B. Le Marec

1.4k citations

66 papers · 1.1k · h-index 19

Impact in

Genetics top 5%
- Connective tissue disorders research
- Cleft Lip and Palate Research
- Genetic and rare skin diseases.
- Genomic variations and chromosomal abnormalities
Developmental Biology top 10%

Papers in

Genetics 31
- Connective tissue disorders research 6
- Genomic variations and chromosomal abnormalities 5
- Genomics and Rare Diseases 5
- Ocular Disorders and Treatments 5
Molecular Biology 13
- Hedgehog Signaling Pathway Studies 6

Co-authors: Sylvie Odent (10 shared papers)Hubert Journel (15 shared papers)Martine Blayau (3 shared papers)M. Roussey (14 shared papers)Véronique David (2 shared papers)P Maroteaux (4 shared papers)M. K. Simon (1 shared paper)M Bourel (1 shared paper)
Journals: Human Genetics (6 papers)Human Molecular Genetics (3 papers)Clinical Genetics (3 papers)Acta Paediatrica (2 papers)Prenatal Diagnosis (2 papers)
Partner nations: France United States Belgium

In The Last Decade

B. Le Marec

65 papers receiving 1.0k citations

Peers

Countries citing papers authored by B. Le Marec

Since Specialization

Citations

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

Fields of papers citing papers by B. Le Marec

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

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#	Work
1	Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly Human Molecular Genetics ·Sylvie Odent, Tania Attié‐Bitach, Martine Blayau, M Mathieu, J. Augé, Anne‐Lise Delezoide, J. Y. Le Gall, B. Le Marec, A Munnich, Véronique David, Michel Vekemans	1999	131
2	Heredity of idiopathic haemochromatosis: A study of 106 families Clinical Genetics ·M. K. Simon, J. Alexandre, M Bourel, B. Le Marec, C Scordia	1977	82
3	Atelosteogenesis American Journal of Medical Genetics ·P Maroteaux, Jürgen W. Spranger, V. Stanescu, B. Le Marec, R. A. Pfeiffer, Peter Beighton, J. F. Mattei, John M. Opitz	1982	52
4	A new mutation in the six-domain of SIX3 gene causes holoprosencephaly European Journal of Human Genetics ·Laurent Pasquier, Christèle Dubourg, Martine Blayau, L. Lázaro, B. Le Marec, Véronique David, Sylvie Odent	2000	52
5	The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28 Human Molecular Genetics ·A. Smahl, Christel Hydén‐Granskog, Borut Peterlin, P. Vabres, S. Heuertz, M.C. Fulchlgnoni-Lataud, Niklas Dahl, Philippe Labrune, B. Le Marec, C Piussan, A. Taleb, H.von Koskul, M. C. Hors‐Cayla	1994	48
6	Central nervous system malformations and early end-stage renal disease in oro-facio-digital syndrome type I: A review American Journal of Medical Genetics ·Sylvie Odent, B. Le Marec, Annick Toutain, Albert David, Jacqueline Vigneron, Catherine Tr�guier, H�l�ne Jouan, Jo�lle Milon, Jean‐Pierre Fryns, Alain Verloès	1998	46
7	Segregation analysis in nonsyndromic holoprosencephaly American Journal of Medical Genetics ·Sylvie Odent, B. Le Marec, Arnold Münnich, Martine Le Merrer, Catherine Bona�ti-Pelli�	1998	42
8	Synapsis and synaptic adjustment in an infertile human male heterozygous for a pericentric inversion in chromosome 1 Human Genetics ·O. Gabriel-Robez, C. Ratomponirina, Y. Rumpler, B. Le Marec, J. M. Luciani, Marie-Roberte Guichaoua	1986	40
9	Genetics: Obstructive azoospermia with agenesis of vas deferens or with bronchiectasia (Young's syndrome): a genetic approach Human Reproduction ·D. Le Lannou, Pascal Jézéquel, Martine Blayau, I Dorval, Pierre Lemoine, A. Dabadie, M. Roussey, B. Le Marec, J.Y. Legall	1995	39
10	Opsismodysplasia: A new type of chondrodysplasia with predominant involvement of the bones of the hand and the vertebrae American Journal of Medical Genetics ·P Maroteaux, V. Stănescu, R Stănescu, B. Le Marec, Claude Moraine, Horacio Lejarraga	1984	38
