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Filomena Cariola

Research Profile

Procedures

Disorders

Living Beings

Infants

Chemicals & Drugs

Physiology

Anatomy

Chromosomes, Human, Pair 22

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Publications

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Lucia Margari; Angela Pansini; Maria Giuseppina Petruzzelli; Antonia Lucia Buonadonna; Maura Buttiglione; Filomena Cariola; Francesco Craig; Maria Luisa Di Cosola; Mattia Gentile
Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication.
Maria Piccione; Marcello Niceta; V Antona; Antonella Di Fiore; Filomena Cariola; Mattia Gentile; Giovanni Corsello
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.
Mattia Gentile; paolo volpe; Filomena Cariola; Antonio Di Carlo; Vincenzo Marotta; Antonia Lucia Buonadonna; Filippo Maria Boscia
Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.

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All Publications

2012: Lucia Margari; Angela Pansini; Maria Giuseppina Petruzzelli; Antonia Lucia Buonadonna; Maura Buttiglione; Filomena Cariola; Francesco Craig; Maria Luisa Di Cosola; Mattia Gentile
Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication.
American journal of medical genetics. Part A 2012;158A(7):1713-8.
2009: Maria Piccione; Marcello Niceta; V Antona; Antonella Di Fiore; Filomena Cariola; Mattia Gentile; Giovanni Corsello
Identification of two new mutations in TRPS 1 gene leading to the tricho-rhino-phalangeal syndrome type I and III.
American journal of medical genetics. Part A 2009;149A(8):1837-41.
2005: Mattia Gentile; paolo volpe; Filomena Cariola; Antonio Di Carlo; Vincenzo Marotta; Antonia Lucia Buonadonna; Filippo Maria Boscia
Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterization.
American journal of medical genetics. Part A 2005;136(1):66-70.
2005: Mattia Gentile; S De Sanctis; Filomena Cariola; T Spezzi; Antonio Di Carlo; Francesco Tontoli; Florigio Lista; Antonia Lucia Buonadonna
FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II.
European journal of medical genetics 2005;48(1):33-9.
2004: Mattia Gentile; Wim Wuyts; S Grittani; Antonio Di Carlo; Filomena Cariola; Pieter Verdyck; Lucia Margari; Tommaso Perniola; Antonia Lucia Buonadonna
Clinical, cytogenetic, and molecular characterization of a patient with a de novo interstitial 22q12 duplication.
American journal of medical genetics. Part A 2004;127A(2):186-90.
2003: Mattia Gentile; P Fiorente; Antonia Lucia Buonadonna; F Macina; Filomena Cariola
A novel mutation in exon 7 in a family with mild tricho-rhino-phalangeal syndrome type I.
Clinical genetics 2003;63(2):166-7.
2003: Pasquale Berloco; Francesco Russo; Filomena Cariola; Mattia Gentile; Piero Giorgio; Maria Lucia Caruso; Anna Maria Valentini; Giovanni Di Matteo; Alfredo Di Leo
Low presence of p53 abnormalities in H pylori-infected gastric mucosa and in gastric adenocarcinoma.
Journal of gastroenterology 2003;38(1):28-36.
2002: Antonia Lucia Buonadonna; Filomena Cariola; E Caroppo; Antonio Di Carlo; P Fiorente; MC Valenzano; G D'Amato; Mattia Gentile
Molecular and cytogenetic characterization of an azoospermic male with a de-novo Y;14 translocation and alternate centromere inactivation.
Human reproduction (Oxford, England) 2002;17(3):564-9.
2001: Maria Notarnicola; R Gristina; Caterina Messa; Filomena Cariola; P Fiorente; Maria Lucia Caruso; Mattia Gentile; Alfredo Di Leo
Oestrogen receptors and microsatellite instability in colorectal carcinoma patients.
Cancer letters 2001;168(1):65-70.
2001: Nicoletta Resta; Alessandro Stella; Francesco C Susca; Mariapina Montera; Mattia Gentile; Filomena Cariola; F Prete; R Tenconi; Maria Grazia Tibiletti; G Logrieco; T Mattina; G Andriulli; Maria Lucia Caruso; P Fiorente; S Russo; O Caputi-Jambrenghi; Cristina Mareni; Ginevra Guanti
Nine novel APC mutations in Italian FAP patients.
Human mutation 2001;17(5):434-5.
2000: Ginevra Guanti; Nicoletta Resta; Cristiano Simone; Filomena Cariola; I Demma; P Fiorente; Mattia Gentile
Involvement of PTEN mutations in the genetic pathways of colorectal cancerogenesis.
Human molecular genetics 2000;9(2):283-7.
1999: Mattia Gentile; Antonia Lucia Buonadonna; Filomena Cariola; P Fiorente; MC Valenzano; Ginevra Guanti
Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Journal of medical genetics 1999;36(1):77-82.
1998: Alessandro Stella; Nicoletta Resta; A Polizzi; Mariapina Montera; Filomena Cariola; Francesco C Susca; Viviana Gismondi; Lucio Bertario; Cristiana Marchese; R Tenconi; Maria Grazia Tibiletti; Paola Izzo; Mattia Gentile; F Prete; O Pannarale; Giovanni Di Matteo; Paola Sala; Liliana Varesco; Cristina Mareni; Ginevra Guanti
The familial adenomatous polyposis region exhibits many different haplotypes.
Human genetics 1998;102(6):624-8.