Jana Malíková - Concepedia

Author

Jana Malíková

Charles University

Also Known As

Jana Krenek Malikova, Jana Křenek Malíková, Jana Malikova, Jana Malíková, Malikova J, Malikova, J., Malíková, Jana

Publications

579

Citations

H-Index

Concepts

All Affiliations

Charles University Carol Davila University of Medicine and Pharmacy Centre for Biomedical Network Research on Rare Diseases Amsterdam Neuroscience University Hospital of Bern

About

Jana Malíková is an author at Charles University specializing in medicine, endocrinology, and clinical genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	289
2	Endocrinology	2	2	60
3	Immunology	1	1	107
4	Obstetrics	1	1	15
5	Pathology	1	1	107

Jana Malíková

Publications

495

Citations

H-Index

Page 1

	Year	Citations
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial Stefan Groeneweg, Robin P. Peeters, Carla Moran, The Lancet Diabetes & Endocrinology Iodine Deficiency DisordersPharmacologyMct8 DeficiencyTri-iodothyronine Analogue TriacThyroid Hormone	2019	122
Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study Stefan Groeneweg, Ferdy S. van Geest, Ayhan Abacı, The Lancet Diabetes & Endocrinology Disease CharacteristicsDisease MechanismGenetic DisorderImmunodeficienciesPathogenesis	2020	107
CYP17A1 inhibitor abiraterone, an anti-prostate cancer drug, also inhibits the 21-hydroxylase activity of CYP21A2 Jana Malíková, Simone Brixius‐Anderko, Sameer S. Udhane, The Journal of Steroid Biochemistry and Molecular Biology	2017	57
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
Human NR5A1/SF-1 Mutations Show Decreased Activity on BDNF (Brain-Derived Neurotrophic Factor), an Important Regulator of Energy Balance: Testing Impact of Novel SF-1 Mutations Beyond Steroidogenesis Jana Malíková, Núria Camats, Mónica Fernández‐Cancio, PLoS ONE	2014	44
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
Clinical and genetic characteristics of a large international cohort of individuals with rare NR5A1/SF-1 variants of sex development Chrysanthi Kouri, Grit Sommer, Idoia Martinez de la Piscina, EBioMedicine	2024	35
Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants Jana Malíková, Alba Kaci, Petra Dušátková, The Journal of Clinical Endocrinology & Metabolism	2020	18
Lessons learned from 5 years of newborn screening for congenital adrenal hyperplasia in the Czech Republic: 17-hydroxyprogesterone, genotypes, and screening performance Felix Votava, Dana Novotná, P Kračmar, European Journal of Pediatrics Adrenal GlandCongenital Adrenal HyperplasiaAdrenal HealthPediatricsGynecology	2012	15
McCune Albright syndrome and bilateral adrenal hyperplasia: the GNAS mutation may only be present in adrenal tissue Anna Angelousi, Filip Fencl, Fábio R. Faucz, HORMONES	2015	10

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