James Lespinasse

4.1k total citations
35 papers, 1.4k citations indexed

About

James Lespinasse is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, James Lespinasse has authored 35 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 18 papers in Molecular Biology and 6 papers in Plant Science. Recurrent topics in James Lespinasse's work include Genomic variations and chromosomal abnormalities (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). James Lespinasse is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). James Lespinasse collaborates with scholars based in France, Germany and Switzerland. James Lespinasse's co-authors include Marc Delpech, Catherine Dodé, Corinne Fouveaut, Vera M. Kalscheuer, Martine Raynaud, Arnaud Murat, Sławomir Wołczyński, Sylvain Briault, Alexandre Moerman and Luís Teixeira and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

James Lespinasse

34 papers receiving 1.3k citations

Peers

James Lespinasse
Renaud Touraine France
Palma Finelli Italy
Koji Muroya Japan
Julie Désir Belgium
Guntram Borck Germany
Anne Guiochon‐Mantel France
Dieter Kotzot Austria
Anne Camus France
Michelle L. Brinkmeier United States
Süleyman Gülsüner United States
Renaud Touraine France
James Lespinasse
Citations per year, relative to James Lespinasse James Lespinasse (= 1×) peers Renaud Touraine

Countries citing papers authored by James Lespinasse

Since Specialization
Citations

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

Fields of papers citing papers by James Lespinasse

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of James Lespinasse

This figure shows the co-authorship network connecting the top 25 collaborators of James Lespinasse. A scholar is included among the top collaborators of James 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 James Lespinasse. James Lespinasse 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.
Haghshenas, Sadegheh, Michael A. Levy, Raissa Relator, et al.. (2025). Identification of an episignature for the MEF2C-associated syndrome. European Journal of Human Genetics. 34(1). 53–60.
2.
Martinez, Guillaume, Françoise Devillard, Véronique Satre, et al.. (2018). Is sperm FISH analysis still useful for Robertsonian translocations? Meiotic analysis for 23 patients and review of the literature. Basic and Clinical Andrology. 28(1). 5–5. 9 indexed citations
3.
Piard, Juliette, James Lespinasse, Markéta Vlčková, et al.. (2018). Cutis laxa and excessive bone growth due to de novo mutations in PTDSS1. American Journal of Medical Genetics Part A. 176(3). 668–675. 9 indexed citations
4.
Lesca, Gaëtan, Marie‐Pierre Moizard, Gérald Bussy, et al.. (2013). Clinical and neurocognitive characterization of a family with a novel MED12 gene frameshift mutation. American Journal of Medical Genetics Part A. 161(12). 3063–3071. 30 indexed citations
5.
Besnard, Thomas, Christel Vaché, David Baux, et al.. (2011). Non-USH2A mutations in USH2 patients. Human Mutation. 33(3). 504–510. 51 indexed citations
6.
Devillard, Françoise, Vincent Guinchat, Daniel Moreno‐De‐Luca, et al.. (2010). Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. American Journal of Medical Genetics Part A. 152A(9). 2346–2354. 14 indexed citations
7.
Harbuz, Radu, James Lespinasse, Christine Francannet, et al.. (2010). Identification of new FOXP3 mutations and prenatal diagnosis of IPEX syndrome. Prenatal Diagnosis. 30(11). 1072–1078. 34 indexed citations
8.
Philibert, Pascal, Delphine Zénaty, E Thibaud, et al.. (2010). Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration. Reproductive Biology and Endocrinology. 8(1). 28–28. 61 indexed citations
9.
Jouk, Pierre‐Simon, Jean-Jacques Roux, Ariane Paoloni‐Giacobino, et al.. (2008). Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome. European Journal of Medical Genetics. 51(5). 472–478. 7 indexed citations
10.
Lespinasse, James, Stefania Gimelli, Frédérique Béna, et al.. (2008). Characterization of an interstitial deletion 6q13–q14.1 in a female with mild mental retardation, language delay and minor dysmorphisms. European Journal of Medical Genetics. 52(1). 49–52. 10 indexed citations
11.
Warcoin, Mathilde, James Lespinasse, Gilles Despouy, et al.. (2008). Fertility defects revealing germline biallelic nonsenseNBNmutations. Human Mutation. 30(3). 424–430. 18 indexed citations
12.
Bhatt, Samarth, Kamran Moradkhani, Kristin Mrasek, et al.. (2008). Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics. 17(1). 44–50. 14 indexed citations
13.
Gasparre, Giuseppe, Éric Hervouet, Marc Colombel, et al.. (2007). Clonal expansion of mutated mitochondrial DNA is associated with tumor formation and complex I deficiency in the benign renal oncocytoma. Human Molecular Genetics. 17(7). 986–995. 109 indexed citations
14.
Paoloni‐Giacobino, Ariane & James Lespinasse. (2006). Chromosome Y polysomy: a non-mosaic 49,XYYYY case. Clinical Dysmorphology. 16(1). 65–66. 7 indexed citations
15.
Lespinasse, James, et al.. (2004). De novo complex chromosomal rearrangements (CCR) involving chromosome 1, 5, and 6 resulting in microdeletion for 6q14 in a female carrier with psychotic disorder. American Journal of Medical Genetics Part A. 128A(2). 199–203. 11 indexed citations
16.
Andrieux, Joris, Sandra Fert‐Ferrer, Marie‐Christine Copin, et al.. (2003). Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32). Cancer Genetics and Cytogenetics. 145(1). 65–69. 9 indexed citations
17.
Vercherat, Cécile, James Lespinasse, Gilbert Lenoir, et al.. (2002). Germline mutation profile ofMEN1in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein. Human Mutation. 20(1). 35–47. 114 indexed citations
18.
Mircher, Clotilde, et al.. (2002). Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)). American Journal of Medical Genetics Part A. 118A(2). 176–179. 14 indexed citations
19.
Robain, Mathieu, Frédéric Davi, Richard Garand, et al.. (2001). A Multicentric Study of 41 Cases of B-Prolymphocytic Leukemia: Two Evolutive Forms: The Groupe Français d'Hématologie Cellulaire. Leukemia & lymphoma. 42(5). 981–987. 25 indexed citations
20.
Kirchhoff, Maria, Hanne Rose, Jan Maahr, et al.. (2000). High resolution comparative genomic hybridisation analysis reveals imbalances in dyschromosomal patients with normal or apparently balanced conventional karyotypes. European Journal of Human Genetics. 8(9). 661–668. 38 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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