Martine Le Merrer

15.8k citations

130 papers · 7.9k indexed · 1 hit paper · h-index 46

Molecular Biology top 1%
Genetics top 0.2%
Rheumatology top 1%
Surgery top 5%
Pulmonary and Respiratory Medicine top 5%

Co-authors: Arnold Münnich Valérie Cormier‐Daire Dominique Rénier Stanislas Lyonnet Geneviève Baujat Elizabeth Lajeunie Daniel Marchac Annachiara De Sandre‐Giovannoli
Topics: Connective tissue disorders research (43 papers)Bone health and treatments (15 papers)Cleft Lip and Palate Research (14 papers)
Cited by: Genetics Molecular Biology Rheumatology
Journals: Science Nature Genetics Blood
Partner nations: France United States United Kingdom

In The Last Decade

Martine Le Merrer

126 papers receiving 7.7k 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.

Lamin A Truncation in Hutchinson-Gilford Progeria

2003 1.1k citations Jeanne Amiel, Stanislas Lyonnet et al. profile →

Peers

Countries citing papers authored by Martine Le Merrer

Since Specialization

Citations

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

Fields of papers citing papers by Martine Le Merrer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martine Le Merrer

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis 2015 ·Pediatric Radiology ·Massimiliano Rossi,Christine M Hall,Raymonde Bouvier,Sophie Collardeau‐Frachon,F. Le Breton,Martine Bucourt,(unknown),Christine Vianey‐Saban,Giancarlo Parenti,Generoso Andria,Martine Le Merrer,Patrick Edery,Amaka C Offiah	11
2	Fibrous dysplasia and McCune–Albright syndrome: Imaging for positive and differential diagnoses, prognosis, and follow-up guidelines 2014 ·European Journal of Radiology ·V. Bousson,(unknown),Jean-Denis Larédo,Martine Le Merrer,N. Martin–Duverneuil,A. Feydy,Sébastien Aubert,Roland Chapurlat,Philippe Orcel	31
3	Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia 2012 ·The American Journal of Human Genetics ·Céline Huber,Eissa Faqeih,Deborah Bartholdi,Christine Bôle‐Feysot,Zvi Borochowitz,Denise P. Cavalcanti,(unknown),Patrick Nitschké,J. Roume,Heloísa G. dos Santos,Stavit Shalev,Andrea Superti‐Furga,Anne‐Lise Delezoide,Martine Le Merrer,Arnold Münnich,Valérie Cormier‐Daire	41
4	Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia? 2012 ·American Journal of Medical Genetics Part A ·Bertrand Isidor,Sylvaine Poignant,G. Picherot,(unknown),Pierre Quartier,Brigitte Bader‐Meunier,Cédric Le Caignec,Martine Le Merrer,Geneviève Baujat,Valérie Cormier‐Daire,Albert David	2
5	Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations 2010 ·American Journal of Medical Genetics Part A ·Shoji Ichikawa,Geneviève Baujat,Aksel Seyahi,(unknown),Erik A. Imel,Leah R. Padgett,Anthony M. Austin,Andrea H. Sorenson,Zagorka Péjin,Vicken Topouchian,Pierre Quartier,Valérie Cormier‐Daire,M Déchaux,(unknown),(unknown),Martine Le Merrer,Michael J. Econs	75
6	Jean Frézal et l'essor de la génétique médicale. 2008 ·médecine/sciences ·S Gilgenkrantz,Arnold Münnich,Marie‐Louise Briard,Martine Le Merrer,Josué Feingold,Jean-François Mattéi	0
7	Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications 2008 ·The American Journal of Human Genetics ·Ruth Bargal,Valérie Cormier‐Daire,Ziva Ben‐Neriah,Martine Le Merrer,Jacob Sosna,Judith Melki,David Zangen,Sarah Smithson,Zvi Borochowitz,Ruth Belostotsky,Annick Raas‐Rothschild	82
8	Fibrodysplasia ossificans progressiva 2008 ·Best Practice & Research Clinical Rheumatology ·Frederick S. Kaplan,Martine Le Merrer,David L. Glaser,Robert J. Pignolo,Robert E. Goldsby,Joseph A. Kitterman,Jay C. Groppe,Eileen M. Shore	235
9	Ellis-Van Creveld syndrome 2007 ·Orphanet Journal of Rare Diseases ·Geneviève Baujat,Martine Le Merrer	155
