The Narrative of a Patient with Leptin Receptor Deficiency: Personalized Medicine for a Rare Genetic Obesity Disorder by Mila S. Welling, Lotte Kleinendorst, Mieke M. van Haelst, Erica L. T. van den Akker

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Structural Models for the Dynamic Effects of Loss-of-Function Variants in the Human SIM1 Protein Transcriptional Activation Domain by Mathew A. Coban, Patrick R. Blackburn, Murray L. Whitelaw, Mieke M. van Haelst, Paldeep S. Atwal, Thomas R. Caulfield

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Genetic analysis in the bariatric clinic; impact of a PTEN gene mutation by Mellody I. Cooiman, Lotte Kleinendorst, Bert van derZwaag, Ignace M. C. Janssen, Frits J. Berends, Mieke M. van Haelst

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Successful naltrexone-bupropion treatment after several treatment failures in a patient with severe monogenic obesity by Mila S. Welling, Mostafa Mohseni, Eline S. van der Valk, Johanna M. van Hagen, Jan Steven Burgerhart, Mieke M. van Haelst, Elisabeth F.C. van Rossum

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<em>GMDS</em> Intragenic Deletions Associate with Congenital Heart Disease including Ebstein Anomaly by Shirley M. Lo-A-Njoe, Eline A. Verberne, Lars T. van der Veken, Eric Arends, J. Peter van Tintelen, Alex V. Postma, Mieke M. van Haelst

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Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders by Federico Tessadori, Helen I. Roessler, Sanne M. C. Savelberg, Sonja Chocron, Sarah M. Kamel, Karen J. Duran, Mieke M. van Haelst, Gijs van Haaften, Jeroen Bakkers

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Extensive Phenotyping for Potential Weight-Inducing Factors in an Outpatient Population with Obesity by Mesut Savas, Vincent L. Wester, Jenny A. Visser, Lotte Kleinendorst, Bert van der Zwaag, Mieke M. van Haelst, Erica L.T. van den Akker, Elisabeth F.C. van Rossum

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Erratum: Identifying underlying medical causes of pediatric obesity: Results of a systematic diagnostic approach in a pediatric obesity center. by Lotte Kleinendorst, Ozair Abawi, Bibian van der Voorn, Mieke H T M Jongejan, Annelies E Brandsma, Jenny A Visser, Elisabeth F C van Rossum, Bert van der Zwaag, Mariëlle Alders, Elles M J Boon, Mieke M van Haelst, Erica L T van den Akker

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Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism. by Suzanne I M Alsters, Anthony P Goldstone, Jessica L Buxton, Anna Zekavati, Alona Sosinsky, Andrianos M Yiorkas, Susan Holder, Robert E Klaber, Nicola Bridges, Mieke M van Haelst, Carel W le Roux, Andrew J Walley, Robin G Walters, Michael Mueller, Alexandra I F Blakemore

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The Diagnostic Journey of a Patient with Prader–Willi-Like Syndrome and a Unique Homozygous <i>SNURF-SNRPN</i> Variant; Bio-Molecular Analysis and Review of the Literature by Karlijn Pellikaan, Geeske M. van Woerden, Lotte Kleinendorst, Anna G. W. Rosenberg, Bernhard Horsthemke, Christian Grosser, Laura J. C. M. van Zutven, Elisabeth F. C. van Rossum, Aart J. van der Lely, James L. Resnick, Hennie T. Brüggenwirth, Mieke M. van Haelst, Laura C. G. de Graaff

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Functional Insight into and Refinement of the Genomic Boundaries of the <i>JARID2</i>-Neurodevelopmental Disorder Episignature by Liselot van der Laan, Kathleen Rooney, Sadegheh Haghshenas, Ananília Silva, Haley McConkey, Raissa Relator, Michael A. Levy, Irene Valenzuela, Laura Trujillano, Amaia Lasa-Aranzasti, Berta Campos, Neus Castells, Eline A. Verberne, Saskia Maas, Mariëlle Alders, Marcel M. A. M. Mannens, Mieke M. van Haelst, Bekim Sadikovic, Peter Henneman

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DNA Methylation Signature for <i>JARID2</i>-Neurodevelopmental Syndrome by Eline A. Verberne, Liselot van der Laan, Sadegheh Haghshenas, Kathleen Rooney, Michael A. Levy, Mariëlle Alders, Saskia M. Maas, Sandra Jansen, Agne Lieden, Britt-Marie Anderlid, Louise Rafael-Croes, Philippe M. Campeau, Ayeshah Chaudhry, David A. Koolen, Rolph Pfundt, Anna C. E. Hurst, Frederic Tran-Mau-Them, Ange-Line Bruel, Laetitia Lambert, Bertrand Isidor, Marcel M. A. M. Mannens, Bekim Sadikovic, Peter Henneman, Mieke M. van Haelst

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Resting Energy Expenditure and Body Composition in Children and Adolescents With Genetic, Hypothalamic, Medication-Induced or Multifactorial Severe Obesity by Ozair Abawi, Ozair Abawi, Emma C. Koster, Emma C. Koster, Mila S. Welling, Mila S. Welling, Mila S. Welling, Sanne C.M. Boeters, Sanne C.M. Boeters, Elisabeth F. C. van Rossum, Elisabeth F. C. van Rossum, Mieke M. van Haelst, Bibian van der Voorn, Bibian van der Voorn, Bibian van der Voorn, Cornelis J. de Groot, Cornelis J. de Groot, Cornelis J. de Groot, Erica L. T. van den Akker, Erica L. T. van den Akker

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Episignature Mapping of <i>TRIP12</i> Provides Functional Insight into Clark–Baraitser Syndrome by Liselot van der Laan, Kathleen Rooney, Mariëlle Alders, Raissa Relator, Haley McConkey, Jennifer Kerkhof, Michael A. Levy, Peter Lauffer, Mio Aerden, Miel Theunis, Eric Legius, Matthew L. Tedder, Lisenka E. L. M. Vissers, Saskia Koene, Claudia Ruivenkamp, Mariette J. V. Hoffer, Dagmar Wieczorek, Nuria C. Bramswig, Theresia Herget, Vanesa López González, Fernando Santos-Simarro, Pernille M. Tørring, Anne-Sophie Denomme-Pichon, Bertrand Isidor, Boris Keren, Sophie Julia, Elise Schaefer, Christine Francannet, Pierre-Yves Maillard, Mala Misra-Isrie, Hilde Van Esch, Marcel M. A. M. Mannens, Bekim Sadikovic, Mieke M. van Haelst, Peter Henneman

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