Françoise Gary

3.8k citations
25 papers · 2.5k · 2 hit papers · h-index 15

Impact in

Papers in

Françoise Gary

24 papers receiving 2.5k citations

Françoise Gary's Hit Papers

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy 1999 · 1.0k citations
1.0k0+9+19Years since publication2505007501000

Peers

Françoise Gary
Comparison fields: 5 of 82
  • Cardiology and Cardiovascular Medicine 971
  • Sensory Systems 171
  • Molecular Biology 1.8k
  • Obstetrics and Gynecology 98
  • Cell Biology 208
Replace Ralph Waldschütz with:
Ralph Waldschütz Germany
Stephanie A. Parsons United States
Andrea L. Portbury United States
Yukinao Shibukawa Japan
Frances Elmslie United Kingdom
Yoshihiro Wakayama Japan
Nestor X. Barrezueta United States
Joana Almaça United States
Elena Popova Germany
Andrea Vettori Italy
Françoise Gary relative to Ralph Waldschütz Germany Ralph Waldschütz's profile →
Citations per field
00.5×3.4×
Ralph Waldschütz · 1×
Citations per year

Countries citing papers authored by Françoise Gary

Since Specialization
Citations

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

Fields of papers citing papers by Françoise Gary

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 25 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
Hit paper breakdown →
19991036
2
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
Hit paper breakdown →
1997661
3 1997239
4 1998125
5 200662
6
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy.
199960
7 201754
8 199947
9 199843
10 199835
11 201830
12 201923
13 201322
14 199918
15 201315
16 201114
17 20199
18 19918
19 20197
20 19933

About Françoise Gary

Françoise Gary is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology, Genetics, Obstetrics and Gynecology and Animal Science and Zoology, having authored 25 papers that have together received 2.5k indexed citations. Recurring topics across this work include Cardiovascular Effects of Exercise (6 papers), Gestational Diabetes Research and Management (5 papers), Genetic and phenotypic traits in livestock (5 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Cardiomyopathy and Myosin Studies (3 papers), Cardiac electrophysiology and arrhythmias (2 papers), Animal Genetics and Reproduction (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (971 citations), Sensory Systems (171 citations), Molecular Biology (1.8k citations), Obstetrics and Gynecology (98 citations) and Cell Biology (208 citations). Françoise Gary has collaborated with scholars based in France, Australia and United States. Frequent co-authors include Ketty Schwartz, Gisèle Bonne, Michel Fardeau, Shaïda Varnous, Denis Duboc, Daniela Toniolo, Henri-Marc Bécane, Luciano Merlini, Cheryl R. Greenberg and Francesco Muntoni. Their work appears in journals such as EP Europace, Diabetes & Metabolism, Nature Genetics, Genetics Selection Evolution and Biochemical and Biophysical Research Communications.

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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