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Dive into the research topics where Francesca Mancini is active.

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Featured researches published by Francesca Mancini.


Orphanet Journal of Rare Diseases | 2014

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

Marta Romani; Alessia Micalizzi; I. Kraoua; Maria Teresa Dotti; Mara Cavallin; László Sztriha; Rosario Ruta; Francesca Mancini; Tommaso Mazza; Stefano Castellana; Benrhouma Hanene; Maria Alessandra Carluccio; Francesca Darra; Adrienn Máté; Alíz Zimmermann; N. Gouider-Khouja; Enza Maria Valente

Joubert syndrome is a clinically and genetically heterogeneous ciliopathy characterized by a typical cerebellar and brainstem malformation (the “molar tooth sign”), and variable multiorgan involvement. To date, 24 genes have been found mutated in Joubert syndrome, of which 13 also cause Meckel syndrome, a lethal ciliopathy with kidney, liver and skeletal involvement. Here we describe four patients with mild Joubert phenotypes who carry pathogenic mutations in either MKS1 or B9D1, two genes previously implicated only in Meckel syndrome.


Human Genetics | 2015

Oral‑facial‑digital syndrome type VI: is C5orf42 really the major gene?

Marta Romani; Francesca Mancini; Alessia Micalizzi; Andrea Poretti; Elide Miccinilli; Patrizia Accorsi; Emanuela Avola; Enrico Bertini; Renato Borgatti; Romina Romaniello; Serdar Ceylaner; Giangennaro Coppola; Stefano D’Arrigo; Lucio Giordano; Andreas R. Janecke; Mario Lituania; Kathrin Ludwig; Loreto Martorell; Tommaso Mazza; Sylvie Odent; Lorenzo Pinelli; Pilar Poo; Margherita Santucci; Sabrina Signorini; Alessandro Simonati; Ronen Spiegel; Franco Stanzial; Maja Steinlin; Brahim Tabarki; Nicole I. Wolf

Oral-facial-digital type VI syndrome (OFDVI) is a rare phenotype of Joubert syndrome (JS). Recently, C5orf42 was suggested as the major OFDVI gene, being mutated in 9 of 11 families (82xa0%). We sequenced C5orf42 in 313 JS probands and identified mutations in 28 (8.9xa0%), most with a phenotype of pure JS. Only 2 out of 17 OFDVI patients (11.7xa0%) were mutated. A comparison of mutated vs. non-mutated OFDVI patients showed that preaxial and mesoaxial polydactyly, hypothalamic hamartoma and other congenital defects may predict C5orf42 mutations, while tongue hamartomas are more common in negative patients.


Orphanet Journal of Rare Diseases | 2013

Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

Alessandro Ferraris; Laura Bernardini; Vesna Sabolic Avramovska; Ginevra Zanni; Sara Loddo; Elena Sukarova-Angelovska; Valentina Parisi; Anna Capalbo; Stefano Tumini; Lorena Travaglini; Francesca Mancini; Filip Duma; Sabina Barresi; Antonio Novelli; Eugenio Mercuri; Luigi Tarani; Enrico Bertini; Bruno Dallapiccola; Enza Maria Valente

BackgroundThe Dandy-Walker malformation (DWM) is one of the commonest congenital cerebellar defects, and can be associated with multiple congenital anomalies and chromosomal syndromes. The occurrence of overlapping 3q deletions including the ZIC1 and ZIC4 genes in few patients, along with data from mouse models, have implicated both genes in the pathogenesis of DWM.Methods and resultsUsing a SNP-array approach, we recently identified three novel patients carrying heterozygous 3q deletions encompassing ZIC1 and ZIC4. Magnetic resonance imaging showed that only two had a typical DWM, while the third did not present any defect of the DWM spectrum. SNP-array analysis in further eleven children diagnosed with DWM failed to identify deletions of ZIC1-ZIC4. The clinical phenotype of the three 3q deleted patients included multiple congenital anomalies and peculiar facial appearance, related to the localization and extension of each deletion. In particular, phenotypes resulted from the variable combination of three recognizable patterns: DWM (with incomplete penetrance); blepharophimosis, ptosis, and epicanthus inversus syndrome; and Wisconsin syndrome (WS), recently mapped to 3q.ConclusionsOur data indicate that the 3q deletion is a rare defect associated with DWM, and suggest that the hemizygosity of ZIC1-ZIC4 genes is neither necessary nor sufficient per se to cause this condition. Furthermore, based on a detailed comparison of clinical features and molecular data from 3q deleted patients, we propose clinical diagnostic criteria and refine the critical region for WS.


