ANNALISA BOTTA

Ricercatore universitario

email: botta@med.uniroma2.it
telefono: 001838



BOTTA Annalisa
Posizione attuale: Associate Professor
Telefono +39 06 7259 6078
S.S.D.: MED/03 Medical Genetics
S.C.: 06/A1
e-mail botta@med.uniroma2.it

ISTRUZIONE E FORMAZIONE
2002: Università “La Sapienza”, Roma. Specializzazione in Genetica Medica conseguita con la votazione 70/70 con lode.
1998: Università degli Studi dell'Aquila. Abilitazione all'esercizio della professione di Biologo.
1995: Università degli studi di Roma “Tor Vergata”, Laurea in Scienze Biologiche conseguita presso la cattedra di Genetica Medica diretta dal Prof. Bruno Dallapiccola con la votazione 110/110 con lode.
1990: Liceo Scientifico “Vito Volterra”, Roma. Diploma di maturità scientifica con votazione 60/60.

ESPERIENZA ACCADEMICA
Posizione attuale:
Professore Associato di Genetica Medica a tempo pieno presso la Sezione di Genetica Medica, Università degli Studi di Roma “Tor Vergata”
Posizioni precedenti:
2004-2022: Ricercatore in Genetica Medica a tempo indeterminato (RTI) presso la Sezione di Genetica Medica, Università degli Studi di Roma “Tor Vergata”

ALTRI INCARICHI PROFESSIONALI
2015-2018: incarico assistenziale di natura professionale (strutturazione assistenziale) presso la UOC di Genetica Medica del PTV Policlinico Tor Vergata, diretta dal Prof. Giuseppe Novelli.
2001-2003 incarico assistenziale di natura professionale per consulenza libero-professionale in qualità di Biologa specialista in Genetica Medica, presso il Laboratorio di Genetica Medica dell’Azienda Ospedaliera Universitaria Policlinico Tor Vergata, diretto dal Prof. Giuseppe Novelli.
15/01/1999-14/01/2001: Vincitrice di borsa di studio biennale relativa a progetto Telethon biennale riservato a ricercatori italiani con esperienze lavorative all'estero (n. 364/bi), Università degli studi di Roma "Tor Vergata". Progetto dal titolo “Approccio funzionale verso la comprensione delle basi molecolarid della sindrome di DiGeorge: ruolo dell’enzima deubiquitinante UFD1L nella patogenesi".
1998: Vincitrice di borsa di studio relativa al progetto "Applicazioni della Tecnica RX BANDING all'analisi Genetica" svolta presso l'Università degli studi di Roma "Tor Vergata". Sezione di Genetica Medica.
1996-1997: Post-doctoral Visiting Research Assistant funded by US National Institute of Health nel Dipartimento di Genetica Umana e Molecolare, Baylor College of Medicine- Houston, Texas- USA.
1998: vincitrice di borsa di relativa al progetto "Applicazioni della Tecnica RX BANDING all'analisi Genetica" svolto presso l'Università degli studi di Roma "Tor Vergata". Sezione di Genetica Medica.

ATTIVITA' SCIENTIFICA

Annalisa Botta è professore Associato di Genetica Medica presso la facoltà di Medicina e Chirurgia dell'Università di Roma Tor Vergata. Ha contribuito alla messa a punto di protocolli molecolari, progettato studi sperimentali e ottenuto risultati innovativi nell'ambito delle malattie ereditarie. Le ricerche di cui si è occupata all’inizio della sua carriera hanno riguardato le basi genetiche delle malattie mendeliane, in particolare la fibrosi cistica, la malattia Thomsen, le sindromi di Williams e di DiGeorge. Parallelamente alla sua attività di ricerca scientifica, la Prof.ssa Botta ha iniziato un percorso orientato sull’attività clinica e ottenuto un incarico come Genetista presso il laboratorio di Genetica Medica dell’Azienda Ospedaliera Policlinico Tor Vergata. In tale ambito ha partecipato alla elaborazione di linee nazionali per la diagnosi molecolare delle Distrofie Miotoniche (DM) e delle Atrofie Muscolari Spinali (SMA). Attualmente coordina una unità che si occupa della comprensione dei meccanismi patogenetici e dello sviluppo di strategie terapeutiche nel campo delle malattie neuromuscolari. Negli ultimi anni, le sue ricerche hanno anche riguardato l’identificazione di fattori genetici di suscettibilità e l’identificazione di biomarcatori delle patologie da fragilità ossea. L'attività scientifica della prof.ssa Botta è documentata numerose pubblicazioni scientifiche inerenti aspetti di ricerca di base (comprensione di meccanismi patogenetici e sviluppo di modelli-malattia cellulari) e medicina traslazionale (protocolli diagnostici, studi di correlazione genotipo-fenotipo, identificazione di biomarcatori) (https://orcid.org/0000-0003-4031-5624). Annalisa Botta è membro della Società Italiana di Genetica Umana (SIGU) e dell’Associazione Italiana di Miologia (AIM). Ha svolto attività di revisore per numerose riviste scientifiche internazionali e partecipato a progetti di ricerca finanziati da enti nazionali ed internazionali.

ATTIVITÀ DIDATTICA

Dal 2004 la dott.ssa Botta è docente titolare per la disciplina di Genetica Medica nei corsi di laurea e di specializzazione afferenti alla Facoltà di Medicina e Chirurgia presso l'Università degli studi di Roma Tor Vergata sia in lingua italiana che in lingua inglese (International School of Medicine). E’ inoltre membro del Collegio dei Docenti del Dottorato di Ricerca in “Dottorato in Biotecnologie Medico Chirurgiche e Medicina Traslazionale”.

