U. Groß

Mutation in the V2 vasopressin receptor gene, AVPR2, causes nephrogenic syndrome of inappropriate diuresis.

L. Hunyady, P. Várnai, D. Morris-Rosendahl, 2015, Kidney international.

Characterization of the RET protooncogene transmembrane domain mutation S649L associated with nonaggressive medullary thyroid carcinoma.

B. Pützer, H. Herbst, N. Senninger, 2008, European journal of endocrinology.

Functional characterization of a missense mutation in the V 2 vasopressin receptor gene , AVPR 2 , causing a nephrogenic syndrome of inappropriate diuresis

L. Hunyady, P. Várnai, D. Morris-Rosendahl, 2015 .

A new mutation in the hepatocyte nuclear factor-1-alpha gene (P224S) in a newly discovered German family with maturity-onset diabetes of the young 3 (MODY 3). Family members carry additionally the homozygous I27L amino acid polymorphism in the HNF1 alpha gene.

H. Fehmann, U. Groß, M. Epe, 2004, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Novel Germline p.Gly42Val MEN1 Mutation in a Family with Multiple Endocrine Neoplasia Type 1 - Excellent Response of Prolactinoma to Cabergoline.

M. Korbonits, D. Iacovazzo, K. Jungheim, 2017, Annals of clinical and laboratory science.

Improvement of fertility in men with adrenal enzyme deficencies

H. Schulte, M. Ludwig, U. Groß, 2005 .