S. Fricke-Otto

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Silver‐Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

R. Siebert, M. Baudis, T. Eggermann, 2011, Clinical genetics.

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

G. Binder, M. Ranke, V. Hesse, 2004, The Journal of clinical endocrinology and metabolism.

Guideline Adherence and Registry Recruitment of Congenital Primary Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (HypoDok)

R. Holl, M. Bettendorf, J. Woelfle, 2020, International journal of neonatal screening.

Submicroscopic chromosomal imbalances in idiopathic Silver–Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome

M. Baudis, T. Eggermann, N. Schoenherr, 2009, Journal of Medical Genetics.

Cross-sectional seroprevalence surveys of SARS-CoV-2 antibodies in children in Germany, June 2020 to May 2021

A. Beyerlein, H. von Bernuth, C. Schwerk, 2022, Nature Communications.

Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment

M. Bullinger, H. Dörr, E. Schönau, 2019, Front. Pediatr..

Height Gains in Response to Growth Hormone Treatment to Final Height Are Similar in Patients with SHOX Deficiency and Turner Syndrome

G. Binder, D. Cao, J. Ross, 2009, Hormone Research in Paediatrics.

Retinoic acid catabolizing enzyme CYP26C1 is a genetic modifier in SHOX deficiency

G. Rappold, T. Ogata, G. Binder, 2016, EMBO molecular medicine.

Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patients

H. Dörr, E. Schönau, R. Holl, 2019, Endocrine connections.

Long-term Surveillance of Children with Congenital Hypothyroidism: Data from the German Registry for Congenital Hypothyroidism (AQUAPE “Hypo Dok”)

H. Dörr, T. Rohrer, E. Schönau, 2015, Klinische Pädiatrie.

Congenital goitrous primary hypothyroidism in two German families caused by novel thyroid peroxidase (TPO) gene mutations.

P. Hermanns, J. Pohlenz,, R. Mühlenberg, 2013, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Twenty years of newborn screening for congenital adrenal hyperplasia and congenital primary hypothyroidism – experiences from the DGKED/AQUAPE study group for quality improvement in Germany

E. Schönau, R. Holl, W. Bonfig, 2022, Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V.

Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose

H. Dörr, E. Schönau, R. Holl, 2017, Hormone Research in Paediatrics.

Identification of growth patterns of preterm and small-for-gestational age children from birth to 4 years – do they catch up?

M. Wabitsch, U. Wittwer-Backofen, R. Mumm, 2019, Journal of perinatal medicine.

Semen quality and testicular adrenal rest tumor development in 46,XY congenital adrenal hyperplasia - the importance of optimal hormonal replacement.

J. Weigel, S. Kliesch, F. Reschke, 2021, European journal of endocrinology.

Mild congenital primary hypothyroidism in a Turkish family caused by a homozygous missense thyrotropin receptor (TSHR) gene mutation (A593 V).

N. Pfarr, J. Pohlenz,, R. Mühlenberg, 2005, Experimental and clinical endocrinology & diabetes.