Géraldine Viot

3.5k citations

56 papers · 1.4k · h-index 21

Impact in

Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in

Genetics 28
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 8
- Genetic Syndromes and Imprinting 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
Pediatrics, Perinatology and Child Health 27
- Prenatal Screening and Diagnostics 24
- Assisted Reproductive Technology and Twin Pregnancy 10

Co-authors: Arnold Münnich (11 shared papers)Michel Vekemans (9 shared papers)Valérie Cormier‐Daire (6 shared papers)Delphine Girlich (2 shared papers)Martine Le Merrer (2 shared papers)Véronica Cusin (2 shared papers)Annick Toutain (2 shared papers)Stanislas Lyonnet (4 shared papers)
Journals: Prenatal Diagnosis (5 papers)Journal of Assisted Reproduction and Genetics (4 papers)Reproductive BioMedicine Online (3 papers)The Journal of Pediatrics (2 papers)Fertility and Sterility (2 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Géraldine Viot

53 papers receiving 1.4k citations

Peers

Countries citing papers authored by Géraldine Viot

Since Specialization

Citations

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

Fields of papers citing papers by Géraldine Viot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Géraldine Viot, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Géraldine Viot Line = papers co-authored together Géraldine Viot links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	SHOX mutations in dyschondrosteosis (Leri-Weill syndrome) Nature Genetics ·Valérie Belin, Véronica Cusin, Géraldine Viot, Delphine Girlich, Annick Toutain, Anne Moncla, Michel Vekemans, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire	1998	257
2	Inversion of the circadian rhythm of melatonin in the Smith-Magenis syndrome The Journal of Pediatrics ·Hélène De Leersnyder, Marie‐Christine de Blois, Bruno Claustrat, Serge Romana, Urs Albrecht, Jürgen‐Christoph von Kleist-Retzow, Bruno Delobel, Géraldine Viot, Stanislas Lyonnet, Michel Vekemans, Arnold Münnich	2001	124
3	Natural history of Barth syndrome: a national cohort study of 22 patients Orphanet Journal of Rare Diseases ·Charlotte Rigaud, Anne-Sophie Lèbre, Renaud Touraine, Blandine Beaupain, Chris Ottolenghi, A. Chabli, Hélène Ansquer, (unknown), Sylvie Di Filippo, Pascale de Lonlay, Betina Borm, François Rivier, Marie-Catherine Vaillant, Michèle Mathieu‐Dramard, Alice Goldenberg, Géraldine Viot, Philippe Charron, Marlène Rio, Damien Bonnet, Jean Donadieu	2013	97
4	Antenatal manifestations of mitochondrial respiratory chain deficiency The Journal of Pediatrics ·Jürgen‐Christoph von Kleist-Retzow, Valérie Cormier‐Daire, Géraldine Viot, Alice Goldenberg, Becky Mardach, Jeanne Amiel, Philippe Saada, Yves Dumez, Françis Brunelle, Jean‐Marie Saudubray, Dominique Chrétien, Agnès Rötig, Pierre Rustin, Arnold Münnich, Pascale de Lonlay	2003	94
5	Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies European Journal of Pediatrics ·Laurence Iserin, Pascale de Lonlay, Géraldine Viot, D. Sidi, J Kachaner, Arnold Münnich, Stanislas Lyonnet, Michel Vekemans, Damien Bonnet	1998	74
6	Atypical findings in Kabuki syndrome: Report of 8 patients in a series of 20 and review of the literature American Journal of Medical Genetics Part A ·David Geneviève, Jeanne Amiel, Géraldine Viot, M. Le Merrer, Damien Sanlaville, Andoni Urtizberea, M. Gérard, A Munnich, Valérie Cormier‐Daire, Stanislas Lyonnet	2004	58
7	Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia Human Mutation ·A. Taillandier, Anne-Sophie Lia-Baldini, M. Mouchard, Blaise Robin, Françoise Müller, Brigitte Simon‐Bouy, J.L. Serre, Anne Béra-Louville, M Bonduelle, Jan Eckhardt, Dominique Gaillard, A. G. Myhre, S. Körtge‐Jung, L Larget-Piet, E. Malou, David Sillence, I. Karen Temple, Géraldine Viot, Étienne Mornet	2001	45
8	Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature Prenatal Diagnosis ·Laurence Faivre, N. Morichon-Delvallez, Géraldine Viot, Françoise Narcy, St�phane Loison, Laurent Mandelbrot, M. C. Aubry, Valérie Raclin, Patrick Edery, Arnold Münnich, Michel Vekemans	1998	41
9	Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1 European Journal of Human Genetics ·Rémi Dufourcq-Lagelouse, Nathalie Lambert, Michel Duval, Géraldine Viot, E Vilmer, Alain Fischer, Marguerite Prieur, Geneviève de Saint Basile	1999	40
