Françoise Gary

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

Françoise Gary

24 papers receiving 2.4k citations

Hit Papers

Mutations in the gene encoding lamin A/C cause autosomal ...1.0k19972026200620162505007501000

Peers

Françoise Gary
Comparison fields: 5 of 85
  • Cardiology and Cardiovascular Medicine 1.0k
  • Sensory Systems 177
  • Molecular Biology 1.9k
  • Cell Biology 224
  • Obstetrics and Gynecology 99
Replace Andrea L. Portbury with:
Andrea L. Portbury United States
Richard J. Lang Australia
Yoshihiro Wakayama Japan
Tania E. Webb United Kingdom
Elena Popova Germany
Lynne H. Liu United States
Colleen Kondo Canada
Inge Brouns Belgium
Sylvia Bähring Germany
M Dvořáková Czechia
Françoise Gary relative to Andrea L. Portbury United States Andrea L. Portbury's profile →
Citations per field
00.5×6.2×
Andrea L. Portbury · 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-authorship network

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
#Work
1 201922
2 201829
3 201750
4 20160
5 201315
6 201322
7 201113
8 200662
9
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
10
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophybreakdown →
19991032
11 199918
12 199947
13 199843
14 199835
15 1998125
16
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndromebreakdown →
1997659
17 1997238
18 19933
19 19911
20 19913

About Françoise Gary

Françoise Gary is a scholar working on Obstetrics and Gynecology, Orthopedics and Sports Medicine and Cardiology and Cardiovascular Medicine, having authored 25 papers that have together received 2.5k indexed citations. Recurring topics across this work include Cardiovascular Effects of Exercise (6 papers), Genetic and phenotypic traits in livestock (5 papers), Gestational Diabetes Research and Management (5 papers), Pregnancy and preeclampsia studies (4 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers), Sports injuries and prevention (4 papers), Cardiac electrophysiology and arrhythmias (3 papers) and Cardiomyopathy and Myosin Studies (3 papers). The work is most often cited by research in Cardiology and Cardiovascular Medicine (1.0k citations), Sensory Systems (177 citations) and Molecular Biology (1.9k citations). Françoise Gary has collaborated with scholars based in France, Ivory Coast and United Kingdom. Frequent co-authors include Ketty Schwartz, Gisèle Bonne, Michel Fardeau, Shaïda Varnous, E. Hammouda, Henri-Marc Bécane, Cheryl R. Greenberg, Marina Raffaele di Barletta, Luciano Merlini and Denis Duboc. Their work appears in journals such as Nature Genetics, Diabetes & Metabolism, EP Europace, Genetics Selection Evolution and European Journal of Human 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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