Shaïda Varnous

4.1k citations
80 papers · 2.6k indexed · 1 hit paper · h-index 22

Shaïda Varnous

75 papers receiving 2.6k citations

Hit Papers

Mutations in the gene encoding lamin A/C cause autosomal ...1.0k19992026200820172505007501000

Peers

Shaïda Varnous
Comparison fields: 5 of 84
  • Transplantation 323
  • Cardiology and Cardiovascular Medicine 597
  • Molecular Biology 1.5k
  • Surgery 627
  • Cell Biology 208
Replace Lennart Rydberg with:
Lennart Rydberg Sweden
Ellen Fietze Germany
Robert L. Yowell United States
Randall Craver United States
Cécile Contin‐Bordes France
Helmut E. Feucht Germany
M Rose United Kingdom
Geetha Chalasani United States
Alan Ting United Kingdom
Hossein C. Nousari United States
Shaïda Varnous relative to Lennart Rydberg Sweden Lennart Rydberg's profile →
Citations per field
00.5×10×16.1×
Lennart Rydberg · 1×
Citations per year

Countries citing papers authored by Shaïda Varnous

Since Specialization
Citations

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

Fields of papers citing papers by Shaïda Varnous

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20240
2 20234
3 20233
4 20235
5 20225
6 20221
7 20221
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9 20203
10 20199
11 201810
12 20181
13 201610
14 201617
15 201354
16 201211
17 20122
18 20088
19 2000169
20
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophybreakdown →
19991032

About Shaïda Varnous

Shaïda Varnous is a scholar working on Transplantation, Surgery and Cardiology and Cardiovascular Medicine, having authored 80 papers that have together received 2.6k indexed citations. Recurring topics across this work include Transplantation: Methods and Outcomes (45 papers), Mechanical Circulatory Support Devices (22 papers), Cardiac Structural Anomalies and Repair (19 papers), Renal Transplantation Outcomes and Treatments (18 papers), Viral Infections and Immunology Research (16 papers), Nuclear Structure and Function (6 papers), Organ Transplantation Techniques and Outcomes (6 papers) and Cytomegalovirus and herpesvirus research (6 papers). The work is most often cited by research in Transplantation (323 citations), Cardiology and Cardiovascular Medicine (597 citations) and Molecular Biology (1.5k citations). Shaïda Varnous has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Gisèle Bonne, Ketty Schwartz, Henri-Marc Bécane, Denis Duboc, Françoise Gary, E. Hammouda, Daniela Toniolo, J.A. Urtizberea, Francesco Muntoni and Cheryl R. Greenberg. Their work appears in journals such as The Journal of Heart and Lung Transplantation, American Journal of Transplantation, Archives of cardiovascular diseases, European Heart Journal and Human Molecular 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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