Woelfle, Joachim

Clinical practice guidelines for the care of girls and women with Turner syndrome: proceedings from the 2016 Cincinnati International Turner syndrome meeting

Gravholt, C. H., Andersen, N. H., Conway, G. S., Dekkers, O. M., Geffner, M. E., Klein, K. O., Lin, A. E., Mauras, N., Quigley, C. A., Rubin, K., et al. (2017) · European Journal of Endocrinology

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 1,101

Clinical practice guidelines for the care of girls and women with Turner syndrome.

Gravholt, C. H., Andersen, N. H., Christin-Maitre, S., Davis, S. M., Duijnhouwer, A., Gawlik, A., Maciel-Guerra, A. T., Gutmark-Little, I., Fleischer, K., Hong, D., et al. (2024) · European Journal of Endocrinology

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 224

DNA methylation signature in peripheral blood reveals distinct characteristics of human X chromosome numerical aberrations

Sharma, A., Jamil, M. A., Nuesgen, N., Schreiner, F., Priebe, L., Hoffmann, P., Herns, S., Nöthen, M. M., Fröhlich, H., Oldenburg, J., et al. (2015) · Clinical Epigenetics

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesEpigenetics and DNA Methylation

Cited by 81

MKRN3 Mutations in Familial Central Precocious Puberty

Schreiner, F., Gohlke, B., Hamm, M., Korsch, E., & Woelfle, J. (2014) · Hormone Research in Paediatrics

Hypothalamic control of reproductive hormonesGenetic Syndromes and Imprinting

Cited by 63

Frequency and characteristics of MODY 1 (HNF4A mutation) and MODY 5 (HNF1B mutation): analysis from the dpv database

Warncke, K., Kummer, S., Raile, K., Grulich-Henn, J., Woelfle, J., Steichen, E., Prinz, N., & Holl, R. W. (2019) · The Journal of Clinical Endocrinology & Metabolism

Diabetes and associated disordersPancreatic function and diabetes

Cited by 52

Inflammatory markers in obese adolescents with type 2 diabetes and their relationship to hepatokines and adipokines

Reinehr, T., Karges, B., Meissner, T., Wiegand, S., Stoffel-Wagner, B., Holl, R. W., & Woelfle, J. (2016) · The Journal of Pediatrics

Adipokines, Inflammation, and Metabolic DiseasesSkin Diseases and Diabetes

Cited by 51

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany

on behalf of the German Society of Pediatric Endocrinology and Diabetology, Dörr, H. G., Wollmann, H. A., Hauffa, B. P., & Woelfle, J. (2018) · BMC Endocrine Disorders

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 22

Secular trends on birth parameters, growth, and pubertal timing in girls with Turner syndrome

Woelfle, J., Lindberg, A., Aydin, F., Ong, K. K., Camacho-Hubner, C., & Gohlke, B. (2018) · Frontiers in Endocrinology

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGrowth Hormone and Insulin-like Growth Factors

Cited by 12