10	A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders 2006 ·Prenatal Diagnosis ·Marina Colombani,Nicole Laurent,Martine Le Merrer,Anne‐Lise Delezoide,Christel Thauvin‐Robinet,Frédéric Huet,(unknown),(unknown),Thierry Rousseau,Stephen P. Robertson,Laurence Faivre	2
11	Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome 2004 ·The American Journal of Human Genetics ·Geneviève Baujat,Marlène Rio,Sylvie Rossignol,Damien Sanlaville,Stanislas Lyonnet,Martine Le Merrer,Arnold Münnich,Christine Gicquel,Valérie Cormier‐Daire,Laurence Colleaux	88
12	Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome 2004 ·The American Journal of Human Genetics ·Nathalie Dagoneau,Déborah Scheffer,Céline Huber,L.I. Al-Gazali,Maja Di Rocco,Anne Godard,Jelena Martinović,Annick Raas‐Rothschild,Sabine Sigaudy,Sheila Unger,Sophie Nicole,Bertrand Fontaine,Jean‐Luc Taupin,Jean-François Moreau,Andrea Superti‐Furga,Martine Le Merrer,Jacky Bonaventure,Arnold Münnich,Laurence Legeai‐Mallet,Valérie Cormier‐Daire	136
13	Recurrence of achondrogenesis type II within the same family: Evidence for germline mosaicism 2003 ·American Journal of Medical Genetics Part A ·Laurence Faivre,Martine Le Merrer,(unknown),Nicole Laurent,Christel Thauvin‐Robinet,Thierry Rousseau,(unknown),(unknown),Anne‐Lise Delezoide,Paul Coucke,Geert Mortier	13
14	Classification moléculaire des maladies osseuses constitutionnelles 2001 ·Valérie Cormier‐Daire,Martine Le Merrer	1
15	Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures 2001 ·The American Journal of Human Genetics ·Jeanne Amiel,Yolanda Espinosa‐Parrilla,Julie Steffann,Philippe Gosset,Anna Pelet,Marguerite Prieur,Odile Boute,Agnès Choiset,Didier Lacombe,Nicole Philip,Martine Le Merrer,Hajime Tanaka,Marianne Till,Renaud Touraine,Annick Toutain,Michel Vekemans,Arnold Münnich,Stanislas Lyonnet	79
16	IMAGe, a New Clinical Association of Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 1999 ·The Journal of Clinical Endocrinology & Metabolism ·Éric Vilain,Martine Le Merrer,C Lecointre,F Desangles,Mark A. Kay,P Maroteaux,Edward R.B. McCabe	78
17	Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification 1998 ·Mechanisms of Development ·Anne‐Lise Delezoide,Catherine Benoist-Lasselin,Laurence Legeai‐Mallet,Martine Le Merrer,Arnold Münnich,Michel Vekemans,Jacky Bonaventure	143
18	Syndromal and nonsyndromal primary trigonocephaly: Analysis of a series of 237 patients 1998 ·American Journal of Medical Genetics ·Elizabeth Lajeunie,Martine Le Merrer,Daniel Marchac,Dominique Rénier	134
19	Genetic study of nonsyndromic coronal craniosynostosis 1995 ·American Journal of Medical Genetics ·Elizabeth Lajeunie,Martine Le Merrer,Catherine Bonaïti‐Pellié,Daniel Marchac,Dominique Rénier	269
20	Metaphyseal acroscyphodysplasia 1991 ·Clinical Genetics ·Alain Verloès,Martine Le Merrer,J. P. Farriaux,P Maroteaux	10

About Martine Le Merrer

Martine Le Merrer is a scholar working on Genetics, Developmental Biology and Rheumatology, having authored 130 papers that have together received 7.9k indexed citations. Recurring topics across this work include Connective tissue disorders research (43 papers), Bone health and treatments (15 papers) and Cleft Lip and Palate Research (14 papers). The work is most often cited by research in Genetics (4.0k citations), Molecular Biology (4.6k citations) and Rheumatology (952 citations). Martine Le Merrer has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Arnold Münnich, Valérie Cormier‐Daire, Dominique Rénier, Stanislas Lyonnet, Geneviève Baujat, Elizabeth Lajeunie, Daniel Marchac, Annachiara De Sandre‐Giovannoli, Nicolas Lévy and Rafaëlle Bernard. Their work appears in journals such as Science, Nature Genetics and Blood.

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.

Explore authors with similar magnitude of impact