Roser Ufartes

686 total citations
11 papers, 520 citations indexed

About

Roser Ufartes is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Roser Ufartes has authored 11 papers receiving a total of 520 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Roser Ufartes's work include Ion channel regulation and function (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cardiac electrophysiology and arrhythmias (2 papers). Roser Ufartes is often cited by papers focused on Ion channel regulation and function (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Cardiac electrophysiology and arrhythmias (2 papers). Roser Ufartes collaborates with scholars based in Germany, Spain and United States. Roser Ufartes's co-authors include Frauke Alves, Alexander Wenk, José‐María Montenegro, Nadine Haberl, Marianne Geiser, Abuelmagd M. Abdelmonem, Idoia Ruiz de Larramendi, Wolfgang G. Kreyling, Zulqurnain Ali and Wolfgang J. Parak and has published in prestigious journals such as PLoS ONE, Nature Nanotechnology and The Journal of Physiology.

In The Last Decade

Roser Ufartes

11 papers receiving 514 citations

Peers

Roser Ufartes
Comparison fields: 5 of 96
  • Molecular Biology 211
  • Biomedical Engineering 153
  • Biomaterials 146
  • Materials Chemistry 125
  • Electronic, Optical and Magnetic Materials 57
Margaret F. Bennewitz United States
Marc D. Roy United States
Ashwath Jayagopal United States
Takayasu Arai United States
J. Röther Germany
Marc Schwarz Germany
Cinzia Stigliano United States
Isabelle Mahieu Belgium
Dan Wilkinson United States
Margaret F. Bennewitz United States View profile →
Citations per field, relative to Roser Ufartes
Roser Ufartes · 1×
Citations per year, relative to Roser Ufartes
Roser Ufartes · 1×

Countries citing papers authored by Roser Ufartes

Since Specialization
Citations

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

Fields of papers citing papers by Roser Ufartes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roser Ufartes

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

All Works

11 of 11 papers shown
# Title Journal Authors Indexed citations
1 FBRSL1 regulates the expression of chromatin regulators BRPF1 and KAT6A Human Genetics Roser Ufartes, Annette Borchers et al. 1
2 Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome Frontiers in Cell and Developmental Biology Silke Pauli, Hanna Berger et al. 9
3 CHARGE syndrome and related disorders: a mechanistic link Human Molecular Genetics Roser Ufartes, Gabriela Salinas et al. 4
4 De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome Human Genetics Roser Ufartes, Hanna Berger et al. 10
5 Sema3a plays a role in the pathogenesis of CHARGE syndrome Human Molecular Genetics Roser Ufartes, Christiane Neuhofer et al. 20
6 3D virtual histology of murine kidneys –high resolution visualization of pathological alterations by micro computed tomography Scientific Reports Jeannine Missbach‐Guentner, Christian Dullin et al. 36
7 μCT of ex-vivo stained mouse hearts and embryos enables a precise match between 3D virtual histology, classical histology and immunochemistry PLoS ONE Christian Dullin, Roser Ufartes et al. 54
8 Periodic expression of Kv10.1 driven by pRb/E2F1 contributes to G2/M progression of cancer and non-transformed cells Cell Cycle Diana Urrego, Roser Ufartes et al. 30
9 In vivo integrity of polymer-coated gold nanoparticles Nature Nanotechnology Wolfgang G. Kreyling, Abuelmagd M. Abdelmonem et al. 281
10 KV10.1 opposes activity‐dependent increase in Ca2+ influx into the presynaptic terminal of the parallel fibre–Purkinje cell synapse The Journal of Physiology Lena Sünke Mortensen, Hartmut Schmidt et al. 34
11 Behavioural and functional characterization of Kv10.1 (Eag1) knockout mice Human Molecular Genetics Roser Ufartes, Tomasz Schneider et al. 41

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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