Catherine Molinas

4.1k total citations · 1 hit paper
57 papers, 3.0k citations indexed

About

Catherine Molinas is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Catherine Molinas has authored 57 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Genetics, 19 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Catherine Molinas's work include Genetic Syndromes and Imprinting (39 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Bacterial Genetics and Biotechnology (9 papers). Catherine Molinas is often cited by papers focused on Genetic Syndromes and Imprinting (39 papers), Genetics and Neurodevelopmental Disorders (18 papers) and Bacterial Genetics and Biotechnology (9 papers). Catherine Molinas collaborates with scholars based in France, Netherlands and United States. Catherine Molinas's co-authors include Patrice Courvalin, Michel Arthur, M. Tauber, Florence Depardieu, Gwénaëlle Diene, Sylvie Dutka‐Malen, Jean‐Pierre Salles, Catherine Arnaud, Gerard D. Wright and Éric Bieth and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, PEDIATRICS and Clinical Infectious Diseases.

In The Last Decade

Catherine Molinas

57 papers receiving 2.9k citations

Hit Papers

align trajectories

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.

Characterization of Tn1546, a Tn3-related transposon conferring glycopeptide resistance by synthesis of depsipeptide peptidoglycan precursors in Enterococcus faecium BM4147

1993 483 citations Michel Arthur, Catherine Molinas et al. profile →

Peers

Catherine Molinas

GENET

PPCH

Taina Härkönen Finland

John K. Crane United States

James M. Fleckenstein United States

Natasha A. Barry United States

Melinda A. Engevik United States

Isabelle Le Huërou‐Luron France

Henry L. Schreiber United States

Richard Holt United Kingdom

William Eisner United States

Karin de Punder Germany

Taina Härkönen Finland

Catherine Molinas

1.4k ×0.9

GENET

1.2k ×1.0

512 ×0.5

56 ×0.2

102 ×0.3

PPCH

Citations per year, relative to Catherine Molinas Catherine Molinas (= 1×) peers Taina Härkönen

Countries citing papers authored by Catherine Molinas

Since Specialization

Citations

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

Fields of papers citing papers by Catherine Molinas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Catherine Molinas

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine Molinas. A scholar is included among the top collaborators of Catherine Molinas 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 Catherine Molinas. Catherine Molinas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Diene, Gwénaëlle, et al.. (2024). Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader–Willi syndrome. Clinical Autonomic Research. 35(2). 243–255. 1 indexed citations

Eddiry, Sanaa, Gwénaëlle Diene, Catherine Molinas, et al.. (2021). SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome. Genetics in Medicine. 23(9). 1664–1672. 12 indexed citations

Salles, Juliette, Sanaa Eddiry, Emmanuelle Lacassagne, et al.. (2021). Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory. Clinical Epigenetics. 13(1). 159–159. 9 indexed citations

Beauloye, Véronique, Gwénaëlle Diene, Renske Kuppens, et al.. (2016). High unacylated ghrelin levels support the concept of anorexia in infants with prader-willi syndrome. Orphanet Journal of Rare Diseases. 11(1). 56–56. 34 indexed citations

Cadoudal, Thomas, Gwénaëlle Diene, Coralie Sengenès, et al.. (2014). Impairment of Adipose Tissue in Prader-Willi Syndrome Rescued by GH Treatment. 82. 1 indexed citations

Tauber, M., Gwénaëlle Diene, Emmanuelle Mimoun, et al.. (2014). Prader-Willi Syndrome as a Model of Human Hyperphagia. Frontiers of hormone research. 42. 93–106. 32 indexed citations

Cadoudal, Thomas, Marie Buléon, Coralie Sengenès, et al.. (2014). Impairment of adipose tissue in Prader–Willi syndrome rescued by growth hormone treatment. International Journal of Obesity. 38(9). 1234–1240. 28 indexed citations

Bieth, Éric, Sanaa Eddiry, Véronique Gaston, et al.. (2014). Highly restricted deletion of the SNORD116 region is implicated in Prader–Willi Syndrome. European Journal of Human Genetics. 23(2). 252–255. 126 indexed citations

Coupaye, Muriel, F. Lorenzini, Célia Lloret‐Linares, et al.. (2013). Growth Hormone Therapy for Children and Adolescents with Prader-Willi Syndrome Is Associated with Improved Body Composition and Metabolic Status in Adulthood. The Journal of Clinical Endocrinology & Metabolism. 98(2). E328–E335. 46 indexed citations

10.

Tauber, M., P. Copet, Gwénaëlle Diene, et al.. (2011). Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients. Orphanet Journal of Rare Diseases. 6(1). 47–47. 82 indexed citations

11.

Diene, Gwénaëlle, Emmanuelle Mimoun, Eva Feigerlová, et al.. (2010). Endocrine Disorders in Children with Prader-Willi Syndrome – Data from 142 Children of the French Database. Hormone Research in Paediatrics. 74(2). 121–128. 125 indexed citations

12.

Copet, P., Virginie Laurier, Virginie Ehlinger, et al.. (2010). Cognitive profile in a large french cohort of adults with Prader–Willi syndrome: differences between genotypes. Journal of Intellectual Disability Research. 54(3). 204–215. 53 indexed citations

13.

Molinas, Catherine, et al.. (2008). French database of children and adolescents with Prader-Willi syndrome. BMC Medical Genetics. 9(1). 89–89. 15 indexed citations

14.

Tauber, M., Wietske A. Ester, Catherine Molinas, et al.. (2007). GH responsiveness in a large multinational cohort of SGA children with short stature (NESTEGG) is related to the exon 3 GHR polymorphism. Clinical Endocrinology. 67(3). 457–461. 37 indexed citations

15.

Salles, Jean‐Pierre, et al.. (2002). Identification of a Region Critical for Proteolysis of the Human Growth Hormone Receptor. Biochemical and Biophysical Research Communications. 290(2). 851–857. 13 indexed citations

16.

Dastot, Florence, et al.. (1998). Heterozygous mutation in the WSXWS equivalent motif of the growth hormone receptor in a child with poor response to growth hormone therapy. Growth Hormone & IGF Research. 8(3). 211–216. 8 indexed citations

17.

Bieth, Éric, Claire Cahoreau, Catherine Molinas, et al.. (1997). Human growth hormone receptor: cloning and expression of the full-length complementary DNA after site-directed inactivation of a cryptic bacterial promoter. Gene. 194(1). 97–105. 6 indexed citations

18.

Arthur, Michel, Florence Depardieu, Catherine Molinas, Peter E. Reynolds, & Patrice Courvalin. (1995). The vanZ gene of Tn1546 from enterococcus faecium BM4147 confers resistance to teicoplanin. Gene. 154(1). 87–92. 131 indexed citations

19.

Leclercq, Roland, Sylvie Dutka‐Malen, A Brisson-Noël, et al.. (1992). Resistance of Enterococci to Aminoglycosides and Glycopeptides. Clinical Infectious Diseases. 15(3). 495–501. 93 indexed citations

20.

Arthur, Michel, Catherine Molinas, Sylvie Dutka‐Malen, & Patrice Courvalin. (1991). Structural relationship between the vancomycin resistance protein VanH and 2-hydroxycarboxylic acid dehydrogenases. Gene. 103(1). 133–134. 87 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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