Štěpánka Průhová

Author

Štěpánka Průhová

Also Known As

L. Drnkova, Pruhova, Stepanka, S Pruhova, S Průhová, S. Pruhova, S. Průhová, S., Pruhova, STEPANKA PRUHOVA, Stepanka Pruhova, Stepanka Pruhova

110

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Charles University University Hospital in Motol Steno Diabetes Centers University of Copenhagen Aarhus University

ŠP

About

Štěpánka Průhová is an author at Charles University specializing in medicine, genetics, and diabetes.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	743
2	Health Sciences	2	2	46
3	Public Health	2	2	134
4	Engineering	1	1	27
5	Cell Biology	1	1	105

Štěpánka Průhová

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection Ewan R. Pearson, Štěpánka Průhová, Cees J. Tack, Diabetologia Phenotypic CharacteristicsHepatologyGenetic DisorderLiver PhysiologyGenetics	2005	231
De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed Juraj Staník, Petra Dušátková, Ondřej Cinek, Diabetologia Genetic DisorderGeneticsMolecular BiologyMolecular GeneticsDisease Gene Identification	2013	117
Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function Sara K. Hansen, Marcelina Párrizas, Maria L. Jensen, Journal of Clinical Investigation Hnf-1α–dependent Transcriptional ControlGeneticsHnf-1alpha Binding SiteInsulin SignalingMetabolic Syndrome	2002	105
Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α Štěpánka Průhová, Jakob Ek, Jan Lebl, Diabetologia Mody Genes Hnf-4αGenetic DisorderGeneticsGenetic EpidemiologyCzech Republic	2003	88
Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function Sara K. Hansen, Marcelina Párrizas, Maria L. Jensen, Journal of Clinical Investigation	2002	84
Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY) Trine Welløv Boesgaard, Štěpánka Průhová, Ehm A. Andersson, BMC Medical Genetics	2010	75
Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations Štěpánka Průhová, Petra Dušátková, Zdenĕk Šumnı́k, Pediatric Diabetes	2010	65
The Common p.R114W <i>HNF4A</i> Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes Thomas W. Laver, Kevin Colclough, Maggie Shepherd, Diabetes	2016	57
Intralymphatic Glutamic Acid Decarboxylase With Vitamin D Supplementation in Recent-Onset Type 1 Diabetes: A Double-Blind, Randomized, Placebo-Controlled Phase IIb Trial Johnny Ludvigsson, Zdenĕk Šumnı́k, Terezie Pelikánová, Diabetes Care	2021	54
Growth data in large series of 587 children and adolescents with type 1 diabetes mellitus. Jan Lebl, Edith Schober, Thomas Zidek, PubMed	2003	50

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