Laurent Pasquier

8.3k total citations
72 papers, 2.0k citations indexed

About

Laurent Pasquier is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laurent Pasquier has authored 72 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 38 papers in Molecular Biology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laurent Pasquier's work include Genomic variations and chromosomal abnormalities (18 papers), Hedgehog Signaling Pathway Studies (16 papers) and Prenatal Screening and Diagnostics (11 papers). Laurent Pasquier is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Hedgehog Signaling Pathway Studies (16 papers) and Prenatal Screening and Diagnostics (11 papers). Laurent Pasquier collaborates with scholars based in France, Australia and United Kingdom. Laurent Pasquier's co-authors include Sylvie Odent, Christèle Dubourg, Claude Bendavid, Cathérine Henry, Véronique David, Véronique David, Sylvie Odent, Daniel Guerrier, Isabelle Pellerin and Philippe Loget and has published in prestigious journals such as Brain, International Journal of Molecular Sciences and European Journal of Operational Research.

In The Last Decade

Laurent Pasquier

67 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurent Pasquier France 28 1.2k 1.1k 502 183 162 72 2.0k
Robert‐Jan H. Galjaard Netherlands 22 859 0.7× 1.2k 1.1× 1.0k 2.1× 111 0.6× 57 0.4× 65 2.2k
Sylvie Odent France 36 2.7k 2.3× 1.5k 1.4× 562 1.1× 333 1.8× 115 0.7× 152 3.8k
Uppala Radhakrishna United States 25 1.0k 0.9× 758 0.7× 174 0.3× 252 1.4× 36 0.2× 81 2.1k
Svetlana A. Yatsenko United States 26 1.5k 1.3× 1.8k 1.7× 628 1.3× 106 0.6× 135 0.8× 110 3.0k
Arie van Haeringen Netherlands 26 1.9k 1.6× 1.3k 1.2× 296 0.6× 154 0.8× 34 0.2× 69 3.0k
Jean‐Pierre Fryns Belgium 21 1.2k 1.0× 909 0.8× 202 0.4× 206 1.1× 30 0.2× 25 2.0k
Lucy R. Osborne Canada 32 1.3k 1.1× 931 0.9× 136 0.3× 163 0.9× 88 0.5× 69 3.1k
Palma Finelli Italy 29 1.2k 1.0× 1.0k 1.0× 211 0.4× 139 0.8× 16 0.1× 95 2.2k
Ian A. Glass United States 36 2.9k 2.4× 2.1k 1.9× 1.1k 2.3× 323 1.8× 61 0.4× 122 4.4k
Hutton M. Kearney United States 21 1.1k 0.9× 2.2k 2.0× 1.0k 2.1× 175 1.0× 27 0.2× 40 3.2k

Countries citing papers authored by Laurent Pasquier

Since Specialization
Citations

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

Fields of papers citing papers by Laurent Pasquier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurent Pasquier. 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 Laurent Pasquier. The network helps show where Laurent Pasquier may publish in the future.

Co-authorship network of co-authors of Laurent Pasquier

This figure shows the co-authorship network connecting the top 25 collaborators of Laurent Pasquier. A scholar is included among the top collaborators of Laurent Pasquier 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 Laurent Pasquier. Laurent Pasquier 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.
Dion, Ludivine, Maud Bidet, Chloé Quēlin, et al.. (2024). Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility. Acta Obstetricia Et Gynecologica Scandinavica. 104(3). 514–521.
2.
Quēlin, Chloé, Laurent Pasquier, Philippe Loget, et al.. (2023). PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect. European Journal of Medical Genetics. 66(11). 104852–104852.
3.
Pasquier, Laurent, et al.. (2023). Attitudes of professional stakeholders towards implementation of reproductive genetic carrier screening: a systematic review. European Journal of Human Genetics. 31(4). 395–408. 1 indexed citations
4.
Borry, Pascal, et al.. (2022). Informing relatives of their genetic risk: an examination of the Belgian legal context. European Journal of Human Genetics. 30(7). 766–771. 11 indexed citations
5.
6.
Schaefer, Élise, Christèle Dubourg, Wilfrid Carré, et al.. (2021). Skraban‐Deardorff syndrome: Six new cases of WDR 26 ‐related disease and expansion of the clinical phenotype. Clinical Genetics. 99(5). 732–739. 4 indexed citations
7.
Fradin, Mélanie, Alinoë Lavillaureix, Sylvie Jaillard, et al.. (2020). ATP7A mutation with occipital horns and distal motor neuropathy: A continuum. European Journal of Medical Genetics. 63(12). 104087–104087. 8 indexed citations
8.
Quēlin, Chloé, Philippe Loget, Lucile Boutaud, et al.. (2018). Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis. American Journal of Medical Genetics Part A. 176(7). 1610–1613. 11 indexed citations
9.
Chassaing, Nicolas, Erica E. Davis, Véronique David, et al.. (2016). Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network. Genome Research. 26(4). 474–485. 36 indexed citations
10.
Pasquier, Laurent, Mélanie Fradin, Dominique Martin‐Coignard, et al.. (2015). Karyotype is not dead (yet)!. European Journal of Medical Genetics. 59(1). 11–15. 31 indexed citations
11.
Habib, Walid Abi, Salah Azzi, Frédéric Brioude, et al.. (2014). Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome. Human Molecular Genetics. 23(21). 5763–5773. 51 indexed citations
12.
Jaillard, Sylvie, Anu Bashamboo, Laurent Pasquier, et al.. (2014). Gene dosage effects in 46, XY DSD: usefulness of CGH technologies for diagnosis. Journal of Assisted Reproduction and Genetics. 32(2). 287–291. 6 indexed citations
13.
Petit, Florence, Joris Andrieux, Geneviève Baujat, et al.. (2013). Split hand/foot malformation with long‐bone deficiency and BHLHA9 duplication: report of 13 new families. Clinical Genetics. 85(5). 464–469. 17 indexed citations
14.
Morcel, Karine, Tanguy Watrin, Laurent Pasquier, et al.. (2011). Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci. Orphanet Journal of Rare Diseases. 6(1). 9–9. 42 indexed citations
15.
Philippe, Christophe, Laurent Villard, Nicolás de Roux, et al.. (2005). Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update. European Journal of Medical Genetics. 49(1). 9–18. 57 indexed citations
16.
Pasquier, Laurent. (2005). Wide clinical variability among 13 new Cockayne syndrome cases confirmed by biochemical assays. Archives of Disease in Childhood. 91(2). 178–182. 31 indexed citations
17.
18.
19.
Bétrémieux, P., Alain Beuchée, Patrick Pladys, et al.. (2002). Perinatal management and outcome of prenatally diagnosed congenital diaphragmatic hernia: a 1995–2000 series in Rennes University Hospital. Prenatal Diagnosis. 22(11). 988–994. 27 indexed citations
20.
Salter–Cid, Luisa, Laurent Pasquier, & Martin F. Flajnik. (1996). RING3 is linked to the Xenopus major histocompatibility complex.. PubMed. 44(5). 397–9. 21 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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