SCIENTIFIC PUBLICATIONS
Link ORCID profile: https://orcid.org/0000-0003-4031-5624
Link SCOPUS profile: https://www.scopus.com/authid/detail.uri?authorId=7005993766
Link PUBMED: https://www.ncbi.nlm.nih.gov/myncbi/1b3Ji7bQpH0kk/bibliography/public/



Produzione scientifica

2108/383463 - 2024 - Cellular Senescence: The Driving Force of Musculoskeletal Diseases
Falvino, Angela; Gasperini, Beatrice; Cariati, Ida; Bonanni, Roberto; Chiavoghilefu, Angela Abby; Gasbarra, Elena; Botta, Annalisa; Tancredi, Virginia; Tarantino, Umberto - 01 - Articolo su rivista
rivista: BIOMEDICINES (Basel: MDPI) pp. - - issn: 2227-9059 - wos: (0) - scopus: (0)

2108/329616 - 2023 - Plasma heavy metal levels correlate with deregulated gene expression of detoxifying enzymes in osteoporotic patients
Greggi, Chiara; Messina, Alessandra; Iundusi, Riccardo; Botta, Annalisa; Palombi, Leonardo; Tarantino, Umberto - 01 - Articolo su rivista
rivista: SCIENTIFIC REPORTS (London: Springer Nature London: Nature Publishing Group) pp. 1-7 - issn: 2045-2322 - wos: WOS:001022800200015 (5) - scopus: 2-s2.0-85164178889 (5)

2108/335563 - 2023 - In Cis Effect of DMPK Expanded Alleles in Myotonic Dystrophy Type 1 Patients Carrying Variant Repeats at 5′ and 3′ Ends of the CTG Array
Visconti, Virginia Veronica; D'apice, Maria Rosaria; Massa, Roberto; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel (Matthaeustrasse 11) : Molecular Diversity Preservation International MDPI) pp. 1-14 - issn: 1661-6596 - wos: WOS:001017278900001 (0) - scopus: 2-s2.0-85163963409 (1)

2108/388103 - 2023 - Methylation of the Vitamin D Receptor Gene in Human Disorders
Gasperini, Beatrice; Falvino, Angela; Piccirilli, Eleonora; Tarantino, Umberto; Botta, Annalisa; Visconti, Virginia Veronica - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel: MDPI Center) pp. - - issn: 1422-0067 - wos: WOS:001140519400001 (4) - scopus: 2-s2.0-85181952563 (3)

2108/388099 - 2023 - Role of the Vitamin D Receptor (VDR) in the Pathogenesis of Osteoporosis: A Genetic, Epigenetic and Molecular Pilot Study
Gasperini, Beatrice; Visconti, Virginia Veronica; Falvino, Angela; Gasbarra, Elena; Iundusi, Riccardo; Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. - - issn: 2073-4425 - wos: WOS:000958089900001 (9) - scopus: 2-s2.0-85151975645 (7)

2108/306579 - 2022 - Circulating MicroRNAs as Biomarkers of Osteoporosis and Fragility Fractures
Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM (-Springfield, Ill. : Charles C. Thomas -Philadelphia : J.B. Lippincott Co. -Baltimore, Md. : Issued for the Endocrine Society by the Williams & Wilkins Co. -Bethesda, MD : Endocrine Society -Chevy Chase, MD : Endocrine Society) pp. 2267-2285 - issn: 0021-972X - wos: WOS:000808216600001 (10) - scopus: 2-s2.0-85134428913 (11)

2108/306239 - 2022 - Deregulated Clusterin as a Marker of Bone Fragility: New Insights into the Pathophysiology of Osteoporosis
Greggi, Chiara; Cariati, Ida; Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. 652- - issn: 2073-4425 - wos: WOS:000786793600001 (3) - scopus: 2-s2.0-85128724914 (4)

2108/306388 - 2022 - Association Between DRD2 and DRD4 Polymorphisms and Eating Disorders in an Italian Population
Ciccacci, Cinzia; Botta, Annalisa - 01 - Articolo su rivista
rivista: FRONTIERS IN NUTRITION (Lausanne : Frontiers Media S.A., 2014-) pp. 838177- - issn: 2296-861X - wos: WOS:000777468600001 (7) - scopus: 2-s2.0-85127795709 (7)

2108/311558 - 2022 - Characterization of full-length CNBP expanded alleles in myotonic dystrophy type 2 patients by Cas9-mediated enrichment and nanopore sequencing
Massa, Roberto; D'apice, Maria Rosaria; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: ELIFE (Cambridge: eLife Sciences Publications) pp. - - issn: 2050-084X - wos: WOS:000921161000001 (7) - scopus: 2-s2.0-85138128565 (8)

2108/311735 - 2022 - Two Different Therapeutic Approaches for SARS-CoV-2 in hiPSCs-Derived Lung Organoids
Spitalieri, Paola; Murdocca, Michela; Di Cesare, Silvia; Orlandi, Augusto; Botta, Annalisa; Sangiuolo, Federica Carla; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CELLS (Basel: mdpi-Molecular Diversity Preservation International) pp. 1-18 - issn: 2073-4409 - wos: WOS:000780993700001 (22) - scopus: 2-s2.0-85127614410 (23)

2108/311731 - 2021 - Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture
Botta, Annalisa; D'apice, Maria Rosaria; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: FRONTIERS IN GENETICS (Lausanne : Frontiers Research Foundation, 2010-) pp. 1-12 - issn: 1664-8021 - wos: WOS:000705469700001 (9) - scopus: 2-s2.0-85116889067 (10)

2108/275408 - 2021 - DNA Methylation Signatures of Bone Metabolism in Osteoporosis and Osteoarthritis Aging-Related Diseases: An Updated Review
Cariati, Ida; Iundusi, Riccardo; Gasbarra, Elena; Tarantino, Umberto; Botta, Annalisa - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel: MDPI Center) pp. 4244- - issn: 1422-0067 - wos: WOS:000644322400001 (27) - scopus: 2-s2.0-85104435934 (26)

2108/311730 - 2021 - A 14-Year Italian Experience in DM2 Genetic Testing: Frequency and Distribution of Normal and Premutated CNBP Alleles
Botta, Annalisa; Massa, Roberto; Sangiuolo, Federica Carla; D'apice, Maria Rosaria; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: FRONTIERS IN GENETICS (Lausanne : Frontiers Research Foundation, 2010-) pp. 1-10 - issn: 1664-8021 - wos: WOS:000669469000001 (2) - scopus: 2-s2.0-85109106084 (3)

2108/306238 - 2021 - The Role of PTX3 in Mineralization Processes and Aging-Related Bone Diseases
Tarantino, Umberto; Greggi, Chiara; Cariati, Ida; Gasbarra, Elena; Botta, Annalisa; Salustri, Antonietta; Scimeca, Manuel - 01 - Articolo su rivista
rivista: FRONTIERS IN IMMUNOLOGY (Lausanne : Frontiers Research Foundation, 2010-) pp. 622772- - issn: 1664-3224 - wos: WOS:000617046500001 (10) - scopus: 2-s2.0-85101034151 (9)

