Laurence Michel‐Calemard

1.6k total citations
22 papers, 438 citations indexed

About

Laurence Michel‐Calemard is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Laurence Michel‐Calemard has authored 22 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Surgery. Recurrent topics in Laurence Michel‐Calemard's work include Muscle Physiology and Disorders (4 papers), Renal and related cancers (4 papers) and Sexual Differentiation and Disorders (4 papers). Laurence Michel‐Calemard is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Renal and related cancers (4 papers) and Sexual Differentiation and Disorders (4 papers). Laurence Michel‐Calemard collaborates with scholars based in France, Tunisia and Monaco. Laurence Michel‐Calemard's co-authors include Yves Morel, M David, Patricia Bretones, Delphine Mallet, Frédérique Dijoud, Francis Jaubert, Nathalie Josso, Cécile Teinturier, Jean‐Louis Chaussain and Pierre Chatelain and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Kidney International and The International Journal of Biochemistry & Cell Biology.

In The Last Decade

Laurence Michel‐Calemard

21 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurence Michel‐Calemard France 9 325 295 76 57 53 22 438
C Lecointre France 10 336 1.0× 203 0.7× 58 0.8× 55 1.0× 119 2.2× 15 506
Ricardo Gracía Spain 11 277 0.9× 241 0.8× 39 0.5× 50 0.9× 8 0.2× 17 461
Monique A. de Vroede United States 10 482 1.5× 257 0.9× 67 0.9× 105 1.8× 42 0.8× 12 687
Yu Ding China 12 219 0.7× 170 0.6× 11 0.1× 35 0.6× 22 0.4× 38 359
Noriyuki Sugiyama Japan 12 531 1.6× 295 1.0× 21 0.3× 59 1.0× 118 2.2× 16 690
Lilia Baldazzi Italy 15 546 1.7× 280 0.9× 99 1.3× 43 0.8× 52 1.0× 28 669
Abdulsalam Abu‐Libdeh Israel 10 187 0.6× 115 0.4× 17 0.2× 66 1.2× 24 0.5× 25 338
José María Cantú Mexico 10 199 0.6× 129 0.4× 49 0.6× 56 1.0× 15 0.3× 17 377
Tossaporn Seeherunvong United States 7 131 0.4× 113 0.4× 29 0.4× 18 0.3× 40 0.8× 14 201
Shinichiro Sano Japan 12 254 0.8× 292 1.0× 18 0.2× 24 0.4× 32 0.6× 32 359

Countries citing papers authored by Laurence Michel‐Calemard

Since Specialization
Citations

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

Fields of papers citing papers by Laurence Michel‐Calemard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurence Michel‐Calemard. 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 Laurence Michel‐Calemard. The network helps show where Laurence Michel‐Calemard may publish in the future.

Co-authorship network of co-authors of Laurence Michel‐Calemard

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

All Works

20 of 20 papers shown
1.
Dorval, Guillaume, Gérald Le Gac, Vincent Morinière, et al.. (2024). Targeted RNAseq from patients’ urinary cells to validate pathogenic noncoding variants in autosomal dominant polycystic kidney disease genes: a proof of concept. Kidney International. 106(3). 532–535. 1 indexed citations
2.
Rendu, John, Laurence Michel‐Calemard, Rita Menassa, et al.. (2023). Muscular phenotype description of abnormal THOC2 splicing. Neuromuscular Disorders. 33(12). 978–982. 2 indexed citations
3.
Menassa, Rita, et al.. (2023). Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation.. PubMed. 42(4). 106–112. 1 indexed citations
4.
Pégat, Antoine, Nathalie Streichenberger, Nicolas Lacoste, et al.. (2022). Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report. Genes. 13(12). 2245–2245. 5 indexed citations
5.
Svahn, Juliette, Pascal Laforêt, Christophe Vial, et al.. (2019). Dilated cardiomyopathy and limb-girdle muscular dystrophy-dystroglycanopathy due to novel pathogenic variants in the DPM3 gene. Neuromuscular Disorders. 29(7). 497–502. 7 indexed citations
6.
Michel‐Calemard, Laurence, et al.. (2019). A novel disease-causing mutation in the Renin gene in a Tunisian family with autosomal dominant tubulointerstitial kidney disease. The International Journal of Biochemistry & Cell Biology. 117. 105625–105625.
7.
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Duval, Hélène, Laurence Michel‐Calemard, Marie Gonzalès, et al.. (2016). Fetal anomalies associated withHNF1Bmutations: report of 20 autopsy cases. Prenatal Diagnosis. 36(8). 744–751. 23 indexed citations
9.
Roucher‐Boulez, Florence, Rita Menassa, Nathalie Streichenberger, et al.. (2015). A splicing mutation in the DMD gene detected by next-generation sequencing and confirmed by mRNA and protein analysis. Clinica Chimica Acta. 448. 146–149. 5 indexed citations
10.
Denamur, Érick, Anne‐Lise Delezoide, Corinne Alberti, et al.. (2009). Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease. Kidney International. 77(4). 350–358. 55 indexed citations
11.
Pichon, Olivier, Antoine Hamel, Yves Héloury, et al.. (2009). Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9. American Journal of Medical Genetics Part A. 149A(6). 1183–1189. 50 indexed citations
12.
Schluth‐Bolard, Caroline, Damien Sanlaville, Audrey Labalme, et al.. (2009). Unexpected diagnosis of 45,X/47,XX,+18 mosaicism in a girl with mild phenotype. American Journal of Medical Genetics Part A. 149A(11). 2584–2587. 2 indexed citations
13.
Chardon, Laurence, et al.. (2008). Identification of two novel mutations and long-term follow-up in abetalipoproteinemia: a report of four cases. European Journal of Pediatrics. 168(8). 983–989. 22 indexed citations
14.
Massardier, Jérôme, et al.. (2008). Campomelic Dysplasia: Echographic Suspicion in the First Trimester of Pregnancy and Final Diagnosis of Two Cases. Fetal Diagnosis and Therapy. 24(4). 452–457. 8 indexed citations
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16.
Morel, Yves, Laurence Michel‐Calemard, & Delphine Mallet. (2005). Anomalies génétiques du récepteur aux androgènes et ambiguïté sexuelle avec fonction testiculaire normale à la naissance. Annales d Endocrinologie. 66(3). 217–224. 1 indexed citations
17.
Michel‐Calemard, Laurence, et al.. (2004). Campomelic acampomelic dysplasia presenting with increased nuchal translucency in the first trimester. Prenatal Diagnosis. 24(7). 519–523. 13 indexed citations
18.
Mallet, Delphine, Patricia Bretones, Laurence Michel‐Calemard, et al.. (2004). Gonadal Dysgenesis Without Adrenal Insufficiency in a 46, XY Patient Heterozygous for the Nonsense C16X Mutation: A Case of SF1 Haploinsufficiency. The Journal of Clinical Endocrinology & Metabolism. 89(10). 4829–4832. 83 indexed citations
19.
Morel, Yves, Rodolfo A. Rey, Cécile Teinturier, et al.. (2001). Aetiological diagnosis of male sex ambiguity: a collaborative study. European Journal of Pediatrics. 161(1). 49–59. 91 indexed citations
20.
Ruffion, A., et al.. (2000). Inhibition of growth and induction of apoptosis by androgens of a variant of LNCaP cell line. The Journal of Steroid Biochemistry and Molecular Biology. 73(5). 237–249. 43 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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