Michèle Mathieu‐Dramard

2.7k citations

15 papers · 363 indexed · h-index 9

Co-authors: Joris Andrieux Philippe Charron Bénédicte Demeer Henri Copin Aline Receveur Alice Goldenberg G Morin Ghislaine Plessis
Topics: Genomic variations and chromosomal abnormalities (7 papers)Genetics and Neurodevelopmental Disorders (3 papers)Chromosomal and Genetic Variations (3 papers)
Cited by: Developmental Biology Genetics Clinical Biochemistry
Journals: SHILAP Revista de lepidopterologíaHuman Mutation Orphanet Journal of Rare Diseases
Partner nations: France United Kingdom Sweden

In The Last Decade

Michèle Mathieu‐Dramard

15 papers receiving 321 citations

Peers

Countries citing papers authored by Michèle Mathieu‐Dramard

Since Specialization

Citations

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

Fields of papers citing papers by Michèle Mathieu‐Dramard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michèle Mathieu‐Dramard. 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 Michèle Mathieu‐Dramard. The network helps show where Michèle Mathieu‐Dramard may publish in the future.

Co-authorship network of co-authors of Michèle Mathieu‐Dramard

This figure shows the co-authorship network connecting the top 25 collaborators of Michèle Mathieu‐Dramard. A scholar is included among the top collaborators of Michèle Mathieu‐Dramard 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 Michèle Mathieu‐Dramard. Michèle Mathieu‐Dramard is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Kleefstra syndrome: Recurrence in siblings due to a paternal mosaic mutation 2021 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Amélie Piton,Anne‐Gaëlle Le Moing,Michèle Mathieu‐Dramard,(unknown),G Morin,Guillaume Jedraszak	2
2	Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants 2020 ·Clinical Genetics ·Emmanuelle Ranza,Anne Guimier,Alain Verloès,Yline Capri,(unknown),Martine Auclair,Michèle Mathieu‐Dramard,Gilles Morin,Julien Thévenon,Laurence Faivre,Christel Thauvin‐Robinet,A. Micheil Innes,David A. Dyment,Corinne Vigouroux,Jeanne Amiel	10
3	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
4	New intragenic rearrangements in non‐Finnish mulibrey nanism 2017 ·American Journal of Medical Genetics Part A ·(unknown),Gilles Morin,Catherine Vincent‐Delorme,(unknown),Rosalie Cabry,Michèle Mathieu‐Dramard,Henri Copin,Jacques Rochette,Guillaume Jedraszak	8
5	Prenatal diagnosis of femoral facial syndrome: Three case reports and literature review 2017 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Céline Klein,(unknown),Bénédicte Demeer,Michèle Mathieu‐Dramard,Guillaume Jedraszak,Catherine Gondry‐Jouet,Jean Gondry,Anne Dieux‐Coëslier,Gilles Morin	5
6	Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: Six new patients 2015 ·American Journal of Medical Genetics Part A ·Guillaume Jedraszak,Bénédicte Demeer,Michèle Mathieu‐Dramard,Joris Andrieux,Aline Receveur,Astrid Weber,Una Maye,Nicola Foulds,I. Karen Temple,John A. Crolla,(unknown),Damien Sanlaville,Lisa Ewans,Meredith Wilson,Ruth Armstrong,(unknown),Henri Copin,Gilles Morin	17
7	Severe Psychomotor Delay in a Severe Presentation of Cat-Eye Syndrome 2015 ·SHILAP Revista de lepidopterología ·Guillaume Jedraszak,Aline Receveur,Joris Andrieux,Michèle Mathieu‐Dramard,Henri Copin,Gilles Morin	3
8	Natural history of Barth syndrome: a national cohort study of 22 patients 2013 ·Orphanet Journal of Rare Diseases ·Charlotte Rigaud,Anne-Sophie Lèbre,Renaud Touraine,Blandine Beaupain,Chris Ottolenghi,A. Chabli,(unknown),(unknown),Sylvie Di Filippo,Pascale de Lonlay,(unknown),François Rivier,(unknown),Michèle Mathieu‐Dramard,Alice Goldenberg,Géraldine Viot,Philippe Charron,Marlène Rio,Damien Bonnet,Jean Donadieu	97
