Sandra Bonache

1.8k total citations
24 papers, 493 citations indexed

About

Sandra Bonache is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Sandra Bonache has authored 24 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 18 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Sandra Bonache's work include DNA Repair Mechanisms (10 papers), BRCA gene mutations in cancer (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Sandra Bonache is often cited by papers focused on DNA Repair Mechanisms (10 papers), BRCA gene mutations in cancer (9 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers). Sandra Bonache collaborates with scholars based in Spain, Palestinian Territory and Sweden. Sandra Bonache's co-authors include Sara Larriba, Lluís Bassas, Orland Dı́ez, Sara Gutiérrez‐Enríquez, Judith Balmañà, Gemma Montalban, María Dolores Burguete Ramos, Estela Carrasco, Holger Heyn and Lluís Bassas and has published in prestigious journals such as PLoS ONE, Human Reproduction and Fertility and Sterility.

In The Last Decade

Sandra Bonache

24 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Bonache Spain 13 293 254 106 82 57 24 493
Beike Leegte Netherlands 11 189 0.6× 428 1.7× 103 1.0× 91 1.1× 63 1.1× 15 531
Estela G. Toraño Spain 9 292 1.0× 82 0.3× 86 0.8× 61 0.7× 29 0.5× 9 431
Feng-Tao Shi China 14 422 1.4× 66 0.3× 65 0.6× 71 0.9× 23 0.4× 18 633
Temuujin Dansranjavin Germany 12 308 1.1× 80 0.3× 85 0.8× 59 0.7× 15 0.3× 15 426
Annemieke H. van der Hout Netherlands 8 227 0.8× 223 0.9× 32 0.3× 88 1.1× 33 0.6× 13 451
Ewa Rajpert-De Meyts Denmark 6 272 0.9× 115 0.5× 140 1.3× 55 0.7× 14 0.2× 6 429
Rachel Linger United Kingdom 4 327 1.1× 256 1.0× 154 1.5× 44 0.5× 15 0.3× 7 557
Caterina Barbieri Italy 9 228 0.8× 79 0.3× 49 0.5× 37 0.5× 54 0.9× 18 392
Tatsuo Kido United States 13 338 1.2× 291 1.1× 109 1.0× 37 0.5× 10 0.2× 20 482
Sofia Dória Portugal 13 244 0.8× 208 0.8× 99 0.9× 50 0.6× 12 0.2× 49 541

Countries citing papers authored by Sandra Bonache

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Bonache

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Bonache

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Bonache. A scholar is included among the top collaborators of Sandra Bonache 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 Sandra Bonache. Sandra Bonache 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.
Rodríguez, Anna Duat, Juan Luís Becerra, Sandra Bonache, et al.. (2022). Neurofibromatosis type 1 families with first-degree relatives harbouring distinct NF1 pathogenic variants. Genetic counselling and familial diagnosis: what should be offered?. Journal of Medical Genetics. 59(10). 1017–1023. 7 indexed citations
2.
Bonache, Sandra, Miguel Torres‐Martín, S.P. Hector, et al.. (2022). Antisense oligonucleotides targeting exon 11 are able to partially rescue the NF2-related schwannomatosis phenotype in vitro. Molecular Therapy — Nucleic Acids. 30. 493–505. 5 indexed citations
3.
Montalban, Gemma, Sandra Bonache, Vanessa Bach, et al.. (2021). BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patients. Cancer Genetics. 258-259. 10–17. 5 indexed citations
4.
Castells‐Roca, Laia, Sara Gutiérrez‐Enríquez, Sandra Bonache, et al.. (2021). Clinical consequences of BRCA2 hypomorphism. npj Breast Cancer. 7(1). 117–117. 6 indexed citations
5.
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
6.
Moles‐Fernández, Alejandro, Gemma Montalban, Sandra Bonache, et al.. (2018). Computational Tools for Splicing Defect Prediction in Breast/Ovarian Cancer Genes: How Efficient Are They at Predicting RNA Alterations?. Frontiers in Genetics. 9. 366–366. 46 indexed citations
7.
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
8.
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
9.
Caragol, Isabel, Carmen Alonso, Teresa Ramón y Cajal, et al.. (2014). Apoptosis for prediction of radiotherapy late toxicity: lymphocyte subset sensitivity and potential effect of TP53 Arg72Pro polymorphism. APOPTOSIS. 20(3). 371–382. 18 indexed citations
10.
Blanco, Ana, Sara Gutiérrez‐Enríquez, Marta Santamariña, et al.. (2014). RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families. Breast Cancer Research and Treatment. 147(1). 133–143. 24 indexed citations
11.
Bonache, Sandra, et al.. (2013). Mutation analysis of the SHFM1 gene in breast/ovarian cancer families. Journal of Cancer Research and Clinical Oncology. 139(3). 529–532. 6 indexed citations
12.
Bonache, Sandra, et al.. (2013). Mutation analysis of the BCCIP gene for breast cancer susceptibility in breast/ovarian cancer families. Gynecologic Oncology. 131(2). 460–463. 4 indexed citations
13.
Garibay, Gorka Ruíz de, Sara Gutiérrez‐Enríquez, Pilar Garré, et al.. (2012). Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their origin. Breast Cancer Research and Treatment. 133(1). 273–283. 12 indexed citations
14.
Heyn, Holger, Humberto J. Ferreira, Lluís Bassas, et al.. (2012). Epigenetic Disruption of the PIWI Pathway in Human Spermatogenic Disorders. PLoS ONE. 7(10). e47892–e47892. 77 indexed citations
15.
Bonache, Sandra, A. Mata, María Dolores Burguete Ramos, Lluís Bassas, & Sara Larriba. (2012). Sperm gene expression profile is related to pregnancy rate after insemination and is predictive of low fecundity in normozoospermic men. Human Reproduction. 27(6). 1556–1567. 39 indexed citations
16.
Terribas, Ernest, et al.. (2010). Changes in the Expression Profile of the Meiosis‐Involved Mismatch Repair Genes in Impaired Human Spermatogenesis. Journal of Andrology. 31(4). 346–357. 61 indexed citations
17.
Bonache, Sandra, et al.. (2007). Single nucleotide polymorphisms in succinate dehydrogenase subunits and citrate synthase genes: association results for impaired spermatogenesis. International Journal of Andrology. 30(3). 144–152. 7 indexed citations
18.
Bonache, Sandra, et al.. (2007). Mutations of SYCP3 are rare in infertile Spanish men with meiotic arrest. Fertility and Sterility. 88(4). 988–989. 21 indexed citations
19.
Bonache, Sandra, et al.. (2005). Spectrum of mutations in CFTR in Finland: 18 years follow-up study and identification of two novel mutations. Journal of Cystic Fibrosis. 4(4). 233–237. 10 indexed citations
20.
Larriba, Sara, Sandra Bonache, Joaquim Sàrquella, et al.. (2005). Molecular evaluation of CFTR sequence variants in male infertility of testicular origin. International Journal of Andrology. 28(5). 284–290. 19 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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