Mehmet Tekman
University of Freiburg(DE)
Publications by Year
Research Areas
Genomics and Rare Diseases, Single-cell and spatial transcriptomics, Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics
Most-Cited Works
- → The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2022 update(2022)1,330 cited
- → A Missense Mutation in KCTD17 Causes Autosomal Dominant Myoclonus-Dystonia(2015)140 cited
- → Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2(2017)111 cited
- → Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure(2018)90 cited
- → STAG3 truncating variant as the cause of primary ovarian insufficiency(2015)81 cited
- → Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue—a case series and genetic exploration(2016)63 cited
- → Noncoding deletions reveal a gene that is critical for intestinal function(2019)39 cited
- → Eomes restricts Brachyury functions at the onset of mouse gastrulation(2023)35 cited
- → A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis—Further evidence of genotype–phenotype correlation(2014)33 cited
- → Delayed boosting improves human antigen-specific Ig and B cell responses to the RH5.1/AS01B malaria vaccine(2023)32 cited