Annie Laquerrière

7.3k total citations · 1 hit paper
109 papers, 3.3k citations indexed

About

Annie Laquerrière is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Annie Laquerrière has authored 109 papers receiving a total of 3.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 26 papers in Pediatrics, Perinatology and Child Health and 15 papers in Genetics. Recurrent topics in Annie Laquerrière's work include Fetal and Pediatric Neurological Disorders (12 papers), Glioma Diagnosis and Treatment (10 papers) and Neonatal and fetal brain pathology (10 papers). Annie Laquerrière is often cited by papers focused on Fetal and Pediatric Neurological Disorders (12 papers), Glioma Diagnosis and Treatment (10 papers) and Neonatal and fetal brain pathology (10 papers). Annie Laquerrière collaborates with scholars based in France, United States and Belgium. Annie Laquerrière's co-authors include Stéphane Marret, Thierry Frébourg, Dominique Campion, Pascale Marcorelles, Didier Hannequin, Anne Rovelet‐Lecrux, Alexis Brice, Anne Vital, Martine Vercelletto and Nathalie Le Meur and has published in prestigious journals such as Nature Genetics, Blood and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Annie Laquerrière

108 papers receiving 3.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

2005 871 citations Didier Hannequin, Annie Laquerrière et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Annie Laquerrière France	32	1.4k	842	584	564	502	109	3.3k
Teresa L. Wood United States	44	2.5k 1.8×	404 0.5×	798 1.4×	422 0.7×	657 1.3×	113	5.1k
Ni‐Chung Lee Taiwan	33	1.7k 1.2×	1.8k 2.1×	798 1.4×	373 0.7×	274 0.5×	218	4.3k
Pascale Cervera France	26	1.4k 1.0×	1.1k 1.3×	285 0.5×	229 0.4×	358 0.7×	69	3.8k
Linda De Meırleır Belgium	33	2.2k 1.6×	783 0.9×	337 0.6×	254 0.5×	345 0.7×	121	3.7k
Annick Raas‐Rothschild Israel	34	1.7k 1.2×	982 1.2×	898 1.5×	197 0.3×	262 0.5×	108	3.8k
I.F.M. de Coo Netherlands	45	4.4k 3.2×	505 0.6×	914 1.6×	493 0.9×	600 1.2×	159	6.1k
Omolara O. Ogunshola Switzerland	28	1.1k 0.8×	462 0.5×	259 0.4×	182 0.3×	361 0.7×	55	2.8k
Nobuyuki Murakami Japan	27	1.2k 0.8×	501 0.6×	628 1.1×	250 0.4×	266 0.5×	112	2.8k
Hubert J.M. Smeets Netherlands	38	3.0k 2.1×	331 0.4×	581 1.0×	335 0.6×	617 1.2×	133	4.6k
Gunnar Buyse Belgium	28	2.2k 1.6×	283 0.3×	359 0.6×	292 0.5×	643 1.3×	89	3.2k

Countries citing papers authored by Annie Laquerrière

Since Specialization

Citations

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

Fields of papers citing papers by Annie Laquerrière

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annie Laquerrière

This figure shows the co-authorship network connecting the top 25 collaborators of Annie Laquerrière. A scholar is included among the top collaborators of Annie Laquerrière 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 Annie Laquerrière. Annie Laquerrière 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

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.

Derambure, Céline, Carole Brasse‐Lagnel, Philippe Leroux, et al.. (2023). Prenatal Alcohol Exposure Impairs the Placenta–Cortex Transcriptomic Signature, Leading to Dysregulation of Angiogenic Pathways. International Journal of Molecular Sciences. 24(17). 13484–13484. 3 indexed citations

Burel, Delphine, Annie Laquerrière, Alexis Lebon, et al.. (2023). In UteroAlcohol Exposure Impairs Retinal Angiogenesis and the Microvessel-Associated Positioning of Calretinin Interneurons. eNeuro. 10(4). ENEURO.0295–22.2022. 1 indexed citations

Capri, Yline, Céline Dupont, Fabien Guimiot, et al.. (2023). DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy. Clinical Genetics. 104(5). 587–592. 2 indexed citations

