Célia Bádenas

6.5k total citations
139 papers, 3.9k citations indexed

About

Célia Bádenas is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Célia Bádenas has authored 139 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 80 papers in Molecular Biology, 59 papers in Genetics and 34 papers in Oncology. Recurrent topics in Célia Bádenas's work include Cutaneous Melanoma Detection and Management (31 papers), Genomic variations and chromosomal abnormalities (23 papers) and Genetics and Neurodevelopmental Disorders (22 papers). Célia Bádenas is often cited by papers focused on Cutaneous Melanoma Detection and Management (31 papers), Genomic variations and chromosomal abnormalities (23 papers) and Genetics and Neurodevelopmental Disorders (22 papers). Célia Bádenas collaborates with scholars based in Spain, United States and Australia. Célia Bádenas's co-authors include Montserrat Milà, Susana Puig, Josep Malvehy, Xavier Estivill, Roser Torrá, Laia Rodríguez‐Revenga, Joan Anton Puig‐Butillé, Cristina Carrera, Alejandro Darnell and Irene Madrigal and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Oncology and Blood.

In The Last Decade

Célia Bádenas

138 papers receiving 3.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Célia Bádenas Spain	33	2.2k	1.4k	952	400	374	139	3.9k
Carla Rosenberg Brazil	38	2.8k 1.3×	2.3k 1.6×	635 0.7×	445 1.1×	341 0.9×	183	5.7k
Michael A. Patton United Kingdom	36	4.1k 1.8×	1.3k 0.9×	597 0.6×	239 0.6×	484 1.3×	82	6.0k
Patrick Edery France	33	2.4k 1.1×	1.6k 1.1×	220 0.2×	250 0.6×	326 0.9×	117	4.5k
Marco Seri Italy	38	2.3k 1.0×	1.4k 0.9×	510 0.5×	202 0.5×	323 0.9×	193	5.3k
Chyuan‐Sheng Lin United States	31	4.3k 1.9×	1.3k 0.9×	512 0.5×	504 1.3×	540 1.4×	70	6.5k
Lies H. Hoefsloot Netherlands	45	3.7k 1.7×	1.7k 1.2×	511 0.5×	220 0.6×	292 0.8×	136	6.6k
Andreas Janecke Austria	37	2.2k 1.0×	1.3k 0.9×	163 0.2×	194 0.5×	694 1.9×	132	4.4k
Masatake Osawa Japan	33	2.2k 1.0×	420 0.3×	888 0.9×	142 0.4×	1.2k 3.1×	92	5.4k
Anita Rauch Germany	48	4.4k 2.0×	3.4k 2.4×	501 0.5×	679 1.7×	408 1.1×	194	7.5k
Lidia Larizza Italy	43	3.7k 1.7×	2.3k 1.6×	530 0.6×	780 1.9×	412 1.1×	271	6.3k

Countries citing papers authored by Célia Bádenas

Since Specialization

Citations

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

Fields of papers citing papers by Célia Bádenas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Célia Bádenas

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

All Works

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20 of 20 papers shown

Mariñó, Zoe, Célia Bádenas, Jesús Quintero, et al.. (2023). Benefits of using exchangeable copper and the ratio of exchangeable copper in a real‐world cohort of patients with Wilson disease. Journal of Inherited Metabolic Disease. 46(5). 982–991. 11 indexed citations

Podlipnik, Sebastián, Cristina Carrera, Míriam Potrony, et al.. (2022). Synchronous primary cutaneous melanomas: a descriptive study of their clinical features, histology, genetic background of the patients and clinical outcomes. Journal of the European Academy of Dermatology and Venereology. 36(12). 2364–2372. 4 indexed citations

Bádenas, Célia, Constantino Fondevila, Wladimiro Jiménez, et al.. (2021). Monitoring of Donor‐Derived Cell‐Free DNA by Short Tandem Repeats: Concentration of Total Cell‐Free DNA and Fragment Size for Acute Rejection Risk Assessment in Liver Transplantation. Liver Transplantation. 28(2). 257–268. 26 indexed citations

