CNR Institutional Research Information System

RICOTTI, ROBERTA
 Distribuzione geografica
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Continente #
NA - Nord America 376
AS - Asia 96
EU - Europa 36
AF - Africa 1
Totale 509
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Nazione #
US - Stati Uniti d'America 364
SG - Singapore 81
CA - Canada 11
IT - Italia 11
GB - Regno Unito 10
KR - Corea 10
DE - Germania 3
BE - Belgio 2
FI - Finlandia 2
LT - Lituania 2
NL - Olanda 2
BD - Bangladesh 1
BG - Bulgaria 1
CH - Svizzera 1
CN - Cina 1
CR - Costa Rica 1
IN - India 1
LA - Repubblica Popolare Democratica del Laos 1
LK - Sri Lanka 1
MA - Marocco 1
PT - Portogallo 1
SE - Svezia 1
Totale 509
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Città #
Santa Clara 321
Singapore 42
Seoul 10
Ottawa 7
London 6
Pavia 6
Ashburn 4
Toronto 4
Brussels 2
Frankfurt am Main 2
Helsinki 2
Los Angeles 2
Rome 2
Buffalo 1
Colombo 1
Dhaka 1
Forest City 1
Mumbai 1
Phoenix 1
Prineville 1
Rabat 1
San José 1
Sofia 1
Springfield 1
Stockholm 1
Vientiane 1
Zurich 1
Totale 424
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Nome #
TFIIH stabilization recovers the DNA repair and transcription dysfunctions in thermo-sensitive trichothiodystrophy 38
Dalla conferma della diagnosi clinica dei pazienti alla dissezione dei pathways coinvolti nella risposta a stress ossidativo e radiazione UV 19
The X-linked DIAPH2 gene is a risk factor for Premature Ovarian Failure (POF) involved in actin dynamics of ovarian granulosa cells 17
Phenotypic variability in xeroderma pigmentosum group G: An uncommon case with severe prenatal-onset Cockayne syndrome features 15
Genotype-phenotype relationships in trichothiodystrophy patients with novel splicing mutations in the XPD Gene. 15
GTF2E2 Mutations Destabilize the General Transcription Factor Complex TFIIE in Individuals with DNA Repair-Proficient Trichothiodystrophy 15
Genotype-phenotype Relationships in Patients with Trichothiodystrophy and Xeroderma Pigmentosum. 14
The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring. 14
Modulation of poly(ADP-ribosylation) during neoplastic transformation: effect of 3-aminobenzamide. 14
The X-linked DIAPH2 gene is a risk-factor for Premature Ovarian Failure (POF) and accounts for female preponderance among POF patients offspring. 14
High throughput screening of candidate genes for X-linked premature ovarian failure 14
Modulation of poly(ADP-ribosylation) during neoplastic transformation 14
Malattie ereditarie difettive nella riparazione dei danni indotti sul DNA dai raggi ultravioletti. Corso di Aggiornamento: Difetti di riparo del DNA: meccanismi e patologie. 14
Malattie ereditarie difettive nella risposta al danno indotto da radiazioni UV 14
Effetto dell inibizione di PARP sulla trasformazione tumorale. 13
A mutation in the X-linked Emery-Dreifuss muscular dystrophy gene in a patient affected with conduction cardiomyopathy 13
Dissecting the genetic basis and molecular mechanisms of Premature Ovarian Failure. 13
HIGH THROUGHPUT SCREENING OF CANDIDATE GENES FOR X-LINKED PREMATURE OVARIAN FAILURE: THE STUDY DESIGN 13
Frequent low penetrance mutations in the Lamin A/C gene, causing Emery Dreifuss muscular dystrophy. 12
Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. 12
Poly (ADP-Ribosylation) and Neoplastic Transformation: Effect of PARP Inhibitors 12
Super-telomeres in transformed human fibroblasts 12
Loss of telomere length homeostasis in telomerase immortalized human fibroblasts. 12
New patient material. 11
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy 11
DIAPH2 is a susceptibility gene for POF 11
Mutations in the C7orf11 (TTDN1) gene in six nonphotosensitive trichothiodystrophy patients: no obvious genotype-phenotype relationships. 11
X; autosome balanced translocations and ovarian failure: chromatin organization around the breakpoints premature 10
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B. 10
DIAPH2 is a susceptibility gene for POF 10
Molecular genetics of POF2 locus in Xq13.3-22 (DACH2; DIAPH2) 10
Association studies of candidate genes for Premature Ovarian Failure (POF) 10
New patient material. 10
Identificazione e caratterizzazione di pazienti difettivi nella riparazione del DNA 10
Dissecting the genetic basis and molecular mechanisms of premature ovarian failure 9
Trichothiodystrophy with normal DNA repair efficiency and mutations in the TTDN1 gene. 9
New patient material. 9
X;autosome balanced translocations and premature ovarian failure: chromatin organization around the breakpoints. 9
Involvement of the TTDN1 gene in the non-photosensitive form of trichothiodystrophy. 9
The human X chromosome in the etiology of Premature Ovarian Failure (POF) 9
Mutations in the human DACH2 gene as risk factors for Premature Ovarian Failure 9
Totale 520
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Categoria #
all - tutte 1.626
article - articoli 538
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.164
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202412 0 0 0 0 0 0 0 0 0 2 10 0
2024/2025508 3 3 57 18 280 90 4 33 20 0 0 0
Totale 520