Pfäffle, Roland

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index

Felix, J. F., Bradfield, J. P., Monnereau, C., van der Valk, R. J. P., Stergiakouli, E., Chesi, A., Gaillard, R., Feenstra, B., Thiering, E., Kreiner-Møller, E., et al. (2016) · Human Molecular Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 343

Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency

Pfäffle, R., & Klammt, J. (2011) · Best Practice & Research Clinical Endocrinology & Metabolism

Pituitary Gland Disorders and TreatmentsGrowth Hormone and Insulin-like Growth Factors

Cited by 115

Compound Heterozygous and Homozygous Mutations of the TSHβ Gene as a Cause of Congenital Central Hypothyroidism in Europe

Karges, B., LeHeup, B., Schoenle, E., Castro-Correia, C., Fontoura, M., Pfäffle, R., Andler, W., Debatin, K.-M., & Karges, W. (2004) · Hormone Research in Paediatrics

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 32

Safety and effectiveness of recombinant human growth hormone in children with Turner syndrome: data from the PATRO children study

Backeljauw, P., Kanumakala, S., Loche, S., Schwab, K. O., Pfäffle, R. W., Höybye, C., Lundberg, E., Battelino, T., Kriström, B., Giemza, T., et al. (2021) · Hormone Research in Paediatrics

Growth Hormone and Insulin-like Growth FactorsBiosimilars and Bioanalytical Methods

Cited by 19