10	CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy Human Mutation ·Karine Poirier, Laurence Hubert, Géraldine Viot, Marlène Rio, Pierre Billuart, Claude Besmond, Thierry Bienvenu	2017	37
11	First‐trimester ultrasound diagnosis of skeletal dysplasia associated with increased nuchal translucency thickness Ultrasound in Obstetrics and Gynecology ·Charlotte Ngô, Géraldine Viot, M. C. Aubry, V. Tsatsaris, G. Grangé, D. Cabrol, E. Pannier	2007	33
12	Prenatal detection of a 1p36 deletion in a fetus with multiple malformations and a review of the literature Prenatal Diagnosis ·Laurence Faivre, N. Morichon-Delvallez, Géraldine Viot, Jelena Martinović, M. P. Pinson, J. P. Aubry, Valérie Raclin, Patrick Edery, Yves Dumez, Arnold Münnich, Michel Vekemans	1999	32
13	Adverse health effects in children of women exposed in utero to diethylstilbestrol (DES) Therapies ·Michel Tournaire, Sylvie Epelboin, Émmanuel Devouche, Géraldine Viot, J. Le Bidois, A Cabau, Annabel Dunbavand, Anne Levadou	2016	31
14	Results of assisted reproductive technique in men with cystic fibrosis Human Reproduction ·D. Hubert, Catherine Patrat, Juliette Guibert, Nicolas Thiounn, Thierry Bienvenu, Géraldine Viot, Pierre Jouannet, Sylvie Epelboin	2006	29
15	Identification of a newDPY19L2mutation and a better definition ofDPY19L2deletion breakpoints leading to globozoospermia Molecular Human Reproduction ·Houda Ghédir, Samira Ibala‐Romdhane, Özlem Okutman, Géraldine Viot, Saad Hasan Mohammed Ali, Stéphane Viville	2015	29
16	Osteopathia striata cranial sclerosis: Non‐random X‐inactivation suggestive of X‐linked dominant inheritance American Journal of Medical Genetics ·Géraldine Viot, Didier Lacombe, Albert David, Michèle Mathieu, A. de Broca, Laurence Faivre, Nadine Gigarel, Arnold Münnich, Stanislas Lyonnet, Martine Le Merrer, Valérie Cormier‐Daire	2002	28
17	Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCR Clinical Chemistry and Laboratory Medicine (CCLM) ·Aurélia Gruber, Mathilde Pacault, Laïla El Khattabi, Nicolas Vaucouleur, Lucie Orhant, Thierry Bienvenu, Emmanuelle Girodon, Dominique Vidaud, France Leturcq, Cathérine Costa, Franck Letourneur, Olivia Anselem, Vassilis Tsatsaris, François Goffinet, Géraldine Viot, Michel Vidaud, Juliette Nectoux	2018	27
18	Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing Clinical Genetics ·Charlotte Mouden, Christèle Dubourg, Wilfrid Carré, Sophie Rose, C. Quelin, Linda Akloul, Houda Hamdi‐Rozé, Géraldine Viot, H. Salhi, P. Darnault, S. Odent, Valérie Dupé, Véronique David	2016	26
19	Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different American Journal of Medical Genetics Part A ·Géraldine Viot, Pascale Sonigo, Isabelle Simon, Brigitte Simon‐Bouy, Frédéric Chadeyron, Chérif Beldjord, Julia Tantau, Jelena Martinović, Chantal Esculpavit, Françis Brunelle, Arnold Münnich, Michel Vekemans, Férechté Encha‐Razavi	2003	23
20	Loss of Function of KCNC1 is associated with intellectual disability without seizures European Journal of Human Genetics ·Karine Poirier, Géraldine Viot, Laura Lombardi, Clémence Jauny, Pierre Billuart, Thierry Bienvenu	2017	23

About Géraldine Viot

Géraldine Viot is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Rheumatology and Public Health, Environmental and Occupational Health, having authored 56 papers that have together received 1.4k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (13 papers), Assisted Reproductive Technology and Twin Pregnancy (10 papers), Genetics and Neurodevelopmental Disorders (8 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Genetics (647 citations), Clinical Biochemistry (101 citations), Pediatrics, Perinatology and Child Health (280 citations), Reproductive Medicine (100 citations) and Developmental Biology (25 citations). Géraldine Viot has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Arnold Münnich, Michel Vekemans, Valérie Cormier‐Daire, Delphine Girlich, Martine Le Merrer, Véronica Cusin, Annick Toutain, Stanislas Lyonnet, Anne Moncla and Jürgen‐Christoph von Kleist-Retzow. Their work appears in journals such as Prenatal Diagnosis, Journal of Assisted Reproduction and Genetics, Reproductive BioMedicine Online, The Journal of Pediatrics and Fertility and Sterility.

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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Géraldine Viot

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