Jan Lebl

5.5k citations

178 papers · 3.5k indexed · h-index 35

Impact in

Endocrinology, Diabetes and Metabolism top 0.5%
- Growth Hormone and Insulin-like Growth Factors
- Diabetes Management and Research
Genetics top 1%
- Diabetes and associated disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders

Papers in ⓘ

Endocrinology, Diabetes and Metabolism 77
- Growth Hormone and Insulin-like Growth Factors 38
- Diabetes Management and Research 14
Genetics 79
- Diabetes and associated disorders 38
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 21
- Genetics and Neurodevelopmental Disorders 10

Co-authors: Štěpánka Průhová (42 shared papers)Ondřej Cinek (37 shared papers)Zdenĕk Šumnı́k (43 shared papers)Torben Hansen (17 shared papers)Oluf Pedersen (17 shared papers)Stanislava Koloušková (42 shared papers)Petra Dušátková (46 shared papers)Marta Šnajderová (33 shared papers)
Journals: Hormone Research in Paediatrics (17 papers)The Journal of Clinical Endocrinology & Metabolism (14 papers)European Journal of Pediatrics (11 papers)European Journal of Endocrinology (5 papers)Pediatric Diabetes (5 papers)
Partner nations: Czechia United Kingdom Denmark

In The Last Decade

Jan Lebl

166 papers receiving 3.4k citations

Peers

Countries citing papers authored by Jan Lebl

Since Specialization

Citations

This map shows the geographic impact of Jan Lebl's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jan Lebl with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jan Lebl more than expected).

Fields of papers citing papers by Jan Lebl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jan Lebl. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jan Lebl. The network helps show where Jan Lebl may publish in the future.