2108/275406 - 2021 - The long pentraxin PTX3: a novel serum marker to improve the prediction of osteoporosis and osteoarthritis bone-related phenotypes
Greggi, Chiara; Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: JOURNAL OF ORTHOPAEDIC SURGERY AND RESEARCH (London : BioMed Central, 2006-) pp. 288- - issn: 1749-799X - wos: WOS:000656145300002 (7) - scopus: 2-s2.0-85105203302 (8)

2108/275363 - 2020 - A pilot study of lncRNAs expression profile in serum of progressive multiple sclerosis patients
Botta, Annalisa - 01 - Articolo su rivista
rivista: EUROPEAN REVIEW FOR MEDICAL AND PHARMACOLOGICAL SCIENCES (Roma: Verduci publisher) pp. 3267-3273 - issn: 2284-0729 - wos: WOS:000525326200050 (16) - scopus: 2-s2.0-85082940628 (17)

2108/275361 - 2020 - Recognition of emotions conveyed by facial expression and body postures in myotonic dystrophy (DM)
Botta, Annalisa - 01 - Articolo su rivista
rivista: CORTEX (Milano: Masson) pp. 58-66 - issn: 1973-8102 - wos: WOS:000534377300005 (17) - scopus: 2-s2.0-85080990548 (21)

2108/275359 - 2020 - Evaluation of mexiletine effect on conduction delay and bradyarrhythmic complications in patients with myotonic dystrophy type 1 over long-term follow-up
Botta, Annalisa - 01 - Articolo su rivista
rivista: HEART RHYTHM (New York, NY : Elsevier, c2004-) pp. 1944-1950 - issn: 1547-5271 - wos: WOS:000583293800016 (11) - scopus: 2-s2.0-85088964602 (14)

2108/306237 - 2020 - Identification of Aberrantly-Expressed Long Non-Coding RNAs in Osteoblastic Cells from Osteoporotic Patients
Rinaldi, Anna Maria; D'arcangelo, Giovanna; Novelli, Giuseppe; Orlandi, Augusto; Tancredi, Virginia; Tarantino, Umberto; Botta, Annalisa - 01 - Articolo su rivista
rivista: BIOMEDICINES (Basel: MDPI) pp. 65- - issn: 2227-9059 - wos: WOS:000530205700024 (18) - scopus: 2-s2.0-85083716439 (17)

2108/306236 - 2020 - Circulating long non-coding rna gas5 is overexpressed in serum from osteoporotic patients and is associated with increased risk of bone fragility
Novelli, Giuseppe; Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (Basel: MDPI Center) pp. 1-12 - issn: 1422-0067 - wos: WOS:000580740200001 (13) - scopus: 2-s2.0-85091517131 (15)

2108/256544 - 2020 - Carrier frequency of CFTR variants in the non-Caucasian populations by genome aggregation database (gnomAD)-based analysis
Novelli, Giuseppe; Sangiuolo, Federica Carla; Botta, Annalisa - 01 - Articolo su rivista
rivista: ANNALS OF HUMAN GENETICS (-MALDEN, USA: WILEY-BLACKWELL PUBLISHING, INC -Cambridge, United Kingdom: Cambridge University Press) pp. 463-468 - issn: 0003-4800 - wos: WOS:000536989000001 (9) - scopus: 2-s2.0-85085690984 (9)

2108/266323 - 2020 - Cutaneous and metabolic defects associated with nuclear abnormalities in a transgenic mouse model expressing R527H lamin A mutation causing mandibuloacral dysplasia type A (MADA) syndrome
De Dominicis, Andrea; Murdocca, Michela; Amati, Francesca; Botta, Annalisa; Sangiuolo, Federica Carla; Federici, Massimo; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: ACTA MYOLOGICA (Gaetano Conte Academy for the study of striated muscle diseases. Napoli) pp. 320-335 - issn: 1128-2460 - wos: (0) - scopus: 2-s2.0-85100325503 (3)

2108/266315 - 2020 - Genetic variability in noncoding RNAs: involvement of miRNAs and long noncoding RNAs in osteoporosis pathogenesis
Tarantino, Umberto; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: EPIGENOMICS (London: Future Medicine, 2009-) pp. 2035-2049 - issn: 1750-1911 - wos: WOS:000595087000001 (4) - scopus: 2-s2.0-85098138145 (6)

2108/266317 - 2020 - Identification, molecular characterization and segregation analysis of a variant DMPK pre-mutation allele in a three-generation Italian family
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: ACTA MYOLOGICA (Gaetano Conte Academy for the study of striated muscle diseases. Napoli) pp. 13-18 - issn: 1128-2460 - wos: (0) - scopus: 2-s2.0-85087090499 (4)

2108/227547 - 2019 - TNNT2 missplicing in skeletal muscle as a cardiac biomarker in myotonic dystrophy type 1 but not in myotonic dystrophy type 2
Botta, Annalisa - 01 - Articolo su rivista
rivista: FRONTIERS IN NEUROLOGY (Lausanne: Frontiers Research Foundation, 2010-) pp. 992- - issn: 1664-2295 - wos: WOS:000488060800001 (7) - scopus: 2-s2.0-85073150290 (8)

2108/227551 - 2019 - Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study
Massa, Roberto; Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF THE NEUROLOGICAL SCIENCES (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 118-124 - issn: 0022-510X - wos: WOS:000465148900021 (29) - scopus: 2-s2.0-85061815728 (33)

2108/227555 - 2019 - Reply to the letter entitled “Predictors of respiratory impairment in patients with myotonic dystrophy type 1”
Massa, Roberto; Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF THE NEUROLOGICAL SCIENCES (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 166-167 - issn: 0022-510X - wos: WOS:000484647600037 (0) - scopus: 2-s2.0-85070665126 (0)

2108/227545 - 2019 - The Role of Motor System in Mental Rotation: New Insights from Myotonic Dystrophy Type 1
Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY (Cambridge University Press:Edinburgh Building, Shaftesbury Road, Cambridge CB2 2RU United Kingdom:011 44 1223 326092, EMAIL: journals@cambridge.org, journals_subscriptions@cambridge.org, INTERNET: http://www.cup.cam.ac.uk, journals_subscriptions@camebridge.org, Fax: 011 44 1223 325959) pp. 1-11 - issn: 1355-6177 - wos: WOS:000530308000004 (4) - scopus: 2-s2.0-85076474830 (4)

