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Genetics Research|June 17, 2020
Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre studyAlvaro Mesoraca, Katia Margiotti, Claudio Dello Russo, et al.
Gene Expression|October 12, 2004
Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarraysFrancesca Amati, Michela Biancolella, Maria Rosaria D'Apice, et al.
Genes|December 23, 2022
Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 GeneMarco Fabiani, Francesco Libotte, Katia Margiotti, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
A de novo proximal 3q29 chromosome microduplication in a patient with oculo auriculo vertebral spectrumValentina Guida, Lorenzo Sinibaldi, Mario Pagnoni, et al.
Plos One|August 5, 2021
Multi-analytical test based on serum miRNAs and proteins quantification for ovarian cancer early detectionPriscila D R Cirillo, Katia Margiotti, Marco Fabiani, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 2, 2009
In vivo knockdown of the androgen receptor results in growth inhibition and regression of well-established, castration-resistant prostate tumorsRobert Snoek, Helen Cheng, Katia Margiotti, et al.
Brain and Behavior|November 22, 2025
Maternal Folate Receptor Alpha Autoantibodies and Increased Fetal Nuchal Translucency as Potential Early Markers of Autism Spectrum DisorderClaudio Giorlandino, Katia Margiotti, Marco Fabiani, et al.
The Prostate|October 1, 2009
Arachidonic acid activation of intratumoral steroid synthesis during prostate cancer progression to castration resistanceJennifer A Locke, Emma S Tomlinson Guns, Melanie L Lehman, et al.
Journal of Assisted Reproduction and Genetics|December 18, 2024
Uniparental disomy (UPD) exclusion in embryos following Preimplantation Genetic Testing for Structural Rearrangements (PGT-SR)Marco Fabiani, Katia Margiotti, Francesco Libotte, et al.
Molecular Genetics & Genomic Medicine|June 11, 2020
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritanceAlice Traversa, Enrica Marchionni, Agnese Giovannetti, et al.
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