Eva Pipiras

1.9k total citations
26 papers, 744 citations indexed

About

Eva Pipiras is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eva Pipiras has authored 26 papers receiving a total of 744 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 11 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eva Pipiras's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Eva Pipiras is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Eva Pipiras collaborates with scholars based in France, United Kingdom and United States. Eva Pipiras's co-authors include Franck Toledo, Arnaud Coquelle, Michelle Debatisse, Gérard Buttin, Brigitte Benzacken, Céline Dupont, Alain Verloès, Andrée Delahaye‐Duriez, Anne‐Claude Tabet and Séverine Drunat and has published in prestigious journals such as Cell, The EMBO Journal and Neurology.

In The Last Decade

Eva Pipiras

26 papers receiving 675 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Pipiras France 15 475 424 110 86 80 26 744
Susanne Morlot Germany 17 631 1.3× 399 0.9× 85 0.8× 82 1.0× 69 0.9× 35 960
Ute Grasshoff Germany 12 463 1.0× 477 1.1× 91 0.8× 100 1.2× 27 0.3× 29 791
Jiong Yan United States 15 650 1.4× 487 1.1× 94 0.9× 35 0.4× 56 0.7× 27 1.0k
Pamela Magini Italy 16 347 0.7× 349 0.8× 47 0.4× 53 0.6× 119 1.5× 38 717
Silvestre Oltra Spain 20 626 1.3× 478 1.1× 75 0.7× 109 1.3× 185 2.3× 69 1.1k
Daniela Orteschi Italy 19 467 1.0× 597 1.4× 58 0.5× 101 1.2× 49 0.6× 37 917
Gotthold Barbi Germany 17 560 1.2× 632 1.5× 127 1.2× 188 2.2× 58 0.7× 59 1.1k
David B. Everman United States 20 657 1.4× 466 1.1× 41 0.4× 146 1.7× 51 0.6× 39 1.1k
Karen Buysse Belgium 15 456 1.0× 633 1.5× 75 0.7× 169 2.0× 66 0.8× 19 959
Alex Magee United Kingdom 12 507 1.1× 537 1.3× 39 0.4× 56 0.7× 30 0.4× 20 913

Countries citing papers authored by Eva Pipiras

Since Specialization
Citations

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

Fields of papers citing papers by Eva Pipiras

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Pipiras

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Pipiras. A scholar is included among the top collaborators of Eva Pipiras 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 Eva Pipiras. Eva Pipiras 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.
Cuisset, Laurence, Sarah Grotto, Corinne Fouveaut, et al.. (2023). Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene. American Journal of Medical Genetics Part A. 194(4). e63479–e63479. 2 indexed citations
2.
Aloui, Chaker, Stéphanie Guey, Eva Pipiras, et al.. (2020). Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome. Journal of Medical Genetics. 57(5). 339–346. 9 indexed citations
3.
Larcher, Lise, Julien Buratti, Brigitte Benzacken, et al.. (2019). New evidence that biallelic loss of function in EEF1B2 gene leads to intellectual disability. Clinical Genetics. 97(4). 639–643. 7 indexed citations
4.
Lévy, Jonathan, Damien Haye, Nicola Marziliano, et al.. (2018). EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder. Clinical Genetics. 93(6). 1141–1147. 19 indexed citations
5.
Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations
6.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
7.
Delahaye‐Duriez, Andrée, Suonavy Khung‐Savatovsky, Azzedine Aboura, et al.. (2012). Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. American Journal of Medical Genetics Part A. 158A(10). 2430–2438. 37 indexed citations
8.
Bitoun, Pierre, Eva Pipiras, & Florence Rigaudière. (2011). Congenital Macular Dystrophy, Corpus Callosum Agenesis, Hippocampi Hypoplasia – A Novel Neuro-Ophthalmic Syndrome: Case Report. Ophthalmic Genetics. 33(1). 39–43. 2 indexed citations
9.
Tabet, Anne‐Claude, Azzedine Aboura, Marion Gérard, et al.. (2010). Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis. American Journal of Medical Genetics Part A. 152A(7). 1781–1788. 20 indexed citations
10.
Toutain, Annick, Céline Dupont, Anne Claude Tabet, et al.. (2009). Chromosome 22q13.3 deletion syndrome with a de novo interstitial 22q13.3 cryptic deletion disrupting SHANK3. European Journal of Medical Genetics. 52(5). 328–332. 41 indexed citations
11.
Aboura, Azzedine, Eva Pipiras, Lionel Carbillon, et al.. (2007). Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype. Prenatal Diagnosis. 27(3). 279–284. 3 indexed citations
12.
Pipiras, Eva, Cyril Touboul, Férechté Encha‐Razavi, et al.. (2007). De novo Subtelomeric Deletion Additional to an Inherited Apparently Balanced Reciprocal Translocation. Fetal Diagnosis and Therapy. 22(4). 306–312. 3 indexed citations
13.
Delahaye‐Duriez, Andrée, Eva Pipiras, Moncef Benkhalifa, et al.. (2006). Retrospective Diagnosis of Pallister-Killian Syndrome by CGH Array. Fetal Diagnosis and Therapy. 21(6). 485–488. 6 indexed citations
14.
Cohen, David, A. J. C. Wilson, Jean-Marc Guilé, et al.. (2006). Brief Report: Visual-Spatial Deficit in a 16-year-old Girl with Maternally Derived Duplication of Proximal 15q. Journal of Autism and Developmental Disorders. 37(8). 1585–1591. 16 indexed citations
15.
16.
Chantot‐Bastaraud, Sandra, Eva Pipiras, Anne Roubergue, et al.. (2004). Clinical findings and cytogenetic analysis of small supernumerary ring chromosomes 7: report of two new cases. Annales de Génétique. 47(3). 241–249. 8 indexed citations
17.
Pipiras, Eva, Céline Dupont, Sandra Chantot‐Bastaraud, et al.. (2004). Structural chromosomal mosaicism and prenatal diagnosis. Prenatal Diagnosis. 24(2). 101–103. 15 indexed citations
18.
Dupont, Céline, Eva Pipiras, Sandra Chantot‐Bastaraud, et al.. (2003). CGH and direct diagnosis of mosaic structural chromosomal abnormalities: description of a mosaic ring chromosome 17 and review of the literature. European Journal of Human Genetics. 11(6). 452–456. 18 indexed citations
19.
20.
Coquelle, Arnaud, Eva Pipiras, Franck Toledo, Gérard Buttin, & Michelle Debatisse. (1997). Expression of Fragile Sites Triggers Intrachromosomal Mammalian Gene Amplification and Sets Boundaries to Early Amplicons. Cell. 89(2). 215–225. 330 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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