Valeska Frank

1.8k total citations
12 papers, 488 citations indexed

About

Valeska Frank is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Valeska Frank has authored 12 papers receiving a total of 488 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Genetics and 1 paper in Surgery. Recurrent topics in Valeska Frank's work include Genetic and Kidney Cyst Diseases (10 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (6 papers). Valeska Frank is often cited by papers focused on Genetic and Kidney Cyst Diseases (10 papers), Renal and related cancers (9 papers) and Genetic Syndromes and Imprinting (6 papers). Valeska Frank collaborates with scholars based in Germany, Netherlands and Türkiye. Valeska Frank's co-authors include Carsten Bergmann, Klaus Zerres, Nadina Ortiz Brüchle, Jan Senderek, Henry Fehrenbach, Lars Pape, Christian Becker, Marijke N. Zonneveld, Nanette Sarioglu and Marcus R. Benz and has published in prestigious journals such as PLoS ONE, Journal of the American Society of Nephrology and Journal of Investigative Dermatology.

In The Last Decade

Valeska Frank

12 papers receiving 467 citations

Peers

Countries citing papers authored by Valeska Frank

Since Specialization

Citations

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

Fields of papers citing papers by Valeska Frank

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeska Frank

This figure shows the co-authorship network connecting the top 25 collaborators of Valeska Frank. A scholar is included among the top collaborators of Valeska Frank 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 Valeska Frank. Valeska Frank 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	Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes 2020 ·Genetics in Medicine ·Ria Schönauer, Sebastian Baatz, (unknown), Valeska Frank, (unknown), (unknown), Bernt Popp, (unknown), (unknown), Carsten Bergmann, Jan Halbritter	24
2	Clinical utility gene card for: Meckel syndrome – update 2016 2016 ·European Journal of Human Genetics ·Carsten Bergmann, Valeska Frank, Riitta Salonen	5
3	An Efficient and Comprehensive Strategy for Genetic Diagnostics of Polycystic Kidney Disease 2015 ·PLoS ONE ·Tobias Eisenberger, Christian Decker, Milan Hiersche, (unknown), Eva L. Decker, (unknown), Valeska Frank, Hanno J. Bolz, Henry Fehrenbach, Lars Pape, Burkhard Toenshoff, Christoph J. Mache, (unknown), Carsten Bergmann	47
4	Transcriptional Complexity in Autosomal Recessive Polycystic Kidney Disease 2014 ·Clinical Journal of the American Society of Nephrology ·Valeska Frank, Klaus Zerres, Carsten Bergmann	13
5	Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies 2014 ·Pediatric Nephrology ·Henry Fehrenbach, Christian Decker, Tobias Eisenberger, Valeska Frank, (unknown), (unknown), Kerstin Amann, (unknown), Hanno J. Bolz, Karsten Häffner, Martin Pöhl, Carsten Bergmann	30
6	Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8 2013 ·Cytogenetic and Genome Research ·Thomas M. Schmidt, Tatjana Bierhals, Fanny Kortüm, Iris Bartels, Thomas Liehr, Peter Burfeind, Moneef Shoukier, Valeska Frank, Carsten Bergmann, Kerstin Kutsche	18
7	Mutations in Multiple PKD Genes May Explain Early and Severe Polycystic Kidney Disease 2011 ·Journal of the American Society of Nephrology ·Carsten Bergmann, (unknown), Nadina Ortiz Brüchle, (unknown), Valeska Frank, Henry Fehrenbach, (unknown), Lars Pape, Annegret Buske, Jón J. Jónsson, Nanette Sarioglu, (unknown), José Carlos Ferreira, Jan U. Becker, Reinhold Cremer, Julia Hoefele, Marcus R. Benz, Lutz T. Weber, Reinhard Buettner, Klaus Zerres	161
8	RSPO4 Is the Major Gene in Autosomal-Recessive Anonychia and Mutations Cluster in the Furin-Like Cysteine-Rich Domains of the Wnt Signaling Ligand R-spondin 4 2007 ·Journal of Investigative Dermatology ·Nadina Ortiz Brüchle, Jorge Frank, Valeska Frank, Jan Senderek, Ahmet Rüçhan Akar, Erol Koç, Dimitris Rigopoulos, Maurice A. M. Van Steensel, Klaus Zerres, Carsten Bergmann	35
9	Aberrant splicing is a common mutational mechanism inMKS1, a key player in Meckel-Gruber syndrome 2007 ·Human Mutation ·Valeska Frank, Nadina Ortiz Brüchle, (unknown), Suzanna G.M. Frints, Axel Bohring, (unknown), (unknown), Heide Seidel, Jan Senderek, Nesrin Beşbaş, Unda Todt, Christian Kubisch, T. Grimm, (unknown), Sevim Balcı, Klaus Zerres, Carsten Bergmann	17
10	Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome 2007 ·Human Mutation ·Valeska Frank, Anneke I. den Hollander, Nadina Ortiz Brüchle, Marijke N. Zonneveld, Gudrun Nürnberg, Christian Becker, (unknown), (unknown), Susanne Roosing, Jan Senderek, Peter Nürnberg, Frans P.M. Cremers, Klaus Zerres, Carsten Bergmann	108
11	Diagnosis, Pathogenesis, and Treatment Prospects in Cystic Kidney Disease 2006 ·Molecular Diagnosis & Therapy ·Carsten Bergmann, Valeska Frank, Fabian Küpper, (unknown), (unknown), (unknown), (unknown), Markus Moser, Jutta Kirfel, Reinhard Büttner, Jan Senderek, Klaus Zerres	12
12	Functional analysis of PKHD1 splicing in autosomal recessive polycystic kidney disease 2006 ·Journal of Human Genetics ·Carsten Bergmann, Valeska Frank, Fabian Küpper, (unknown), Jan Senderek, Klaus Zerres	18

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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