9	A severe prenatal presentation of Cat Eye Syndrome 2013 ·Clinical Dysmorphology ·Guillaume Jedraszak,Aline Receveur,Joris Andrieux,(unknown),Michèle Mathieu‐Dramard,Dominique Brémond‐Gignac,Henri Sevestre,Henri Copin,Jacques Rochette	2
10	A patient with Simpson–Golabi–Behmel syndrome, biliary cirrhosis and successful liver transplantation 2013 ·American Journal of Medical Genetics Part A ·Guillaume Jedraszak,M Girard,(unknown),D. Djeddi,Christophe Chardot,(unknown),Marie‐Pierre Moizard,Jean Gondry,Henri Sevestre,Michèle Mathieu‐Dramard,Florence Lacaille,Bénédicte Demeer	5
11	A novel microdeletion syndrome at 9q21.13 characterised by mental retardation, speech delay, epilepsy and characteristic facial features 2012 ·European Journal of Medical Genetics ·(unknown),Bénédicte Demeer,Cédric Le Caignec,Bertrand Isidor,Michèle Mathieu‐Dramard,Ghislaine Plessis,Alice M. George,Juliet Taylor,Salim Aftimos,Adelheid Wiemer‐Kruel,Jürgen Kohlhase,Göran Annerén,Helen V. Firth,Ingrid Simonic,Joris Vermeesch,Ann‐Charlotte Thuresson,Henri Copin,Donald R. Love,Joris Andrieux	41
12	Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: Two cases and expansion of the phenotype to radial agenesis 2012 ·European Journal of Medical Genetics ·Florence Petit,Joris Andrieux,Bénédicte Demeer,(unknown),Henri Copin,(unknown),Fabienne Escande,Sylvie Manouvrier‐Hanu,Michèle Mathieu‐Dramard	11
13	Duplication 16p13.3 and the CREBBP gene: Confirmation of the phenotype 2012 ·European Journal of Medical Genetics ·Bénédicte Demeer,Joris Andrieux,Aline Receveur,G Morin,Florence Petit,Sophie Julia,Ghislaine Plessis,Dominique Martin‐Coignard,Bruno Delobel,Helen V. Firth,Ann‐Charlotte Thuresson,(unknown),(unknown),Cédric Le Caignec,Koenraad Devriendt,Michèle Mathieu‐Dramard	41
14	Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients 2010 ·American Journal of Medical Genetics Part A ·Eleni Katzaki,Gilles Morin,Marzia Pollazzon,Filomena Tiziana Papa,Sabrina Buoni,Joussef Hayek,Joris Andrieux,Laure Lecerf,Cornel Popovici,Aline Receveur,Michèle Mathieu‐Dramard,Alessandra Renieri,Francesca Mari,Nicole Philip	19
15	TCF4Deletions in Pitt-Hopkins Syndrome 2008 ·Human Mutation ·Irina Giurgea,Chantal Missirian,Pierre Cacciagli,Sandra Whalen,Tessa Fredriksen,(unknown),Julia Rankin,Michèle Mathieu‐Dramard,G Morin,Dominique Martin‐Coignard,Christèle Dubourg,B. Chabrol,(unknown),Fabienne Giuliano,(unknown),Nicole Philip,Pierre Sarda,Laurent Villard,Michel Goossens,Anne Moncla	45

About Michèle Mathieu‐Dramard

Michèle Mathieu‐Dramard is a scholar working on Developmental Biology, Genetics and Genetics, having authored 15 papers that have together received 363 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Developmental Biology (20 citations), Genetics (170 citations) and Clinical Biochemistry (27 citations). Michèle Mathieu‐Dramard has collaborated with scholars based in France, United Kingdom and Sweden. Frequent co-authors include Joris Andrieux, Philippe Charron, Bénédicte Demeer, Henri Copin, Aline Receveur, Alice Goldenberg, G Morin, Ghislaine Plessis, Gilles Morin and Sylvie Di Filippo. Their work appears in journals such as SHILAP Revista de lepidopterología, Human Mutation and Orphanet Journal of Rare Diseases.

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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