2108/227535 - 2018 - Workload measurement for molecular genetics laboratory: A survey study
Botta, Annalisa - 01 - Articolo su rivista
rivista: PLOS ONE (San Francisco, CA : Public Library of Science) pp. e0206855- - issn: 1932-6203 - wos: WOS:000451440000006 (6) - scopus: 2-s2.0-85057270582 (6)

2108/227530 - 2018 - Validation of the Nine Hole Peg Test as a measure of dexterity in myotonic dystrophy type 1
Botta, Annalisa; Massa, Roberto - 01 - Articolo su rivista
rivista: NEUROMUSCULAR DISORDERS (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 947-951 - issn: 0960-8966 - wos: WOS:000453497300006 (5) - scopus: 2-s2.0-85054191926 (5)

2108/226329 - 2018 - AFM nano-mechanical study of the beating profile of hiPSC-derived cardiomyocytes beating bodies WT and DM1
Spitalieri, Paola; Murdocca, Michela; Botta, Annalisa; Novelli, Giuseppe; Sangiuolo, Federica Carla - 01 - Articolo su rivista
rivista: JOURNAL OF MOLECULAR RECOGNITION ([London, UK : Heydon & Son] : John Wiley & Sons, Ltd., c1988-) pp. e2725- - issn: 1099-1352 - wos: WOS:000444465000001 (5) - scopus: 2-s2.0-85046747639 (8)

2108/227060 - 2018 - SCN4A as modifier gene in patients with myotonic dystrophy type 2
Botta, Annalisa - 01 - Articolo su rivista
rivista: SCIENTIFIC REPORTS (London: Springer Nature London: Nature Publishing Group) pp. 11058- - issn: 2045-2322 - wos: WOS:000439421600026 (10) - scopus: 2-s2.0-85050608480 (14)

2108/243170 - 2018 - Vitamin D Receptor in Muscle Atrophy of Elderly Patients: A Key Element of Osteoporosis-Sarcopenia Connection
Scimeca, Manuel; Gasbarra, Elena; Novelli, Giuseppe; Botta, Annalisa; Tarantino, Umberto - 01 - Articolo su rivista
rivista: AGING AND DISEASE (California : JKL International) pp. 952-964 - issn: 2152-5250 - wos: WOS:000457497300001 (32) - scopus: 2-s2.0-85060383729 (34)

2108/195122 - 2018 - Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients
Maiorca, Francesca; Massa, Roberto; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: BIOCHIMICA ET BIOPHYSICA ACTA. MOLECULAR BASIS OF DISEASE (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 917-924 - issn: 0925-4439 - wos: WOS:000425477500026 (10) - scopus: 2-s2.0-85039993111 (11)

2108/195116 - 2018 - A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre
Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF NEUROLOGY (Heidelberg Germany: Springer Verlag) pp. 1-11 - issn: 0340-5354 - wos: WOS:000428928200017 (10) - scopus: 2-s2.0-85041930746 (14)

2108/211139 - 2018 - Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2
Spitalieri, Paola; Murdocca, Michela; Campione, Elena; Massa, Roberto; Novelli, Giuseppe; Sangiuolo, Federica Carla; Botta, Annalisa - 01 - Articolo su rivista
rivista: FRONTIERS IN PHYSIOLOGY (Lausanne: Frontiers Research Foundation, 2010-) pp. 967- - issn: 1664-042X - wos: WOS:000440033300001 (3) - scopus: 2-s2.0-85065959333 (3)

2108/211427 - 2018 - Modelling the pathogenesis of Myotonic Dystrophy type 1 cardiac phenotype through human iPSC-derived cardiomyocytes
Spitalieri, Paola; Caioli, Silvia; Murdocca, Michela; Pucci, Sabina; Botta, Annalisa; Novelli, Giuseppe; Zona, Cristina; Sangiuolo, Federica Carla - 01 - Articolo su rivista
rivista: JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 95-109 - issn: 0022-2828 - wos: WOS:000432499700008 (19) - scopus: 2-s2.0-85044483318 (22)

2108/227062 - 2018 - Activation of the interferon type I response rather than autophagy contributes to myogenesis inhibition in congenital DM1 myoblasts
Botta, Annalisa - 01 - Articolo su rivista
rivista: CELL DEATH & DISEASE (Nature Group) pp. 1071- - issn: 2041-4889 - wos: WOS:000447648300005 (14) - scopus: 2-s2.0-85055073058 (14)

2108/180110 - 2017 - Targeted Next Generation Sequencing in patients with Myotonia Congenita
Ferradini, Valentina; D'apice, Maria Rosaria; Botta, Annalisa; Novelli, Giuseppe; Sangiuolo, Federica Carla - 01 - Articolo su rivista
rivista: CLINICA CHIMICA ACTA (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 1-7 - issn: 0009-8981 - wos: WOS:000405883100001 (9) - scopus: 2-s2.0-85018634249 (12)

2108/256290 - 2017 - Erratum: Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1
Botta, Annalisa; Massa, Roberto - 99 - Altro

2108/169501 - 2017 - Identification and characterization of 5' CCG interruptions in complex DMPK expanded alleles
Botta, Annalisa; Massa, Roberto; Sangiuolo, Federica Carla; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: EUROPEAN JOURNAL OF HUMAN GENETICS (-NATURE PUBLISHING GROUP, MACMILLAN BUILDING, 4 CRINAN ST, LONDON, ENGLAND, N1 9XW -S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 257-261 - issn: 1018-4813 - wos: WOS:000394122900021 (31) - scopus: 2-s2.0-84996844847 (32)

2108/166152 - 2017 - Cutaneous features of myotonic dystrophy types 1 and 2: implication of premature aging and vitamin d homeostasis
Campione, Elena; Botta, Annalisa; Bernardini, Sergio; Novelli, Giuseppe; Bianchi, Luca; Orlandi, Augusto; Massa, Roberto - 01 - Articolo su rivista
rivista: NEUROMUSCULAR DISORDERS (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 163-169 - issn: 0960-8966 - wos: WOS:000394474600009 (14) - scopus: 2-s2.0-85008455618 (17)

