Cécile Mignon‐Ravix

1.1k citations

26 papers · 727 indexed · h-index 15

Co-authors: Laurent Villard Pierre Cacciagli Marie‐Geneviève Mattéi D. Depétris B. Chabrol Mathieu Milh Chantal Missirian Judith Luciani
Topics: Genetics and Neurodevelopmental Disorders (11 papers)Genomic variations and chromosomal abnormalities (10 papers)Cellular transport and secretion (3 papers)
Cited by: Aging Genetics Molecular Biology
Journals: Neurology Scientific Reports Journal of Cell Science
Partner nations: France Lebanon Germany

In The Last Decade

Cécile Mignon‐Ravix

25 papers receiving 706 citations

Peers

Countries citing papers authored by Cécile Mignon‐Ravix

Since Specialization

Citations

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

Fields of papers citing papers by Cécile Mignon‐Ravix

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Cécile Mignon‐Ravix. 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 Cécile Mignon‐Ravix. The network helps show where Cécile Mignon‐Ravix may publish in the future.

Co-authorship network of co-authors of Cécile Mignon‐Ravix

This figure shows the co-authorship network connecting the top 25 collaborators of Cécile Mignon‐Ravix. A scholar is included among the top collaborators of Cécile Mignon‐Ravix 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 Cécile Mignon‐Ravix. Cécile Mignon‐Ravix 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	NAPB and developmental and epileptic encephalopathy: Description of the electroclinical profile associated with a novel pathogenic variant 2023 ·Epilepsia ·Cécile Mignon‐Ravix,(unknown),Géraldine Daquin,Pierre Cacciagli,(unknown),Laurent Villard,Nathalie Villeneuve,Florence Molinari	5
2	Loss of NDST1 N-sulfotransferase activity is associated with autosomal recessive intellectual disability 2023 ·Human Molecular Genetics ·(unknown),Cécile Mignon‐Ravix,(unknown),Pierre Cacciagli,Béatrice Desnous,Sabine Sigaudy,Mathieu Milh,Laurent Villard,Lena Kjellén,Florence Molinari	0
3	TRAPPC2L-related disorder: first homozygous protein-truncating variant and further delineation of the phenotype 2023 ·Journal of Medical Genetics ·(unknown),Cécile Mignon‐Ravix,Svetlana Gorokhova,Pierre Cacciagli,(unknown),Florence Molinari,B. Chabrol,Sabine Sigaudy,Laurent Villard,(unknown)	1
4	A large consanguineous family with a homozygous Metabotropic Glutamate Receptor 7 (mGlu7) variant and developmental epileptic encephalopathy: Effect on protein structure and ligand affinity 2021 ·Orphanet Journal of Rare Diseases ·(unknown),Cécile Mignon‐Ravix,(unknown),(unknown),Faiza Fakhfakh,Laurent Villard,Chahnez Triki	9
5	Molecular characterization of a 1p36 chromosomal duplication and in utero interference define ENO1 as a candidate gene for polymicrogyria 2020 ·European Journal of Human Genetics ·Bilal El Waly,Cécile Mignon‐Ravix,Pierre Cacciagli,Emmanuelle Buhler,Bruria Ben Zeev,Laurent Villard	4
6	Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration 2017 ·European Journal of Paediatric Neurology ·Nathalie Villeneuve,(unknown),Pierre Cacciagli,Cécile Mignon‐Ravix,B. Chabrol,Laurent Villard,Mathieu Milh	12
7	Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients 2015 ·Molecular Cytogenetics ·(unknown),Joelle Abou Ghoch,Sandra Corbani,Pierre Cacciagli,Cécile Mignon‐Ravix,Nabiha Salem,Nadine Jalkh,Sandra Sabbagh,Ali Fawaz,Tony Ibrahim,Laurent Villard,André Mégarbané,Éliane Chouery	6
8	Evidence that homozygous PTPRD gene microdeletion causes trigonocephaly, hearing loss, and intellectual disability 2015 ·Molecular Cytogenetics ·(unknown),Cécile Mignon‐Ravix,Pierre Cacciagli,Joelle Abou Ghoch,Ali Fawaz,André Mégarbané,Laurent Villard,Éliane Chouery	31
9	Intragenic rearrangements in X‐linked intellectual deficiency: Results of a‐CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes 2014 ·American Journal of Medical Genetics Part A ·Cécile Mignon‐Ravix,Pierre Cacciagli,(unknown),Cornel Popovici,Chantal Missirian,Mathieu Milh,André Mégarbané,Tiffany Busa,Sophie Julia,Nadine Girard,Catherine Badens,Sabine Sigaudy,Nicole Philip,Laurent Villard	23
