T. Diemer

Patients' choices and opinions on chorionic villous sampling and non‐invasive alternatives for prenatal testing following preimplantation genetic testing for hereditary disorders: A cross‐sectional questionnaire study

U. Kesmodel, I. Pedersen, H. J. Ingerslev, 2022, Prenatal diagnosis.

Developmental and genetic disorders in spermatogenesis.

C. Desjardins, T. Diemer, Claude Desjardins, 1999, Human reproduction update.

A systematic review on concurrent aneuploidy screening and preimplantation genetic testing for hereditary disorders: What is the prevalence of aneuploidy and is there a clinical effect from aneuploidy screening?

H. Okkels, U. Kesmodel, I. Pedersen, 2020, Acta obstetricia et gynecologica Scandinavica.

Preimplantation genetic testing in two Danish couples affected by Peutz–Jeghers syndrome

A. Byrjalsen, J. Karstensen, A. M. Jelsig, 2022, Scandinavian journal of gastroenterology.

Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.

Robert W. Taylor, R. Horvath, E. Ostergaard, 2021, Human molecular genetics.

Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy.

E. Eichler, H. Lerche, R. Møller, 2021, Brain : a journal of neurology.

A method for estimation of plasma albumin concentration from the buffering properties of whole blood.

S. Rees, S. Kristensen, T. Diemer, 2012, Journal of critical care.