Sara Bernal

49 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 · 313 citations
3130+2+5Years since publication100200300

Peers

Sara Bernal
Comparison fields: 5 of 60
  • Genetics 908
  • Sensory Systems 141
  • Molecular Biology 1.0k
  • Ophthalmology 91
  • Surgery 361
Replace Masatoshi Hirayama with:
Masatoshi Hirayama Japan
Félix Prieto Spain
Shalini Jadeja United Kingdom
Tuula Rinne Netherlands
Silvestre Oltra Spain
T.J. Yoo United States
Benjamin Bakondi United States
Constanze Kaiser United States
Simon R. Bababeygy United States
Sanford L. Boye United States
Sara Bernal relative to Masatoshi Hirayama Japan Masatoshi Hirayama's profile →
Citations per field
00.5×9.8×
Masatoshi Hirayama · 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 54 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 →
2018313
2 2008132
3 200976
4 200371
5 201970
6 201268
7 201362
8 200355
9 201153
10 201052
11 201147
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 202038
15 200834
16 201134
17 201332
18 202131
19 201430
20 201128

About Sara Bernal

Sara Bernal is a scholar working on Molecular Biology, Genetics, Surgery, Cellular and Molecular Neuroscience and Rheumatology, having authored 54 papers that have together received 1.6k indexed citations. Recurring topics across this work include Neurogenetic and Muscular Disorders Research (21 papers), RNA modifications and cancer (11 papers), Congenital Anomalies and Fetal Surgery (9 papers), Retinal Development and Disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers), Genetic Neurodegenerative Diseases (4 papers), Rheumatoid Arthritis Research and Therapies (4 papers) and Retinal Diseases and Treatments (3 papers). The work is most often cited by research in Genetics (908 citations), Sensory Systems (141 citations), Molecular Biology (1.0k citations), Ophthalmology (91 citations) and Surgery (361 citations). Sara Bernal has collaborated with scholars based in Spain, United States and Italy. 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 Carmen Ayuso. Their work appears in journals such as Neuromuscular Disorders, Clinical Genetics, European Journal of Human Genetics, Annals of Clinical and Translational Neurology and Ophthalmic Genetics.

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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