Berta Campos

628 total citations
21 papers, 254 citations indexed

About

Berta Campos is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Berta Campos has authored 21 papers receiving a total of 254 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Berta Campos's work include BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Berta Campos is often cited by papers focused on BRCA gene mutations in cancer (10 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Berta Campos collaborates with scholars based in Spain, France and Chile. Berta Campos's co-authors include Orland Dı́ez, Montserrat Domènech, Carmen Alonso, Montserrat Baiget, Manel Baena, Judith Balmañà, Ángel Carracedo, Carles Pericay, Brigitte Bressac–de Paillerets and Ana Vega and has published in prestigious journals such as International Journal of Molecular Sciences, Annals of Oncology and Breast Cancer Research and Treatment.

In The Last Decade

Berta Campos

20 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Berta Campos Spain 8 155 144 47 37 35 21 254
Jocelyne Attia‐Sobol France 8 99 0.6× 64 0.4× 45 1.0× 43 1.2× 17 0.5× 10 240
Mary Haddadin United States 6 210 1.4× 103 0.7× 23 0.5× 29 0.8× 17 0.5× 7 343
Xue‐Xue Zhu United States 7 118 0.8× 108 0.8× 42 0.9× 34 0.9× 35 1.0× 11 393
Erika Della Mina Italy 8 124 0.8× 167 1.2× 25 0.5× 20 0.5× 17 0.5× 16 263
Wendy Alcaraz United States 8 144 0.9× 140 1.0× 14 0.3× 28 0.8× 19 0.5× 14 264
Bandarigoda N. Somatilaka United States 10 323 2.1× 287 2.0× 44 0.9× 20 0.5× 34 1.0× 14 432
Hafdís T. Helgadóttir Sweden 7 160 1.0× 64 0.4× 30 0.6× 15 0.4× 35 1.0× 21 267
Hirofumi Ohashi Japan 11 198 1.3× 125 0.9× 15 0.3× 28 0.8× 19 0.5× 12 321
Juliane Eckhold Germany 8 116 0.7× 66 0.5× 16 0.3× 16 0.4× 10 0.3× 10 202
C. Verellen‐Dumoulin Belgium 9 166 1.1× 170 1.2× 28 0.6× 35 0.9× 25 0.7× 17 289

Countries citing papers authored by Berta Campos

Since Specialization
Citations

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

Fields of papers citing papers by Berta Campos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Berta Campos

