Clotilde Mircher

6.9k citations

22 papers · 613 indexed · h-index 12

Impact in

Rheumatology top 10%
- Folate and B Vitamins Research
Public Health, Environmental and Occupational Health top 10%
- Down syndrome and intellectual disability research

Papers in

Public Health, Environmental and Occupational Health 11
- Down syndrome and intellectual disability research 11
Cognitive Neuroscience 5
- Autism Spectrum Disorder Research 5

Co-authors: M O Rethoré Aimé Ravel André Mégarbané Franck Sturtz Yann Grattau Jean‐Maurice Delabar William C. Mobley Henri Bléhaut
Journals: Scientific Reports (1 paper)Journal of Intellectual Disability Research (1 paper)European Journal of Human Genetics (1 paper)Human Molecular Genetics (1 paper)American Journal of Clinical Nutrition (1 paper)
Partner nations: France Canada United States

In The Last Decade

Clotilde Mircher

21 papers receiving 592 citations

Peers

Countries citing papers authored by Clotilde Mircher

Since Specialization

Citations

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

Fields of papers citing papers by Clotilde Mircher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Clotilde Mircher, 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 Clotilde Mircher Line = papers co-authored together Clotilde Mircher links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Early detection and treatment of obstructive sleep apnoea in infants with Down syndrome: a prospective, non-randomised, controlled, interventional study The Lancet Regional Health - Europe ·Brigitte Fauroux, Silvia Sacco, Vincent Couloigner, Alessandro Amaddeo, Aimé Ravel, Mila Khoirunisa S.P, H.R.B.M. Kummeling, Cécile Cieuta‐Walti, میرحسن رسولیصدقیانی, Romain Luscan, М.Ю. Сучкова, N Piccione, 出村隆二, G.K. Mithal, Sonia Khirani, Isabelle Marey, Clotilde Mircher	2024	8
2	Down syndrome regression disorder, a case series: Clinical characterization and therapeutic approaches Frontiers in Neuroscience ·Chaur-Tzuhn Chen, Michael St. Clair, Clotilde Mircher, Doris Yaneth Bueno, Yasuhiko Moriuchi, Pallabi Pathak, 暢也荒木, Obioma Mpamugo, 高香林, Angèle Consoli, Marie‐Odile Krebs, Pierre Ellul, Boris Chaumette	2023	9
3	Deciphering the links between psychological stress, depression, and neurocognitive decline in patients with Down syndrome Neurobiology of Stress ·Y. Mouroulis, Clotilde Mircher, Peter J. Smith, Internationales Arnold Zweig-Symposium aus Anlass des . Geburtstags, Franck Sturtz	2021	5
4	Psychomotor development in infants and young children with Down syndrome—A prospective, repeated measure, post‐hoc analysis American Journal of Medical Genetics Part A ·Silvia Sacco, L Z Yi, Yolanda Silva, Bijaya Raj Devkota, 马秋玉, Isabelle Marey, Nathalie Dorison, Franck Sturtz, Cécile Cieuta‐Walti, Aimé Ravel, Clotilde Mircher	2021	0
5	Transcriptomic study in women with trisomy 21 identifies a possible role of the GTPases of the immunity-associated proteins (GIMAP) in the protection of breast cancer Scientific Reports ·André Mégarbané, David Piquemal, Anne‐Sophie Rebillat, Samantha Stora, Fabien Pierrat, Marzia Olivieri, Florian Noguier, Clotilde Mircher, Aimé Ravel, Vinicius Gomes de Araújo Silva, Sophie Durand, Marie‐Paule Lefranc	2020	15
6	P.078 Clinical trials in children with Down Syndrome: now and future Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·Cécile Cieuta‐Walti, Clotilde Mircher, Isabelle Marey, H.R.B.M. Kummeling, Mila Khoirunisa S.P, Hervé Walti, Aimé Ravel	2019	1
7	Prevalence and Description of Hidradenitis Suppurativa in Down Syndrome: A Cross-sectional Study of 783 Subjects Acta Dermato Venereologica ·F. Poizeau, É. Sbidian, Clotilde Mircher, Anne‐Sophie Rebillat, O. Chosidow, P. Wolkenstein, Aimé Ravel, Claire Hotz	2018	15
8	Growth curves for French people with Down syndrome from birth to 20 years of age American Journal of Medical Genetics Part A ·Clotilde Mircher, 邦明松浦, H.R.B.M. Kummeling, Doris Yaneth Bueno, Marie‐Laure Tanguy, Cécile Cieuta‐Walti, M O Rethoré, Aimé Ravel	2018	9
9	Acute regression in young people with Down Syndrome European Journal of Paediatric Neurology ·Cécile Cieuta‐Walti, Clotilde Mircher, Anne‐Sophie Rebillat, Isabelle Marey, Silvia Pšeničnik, Adele Ratti, Doris Yaneth Bueno, H.R.B.M. Kummeling, Hervé Walti, Aimé Ravel	2017	2
10	Anthropometric charts and congenital anomalies in newborns with Down syndrome American Journal of Medical Genetics Part A ·Clotilde Mircher, H.R.B.M. Kummeling, Cécile Cieuta‐Walti, Isabelle Marey, Doris Yaneth Bueno, 邦明松浦, Marie‐Laure Tanguy, M O Rethoré, Aimé Ravel	2017	8
