Gwenaelle DIENE

25
Documents

Publications

Publications

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Longitudinal Changes in Acylated versus Unacylated Ghrelin Levels May Be Involved in the Underlying Mechanisms of the Switch in Nutritional Phases in Prader-Willi Syndrome

Lionne Grootjen , Gwenaelle Diene , Catherine Molinas , Véronique Beauloye , T Martin Huisman et al.
Hormone Research in Paediatrics, 2024, 97 (4), pp.343-352. ⟨10.1159/000534560⟩
Article dans une revue hal-04946162 v1

Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader–Willi syndrome

Rachel Debs , Gwenaëlle Diene , Julie Cortadellas , Catherine Molinas , Marc Kermorgant et al.
Clinical Autonomic Research, 2024, 35 (2), pp.243-255. ⟨10.1007/s10286-024-01083-8⟩
Article dans une revue hal-04946149 v1
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Liraglutide for Weight Management in Children and Adolescents With Prader–Willi Syndrome and Obesity

Gwenaëlle Diene , Moris Angulo , Paula M Hale , Cecilie H Jepsen , Paul L Hofman et al.
Journal of Clinical Endocrinology and Metabolism, 2023, 108 (1), pp.4-12. ⟨10.1210/clinem/dgac549⟩
Article dans une revue hal-04233036 v1

Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young Adults

Gaëlle Nannette , Céline Bar , Gwenaëlle Diene , Catherine Pienkowski , Isabelle Oliver-Petit et al.
Journal of Clinical Endocrinology and Metabolism, 2023, 108 (2), pp.323-330. ⟨10.1210/clinem/dgac583⟩
Article dans une revue hal-04233001 v1
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A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

Anne-Sophie Denommé-Pichon , Leslie Matalonga , Elke de Boer , Adam Jackson , Elisa Benetti et al.
Genetics in Medicine, 2023, 25 (4), pp.100018. ⟨10.1016/j.gim.2023.100018⟩
Article dans une revue hal-05290572 v1
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What underlies emotion regulation abilities? An innovative programme based on an integrative developmental approach to improve emotional competencies: Promising results in children with Prader–Willi syndrome

Nawelle Famelart , Gwenaelle Diene , Sophie Çabal-Berthoumieu , Mélanie Glattard , Catherine Molinas et al.
Frontiers in Psychiatry, 2022, 13, pp.1038223. ⟨10.3389/fpsyt.2022.1038223⟩
Article dans une revue hal-04946279 v1

First step towards a consensus strategy for multi-locus diagnostic testing of imprinting disorders

Deborah Mackay , Jet Bliek , Masayo Kagami , Jair Tenorio-Castano , Arrate Pereda et al.
Clinical Epigenetics, 2022, 14 (1), pp.143. ⟨10.1186/s13148-022-01358-9⟩
Article dans une revue hal-04946295 v1
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Impact of Deprivation on Obesity in Children with PWS

Sabrina Grolleau , Marine Delagrange , Melina Souquiere , Catherine Molinas , Gwenaëlle Diene et al.
Journal of Clinical Medicine, 2022, 11 (8), pp.2255. ⟨10.3390/jcm11082255⟩
Article dans une revue hal-04233601 v1
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SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome

Sanaa Eddiry , Gwenaelle Diene , Catherine Molinas , Juliette Salles , Françoise Conte Auriol et al.
Genetics in Medicine, 2021, 23 (9), pp.1664-1672. ⟨10.1038/s41436-021-01185-y⟩
Article dans une revue hal-04946344 v1
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Is ghrelin a biomarker of early-onset scoliosis in children with Prader–Willi syndrome?

Dibia Liz Pacoricona Alfaro , Gwenaelle Diene , Graziella Pinto , Jean-Pierre Salles , Isabelle Gennero et al.
Orphanet Journal of Rare Diseases, 2021, 16 (1), pp.305. ⟨10.1186/s13023-021-01930-1⟩
Article dans une revue hal-03763771 v1
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Diabetes Mellitus in Prader-Willi Syndrome: Natural History during the Transition from Childhood to Adulthood in a Cohort of 39 Patients

Alice Clerc , Muriel Coupaye , Héléna Mosbah , Graziella Pinto , Virginie Laurier et al.
Journal of Clinical Medicine, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩
Article dans une revue hal-03457276 v1
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Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients

Muriel Coupaye , Virginie Laurier , Grégoire Benvegnu , Christine Poitou , Pauline Faucher et al.
Orphanet Journal of Rare Diseases, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩
Article dans une revue hal-03298534 v1

Evolution of Hip Dysplasia in Pediatric Patients With Prader-Willi Syndrome Treated With Growth Hormone Early in Development

Pierre Laumonerie , Meagan Tibbo , Aissa Ibnoulkhatib , Panagiotis Kerezoudis , Gwenaëlle Diene et al.
Journal of Pediatric Orthopaedics, 2020, 40 (5), pp.e357-e361. ⟨10.1097/BPO.0000000000001443⟩
Article dans une revue hal-04542369 v1
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Equivocal expression of emotions in children with Prader-Willi syndrome : what are the consequences for emotional abilities and social adjustment?

