Caroline Michot

3.0k total citations
43 papers, 823 citations indexed

About

Caroline Michot is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Caroline Michot has authored 43 papers receiving a total of 823 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 20 papers in Genetics and 11 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Caroline Michot's work include Connective tissue disorders research (11 papers), Bone health and treatments (5 papers) and Obstructive Sleep Apnea Research (4 papers). Caroline Michot is often cited by papers focused on Connective tissue disorders research (11 papers), Bone health and treatments (5 papers) and Obstructive Sleep Apnea Research (4 papers). Caroline Michot collaborates with scholars based in France, Italy and United Kingdom. Caroline Michot's co-authors include Valérie Cormier‐Daire, Geneviève Baujat, Carine Le Goff, Stanislas Lyonnet, Arnold Münnich, Céline Huber, Sophie Monnot, L. Meunier, L Durand and Kim‐Hanh Le Quan Sang and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Caroline Michot

40 papers receiving 806 citations

Peers

Countries citing papers authored by Caroline Michot

Since Specialization

Citations

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

Fields of papers citing papers by Caroline Michot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caroline Michot

This figure shows the co-authorship network connecting the top 25 collaborators of Caroline Michot. A scholar is included among the top collaborators of Caroline Michot 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 Caroline Michot. Caroline Michot 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	Gnathodiaphyseal dysplasia: Diagnostic clues from two fetal cases and literature review 2024 ·Prenatal Diagnosis ·(unknown), Detlef Trost, (unknown), Caroline Michot, Valérie Cormier‐Daire, Nathalie Boutry, (unknown), Catherine Vincent‐Delorme	2
2	Identification ofkinesin family member (KIF22)homozygous variants in spondyloepimetaphyseal dysplasia with joint laxity, lepdodactylic type and demonstration of proteoglycan biosynthesis impairment 2024 ·Journal of Bone and Mineral Research ·Johanne Dubail, Sophie Rondeau, Caroline Michot, Geneviève Baujat, Yline Capri, Julien Thévenon, (unknown), Zagorka Péjin, Gilles Phan, Céline Huber, Valérie Cormier‐Daire	0
3	Clinical spectrum of rare bone fragility disorders and response to bisphosphonate treatment: a retrospective study 2024 ·European Journal of Human Genetics ·(unknown), Perrine Brunelle, Geneviève Baujat, Caroline Michot, Julien Van‐Gils, Bruno Leheup, Élise Schaefer, Eugénie Koumakis, Zagorka Péjin, Graziella Pinto, Sophie Monnot, Valérie Cormier‐Daire	0
4	Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature 2023 ·Journal of Medical Genetics ·Pauline Marzin, Sophie Rondeau, Jean‐Luc Alessandri, Klaus Dieterich, Carine Le Goff, Clémentine Mahaut, Sandra Mercier, Caroline Michot, Oana Moldovan, Gianmaria Miolo, Massimiliano Rossi, Julien Van‐Gils, Christine Francannet, Matthieu P. Robert, Jean-Philippe Jaı̈s, Céline Huber, Valérie Cormier‐Daire	7
5	SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients 2022 ·Orphanet Journal of Rare Diseases ·(unknown), (unknown), Sylvain Breton, Marie‐Liesse Piketty, Alexandra Afenjar, J. Amiel, Yline Capri, Alice Goldenberg, Christine Francannet, Caroline Michot, Cyril Mignot, Laurence Perrin, Chloé Quēlin, (unknown), Giulia Barcia, Véronique Pingault, Gérard Maruani, Eugénie Koumakis, Valérie Cormier‐Daire	10
6	Ellis-Van Creveld Syndrome: Clinical and Molecular Analysis of 50 Individuals 2022 ·Journal of Medical Genetics ·(unknown), Céline Huber, Geneviève Baujat, Caroline Michot, Mohammed Zarhrate, Marc Bras, Lucile Boutaud, Valérie Malan, Tania Attié‐Bitach, Valérie Cormier‐Daire	8
7	A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder 2021 ·SHILAP Revista de lepidopterología ·(unknown), Philippe de Mazancourt, Corinne Métay, Robert Carlier, Valérie Allamand, Corine Gartioux, (unknown), (unknown), (unknown), Ahmed Mekki, Pascale Richard, Caroline Michot, Karelle Bénistan	6
