Gwenaelle DIENE

Publications

Article dans une revue (23)

Genomic newborn screening as a paradigm shift in rare disease management, with emphasis on endocrine conditions Laurence Faivre,Camille Level,Régis Coutant,Patrice Rodien,Anne Barlieret al. Annales d'Endocrinologie = Annals of Endocrinology, 2026, pp.102517. ⟨10.1016/j.ando.2026.102517⟩ Article dans une revue hal-05582204v1
Early oxytocin treatment in infants with Prader–Willi syndrome is safe and is associated with better endocrine, metabolic and behavioral outcomes Marion Valette,Gwenaelle Diene,Mélanie Glattard,Julie Cortadellas,Catherine Molinaset al. Orphanet Journal of Rare Diseases, 2025, 20 (1), pp.96. ⟨10.1186/s13023-025-03560-3⟩ Article dans une revue hal-05524049v1
Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader–Willi syndrome Rachel Debs,Gwenaëlle Diene,Julie Cortadellas,Catherine Molinas,Marc Kermorgantet al. Clinical Autonomic Research, 2024, 35 (2), pp.243-255. ⟨10.1007/s10286-024-01083-8⟩ Article dans une revue hal-04946149v1
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 Huismanet al. Hormone Research in Paediatrics, 2024, 97 (4), pp.343-352. ⟨10.1159/000534560⟩ Article dans une revue hal-04946162v1
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 Hofmanet al. Journal of Clinical Endocrinology and Metabolism, 2023, 108 (1), pp.4-12. ⟨10.1210/clinem/dgac549⟩ Article dans une revue hal-04233036v1
Obesity, Overweight, and Pituitary Stalk Interruption Syndrome in Children and Young Adults Gaëlle Nannette,Céline Bar,Gwenaëlle Diene,Catherine Pienkowski,Isabelle Oliver-Petitet al. Journal of Clinical Endocrinology and Metabolism, 2023, 108 (2), pp.323-330. ⟨10.1210/clinem/dgac583⟩ Article dans une revue hal-04233001v1
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 Benettiet al. Genetics in Medicine, 2023, 25 (4), pp.100018. ⟨10.1016/j.gim.2023.100018⟩ Article dans une revue hal-05290572v1
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 Molinaset al. Frontiers in Psychiatry, 2022, 13, pp.1038223. ⟨10.3389/fpsyt.2022.1038223⟩ Article dans une revue hal-04946279v1
Impact of Deprivation on Obesity in Children with PWS Sabrina Grolleau,Marine Delagrange,Melina Souquiere,Catherine Molinas,Gwenaëlle Dieneet al. Journal of Clinical Medicine, 2022, 11 (8), pp.2255. ⟨10.3390/jcm11082255⟩ Article dans une revue hal-04233601v1
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 Genneroet al. Orphanet Journal of Rare Diseases, 2021, 16 (1), pp.305. ⟨10.1186/s13023-021-01930-1⟩ Article dans une revue hal-03763771v1
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 Laurieret al. Journal of Clinical Medicine, 2021, 10 (22), pp.5310. ⟨10.3390/jcm10225310⟩ Article dans une revue hal-03457276v1
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 Faucheret al. Orphanet Journal of Rare Diseases, 2021, 16, pp.325. ⟨10.1186/s13023-021-01949-4⟩ Article dans une revue hal-03298534v1
SNORD116 and growth hormone therapy impact IGFBP7 in Prader–Willi syndrome Sanaa Eddiry,Gwenaelle Diene,Catherine Molinas,Juliette Salles,Françoise Conte Auriolet al. Genetics in Medicine, 2021, 23 (9), pp.1664-1672. ⟨10.1038/s41436-021-01185-y⟩ Article dans une revue hal-04946344v1
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 Dieneet al. Journal of Pediatric Orthopaedics, 2020, 40 (5), pp.e357-e361. ⟨10.1097/BPO.0000000000001443⟩ Article dans une revue hal-04542369v1
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 Molinaset al. Orphanet Journal of Rare Diseases, 2020, 15 (1), pp.55. ⟨10.1186/s13023-020-1333-9⟩ Article dans une revue hal-02502455v1
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 Dieneet al. Orphanet Journal of Rare Diseases, 2019, 14 (1), pp.238. ⟨10.1186/s13023-019-1214-2⟩ Article dans une revue hal-04946367v1
Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing Ange-Line Bruel,Sophie Nambot,Virginie Quéré,Antonio Vitobello,Julien Thevenonet al. European Journal of Human Genetics, 2019, 27 (10), pp.1519-1531. ⟨10.1038/s41431-019-0442-1⟩ Article dans une revue hal-04947373v1
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 Thuilleauxet al. PLoS ONE, 2018, 13 (1), pp.e0190849. ⟨10.1371/journal.pone.0190849⟩ Article dans une revue hal-04013074v1
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 Ehlingeret al. Pediatrics, 2017, 139 (2), pp.e20162976. ⟨10.1542/peds.2016-2976⟩ Article dans une revue hal-03436895v1
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 Tauberet al. Enfance, 2017, 69 (4), pp.563-569 Article dans une revue hal-02052706v1
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-Berthoumieuet al. Journal of Physiology - Paris, 2016, 110 (4), pp.427 - 433. ⟨10.1016/j.jphysparis.2017.08.001⟩ Article dans une revue hal-01685410v1
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 Demeeret al. Orphanet Journal of Rare Diseases, 2011, 6 (1), pp.47. ⟨10.1186/1750-1172-6-47⟩ Article dans une revue inserm-00663634v1
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 Rousselet al. Journal of Neuroscience, 2008, 28 (7), pp.1745-55. ⟨10.1523/JNEUROSCI.4334-07.2008⟩ Article dans une revue hal-00321665v1

Chapitre d'ouvrage (2)

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-03764492v1
Prader-Willi Syndrome as a Model of Human Hyperphagia Maithe Tauber,Gwenaelle Diene,Emmanuelle Mimoun,Sophie Çabal-Berthoumieu,Carine Mantoulanet 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-03436957v1

Poster de conférence (1)

Gonadal function of female patients with Noonan syndrome Sophie Moniez,Yline Capri,Catherine Pienkowski,Benoît Lepage,Safouane Mohammed Hamdiet 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-04888195v1