Charbit‐Henrion, Fabienne, et al.. (2022). Tubulin mutations in human neurodevelopmental disorders. Seminars in Cell and Developmental Biology. 137. 87–95. 23 indexed citations

Gilard, Vianney, Florent Marguet, Maxime Fontanilles, et al.. (2021). Integrative Metabolomics Reveals Deep Tissue and Systemic Metabolic Remodeling in Glioblastoma. Cancers. 13(20). 5157–5157. 14 indexed citations

Gilard, Vianney, Abdellah Tebani, Ivana Dabaj, et al.. (2021). Diagnosis and Management of Glioblastoma: A Comprehensive Perspective. Journal of Personalized Medicine. 11(4). 258–258. 45 indexed citations

Joncour, Vadim Le, Pierre‐Olivier Guichet, Laurence Desrues, et al.. (2021). Targeting the Urotensin II/UT G Protein-Coupled Receptor to Counteract Angiogenesis and Mesenchymal Hypoxia/Necrosis in Glioblastoma. Frontiers in Cell and Developmental Biology. 9. 652544–652544. 9 indexed citations

Marguet, Florent, Annie Laquerrière, Stéphane Marret, et al.. (2019). A new optimization strategy for MALDI FTICR MS tissue analysis for untargeted metabolomics using experimental design and data modeling. Analytical and Bioanalytical Chemistry. 411(17). 3891–3903. 12 indexed citations

10.

Marguet, Florent, John Rendu, Catherine Vanhulle, et al.. (2019). Association of fingerprint bodies with rods in a case with mutations in the LMOD3 gene. Neuromuscular Disorders. 30(3). 207–212. 6 indexed citations

11.

Marguet, Florent, Ludivine Beaussire, Christophe Peillon, et al.. (2019). TERTp Mutation Detection in Plasma by Droplet-Digital Polymerase Chain Reaction in Spinal Myxopapillary Ependymoma with Lung Metastases. World Neurosurgery. 130. 405–409. 9 indexed citations

12.

Saugier-Véber, Pascale, Florent Marguet, François Lecoquierre, et al.. (2017). Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene. Acta Neuropathologica Communications. 5(1). 36–36. 23 indexed citations

13.

Tauziède‐Espariat, Arnault, Julien Masliah‐Planchon, Laurence Brugières, et al.. (2017). Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor. European Journal of Human Genetics. 25(10). 1170–1172. 8 indexed citations

14.

Crahès, Marie, Homa Adle‐Biassette, Martine Bucourt, et al.. (2016). Phenotypic and Neuropathological Characterization of Fetal Pyruvate Dehydrogenase Deficiency. Journal of Neuropathology & Experimental Neurology. 75(3). 227–238. 25 indexed citations

15.

Nolent, Flora, Jérôme Maluenda, Fabienne Giuliano, et al.. (2015). Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis. The American Journal of Human Genetics. 97(4). 616–620. 48 indexed citations

16.

Marguet, Florent, F. Proust, Marie Crahès, et al.. (2014). Le méningiome malin avec métaplasie adénocarcinomateuse : une entité rare à ne pas méconnaître. Annales de Pathologie. 34(3). 223–227. 4 indexed citations

17.

Jurici, Snejana, Annie Laquerrière, Anne‐Laure Bédat‐Millet, et al.. (2011). An Autopsy Case of Amyotrophic Lateral Sclerosis with Waldenström Macroglobulinemia and Anti-MAG Gammopathy. Case Reports in Neurology. 3(3). 294–300. 4 indexed citations

18.

Laquerrière, Annie. (2010). Mise en place des voies de la douleur chez le fœtus. 12(2). 111–115. 1 indexed citations

19.

Derrey, Stéphane, F. Proust, Bertrand Debono, et al.. (2004). Association between Cowden syndrome and Lhermitte-Duclos disease. Surgical Neurology. 61(5). 447–454. 33 indexed citations

20.

Diguet, A., Annie Laquerrière, D. Eurin, et al.. (2002). Fetal capillary haemangioblastoma: an exceptional tumour. A review of the literature. Prenatal Diagnosis. 22(11). 979–983. 9 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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