Friedel Wenzel
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Genomic variations and chromosomal abnormalities, Genetic factors in colorectal cancer, RNA modifications and cancer, Acute Myeloid Leukemia Research
Most-Cited Works
- → aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis(2011)86 cited
- → Novel Real-Time Quantitative PCR Test for Trisomy 21(2002)85 cited
- → Mosaic ring chromosome 8: Clinical and array‐CGH findings in partial trisomy 8(2008)73 cited
- → Deletion in Xp22.11: PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism(2010)60 cited
- → Genotyping fetal paternally inherited SNPs by MALDI‐TOF MS using cell‐free fetal DNA in maternal plasma: Influence of size fractionation(2006)42 cited
- → Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype–genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome(2010)32 cited
- → Somatic alterations in juvenile polyps from BMPR1A and SMAD4 mutation carriers(2015)26 cited
- → Reliable detection of Trisomy 21 using MALDI-TOF mass spectrometry(2006)21 cited
- → Morphogenesis of the micropylar apparatus in ovarian follicles of the fungus gnatBradysia tritici (syn.Sciara ocellaris)(1990)20 cited
- → Discordant Gene Expression Signatures and Related Phenotypic Differences in Lamin A- and A/C-Related Hutchinson-Gilford Progeria Syndrome (HGPS)(2011)18 cited