Anna Benet‐Pagès

6.9k citations

34 papers · 2.5k indexed · 1 hit paper · h-index 15

Impact in

Nephrology top 0.2%
- Parathyroid Disorders and Treatments
Genetics top 2%
- Genetic Syndromes and Imprinting

Papers in

Nephrology 6
- Parathyroid Disorders and Treatments 6
Cancer Research 12
- Cancer Genomics and Diagnostics 11

Co-authors: Tim M. Strom Bettina Lorenz‐Depiereux Kenneth E. White Michael J. Econs Peter Orlik Gwénaëlle Carn Janine Wagenstaller Eric Bennett
Journals: Familial Cancer (3 papers)Human Mutation (2 papers)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)Leukemia (1 paper)
Partner nations: Germany United States United Kingdom

In The Last Decade

Anna Benet‐Pagès

33 papers receiving 2.5k citations

Hit Papers

align trajectories log scale

The UCSC Genome Browser database: 2025 update 2024 · 113 citations

Peers

Countries citing papers authored by Anna Benet‐Pagès

Since Specialization

Citations

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

Fields of papers citing papers by Anna Benet‐Pagès

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Benet‐Pagès. 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 Anna Benet‐Pagès. The network helps show where Anna Benet‐Pagès may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Anna Benet‐Pagès, 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 Anna Benet‐Pagès Line = papers co-authored together Anna Benet‐Pagès links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The UCSC Genome Browser database: 2025 update Nucleic Acids Research ·GS Melah, Galt P Barber, Anna Benet‐Pagès, Jonathan D. Casper, Hiram Clawson, Mark Diekhans, Clay Fischer, Jairo Navarro Gonzalez, Angie S. Hinrichs, Christopher M. Lee, Luis R Nassar, Brian J. Raney, Matthew L Speir, Marijke J. van Baren, Charles Vaske, D. Haussler, W. James Kent, Maximilian Haeussler Hit paper breakdown →	2024	113
2	Quality assurance within the context of genome diagnostics (a german perspective) Medizinische Genetik ·Florian Kraft, Anna Benet‐Pagès, Daniel Berner, Anna Teubert, Sebastian Eck, Norbert Arnold, Peter Bauer, Matthias Begemann, Marc Sturm, Stephanie Kleinle, Tobias B. Haack, Thomas Eggermann	2023	1
3	Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes Human Mutation ·Isabel Diebold, Christopoher Allison, Lauren D Boczkowski, Anna Benet‐Pagès, Andreas Laner, Elke Holinski‐Feder, Angela Abicht	2020	8
4	Analysis of 3297 individuals suggests that the pathogenic germline 5′-UTR variant BRCA1 c.-107A > T is not common in south-east Germany Familial Cancer ·Andreas Laner, Anna Benet‐Pagès, Maria da Conceição Camps, Elke Holinski‐Feder	2020	7
5	Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics Familial Cancer ·Monika Morak, Verena Steinke‐Lange, Rhayssa Gabriela Lopes Alves, Anna Benet‐Pagès, Leon Homola, Andreas Laner, Katrin Kayser, Stefan Aretz, Elke Holinski‐Feder	2020	9
6	Targeted deep-intronic sequencing in a cohort of unexplained cases of suspected Lynch syndrome European Journal of Human Genetics ·Barmen Als Thema Einer Kurzen Unterrichtseinheit, Monika Morak, Anna Benet‐Pagès, Andreas Laner, مرتضی نورعلیزاده اطاق سرا, Elke Holinski‐Feder	2019	11
7	Mitochondrial and nuclear disease panel (Mito‐aND‐Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost‐effective and sensitive NGS‐based method Molecular Genetics & Genomic Medicine ·Angela Abicht, Lauren D Boczkowski, Stephanie Kleinle, Christopoher Allison, Elke Holinski‐Feder, Rita Horváth, Anna Benet‐Pagès, Isabel Diebold	2018	23
8	Extending the critical regions for mutations in the non‐coding gene RNU4ATAC in another patient with Roifman Syndrome Clinical Case Reports ·Estefanía Comesaña-Da Vila, 魏敬群, Udo Koehler, Andreas Laner, Lirije Ameti, Anna Benet‐Pagès, Elke Holinski‐Feder	2018	7
9	Early-onset leukoencephalopathy due to a homozygous missense mutation in the DARS2 gene Molecular and Cellular Probes ·Cornelia Köhler, Christoph M. Heyer, Sabine Hoffjan, Susanne Stemmler, Thomas Lücke, Charlotte Thiels, Alfried Kohlschütter, Ulrike Löbel, Rita Horváth, Stephanie Kleinle, Anna Benet‐Pagès, Angela Abicht	2015	14
