Vytautas Ivaškevičius

Author

Also Known As

A. Biswas, B. Pezeshkpoor, B. Pötzsch, H. Rühl, Hans-Jörg Hertfelder, S. Horneff, V Ivaskevicius, V Ivaškevičius, V. IVASKEVICIUS, V. Ivaskevicius

Publications

Citations

H-Index

Concepts

All Affiliations

University of Bonn University of Bern University Hospital Bonn German Red Cross Paul Ehrlich Institut

About

Vytautas Ivaškevičius is an author at University of Bonn specializing in medicine, pathology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	1.4K
2	Natural Sciences	2	2	55
3	Engineering	1	1	22
4	Public Health	1	1	13
5	Biochemistry	1	1	41

Vytautas Ivaškevičius

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2 Simone Rost, Andreas Fregin, Vytautas Ivaškevičius, Nature ThrombosisDisease MechanismGenetic DisorderMedicineGenetics	2004	1.1K
International Registry on Factor XIII Deficiency: A basis formed mostly on European data Rainer Seitz, H Köhler, Verena Schroeder, Thrombosis and Haemostasis	2007	143
Evaluation of DHPLC in the analysis of hemophilia A Johannes Oldenburg, Vytautas Ivaškevičius, Simone Rost, Journal of Biochemical and Biophysical Methods Laboratory HematologyGranulocyteMedicineHematologyPathology	2001	82
Protection From Type 1 Diabetes by Vitamin D Receptor Haplotypes Elizabeth Ramos‐Lopez, Thomas Jansen, Vytautas Ivaškevičius, Annals of the New York Academy of Sciences	2006	69
Elastin Polymorphism Haplotype and Intracranial Aneurysms Are Not Associated in Central Europe Anne Höfer, Marcella Hermans, Nina Kubassek, Stroke	2003	48
Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function Vytautas Ivaškevičius, Arijit Biswas, Carville G. Bevans, Haematologica	2010	45
Revisiting the mechanism of coagulation factor XIII activation and regulation from a structure/functional perspective Sneha Gupta, Arijit Biswas, Mohammad Suhail Akhter, Scientific Reports Protein AssemblyMolecular RegulationImmunologyZymogenic FxiiiMolecular Biology	2016	41
Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5′ splice site Hamideh Yadegari, Arijit Biswas, Mohammad Suhail Akhter, Blood	2016	39
Mutations affecting disulphide bonds contribute to a fairly common prevalence of <i>F13B</i> gene defects: results of a genetic study in 14 families with factor XIII B deficiency Vytautas Ivaškevičius, Arijit Biswas, Ralph M. Loreth, Haemophilia Disulphide BondsGeneticsGenetic EpidemiologyMolecular BiologyPathology	2010	33
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic data Vytautas Ivaškevičius, Romualdas Jurgutis, Simone Rost, British Journal of Haematology	2001	32

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