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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems 2021 ·Neurogenetics ·(unknown), Marion Gérard, (unknown), Olivier Pichon, (unknown), (unknown), Madeleine Joubert, Stéphane Bezieau, Claire Bénéteau	1
2	FLNC pathogenic variants in patients with cardiomyopathies: Prevalence and genotype‐phenotype correlations 2019 ·Clinical Genetics ·Flavie Ader, Pascal de Groote, Patricia Réant, Caroline Rooryck, Delphine Dupin‐Deguine, Caroline Rambaud, Diala Khraiche, Claire Perret, (unknown), Michèle Mathieu‐Dramard, Marion Gérard, (unknown), Laurent Gouya, Xavier Jeunemaı̂tre, Lionel Van Maldergem, Albert Hagège, Eric Villard, Philippe Charron, Pascale Richard	57
3	RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation 2019 ·Journal of Medical Genetics ·Nicole Revençu, (unknown), Marie Ravoet, Raphaël Helaers, Pascal Brouillard, (unknown), (unknown), Marion Gérard, Veronika Dvořáková, Alan D. Irvine, Louis Boon, Miikka Vikkula	46
4	A 2 bp deletion in the mitochondrial ATP 6 gene responsible for the NARP (neuropathy, ataxia, and retinitis pigmentosa) syndrome 2017 ·Biochemical and Biophysical Research Communications ·(unknown), S. Schaeffer, (unknown), (unknown), Marion Gérard, Françoise Chapon, Stéphane Allouche	23
5	Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene 2017 ·Acta Neuropathologica Communications ·Pascale Saugier-Véber, Florent Marguet, François Lecoquierre, Homa Adle‐Biassette, Fabien Guimiot, Sara Cipriani, Sophie Patrier, M. Brasseur‐Daudruy, Alice Goldenberg, Valérie Layet, Yline Capri, Marion Gérard, Thierry Frébourg, Annie Laquerrière	23
6	Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature 2016 ·American Journal of Medical Genetics Part A ·(unknown), Sophie Scheidecker, M. Köhler, (unknown), Anne‐Lise Delezoide, (unknown), Stéphane Triau, Estelle Colin, Marion Gérard, Karl‐Heinz Grzeschik, Hélène Dollfus, Maria Cristina Antal	5
7	Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorder 2015 ·European Journal of Medical Genetics ·Marion Gérard, Gilles Morin, A. Bourillon, Cindy Colson, Sophie Mathieu, Daniel Rabier, Thierry Billette de Villemeur, H. Ogier de Baulny, Jean François Benoist	21
8	An Integrated Diagnosis Strategy for Congenital Myopathies 2013 ·PLoS ONE ·Johann Böhm, Nasim Vasli, Edoardo Malfatti, Stéphanie Le Gras, Claire Feger, Bernard Jost, Nicole Monnier, Julie Brocard, Hatice Karasoy, Marion Gérard, Maggie C. Walter, Peter Reilich, Valérie Biancalana, Christine Kretz, Nadia Messaddeq, Isabelle Marty, Joël Lunardi, Norma B. Romero, Jocelyn Laporte	43
9	Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication 2012 ·American Journal of Medical Genetics Part A ·Jérôme Rambaud, Isabelle Marey, Céline Dupont, (unknown), Yline Capri, Anne Claude Tabet, Brigitte Benzacken, Alain Verloès, Azzedine Aboura, Marion Gérard	2
10	Sirenomelia and caudal malformations in two families 2012 ·American Journal of Medical Genetics Part A ·Marion Gérard, Valérie Layet, (unknown), (unknown), (unknown), (unknown), Bénédicte Gérard	9
11	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 2012 ·Journal of Medical Genetics ·Vincent Marion, Fanny Stutzmann, Marion Gérard, (unknown), Élise Schaefer, (unknown), Sophie Hellé, Valérie Delague, Eric H. Souied, Catherine Barrey, Alain Verloès, Corinne Stoetzel, Hélène Dollfus	101
12	Pre‐ and postnatal phenotype of 6p25 deletions involving the FOXC1 gene 2012 ·American Journal of Medical Genetics Part A ·Andrée Delahaye‐Duriez, Suonavy Khung‐Savatovsky, Azzedine Aboura, Fabien Guimiot, Séverine Drunat, Jean‐Luc Alessandri, Marion Gérard, Pierre Bitoun, (unknown), Stéphanie Robin, C. Huel, (unknown), Stéphane Serero, Pierre Gressèns, Jacques Élion, Alain Verloès, Brigitte Benzacken, Anne‐Lise Delezoide, Eva Pipiras	37
13	A new lysosomal storage disorder resembling Morquio syndrome in sibs 2012 ·European Journal of Medical Genetics ·Laurence Perrin, Odile Fenneteau, Brice Ilharreborde, Yline Capri, Marion Gérard, E. Bui Quoc, Sandrine Passemard, Jamal Ghoumid, Catherine Caillaud, Roseline Froissart, Anne‐Claude Tabet, Sophie Lebon, Vincent El Ghouzzi, Keyvan Mazda, Alain Verloès	1
14	Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis 2010 ·American Journal of Medical Genetics Part A ·Anne‐Claude Tabet, Azzedine Aboura, Marion Gérard, Marion Pilorge, Céline Dupont, Jean‐François Gadisseux, (unknown), Eva Pipiras, Andrée Delahaye‐Duriez, (unknown), Alain Verloès, Brigitte Benzacken, Catalina Betancur	20
15	Temple–Baraitser syndrome: A rare and possibly unrecognized condition 2010 ·American Journal of Medical Genetics Part A ·Adeline Jacquinet, Marion Gérard, Michael T. Gabbett, (unknown), Jean‐Paul Misson, Björn Menten, Geert Mortier, Lionel Van Maldergem, Alain Verloès, François‐Guillaume Debray	10
16	The three stages of epilepsy in patients with CDKL5 mutations 2008 ·Epilepsia ·Nadia Bahi‐Buisson, Anna Kamińska, Nathalie Boddaert, Marlène Rio, Alexandra Afenjar, Marion Gérard, Fabienne Giuliano, Jacques Motté, Delphine Héron, (unknown), Perrine Plouin, Christian Richelme, Vincent des Portes, Olivier Dulac, Christophe Philippe, Catherine Chiron, Rima Nabbout, Thierry Bienvenu	139
17	Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity 2007 ·European Journal of Human Genetics ·F. Caux, Henri Plauchu, Frédéric Chibon, Laurence Faivre, Olivier Fain, P. Vabres, Françoise Bonnet, (unknown), L. Laroche, Marion Gérard, Michel Longy	94
18	Improved Fluorescent PCR-Based Assay for Sizing CGG Repeats at the FRAXA Locus 1999 ·Clinical Chemistry and Laboratory Medicine (CCLM) ·Claude Houdayer, Alban Le Monnier, Marion Gérard, (unknown), Mohammed Tredano, Thierry Billette de Villemeur, P Aymard, Jean‐Paul Bonnefont, Delphine Feldmann	18
19	Remethylation defects: guidelines for clinical diagnosis and treatment 1998 ·European Journal of Pediatrics ·H. Ogier de Baulny, Marion Gérard, Jean‐Marie Saudubray, J Zittoun	103
20	The rat phospholipase Cβ 4 gene is expressed at high abundance in cerebellar Purkinje cells 1995 ·Neuroreport ·(unknown), Marc Abitbol, Christian Ménini, (unknown), Marion Gérard, Michel Vekemans, Jacques Mallet, Jean‐Louis Dufier	38

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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