Francesca Vidal

5.8k citations
136 papers · 4.0k · h-index 38

Impact in

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 35
    • Genomic variations and chromosomal abnormalities 19
    • Animal Genetics and Reproduction 18
    • Prenatal Screening and Diagnostics 53
    • Assisted Reproductive Technology and Twin Pregnancy 14

Francesca Vidal

134 papers receiving 3.7k citations

Peers

Francesca Vidal
Comparison fields: 5 of 90
  • Reproductive Medicine 1.6k
  • Pediatrics, Perinatology and Child Health 1.9k
  • Genetics 2.0k
  • Public Health, Environmental and Occupational Health 1.7k
  • Plant Science 797
Replace J. Egozcue with:
J. Egozcue Spain
E. Fragouli United Kingdom
Joan Blanco Spain
Xiaoxi Sun China
Asangla Ao Canada
M.C. Magli United States
Frank L. Barnes United States
Charlotte E. Farin United States
M. Oliver‐Bonet Spain
Geraldine Hartshorne United Kingdom
Francesca Vidal relative to J. Egozcue Spain J. Egozcue's profile →
Citations per field
00.5×10.3×
J. Egozcue · 1×
Citations per year

Countries citing papers authored by Francesca Vidal

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Vidal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Francesca Vidal, 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 Francesca Vidal Line = papers co-authored together Francesca Vidal links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 136 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2003215
2 2011157
3 2001142
4 1999113
5 1983104
6 1996102
7 199995
8 200194
9 200588
10 199888
11 201585
12 201179
13 199878
14 201469
15 199768
16 199368
17 201167
18 199966
19 199161
20 199861

About Francesca Vidal

Francesca Vidal is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Public Health, Environmental and Occupational Health, Reproductive Medicine and Molecular Biology, having authored 136 papers that have together received 4.0k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (53 papers), Reproductive Biology and Fertility (53 papers), Sperm and Testicular Function (46 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (35 papers), Chromosomal and Genetic Variations (35 papers), Genomic variations and chromosomal abnormalities (19 papers), Animal Genetics and Reproduction (18 papers) and Assisted Reproductive Technology and Twin Pregnancy (14 papers). The work is most often cited by research in Reproductive Medicine (1.6k citations), Pediatrics, Perinatology and Child Health (1.9k citations), Genetics (2.0k citations), Public Health, Environmental and Occupational Health (1.7k citations) and Plant Science (797 citations). Francesca Vidal has collaborated with scholars based in Spain, France and United Kingdom. Frequent co-authors include Joan Blanco, Ester Antón, J. Egozcue, C. Templado, Carlos Simón, J. Egozcue, António Pellicer, J. Navarro, Josep Egozcue and Zaida Sarrate. Their work appears in journals such as Human Reproduction, Human Genetics, Fertility and Sterility, Journal of Assisted Reproduction and Genetics and Cytogenetic and Genome Research.

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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