Kircher, Martin

Expanding the clinical and genetic heterogeneity of hereditary disorders of connective tissue

Alazami, A. M., Al-Qattan, S. M., Faqeih, E., Alhashem, A., Alshammari, M., Alzahrani, F., Al-Dosari, M. S., Patel, N., Alsagheir, A., Binabbas, B., et al. (2016) · Human Genetics

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 110

Predicting the pathogenicity of missense variants using features derived from AlphaFold2

Schmidt, A., Röner, S., Mai, K., Klinkhammer, H., Kircher, M., & Ludwig, K. U. (2022) · Bioinformatics

Genomics and Rare DiseasesProtein Structure and Dynamics

Cited by 79

Predicting the pathogenicity of missense variants using features derived from AlphaFold2

Schmidt, A., Röner, S., Mai, K., Klinkhammer, H., Kircher, M., & Ludwig, K. U. (2023) · Bioinformatics

Genomics and Rare DiseasesProtein Structure and Dynamics

Cited by 79

Road blocks on paleogenomes—polymerase extension profiling reveals the frequency of blocking lesions in ancient DNA

Heyn, P., Stenzel, U., Briggs, A. W., Kircher, M., Hofreiter, M., & Meyer, M. (2010) · Nucleic Acids Research

Forensic and Genetic ResearchGenomics and Phylogenetic Studies

Cited by 56