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New Horizons in Short Children Born Small for Gestational Age

Irène Netchine , Manouk van Der Steen , Abel López-Bermejo , Ekaterina Koledova , Mohamad Maghnie
Frontiers in Pediatrics, 2021, 9, pp.655931. ⟨10.3389/fped.2021.655931⟩
Journal articles hal-03244959v1
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11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome

Walid Abi Habib , Frederic Brioude , Salah Azzi , Jennifer Salem , Cristina das Neves , et al.
Human Mutation, 2017, 38 (1), pp.105-111. ⟨10.1002/humu.23131⟩
Journal articles hal-04026539v1
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Quality of life and mental health of adolescents and adults with Silver-Russell syndrome

Mélissa Burgevin , Agnès Lacroix , Karine Bourdet , Régis Coutant , Bruno Donadille , et al.
European Journal of Medical Genetics, 2022, 65 (5), pp.104482. ⟨10.1016/j.ejmg.2022.104482⟩
Journal articles hal-03629998v1
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A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome

Salah Azzi , Jennifer Salem , Nathalie Thibaud , Sandra Chantot-Bastaraud , Eli Lieber , et al.
Journal of Medical Genetics, 2015, 52 (7), pp.446-453. ⟨10.1136/jmedgenet-2014-102979⟩
Journal articles hal-01293084v1

National cohort on imprinting disorders and their metabolic consequences (RaDiCo-IDMet)

Eve Klising-Sireul , Radico Team , Irène Netchine , Agnès Linglart , Laure Jamot
4th ID school of the Imprinting disorder network, Mar 2017, Behoust, France
Conference papers inserm-04059036v1
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Growth Restriction and Genomic Imprinting-Overlapping Phenotypes Support the Concept of an Imprinting Network

Thomas Eggermann , Justin H Davies , Maithé Tauber , Erica van den Akker , Anita Hokken-Koelega , et al.
Genes, 2021, 12 (4), pp.585. ⟨10.3390/genes12040585⟩
Journal articles hal-03215322v1
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Maintenance of methylation profile in imprinting control regions in human induced pluripotent stem cells

A Pham , C Selenou , E Giabicani , V Fontaine , S Marteau , et al.
Clinical Epigenetics, 2022, 14, ⟨10.1186/s13148-022-01410-8⟩
Journal articles hal-03933584v1

11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome

Walid Abi Habib , Frederic Brioude , Salah Azzi , Jennifer Salem , Cristina das Neves , et al.
Human Mutation, 2017, 38 (1), pp.105-111. ⟨10.1002/humu.23131⟩
Journal articles inserm-04032178v1

Clinical characteristics, puberty pattern and adult or near-adult-height data in a group of patients with growth failure due to severe primary IGF-1 deficiency (GROWPATI study).

Athanasia Stoupa , Christine Lorraud , Isabelle Flechtner , Magali Viaud , Graziella Pinto , et al.
European Society for Paediatric Endocrinology 58th Annual Meeting, Sep 2019, Vienna, Austria
Conference poster inserm-04163446v1

Fetal and post-natal growth are impaired in children with deletions of the GH1 gene: description of a cohort of 14 patients. European Society for Paediatric

E Darvish , Marie Legendre , Irène Netchine , Serge Amselem , Frédéric Brioude
Endocrinology 58th Annual Meeting, Sep 2019, Vienna, Austria
Conference poster inserm-04159171v1
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IGF2: Development, Genetic and Epigenetic Abnormalities

Céline Sélénou , Frédéric Brioude , Eloïse Giabicani , Marie-Laure Sobrier , Irène Netchine
Cells, 2022, 11 (12), pp.1886. ⟨10.3390/cells11121886⟩
Journal articles hal-03711849v1
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Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth

Aurelie Pham , Delphine Mitanchez , Anne Forhan , Laurence Perin , Yves Le Bouc , et al.
Frontiers in Endocrinology, 2022, 13, pp.836731. ⟨10.3389/fendo.2022.836731⟩
Journal articles hal-04026820v1
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Increasing knowledge in IGF1R defects: lessons from 35 new patients

Eloïse Giabicani , Marjolaine Willems , Virginie Steunou , Sandra Chantot-Bastaraud , Nathalie Thibaud , et al.
Journal of Medical Genetics, In press, ⟨10.1136/jmedgenet-2019-106328⟩
Journal articles hal-02435128v1