2108/177668 - 2017 - Myotonic dystrophy type 1: Role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosis
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: CLINICAL GENETICS (Blackwell Munksgaard:PO Box 2148, Periodicals Department, DK-1016 Copenhagen K Denmark:011 45 33 755913, EMAIL: agentservices@oxon.blackwellpublishing.com, INTERNET: http://www.blackwellmunksgaard.com, Fax: 011 45 77 333377) pp. 355-364 - issn: 0009-9163 - wos: WOS:000411478400001 (35) - scopus: 2-s2.0-85013384803 (44)

2108/166248 - 2016 - Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency
Botta, Annalisa - 01 - Articolo su rivista
rivista: AMERICAN JOURNAL OF HUMAN GENETICS (Chicago, Ill. : University of Chicago Press for the American Society of Human Genetics) pp. 1130-1145 - issn: 1537-6605 - wos: WOS:000377286000008 (99) - scopus: 2-s2.0-84971568098 (116)

2108/166250 - 2016 - Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors (J Nerol, 10.1007/s00415-015-8006-y)
Massa, Roberto; Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF NEUROLOGY (Heidelberg Germany: Springer Verlag) pp. 499-499 - issn: 0340-5354 - wos: WOS:000372433600012 (2) - scopus: 2-s2.0-84960405698 (1)

2108/166252 - 2016 - Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts
Giardina, Emiliano; Sangiuolo, Federica Carla; Botta, Annalisa - 01 - Articolo su rivista
rivista: EXPERIMENTAL CELL RESEARCH (Academic Press Incorporated:6277 Sea Harbor Drive:Orlando, FL 32887:(800)543-9534, (407)345-4100, EMAIL: ap@acad.com, INTERNET: http://www.idealibrary.com, Fax: (407)352-3445) pp. 39-51 - issn: 0014-4827 - wos: WOS:000372766600005 (22) - scopus: 2-s2.0-84962798228 (21)

2108/163050 - 2016 - An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy
Botta, Annalisa; Novelli, Giuseppe; Massa, Roberto - 01 - Articolo su rivista
rivista: NEUROEPIDEMIOLOGY (S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 191-197 - issn: 0251-5350 - wos: WOS:000373864300006 (32) - scopus: 2-s2.0-84958818835 (35)

2108/172614 - 2016 - Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1
Botta, Annalisa; Massa, Roberto - 01 - Articolo su rivista
rivista: SCIENTIFIC REPORTS (London: Springer Nature London: Nature Publishing Group) pp. 38174- - issn: 2045-2322 - wos: WOS:000388983400001 (41) - scopus: 2-s2.0-85000501065 (44)

2108/119217 - 2015 - Generation of human induced pluripotent stem cells from extraembryonic tissues of fetuses affected by monogenic diseases
Botta, Annalisa; Murdocca, Michela; Orlandi, Augusto; Giardina, Emiliano; Novelli, Giuseppe; Sangiuolo, Federica Carla - 01 - Articolo su rivista
rivista: CELLULAR REPROGRAMMING (New Rochelle, NY : Mary Ann Liebert, Inc.) pp. 275-287 - issn: 2152-4971 - wos: WOS:000359621100005 (18) - scopus: 2-s2.0-84938693781 (19)

2108/119158 - 2015 - Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1)
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: BIOCHIMICA ET BIOPHYSICA ACTA (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 2645-2652 - issn: 0006-3002 - wos: WOS:000363827300008 (26) - scopus: 2-s2.0-84942694221 (28)

2108/119227 - 2015 - Variant interrupted DMPK alleles: implications in the pathogenesis and molecular diagnosis of myotonic dystrophy type 1 (DM1)
Novelli, Giuseppe; Botta, Annalisa - 03 - Contributo in libro
libro: Myotonic dystrophies: epidemiology, diagnosis and therapeutic challenges - (978-163482917-5)

2108/119192 - 2015 - SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype
Botta, Annalisa - 01 - Articolo su rivista
rivista: NEUROMUSCULAR DISORDERS (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 301-307 - issn: 0960-8966 - wos: WOS:000353081700004 (30) - scopus: 2-s2.0-84925279853 (39)

2108/119187 - 2015 - Epstein-Barr virus infection induces miR-21 in terminally differentiated malignant B cells
Botta, Annalisa - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF CANCER (Hoboken N.J.: Wiley New York NY: Wiley-Liss) pp. 1491-1497 - issn: 0020-7136 - wos: WOS:000357808900029 (30) - scopus: 2-s2.0-84936846039 (31)

2108/119206 - 2014 - Progression of muscle histopathology but not of spliceopathy in myotonic dystrophy type 2
Botta, Annalisa - 01 - Articolo su rivista
rivista: EUROPEAN JOURNAL OF HISTOCHEMISTRY (Tipolitografia l Ponzio:Viale Montegrappa 2, I 27100 Pavia Italy:011 39 0382 576600, Fax: 011 39 0382 574200) pp. 1042-1053 - issn: 1121-760X - wos: WOS:000347770100003 (12) - scopus: 2-s2.0-84919461424 (14)

2108/119201 - 2014 - Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 induction
Botta, Annalisa - 01 - Articolo su rivista
rivista: EUROPEAN JOURNAL OF HISTOCHEMISTRY (Pavia : PagePress Publications, 2010) pp. 275-286 - issn: 2038-8306 - wos: WOS:000347228000003 (25) - scopus: 2-s2.0-84908292875 (27)

2108/85951 - 2013 - MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases
Botta, Annalisa; Bellocchi, Maria Concetta; Novelli, Giuseppe; Rossi, Gabriele - 01 - Articolo su rivista
rivista: CELL DEATH & DISEASE (Nature Group) pp. e770-e770 - issn: 2041-4889 - wos: WOS:000324146000027 (24) - scopus: 2-s2.0-84882733817 (25)

2108/88076 - 2013 - Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cells.
Botta, Annalisa - 01 - Articolo su rivista
rivista: GENES (Basel : Molecular Diversity Preservation International) pp. 275-292 - issn: 2073-4425 - wos: WOS:000209242800009 (30) - scopus: 2-s2.0-84880781160 (31)

