Éloïse Giabicani

1.2k total citations
24 papers, 358 citations indexed

About

Éloïse Giabicani is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Éloïse Giabicani has authored 24 papers receiving a total of 358 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 14 papers in Molecular Biology and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Éloïse Giabicani's work include Genetic Syndromes and Imprinting (15 papers), Epigenetics and DNA Methylation (11 papers) and Prenatal Screening and Diagnostics (6 papers). Éloïse Giabicani is often cited by papers focused on Genetic Syndromes and Imprinting (15 papers), Epigenetics and DNA Methylation (11 papers) and Prenatal Screening and Diagnostics (6 papers). Éloïse Giabicani collaborates with scholars based in France, United Kingdom and United States. Éloïse Giabicani's co-authors include Irène Netchine, Frédéric Brioude, Marie‐Laure Sobrier, Raja Brauner, Annick Toutain, Valérie Cormier‐Daire, Delphine Mitanchez, Yves Le Bouc, Salah Azzi and Sylvie Rossignol and has published in prestigious journals such as PLoS ONE, Annals of the New York Academy of Sciences and Science Advances.

In The Last Decade

Éloïse Giabicani

23 papers receiving 353 citations

Peers

Countries citing papers authored by Éloïse Giabicani

Since Specialization

Citations

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

Fields of papers citing papers by Éloïse Giabicani

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Éloïse Giabicani

This figure shows the co-authorship network connecting the top 25 collaborators of Éloïse Giabicani. A scholar is included among the top collaborators of Éloïse Giabicani 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 Éloïse Giabicani. Éloïse Giabicani 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	Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylation 2024 ·Frontiers in Pediatrics ·(unknown), Éloïse Giabicani, Irène Netchine, (unknown)	0
2	Imprinting disorders 2023 ·Nature Reviews Disease Primers ·Thomas Eggermann, David Monk, Guiomar Pérez de Nanclares, Masayo Kagami, Éloïse Giabicani, Andrea Riccio, Zeynep Tümer, Jennifer M. Kalish, M. Tauber, Jessica Duis, Rosanna Weksberg, Eamonn R. Maher, Matthias Begemann, Miriam Elbracht	34
3	IGF2: Development, Genetic and Epigenetic Abnormalities 2022 ·Cells ·(unknown), Frédéric Brioude, Éloïse Giabicani, Marie‐Laure Sobrier, Irène Netchine	57
4	Impact of claudin‐10 deficiency on amelogenesis: Lesson from a HELIX tooth 2022 ·Annals of the New York Academy of Sciences ·(unknown), Adeline Le Cabec, (unknown), Éloïse Giabicani, Stijn J. M. Van Malderen, Jan Garrevoet, Aline Percot, Céline Paris, Christopher Dean, S. Hadj‐Rabia, Pascal Houillier, Tilman Breiderhoff, Claire Bardet, Thibaud Coradin, Fernando Ramírez Rozzi, Catherine Chaussain	4
5	Dental pulp stem cells as a promising model to study imprinting diseases 2022 ·International Journal of Oral Science ·Éloïse Giabicani, (unknown), (unknown), Marie‐Laure Sobrier, (unknown), Julie Lesieur, Agnès Linglart, Anne Poliard, Catherine Chaussain, Irène Netchine	5
6	Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells 2022 ·Clinical Epigenetics ·(unknown), (unknown), Éloïse Giabicani, Vincent Fontaine, (unknown), Frédéric Brioude, Laurent David, Delphine Mitanchez, Marie‐Laure Sobrier, Irène Netchine	4
7	Height and body mass index in molecularly confirmed Silver–Russell syndrome and the long‐term effects of growth hormone treatment 2022 ·Clinical Endocrinology ·Oluwakemi Lokulo‐Sodipe, Éloïse Giabicani, Ana Pinheiro Machado Canton, (unknown), (unknown), Emma Wakeling, Gerhard Binder, Irène Netchine, Deborah Mackay, Hazel Inskip, Christopher D. Byrne, I. Karen Temple, Justin H. Davies	6
8	Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants 2021 ·European Journal of Human Genetics ·(unknown), Marie‐Laure Sobrier, Éloïse Giabicani, (unknown), Delphine Mitanchez, Frédéric Brioude, Irène Netchine	3
9	Case report of nutritional rickets in an infant following a vegan diet 2020 ·Archives de Pédiatrie ·(unknown), Éloïse Giabicani, (unknown), E. Grimprel, Patrick Tounian	13
10	Paroxysmal strabismus and stridor acquired in childhood: Do not overlook calcemia! 2020 ·Archives de Pédiatrie ·(unknown), Éloïse Giabicani, Bénédicte Neven, (unknown), M. Blanchard, Arnaud Isapof, (unknown), (unknown)	1
11	Overgrowth syndromes — clinical and molecular aspects and tumour risk 2019 ·Nature Reviews Endocrinology ·Frédéric Brioude, Annick Toutain, Éloïse Giabicani, (unknown), Valérie Cormier‐Daire, Irène Netchine	56
12	Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders 2019 ·Science Advances ·Walid Abi Habib, Frédéric Brioude, Salah Azzi, Sylvie Rossignol, Agnès Linglart, Marie‐Laure Sobrier, Éloïse Giabicani, Virginie Steunou, Madeleine D. Harbison, Yves Le Bouc, Irène Netchine	33
13	Sleep disordered breathing in Silver−Russell syndrome patients: a new outcome 2019 ·Sleep Medicine ·Éloïse Giabicani, Michèle Boulé, Guillaume Aubertin, (unknown), Frédéric Brioude, Béatrice Dubern, Irène Netchine	5
14	Roles of Type 1 Insulin-Like Growth Factor (IGF) Receptor and IGF-II in Growth Regulation: Evidence From a Patient Carrying Both an 11p Paternal Duplication and 15q Deletion 2019 ·Frontiers in Endocrinology ·Éloïse Giabicani, Sandra Chantot‐Bastaraud, (unknown), (unknown), Sandra Whalen, Irène Netchine, Frédéric Brioude	8
15	Diagnosis and management of postnatal fetal growth restriction 2018 ·Best Practice & Research Clinical Endocrinology & Metabolism ·Éloïse Giabicani, (unknown), Frédéric Brioude, Delphine Mitanchez, Irène Netchine	24
16	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
17	Imprinted disorders and growth 2017 ·Annales d Endocrinologie ·Éloïse Giabicani, Frédéric Brioude, Yves Le Bouc, Irène Netchine	5
18	Chronic intestinal pseudo-obstruction in a child with Treacher Collins syndrome 2017 ·Archives de Pédiatrie ·Éloïse Giabicani, Julie Lemale, Linda Dainese, Sabah Boudjemaa, Aurore Coulomb, P. Tounian, B. Dubern	2
19	Sleep Apneas in Silver Russell Syndrome: A Constant Finding 2015 ·Éloïse Giabicani, Michèle Boulé, (unknown), Irène Netchine	2
20	Presentation of 493 Consecutive Girls with Idiopathic Central Precocious Puberty: A Single-Center Study 2013 ·PLoS ONE ·Éloïse Giabicani, Slimane Allali, (unknown), (unknown), (unknown), Raja Brauner	30

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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