Martine LeMerrer

3.0k total citations · 2 hit papers
20 papers, 1.9k citations indexed

About

Martine LeMerrer is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Martine LeMerrer has authored 20 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Martine LeMerrer's work include Bone Tumor Diagnosis and Treatments (3 papers), Genetic and rare skin diseases. (2 papers) and Heterotopic Ossification and Related Conditions (2 papers). Martine LeMerrer is often cited by papers focused on Bone Tumor Diagnosis and Treatments (3 papers), Genetic and rare skin diseases. (2 papers) and Heterotopic Ossification and Related Conditions (2 papers). Martine LeMerrer collaborates with scholars based in France, United States and United Kingdom. Martine LeMerrer's co-authors include J. M. Connor, Eileen M. Shore, George Feldman, Roger Smith, Frederick S. Kaplan, James T. Triffitt, Jon Andoni Urtizberea, Rolf Morhart, Tae‐Joon Cho and Patricia Delai and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Journal of the American Academy of Dermatology.

In The Last Decade

Martine LeMerrer

19 papers receiving 1.9k 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.

A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva

2006 866 citations Eileen M. Shore, Meiqi Xu et al. Nature Genetics profile →
Nosology and classification of genetic skeletal disorders: 2010 revision

2011 450 citations Matthew L. Warman, Valérie Cormier‐Daire et al. American Journal of Medical Genetics Part A profile →

Peers

Martine LeMerrer

RHEUM

GENET

PRM

NEPHR

George Feldman United States

Vitali Lounev United States

Dimitra Micha Netherlands

M. Le Merrer France

Christine Verellen‐Dumoulin Belgium

Michael C. Naski United States

Ernie M.H.F. Bongers Netherlands

Kuber T. Sampath United States

Branka Dabovic United States

Allan J. Richards United Kingdom

George Feldman United States

Martine LeMerrer

881 ×0.9

RHEUM

695 ×1.0

GENET

611 ×0.9

PRM

887 ×1.3

354 ×1.2

NEPHR

Citations per year, relative to Martine LeMerrer Martine LeMerrer (= 1×) peers George Feldman

Countries citing papers authored by Martine LeMerrer

Since Specialization

Citations

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

Fields of papers citing papers by Martine LeMerrer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine LeMerrer

This figure shows the co-authorship network connecting the top 25 collaborators of Martine LeMerrer. A scholar is included among the top collaborators of Martine LeMerrer 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 Martine LeMerrer. Martine LeMerrer 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

Barthélémy, Florian, Claire Navarro, Nathalie Da Silva, et al.. (2015). Truncated prelamin A expression in HGPS-like patients: a transcriptional study. European Journal of Human Genetics. 23(8). 1051–1061. 21 indexed citations

Dieux, Anne, et al.. (2012). Oral manifestations of patients with Kenny–Caffey Syndrome. European Journal of Medical Genetics. 55(8-9). 441–445. 18 indexed citations

Boulé, Michèle, Geneviève Baujat, Adriana Ramirez, et al.. (2012). Lung function, diagnosis, and treatment of sleep‐disordered breathing in children with achondroplasia. American Journal of Medical Genetics Part A. 158A(8). 1987–1993. 45 indexed citations

Warman, Matthew L., Valérie Cormier‐Daire, Christine M Hall, et al.. (2011). Nosology and classification of genetic skeletal disorders: 2010 revision. American Journal of Medical Genetics Part A. 155(5). 943–968. 450 indexed citations breakdown →

Saussine, A., Karine Marrou, N. Bodak, et al.. (2011). Connective tissue nevi: An entity revisited. Journal of the American Academy of Dermatology. 67(2). 233–239. 15 indexed citations

Shore, Eileen M., Meiqi Xu, George Feldman, et al.. (2006). A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nature Genetics. 38(5). 525–527. 866 indexed citations breakdown →

