Clemens Freiberg

563 total citations
15 papers, 287 citations indexed

About

Clemens Freiberg is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Clemens Freiberg has authored 15 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Clemens Freiberg's work include Diabetes and associated disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Pancreatic function and diabetes (3 papers). Clemens Freiberg is often cited by papers focused on Diabetes and associated disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers) and Pancreatic function and diabetes (3 papers). Clemens Freiberg collaborates with scholars based in Germany, Austria and United States. Clemens Freiberg's co-authors include Reinhard W. Holl, Christina Lißewski, Petra Fallier‐Becker, Sascha R. Tittel, Helmuth‐Günther Dörr, Gunnar Blumenstock, Richard Zimmermann, Markus Greiner, Klemens Raile and Martin Zenker and has published in prestigious journals such as Diabetes Care, The American Journal of Human Genetics and The Journal of Pediatrics.

In The Last Decade

Clemens Freiberg

14 papers receiving 273 citations

Peers

Countries citing papers authored by Clemens Freiberg

Since Specialization

Citations

This map shows the geographic impact of Clemens Freiberg'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 Clemens Freiberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Clemens Freiberg more than expected).

Fields of papers citing papers by Clemens Freiberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Clemens Freiberg. 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 Clemens Freiberg. The network helps show where Clemens Freiberg may publish in the future.