Annals of Nutrition and Metabolism | 2017

Chronic Consumption of Artificial Sweetener in Packets or Tablets and Type 2 Diabetes Risk: Evidence from the E3N-European Prospective Investigation into Cancer and Nutrition Study

Guy Fagherazzi; Gaëlle Gusto; Aurélie Affret; Francesca Mancini; Courtney Dow; Beverley Balkau; Françoise Clavel-Chapelon; Fabrice Bonnet; Marie-Christine Boutron-Ruault

Background: The influence of artificial sweeteners on metabolic diseases is controversial. Artificially sweetened beverages have been associated with an increased risk of type 2 diabetes (T2D) but biases and reverse causation have been suspected to have influenced the observed association. In addition, it has been suggested that investigation into the relationship between the frequency and duration of the consumption of packet or tablet artificial sweeteners and T2D risk is necessary. Methods: We used data from 61,440 women in the prospective E3N-European Prospective Investigation into Cancer and Nutrition study, conducted between 1993 and 2011. We estimated hazards ratios (HRs) and 95% CIs of T2D risk associated with both the frequency and the duration of use of artificial sweeteners consumed in packets or tablets. Results: Compared to “never or rare” consumers of artificial sweeteners, those using them “always or almost always” had an increased risk of T2D (HR = 1.83 [95% CI 1.66-2.02] in the multivariate model [MM], HR = 1.33 [95% CI 1.20-1.47] when further adjusted for body mass index, BMI). Women consuming artificial sweeteners in packets or tablets for more than 10 years also had an increased risk of T2D compared to never or rare users (HR = 2.10 [95% CI 1.83-2.40] in the MM and HR = 1.15 [95% CI 1.00-1.33] when adjusted for BMI, respectively). Conclusions: Our data suggest that both a higher frequency and a longer consumption of artificial sweeteners in packets or tablets was associated with T2D risk, independently of major T2D risk factors, but partially mediated by adiposity. A precautionary principle should be applied to the promotion of these products that are still largely recommended as healthy sugar substitutes.


American Journal of Medical Genetics Part A | 2016

Cognitive, adaptive, and behavioral features in Joubert syndrome

Sara Bulgheroni; Stefano D'Arrigo; Sabrina Signorini; Marilena Briguglio; Maria Lucia Di Sabato; Manuela Casarano; Francesca Mancini; Marta Romani; Paolo Alfieri; Roberta Battini; Marina Zoppello; Gaetano Tortorella; Enrico Bertini; Vincenzo Leuzzi; Enza Maria Valente; Daria Riva

Joubert syndrome (JS) is a recessive neurodevelopmental disorder characterized by a distinctive cerebellar and brainstem malformation recognizable on brain imaging, the so‐called molar tooth sign. The full spectrum of cognitive and behavioral phenotypes typical of JS is still far from being elucidated. The aim of this multicentric study was to define the clinical phenotype and neurobehavioral features of a large cohort of subjects with a neuroradiologically confirmed diagnosis of JS. Fifty‐four patients aged 10 months to 29 years were enrolled. Each patient underwent a neurological evaluation as well as psychiatric and neuropsychological assessments. Global cognitive functioning was remarkably variable with Full IQ/General Quotient ranging from 32 to 129. Communication skills appeared relatively preserved with respect to both Daily Living and Socialization abilities. The motor domain was the area of greatest vulnerability, with a negative impact on personal care, social, and academic skills. Most children did not show maladaptive behaviors consistent with a psychiatric diagnosis but approximately 40% of them presented emotional and behavioral problems. We conclude that intellectual disability remains a hallmark but cannot be considered a mandatory diagnostic criterion of JS. Despite the high variability in the phenotypic spectrum and the extent of multiorgan involvement, nearly one quarter of JS patients had a favorable long‐term outcome with borderline cognitive deficit or even normal cognition. Most of JS population also showed relatively preserved communication skills and overall discrete behavioral functioning in everyday life, independently from the presence and/or level of intellectual disability.


Nutrients | 2017

Identification of Urinary Polyphenol Metabolite Patterns Associated with Polyphenol-Rich Food Intake in Adults from Four European Countries

Hwayoung Noh; Heinz Freisling; Nada Assi; Raul Zamora-Ros; David Achaintre; Aurélie Affret; Francesca Mancini; Marie-Christine Boutron-Ruault; Anna Flögel; Heiner Boeing; Tilman Kühn; Ruth Schübel; Antonia Trichopoulou; Androniki Naska; Maria Kritikou; Domenico Palli; Valeria Pala; Rosario Tumino; Fulvio Ricceri; Maria Santucci de Magistris; Amanda J. Cross; Nadia Slimani; Augustin Scalbert; Pietro Ferrari

