• 1 Citations
  • 1 h-Index
20182019
If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Milena Crippa is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Rubinstein-Taybi Syndrome Medicine & Life Sciences
Induced Pluripotent Stem Cells Medicine & Life Sciences
Exons Medicine & Life Sciences
Mutation Medicine & Life Sciences
Exome Medicine & Life Sciences
Cell Line Medicine & Life Sciences
Genes Medicine & Life Sciences
Comparative Genomic Hybridization Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2018 2019

  • 1 Citations
  • 1 h-Index
  • 5 Article

9q34.3 microduplications lead to neurodevelopmental disorders through EHMT1 overexpression

Bonati, M. T., Castronovo, C., Sironi, A., Zimbalatti, D., Bestetti, I., Crippa, M., Novelli, A., Loddo, S., Dentici, M. L., Taylor, J., Devillard, F., Larizza, L. & Finelli, P., Jun 17 2019, In : Neurogenetics.

Research output: Contribution to journalArticle

Genes
Cytogenetics
Computer Simulation
Neurodevelopmental Disorders
Phenotype
1 Citation (Scopus)

Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein–Taybi syndrome: the interconnections of epigenetic machinery disorders

Negri, G., Magini, P., Milani, D., Crippa, M., Biamino, E., Piccione, M., Sotgiu, S., Perrìa, C., Vitiello, G., Frontali, M., Boni, A., Di Fede, E., Gandini, M. C., Colombo, E. A., Bamshad, M. J., Nickerson, D. A., Smith, J. D., Loddo, I., Finelli, P., Seri, M. & 3 others, Pippucci, T., Larizza, L. & Gervasini, C., Mar 4 2019, In : Human Genetics. 138, 3, p. 257-269 13 p.

Research output: Contribution to journalArticle

Exome
Epigenomics
Genes
Intellectual Disability
Mutation

Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

Crippa, M., Bonati, M. T., Calzari, L., Picinelli, C., Gervasini, C., Sironi, A., Bestetti, I., Guzzetti, S., Bellone, S., Selicorni, A., Mussa, A., Riccio, A., Ferrero, G. B., Russo, S., Larizza, L. & Finelli, P., Oct 15 2019, In : Frontiers in Genetics. 10, 955.

Research output: Contribution to journalArticle

Open Access
Comparative Genomic Hybridization
Phenotype
Growth Disorders
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 7
Rubinstein-Taybi Syndrome
Induced Pluripotent Stem Cells
Exons
Cell Line
Mutation
Rubinstein-Taybi Syndrome
Induced Pluripotent Stem Cells
Exons
Cell Line
Mutation