11	De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy Human Genetics ·Jamel Chelly, F. Marlhens, B. Le Marec, Marc Jeanpierre, M. Lambert, G. Hamard, Bernard Dutrillaux, J.‐C. Kaplan	1986	37
12	Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses Human Genetics ·Claude Férec, C. Verlingue, Philippe Parent, Julie Morin, Jean-Pierre Codet, G. Rault, M. Dagorne, A. Lemoigne, Hubert Journel, M. Roussey, B. Le Marec, Michel Catheline, M.‐P. Audrézet, Bernard Mercier	1995	34
13	Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred British Journal of Dermatology ·C Blanchet‐Bardon, V. Nazzaro, J Chevrant‐Breton, Marc Espié, Pierre Kerbrat, B. Le Marec	1987	30
14	Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome Human Genetics ·S. Szpiro‐Tapia, A. Sefiani, M Guilloud-Bataille, S. Heuertz, B. Le Marec, J Frézal, P Maroteaux, M. C. Hors‐Cayla	1988	29
15	Magnetic resonance imaging in Pelizaeus-Merzbacher disease Neuroradiology ·Hubert Journel, M Roussey, Y. Gandon, Catherine Allaire, M. Carsin, B. Le Marec	1987	27
16	MCA/MR syndrome with oligodactyly and Möbius anomaly in first cousins: New syndrome or familial facial‐limb disruption sequence? American Journal of Medical Genetics ·Hubert Journel, M. Roussey, B. Le Marec	1989	26
17	Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus Human Genetics ·Monique Berthelon, Catherine Caillaud, Françoise Rey, Philippe Labrune, Dominique Melle, Josué Feingold, J Frézal, Marie‐Louise Briard, J. P. Farriaux, P Guibaud, Hubert Journel, B. Le Marec, Nicole Maurin, J L Nivelon, Henri Plauchu, Jean‐Marie Saudubray, Philippe Tron, Jean Rey, Arnold Münnich, Stanislas Lyonnet	1991	26
18	Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28 Human Genetics ·Valérie Biancalana, B. Le Marec, Sylvie Odent, J. A. M. J. van den Hurk, André Hanauer	1991	25
19	Prenatal diagnosis of familial tuberous sclerosis following detection of cardiac rhabdomyoma by ultrasound Prenatal Diagnosis ·Hubert Journel, M. Roussey, M. H. Plais, J Milon, C Almange, B. Le Marec	1986	23
20	Retinoblastoma, deletion 13q14, and esterase D: Application of gene dosage effect to prenatal diagnosis Cancer Genetics and Cytogenetics ·Claudine Junien, Suzy Despoisse, C Turleau, Henriette Nicolas, François Picard, B. Le Marec, Jean‐Claude Kaplan, J. de Grouchy	1982	18

About B. Le Marec

B. Le Marec is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Genetics, having authored 66 papers that have together received 1.1k indexed citations. Recurring topics across this work include Hedgehog Signaling Pathway Studies (6 papers), Connective tissue disorders research (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (5 papers), Ocular Disorders and Treatments (5 papers), Fetal and Pediatric Neurological Disorders (4 papers), Prenatal Screening and Diagnostics (4 papers) and Congenital limb and hand anomalies (4 papers). The work is most often cited by research in Genetics (493 citations), Developmental Biology (35 citations), Clinical Biochemistry (59 citations), Genetics (86 citations) and Molecular Biology (512 citations). B. Le Marec has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Sylvie Odent, Hubert Journel, Martine Blayau, M. Roussey, Véronique David, P Maroteaux, M. K. Simon, M Bourel, M Mathieu and Michel Vekemans. Their work appears in journals such as Human Genetics, Human Molecular Genetics, Clinical Genetics, Acta Paediatrica and Prenatal Diagnosis.

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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