Bettina Lorenz

2.4k total citations
12 papers, 703 citations indexed

About

Bettina Lorenz is a scholar working on Molecular Biology, Nephrology and Physiology. According to data from OpenAlex, Bettina Lorenz has authored 12 papers receiving a total of 703 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 2 papers in Nephrology and 2 papers in Physiology. Recurrent topics in Bettina Lorenz's work include Retinal Development and Disorders (2 papers), Parathyroid Disorders and Treatments (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Bettina Lorenz is often cited by papers focused on Retinal Development and Disorders (2 papers), Parathyroid Disorders and Treatments (2 papers) and Amino Acid Enzymes and Metabolism (1 paper). Bettina Lorenz collaborates with scholars based in Germany, United States and United Kingdom. Bettina Lorenz's co-authors include Thomas Meitinger, Tim M. Strom, Michael J. Econs, Annett Böddrich, Hans Lehrach, Fiona Francis, Kathryn Woods‐Townsend, David I. Wilson, Stephanie Spranger and Peter Freisinger and has published in prestigious journals such as Nature Genetics, Genome Research and Human Molecular Genetics.

In The Last Decade

Bettina Lorenz

12 papers receiving 685 citations

Peers

Countries citing papers authored by Bettina Lorenz

Since Specialization

Citations

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

Fields of papers citing papers by Bettina Lorenz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bettina Lorenz

This figure shows the co-authorship network connecting the top 25 collaborators of Bettina Lorenz. A scholar is included among the top collaborators of Bettina Lorenz 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 Bettina Lorenz. Bettina Lorenz is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Die Discountisierung der Gesellschaft : Dimensionen eines Megatrends 2007 ·Wolfgang Fritz, Bettina Lorenz, Ulrike Hauser	2
2	Die Discountisierung der Gesellschaft 2007 ·Duncker & Humblot eBooks ·Wolfgang Fritz, Bettina Lorenz, Ulrike Hauser	2
3	Klinische und molekulargenetische Befunde beim isolierten sporadischen Retraktionssyndrom nach Stilling-Türk-Duane 2004 ·Klinische Monatsblätter für Augenheilkunde ·Bettina Wabbels, J. Kohlhase, Bettina Lorenz	2
4	Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis 2000 ·Nature Genetics ·Víctor L. Ruiz‐Pérez, Susan Ide, Tim M. Strom, Bettina Lorenz, David I. Wilson, Kathryn Woods‐Townsend, Lynn King, Clair A. Francomano, Peter Freisinger, Stephanie Spranger, Bruno Marino, Bruno Dallapiccola, Michael Wright, Thomas Meitinger, Mihael H. Polymeropoulos, Judith Goodship	224
5	Molecular cloning of a novel human UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene 2000 ·Gene ·Kenneth E. White, Bettina Lorenz, W. Evans, Thomas Meitinger, Tim M. Strom, Michael J. Econs	64
6	Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse 1998 ·European Journal of Human Genetics ·Bettina Lorenz, Carmela Migliaccio, Peter Lichtner, Carsten Meyer, Tim M. Strom, Michele D’Urso, Jörg D. Becker, Alfredo Ciccodicola, Thomas Meitinger	14
7	Spermine deficiency in Gy mice caused by deletion of the spermine synthase gene 1998 ·Human Molecular Genetics ·Bettina Lorenz	51
8	Genomic Organization of the Human PEX Gene Mutated in X-Linked Dominant Hypophosphatemic Rickets 1997 ·Genome Research ·Fiona Francis, Tim M. Strom, Steffen Hennig, Annett Böddrich, Bettina Lorenz, Oliver Brandau, Klaus Mohnike, (unknown), (unknown), Sven Klages, Katja Borzym, Thomas Pohl, C Oudet, Michael J. Econs, Peter Rowe, Richard Reinhardt, Thomas Meitinger, Hans Lehrach	129
9	Pex Gene Deletions in Gy and Hyp Mice Provide Mouse Models for X-Linked Hypophosphatemia 1997 ·Human Molecular Genetics ·Tim M. Strom, Fiona Francis, Bettina Lorenz, Annett Böddrich, Hans Lehrach, Michael J. Econs, Thomas Meitinger	155
10	A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa 1995 ·Human Molecular Genetics ·Alfons Meindl, Maria Raquel Santos Carvalho, Klaus M. Herrmann, Bettina Lorenz, Helene Achatz, Birgit Lorenz, Eckart Apfelstedt-Sylla, B Wittwer, Mark T. Ross, Thomas Meitinger	49
11	Berger, W. et al. Isolation of a candidate gene for Norrie disease by positional cloning. Nature Genet. 1, 199-203 1992 ·Wilhelm Berger, A Meindl, T.J.R. van de Pol, Frans P.M. Cremers, H.H. Ropers, (unknown), Anthony P. Monaco, Arthur A. Bergen, L Zergollern, R V Lebo, Bettina Lorenz, (unknown), András Gál, E. M. Bleeker‐Wagemakers, Thomas Meitinger	1
12	Contribution of mitochondrial and cytoplasmic protein synthesis to the formation of cytochrome b and cytochrome aa3 1973 ·Biochimie ·H. Weiss, Walter Sebald, A. J. Schwab, W. Kleinow, Bettina Lorenz	10

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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