B. Le Marec

1.4k total citations
67 papers, 1.0k citations indexed

About

B. Le Marec is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, B. Le Marec has authored 67 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Genetics, 13 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in B. Le Marec's work include Connective tissue disorders research (6 papers), Hedgehog Signaling Pathway Studies (6 papers) and Genomics and Rare Diseases (5 papers). B. Le Marec is often cited by papers focused on Connective tissue disorders research (6 papers), Hedgehog Signaling Pathway Studies (6 papers) and Genomics and Rare Diseases (5 papers). B. Le Marec collaborates with scholars based in France, Belgium and United States. B. Le Marec's co-authors include Sylvie Odent, Hubert Journel, Martine Blayau, M. Roussey, Véronique David, P Maroteaux, M. K. Simon, M Bourel, A Munnich and J. Y. Le Gall and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Human Reproduction.

In The Last Decade

B. Le Marec

66 papers receiving 967 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
B. Le Marec France	19	506	474	150	115	88	67	1.0k
J. Spranger Germany	19	407 0.8×	508 1.1×	93 0.6×	103 0.9×	61 0.7×	55	930
E. Gandini Italy	18	419 0.8×	287 0.6×	100 0.7×	125 1.1×	47 0.5×	62	1.0k
C McKeown United Kingdom	13	735 1.5×	551 1.2×	129 0.9×	168 1.5×	59 0.7×	25	1.3k
James V. Higgins United States	18	332 0.7×	414 0.9×	182 1.2×	241 2.1×	65 0.7×	39	927
Ann Haskins Olney United States	19	842 1.7×	716 1.5×	214 1.4×	169 1.5×	93 1.1×	43	1.4k
R. Sid Wilroy United States	21	635 1.3×	778 1.6×	275 1.8×	166 1.4×	61 0.7×	53	1.3k
Brad Angle United States	18	444 0.9×	527 1.1×	117 0.8×	191 1.7×	43 0.5×	33	1000
M Shohat Israel	15	329 0.7×	387 0.8×	134 0.9×	88 0.8×	35 0.4×	29	911
Georg Klaus Hinkel Germany	17	498 1.0×	528 1.1×	107 0.7×	90 0.8×	59 0.7×	41	933
Pamela S. Karnes United States	17	430 0.8×	199 0.4×	89 0.6×	200 1.7×	105 1.2×	29	992

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-authorship network of co-authors of B. Le Marec

This figure shows the co-authorship network connecting the top 25 collaborators of B. Le Marec. A scholar is included among the top collaborators of B. Le Marec 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 B. Le Marec. B. Le Marec 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

Odent, Sylvie, et al.. (2001). Prader–Willi syndrome and polygonosomal abnormalities in males:about a Prader–Willi/47,XYY patient. Annales de Génétique. 44(1). 1–3. 3 indexed citations

Pasquier, Laurent, Christèle Dubourg, Martine Blayau, et al.. (2000). A new mutation in the six-domain of SIX3 gene causes holoprosencephaly. European Journal of Human Genetics. 8(10). 797–800. 52 indexed citations

Odent, Sylvie, Tania Attié‐Bitach, Martine Blayau, et al.. (1999). Expression of the Sonic hedgehog (SHH) Gene during Early Human Development and Phenotypic Expression of New Mutations Causing Holoprosencephaly. Human Molecular Genetics. 8(9). 1683–1689. 123 indexed citations

Rouillac, Christelle, Dominique Marchant, Lucien Bachner, et al.. (1998). Mapping of a Congenital Microcoria Locus to 13q31-q32. The American Journal of Human Genetics. 62(5). 1117–1122. 15 indexed citations

Férec, Claude, C. Verlingue, Philippe Parent, et al.. (1995). Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses. Human Genetics. 96(5). 542–548. 32 indexed citations

Poulain, Patrice, et al.. (1994). Remarks about the prognosis in case of antenatal diagnosis of gastroschisis. European Journal of Obstetrics & Gynecology and Reproductive Biology. 54(3). 185–190. 9 indexed citations

Oriot, Denis, P. Bétrémieux, Nicole Baumann, C Lefrançois, & B. Le Marec. (1992). CSF ascorbic acid and lactate levels after neonatal asphyxia: preliminary results. Acta Paediatrica. 81(10). 845–846. 8 indexed citations

Caillaud, Catherine, Françoise Rey, Philippe Labrune, et al.. (1991). Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus. Human Genetics. 86(4). 355–358. 25 indexed citations

Biancalana, Valérie, et al.. (1991). Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28. Human Genetics. 88(2). 228–230. 23 indexed citations

10.

Marec, B. Le, et al.. (1988). L'Alsace dans la guerre, 1939-1945. 3 indexed citations

11.

Roussey, M., et al.. (1988). Nephrotic Syndrome in a Child with Cystic Fibrosis. Acta Paediatrica. 77(6). 920–921. 3 indexed citations

12.

Sefiani, A., M Guilloud-Bataille, S. Heuertz, et al.. (1988). Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosome. Human Genetics. 81(1). 61–63. 29 indexed citations

13.

Marec, B. Le, et al.. (1988). [Oto-palato-digital type I syndrome in five generations. Relationship to the type II form].. PubMed. 31(3). 155–61. 7 indexed citations

14.

Blanchet‐Bardon, C, et al.. (1987). Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred. British Journal of Dermatology. 117(3). 363–370. 28 indexed citations

15.

Journel, Hubert, et al.. (1986). Manifestations oculaires de la trisomie 21. Etude de cinquante-trois cas et revue de la littérature.. 33(5). 3428–3433. 1 indexed citations

16.

Carsin, Anne‐Elie, Hubert Journel, M. Roussey, & B. Le Marec. (1986). [Incidence of occult lumbro-sacral spina bifida in parents of children with spina bifida (concerning 80 pairs of parents with affected children)].. PubMed. 34(3-4). 285–92. 2 indexed citations

17.

Journel, Hubert, et al.. (1986). [Evaluation of the incidence of anencephaly and spina bifida in Brittany (1975-1984)].. PubMed. 34(6). 373–81. 1 indexed citations

18.

Marec, B. Le, et al.. (1984). [Colobomatous microphthalmos with cyst and 4 P- syndrome].. PubMed. 84(1). 67–8. 1 indexed citations

19.

Marec, B. Le, et al.. (1981). Cancer de la thyroïde à stroma amyloïde, syndrome de Sipple, mégacolon congénital avec hyperplasie des plexus: une seule et même affection autosomique dominante à pénetrance complète.. 28(5). 4 indexed citations

20.

Deshaies, Yves, et al.. (1979). [Recessive microencephaly linked to the X chromosome].. PubMed. 27(3). 221–36. 2 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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