Researcher profile · Semantic Scholar

Linda Mannini

h-index: 18
Works: 28
Citations: 1,247

Most-cited papers

Mutation Spectrum and Genotype–Phenotype Correlation in Cornelia de Lange Syndrome
Linda Mannini, F. Cucco, Valentina Quarantotti, I. Krantz +1 more
2013Human Mutation190 citations Open access
Semantic Scholar
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.
Frank J. Kaiser, Morad Ansari, D. Braunholz, María Concepción Gil-Rodríguez +79 more
2014Human Molecular Genetics163 citations Open access
Semantic Scholar
Cornelia de Lange syndrome mutations in SMC1A or SMC3 affect binding to DNA.
E. Revenkova, Maria Luisa Focarelli, L. Susani, M. Paulis +8 more
2009Human Molecular Genetics117 citations Open access
Semantic Scholar
Deciphering the molecular machinery of stem cells: a look at the neoblast gene expression profile
L. Rossi, A. Salvetti, F. Marincola, A. Lena +5 more
2007Genome Biology107 citations Open access
Semantic Scholar
Djeyes absent (Djeya) controls prototypic planarian eye regeneration by cooperating with the transcription factor Djsix-1.
Linda Mannini, L. Rossi, P. Deri, V. Gremigni +3 more
2004Developmental Biology90 citations Open access
Semantic Scholar
Spectrum and Consequences of SMC1A Mutations: The Unexpected Involvement of a Core Component of Cohesin in Human Disease
Linda Mannini, Jinglan Liu, I. Krantz, A. Musio
2010Human Mutation75 citations Open access
Semantic Scholar
A conserved role for the mitochondrial citrate transporter Sea/SLC25A1 in the maintenance of chromosome integrity.
P. Morciano, C. Carrisi, L. Capobianco, Linda Mannini +6 more
2009Human Molecular Genetics66 citations Open access
Semantic Scholar
The expanding universe of cohesin functions: a new genome stability caretaker involved in human disease and cancer
Linda Mannini, Stefania Menga, A. Musio
2010Human Mutation54 citations Open access
Semantic Scholar
Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome
Linda Mannini, Fabien C. Lamaze, F. Cucco, Clelia Amato +5 more
2015Scientific Reports48 citations Open access
Semantic Scholar
Proteomic Profile Identifies Dysregulated Pathways in Cornelia de Lange Syndrome Cells With Distinct Mutations in SMC1A and SMC3 Genes
A. Gimigliano, Linda Mannini, L. Bianchi, M. Puglia +5 more
2012Journal of Proteome Research47 citations Open access
Semantic Scholar
Mutant cohesin drives chromosomal instability in early colorectal adenomas.
F. Cucco, Adele Servadio, V. Gatti, P. Bianchi +9 more
2014Human Molecular Genetics36 citations
Semantic Scholar
SMC1B is present in mammalian somatic cells and interacts with mitotic cohesin proteins
Linda Mannini, F. Cucco, Valentina Quarantotti, Clelia Amato +7 more
2015Scientific Reports33 citations Open access
Semantic Scholar
Claspin inhibition leads to fragile site expression
Maria Luisa Focarelli, S. Soza, Linda Mannini, M. Paulis +2 more
2009Genes, Chromosomes and Cancer33 citations
Semantic Scholar
A mortalin-like gene is crucial for planarian stem cell viability.
M. Conte, P. Deri, M. Isolani, Linda Mannini +1 more
2009Developmental Biology32 citations Open access
Semantic Scholar
The dark side of cohesin: the carcinogenic point of view.
Linda Mannini, A. Musio
2011Mutation research27 citations
Semantic Scholar
CEP57 mutation in a girl with mosaic variegated aneuploidy syndrome
L. Pinson, Linda Mannini, M. Willems, F. Cucco +10 more
2014American Journal of Medical Genetics. Part A25 citations
Semantic Scholar
A role for Separase in telomere protection
F. Cipressa, P. Morciano, Giuseppe Bosso, Linda Mannini +5 more
2016Nature Communications23 citations Open access
Semantic Scholar
Two msh/msx-related genes, Djmsh1 and Djmsh2, contribute to the early blastema growth during planarian head regeneration.
Linda Mannini, P. Deri, V. Gremigni, L. Rossi +2 more
2008International Journal of Developmental Biology23 citations Open access
Semantic Scholar
SMC1A codon 496 mutations affect the cellular response to genotoxic treatments
Linda Mannini, Stefania Menga, A. Tonelli, S. Zanotti +3 more
2012American Journal of Medical Genetics. Part A18 citations
Semantic Scholar
Expression of hsp90 mediates cytoprotective effects in the gastrodermis of planarians
M. Conte, M. Isolani, P. Deri, Linda Mannini +1 more
2010Cell stress & chaperones (Print)18 citations Open access
Semantic Scholar
Erratum to “Djeyes absent (Djeya) controls prototypic planarian eye regeneration by cooperating with the transcription factor Djsix-1” [Dev. Biol. 269 (2004) 346–359]
Linda Mannini, L. Rossi, P. Deri, V. Gremigni +3 more
200412 citations Open access
Semantic Scholar
Expression of a retinal homeobox (Rx) gene during planarian regeneration.
Linda Mannini, P. Deri, Jacopo Picchi, R. Batistoni
2008International Journal of Developmental Biology10 citations Open access
Semantic Scholar
Genetic regulation of planarian head morphogenesis during regeneration
R. Batistoni, Linda Mannini, A. Salvetti, L. Rossi +2 more
20063 citations
Semantic Scholar
Proteomic Approach to the Study of Cornelia de Lange Syndrome
L. Bianchi, Linda Mannini, A. Gimigliano, C. Landi +5 more
20100 citations
Semantic Scholar
Protein expression variations in Cornelia de Lange Syndrome
L. Bianchi, A. Gimigliano, C. Landi, M. Puglia +4 more
20090 citations
Semantic Scholar
Planarian stem cell restricted genes
L. Rossi, A. Salvetti, F. Marincola, R. Batistoni +5 more
20060 citations
Semantic Scholar
Chromosomes and genetic organization of rdna in planarians of the genus schmidtea (platyhelminthes, tricladida)
P. Deri, G. Stocchino, S. Casu, M. Pala +2 more
20050 citations Open access
Semantic Scholar
Il controllo genetico della formazione delle strutture visive nelle planarie
L. Rossi, Renata Batistoni, A. Salvetti, P. Deri +3 more
20010 citations
Semantic Scholar

A. Salvetti

×6

V. Gremigni×6

F. Cucco×5

Valentina Quarantotti×4

Ian D. Krantz×4

I. Krantz×3

Stefania Menga×3

A. Gimigliano×3