Petra Dušátková - Concepedia

Author

Petra Dušátková

Also Known As

Dusatkova P, Dusatkova, P., Dusatkova, Petra, Dušátková, Petra, P. Dusatkova, P. Dušátková, P., Dušátková, Petra Dusatkova, Petra Dušatkova, Petra Dušátková

105

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

Charles University University Hospital in Motol University of Copenhagen University of Bergen University of Southern Denmark

About

Petra Dušátková is an author at Charles University specializing in genetics, medicine, and endocrinology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	244
2	Endocrinology	3	3	95
3	Diabetes	2	2	36
4	Health Sciences	1	1	22
5	Molecular Biology	1	1	117

Petra Dušátková

Publications

Citations

H-Index

Page 1

	Year	Citations
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
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
High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH Lukáš Plachý, Veronika Strakova, Lenka Elblová, The Journal of Clinical Endocrinology & Metabolism	2019	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
The Relationship Between Serum Bilirubin and Crohn’s Disease Martin Leníček, Dana Ďuricová, Ondřej Hradský, Inflammatory Bowel Diseases	2014	51
Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations Petra Dušátková, Roland Pfäffle, Milton R. Brown, European Journal of Human Genetics Developmental BiologyPituitary GlandGenetic DisorderGeneticsGenetic Epidemiology	2015	45
Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a <b><i>STAT3</i></b> Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised? Hana Šedivá, Petra Dušátková, Veronika Kanderová, Hormone Research in Paediatrics	2017	45
High Incidence of Heterozygous<i>ABCC8</i>and<i>HNF1A</i>Mutations in Czech Patients With Congenital Hyperinsulinism Klára Roženková, Jana Malíková, Azizun Nessa, The Journal of Clinical Endocrinology & Metabolism	2015	42
<i>NPR2</i> Variants Are Frequent among Children with Familiar Short Stature and Respond Well to Growth Hormone Therapy Lukáš Plachý, Petra Dušátková, Klára Maratová, The Journal of Clinical Endocrinology & Metabolism	2020	42
HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes Petra Dušátková, Štěpánka Průhová, Zdenĕk Šumnı́k, Journal of Pediatric Endocrinology and Metabolism	2011	37

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