Martine Le Merrer

15.8k citations

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

Genetics top 0.2%
- Connective tissue disorders research 43
- Cleft Lip and Palate Research 14
- Genetic Syndromes and Imprinting 12
- Craniofacial Disorders and Treatments 12
- Dermatological and Skeletal Disorders 8
Molecular Biology top 1%
Rheumatology top 1%
Developmental Biology top 2%
Immunology and Allergy top 2%
- Cell Adhesion Molecules Research 9
Oncology
- Bone health and treatments 15
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 8

Co-authors: Arnold Münnich Valérie Cormier‐Daire Dominique Rénier Stanislas Lyonnet Geneviève Baujat Elizabeth Lajeunie Daniel Marchac Annachiara De Sandre‐Giovannoli
Cited by: Genetics Molecular Biology Rheumatology
Journals: Science (1 paper)Nature Genetics (8 papers)Blood (1 paper)
Partner nations: France United States United Kingdom

In The Last Decade

Martine Le Merrer

126 papers receiving 7.7k citations

Hit Papers

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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

The 25 scholars most cited alongside Martine Le Merrer, 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 Martine Le Merrer Line = papers co-authored together Martine Le Merrer links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis Pediatric Radiology ·Massimiliano Rossi,Christine M Hall,Raymonde Bouvier,Sophie Collardeau‐Frachon,F. Le Breton,Martine Bucourt,Marie Pierre Cordier,Christine Vianey‐Saban,Giancarlo Parenti,Generoso Andria,Martine Le Merrer,Patrick Edery,Amaka C Offiah	2015	11
2	Fibrous dysplasia and McCune–Albright syndrome: Imaging for positive and differential diagnoses, prognosis, and follow-up guidelines European Journal of Radiology ·V. Bousson,Caroline Rey-Jouvin,Jean-Denis Larédo,Martine Le Merrer,N. Martin–Duverneuil,A. Feydy,Sébastien Aubert,Roland Chapurlat,Philippe Orcel	2014	31
3	Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia The American Journal of Human Genetics ·Céline Huber,Eissa Faqeih,Deborah Bartholdi,Christine Bôle‐Feysot,Zvi Borochowitz,Denise P. Cavalcanti,Amandine Frigo,Patrick Nitschké,J. Roume,Heloísa G. dos Santos,Stavit Shalev,Andrea Superti‐Furga,Anne‐Lise Delezoide,Martine Le Merrer,Arnold Münnich,Valérie Cormier‐Daire	2012	41
4	Progressive polyepiphyseal dysplasia with arthropathy: A distinct disorder from idiopathic juvenile arthritis and pseudorheumatoid dysplasia? American Journal of Medical Genetics Part A ·Bertrand Isidor,Sylvaine Poignant,G. Picherot,André Megabarne,Pierre Quartier,Brigitte Bader‐Meunier,Cédric Le Caignec,Martine Le Merrer,Geneviève Baujat,Valérie Cormier‐Daire,Albert David	2012	2
5	Clinical variability of familial tumoral calcinosis caused by novel GALNT3 mutations American Journal of Medical Genetics Part A ·Shoji Ichikawa,Geneviève Baujat,Aksel Seyahi,Anastasia G. Garoufali,Erik A. Imel,Leah R. Padgett,Anthony M. Austin,Andrea H. Sorenson,Zagorka Péjin,Vicken Topouchian,Pierre Quartier,Valérie Cormier‐Daire,M Déchaux,Fotini Malandrinou,P.N. Singhellakis,Martine Le Merrer,Michael J. Econs	2010	75
6	Jean Frézal et l'essor de la génétique médicale. médecine/sciences ·S Gilgenkrantz,Arnold Münnich,Marie‐Louise Briard,Martine Le Merrer,Josué Feingold,Jean-François Mattéi	2008	0
7	Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications 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	2008	82
8	Fibrodysplasia ossificans progressiva 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	2008	235
9	Ellis-Van Creveld syndrome Orphanet Journal of Rare Diseases ·Geneviève Baujat,Martine Le Merrer	2007	155
10	A new osteochondrodysplasia with severe osteopenia, preaxial polydactyly, clefting and dysmorphic features resembling filamin-related disorders Prenatal Diagnosis ·Marina Colombani,Nicole Laurent,Martine Le Merrer,Anne‐Lise Delezoide,Christel Thauvin‐Robinet,Frédéric Huet,P. Sagot,Stéphanie Couvreur,Thierry Rousseau,Stephen P. Robertson,Laurence Faivre	2006	2
11	Paradoxical NSD1 Mutations in Beckwith-Wiedemann Syndrome and 11p15 Anomalies in Sotos Syndrome 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	2004	88
12	Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome 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	2004	136
13	Recurrence of achondrogenesis type II within the same family: Evidence for germline mosaicism American Journal of Medical Genetics Part A ·Laurence Faivre,Martine Le Merrer,Serges Douvier,Nicole Laurent,Christel Thauvin‐Robinet,Thierry Rousseau,Inge Vereecke,P. Sagot,Anne‐Lise Delezoide,Paul Coucke,Geert Mortier	2003	13
14	Classification moléculaire des maladies osseuses constitutionnelles Valérie Cormier‐Daire,Martine Le Merrer	2001	1
15	Large-Scale Deletions and SMADIP1 Truncating Mutations in Syndromic Hirschsprung Disease with Involvement of Midline Structures 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	2001	79
16	IMAGe, a New Clinical Association of Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies The Journal of Clinical Endocrinology & Metabolism ·Éric Vilain,Martine Le Merrer,C Lecointre,F Desangles,Mark A. Kay,P Maroteaux,Edward R.B. McCabe	1999	78
17	Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification Mechanisms of Development ·Anne‐Lise Delezoide,Catherine Benoist-Lasselin,Laurence Legeai‐Mallet,Martine Le Merrer,Arnold Münnich,Michel Vekemans,Jacky Bonaventure	1998	143
18	Syndromal and nonsyndromal primary trigonocephaly: Analysis of a series of 237 patients American Journal of Medical Genetics ·Elizabeth Lajeunie,Martine Le Merrer,Daniel Marchac,Dominique Rénier	1998	134
19	Genetic study of nonsyndromic coronal craniosynostosis American Journal of Medical Genetics ·Elizabeth Lajeunie,Martine Le Merrer,Catherine Bonaïti‐Pellié,Daniel Marchac,Dominique Rénier	1995	269
20	Metaphyseal acroscyphodysplasia Clinical Genetics ·Alain Verloès,Martine Le Merrer,J. P. Farriaux,P Maroteaux	1991	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), Cleft Lip and Palate Research (14 papers), Genetic Syndromes and Imprinting (12 papers), Craniofacial Disorders and Treatments (12 papers), Cell Adhesion Molecules Research (9 papers), Prenatal Screening and Diagnostics (8 papers) and Dermatological and Skeletal Disorders (8 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.

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