Contact
Email: | |
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Phone: | +420 54949 6997 |
Research group: | CF: Genomics Core Facility, Medical Genomics - Šárka Pospíšilová |
Workplace: |
Publications that are part of the Web of Science database, possibly also other publications chosen by authors.
2021
- Hrabovsky, S; Vrzalova, Z; Stika, J; Jelinkova, H; Jarosova, M; Navrkalova, V; Martenek, J; Folber, F; Salek, C; Horacek, JM; Pospisilova, S; Mayer, J; Doubek, M, 2021: Genomic landscape of B-other acute lymphoblastic leukemia in an adult retrospective cohort with a focus on BCR-ABL1-like subtype. ACTA ONCOLOGICA 60(6), p. 760 - 770, doi: 10.1080/0284186X.2021.1900908
- Navrkalova, V; Plevova, K; Hynst, J; Pal, K; Mareckova, A; Reigl, T; Jelinkova, H; Vrzatova, Z; Starska, K; Pavlova, S; Panovska, A; Janikova, A; Doubek, M; Kotaskova, J; Pospisilova, S, 2021: LYmphoid NeXt-Generation Sequencing (LYNX) Panel A Comprehensive Capture-Based Sequencing Tool for the Analysis of Prognostic and Predictive Markers in Lymphoid Malignancies. JOURNAL OF MOLECULAR DIAGNOSTICS 23(8), p. 959 - 974, doi: 10.1016/j.jmoldx.2021.05.007
2020
- Trizuljak, J; Petruchova, T; Blahakova, I; Vrzalova, Z; Horinova, V; Doubkova, M; Michalka, J; Mayer, J; Pospisilova, S; Doubek, M, 2020: Diagnosis of Bloom Syndrome in a Patient with Short Stature, Recurrence of Malignant Lymphoma, and Consanguineous Origin. MOLECULAR SYNDROMOLOGY 11(2), p. 73 - 82, doi: 10.1159/000507006
2019
- Doubkova, M; Kozubik, KS; Radova, L; Pesova, M; Trizuljak, J; Pal, K; Svobodova, K; Reblova, K; Svozilova, H; Vrzalova, Z; Pospisilova, S; Doubek, M, 2019: A novel germline mutation of the SFTPA1 gene in familial interstitial pneumonia. HUMAN GENOME VARIATION 6, doi: 10.1038/s41439-019-0044-z
- Trizuljak, J; Doubkova, M; Hrazdirova, A; Vrzalova, Z; Blahakova, I; Radova, L; Pospisilova, S; Doubek, M, 2019: A rare diagnosis: Hermansky-Pudlak syndrome in a patient with pulmonary fibrosis, oculocutaneous albinism and thrombocytopathy. EUROPEAN JOURNAL OF HUMAN GENETICS 27, p. 1252 - 1252
- Doubkova, M; Trizuljak, J; Vrzalova, Z; Hrazdirova, A; Blahakova, I; Radova, L; Pospisilova, S; Doubek, M, 2019: Novel genetic variant of HPS1 gene in Hermansky-Pudlak syndrome with fulminant progression of pulmonary fibrosis: a case report. BMC PULMONARY MEDICINE 19(1), doi: 10.1186/s12890-019-0941-4
2018
- Vrzalova, Z; Jelinkova, H; Hrabovsky, S; Folber, F; Salek, C; Horacek, J; Zaliova, M; Stika, J; Slavikova, M; Pospisilova, S; Doubek, M, 2018: Gene Aberrations in Adult Patients with Ph-Negative ALL in the Czech Republic. BLOOD 132, doi: 10.1182/blood-2018-99-118308
2012
- Votava, F; Novotna, D; Kracmar, P; Vinohradska, H; Stahlova-Hrabincova, E; Vrzalova, Z; Neumann, D; Malikova, J; Lebl, J; Matern, D, 2012: Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance. EUROPEAN JOURNAL OF PEDIATRICS 171(6), p. 935 - 940, doi: 10.1007/s00431-011-1656-6
- Vyhledávání a funkční testování variant genů predisponujících k familiárním onemocněním krvetvorby, , 2020 - 2023
- Creating synergies between research infrastructures to stimulate innovation in the cross-border region (ATCZ40), Ministerstvo pro místní rozvoj ČR, 2016 - 2020
- Národní centrum lékařské genomiky (LM2015091), Ministerstvo školství, mládeže a tělovýchovy ČR, 2016 - 2019
- NCLG - Národní centrum lékařské genomiky - modernizace infrastruktury a výzkum genetické variability populace (CZ.02.1.01/0.0/0.0/16_013/0001634), Ministerstvo školství, mládeže a tělovýchovy ČR, 2017 - 2019
- Expression and function of activation-induced cytidine deaminase splice variants in normal B cell physiology and chronic lymphocytic leukemia (3SGA5792), Jihomoravský kraj, 2013 - 2016
- Functional and structural changes of microRNAs in lymphoproliferative malignancies and their impact on prognosis and prediction of therapy response (NT11218), Ministry of Health - Ministry of Health´s Departmental Research and Development Programme III (2010-2015), 2010 - 2015
- NGS-PTL - Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia (306242), Evropská unie, 2012 - 2015
- SuPReMMe - Podpora profesního růstu a mezinárodní integrace výzkumných týmů v oblasti molekulární medicíny (CZ.1.07/2.3.00/20.0045), Ministerstvo školství, mládeže a tělovýchovy ČR, 2011 - 2014
- Real-time PCR soupravy pro diagnostiku v onkologii (FR-TI2/254), Ministerstvo průmyslu a obchodu ČR, 2010 - 2013
- Functional and molecular characteristics of cancer and normal stem cells - identification of targets for novel therapeutics and therapeutic strategies (MSM0021622430), Ministerstvo školství, mládeže a tělovýchovy ČR, 2007 - 2013
- Involvement of nuclear HMGB proteins in sensitizing of human cells to anticancer drugs inhibiting DNA topoizomerases (GAP301/10/0590), Czech Science Foundation - Standard Grants, 2010 - 2012
- Analysis of changes in genome and its expression in chronic lymphocytic leukemia patients during the disease development (NS10439), Ministry of Health - Departmental Programme of Research and Development (2008-2011), 2009 - 2011