| De novo loss-of-function mutations in USP9X cause a female-specific recognizable syndrome with developmental delay and congenital malformations MRF Reijnders, V Zachariadis, B Latour, L Jolly, GM Mancini, R Pfundt, ... The American Journal of Human Genetics 98 (2), 373-381, 2016 | 93 | 2016 |
| DNA methylation-based subtype prediction for pediatric acute lymphoblastic leukemia J Nordlund, CL Bäcklin, V Zachariadis, L Cavelier, J Dahlberg, ... Clinical epigenetics 7, 1-12, 2015 | 77 | 2015 |
| Impact of IKZF1 deletions and PAX5 amplifications in pediatric B-cell precursor ALL treated according to NOPHO protocols I Öfverholm, AN Tran, M Heyman, V Zachariadis, M Nordenskjöld, ... Leukemia 27 (9), 1936-1939, 2013 | 67 | 2013 |
| Whole‐genome sequencing of cytogenetically balanced chromosome translocations identifies potentially pathological gene disruptions and highlights the importance of … D Nilsson, M Pettersson, P Gustavsson, A Förster, W Hofmeister, ... Human mutation 38 (2), 180-192, 2017 | 65 | 2017 |
| The clinical impact of IKZF1 deletions in paediatric B‐cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in … L Olsson, I Ivanov Öfverholm, U Norén‐Nyström, V Zachariadis, ... British journal of haematology 170 (6), 847-858, 2015 | 61 | 2015 |
| A highly scalable method for joint whole-genome sequencing and gene-expression profiling of single cells V Zachariadis, H Cheng, N Andrews, M Enge Molecular Cell 80 (3), 541-553. e5, 2020 | 60 | 2020 |
| Tooth agenesis in osteogenesis imperfecta related to mutations in the collagen type I genes B Malmgren, K Andersson, K Lindahl, A Kindmark, G Grigelioniene, ... Oral diseases 23 (1), 42-49, 2017 | 56 | 2017 |
| Mesenchymal stem cells transplanted into spinal cord injury adopt immune cell-like characteristics R Hakim, R Covacu, V Zachariadis, A Frostell, SR Sankavaram, L Brundin, ... Stem Cell Research & Therapy 10, 1-16, 2019 | 43 | 2019 |
| Transcription-coupled genetic instability marks acute lymphoblastic leukemia structural variation hotspots M Heinäniemi, T Vuorenmaa, S Teppo, MU Kaikkonen, M Bouvy-Liivrand, ... Elife 5, e13087, 2016 | 43 | 2016 |
| Metabolic reprogramming of acute lymphoblastic leukemia cells in response to glucocorticoid treatment M Dyczynski, M Vesterlund, AC Björklund, V Zachariadis, J Janssen, ... Cell death & disease 9 (9), 846, 2018 | 41 | 2018 |
| The frequency and prognostic impact of dic (9; 20)(p13. 2; q11. 2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial V Zachariadis, F Gauffin, E Kuchinskaya, M Heyman, J Schoumans, ... Leukemia 25 (4), 622-628, 2011 | 38 | 2011 |
| Spinal cord injury induces permanent reprogramming of microglia into a disease-associated state which contributes to functional recovery R Hakim, V Zachariadis, SR Sankavaram, J Han, RA Harris, L Brundin, ... Journal of Neuroscience 41 (40), 8441-8459, 2021 | 26 | 2021 |
| Single nucleotide polymorphism genomic arrays analysis of t (8; 21) acute myeloid leukemia cells T Akagi, LY Shih, S Ogawa, J Gerss, SR Moore, R Schreck, N Kawamata, ... haematologica 94 (9), 1301, 2009 | 20 | 2009 |
| Predisposition to childhood acute lymphoblastic leukemia caused by a constitutional translocation disrupting ETV6 T Järviaho, B Bang, V Zachariadis, F Taylan, J Moilanen, M Möttönen, ... Blood Advances 3 (18), 2722-2731, 2019 | 16 | 2019 |
| Homozygous deletions of CDKN2A are present in all dic (9; 20)(p13· 2; q11· 2)-positive B-cell precursor acute lymphoblastic leukaemias and may be important for leukaemic … V Zachariadis, J Schoumans, G Barbany, M Heyman, E Forestier, ... British journal of haematology 159 (4), 2012 | 16 | 2012 |
| Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth S Frisk, F Taylan, I Blaszczyk, I Nennesmo, G Annerén, B Herm, EL Stattin, ... Clinical Genetics 96 (2), 118-125, 2019 | 15 | 2019 |
| High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing AN Tran, F Taylan, V Zachariadis, I Ivanov Öfverholm, A Lindstrand, ... Plos one 13 (3), e0193928, 2018 | 15 | 2018 |
| Detailed gene dose analysis reveals recurrent focal gene deletions in pediatric B-cell precursor acute lymphoblastic leukemia I Ivanov Öfverholm, AN Tran, L Olsson, V Zachariadis, M Heyman, E Rudd, ... Leukemia & Lymphoma 57 (9), 2161-2170, 2016 | 15 | 2016 |
| PAX5-ESRRB is a recurrent fusion gene in B-cell precursor pediatric acute lymphoblastic leukemia Y Marincevic-Zuniga, V Zachariadis, L Cavelier, A Castor, G Barbany, ... Haematologica 101 (1), e20, 2016 | 9 | 2016 |
| A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins B Bang, J Eisfeldt, G Barbany, A Harila-Saari, M Heyman, V Zachariadis, ... Blood Advances 6 (7), 2275-2289, 2022 | 7 | 2022 |
Jessica NordlundAssociate Professor - Uppsala University and SciLifeLab National Genomics InfrastructureVerifierad e-postadress på medsci.uu.se
