Thomas J. Corydon

Clinical and molecular evidence of abnormal processing and trafficking of the vasopressin preprohormone in a large kindred with familial neurohypophyseal diabetes insipidus due to a signal peptide mutation.

L. Bolund, T. Jensen, B. Andresen, 1999, The Journal of clinical endocrinology and metabolism.

Evidence implicating BRD1 with brain development and susceptibility to both schizophrenia and bipolar affective disorder

D. Blackwood, W. Muir, O. Mors, 2006, Molecular Psychiatry.

A human homologue of Escherichia coli ClpP caseinolytic protease: recombinant expression, intracellular processing and subcellular localization.

K. Kristiansen, L. Bolund, P. Bross, 1998, The Biochemical journal.

Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism.

L. D. Schroeder, R. Wanders, P. Bross, 2000, American journal of human genetics.

SNAP-25-associated Hrs-2 protein colocalizes with AQP2 in rat kidney collecting duct principal cells.

R. Dahl, S. Nielsen, H. Li, 2001, American journal of physiology. Renal physiology.

A novel deletion partly removing the AVP gene causes autosomal recessive inheritance of early‐onset neurohypophyseal diabetes insipidus

N. Gregersen, S. Rittig, G. Shaikh, 2013, Clinical genetics.