Caracausi, Maria
University of Bologna
5 papers on CoChatORCID 0000-0001-8957-8391
Most cited papers
- Verified
On the length, weight and GC content of the human genome
Piovesan, A., Pelleri, M. C., Antonaros, F., Strippoli, P., Caracausi, M., & Vitale, L. (2019) · BMC Research Notes
Genomics and Phylogenetic StudiesChromosomal and Genetic Variations
Cited by 283
- Verified
Plasma and urinary metabolomic profiles of Down syndrome correlate with alteration of mitochondrial metabolism
Caracausi, M., Ghini, V., Locatelli, C., Mericio, M., Piovesan, A., Antonaros, F., Pelleri, M. C., Vitale, L., Vacca, R. A., Bedetti, F., et al. (2018) · Scientific Reports
Down syndrome and intellectual disability researchMetabolomics and Mass Spectrometry Studies
Cited by 84
- Verified
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype
Pelleri, M. C., Cicchini, E., Locatelli, C., Vitale, L., Caracausi, M., Piovesan, A., Rocca, A., Poletti, G., Seri, M., Strippoli, P., et al. (2016) · Human Molecular Genetics
Down syndrome and intellectual disability researchGenomic variations and chromosomal abnormalities
Cited by 83
- Verified
Integrated Quantitative Transcriptome Maps of Human Trisomy 21 Tissues and Cells
Pelleri, M. C., Cattani, C., Vitale, L., Antonaros, F., Strippoli, P., Locatelli, C., Cocchi, G., Piovesan, A., & Caracausi, M. (2018) · Frontiers in Genetics
Down syndrome and intellectual disability researchGenomic variations and chromosomal abnormalities
Cited by 61
- Verified
Difficulty in obtaining the complete mRNA coding sequence at 5′ region (5′ end mRNA artifact): Causes, consequences in biology and medicine and possible solutions for obtaining the actual amino acid sequence of proteins (Review)
Vitale, L., Caracausi, M., Casadei, R., Pelleri, M. C., & Piovesan, A. (2017) · International Journal of Molecular Medicine
Genomics and Phylogenetic StudiesRNA Research and Splicing
Cited by 4
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