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Dragica Radojkovic
Dragica Radojkovic
IMGGE
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Title
Cited by
Cited by
Year
Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice
C Castellani, H Cuppens, M Macek Jr, JJ Cassiman, E Kerem, P Durie, ...
Journal of cystic fibrosis 7 (3), 179-196, 2008
8642008
Recommendations for the classification of diseases as CFTR-related disorders
C Bombieri, M Claustres, K De Boeck, N Derichs, J Dodge, E Girodon, ...
Journal of Cystic Fibrosis 10, S86-S102, 2011
4762011
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
W Dondorp, G De Wert, Y Bombard, DW Bianchi, C Bergmann, P Borry, ...
European Journal of Human Genetics 23 (11), 1438-1450, 2015
4592015
The use of D-dimer with new cutoff can be useful in diagnosis of venous thromboembolism in pregnancy
M Kovac, Z Mikovic, L Rakicevic, S Srzentic, V Mandic, V Djordjevic, ...
European Journal of Obstetrics & Gynecology and Reproductive Biology 148 (1 …, 2010
1892010
Reconstructing the population history of European Romani from genome-wide data
I Mendizabal, O Lao, UM Marigorta, A Wollstein, L Gusmăo, V Ferak, ...
Current Biology 22 (24), 2342-2349, 2012
1762012
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
T Dörk, M Macek Jr, F Mekus, B Tümmler, J Tzountzouris, T Casals, ...
Human genetics 106, 259-268, 2000
1692000
Mutations in the amiloride‐sensitive epithelial sodium channel in patients with cystic fibrosis‐like disease
AK Azad, R Rauh, F Vermeulen, M Jaspers, J Korbmacher, B Boissier, ...
Human mutation 30 (7), 1093-1103, 2009
1082009
Thrombophilia in women with pregnancy-associated complications: fetal loss and pregnancy-related venous thromboembolism
M Kovac, G Mitic, Z Mikovic, V Djordjevic, O Savic, V Mandic, LJ Rakicevic, ...
Gynecologic and obstetric investigation 69 (4), 233-238, 2010
932010
Silver staining of denaturing gradient gel electrophoresis gels
D Radojkovic, J Kušic
Clinical chemistry 46 (6), 883-884, 2000
922000
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
F Fellmann, CG Van El, P Charron, K Michaud, HC Howard, SN Boers, ...
European journal of human genetics 27 (12), 1763-1773, 2019
902019
Muscle ankyrin repeat proteins: their role in striated muscle function in health and disease
S Kojic, D Radojkovic, G Faulkner
Critical reviews in clinical laboratory sciences 48 (5-6), 269-294, 2011
902011
Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype
J Yarden, D Radojkovic, K De Boeck, M Macek, D Zemkova, V Vavrova, ...
Journal of medical genetics 41 (8), 629-633, 2004
872004
Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype
J Yarden, D Radojkovic, K De Boeck, M Macek, D Zemkova, V Vavrova, ...
Thorax 60 (4), 320-325, 2005
762005
A novel prothrombin mutation in two families with prominent thrombophilia–the first cases of antithrombin resistance in a Caucasian population
V Djordjevic, M Kovac, P Miljic, M Murata, A Takagi, I Pruner, D Francuski, ...
Journal of Thrombosis and Haemostasis 11 (10), 1936-1939, 2013
722013
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia
F Stanke, T Becker, V Kumar, S Hedtfeld, C Becker, H Cuppens, S Tamm, ...
Journal of medical genetics 48 (1), 24-31, 2011
722011
One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans
HC Howard, CG van El, F Forzano, D Radojkovic, E Rial-Sebbag, ...
European Journal of Human Genetics 26 (1), 1-11, 2018
712018
Prevalence of factor V leiden, factor V cambridge, factor II G20210A and methylenetetrahydrofolate reductase C677T mutations in healthy and thrombophilic Serbian populations
V Djordjevic, LJ Rakicevic, D Mikovic, M Kovac, P Miljic, D Radojkovic, ...
Acta haematologica 112 (4), 227-229, 2004
592004
Responsible innovation in human germline gene editing. Background document to the recommendations of ESHG and ESHRE
G De Wert, B Heindryckx, G Pennings, A Clarke, U Eichenlaub-Ritter, ...
Human reproduction open 2018 (1), hox024, 2018
562018
The TNFα receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis
F Stanke, T Becker, H Cuppens, V Kumar, JJ Cassiman, S Jansen, ...
Human genetics 119, 331-343, 2006
552006
Human germline gene editing. Recommendations of ESHG and ESHRE
G De Wert, G Pennings, A Clarke, U Eichenlaub-Ritter, CG Van El, ...
Human reproduction open 2018 (1), hox025, 2018
492018
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