Françoise Gary

3.8k total citations · 2 hit papers
25 papers, 2.5k citations indexed

About

Françoise Gary is a scholar working on Cardiology and Cardiovascular Medicine, Molecular Biology and Genetics. According to data from OpenAlex, Françoise Gary has authored 25 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cardiology and Cardiovascular Medicine, 7 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Françoise Gary's work include Cardiovascular Effects of Exercise (6 papers), Gestational Diabetes Research and Management (5 papers) and Genetic and phenotypic traits in livestock (5 papers). Françoise Gary is often cited by papers focused on Cardiovascular Effects of Exercise (6 papers), Gestational Diabetes Research and Management (5 papers) and Genetic and phenotypic traits in livestock (5 papers). Françoise Gary collaborates with scholars based in France, Burundi and United Kingdom. Françoise Gary's co-authors include Ketty Schwartz, Gisèle Bonne, Michel Fardeau, Shaïda Varnous, Luciano Merlini, E. Hammouda, Henri-Marc Bécane, J.A. Urtizberea, Denis Duboc and Francesco Muntoni and has published in prestigious journals such as Nature Genetics, PLoS ONE and Circulation Research.

In The Last Decade

Françoise Gary

24 papers receiving 2.4k citations

Hit Papers

Mutations in the gene encoding lamin A/C cause autosomal ... 1997 2026 2006 2016 1999 1997 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
    1999 1.0k citations Gisèle Bonne, Marina Raffaele di Barletta et al. Nature Genetics profile →
  2. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    1997 659 citations Nathalie Neyroud, Frédérique Tesson et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Françoise Gary France 15 1.9k 1.0k 224 220 177 25 2.5k
Andrea L. Portbury United States 18 918 0.5× 165 0.2× 233 1.0× 552 2.5× 56 0.3× 28 1.5k
Yoshihiro Wakayama Japan 22 1.4k 0.7× 207 0.2× 238 1.1× 207 0.9× 21 0.1× 114 1.7k
Elena Popova Germany 18 696 0.4× 475 0.5× 40 0.2× 144 0.7× 10 0.1× 39 1.3k
Richard J. Lang Australia 20 661 0.3× 159 0.2× 28 0.1× 143 0.7× 172 1.0× 52 1.2k
Andrea Vettori Italy 20 597 0.3× 432 0.4× 294 1.3× 221 1.0× 7 0.0× 43 1.5k
Yukio Hirata Japan 8 1.1k 0.6× 273 0.3× 32 0.1× 316 1.4× 34 0.2× 9 1.6k
Tania E. Webb United Kingdom 24 989 0.5× 280 0.3× 21 0.1× 394 1.8× 41 0.2× 39 2.2k
Jesun Lee South Korea 7 1.1k 0.6× 225 0.2× 76 0.3× 472 2.1× 447 2.5× 8 1.4k
Andrea A. Domenighetti United States 19 882 0.5× 725 0.7× 123 0.5× 198 0.9× 10 0.1× 34 1.4k
Lynne H. Liu United States 11 871 0.5× 340 0.3× 203 0.9× 140 0.6× 194 1.1× 11 1.2k

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 of co-authors of Françoise Gary