8	Geleophysic and acromicric dysplasias: natural history, genotype–phenotype correlations, and management guidelines from 38 cases 2020 ·Genetics in Medicine ·Pauline Marzin, Briac Thierry, (unknown), (unknown), Caroline Michot, Sophie Rondeau, Geneviève Baujat, Gilles Phan, Maryse Bonnière, Muriel Le Bourgeois, Diala Khraiche, Zagorka Péjin, Damien Bonnet, Christophe Delacourt, Valérie Cormier‐Daire	20
9	Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review 2019 ·Clinical Genetics ·(unknown), Caroline Michot, Geneviève Baujat, (unknown), S. Baron, Yline Capri, Martine Cohen‐Solal, Corinne Collet, Anne Dieux, David Geneviève, Bertrand Isidor, Sophie Monnot, Massimiliano Rossi, Anya Rothenbühler, Élise Schaefer, Valérie Cormier‐Daire	31
10	Expanding the phenotype in Adams–Oliver syndrome correlating with the genotype 2019 ·American Journal of Medical Genetics Part A ·(unknown), Céline Huber, Caroline Michot, Federico Di Rocco, M Girard, Stanislas Lyonnet, Marlène Rio, (unknown), Valérie Cormier‐Daire, Geneviève Baujat	14
11	Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences 2017 ·Journal of Medical Genetics ·Solveig Heide, Sandra Chantot‐Bastaraud, Boris Keren, Madeleine D. Harbison, Salah Azzi, Sylvie Rossignol, Caroline Michot, (unknown), Bénédicte Demeer, Claudine Heinrichs, Ron S. Newfield, Pierre Sarda, Lionel Van Maldergem, (unknown), Éloïse Giabicani, Jean‐Pierre Siffroi, Yves Le Bouc, Irène Netchine, Frédéric Brioude	34
12	Prevalence of fibrodysplasia ossificans progressiva (FOP) in France: an estimate based on a record linkage of two national databases 2017 ·Orphanet Journal of Rare Diseases ·Geneviève Baujat, Rémy Choquet, S. Bouée, Viviane Jeanbat, (unknown), (unknown), Caroline Michot, Kim‐Hanh Le Quan Sang, (unknown), Claude Messiaen, Paul Landais, Valérie Cormier‐Daire	66
13	Perinatal and infantile hypophosphatasia: clinical features and treatment 2017 ·Archives de Pédiatrie ·Geneviève Baujat, Caroline Michot, Kim‐Hanh Le Quan Sang, Valérie Cormier‐Daire	10
14	Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndrome 2016 ·American Journal of Medical Genetics Part A ·Angela E. Lin, Caroline Michot, Valérie Cormier‐Daire, Thomas J. L’Ecuyer, G. Paul Matherne, Peter J. Barnes, Jennifer B. Humberson, Andrew C. Edmondson, Elaine H. Zackai, Matthew J. O’Connor, Julie Kaplan, Makram R. Ebeid, Joel B. Krier, Elizabeth L. Krieg, Brian Ghoshhajra, Mark E. Lindsay	45
15	RPL10 mutation segregating in a family with X‐linked syndromic Intellectual Disability 2015 ·American Journal of Medical Genetics Part A ·Julien Thévenon, Caroline Michot, Christine Bole, Patrick Nitschké, Mathilde Nizon, Laurence Faivre, Arnold Münnich, Stanislas Lyonnet, Jean‐Paul Bonnefont, Vincent des Portes, Jeanne Amiel	22
16	Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome 2014 ·Human Molecular Genetics ·Walid Abi Habib, Salah Azzi, Frédéric Brioude, Virginie Steunou, Nathalie Thibaud, (unknown), (unknown), Sandra Chantot‐Bastaraud, Boris Keren, Stanislas Lyonnet, Caroline Michot, Massimiliano Rossi, Laurent Pasquier, Christine Gicquel, Sylvie Rossignol, Yves Le Bouc, Irène Netchine	51
17	Parental mosaicism is a pitfall in preimplantation genetic diagnosis of dominant disorders 2013 ·European Journal of Human Genetics ·Julie Steffann, Caroline Michot, (unknown), (unknown), Sophie Monnot, Jean‐Paul Bonnefont, Arnold Münnich	5
18	Monozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid 2013 ·European Journal of Medical Genetics ·M. Essaoui, Mathilde Nizon, (unknown), (unknown), Julia Tantau, (unknown), (unknown), Caroline Michot, Jeanne Amiel, J. P. Bernard, Tania Attié‐Bitach, Michel Vekemans, C Turleau, Y. Ville, Valérie Malan	12
19	Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis 2012 ·The American Journal of Human Genetics ·Caroline Michot, Carine Le Goff, Alice Goldenberg, Avinash Abhyankar, Céline Klein, Esther Kinning, Anne‐Marie Guerrot, (unknown), (unknown), Geneviève Baujat, Stanislas Lyonnet, Caroline Thalassinos, Patrick Nitschké, Jean‐Laurent Casanova, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire	84
20	Treatment of multiple myeloma with etidronate: results of a multicentre double-blind study. Groupe d'Etudes et de Recherches sur le Myélome (GERM). 1994 ·PubMed ·A Daragon, (unknown), Caroline Michot, (unknown), B. Grosbois, (unknown), L Euller-Ziegler, I Azaïs, (unknown), (unknown)	32

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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