| An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic characterization and outcome CJ Harrison, AV Moorman, C Schwab, AJ Carroll, EA Raetz, M Devidas, ... Leukemia 28 (5), 1015-1021, 2014 | 230 | 2014 |
| Dysfunction of SHANK2 and CHRNA7 in a patient with intellectual disability and language impairment supports genetic epistasis of the two loci B Chilian, H Abdollahpour, T Bierhals, I Haltrich, G Fekete, I Nagel, ... Clinical genetics 84 (6), 560-565, 2013 | 93 | 2013 |
| Parallel evolution under chemotherapy pressure in 29 breast cancer cell lines results in dissimilar mechanisms of resistance B Tegze, Z Szallasi, I Haltrich, Z Penzvalto, Z Toth, I Liko, B Győrffy PloS one 7 (2), e30804, 2012 | 72 | 2012 |
| Validation of the United Kingdom copy-number alteration classifier in 3239 children with B-cell precursor ALL L Hamadeh, A Enshaei, C Schwab, CN Alonso, A Attarbaschi, G Barbany, ... Blood advances 3 (2), 148-157, 2019 | 68 | 2019 |
| Normal karyotype is a poor prognostic factor in myeloid leukemia of Down syndrome: a retrospective, international study M Blink, M Zimmermann, C von Neuhoff, D Reinhardt, V de Haas, H Hasle, ... Haematologica 99 (2), 299, 2014 | 47 | 2014 |
| Ponte di Legno International Workshop in Childhood Acute Lymphoblastic Leukemia. An international study of intrachromosomal amplification of chromosome 21 (iAMP21): cytogenetic … CJ Harrison, AV Moorman, C Schwab, AJ Carroll, EA Raetz, M Devidas, ... Leukemia 28 (5), 1015-1021, 2014 | 37 | 2014 |
| Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure A Beke, H Piko, I Haltrich, J Csomor, A Matolcsy, G Fekete, J Rigo, ... Molecular cytogenetics 6, 1-8, 2013 | 31 | 2013 |
| Donor-cell myelodysplastic syndrome developing 13 years after marrow grafting for aplastic anemia I Haltrich, J Müller, J Szabó, G Kovács, R Kóos, A Poros, M Dobos, ... Cancer genetics and cytogenetics 142 (2), 124-128, 2003 | 21 | 2003 |
| A transgenic mouse model for detection of tissue-specific thyroid hormone action P Mohácsik, F Erdélyi, M Baranyi, B Botz, G Szabó, M Tóth, I Haltrich, ... Endocrinology 159 (2), 1159-1171, 2018 | 20 | 2018 |
| Gonadoblastoma: Case report of two young patients with isochromosome 12p found in the dysgerminoma overgrowth component in one case YC Changchien, I Haltrich, T Micsik, E Kiss, L Fónyad, G Papp, Z Sápi Pathology-Research and Practice 208 (10), 628-632, 2012 | 18 | 2012 |
| Multipoint interphase FISH analysis of chromosome 3 abnormalities in 28 childhood AML patients I Haltrich, M Kost‐Alimova, G Kovács, G Klein, G Fekete, S Imreh European journal of haematology 76 (2), 124-133, 2006 | 18 | 2006 |
| Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia R Kiss, A Gángó, A Benard-Slagter, B Egyed, I Haltrich, L Hegyi, ... Modern Pathology 33 (5), 812-824, 2020 | 15 | 2020 |
| Diagnostic difficulties and possibilities of NF1-like syndromes in childhood E Pinti, K Nemeth, K Staub, A Lengyel, G Fekete, I Haltrich BMC pediatrics 21, 1-14, 2021 | 14 | 2021 |
| A de novo atypical ring sSMC (22) characterized by array CGH in a boy with cat-eye syndrome I Haltrich, H Pikó, E Kiss, Z Tóth, V Karcagi, G Fekete Molecular cytogenetics 7, 1-8, 2014 | 12 | 2014 |
| Six cases of rare gene amplifications and multiple copy of fusion gene in childhood acute lymphoblastic leukemia I Haltrich, M Csóka, G Kovács, D Török, D Alpár, G Ottoffy, G Fekete Pathology & Oncology Research 19, 123-128, 2013 | 12 | 2013 |
| Complex X chromosome rearrangement associated with multiorgan autoimmunity I Haltrich, H Pikó, H Pamjav, A Somogyi, A Völgyi, D David, A Beke, ... Molecular Cytogenetics 8, 1-11, 2015 | 10 | 2015 |
| Generation of multiple iPSC clones from a male schizophrenia patient carrying de novo mutations in genes KHSRP, LRRC7, and KIR2DL1, and his parents E Hathy, E Szabó, K Vincze, I Haltrich, E Kiss, N Varga, Z Erdei, G Várady, ... Stem Cell Research 51, 102140, 2021 | 9 | 2021 |
| What should we consider in the case of combined Down-and 47, XY,+ i (X)(q10) Klinefelter syndromes? The unique case of a male newborn and review of the literature E Pinti, A Lengyel, G Fekete, I Haltrich BMC pediatrics 20, 1-8, 2020 | 7 | 2020 |
| An ultra-rare manifestation of an X-linked recessive disorder: Duchenne muscular dystrophy in a female patient Z Szűcs, É Pinti, I Haltrich, OP Szén, T Nagy, E Barta, G Méhes, L Bidiga, ... International Journal of Molecular Sciences 23 (21), 13076, 2022 | 6 | 2022 |
| Similar cause, different phenotype: SOX9 enhancer duplication in a family E Pinti, H Piko, A Lengyel, A Luczay, V Karcagi, G Fekete, I Haltrich Hormone Research in Paediatrics 92 (5), 335-339, 2020 | 6 | 2020 |