Nawelle Famelart , Gwenaëlle Diene , Sophie Çabal-Berthoumieu , Mélanie Glattard , Catherine Molinas et al.
Orphanet Journal of Rare Diseases, 2020, 15 (1), pp.55. ⟨10.1186/s13023-020-1333-9⟩
Article dans une revue hal-02502455 v1
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Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center

Dibia Liz Pacoricona Alfaro , Perrine Lemoine , Virginie Ehlinger , Catherine Molinas , Gwénaëlle Diene et al.
Orphanet Journal of Rare Diseases, 2019, 14 (1), pp.238. ⟨10.1186/s13023-019-1214-2⟩
Article dans une revue hal-04946367 v1

Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing

Ange-Line Bruel , Sophie Nambot , Virginie Quéré , Antonio Vitobello , Julien Thevenon et al.
European Journal of Human Genetics, 2019, 27 (10), pp.1519-1531. ⟨10.1038/s41431-019-0442-1⟩
Article dans une revue hal-04947373 v1
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AZP-531, an unacylated ghrelin analog, improves food-related behavior in patients with Prader-Willi syndrome: A randomized placebo-controlled trial

Soraya Allas , Assumpta Caixàs , Christine Poitou , Muriel Coupaye , Denise Thuilleaux et al.
PLoS ONE, 2018, 13 (1), pp.e0190849. ⟨10.1371/journal.pone.0190849⟩
Article dans une revue hal-04013074 v1

The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader–Willi Syndrome

Maïthé Tauber , Kader Boulanouar , Gwenaelle Diene , Sophie Çabal-Berthoumieu , Virginie Ehlinger et al.
Pediatrics, 2017, 139 (2), pp.e20162976. ⟨10.1542/peds.2016-2976⟩
Article dans une revue hal-03436895 v1

Apprendre les émotions aux enfants porteurs d’un syndrome de Prader-Willi : le programme EMOT

Nawelle Famelart , Gwenaëlle Diene , Sophie Çabal-Berthoumieu , Mélanie Glattard , Maïthé Tauber et al.
Enfance, 2017, 69 (4), pp.563-569
Article dans une revue hal-02052706 v1
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Dyssynchrony and perinatal psychopathology impact of child disease on parents-child interactions, the paradigm of Prader Willi syndrom

Sylvie Viaux-Savelon , Ouriel Rosenblum , Antoine Guedeney , Gwenaëlle Diene , Sophie Çabal-Berthoumieu et al.
Journal of Physiology - Paris, 2016, 110 (4), pp.427 - 433. ⟨10.1016/j.jphysparis.2017.08.001⟩
Article dans une revue hal-01685410 v1
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Oxytocin may be useful to increase trust in others and decrease disruptive behaviours in patients with Prader-Willi syndrome: a randomised placebo-controlled trial in 24 patients.

Maïthé Tauber , Carine Mantoulan , Pierre Copet , Joseba Jauregui , Genevieve Demeer et al.
Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.47. ⟨10.1186/1750-1172-6-47⟩
Article dans une revue inserm-00663634 v1

Necdin plays a role in the serotonergic modulation of the mouse respiratory network: implication for Prader-Willi syndrome.

Sébastien Zanella , Françoise Watrin , Saïda Mebarek , Fabienne Marly , Michel Roussel et al.
Journal of Neuroscience, 2008, 28 (7), pp.1745-55. ⟨10.1523/JNEUROSCI.4334-07.2008⟩
Article dans une revue hal-00321665 v1

Prader–Willi syndrome: Hormone therapies

Maithé Tauber , Gwenaelle Diene
Dick F. Swaab; Ruud M. Buijs; Paul J. Lucassen; Ahmad Salehi; Felix Kreier. The Human Hypothalamus - Neuroendocrine Disorders, 181, Elsevier, pp.351-367, 2021, Handbook of Clinical Neurology, ⟨10.1016/B978-0-12-820683-6.00026-9⟩
Chapitre d'ouvrage hal-03764492 v1

Prader-Willi Syndrome as a Model of Human Hyperphagia

Maithe Tauber , Gwenaelle Diene , Emmanuelle Mimoun , Sophie Çabal-Berthoumieu , Carine Mantoulan et al.
How Gut and Brain Control Metabolism, 42, S. KARGER AG, pp.93-106, 2014, Frontiers of Hormone Research, ⟨10.1159/000358317⟩
Chapitre d'ouvrage hal-03436957 v1

Gonadal function of female patients with Noonan syndrome

Sophie Moniez , Yline Capri , Catherine Pienkowski , Benoît Lepage , Safouane Mohammed Hamdi et al.
58th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Sep 2019, Vienne (Austria), Austria. HORMONE RESEARCH INPÆDIATRICS, 91 (S1), pp.P1-139, 2019
Poster de conférence hal-04888195 v1