Sara Bernal

50 papers receiving 1.5k citations

Sara Bernal's Hit Papers

Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases 2018 · 298 citations
2980+2+5Years since publication50100150200250

Peers

Sara Bernal
Comparison fields: 5 of 66
  • Genetics 890
  • Sensory Systems 139
  • Ophthalmology 173
  • Molecular Biology 1.2k
  • Surgery 481
Replace Raoul Heller with:
Raoul Heller Germany
Masatoshi Hirayama Japan
Anthony J. Vivian United Kingdom
Silvestre Oltra Spain
Tuula Rinne Netherlands
Shalini Jadeja United Kingdom
Turgut Tükel Türkiye
T.J. Yoo United States
Abdulrahman Alswaid Saudi Arabia
Yasuhiko Hirami Japan
Sara Bernal relative to Raoul Heller Germany Raoul Heller's profile →
Citations per field
00.5×9.6×
Raoul Heller · 1×
Citations per year

Countries citing papers authored by Sara Bernal

Since Specialization
Citations

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

Fields of papers citing papers by Sara Bernal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 53 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Correlation between SMA type and SMN2 copy number revisited: An analysis of 625 unrelated Spanish patients and a compilation of 2834 reported cases
Hit paper breakdown →
2018298
2 2008131
3 200976
4 200371
5 201969
6 201267
7 201360
8 200354
9 201153
10 201051
11 201146
12
Microarray-based mutation analysis of the ABCA4 gene in Spanish patients with Stargardt disease: evidence of a prevalent mutated allele.
200644
13 200542
14 202036
15 200833
16 201133
17 201430
18 201330
19 202129
20 201127

About Sara Bernal

Sara Bernal is a scholar working on Molecular Biology, Genetics, Surgery, Cellular and Molecular Neuroscience and Ophthalmology, having authored 53 papers that have together received 1.5k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (21 papers), RNA modifications and cancer (13 papers), Congenital Anomalies and Fetal Surgery (11 papers), Retinal Development and Disorders (8 papers), Retinal Diseases and Treatments (6 papers), Genetic Neurodegenerative Diseases (5 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Rheumatoid Arthritis Research and Therapies (4 papers). The work is most often cited by research in Genetics (890 citations), Sensory Systems (139 citations), Ophthalmology (173 citations), Molecular Biology (1.2k citations) and Surgery (481 citations). Sara Bernal has collaborated with scholars based in Spain, United Kingdom and United States. Frequent co-authors include Eduardo F. Tizzano, Laura Alías, Montserrat Baiget, Rebeca Martínez‐Hernández, José M. Millán, Pablo Fuentes‐Prior, Francisco Javier Álvarez Rodríguez, Concepción Hernández-Chico, Elena Aller and Salud Borrego. Their work appears in journals such as Neuromuscular Disorders, European Journal of Human Genetics, Clinical Genetics, Orphanet Journal of Rare Diseases and Annals of Clinical and Translational Neurology.

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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