This figure shows the co-authorship network connecting the top 25 collaborators of Françoise Gary. A scholar is included among the top collaborators of Françoise Gary based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Françoise Gary. Françoise Gary is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Cosson, Emmanuel, Éric Vicaut, Françoise Gary, et al.. (2019). Performance of a selective screening strategy for diagnosis of hyperglycaemia in pregnancy as defined by IADPSG/WHO criteria. Diabetes & Metabolism. 46(4). 311–318. 22 indexed citations
2.
3.
Cosson, Emmanuel, Éric Vicaut, Françoise Gary, et al.. (2018). Early screening for gestational diabetes mellitus is not associated with improved pregnancy outcomes: an observational study including 9795 women. Diabetes & Metabolism. 45(5). 465–472. 29 indexed citations
4.
Cosson, Emmanuel, Françoise Gary, I. Pharisien, et al.. (2017). Poor Reliability and Poor Adherence to Self-Monitoring of Blood Glucose Are Common in Women With Gestational Diabetes Mellitus and May Be Associated With Poor Pregnancy Outcomes. Diabetes Care. 40(9). 1181–1186. 50 indexed citations
5.
Gandjbakhch, Estelle, Alexia Vite, Françoise Gary, et al.. (2013). Screening of genes encoding junctional candidates in arrhythmogenic right ventricular cardiomyopathy/dysplasia. EP Europace. 15(10). 1522–1525. 15 indexed citations
6.
Vite, Alexia, Estelle Gandjbakhch, Cathérine Prost, et al.. (2013). Desmosomal Cadherins Are Decreased in Explanted Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patient Hearts. PLoS ONE. 8(9). e75082–e75082. 22 indexed citations
7.
Gandjbakhch, Estelle, Philippe Charron, Véronique Fressart, et al.. (2011). Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy. Heart. 97(10). 844–849. 13 indexed citations
8.
Fagart, Jérôme, Françoise Gary, Dimitrios T. Papadimitriou, et al.. (2006). Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism. Human Mutation. 28(1). 33–40. 62 indexed citations
9.
Bonne, Gisèle, Marina Raffaele di Barletta, Shaïda Varnous, et al.. (1999). Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nature Genetics. 21(3). 285–288. 1032 indexed citations breakdown →
10.
Richard, Pascale, Richard Isnard, Lucie Carrier, et al.. (1999). 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.. PubMed. 36(7). 542–5. 60 indexed citations
11.
Richard, Pascale, Richard Isnard, Lucie Carrier, et al.. (1999). Double heterozygosity for mutations in the β-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy. Journal of Medical Genetics. 36(7). 542–545. 47 indexed citations
12.
Vignier, Nicolas, Behzad Moghadaszadeh, Françoise Gary, et al.. (1999). Structure, Genetic Localization, and Identification of the Cardiac and Skeletal Muscle Transcripts of the Human Integrin α7 Gene (ITGA7). Biochemical and Biophysical Research Communications. 260(2). 357–364. 18 indexed citations
13.
Duclos, Franck, Odile Broux, Nathalie Bourg, et al.. (1998). β-Sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolate. Neuromuscular Disorders. 8(1). 30–38. 43 indexed citations
14.
Neyroud, Nathalie, Isabelle Denjoy, Claire Donger, et al.. (1998). Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome. European Journal of Human Genetics. 6(2). 129–133. 35 indexed citations
15.
Donger, Claire, Éric Krejci, B. Eymard, et al.. (1998). Mutation in the Human Acetylcholinesterase-Associated Collagen Gene, COLQ, Is Responsible for Congenital Myasthenic Syndrome with End-Plate Acetylcholinesterase Deficiency (Type Ic). The American Journal of Human Genetics. 63(4). 967–975. 125 indexed citations
16.
17.
Neyroud, Nathalie, Frédérique Tesson, Isabelle Denjoy, et al.. (1997). A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genetics. 15(2). 186–189. 659 indexed citations breakdown →
18.
Gary, Françoise, et al.. (1993). Effects of the 6/15 Robertsonian Translocation in Saanen Goats. Reproduction in Domestic Animals. 28(1). 28–32. 3 indexed citations
19.
Gary, Françoise, et al.. (1991). Does the Robertsonian translocation affect the fertility of Blonde d'Aquitaine breed bulls?. Theriogenology. 36(3). 419–425. 1 indexed citations
20.
Gary, Françoise, et al.. (1991). 1/29 Robertsonian translocation in Blonde d'Aquitaine bulls: frequency and effects on semen characteristics. Genetics Selection Evolution. 23(S1). 3 indexed citations

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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