T. Klemm

Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis

S. Maurer-Stroh, P. Calvas, S. Rozen, 2013, Journal of Medical Genetics.

CYP1B1, MYOC, and LTBP2 mutations in primary congenital glaucoma patients in the United States.

S. Rozen, R. Metlapally, K. Tran-Viet, 2013, American journal of ophthalmology.

Rapid and accurate detection of Giardia lamblia and Cryptosporidium spp. antigens in human fecal specimens by new commercially available qualitative immunochromatographic assays

R. Ignatius, T. Regnath, T. Klemm, 2006, European Journal of Clinical Microbiology and Infectious Diseases.

Highly specific detection of Cryptosporidium spp. oocysts in human stool samples by undemanding and inexpensive phase contrast microscopy

F. Mockenhaupt, J. Gahutu, R. Ignatius, 2016, Parasitology Research.

Mutations in SCO2 are associated with autosomal-dominant high-grade myopia.

Yi-Ju Li, S. Maurer-Stroh, S. Saw, 2013, American journal of human genetics.

Reduced penetrance in a large Caucasian pedigree with Stickler syndrome

E. Stone, S. Rozen, D. Abbott, 2017, Ophthalmic genetics.

Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility

S. Saw, K. Tran-Viet, T. Young, 2012, Molecular vision.

Highly specific detection of Cryptosporidium spp. oocysts in human stool samples by undemanding and inexpensive phase contrast microscopy

F. Mockenhaupt, J. Gahutu, R. Ignatius, 2016, Parasitology Research.