Marion Gérard

5.0k total citations
29 papers, 837 citations indexed

About

Marion Gérard is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marion Gérard has authored 29 papers receiving a total of 837 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 15 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marion Gérard's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (4 papers). Marion Gérard is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Rare Diseases (4 papers). Marion Gérard collaborates with scholars based in France, Australia and United States. Marion Gérard's co-authors include H. Ogier de Baulny, Jean‐Marie Saudubray, J Zittoun, Alain Verloès, Laurence Faivre, Olivier Fain, Françoise Bonnet, Michel Longy, L. Laroche and F. Caux and has published in prestigious journals such as PLoS ONE, Biochemical and Biophysical Research Communications and Journal of Bone and Mineral Research.

In The Last Decade

Marion Gérard

28 papers receiving 799 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marion Gérard France 14 436 386 111 107 94 29 837
Pagon Ra United States 6 450 1.0× 260 0.7× 39 0.4× 55 0.5× 59 0.6× 291 791
Boris Keren France 21 649 1.5× 515 1.3× 61 0.5× 44 0.4× 49 0.5× 70 1.1k
Maja Hempel Germany 19 511 1.2× 342 0.9× 33 0.3× 58 0.5× 112 1.2× 58 855
Yaping Yang United States 16 322 0.7× 292 0.8× 35 0.3× 39 0.4× 76 0.8× 37 654
Angus Dobbie United Kingdom 12 402 0.9× 284 0.7× 31 0.3× 108 1.0× 67 0.7× 20 675
Amal Y. Kentab Saudi Arabia 13 443 1.0× 196 0.5× 25 0.2× 39 0.4× 127 1.4× 44 780
Elizabeth A. Geiger United States 16 963 2.2× 473 1.2× 86 0.8× 97 0.9× 84 0.9× 20 1.2k
Birgit Zirn Germany 19 689 1.6× 419 1.1× 27 0.2× 51 0.5× 66 0.7× 33 1.1k
Shanaz Pasha United Kingdom 14 515 1.2× 295 0.8× 37 0.3× 48 0.4× 45 0.5× 14 919
Gerarda Cappuccio Italy 15 348 0.8× 287 0.7× 29 0.3× 62 0.6× 73 0.8× 59 611

Countries citing papers authored by Marion Gérard

Since Specialization
Citations

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

Fields of papers citing papers by Marion Gérard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marion Gérard

This figure shows the co-authorship network connecting the top 25 collaborators of Marion Gérard. A scholar is included among the top collaborators of Marion Gérard 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 Marion Gérard. Marion Gérard 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.
Gérard, Marion, et al.. (2021). Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems. Neurogenetics. 22(3). 195–206. 1 indexed citations
2.
Ader, Flavie, Pascal de Groote, Patricia Réant, et al.. (2019). FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations. Clinical Genetics. 96(4). 317–329. 57 indexed citations
3.
Revençu, Nicole, Marie Ravoet, Raphaël Helaers, et al.. (2019). RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation. Journal of Medical Genetics. 57(1). 48–52. 46 indexed citations
4.
Schaeffer, S., et al.. (2017). A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome. Biochemical and Biophysical Research Communications. 494(1-2). 133–137. 23 indexed citations
5.
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
6.
Scheidecker, Sophie, M. Köhler, Anne‐Lise Delezoide, et al.. (2016). Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature. American Journal of Medical Genetics Part A. 173(2). 479–486. 5 indexed citations
7.
Gérard, Marion, Gilles Morin, A. Bourillon, et al.. (2015). Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorder. European Journal of Medical Genetics. 58(3). 148–153. 21 indexed citations
8.
Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations
9.
Rambaud, Jérôme, Isabelle Marey, Céline Dupont, et al.. (2012). Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication. American Journal of Medical Genetics Part A. 158A(9). 2277–2282. 2 indexed citations
10.
Gérard, Marion, et al.. (2012). Sirenomelia and caudal malformations in two families. American Journal of Medical Genetics Part A. 158A(7). 1801–1807. 9 indexed citations
11.
Marion, Vincent, Fanny Stutzmann, Marion Gérard, et al.. (2012). Exome sequencing identifies mutations in LZTFL1, a BBSome and smoothened trafficking regulator, in a family with Bardet–Biedl syndrome with situs inversus and insertional polydactyly. Journal of Medical Genetics. 49(5). 317–321. 101 indexed citations
12.
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
13.
Perrin, Laurence, Odile Fenneteau, Brice Ilharreborde, et al.. (2012). A new lysosomal storage disorder resembling Morquio syndrome in sibs. European Journal of Medical Genetics. 55(3). 157–162. 1 indexed citations
14.
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
15.
Jacquinet, Adeline, Marion Gérard, Michael T. Gabbett, et al.. (2010). Temple–Baraitser syndrome: A rare and possibly unrecognized condition. American Journal of Medical Genetics Part A. 152A(9). 2322–2326. 10 indexed citations
16.
Bahi‐Buisson, Nadia, Anna Kamińska, Nathalie Boddaert, et al.. (2008). The three stages of epilepsy in patients with CDKL5 mutations. Epilepsia. 49(6). 1027–1037. 139 indexed citations
17.
Caux, F., Henri Plauchu, Frédéric Chibon, et al.. (2007). Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity. European Journal of Human Genetics. 15(7). 767–773. 94 indexed citations
18.
Houdayer, Claude, Alban Le Monnier, Marion Gérard, et al.. (1999). Improved Fluorescent PCR-Based Assay for Sizing CGG Repeats at the FRAXA Locus. Clinical Chemistry and Laboratory Medicine (CCLM). 37(4). 397–402. 18 indexed citations
19.
Baulny, H. Ogier de, Marion Gérard, Jean‐Marie Saudubray, & J Zittoun. (1998). Remethylation defects: guidelines for clinical diagnosis and treatment. European Journal of Pediatrics. 157(S2). S77–S83. 103 indexed citations
20.
Abitbol, Marc, Christian Ménini, Marion Gérard, et al.. (1995). The rat phospholipase Cβ 4 gene is expressed at high abundance in cerebellar Purkinje cells. Neuroreport. 6(14). 1837–1841. 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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