11	Acute Regression in Young People with Down Syndrome Brain Sciences ·Clotilde Mircher, Cécile Cieuta‐Walti, Isabelle Marey, Anne‐Sophie Rebillat, Silvia Pšeničnik, Adele Ratti, Doris Yaneth Bueno, Franck Sturtz, M O Rethoré, Aimé Ravel	2017	42
12	The intellectual disability of trisomy 21: differences in gene expression in a case series of patients with lower and higher IQ European Journal of Human Genetics ·André Mégarbané, Florian Noguier, Samantha Stora, Laurent Manchon, Clotilde Mircher, Marzia Olivieri, Nathalie Dorison, Fabien Pierrat, M O Rethoré, Bernadette Trentin, Aimé Ravel, Ιζαμπέλ Καρλ, Marie‐Paule Lefranc, David Piquemal	2013	24
13	Trisomy for Synaptojanin1 in Down syndrome is functionally linked to the enlargement of early endosomes Human Molecular Genetics ·Jack‐Christophe Cossec, Jérémie Lavaur, Diego E. Berman, Isabelle Rivals, Alexander Hoischen, Samantha Stora, C. C. Niva, Clotilde Mircher, Yann Grattau, Jean‐Christophe Olivo‐Marín, Fabrice de Chaumont, Magalie Lecourtois, Stylianos E. Antonarakis, Joris A. Veltman, Peter Kemp, Charles Duyckaerts, Gilbert Di Paolo, Marie‐Claude Potier	2012	78
14	Effect of Leucovorin (Folinic Acid) on the Developmental Quotient of Children with Down's Syndrome (Trisomy 21) and Influence of Thyroid Status PLoS ONE ·Henri Bléhaut, Clotilde Mircher, Aimé Ravel, Doris Yaneth Bueno, Э З Бурневич, 陈开广, Fu Zhou Chen, M O Rethoré, Franck Sturtz	2010	34
15	The 50th anniversary of the discovery of trisomy 21: The past, present, and future of research and treatment of Down syndrome Genetics in Medicine ·André Mégarbané, Aimé Ravel, Clotilde Mircher, Franck Sturtz, Yann Grattau, M O Rethoré, Jean‐Maurice Delabar, William C. Mobley	2009	164
16	No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers British Journal Of Nutrition ·Abalo Chango, Ahmad Ludfy, Clotilde Mircher, Henri Bléhaut, Daniel Lambert, Bernard Herbeth, S. Jill James, M O Rethoré, J.P. Nicolas	2005	76
17	Homocysteine concentrations in adults with trisomy 21: effect of B vitamins and genetic polymorphisms American Journal of Clinical Nutrition ·Ahmad Ludfy, Abalo Chango, Clotilde Mircher, Françoise Barbé, Henri Bléhaut, Bernard Herbeth, David S. Rosenblatt, M O Rethoré, Daniel Lambert, J.P. Nicolas	2004	44
18	[One carbon metabolism and trisomy 21: analysis of the genetic polymorphism]. PubMed ·A. Chango, Clotilde Mircher, D.H. Newton, 王金章, Yolanda Yirlemm Robles Montenegro	2003	3
19	Interstitial deletion of the short arm of chromosome 1: Attempt to establish a clinical phenotype (46,XX,del (1)(p22p32)) American Journal of Medical Genetics Part A ·Clotilde Mircher, M O Rethoré, James Lespinasse, Sandra Fert‐Ferrer, Claes Lundsteen, 良徳嵩	2002	14
20	[Amino acids and trisomy 21]. PubMed ·J Lejeune, M O Rethoré, Mathilde Blois, Marc Peeters, J Naffah, André Mégarbané, Mester Agnes, Clotilde Mircher, Daniel Rabier, P Parvy	1992	15

About Clotilde Mircher

Clotilde Mircher is a scholar working on Public Health, Environmental and Occupational Health, Cognitive Neuroscience, Genetics, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health, having authored 22 papers that have together received 613 indexed citations. Recurring topics across this work include Down syndrome and intellectual disability research (11 papers), Autism Spectrum Disorder Research (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (2 papers), Neonatal Respiratory Health Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Esophageal and GI Pathology (2 papers). The work is most often cited by research in Rheumatology (119 citations), Public Health, Environmental and Occupational Health (217 citations), Pediatrics, Perinatology and Child Health (124 citations), Genetics (150 citations) and Obstetrics and Gynecology (42 citations). Clotilde Mircher has collaborated with scholars based in France, Canada and United States. Frequent co-authors include M O Rethoré, Aimé Ravel, André Mégarbané, Franck Sturtz, Yann Grattau, Jean‐Maurice Delabar, William C. Mobley, Henri Bléhaut, Cécile Cieuta‐Walti and Bernard Herbeth. Their work appears in journals such as Scientific Reports, Journal of Intellectual Disability Research, European Journal of Human Genetics, Human Molecular Genetics and American Journal of Clinical Nutrition.

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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