J. Lespinasse

783 total citations
25 papers, 310 citations indexed

About

J. Lespinasse is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science. According to data from OpenAlex, J. Lespinasse has authored 25 papers receiving a total of 310 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 9 papers in Pediatrics, Perinatology and Child Health and 8 papers in Plant Science. Recurrent topics in J. Lespinasse's work include Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (8 papers). J. Lespinasse is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (8 papers). J. Lespinasse collaborates with scholars based in France, United States and Switzerland. J. Lespinasse's co-authors include Christine Gicquel, M Robert, Yves Le Bouc, B Sèle, Sophie Rousseaux, Edith Chevret, J. Cozzi, Françoise Devillard, Michèle Monteil and R. Pelletier and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Epidemiology and Journal of Allergy and Clinical Immunology.

In The Last Decade

J. Lespinasse

21 papers receiving 273 citations

Peers

J. Lespinasse

GENET

PPCH

Yue-Qiu Tan China

Capucine Hyon France

Stéphane Serero France

Yi-Hui Lin Taiwan

Francisco Álvarez‐Nava Venezuela

M.R. Guichaoua France

Deepika Jaiswal India

Jennifer Eccles United States

Brenda McInnes Canada

R. Martin Canada

Yue-Qiu Tan China

J. Lespinasse

134 ×0.7

GENET

153 ×0.9

PPCH

42 ×0.4

60 ×0.9

29 ×0.7

Citations per year, relative to J. Lespinasse J. Lespinasse (= 1×) peers Yue-Qiu Tan

Countries citing papers authored by J. Lespinasse

Since Specialization

Citations

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

Fields of papers citing papers by J. Lespinasse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Lespinasse

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

Lespinasse, J., et al.. (2026). Stiripentol: Unpublished results from the first phase 2 clinical trial in Lennox–Gastaut syndrome conducted in the early 1990s. Epilepsia.

Diallo, Alpha Oumar, et al.. (2023). Malignant hypercalcemia revealing a diffuse large B‐cell lymphoma in a patient with a previous diagnosis of chronic myelomonocytic leukemia: An uncommon hematological coexistence. SHILAP Revista de lepidopterología. 11(9). e7885–e7885. 1 indexed citations

Lespinasse, J., Carole Dufouil, & Cécile Proust‐Lima. (2023). Disease progression model anchored around clinical diagnosis in longitudinal cohorts: example of Alzheimer’s disease and related dementia. BMC Medical Research Methodology. 23(1). 199–199.

Lespinasse, J., Geneviève Chêne, Jean‐François Mangin, et al.. (2022). Associations among hypertension, dementia biomarkers, and cognition: The MEMENTO cohort. Alzheimer s & Dementia. 19(6). 2332–2342. 9 indexed citations

Dugravot, Aline, J. Lespinasse, Richard L. Merrick, et al.. (2021). How Selection Over Time Contributes to the Inconsistency of the Association Between Sex/Gender and Cognitive Decline Across Cognitive Aging Cohorts. American Journal of Epidemiology. 191(3). 441–452. 9 indexed citations

Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations

Paoloni‐Giacobino, Ariane, Nicole Lemieux, Emmanuelle Lemyre, & J. Lespinasse. (2007). Specific language impairment as the prominent feature in a patient with a low‐level trisomy 21 mosaicism. Journal of Intellectual Disability Research. 51(5). 401–405. 4 indexed citations

Bhatt, Samarth, Kamran Moradkhani, Kristin Mrasek, et al.. (2007). Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Molecular Human Reproduction. 13(10). 751–756. 15 indexed citations

Bugge, Merete, Andrew Collins, Jens Michael Hertz, et al.. (2007). Non-disjunction of chromosome 13. Human Molecular Genetics. 16(16). 2004–2010. 43 indexed citations

10.

Moradkhani, Kamran, Jacques Puechberty, Samarth Bhatt, et al.. (2006). Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report. Human Reproduction. 21(12). 3193–3198. 26 indexed citations

11.

Lespinasse, J. & Gwenaël Nadeau. (2005). Apport de la génétique chromosomique moléculaire au diagnostic prénatal et périnatal des anomalies chromosomiques et des maladies géniques. La Presse Médicale. 34(17). 1257–1263.

12.

Lespinasse, J., et al.. (2004). Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases. Annales de Génétique. 47(3). 315–324. 11 indexed citations

13.

Lespinasse, J., Hervé Testard, Marianne Till, et al.. (2004). A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES). Annales de Génétique. 47(4). 405–417. 14 indexed citations

14.

Lespinasse, J., P. Hoffmann, Anthony Laugé, et al.. (2004). Chromosomal instability in two siblings with gonad deficiency: Case report. Human Reproduction. 20(1). 158–162. 18 indexed citations

15.

Lespinasse, J.. (2003). A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure. Human Reproduction. 18(10). 2058–2066. 21 indexed citations

16.

Paoloni‐Giacobino, Ariane, et al.. (2001). A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH. Annales de Génétique. 44(3). 117–119. 2 indexed citations

17.

Lespinasse, J., Christine Gicquel, M Robert, & Yves Le Bouc. (1998). Phenotypic and genotypic variability in monozygotic triplets with Turner syndrome. Clinical Genetics. 54(1). 56–59. 33 indexed citations

18.

Verschraegen-Spae, M.R., B Quack, Sophie Rousseaux, et al.. (1998). Application of fluorescence in situ hybridization to the identification of different marker chromosomes.. PubMed. 41(1). 5–10. 1 indexed citations

19.

Bouvier, R, et al.. (1998). Néphroblastomatose de présentation inhabituelle. Archives de Pédiatrie. 5(6). 627–632. 1 indexed citations

20.

Rousseaux, Sophie, Edith Chevret, Michèle Monteil, et al.. (1995). Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization. Cytogenetic and Genome Research. 71(3). 240–246. 54 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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