Marc Le Lorc’h

812 total citations
19 papers, 476 citations indexed

About

Marc Le Lorc’h is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Marc Le Lorc’h has authored 19 papers receiving a total of 476 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 7 papers in Molecular Biology. Recurrent topics in Marc Le Lorc’h's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (3 papers). Marc Le Lorc’h is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (3 papers). Marc Le Lorc’h collaborates with scholars based in France, Tunisia and Lebanon. Marc Le Lorc’h's co-authors include Serge Romana, Jean‐Thomas Vilquin, Alvine Bissery, Patrick Bruneval, Philippe Menasché, Albert Hagège, Sophie Brisset, Damien Sanlaville, Michel Vekemans and Saïd Ghostine and has published in prestigious journals such as JAMA, Journal of the American College of Cardiology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Marc Le Lorc’h

19 papers receiving 428 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marc Le Lorc’h France 12 183 171 168 137 101 19 476
Bogdan Yatsula United States 13 47 0.3× 193 1.1× 235 1.4× 77 0.6× 4 0.0× 20 618
Xiang-Xu Jia China 7 44 0.2× 124 0.7× 216 1.3× 105 0.8× 17 0.2× 12 441
Soula Danopoulos United States 15 82 0.4× 331 1.9× 396 2.4× 27 0.2× 22 0.2× 35 720
Shuang You China 11 52 0.3× 48 0.3× 183 1.1× 29 0.2× 12 0.1× 17 414
Luciana Cacciottola Belgium 14 47 0.3× 105 0.6× 200 1.2× 40 0.3× 46 0.5× 36 747
Christa N. Grant United States 13 39 0.2× 218 1.3× 95 0.6× 17 0.1× 24 0.2× 43 433
Olga Katsara United States 10 24 0.1× 63 0.4× 240 1.4× 102 0.7× 10 0.1× 19 388
Abinaya Nathan United States 8 46 0.3× 33 0.2× 271 1.6× 15 0.1× 124 1.2× 10 538
Pierfranco Pignatti Italy 10 74 0.4× 67 0.4× 65 0.4× 101 0.7× 29 0.3× 17 416
Hans‐Peter Hohn Germany 10 24 0.1× 48 0.3× 165 1.0× 63 0.5× 21 0.2× 11 381

Countries citing papers authored by Marc Le Lorc’h

Since Specialization
Citations

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

Fields of papers citing papers by Marc Le Lorc’h

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marc Le Lorc’h. 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 Marc Le Lorc’h. The network helps show where Marc Le Lorc’h may publish in the future.

Co-authorship network of co-authors of Marc Le Lorc’h

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

All Works

19 of 19 papers shown
1.
Malan, Valérie, L. Bussières, Norbert Winer, et al.. (2019). Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial. Obstetrical & Gynecological Survey. 74(1). 16–17. 3 indexed citations
2.
Malan, Valérie, L. Bussières, Norbert Winer, et al.. (2018). Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21. JAMA. 320(6). 557–557. 43 indexed citations
3.
Alberti, Adriana, Laurent Salomon, Marc Le Lorc’h, et al.. (2015). Non‐invasive prenatal testing for trisomy 21 based on analysis of cell‐free fetal DNA circulating in the maternal plasma. Prenatal Diagnosis. 35(5). 471–476. 14 indexed citations
4.
Mougou, Soumaya, et al.. (2013). Molecular and Phenotypic Characterization of Ring Chromosome 22 in Two Unrelated Patients. Cytogenetic and Genome Research. 140(1). 1–11. 19 indexed citations
5.
Frydman, René, Nelly Frydman, Julie Steffann, et al.. (2011). Diagnostic pré-implantatoire : dix ans d’expérience en région parisienne : impasse actuelle et solutions à venir. Bulletin de l Académie Nationale de Médecine. 195(4-5). 1005–1014. 2 indexed citations
6.
Labrune, Philippe, Sophie Brisset, Marc Le Lorc’h, et al.. (2009). Molecular cytogenetic characterization of a 4p15.1‐pter duplication and a 4q35.1‐qter deletion in a recombinant of chromosome 4 pericentric inversion. American Journal of Medical Genetics Part A. 149A(2). 226–231. 24 indexed citations
7.
Benjelloun, Fatine, Alexandrine Garrigue, Corinne Demerens, et al.. (2008). Stable and Functional Lymphoid Reconstitution in Artemis-deficient Mice Following Lentiviral Artemis Gene Transfer Into Hematopoietic Stem Cells. Molecular Therapy. 16(8). 1490–1499. 47 indexed citations
8.
Schluth‐Bolard, Caroline, Marianne Till, Audrey Labalme, et al.. (2008). Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterization. European Journal of Medical Genetics. 51(6). 622–630. 14 indexed citations
9.
Damaj, Léna, Marc Le Lorc’h, Virginie Verkarre, et al.. (2008). Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal Hyperinsulinism. The Journal of Clinical Endocrinology & Metabolism. 93(12). 4941–4947. 59 indexed citations
10.
Sanlaville, Damien, et al.. (2007). Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q. European Journal of Medical Genetics. 50(5). 379–385. 8 indexed citations
11.
Schluth‐Bolard, Caroline, Marianne Till, Audrey Labalme, et al.. (2007). TWIST microdeletion identified by array CGH in a patient presenting Saethre–Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7. European Journal of Medical Genetics. 51(2). 156–164. 16 indexed citations
12.
Brisset, Sophie, Marc Le Lorc’h, Valérie Poncet, et al.. (2006). Terminal 14q32.33 deletion: Genotype–phenotype correlation. American Journal of Medical Genetics Part A. 140A(21). 2324–2329. 22 indexed citations
13.
Ribes, Agnès, Kasra Azarnoush, Laurent Sabbah, et al.. (2005). Can Cold or Heat Shock Improve Skeletal Myoblast Engraftment in Infarcted Myocardium?. Transplantation. 80(5). 660–665. 53 indexed citations
14.
Agbulut, Onnik, Nawwar Al Attar, Jérôme Larghero, et al.. (2004). Comparison of human skeletal myoblasts and bone marrow-derived CD133+progenitors for the repair of infarcted myocardium. Journal of the American College of Cardiology. 44(2). 458–463. 108 indexed citations
15.
Sanlaville, Damien, Marc Le Lorc’h, M Prieur, et al.. (2004). [A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances].. PubMed. 62(2). 203–12. 9 indexed citations
16.
Gérard‐Blanluet, Marion, Serge Romana, Marc Le Lorc’h, et al.. (2004). Classical West “syndrome” phenotype with a subtelomeric 4p trisomy. American Journal of Medical Genetics Part A. 130A(3). 299–302. 10 indexed citations
17.
Sanlaville, Damien, Serge Romana, Jeanne Amiel, et al.. (2002). A CGH study of 27 patients with CHARGE association. Clinical Genetics. 61(2). 135–138. 21 indexed citations
18.
Romana, Serge, Philippe Gosset, Hatem Elghezal, et al.. (2001). [Value of molecular cytogenetics in pre- and postnatal diagnostic of chromosome abnormalities].. PubMed. 30(1 Suppl). 75–9. 2 indexed citations
19.
Frydman, R., et al.. (1993). Per-urethral transvesical first-trimester amniocentesis. European Journal of Obstetrics & Gynecology and Reproductive Biology. 48(2). 99–101. 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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