Liehr, Thomas

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Maass, P. G., Aydin, A., Luft, F. C., Schächterle, C., Weise, A., Stricker, S., Lindschau, C., Vaegler, M., Qadri, F., Toka, H. R., et al. (2015) · Nature Genetics

Phosphodiesterase function and regulationBlood Pressure and Hypertension Studies

Cited by 166

First Molecular Cytogenetic High Resolution Characterization of the NIH 3T3 Cell Line by Murine Multicolor Banding

Leibiger, C., Kosyakova, N., Mkrtchyan, H., Glei, M., Trifonov, V., & Liehr, T. (2013) · Journal of Histochemistry & Cytochemistry

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 92

16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2

Barber, J. C. K., Hall, V., Maloney, V. K., Huang, S., Roberts, A. M., Brady, A. F., Foulds, N., Bewes, B., Volleth, M., Liehr, T., et al. (2013) · European Journal of Human Genetics

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 74

Systems genetics view of endometriosis: a common complex disorder

Baranov, V. S., Ivaschenko, T. E., Liehr, T., & Yarmolinskaya, M. I. (2015) · European Journal of Obstetrics & Gynecology and Reproductive Biology

Endometriosis Research and TreatmentPlant and fungal interactions

Cited by 62

Multiple Sex Chromosomes and Evolutionary Relationships in Amazonian Catfishes: The Outstanding Model of the Genus Harttia (Siluriformes: Loricariidae)

Sassi, F. D. M. C., Deon, G. A., Moreira-Filho, O., Vicari, M. R., Bertollo, L. A. C., Liehr, T., de Oliveira, E. A., & Cioffi, M. B. (2020) · Genes

Chromosomal and Genetic VariationsGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Cited by 31