10	Ambiguous genitalia, microcephaly, seizures, bone malformations, and early death: A distinct MCA/MR syndrome 2011 ·American Journal of Medical Genetics Part A ·André Mégarbané,Éliane Chouery,Cécile Mignon‐Ravix,Sandra Sabbagh,Sandra Corbani,Joelle Abou Ghoch,Nadine Jalkh,Cybel Mehawej,Nicolas Lévy,Laurent Villard	2
11	Epileptic and nonepileptic features in patients with early onset epileptic encephalopathy and STXBP1 mutations 2011 ·Epilepsia ·Mathieu Milh,Nathalie Villeneuve,Mondher Chouchane,Anna Kamińska,Cécile Laroche,Marie Anne Barthez,Cyril Gitiaux,(unknown),(unknown),Pierre Cacciagli,Cécile Mignon‐Ravix,(unknown),B. Chabrol,Laurent Villard	94
12	Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype 2010 ·European Journal of Human Genetics ·Pierre Cacciagli,(unknown),Cécile Mignon‐Ravix,Bilal El Waly,Anne Moncla,Chantal Missirian,B. Chabrol,Laurent Villard	66
13	Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features 2009 ·European Journal of Medical Genetics ·(unknown),Cécile Mignon‐Ravix,Pierre Cacciagli,André Mégarbané,Laurent Villard	1
14	In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin 2008 ·Chromosome Research ·Catherine Metzler‐Guillemain,D. Depétris,Judith Luciani,Cécile Mignon‐Ravix,Michael Mitchell,Marie‐Geneviève Mattéi	28
15	Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations 2007 ·European Journal of Human Genetics ·Cécile Mignon‐Ravix,D. Depétris,Judith Luciani,Cristina Cuoco,Małgorzata Krajewska‐Walasek,Chantal Missirian,Patrick Collignon,Bruno Delobel,Marie‐Françoise Croquette,Anne Moncla,Peter M. Kroisel,Marie‐Geneviève Mattéi	38
16	Intrachromosomal triplication for the distal part of chromosome 15q 2005 ·American Journal of Medical Genetics Part A ·C Schluth,Marie‐Geneviève Mattéi,Cécile Mignon‐Ravix,(unknown),Yves Alembik,(unknown),Emmanuelle Ginglinger,Éric Jeandidier	13
17	Subcellular distribution of HP1 proteins is altered in ICF syndrome 2004 ·European Journal of Human Genetics ·Judith Luciani,D. Depétris,Chantal Missirian,Cécile Mignon‐Ravix,Catherine Metzler‐Guillemain,André Mégarbané,Anne Moncla,Marie‐Geneviève Mattéi	28
18	XNP-1/ATR-X acts with RB, HP1 and the NuRD complex during larval development in C. elegans 2004 ·Developmental Biology ·Carlos Cardoso,Carole Couillault,Cécile Mignon‐Ravix,Anne Millet,Jonathan J. Ewbank,Michel Fontés,Nathalie Pujol	30
19	Mechanism of intrachromosomal triplications 15q11‐q13: A new clinical report 2003 ·American Journal of Medical Genetics Part A ·François Vialard,Cécile Mignon‐Ravix,D. Parain,D. Depétris,Marie‐France Portnoï,Hélène Moirot,Marie‐Geneviève Mattéi	25
20	A human interstitial telomere associates in vivo with specific TRF2 and TIN2 proteins 2002 ·European Journal of Human Genetics ·Cécile Mignon‐Ravix,D. Depétris,Bruno Delobel,Marie‐Françoise Croquette,Marie‐Geneviève Mattéi	21

About Cécile Mignon‐Ravix

Cécile Mignon‐Ravix is a scholar working on Genetics, Aging and Cell Biology, having authored 26 papers that have together received 727 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (11 papers), Genomic variations and chromosomal abnormalities (10 papers) and Cellular transport and secretion (3 papers). The work is most often cited by research in Aging (26 citations), Genetics (320 citations) and Molecular Biology (475 citations). Cécile Mignon‐Ravix has collaborated with scholars based in France, Lebanon and Germany. Frequent co-authors include Laurent Villard, Pierre Cacciagli, Marie‐Geneviève Mattéi, D. Depétris, B. Chabrol, Mathieu Milh, Chantal Missirian, Judith Luciani, André Mégarbané and Catherine Metzler‐Guillemain. Their work appears in journals such as Neurology, Scientific Reports and Journal of Cell Science.

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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