Co-authorship network of co-authors of Clemens Freiberg

This figure shows the co-authorship network connecting the top 25 collaborators of Clemens Freiberg. A scholar is included among the top collaborators of Clemens Freiberg based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Clemens Freiberg. Clemens Freiberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Health-related quality of life of children with X-linked hypophosphatemia in Germany 2024 ·Pediatric Nephrology ·Martin Klein, (unknown), (unknown), (unknown), Mirko Rehberg, Karl P. Schlingmann, (unknown), (unknown), (unknown), (unknown), Markus J. Kemper, Marcus Weitz, Elke Wühl, Norbert Jorch, Ludwig Patzer, Clemens Freiberg, Sabine Heger, (unknown), Dirk Schnabel, Dieter Haffner, (unknown)	5
2	Continuous glucose monitoring versus blood glucose monitoring for risk of severe hypoglycaemia and diabetic ketoacidosis in children, adolescents, and young adults with type 1 diabetes: a population-based study 2023 ·The Lancet Diabetes & Endocrinology ·Beate Karges, Sascha R. Tittel, (unknown), Clemens Freiberg, Christof Klinkert, Olga Kordonouri, (unknown), Carmen Schröder, Claudia Steigleder‐Schweiger, Reinhard W. Holl	30
3	Clinical characteristics and cardiovascular risk profile in children and adolescents with latent autoimmune diabetes: Results from the German/Austrian prospective diabetes follow‐up registry 2022 ·Pediatric Diabetes ·Alena Welters, Sascha R. Tittel, Thomas Reinehr, Daniel Weghuber, Susanna Wiegand, Wölfram Karges, Clemens Freiberg, Thomas Meißner, Nanette C. Schloot, Reinhard W. Holl	2
4	Diabetes management in Wolcott-Rallison syndrome: analysis from the German/Austrian DPV database 2020 ·Orphanet Journal of Rare Diseases ·Alena Welters, Thomas Meißner, Katja Konrad, Clemens Freiberg, Katharina Warncke, (unknown), Olga Kordonouri, Michael Wurm, (unknown), (unknown), (unknown), Sascha R. Tittel, Reinhard W. Holl	9
5	Deficient knowledge in adult Turner syndrome care as an incentive to found Turner centers in Germany 2019 ·Endocrine Connections ·(unknown), Martina Blaschke, Knut Brockmann, Clemens Freiberg, Onno E. Janßen, N Stahnke, (unknown), Martin Merkel, Alexander Mann, (unknown), Heide Siggelkow	9
6	Continuing role for classical cytogenetics: Case report of a boy with ring syndrome caused by complete ring chromosome 4 and review of literature 2017 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), C. Klett, Clemens Freiberg, Wiebke Stark, (unknown), (unknown), G. Rettenberger, Karl Mehnert, Birgit Zirn	17
7	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration 2015 ·The American Journal of Human Genetics ·Matthis Synofzik, Tobias B. Haack, Robert Kopajtich, Matteo Gorza, Doron Rapaport, Markus Greiner, Caroline Schönfeld, Clemens Freiberg, Stefan Schorr, Reinhard W. Holl, Michael Gonzalez, Andreas Fritsche, Petra Fallier‐Becker, Richard Zimmermann, Tim M. Strom, Thomas Meitinger, Stephan Züchner, Rebecca Schüle, Lüdger Schöls, Holger Prokisch	3
8	Novel Insights into 46,XY Disorders of Sex Development due to <b><i>NR5A1</i></b> Gene Mutation 2015 ·Sexual Development ·Ralf Werner, (unknown), (unknown), Clemens Freiberg, (unknown), Benedikt Reiz, Lutz Wünsch, Paul‐Martin Holterhus, Alexandra Kulle, (unknown), Stefan A. Wudy, Annette Richter-Unruh, Christoph Thorns, Olaf Hiort	10
9	Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration 2014 ·The American Journal of Human Genetics ·Matthis Synofzik, Tobias B. Haack, Robert Kopajtich, Matteo Gorza, Doron Rapaport, Markus Greiner, Caroline Schönfeld, Clemens Freiberg, Stefan Schorr, Reinhard W. Holl, Michael Gonzalez, Andreas Fritsche, Petra Fallier‐Becker, Richard Zimmermann, Tim M. Strom, Thomas Meitinger, Stephan Züchner, Rebecca Schüle, Lüdger Schöls, Holger Prokisch	82
10	Two Cases of Thyroid Dysgenesis Caused by Different Novel PAX8 Mutations in the DNA-Binding Region: In Vitro Studies Reveal Different Pathogenic Mechanisms 2013 ·Thyroid ·Pia Hermanns, Helmut Grasberger, Ronald Cohen, Clemens Freiberg, Helmuth‐Günther Dörr, Samuel Refetoff, Joachim Pohlenz	27
11	Higher Relative Risk for Multiple Sclerosis in a Pediatric and Adolescent Diabetic Population: Analysis From DPV Database 2013 ·Diabetes Care ·Susanne Bechtold, Astrid Blaschek, Klemens Raile, Axel Dost, Clemens Freiberg, (unknown), Elke Fröhlich‐Reiterer, E Molz, Reinhard W. Holl	33
12	A de novo interstitial deletion of 2p23.3–24.3 in a boy presenting with intellectual disability, overgrowth, dysmorphic features, skeletal myopathy, dilated cardiomyopathy 2012 ·American Journal of Medical Genetics Part A ·Moneef Shoukier, (unknown), Barbara Zoll, Peter Burfeind, Clemens Freiberg, Lars Klinge, Thomas Kriebel, (unknown), Alexander Mohr, Knut Brockmann	11
13	Health and Quality of Life in Adults with Noonan Syndrome 2012 ·The Journal of Pediatrics ·Gerhard Binder, (unknown), (unknown), Gunnar Blumenstock, Renate Kaulitz, Clemens Freiberg, (unknown), Christina Lißewski, Martin Zenker, Thomas A. Paul	35
14	Two Cases of Thyroid Dysgenesis Caused by Different Novel PAX8 Mutations in the DNA Binding Region: In vitro studies reveal different pathogenic mechanisms. 2012 ·Thyroid ·Pia Hermanns, Helmut Grasberger, Ronald A. Cohen, Clemens Freiberg, Helmuth‐Günther Dörr, Samuel Refetoff, Joachim Pohlenz	0
15	Effective aromatase inhibition by anastrozole in a patient with gonadotropin-independent precocious puberty in McCune-Albright syndrome. 2002 ·PubMed ·Christian Roth, Clemens Freiberg, H. Zappel, Norbert Albers	14

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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