M. Ogorelkova

Mutational Spectrum in the Δ7-Sterol Reductase Gene and Genotype-Phenotype Correlation in 84 Patients with Smith-Lemli-Opitz Syndrome

Martina Witsch‐Baumgartner, Barbara U. Fitzky, M. Ogorelkova et al. · The American Journal of Human Genetics · 2000 · 188 citations · Full text

Smith-lemli-opitz Syndrome, Mendelian Disorder, Genetic Disorder +9

Molecular basis of congenital lp(a) deficiency: a frequent apo(a) 'null' mutation in caucasians

M. Ogorelkova · Human Molecular Genetics · 1999 · 83 citations

Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6 to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians

M. Ogorelkova · Human Molecular Genetics · 2001 · 64 citations · Full text

Genetics, Genetic Epidemiology, Immunology +22

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

Martina Witsch‐Baumgartner, Ilona Schwentner, Mijail Gruber et al. · Journal of Medical Genetics · 2007 · 57 citations

DNA Delivery to Cells in Culture: Generation of Adenoviral Libraries for High-Throughput Functional Screening

M. Ogorelkova, Seyyed Mehdy Elahi, David Gagnon et al. · Humana Press eBooks · 2004 · 12 citations

Molecular Biology, Gene Delivery, Dna Variants +22