Co-authors

The 25 scholars most cited alongside Jan Lebl, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jan Lebl Line = papers co-authored together Jan Lebl links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 178 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection Diabetologia ·Ewan R. Pearson, Štěpánka Průhová, Cees J. Tack, Anders Johansen, Harriet Castleden, P Lumb, Anthony S. Wierzbicki, P M Clark, Jan Lebl, Oluf Pedersen, Sian Ellard, Torben Hansen, Andrew T. Hattersley	2005	174
2	Tumor Risk in Disorders of Sex Development Sexual Development ·J. Pleskacova, Remko Hersmus, J. Wolter Oosterhuis, B.A. Setyawati, S.M. Faradz, Martine Cools, K.P. Wolffenbuttel, Jan Lebl, S L S Drop, Leendert H. J. Looijenga	2010	117
3	Gonadal Pathology and Tumor Risk in Relation to Clinical Characteristics in Patients with 45,X/46,XY Mosaicism The Journal of Clinical Endocrinology & Metabolism ·Martine Cools, J. Pleskacova, Hans Stoop, Piet Hoebeke, Erik Van Laecke, Stenvert L. S. Drop, Jan Lebl, J. Wolter Oosterhuis, Leendert H. J. Looijenga, Katja P. Wolffenbuttel, (unknown)	2011	107
4	De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed Diabetologia ·Juraj Staník, Petra Dušátková, Ondřej Cinek, Lucia Valentínová, Miroslava Hučková, Martina Škopková, Lenka Dušátková, Daniela Staníková, M Pura, I Klimeś, Jan Lebl, Daniela Gašperíková, Štěpánka Průhová	2013	97
5	Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function Journal of Clinical Investigation ·Sara K. Hansen, Marcelina Párrizas, Maria L. Jensen, Štěpánka Průhová, Jakob Ek, Sylvia F. Boj, Anders Johansen, M.A. Maestro, Francisca Rivera, Hans Eiberg, Michal Anděl, Jan Lebl, Oluf Pedersen, Jorge Ferrer, Torben Hansen	2002	91
6	Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia European Journal of Endocrinology ·(unknown), J. Sólyom, G. Fekete, József Kovács, V Rakosnikova, Felix Votava, Jan Lebl, Z. Pribilincová, Sabina Baumgartner‐Parzer, Stefan Riedl, Franz Waldhauser, H Frisch, M Stopar-Obreza, (unknown), Tadej Battelino	2005	78
7	Genetic evidence that HNF-1α–dependent transcriptional control of HNF-4α is essential for human pancreatic β cell function Journal of Clinical Investigation ·Sara K. Hansen, Marcelina Párrizas, Maria L. Jensen, Štěpánka Průhová, Jakob Ek, Sylvia F. Boj, Anders Johansen, M.A. Maestro, Francisca Rivera, Hans Eiberg, Michal Anděl, Jan Lebl, Oluf Pedersen, Jorge Ferrer, Torben Hansen	2002	77
8	Screening for mutations in transcription factors in a Czech cohort of 170 patients with congenital and early-onset hypothyroidism: identification of a novel PAX8 mutation in dominantly inherited early-onset non-autoimmune hypothyroidism European Journal of Endocrinology ·Eva Al Taji, Heike Biebermann, Z Límanová, O Hníková, Jaroslav Zikmund, Christof Dame, Annette Grüters, Jan Lebl, Heiko Krude	2007	76
9	Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α Diabetologia ·Štěpánka Průhová, Jakob Ek, Jan Lebl, (unknown), F Saudek, Michal Anděl, Oluf Pedersen, Torben Hansen	2003	76
10	Continued Growth Hormone (GH) Treatment after Final Height Is Necessary to Complete Somatic Development in Childhood-Onset GH-Deficient Patients The Journal of Clinical Endocrinology & Metabolism ·Andrea Attanasio, Elena P. Shavrikova, Werner Blum, Morris Cromer, Christopher J. Child, Magdalena Paskova, Jan Lebl, John J. Chipman, Stephen M. Shalet	2004	73
11	Melanocortin 4 Receptor Mutations in Obese Czech Children: Studies of Prevalence, Phenotype Development, Weight Reduction Response, and Functional Analysis The Journal of Clinical Endocrinology & Metabolism ·Irena Aldhoon Hainerová, Lesli H. Larsen, Birgitte Holst, Marie Finková, Vojtěch Hainer, Jan Lebl, Torben Hansen, Oluf Pedersen	2007	71
12	Further evidence that mutations in INScan be a rare cause of Maturity-Onset Diabetes of the Young (MODY) BMC Medical Genetics ·Trine Welløv Boesgaard, Štěpánka Průhová, Ehm A. Andersson, Ondřej Cinek, Barbora Obermannová, Jeannet Lauenborg, Peter Damm, Regine Bergholdt, Flemming Pociot, Charlotta Pisinger, Fabrizio Barbetti, Jan Lebl, Oluf Pedersen, Torben Hansen	2010	67
13	Long-Term Stability of Amino Acids and Acylcarnitines in Dried Blood Spots Clinical Chemistry ·Kristina Anna Strnadová, Margareta Holub, Adolf Mühl, Georg Heinze, Rene Ratschmann, Hermann Mascher, Sylvia Stöckler‐Ipsiroglu, Franz Waldhauser, Felix Votava, Jan Lebl, Olaf A. Bodamer	2007	67
14	Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED Human Mutation ·Daniela Čiháková, Katarina Trebusak, Maarit Heino, Valentin Fadeyev, Anatoly Tiulpakov, Tadej Battelino, Attila Tar, Zita Halász, Peter Blümel, Sameh Tawfik, Kai Krohn, Jan Lebl, Pärt Peterson, (unknown)	2001	62
15	Lessons From 30 Years of Clinical Diagnosis and Treatment of Congenital Adrenal Hyperplasia in Five Middle European Countries¹ The Journal of Clinical Endocrinology & Metabolism ·József Kovács, Felix Votava, Georg Heinze, J. Sólyom, Jan Lebl, Zuzana Pribilincová, H Frisch, Tadej Battelino, Franz Waldhauser	2001	61
16	Growth Patterns and Final Height in Congenital Adrenal Hyperplasia due to Classical 21-Hydroxylase Deficiency Hormone Research in Paediatrics ·G. Hargitai, J. Sólyom, Tadej Battelino, Jan Lebl, Z. Pribilincová, Roland Hauspie, József Kovács, Franz Waldhauser, Herwig Frisch	2001	60
17	Absence of breast-feeding is associated with the risk of type 1 diabetes: a case–control study in a population with rapidly increasing incidence European Journal of Pediatrics ·Hana Malcová, Zdenĕk Šumnı́k, Pavel Dřevı́nek, Jitřenka Venháčová, Jan Lebl, Ondřej Cinek	2005	54
18	Screening Detected Celiac Disease in Children with Type 1 Diabetes Mellitus: Effect on the Clinical Course (A Case Control Study) Journal of Pediatric Gastroenterology and Nutrition ·Birgit Rami‐Merhar, Zdenĕk Šumnı́k, Edith Schober, Thomas Waldhör, Tadej Battelino, Nina Bratanič, K Kürti, Jan Lebl, Catarina Limbert, L Madácsy, Roetloef J. H Odink, Magdalena Paskova, Gyula Soltész	2005	54
19	Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations Pediatric Diabetes ·Štěpánka Průhová, Petra Dušátková, Zdenĕk Šumnı́k, Stanislava Koloušková, Oluf Pedersen, Torben Hansen, Ondřej Cinek, Jan Lebl	2010	51
20	High Prevalence of Growth Plate Gene Variants in Children With Familial Short Stature Treated With GH The Journal of Clinical Endocrinology & Metabolism ·Lukáš Plachý, Veronika Strakova, Lenka Elblová, Barbora Obermannová, Stanislava Koloušková, Marta Šnajderová, D Zemková, Petra Dušátková, Zdenĕk Šumnı́k, Jan Lebl, Štěpánka Průhová	2019	49

About Jan Lebl

Jan Lebl is a scholar working on Endocrinology, Diabetes and Metabolism, Genetics, Clinical Biochemistry, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 178 papers that have together received 3.5k indexed citations. Recurring topics across this work include Diabetes and associated disorders (38 papers), Growth Hormone and Insulin-like Growth Factors (38 papers), Pancreatic function and diabetes (33 papers), Sexual Differentiation and Disorders (25 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Diabetes Management and Research (14 papers), Metabolism, Diabetes, and Cancer (12 papers) and Genetics and Neurodevelopmental Disorders (10 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (1.4k citations), Genetics (1.8k citations), Surgery (1.2k citations), Clinical Biochemistry (185 citations) and Urology (172 citations). Jan Lebl has collaborated with scholars based in Czechia, United Kingdom and Denmark. Frequent co-authors include Štěpánka Průhová, Ondřej Cinek, Zdenĕk Šumnı́k, Torben Hansen, Oluf Pedersen, Stanislava Koloušková, Petra Dušátková, Marta Šnajderová, Tadej Battelino and Barbora Obermannová. Their work appears in journals such as Hormone Research in Paediatrics, The Journal of Clinical Endocrinology & Metabolism, European Journal of Pediatrics, European Journal of Endocrinology and Pediatric Diabetes.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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