• 4996 Citations
  • 36 h-Index
1991 …2019
If you made any changes in Pure these will be visible here soon.

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

  • 3 Similar Profiles
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Phenotype Medicine & Life Sciences
MicroRNAs Medicine & Life Sciences
Neoplasms Medicine & Life Sciences
Intellectual Disability Medicine & Life Sciences
Colorectal Neoplasms Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences

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

Research Output 1991 2019

  • 4996 Citations
  • 36 h-Index
  • 197 Article
  • 2 Conference contribution
  • 1 Comment/debate
  • 1 Review article

1q23.1 homozygous deletion and downregulation of Fc receptor-like family genes confer poor prognosis in chronic lymphocytic leukemia

Daniele, G., L’Abbate, A., Turchiano, A., Palumbo, O., Carella, M., Lo Cunsolo, C., Iuzzolino, P., Lonoce, A., Hernández-Sánchez, M., Minoia, C., Leone, P., Hernandez-Rivas, J. M. & Storlazzi, C. T., Jan 1 2019, In : Clinical and Experimental Medicine.

Research output: Contribution to journalArticle

Fc Receptors
B-Cell Chronic Lymphocytic Leukemia
Down-Regulation
Genes
Chromosomes, Human, Pair 1

A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway

Palumbo, P., Petracca, A., Maggi, R., Biagini, T., Nardella, G., Sacco, M. C., Di Schiavi, E., Carella, M., Micale, L. & Castori, M., Jan 1 2019, In : European Journal of Human Genetics.

Research output: Contribution to journalArticle

MAP Kinase Signaling System
Fibroblast Growth Factor 2
Holoprosencephaly
Exome
Autophagy

Concurrent chromothripsis events in a case of TP53 depleted acute myeloid leukemia with myelodysplasia-related changes

Tolomeo, D., L'Abbate, A., Lonoce, A., D'Addabbo, P., Miccoli, M. F., Lo Cunsolo, C., Iuzzolino, P., Palumbo, O., Carella, M., Racanelli, V., Mazza, T., Ottaviani, E., Martinelli, G., Macchia, G. & Storlazzi, C. T., Sep 1 2019, In : Cancer genetics. 237, p. 63-68 6 p.

Research output: Contribution to journalArticle

Acute Myeloid Leukemia
Chromosomes, Human, Pair 19
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 12
Genetic Markers
Open Access
Hypertrophic Cardiomyopathy
Missense Mutation
Cerebral Palsy
Cardiomyopathies
Physicians

Free D-aspartate triggers NMDA receptor-dependent cell death in primary cortical neurons and perturbs JNK activation, Tau phosphorylation, and protein SUMOylation in the cerebral cortex of mice lacking D-aspartate oxidase activity

Nuzzo, T., Feligioni, M., Cristino, L., Pagano, I., Marcelli, S., Iannuzzi, F., Imperatore, R., D'Angelo, L., Petrella, C., Carella, M., Pollegioni, L., Sacchi, S., Punzo, D., De Girolamo, P., Errico, F., Canu, N. & Usiello, A., Jul 1 2019, In : Experimental Neurology. 317, p. 51-65 15 p.

Research output: Contribution to journalArticle

D-Aspartate Oxidase
Sumoylation
D-Aspartic Acid
tau Proteins
N-Methyl-D-Aspartate Receptors