Katrin Koehler

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 3

Top Topics

Autism Spectrum Disorder

Transcription Factor

Top Venues

Journal of the Endocrine Society

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Tina Schubert, Nicole Reisch, Ronald Naumann, Ilka Reichardt, Dana Landgraf, Friederike Quitter, Shamini Ramkumar Thirumalasetty, Anne-Kristin Heninger, Mihail Sarov, Mirko Peitzsch, Angela Huebner, Katrin Koehler
CYP21A2 Gene Expression in a Humanized 21-Hydroxylase Mouse Model Does Not Affect Adrenocortical Morphology and Function. Journal of the Endocrine Society 6 (6) (2022)
Federica Buonocore, Avinaash V Maharaj, Younus Qamar, Katrin Koehler, Jenifer P Suntharalingham, Li F Chan, Bruno Ferraz-de-Souza, Claire R Hughes, Lin Lin, Rathi Prasad, Jeremy Allgrove, Edward Thomas Andrews, Charles R Buchanan, Timothy D Cheetham, Elizabeth C Crowne, Justin Huw Davies, John W Gregory, Peter C Hindmarsh, Tony Hulse, Nils P Krone, Prateek Shanmugananda, Mohamad Guftar Shaikh, Catherine Roberts, Peter Ellis Clayton, Mehul Tulsidas Dattani, N Simon Thomas, Angela Huebner, Adrian J L Clark, Louise A Metherell, John C Achermann
Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK. Journal of the Endocrine Society 5 (8) (2021)
Katrin Koehler, Markus Schuelke, Anna K Hell, Michael Schittkowski, Angela Huebner, Knut Brockmann
A novel homozygous nonsense mutation of VPS13B associated with previously unreported features of Cohen syndrome. American journal of medical genetics. Part A 182 (3) (2019)