Renella, Raffaele, Martine LeMerrer, Yasemin Alanay, et al.. (2006). Spondyloenchondrodysplasia with spasticity, cerebral calcifications, and immune dysregulation: Clinical and radiographic delineation of a pleiotropic disorder. American Journal of Medical Genetics Part A. 140A(6). 541–550. 37 indexed citations

Benoist-Lasselin, Catherine, Emmanuel de Margerie, Linda Gibbs, et al.. (2006). Defective chondrocyte proliferation and differentiation in osteochondromas of MHE patients. Bone. 39(1). 17–26. 43 indexed citations

Lévy, Nicolas, Claire Navarro, Irène Boccaccio, et al.. (2003). Functional exploration of A type lamins and associated proteins in patients affected with Hutchinson-Gilford progeria syndrome caused by G608G mutation in LMNA. The American Journal of Human Genetics. 73(5). 554. 1 indexed citations

10.

Faivre, Laurence, A Nivelon‐Chevallier, Philippe Khau Van Kien, et al.. (2001). Mazabraud syndrome in two patients: Clinical overlap with McCune-Albright syndrome. American Journal of Medical Genetics. 99(2). 132–136. 42 indexed citations

11.

Mahieu‐Caputo, D., P. Sonigo, Jeanne Amiel, et al.. (2000). Prenatal Diagnosis of Sporadic Apert Syndrome: A Sequential Diagnostic Approach Combining Three-Dimensional Computed Tomography and Molecular Biology. Fetal Diagnosis and Therapy. 16(1). 10–12. 25 indexed citations

12.

Feldman, George, Ming Li, Margrit Urbanek, et al.. (2000). Fibrodysplasia Ossificans Progressiva, a Heritable Disorder of Severe Heterotopic Ossification, Maps to Human Chromosome 4q27-31. The American Journal of Human Genetics. 66(1). 128–135. 74 indexed citations

13.

Dureau, P., et al.. (2000). SHORT syndrome: a case with high hyperopia and astigmatism. Ophthalmic Genetics. 21(4). 235–238. 2 indexed citations

14.

Cormier‐Daire, Valérie, Véronique Abadie, Jeanne Amiel, et al.. (1998). CHARGE syndrome: Report of 47 cases and review. American Journal of Medical Genetics. 76(5). 402–409. 180 indexed citations

15.

Lévy, A., Gérard Michel, Martine LeMerrer, & N. Philip. (1997). Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: A new component manifestation of deletion 22q11?. American Journal of Medical Genetics. 69(4). 356–359. 35 indexed citations

16.

Dommergues, Marc, Martine LeMerrer, G Couly, A. L. Delezoide, & Yves Dumez. (1995). Prenatal diagnosis of cleft lip at 11 menstrual weeks using embryoscopy in the Van der Woude syndrome. Prenatal Diagnosis. 15(4). 378–381. 12 indexed citations

17.

Dumez, Yves, Marc Dommergues, Marie-Claire Gübler, et al.. (1994). Meckel‐Gruber syndrome: Prenatal diagnosis at 10 menstrual weeks using embryoscopy. Prenatal Diagnosis. 14(2). 141–144. 9 indexed citations

18.

Bouloc, Anne, Martine LeMerrer, & C Blanchet‐Bardon. (1993). [The neurofibromatosis-Noonan syndrome: 4 cases].. PubMed. 120(11). 763–5.

19.

LeMerrer, Martine, I D Young, V. Stănescu, & P Maroteaux. (1991). Desbuquois syndrome. European Journal of Pediatrics. 150(11). 793–796. 26 indexed citations

20.

Léger, Juliane, Martine LeMerrer, Marie‐Louise Briard, & P Czernichow. (1987). Hypothyroidism in Children with Filter Paper TSH of 30 to 50 μU/ml at Initial Screening Implication of the TSH Cut‐off Point for Recalling of Infants at Risk. Acta Paediatrica. 76(4). 599–602. 4 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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