Sylvie Jaillard

3.5k total citations
54 papers, 802 citations indexed

About

Sylvie Jaillard is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Sylvie Jaillard has authored 54 papers receiving a total of 802 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 26 papers in Genetics and 13 papers in Reproductive Medicine. Recurrent topics in Sylvie Jaillard's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Reproductive Biology and Fertility (10 papers). Sylvie Jaillard is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Genomic variations and chromosomal abnormalities (11 papers) and Reproductive Biology and Fertility (10 papers). Sylvie Jaillard collaborates with scholars based in France, Australia and United States. Sylvie Jaillard's co-authors include Sylvie Odent, Christèle Dubourg, Célia Ravel, Laurent Pasquier, Marc‐Antoine Belaud‐Rotureau, Hubert Journel, Claude Bendavid, Thierry Frébourg, Véronique David and Pascale Saugier-Véber and has published in prestigious journals such as Human Reproduction, Fertility and Sterility and Biology of Reproduction.

In The Last Decade

Sylvie Jaillard

50 papers receiving 769 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sylvie Jaillard France 16 435 397 148 123 114 54 802
Michela Barbaro Sweden 22 885 2.0× 596 1.5× 139 0.9× 53 0.4× 81 0.7× 47 1.3k
Dilek Aktaş Türkiye 17 423 1.0× 455 1.1× 104 0.7× 60 0.5× 49 0.4× 68 873
Osman Demırhan Türkiye 14 222 0.5× 235 0.6× 139 0.9× 138 1.1× 40 0.4× 72 662
Jens Schuster Sweden 19 712 1.6× 247 0.6× 42 0.3× 117 1.0× 50 0.4× 49 1.1k
Julien Thévenon France 15 450 1.0× 474 1.2× 54 0.4× 91 0.7× 47 0.4× 51 798
Alina T. Midro Poland 16 436 1.0× 575 1.4× 244 1.6× 77 0.6× 57 0.5× 74 943
Roel Hordijk Netherlands 15 409 0.9× 520 1.3× 184 1.2× 23 0.2× 62 0.5× 22 739
Nico Ruf Germany 13 1.2k 2.7× 849 2.1× 352 2.4× 100 0.8× 42 0.4× 16 1.6k
Sandra Chantot‐Bastaraud France 24 759 1.7× 939 2.4× 404 2.7× 142 1.2× 304 2.7× 67 1.4k
Sophia Kitsiou‐Tzeli Greece 16 422 1.0× 407 1.0× 77 0.5× 29 0.2× 44 0.4× 39 656

Countries citing papers authored by Sylvie Jaillard

Since Specialization
Citations

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

Fields of papers citing papers by Sylvie Jaillard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sylvie Jaillard

This figure shows the co-authorship network connecting the top 25 collaborators of Sylvie Jaillard. A scholar is included among the top collaborators of Sylvie Jaillard 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 Sylvie Jaillard. Sylvie Jaillard 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.
Tucker, Elena J., Michael F. Sharp, Katrina M. Bell, et al.. (2024). Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency. Clinical Genetics. 106(3). 321–335. 2 indexed citations
2.
Dion, Ludivine, Karim Boudjéma, David Val‐Laillet, et al.. (2023). Hypothermic machine perfusion for uterus transplantation. Fertility and Sterility. 120(6). 1259–1261. 3 indexed citations
3.
Leclerc, Delphine, Sylvie Jaillard, Léna Damaj, et al.. (2023). Gene Editing Corrects In Vitro a G > A GLB1 Transition from a GM1 Gangliosidosis Patient. The CRISPR Journal. 6(1). 17–31. 2 indexed citations
4.
Leclerc, Delphine, Audrey Labalme, Pascale Bellaud, et al.. (2023). Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing. Genes. 14(2). 273–273. 1 indexed citations
5.
Leclerc, Delphine, et al.. (2022). The TALE never ends: A comprehensive overview of the role of PBX1, a TALE transcription factor, in human developmental defects. Human Mutation. 43(9). 1125–1148. 8 indexed citations
6.
Tucker, Elena J., Linda Akloul, Erika Launay, et al.. (2022). Pseudodicentric Chromosome Originating from an X-Autosome Translocation in a Male Patient with Cryptozoospermia. Cytogenetic and Genome Research. 162(3). 124–131. 1 indexed citations
7.
Lavillaureix, Alinoë, Philippe Loget, Erika Launay, et al.. (2022). Prenatal phenotype of 22q11 micro-duplications: A systematic review and report on 12 new cases. European Journal of Medical Genetics. 65(2). 104422–104422. 7 indexed citations
8.
Tucker, Elena J., Katrina M. Bell, Gorjana Robevska, et al.. (2021). Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes. European Journal of Human Genetics. 30(2). 219–228. 23 indexed citations
9.
Dion, Ludivine, Sylvie Jaillard, Krystel Nyangoh Timoh, et al.. (2020). The Landscape and Therapeutic Implications of Molecular Profiles in Epithelial Ovarian Cancer. Journal of Clinical Medicine. 9(7). 2239–2239. 23 indexed citations
10.
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
11.
Dion, Ludivine, et al.. (2020). Ovarian response to stimulation for fertility preservation in women with hematologic cancer. Journal of Gynecology Obstetrics and Human Reproduction. 50(5). 101925–101925. 5 indexed citations
12.
Tucker, Elena J., Erika Launay, Linda Akloul, et al.. (2019). Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia. Cytogenetic and Genome Research. 159(4). 201–207. 3 indexed citations
13.
Ravel, Célia, et al.. (2019). Autophagy is increased in cryptorchid testis resulting in abnormal spermatozoa. Asian Journal of Andrology. 21(6). 570–570. 36 indexed citations
14.
Dugay, Frédéric, Solène‐Florence Kammerer‐Jacquet, Sylvie Jaillard, et al.. (2019). Diagnosis of uncommon renal epithelial neoplasms: performances of fluorescence in situ hybridization. Human Pathology. 92. 81–90. 4 indexed citations
15.
Jaillard, Sylvie, Rajini Sreenivasan, Gorjana Robevska, et al.. (2019). Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility. Maturitas. 131. 78–86. 26 indexed citations
16.
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
17.
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
18.
Vauthier, Virginie, Sylvie Jaillard, Hubert Journel, et al.. (2012). Homozygous deletion of an 80 kb region comprising part of DNAJC6 and LEPR genes on chromosome 1P31.3 is associated with early onset obesity, mental retardation and epilepsy. Molecular Genetics and Metabolism. 106(3). 345–350. 36 indexed citations
19.
Meur, Nathalie Le, Muriel Holder‐Espinasse, Sylvie Jaillard, et al.. (2009). MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations. Journal of Medical Genetics. 47(1). 22–29. 150 indexed citations
20.
Bendavid, Claude, Lucie Rochard, Jonathan Séguin, et al.. (2009). Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: An updated map of candidate loci. Human Mutation. 30(8). 1175–1182. 35 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Michela Barbaro Breakdown of academic impact, for papers by Dilek Aktaş Breakdown of academic impact, for papers by Osman Demırhan Breakdown of academic impact, for papers by Jens Schuster Breakdown of academic impact, for papers by Julien Thévenon Breakdown of academic impact, for papers by Alina T. Midro Breakdown of academic impact, for papers by Roel Hordijk Breakdown of academic impact, for papers by Nico Ruf Breakdown of academic impact, for papers by Sandra Chantot‐Bastaraud Breakdown of academic impact, for papers by Sophia Kitsiou‐Tzeli
Rankless by CCL
2026