Pauta, Montse, et al.. (2021). The Contribution of QF-PCR and Pathology Studies in the Diagnosis of Diandric Triploidy/Partial Mole. Diagnostics. 11(10). 1811–1811. 2 indexed citations

Rodríguez‐Revenga, Laia, Irene Madrigal, A. Borrell, et al.. (2020). Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result. Clinical Genetics. 98(4). 379–383. 8 indexed citations

Sastre, Lydia, Jordi To‐Figueras, Sabela Lens, et al.. (2020). Resolution of subclinical porphyria cutanea tarda after hepatitis C eradication with direct‐acting anti‐virals. Alimentary Pharmacology & Therapeutics. 51(10). 968–973. 6 indexed citations

Tell‐Martí, Gemma, Míriam Potrony, Célia Bádenas, et al.. (2017). Melanocortin 1 receptor (MC1R) polymorphisms’ influence on size and dermoscopic features of nevi. Pigment Cell & Melanoma Research. 31(1). 39–50. 17 indexed citations

Borrell, A., Maribel Grande, E. Meler, et al.. (2016). Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study. Fetal Diagnosis and Therapy. 42(3). 174–180. 38 indexed citations

Carrera, Cristina, Joan Anton Puig‐Butillé, Gemma Tell‐Martí, et al.. (2015). MultipleBRAFWild-Type Melanomas During Dabrafenib Treatment for MetastaticBRAF-Mutant Melanoma. JAMA Dermatology. 151(5). 544–544. 10 indexed citations

10.

Puig‐Butillé, Joan Anton, Cristina Carrera, Paula Aguilera, et al.. (2014). Dermoscopic criteria associated with BRAF and NRAS mutation status in primary cutaneous melanoma. British Journal of Dermatology. 171(4). 754–759. 18 indexed citations

11.

Carrera, Cristina, Alba Díaz, Joan Anton Puig‐Butillé, et al.. (2014). Multiple Primary Acral Melanomas in Two Young Caucasian Patients. Dermatology. 228(4). 307–310. 7 indexed citations

12.

Carrera, Cristina, Rajiv Kumar, Zaida García‐Casado, et al.. (2013). Distribution ofMC1Rvariants among melanoma subtypes: p.R163Q is associated with lentigo maligna melanoma in a Mediterranean population. British Journal of Dermatology. 169(4). 804–811. 22 indexed citations

13.

Salerni, Gabriel, Cristina Carrera, Louise Lovatto, et al.. (2011). Benefits of total body photography and digital dermatoscopy (“two-step method of digital follow-up”) in the early diagnosis of melanoma in patients at high risk for melanoma. Journal of the American Academy of Dermatology. 67(1). e17–e27. 145 indexed citations

14.

Bádenas, Célia, et al.. (2009). Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives. Clinical Genetics. 75(4). 346–353. 25 indexed citations

15.

Rodríguez‐Revenga, Laia, Aurora Sánchez, Montserrat Pujol, et al.. (2008). Screening for FXTAS in 95 Spanish Patients Negative for Huntington Disease. Genetic Testing. 12(1). 135–138. 12 indexed citations

16.

Madrigal, Irene, Laia Rodríguez‐Revenga, Lluı́s Armengol, et al.. (2007). X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation. BMC Genomics. 8(1). 443–443. 48 indexed citations

17.

Madrigal, Irene, Laia Rodríguez‐Revenga, Célia Bádenas, et al.. (2007). MLPA as first screening method for the detection of microduplications and microdeletions in patients with X-linked mental retardation. Genetics in Medicine. 9(2). 117–122. 23 indexed citations

18.

Rifé, M., Célia Bádenas, Josep Mallolas, et al.. (2003). Incidence of Fragile X in 5,000 Consecutive Newborn Males. Genetic Testing. 7(4). 339–343. 44 indexed citations

19.

Torrá, Roser, et al.. (1999). Autosomal recessive Alport syndrome: linkage analysis and clinical features in two families. Nephrology Dialysis Transplantation. 14(3). 627–630. 12 indexed citations

20.

Milà, Montserrat, Sergi Castellvı́-Bel, Carlos Vázquez, et al.. (1996). A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion. Human Genetics. 98(4). 419–421. 10 indexed citations

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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