Sandra Bonache

1.8k citations
24 papers · 537 · h-index 13

Impact in

    • Sperm and Testicular Function
  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomics and Rare Diseases

Papers in

    • BRCA gene mutations in cancer 8
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 6
    • DNA Repair Mechanisms 5
    • CRISPR and Genetic Engineering 3
    • RNA Research and Splicing 3

Sandra Bonache

24 papers receiving 503 citations

Peers

Sandra Bonache
Comparison fields: 5 of 57
  • Reproductive Medicine 112
  • Genetics 253
  • Cancer Research 75
  • Molecular Biology 266
  • Pathology and Forensic Medicine 45
Replace Estela G. Toraño with:
Estela G. Toraño Spain
Beike Leegte Netherlands
Temuujin Dansranjavin Germany
S E Rowell United States
Ewa Rajpert-De Meyts Denmark
Sofia Dória Portugal
Noriyuki Sugiyama Japan
Matthew Lubin United States
Kristin Bosse Germany
Bela Patel United States
Sandra Bonache relative to Estela G. Toraño Spain Estela G. Toraño's profile →
Citations per field
00.5×3.1×
Estela G. Toraño · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Sandra Bonache, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sandra Bonache Line = papers co-authored together Sandra Bonache links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 201283
2 201079
3 201850
4 201849
5 201242
6 201827
7 201424
8 200523
9 200721
10 201418
11 201617
12 201415
13 201212
14 200510
15 20199
16 20199
17 20228
18 20217
19 20077
20 20226

About Sandra Bonache

Sandra Bonache is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Reproductive Medicine and Neurology, having authored 24 papers that have together received 537 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers), DNA Repair Mechanisms (5 papers), Sperm and Testicular Function (3 papers), Genetic factors in colorectal cancer (3 papers), CRISPR and Genetic Engineering (3 papers), RNA Research and Splicing (3 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). The work is most often cited by research in Reproductive Medicine (112 citations), Genetics (253 citations), Cancer Research (75 citations), Molecular Biology (266 citations) and Pathology and Forensic Medicine (45 citations). Sandra Bonache has collaborated with scholars based in Spain, Finland and Portugal. Frequent co-authors include Sara Larriba, Lluís Bassas, Sara Gutiérrez‐Enríquez, Orland Dı́ez, Judith Balmañà, Gemma Montalban, María Dolores Burguete Ramos, Ernest Terribas, Marta García‐Arévalo and Estela Carrasco. Their work appears in journals such as Breast Cancer Research and Treatment, Journal of Cancer Research and Clinical Oncology, International Journal of Andrology, Journal of Medical Genetics and Human Mutation.

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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