2108/85953 - 2013 - Overexpression of CUGBP1 in skeletal muscle from adult classic myotonic dystrophy type 1 but not from myotonic dystrophy type 2
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: PLOS ONE (San Francisco, CA : Public Library of Science) pp. e83777- - issn: 1932-6203 - wos: WOS:000328745100139 (21) - scopus: 2-s2.0-84893518233 (27)

2108/39931 - 2012 - Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues
Massa, Roberto; Di Girolamo, Stefano; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: NEUROBIOLOGY OF DISEASE (Academic Press Incorporated:6277 Sea Harbor Drive:Orlando, FL 32887:(800)543-9534, (407)345-4100, EMAIL: ap@acad.com, INTERNET: http://www.idealibrary.com, Fax: (407)352-3445) pp. 264-271 - issn: 0969-9961 - wos: WOS:000297883500029 (19) - scopus: 2-s2.0-81955167967 (22)

2108/88077 - 2012 - Co-segregation of DM2 with a recessive CLCN1 mutation in juvenile onset of myotonic dystrophy type 2
Botta, Annalisa; Morgante, Alessandra; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: JOURNAL OF NEUROLOGY (Heidelberg Germany: Springer Verlag) pp. 2090-2099 - issn: 0340-5354 - wos: WOS:000309562800009 (33) - scopus: 2-s2.0-84867332225 (40)

2108/102989 - 2011 - Early subclinical cochlear dysfunction in myotonic dystrophy type 1.
Botta, Annalisa; Novelli, Giuseppe; Bernardi, Giorgio; Massa, Roberto; Di Girolamo, Stefano - 01 - Articolo su rivista
rivista: EUROPEAN JOURNAL OF NEUROLOGY (Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320) pp. 1412-1416 - issn: 1351-5101 - wos: WOS:000297162800016 (9) - scopus: 2-s2.0-81855161645 (11)

2108/10344 - 2010 - Validation of sensitivity and specificity of tetraplet-primed PCR (TP-PCR) in the molecular diagnosis of myotonic dystrophy type 2 (DM2)
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: THE JOURNAL OF MOLECULAR DIAGNOSTICS (Bethesda, MD : American Society for Investigative Pathology and the Association for Molecular Pathology, 1999-) pp. 601-606 - issn: 1525-1578 - wos: WOS:000281690800007 (14) - scopus: 2-s2.0-77956811925 (18)

2108/11094 - 2010 - The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles
Massa, Roberto; Caldarola, Sara; Botta, Annalisa; Novelli, Giuseppe; Bernardi, Giorgio; Loreni, Fabrizio - 01 - Articolo su rivista
rivista: NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (Blackwell Science Limited:PO Box 88, Oxford OX2 0NE United Kingdom:011 44 1865 776868, 011 44 1865 206038, EMAIL: journals.cs@blacksci.co.uk, INTERNET: http://www.blackwell-science.com, Fax: 011 44 1865 721205) pp. 275-284 - issn: 0305-1846 - wos: WOS:000277712100002 (13) - scopus: 2-s2.0-77952375211 (14)

2108/10348 - 2010 - Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients
Gambardella, Sergio; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF TRANSLATIONAL MEDICINE (London: BioMed Central, London) pp. 48- - issn: 1479-5876 - wos: WOS:000278296700001 (84) - scopus: 2-s2.0-77952369117 (100)

2108/10928 - 2010 - Normal myogenesis and increased apoptosis in myotonic dystrophy type 1 muscle cells
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: CELL DEATH AND DIFFERENTIATION (Nature Publishing Group:Brunel Road Houndmills, Basingstoke RG21 6XS United Kingdom:011 44 20 78334000, EMAIL: institutions@natureny.com, INTERNET: http://www.nature.com, Fax: 011 44 20 78434640) pp. 1314-1324 - issn: 1350-9047 - wos: WOS:000279725900011 (68) - scopus: 2-s2.0-77954659835 (73)

2108/11028 - 2009 - Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 gene
Botta, Annalisa; Sangiuolo, Federica Carla; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENETIC TESTING AND MOLECULAR BIOMARKERS (New Rochelle, NY : Mary Ann Liebert, Inc.) pp. 127-131 - issn: 1945-0265 - wos: WOS:000265065900021 (11) - scopus: 2-s2.0-67049133473 (10)

2108/38881 - 2009 - Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: NEUROMUSCULAR DISORDERS (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 335-343 - issn: 0960-8966 - wos: WOS:000266794600006 (23) - scopus: 2-s2.0-67349117382 (26)

2108/10995 - 2008 - Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: ACTA MYOLOGICA (Gaetano Conte Academy for the study of striated muscle diseases. Napoli) pp. 82-89 - issn: 1128-2460 - wos: (0) - scopus: 2-s2.0-64949107173 (1)

2108/38332 - 2008 - The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: JOURNAL OF MEDICAL GENETICS (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 639-646 - issn: 0022-2593 - wos: WOS:000259710100005 (42) - scopus: 2-s2.0-54049141673 (44)

2108/11006 - 2007 - Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients
Botta, Annalisa; Vallo, Laura; Massa, Roberto; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENETIC TESTING (Mary Ann Liebert Incorporated:2 Madison Avenue:Larchmont, NY 10538:(914)834-3100, EMAIL: info@liebertpub.com, swilliams@liebertpub.com, INTERNET: http://www.liebertpub.com, Fax: (914)834-3688) pp. 84-90 - issn: 1090-6576 - wos: WOS:000245435000010 (44) - scopus: 2-s2.0-34147135054 (48)

2108/26589 - 2007 - Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.
Botta, Annalisa; Amati, Francesca; Biancolella, Michela; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENE EXPRESSION (North Chicago, IL, USA : Chicago Medical School Press, c1991- Elmsford, NY: Cognizant Communication Corporation) pp. 339-351 - issn: 1052-2166 - wos: WOS:000248602800005 (34) - scopus: 2-s2.0-34548072824 (40)

2108/169683 - 2007 - Myotonic dystrophy unlinked to DM1 and DM2 mutations in three siblings
Pisani, Valerio; Botta, Annalisa; Marfia, Girolama Alessandra; Bernardi, Giorgio; Novelli, Giuseppe; Massa, Roberto - 01 - Articolo su rivista
rivista: NEUROMUSCULAR DISORDERS (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 857-857 - issn: 0960-8966 - wos: WOS:000250258000322 (0) - scopus: (0)

