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Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review2023 The Journal of Clinical Endocrinology & Metabolism article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Muriel Coupaye, Anthony Peter Goldstone, Charlotte Höybye, +9 more
13citations -
Role of mitochondrial function in the oxidative stress profile of children with Prader-Willi syndrome2025 Free Radical Biology and Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Álvaro Carrasco‐García, Guadalupe Herrera, Laura C. G. de Graaff, Jenny A. Visser, Francisco Dası́, Pilar Codoñer‐Franch
2citations -
Hypogonadism in Women with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion2021 Journal of Clinical Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Karlijn Pellikaan, Yassine Ben Brahim, Anna G. W. Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, +16 more
29citations -
Hypogonadism in Adult Males with Prader-Willi Syndrome—Clinical Recommendations Based on a Dutch Cohort Study, Review of the Literature and an International Expert Panel Discussion
Karlijn Pellikaan, Yassine Ben Brahim, Anna G. W. Rosenberg, Kirsten Davidse, Christine Poitou, Muriel Coupaye, +14 more
28citations -
Hyperprolactinemia in Adults with Prader-Willi Syndrome2021 Journal of Clinical Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Anna Sjöström, Karlijn Pellikaan, Henrik Sjöström, Anthony Peter Goldstone, Graziano Grugni, Antonino Crinò, +2 more
6citations -
Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review2023 Frontiers in Endocrinology review Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, +10 more
5citations -
In vivo structural neuroimaging evaluation of the hypothalamus in Prader-Willi Syndrome sub-genotypes2026 Journal of Rare Diseases article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Marten J. Peters, Esther M. Speksnijder, I. Caroline van Nieuwpoort, Alberto M. Pereira, Madeleine L. Drent, Dirk Jan Stenvers, +1 more
0citations -
Corrigendum: Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review2024 Frontiers in Endocrinology erratum Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Denise H. van Abswoude, Karlijn Pellikaan, Naomi Nguyen, Anna G. W. Rosenberg, Kirsten Davidse, Franciska M. E. Hoekstra, +10 more
0citations -
Bone Health in Adults With Prader–Willi Syndrome: Clinical Recommendations Based on a Multicenter Cohort Study2022 The Journal of Clinical Endocrinology & Metabolism article Medicine Bone health and osteoporosis research Open access
Denise H. van Abswoude, Karlijn Pellikaan, Anna G. W. Rosenberg, Kirsten Davidse, Muriel Coupaye, Charlotte Höybye, +13 more
20citations -
Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome2020 The Journal of Clinical Endocrinology & Metabolism article Medicine Adrenal Hormones and Disorders Open access
Anna G. W. Rosenberg, Karlijn Pellikaan, Christine Poitou, Anthony Peter Goldstone, Charlotte Höybye, Tania Markovic, +7 more
45citations -
Cognitive function during 3 years of growth hormone in previously growth hormone-treated young adults with Prader–Willi syndrome2023 European Journal of Endocrinology article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Demi J. Trueba-Timmermans, Lionne N. Grootjen, Alicia F. Juriaans, Eva F. Mahabier, Gerthe Femke Kerkhof, Edmond H.H.M. Rings, +1 more
9citations -
Health Problems in Adults with Prader–Willi Syndrome of Different Genetic Subtypes: Cohort Study, Meta-Analysis and Review of the Literature2022 Journal of Clinical Medicine article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Anna G. W. Rosenberg, Charlotte Wellink, Juan M. Tellez Garcia, Karlijn Pellikaan, Denise H. van Abswoude, Kirsten Davidse, +5 more
22citations -
PHIP-associated Chung-Jansen syndrome: Report of 23 new individuals2023 Frontiers in Cell and Developmental Biology article Biochemistry, Genetics and Molecular Biology Genomics and Rare Diseases Open access
Antje Kampmeier, Elsa Leitão, Ilaria Parenti, Jasmin Beygo, Christel Depienne, Nuria C. Bramswig, +31 more
24citations -
EndoCompass Project: Research Roadmap for Growth Disorders2025 Hormone Research in Paediatrics article Medicine Growth Hormone and Insulin-like Growth Factors Open access
Evelien F. Gevers, Anita C. S. Hokken‐Koelega, M. Tauber, Gerhard Binder, Elena G. Bochukova, Sébastien G. Bouret, +14 more
0citations -
EndoCompass project: research roadmap for growth disorders2025 European Journal of Endocrinology article Medicine Growth Hormone and Insulin-like Growth Factors Open access
Evelien F. Gevers, Anita C. S. Hokken‐Koelega, M. Tauber, Gerhard Binder, Elena G. Bochukova, Sébastien G. Bouret, +14 more
0citations -
Spinale Muskelatrophie (5q-SMA) bei unauffälligem Neugeborenenscreening: eine diagnostische Herausforderung2026 Zeitschrift für Geburtshilfe und Neonatologie article Medicine Neurogenetic and Muscular Disorders Research
H Cipowicz, Christine Pinkwart, H Proquitte, A Schulz, C Petersen, F Kraft, +3 more
0citations -
Copy Number Variants in the 11p15.5 Associated Imprinting Disorders: An Attempt to Establish a Genotype–Phenotype Correlation2026 Clinical Genetics article Biochemistry, Genetics and Molecular Biology Genetic Syndromes and Imprinting Open access
Anastasia Maria Licata, Elke Botzenhart, Katja Kloth‐Stachnau, Thomas Eggermann
0citations -
Clinical management of patients with genetic obesity during COVID-19 pandemic: position paper of the ESE Growth & Genetic Obesity COVID-19 Study Group and Rare Endo-ERN main thematic group on Growth and Obesity
C. Groot, Christine Poitou, Muriel Coupaye, Karine Clément, Stavroula Α. Paschou, Evangelia Charmandari, +7 more
9citations
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