We identified urinary polyphenol metabolite patterns by a novel algorithm that combines dimension reduction and variable selection methods to explain polyphenol-rich food intake, and compared their respective performance with that of single biomarkers in the European Prospective Investigation into Cancer and Nutrition (EPIC) study. The study included 475 adults from four European countries (Germany, France, Italy, and Greece). Dietary intakes were assessed with 24-h dietary recalls (24-HDR) and dietary questionnaires (DQ). Thirty-four polyphenols were measured by ultra-performance liquid chromatography–electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS-MS) in 24-h urine. Reduced rank regression-based variable importance in projection (RRR-VIP) and least absolute shrinkage and selection operator (LASSO) methods were used to select polyphenol metabolites. Reduced rank regression (RRR) was then used to identify patterns in these metabolites, maximizing the explained variability in intake of pre-selected polyphenol-rich foods. The performance of RRR models was evaluated using internal cross-validation to control for over-optimistic findings from over-fitting. High performance was observed for explaining recent intake (24-HDR) of red wine (r = 0.65; AUC = 89.1%), coffee (r = 0.51; AUC = 89.1%), and olives (r = 0.35; AUC = 82.2%). These metabolite patterns performed better or equally well compared to single polyphenol biomarkers. Neither metabolite patterns nor single biomarkers performed well in explaining habitual intake (as reported in the DQ) of polyphenol-rich foods. This proposed strategy of biomarker pattern identification has the potential of expanding the currently still limited list of available dietary intake biomarkers.


Public Health Nutrition | 2017

Socio-economic factors associated with an increase in fruit and vegetable consumption: a 12-year study in women from the E3N-EPIC study

Aurélie Affret; Gianluca Severi; Courtney Dow; Francesca Mancini; Grégoire Rey; Cyrille Delpierre; Françoise Clavel-Chapelon; Marie-Christine Boutron-Ruault; Guy Fagherazzi

OBJECTIVEnTo identify individual and contextual socio-economic factors associated with an increase in fruit and vegetable (F&V) consumption over a 12-year period and evaluate if some socio-economic factors were differentially associated with the change in consumption of some types of F&V.nnnDESIGNnAssociations between increased F&V consumption and socio-economic factors were studied with multivariate logistic regression.nnnSETTINGnE3N, a French prospective cohort study of 98 995 women.nnnSUBJECTSnE3N participants (n 58 193) with information on diet in 1993 and 2005, and numerous individual and contextual socio-economic factors available.nnnRESULTSnAssociations between some individual socio-economic factors and changes in F&V consumption were observed. For instance, women who lived in a large household (>3 children v. no child) had higher probability of increasing their vegetable consumption (OR=1·33; 95 % CI 1·24, 1·42). This association was driven by higher consumption of courgette and raw cucumber. Living with a partner was associated with higher odds of increasing consumption of fruits (OR=1·07; 95 % CI 1·02, 1·13) such as pear, peach and grape.nnnCONCLUSIONSnCertain individual socio-economic factors, but none of the contextual socio-economic factors examined, were associated with an increase in F&V consumption. Factors associated with an increase in total F&V consumption were not necessarily associated with an increase in fruit or vegetable consumption separately, or with an increase in each subtype of fruit or vegetable. Magnitudes of the different associations observed also differed when F&V were considered together, separately or by subtype. Increases in F&V consumption were mostly observed in women with high socio-economic position. To develop effective nutritional interventions and policies that take the socio-economic environment of individuals into account, we recommend future research to further focus on (i) pathways through which population characteristics might influence changes in F&V consumption and (ii) existing interactions between individual and contextual socio-economic factors.


eLS | 2014

Molecular Genetics of Joubert Syndrome

Francesca Mancini; Marta Romani; Alessia Micalizzi; Enza Maria Valente


Diabetes & Metabolism | 2017

Utilisation d’édulcorants dans l’alimentation et risque de diabète de type 2 : résultats de l’étude E3N

Guy Fagherazzi; Gaëlle Gusto; Aurélie Affret; Francesca Mancini; Courtney Dow; Beverley Balkau; Françoise Clavel-Chapelon; Fabrice Bonnet; Marie-Christine Boutron-Ruault


Diabetes & Metabolism | 2017

Société Francophone du Diabète (SFD): Communications Affichées Et DiscutéesCAD-7 - Utilisation d’édulcorants dans l’alimentation et risque de diabète de type 2 : résultats de l’étude E3N

Guy Fagherazzi; Gaëlle Gusto; Aurélie Affret; Francesca Mancini; Courtney Dow; Beverley Balkau; Françoise Clavel-Chapelon; Fabrice Bonnet; Marie-Christine Boutron-Ruault

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Marta Romani

Casa Sollievo della Sofferenza

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Alessia Micalizzi

Casa Sollievo della Sofferenza

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Beverley Balkau

French Institute of Health and Medical Research

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Marie-Christine Boutron-Ruault

French Institute of Health and Medical Research

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Enrico Bertini

Boston Children's Hospital

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Tommaso Mazza

Casa Sollievo della Sofferenza

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Alessandro Ferraris

Casa Sollievo della Sofferenza

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