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

All Works

20 of 20 papers shown
1.
Campos, Berta, et al.. (2024). Parvovirus B19-Induced Pancytopenia: A Case Report of Aplastic Crisis. Cureus. 16(12). e76660–e76660. 1 indexed citations
2.
Pingault, Véronique, Berta Campos, Esther Nibbeling, et al.. (2024). Chromatin assembly factor subunit CHAF1A as a monogenic cause for oculo-auriculo-vertebral spectrum. European Journal of Human Genetics. 33(1). 131–136. 1 indexed citations
3.
Rooney, Kathleen, Sadegheh Haghshenas, Haley McConkey, et al.. (2023). Functional Insight into and Refinement of the Genomic Boundaries of the JARID2-Neurodevelopmental Disorder Episignature. International Journal of Molecular Sciences. 24(18). 14240–14240. 3 indexed citations
4.
Biagetti, Betina, Irene Valenzuela, Ariadna Campos-Martorell, et al.. (2023). Contribution of Dynamic and Genetic Tests for Short Stature Diagnosing: A Case Report. Diagnostics. 13(13). 2259–2259. 1 indexed citations
5.
Frigola, Gerard, V. Borobio, Berta Campos, et al.. (2021). Histopathology of recurrent Steel syndrome in fetuses caused by novel variants of COL27A1 gene. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 479(2). 413–418. 1 indexed citations
6.
Pauta, Montse, Berta Campos, Gemma Arca, et al.. (2021). Next-Generation Sequencing Gene Panels and “Solo” Clinical Exome Sequencing Applied in Structurally Abnormal Fetuses. Fetal Diagnosis and Therapy. 48(10). 746–756. 8 indexed citations
7.
Serrano, Carmen, Marc Corral‐Juan, Giovanni Stévanin, et al.. (2013). New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32. JAMA Neurology. 70(6). 764–764. 29 indexed citations
8.
Campos, Berta, Judith Balmañà, Irene Valenzuela, et al.. (2013). Germline mutations in NF1 and BRCA1 in a family with neurofibromatosis type 1 and early-onset breast cancer. Breast Cancer Research and Treatment. 139(2). 597–602. 25 indexed citations
9.
Campos, Berta, et al.. (2012). Characterization of NF1 allele containing two nonsense mutations in exon 37 that segregates with neurofibromatosis type 1. Clinical Genetics. 83(5). 462–466. 4 indexed citations
10.
Quintáns, Beatriz, José Ruiz Pardo, Berta Campos, et al.. (2011). Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing. Case Reports in Neurology. 3(1). 86–90. 12 indexed citations
11.
Balmañà, Judith, Orland Dı́ez, Berta Campos, et al.. (2005). Sex Ratio Distortion in Offspring of Families with BRCA1 or BRCA2 Mutant Alleles: An Ascertainment Bias Phenomenon?. Breast Cancer Research and Treatment. 92(3). 273–277. 1 indexed citations
12.
Campos, Berta, Orland Dı́ez, Carolina Álvarez, et al.. (2004). Análisis del haplotipo en portadores de la mutación 6857delAA en el gen BRCA2 en 4 familias con cáncer de mama u ovario hereditario. Medicina Clínica. 123(14). 543–545. 3 indexed citations
13.
Campos, Berta, Orland Dı́ez, Montserrat Domènech, et al.. (2003). RNA analysis of eightBRCA1andBRCA2unclassified variants identified in breast/ovarian cancer families from Spain. Human Mutation. 22(4). 337–337. 35 indexed citations
14.
Campos, Berta, Orland Dı́ez, Fabrice Odefrey, et al.. (2003). Haplotype analysis of theBRCA29254delATCAT recurrent mutation in breast/ovarian cancer families from Spain. Human Mutation. 21(4). 452–452. 18 indexed citations
15.
Baiget, Montserrat, et al.. (2001). Bases moleculares del cáncer de mama hereditario. Revista de Senología y Patología Mamaria. 14(1). 20–24.
16.
Campos, Berta, Orland Dı́ez, Montserrat Domènech, et al.. (2001). Conditions for Single-Strand Conformation Polymorphism (SSCP) Analysis of BRCA1 Gene Using an Automated Electrophoresis Unit. Clinical Chemistry and Laboratory Medicine (CCLM). 39(5). 401–4. 5 indexed citations
17.
Campos, Berta, Orland Dı́ez, Montserrat Domènech, et al.. (2001). BRCA2 mutation analysis of 87 Spanish breast/ovarian cancer families. Annals of Oncology. 12(12). 1699–1703. 12 indexed citations
18.
Vega, Ana, Berta Campos, Brigitte Bressac–de Paillerets, et al.. (2001). The R71GBRCA1is a founder Spanish mutation and leads to aberrant splicing of the transcript. Human Mutation. 17(6). 520–521. 92 indexed citations
19.
Pericay, Carles, Orland Dı́ez, Berta Campos, et al.. (2001). Características clinicopatológicas y evolución clínica de pacientes con cáncer de mama y mutaciones en los genes BRCA1 o BRCA2. Medicina Clínica. 117(5). 161–166. 1 indexed citations
20.
Dı́ez, Orland, Berta Campos, & Montserrat Baiget. (2000). Diagnóstico molecular del cáncer hereditario. Medicina Clínica. 115(5). 190–197. 1 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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