10	Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2 Brain ·Elisabeth Stögmann, Eva M. Reinthaler, Salwa El Tawil, Jingxiang Cao, Wa Qd, Nevine El Nahas, V Gómez, Khai Wooi Lee, Sherif Edris, Anna Benet‐Pagès, Sebastian Eck, Ekaterina Pataraia, Davide Mei, Alexis Brice, Sada F. Mohammed, Renzo Guerrini, Fritz Zimprich, Tim M. Strom, Alexander Zimprich	2013	51
11	Assessment of the genomic variation in a cattle population by re-sequencing of key animals at low to medium coverage BMC Genomics ·Sandra Jansen, Bernhard Aigner, Hubert Pausch, Michał Wysocki, Sebastian Eck, Anna Benet‐Pagès, Elisabeth Graf, Thomas Wieland, Tim M. Strom, Thomas Meitinger, Ruedi Fries	2013	54
12	Identification of recurring tumor-specific somatic mutations in acute myeloid leukemia by transcriptome sequencing Leukemia ·Philipp A. Greif, Sebastian Eck, Nikola P. Konstandin, Anna Benet‐Pagès, Bianka Ksienzyk, A Dufour, Alexandra Vetter, Henning D. Popp, Bettina Lorenz‐Depiereux, Thomas Meitinger, Stefan K. Bohlander, Tim M. Strom	2011	44
13	CpG-Methylation Regulates a Class of Epstein-Barr Virus Promoters PLoS Pathogens ·Jianting Ke, Markus Kalla, J EHeiserman, Christine Göbel, Ulrich Rothbauer, Sebastian Eck, Anna Benet‐Pagès, Tim M. Strom, Wolfgang Hammerschmidt	2010	91
14	Whole genome sequencing of a single Bos taurusanimal for single nucleotide polymorphism discovery Genome biology ·Sebastian Eck, Anna Benet‐Pagès, Krzysztof Flisikowski, Thomas Meitinger, Ruedi Fries, Tim M. Strom	2009	93
15	Polypeptide GalNAc-transferase T3 and Familial Tumoral Calcinosis Journal of Biological Chemistry ·Kentaro Kato, Charlotte Jeanneau, Mads A. Tarp, Anna Benet‐Pagès, Bettina Lorenz‐Depiereux, Eric Bennett, Ulla Mandel, Tim M. Strom, Henrik Clausen	2006	342
16	DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis Nature Genetics ·Bettina Lorenz‐Depiereux, Murat Bastepe, Anna Benet‐Pagès, Mustapha Amyere, Janine Wagenstaller, Chenyang Zhuang, Klaus Badenhoop, Stéphanie Kaiser, Roger S. Rittmaster, Mariam Kiran, José L. Olivares, C Loris, Feliciano J. Ramos, Francis H. Glorieux, Miikka Vikkula, Harald Jüppner, Tim M. Strom	2006	373
17	An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia Human Molecular Genetics ·Anna Benet‐Pagès, Peter Orlik, Tim M. Strom, Bettina Lorenz‐Depiereux	2004	373
18	A Gene Locus Responsible for the Familial Hair Shaft Abnormality Pili Annulati Maps to Chromosome 12q24.32–24.33 Journal of Investigative Dermatology ·Kathrin Giehl, Gertrud Eckstein, Anna Benet‐Pagès, Antonellá Tosti, D. A. R. de Berker, Thomas Meitinger, Bertram Müller‐Myhsok, Tim M. Strom	2004	10
19	FGF23 is processed by proprotein convertases but not by PHEX Bone ·Anna Benet‐Pagès, Bettina Lorenz‐Depiereux, Hans Zischka, Kenneth E. White, Michael J. Econs, Tim M. Strom	2004	191
20	Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23 Kidney International ·Kenneth E. White, Gwénaëlle Carn, Bettina Lorenz‐Depiereux, Anna Benet‐Pagès, Tim M. Strom, Michael J. Econs	2001	385

About Anna Benet‐Pagès

Anna Benet‐Pagès is a scholar working on Nephrology, Cancer Research, Genetics, Pathology and Forensic Medicine and Virology, having authored 34 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), Cancer Genomics and Diagnostics (11 papers), Genetic factors in colorectal cancer (8 papers), Parathyroid Disorders and Treatments (6 papers), BRCA gene mutations in cancer (3 papers), Genomics and Phylogenetic Studies (3 papers), Genetic Mapping and Diversity in Plants and Animals (3 papers) and Cardiac pacing and defibrillation studies (2 papers). The work is most often cited by research in Nephrology (1.5k citations), Genetics (1.1k citations), Rheumatology (444 citations), Nutrition and Dietetics (398 citations) and Pathology and Forensic Medicine (327 citations). Anna Benet‐Pagès has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Tim M. Strom, Bettina Lorenz‐Depiereux, Kenneth E. White, Michael J. Econs, Peter Orlik, Gwénaëlle Carn, Janine Wagenstaller, Eric Bennett, Kentaro Kato and Sebastian Eck. Their work appears in journals such as Familial Cancer, Human Mutation, Human Molecular Genetics, European Journal of Human Genetics and Leukemia.

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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