2108/29393 - 2006 - Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CLINICAL CHEMISTRY (-Washington, DC: American Association of Clinical Chemistry -Baltimore, Md. : P.B. Hoeber, [c1955-) pp. 319-322 - issn: 0009-9147 - wos: WOS:000235069600024 (17) - scopus: 2-s2.0-31844441030 (20)

2108/119438 - 2006 - Therapeutic strategies for the treatment of Spinal Muscular Atrophy (SMA) disease
Sangiuolo, Federica Carla; Botta, Annalisa; Filareto, Antonio; Spitalieri, Paola; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CURRENT GENOMICS (Bentham Science Publishers BV:PO Box 7917, Exec Ste Y 26, Saif Zone Sharjah Uae:011 971 6 5571132, EMAIL: benthams@emirates.net.ae, INTERNET: http://www.bentham.org, Fax: 011 971 6 5571134 (Hilversum : Bentham Science Publishers )) pp. 381-386 - issn: 1389-2029 - wos: WOS:000242750400004 (2) - scopus: 2-s2.0-33751435417 (2)

2108/40402 - 2006 - Italian guidelines for molecular analysis in myotonic dystrophies
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: ACTA MYOLOGICA (Gaetano Conte Academy for the study of striated muscle diseases. Napoli) pp. 23-33 - issn: 1128-2460 - wos: (0) - scopus: 2-s2.0-33747517559 (29)

2108/38832 - 2006 - Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2)
Botta, Annalisa; Caldarola, Sara; Vallo, Laura; Massa, Roberto; Novelli, Giuseppe; Loreni, Fabrizio - 01 - Articolo su rivista
rivista: BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (Elsevier BV:PO Box 211, 1000 AE Amsterdam Netherlands:011 31 20 4853757, 011 31 20 4853642, 011 31 20 4853641, EMAIL: nlinfo-f@elsevier.nl, INTERNET: http://www.elsevier.nl, Fax: 011 31 20 4853598) pp. 329-334 - issn: 0304-4165 - wos: WOS:000235439000008 (40) - scopus: 2-s2.0-31644446676 (43)

2108/29383 - 2005 - Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population
Vallo, Laura; Borgiani, Paola; Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: MOLECULAR AND CELLULAR PROBES (Elsevier Science Limited:Oxford Fulfillment Center, PO Box 800, Kidlington Oxford OX5 1DX United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: asianfo@elsevier.com, tcb@elsevier.co.UK, INTERNET: http://www.elsevier.com, http://www.elsevier.com/locate/shpsa/, Fax: 011 44 1865 843010) pp. 71-74 - issn: 0890-8508 - wos: WOS:000226802300009 (4) - scopus: 2-s2.0-11844264812 (3)

2108/119441 - 2005 - Progress in Gene Therapy Research (Horizons in Cancer Research; Vol. 20)
Botta, Annalisa; Sangiuolo, Federica Carla; Novelli, Giuseppe - 03 - Contributo in libro
libro: Gene Therapy in Cancer - (1-59454-288-0)

2108/29396 - 2005 - Transmission ratio distortion in the spinal muscular atrophy locus: Data from 314 prenatal tests
Botta, Annalisa; Giardina, Emiliano; Pietropolli, Adalgisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: NEUROLOGY (Wolters Kluwer Hagerstown MD: Lippincott Williams & Wilkins Cleveland Ohio: Advanstar Communications) pp. 1631-1635 - issn: 0028-3878 - wos: WOS:000233428100022 (12) - scopus: 2-s2.0-28044453501 (13)

2108/40852 - 2004 - Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues.
Amati, Francesca; Pucci, Sabina; Botta, Annalisa; Sangiuolo, Federica Carla; Spagnoli, Luigi Giusto; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENE (Amsterdam Netherlands: Elsevier BV) pp. 69-74 - issn: 0378-1119 - wos: WOS:000220537400007 (21) - scopus: 2-s2.0-12144287243 (21)

2108/34705 - 2004 - A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2
Vallo, Laura; Giardina, Emiliano; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: DIAGNOSTIC MOLECULAR PATHOLOGY (Lippincott, Williams & Wilkins:530 Walnut Street:Philadelphia, PA 19106:(800)638-3030, (301)223-2300, EMAIL: orders@lww.com, INTERNET: http://www.lww.com, Fax: (301)223-2320, (301)223-2320) pp. 164-166 - issn: 1052-9551 - wos: WOS:000223575800006 (19) - scopus: 2-s2.0-4344666094 (28)

2108/117957 - 2002 - Functional characterization of the 5′ flanking region of human Ubiquitin Fusion Degradation 1 Like gene (UFD1L)
Amati, Francesca; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CELL BIOCHEMISTRY AND FUNCTION (John Wiley & Sons Limited:1 Oldlands Way, Bognor Regis, P022 9SA United Kingdom:011 44 1243 779777, EMAIL: cs-journals@wiley.co.uk, INTERNET: http://www.wiley.co.uk, Fax: 011 44 1243 843232) pp. 163-170 - issn: 0263-6484 - wos: WOS:000175598700013 (5) - scopus: 2-s2.0-0036098381 (6)

2108/119238 - 2002 - Evidence for differential S100 gene over-expression in psoriatic patients from genetically heterogeneous pedigrees
Capon, Francesca; Giardina, Emiliano; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: HUMAN GENETICS (Germany: Springer Verlag Germany) pp. 310-313 - issn: 0340-6717 - wos: (0) - scopus: 2-s2.0-0036820794 (71)

2108/119240 - 2001 - Letter to the editor: Exclusion of the elastin gene in the pathogenesis of Costello syndrome
Botta, Annalisa; Sangiuolo, Federica Carla; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 286-287 - issn: 0148-7299 - wos: WOS:000166718600016 (11) - scopus: 2-s2.0-0035931602 (11)

2108/51948 - 2001 - Letter to the editor: exclusion of the elastin gene in the pathogenesis of Costello syndrome [4]
Botta, Annalisa; Sangiuolo, Federica Carla; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 286-287 - issn: 0148-7299 - wos: WOS:000166718600016 (11) - scopus: 2-s2.0-0035931602 (11)

2108/117968 - 2001 - Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster
Amati, Francesca; Sangiuolo, Federica Carla; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CYTOGENETICS AND CELL GENETICS (S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 279-282 - issn: 0301-0171 - wos: WOS:000169735500019 (6) - scopus: 2-s2.0-0034943605 (6)

