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Fenna de Freitas

University of Antwerp

24

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492

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Investigation of common and rare genetic variation in the BAMBI genomic region in light of human obesity

2016 Endocrine
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Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients

2016 Clinics and Research in Hepatology and Gastroenterology
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Screening for rare variants in the PNPLA3 gene in obese liver biopsy patients

2016 Clinics and Research in Hepatology and Gastroenterology
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A common LRP4 haplotype is associated with bone mineral density and hip geometry in men : data from the Odense Androgen Study (OAS)

2013 Bone
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No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disorders.

2013 Bone
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Identification of mutations in the NUCB2/nesfatin gene in children with severe obesity.

2012 Molecular Genetics and Metabolism
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Association Study of Polymorphisms in the SOST Gene Region and Parameters of Bone Strength and Body Composition in Both Young and Elderly Men: Data from the Odense Androgen Study

2012 Calcified Tissue International
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Identification and functional characterization of a missense mutation in resistin in two patients with severe obesity and insulin resistance

2011 European Journal of Endocrinology
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Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphisms

2011 Molecular Genetics and Metabolism
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Association study of MC4R with complex obesity and replication of the rs17782313 association signal.

2011 Molecular Genetics and Metabolism
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Citations (27)