Cecilia Rios
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Williams Syndrome Research, Reproductive Biology and Fertility, Retinal Development and Disorders, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Generation of an Inbred Miniature Pig Model of Retinitis Pigmentosa(2012)154 cited
- → Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome(2010)84 cited
- → Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndrome(2010)20 cited
- → Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome(2010)15 cited
- → Stress relief: can continuous culture in a low lactate culture media reduce numerical chromosomal abnormalities and therefore improve euploidy rates?(2018)10 cited
- → Artificial intelligence: non-invasive detection of morphological features associated with abnormalities in chromosomes 21 and 16(2019)4 cited
- → PP.17 Stereotactic Ablative Radiotherapy in Oligometastatic Pulmonary Disease. First Institutional Experience(2023)
- Inversion Common Polymorphism of the Williams Found Syndrome More Region Frequently Is a in Parents of Children With Williams Syndrome(2010)
- Alpha Associated 1 Antitrypsin With Joint Deficiency Dislocation Alleles and Scoliosis Are(2010)
- → Vaginal neuroendocrine carcinoma: regarding a clinical case(2022)