Group of MDS in Children (EWOG-MDS) SS Sahoo, VB Pastor, C Goodings, RK Voss, EJ Kozyra, A Szvetnik, ... Clinical evolution, genetic landscape and trajectories of clonal …, 2021 | 8 | 2021 |
| Diamond-Blackfan anemia phenotype caused by deficiency of adenosine deaminase 2 EA Szvetnik, C Klemann, I Hainmann, T Farkas, M Niewisch, R Grosse, ... Blood 130, 874, 2017 | 7 | 2017 |
| Impaired overall survival in young patients with acute myeloid leukemia and variants in genes predisposing for myeloid malignancies M Kirschner, B Rolles, M Crysandt, C Röllig, F Stölzel, M Kramer, ... HemaSphere 6 (11), e787, 2022 | 3 | 2022 |
| Monosomy 7 as the initial hit followed by sequential acquisition of SETBP1 and ASXL1 driver mutations in childhood myelodysplastic syndromes VP Loyola, PK Panda, SS Sahoo, EA Szvetnik, EJ Kozyra, RK Voss, ... Blood 132, 105, 2018 | 3 | 2018 |
| Systematic assessment of GATA2 genetic variation reveals the presence of novel disease-causing synonymous exonic mutations EJ Kozyra, V Pastor Loyola, C Wehr, SS Sahoo, R Voss, EA Szvetnik, ... Blood, The Journal of the American Society of Hematology 130 (Suppl_1), 2449 …, 2017 | 2 | 2017 |
| Constitutional SAMD9L mutations cause familial myelodisplastic syndrome with monosomy 7 and stable revertant mosaicism VP Loyola, SS Sahoo, J Boklan, G Schwabe, B Strahm, D Lebrecht, ... Blood 130, 1672, 2017 | 1 | 2017 |
Victor PastorSt.Jude Children’s Research HospitalVerified email at stjude.org
