Neus Gadea

915 total citations
15 papers, 242 citations indexed

About

Neus Gadea is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Neus Gadea has authored 15 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Neus Gadea's work include BRCA gene mutations in cancer (9 papers), DNA Repair Mechanisms (6 papers) and Genetic factors in colorectal cancer (3 papers). Neus Gadea is often cited by papers focused on BRCA gene mutations in cancer (9 papers), DNA Repair Mechanisms (6 papers) and Genetic factors in colorectal cancer (3 papers). Neus Gadea collaborates with scholars based in Spain and Palestinian Territory. Neus Gadea's co-authors include Judith Balmañà, Joan Brunet, Esther Darder, Àngela Velasco, Begoña Graña, Orland Dı́ez, Sara Gutiérrez‐Enríquez, Teresa Ramón y Cajal, Sandra Bonache and Estela Carrasco and has published in prestigious journals such as Journal of Clinical Oncology, Annals of Oncology and Human Reproduction.

In The Last Decade

Neus Gadea

14 papers receiving 238 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Neus Gadea Spain	9	178	78	62	43	39	15	242
Àngela Velasco Spain	8	144 0.8×	57 0.7×	61 1.0×	49 1.1×	36 0.9×	16	202
Joyce Seldon United States	5	200 1.1×	69 0.9×	33 0.5×	45 1.0×	20 0.5×	5	256
Karina L. Brierley United States	8	305 1.7×	94 1.2×	85 1.4×	70 1.6×	24 0.6×	10	416
Elana Levinson United States	6	195 1.1×	49 0.6×	36 0.6×	32 0.7×	8 0.2×	9	282
E. Wadsworth United States	5	214 1.2×	72 0.9×	56 0.9×	73 1.7×	42 1.1×	7	278
Sara Pirzadeh‐Miller United States	9	318 1.8×	67 0.9×	50 0.8×	101 2.3×	17 0.4×	25	410
Gayun Chan–Smutko United States	7	120 0.7×	40 0.5×	39 0.6×	112 2.6×	13 0.3×	14	276
Sari Lieberman Israel	9	207 1.2×	74 0.9×	33 0.5×	54 1.3×	17 0.4×	19	276
Kelly Kohut United Kingdom	7	117 0.7×	56 0.7×	44 0.7×	59 1.4×	19 0.5×	10	200
Julie Mak United States	7	135 0.8×	55 0.7×	26 0.4×	27 0.6×	55 1.4×	13	213

Countries citing papers authored by Neus Gadea

Since Specialization

Citations

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

Fields of papers citing papers by Neus Gadea

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neus Gadea

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

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

López‐Fernández, Adrià, Guillermo Villacampa, Èlia Grau, et al.. (2021). Patients’ and professionals’ perspective of non-in-person visits in hereditary cancer: predictors and impact of the COVID-19 pandemic. Genetics in Medicine. 23(8). 1450–1457. 4 indexed citations

Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2019). Incorporation of semi‐quantitative analysis of splicing alterations for the clinical interpretation of variants inBRCA1andBRCA2genes. Human Mutation. 40(12). 2296–2317. 9 indexed citations

Bonache, Sandra, Alejandro Moles‐Fernández, Gemma Montalban, et al.. (2018). Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of Cancer Research and Clinical Oncology. 144(12). 2495–2513. 49 indexed citations

Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2018). Alternative transcript imbalance underlying breast cancer susceptibility in a family carrying PALB2 c.3201+5G>T. Breast Cancer Research and Treatment. 174(2). 543–550. 4 indexed citations

Moreno, Laura, Neus Gadea, Estela Carrasco, et al.. (2016). Germline BRCA testing is moving from cancer risk assessment to a predictive biomarker for targeting cancer therapeutics. Clinical & Translational Oncology. 18(10). 981–987. 17 indexed citations

Gadea, Neus, Joan Brunet, Teresa Ramón y Cajal, et al.. (2012). What factors may influence psychological well being at three months and one year post BRCA genetic result disclosure?. The Breast. 21(6). 755–760. 32 indexed citations

Balmañà, Judith, Neus Gadea, Cristina Díaz de Heredia, et al.. (2012). Surveillance of Adolescents and Young Adult Patients with Fanconi Anemia (FA): Awareness of Diagnosing Solid Tumors at a Young Age. Annals of Oncology. 23. ixe18–ixe18. 1 indexed citations

Dı́ez, Orland, A. Pelegrí, Neus Gadea, et al.. (2011). Novel BRCA1 deleterious mutation (c.1949_1950delTA) in a woman of Senegalese descent with triple-negative early-onset breast cancer. Oncology Letters. 2(6). 1287–1289. 8 indexed citations

Saura, Cristina, et al.. (2010). High prevalence of BRCA1/2 germline mutations in female breast cancer patients with triple-negative phenotype (TNBC) and family history.. Journal of Clinical Oncology. 28(15_suppl). 1534–1534. 2 indexed citations

10.

Dı́ez, Orland, Sara Gutiérrez‐Enríquez, C. Mediano, et al.. (2009). A novel de novo BRCA2 mutation of paternal origin identified in a Spanish woman with early onset bilateral breast cancer. Breast Cancer Research and Treatment. 121(1). 221–225. 9 indexed citations

11.

Sanz, Judit, Teresa Ramón y Cajal, Esther Darder, et al.. (2009). Uptake of predictive testing among relatives of BRCA1 and BRCA2 families: a multicenter study in northeastern Spain. Familial Cancer. 9(3). 297–304. 34 indexed citations

12.

Balmañà, Judith, Begoña Graña, Esther Darder, et al.. (2008). Opinion about reproductive decision making among individuals undergoing BRCA1/2 genetic testing in a multicentre Spanish cohort. Human Reproduction. 24(4). 1000–1006. 59 indexed citations

13.

Gadea, Neus, et al.. (2004). Bocio. Bocio difuso y multinodular normofuncionante. Medicine - Programa de Formación Médica Continuada Acreditado. 9(14). 831–837.

14.

Gadea, Neus, et al.. (2000). Protocolo terapéutico del enfermo diabético sometido a cirugía. Medicine - Programa de Formación Médica Continuada Acreditado. 8(20). 1086–1088. 1 indexed citations

15.

Gadea, Neus. (2000). Neuropatía diabética periférica. Medicine - Programa de Formación Médica Continuada Acreditado. 8(19). 1009–1016. 13 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.

Explore authors with similar magnitude of impact