2108/51947 - 2001 - Causes of the phenotype-genotype dissociation in DiGeorge syndrome: Clues from mouse models
Botta, Annalisa; Amati, Francesca; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: TRENDS IN GENETICS (Elsevier Applied Science:An Imprint of Elsevier Science Ltd, The Boulevard, Langford Lane, Kidlington Oxford OX5 1GB United Kingdom:011 44 1865 843000, 011 44 1865 843699, EMAIL: nlinfo-f@elsevier.nl OR usinfo-f@elsevier.com OR forinfo-kyf04035@niftyserve.or.jp, INTERNET: http://www.elsevier.nl/, Fax: 011 44 1865 843010) pp. 551-554 - issn: 0168-9525 - wos: WOS:000171456500002 (5) - scopus: 2-s2.0-0035479014 (7)

2108/49982 - 2001 - Association study of a promoter polymorphism of UFD1L gene with schizophrenia
Pasini, Augusto; Amati, Francesca; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 529-533 - issn: 0148-7299 - wos: WOS:000170244500009 (29) - scopus: 2-s2.0-0035828111 (35)

2108/11005 - 2001 - Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L)
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENE (Amsterdam Netherlands: Elsevier BV) pp. 39-46 - issn: 0378-1119 - wos: WOS:000171588300004 (8) - scopus: 2-s2.0-0035812287 (10)

2108/49980 - 2000 - Association between schizohprenia and UFD1L. A developmental gene mapped to chromosome 22
Pasini, Augusto; Amati, Francesca; Botta, Annalisa; Novelli, Giuseppe - 02 - Intervento a convegno
rivista: AMERICAN JOURNAL OF MEDICAL GENETICS (New York, N.Y. : Wiley-Liss, Inc., c1978-c2002.) pp. - - issn: 1096-8628 - wos: WOS:000088565900289 (0) - scopus: 2-s2.0-33749107499 (0)
congresso: World Congress on Psychiatric Genetics, (Versailles, France)

2108/11029 - 1999 - Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome
Botta, Annalisa; Sangiuolo, Federica Carla; Potenza, Saverio; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: GENOMICS (Amsterdam The Netherlands; Boston: Elsevier :Orlando, FL: Academic Press Incorporated) pp. 525-528 - issn: 0888-7543 - wos: WOS:000085089400024 (25) - scopus: 2-s2.0-0033572591 (25)

2108/10994 - 1999 - Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genes
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: JOURNAL OF MEDICAL GENETICS (BMJ / British Medical Journal Publishing Group:PO Box 299, London WC1H 9TD United Kingdom:011 44 20 73836270, EMAIL: subscriptions@bmjgroup.com, INTERNET: http://www.bmjpg.com/bmj, Fax: 011 44 20 73836402) pp. 478-480 - issn: 0022-2593 - wos: WOS:000080797600010 (68) - scopus: 2-s2.0-0032999601 (80)

2108/10927 - 1999 - Congenital heart disease in mice deficient for the DiGeorge Syndrome region
Botta, Annalisa - 01 - Articolo su rivista
rivista: NATURE (London: Nature Pubihing. Group-Springer Nature Limited -London : Macmillan, 1869- -New York, NY; Nature America Incorporated) pp. 379-383 - issn: 0028-0836 - wos: WOS:000082822600052 (318) - scopus: 2-s2.0-0033598389 (369)

2108/119242 - 1999 - Searching for psoriasis susceptibility genes in Italy: Genome scan and evidence for a new locus on chromosome 1
Novelli, Giuseppe; Botta, Annalisa - 01 - Articolo su rivista
rivista: JOURNAL OF INVESTIGATIVE DERMATOLOGY (Elsevier Science Incorporated / NY Journals:Madison Square Station, PO Box 882:New York, NY 10159:(212)633-3730, EMAIL: usinfo-f@elsevier.com, INTERNET: http://www.elsevier.com, Fax: (212)633-3680) pp. 32-35 - issn: 0022-202X - wos: WOS:000077813300005 (145) - scopus: 2-s2.0-0032900956 (171)

2108/119434 - 1998 - Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. Online
Sangiuolo, Federica Carla; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: HUMAN MUTATION (John Wiley & Sons Incorporated:Customer Service, 111 River Street:Hoboken, NJ 07030:(800)225-5945, (201)748-6000, EMAIL: societyinfo@wiley.com, INTERNET: http://www.wiley.com, Fax: (212)748-6551) pp. 331-331 - issn: 1059-7794 - wos: WOS:000072859000013 (27) - scopus: 2-s2.0-0032242278 (28)

2108/119428 - 1997 - Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation
Botta, Annalisa - 01 - Articolo su rivista
rivista: MAMMALIAN GENOME (Springer-Verlag New York Incorporated:175 Fifth Avenue:New York, NY 10010:(212)460-1500, EMAIL: orders@springer-ny.com, INTERNET: http://www.springer-ny.com, Fax: (212)533-3503) pp. 890-895 - issn: 0938-8990 - wos: WOS:A1997YH38100003 (37) - scopus: 2-s2.0-0031542284 (36)

2108/119432 - 1997 - Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene
Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: CYTOGENETICS AND CELL GENETICS (S Karger AG:Allschwilerstrasse 10, CH-4009 Basel Switzerland:011 41 61 3061111, EMAIL: orders@karger.ch, INTERNET: http://www.karger.com, Fax: 011 41 61 3061234) pp. 264-265 - issn: 0301-0171 - wos: WOS:A1997XQ68000028 (4) - scopus: 2-s2.0-0030755247 (4)

2108/119436 - 1995 - Simultaneous detection of delta F508, G542X, N1303K, G551D, and 1717-1G-->A cystic fibrosis alleles by a multiplex DNA enzyme immunoassay
Sangiuolo, Federica Carla; Botta, Annalisa; Novelli, Giuseppe - 01 - Articolo su rivista
rivista: INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH (Springer Verlag Germany:Tiergartenstrasse 17, D 69121 Heidelberg Germany:011 49 6221 3450, EMAIL: g.braun@springer.de, INTERNET: http://www.springer.de, Fax: 011 49 6221 345229) pp. 142-145 - issn: 0940-5437 - wos: WOS:A1995RV42200004 (6) - scopus: 2-s2.0-0028980615 (7)

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