GASPARINI, ALESSANDRA

GASPARINI, ALESSANDRA  

Dipartimento di Scienze Biomediche - DSB  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
TARGETED GENE PANEL FOR COMORBID NEUROLOGICAL DISORDERS 2016 Maria Cristina AspromonteAlessandra GaspariniMarco CarraroElisa BettellaRoberta PolliFederica CescaStefano SartoriIrene ToldoSilvio C. E. TosattoAlessandra MurgiaEmanuela Leonardi + - - TARGETED GENE PANEL FOR COMORBID NEUROLOGICAL DISORDERS
Dynamic scaffolds for neuronal signaling: in silico analysis of the TANC protein family 2017 Alessandra GaspariniSilvio C. E. TosattoAlessandra MurgiaEmanuela Leonardi SCIENTIFIC REPORTS - -
Lessons from the CAGI-4 Hopkins clinical panel challenge 2017 CARRARO, MARCOGASPARINI, ALESSANDRALEONARDI, EMANUELATOSATTO, SILVIO + HUMAN MUTATION - -
DisProt 7.0: A major update of the database of disordered proteins 2017 PIOVESAN, DAMIANOMICETIC, IVANNECCI, MARCOQUAGLIA, FEDERICAAspromonte, Maria CristinaGASPARINI, ALESSANDRAHATOS, ANDRÁSLEONARDI, EMANUELAMINERVINI, GIOVANNITONELLO, FIORELLATOSATTO, SILVIO + NUCLEIC ACIDS RESEARCH - -
TRIO variants in individuals with variable intellectual deficits 2017 Maria Cristina AspromonteAlessandra GaspariniRoberta PolliElisa BettellaFederica CescaStefano SartoriMarco CarraroSilvio C. E. TosattoAlessandra MurgiaEmanuela Leonardi + - - TRIO variants in individuals with variable intellectual deficits
High incidence of SHANK3 loss of function mutations in individuals with intellectual disability and autistic traits 2018 M. C. AspromonteAlessandra GaspariniRoberta PolliElisa BettellaFederica CescaM. BelliniStefano SartoriM. CarraroS. C. E. TosattoA. MurgiaE. Leonardi + - - High incidence of SHANK3 loss of function mutations in individuals with intellectual disability and autistic traits
Effective Diagnosis of Neurodevelopmental Disorders (NDDs) by Computational Analysis and Next Generation Sequencing 2018 Maria Cristina AspromonteAlessandra GaspariniRoberta PolliElisa BettellaFederica CescaMarco CarraroStefano SartoriSilvio C. E. TosattoAlessandra MurgiaEmanuela Leonardi - - Effective Diagnosis of Neurodevelopmental Disorders (NDDs) by Computational Analysis and Next Generation Sequencing
From High-Throughput Analysis of Genetic Variants to the Experimental Validation of Putative Protein Function 2018 Gasparini, Alessandra - - -
Characterization of intellectual disability and autism comorbidity through gene panel sequencing 2019 Aspromonte M. C.BELLINI, MARIAGRAZIAGasparini A.Carraro M.Bettella E.Polli R.Cesca F.MILANI, DUCCIOSartori S.Toldo I.MARINO BUSLJE, CRISTINA ESTERTosatto S. C. E.Murgia A.Leonardi E. + HUMAN MUTATION - -
Genetic, epigenetic and immunologic profiling of MMR-deficient relapsed glioblastoma 2019 Indraccolo, StefanoLombardi, GiuseppeFassan, MatteoGiunco, SilviaGasparini, AlessandraFanelli, Giuseppe NicolòPambuku, ArdiD'Avella, DomenicoGardiman, Marina PDe Rossi, AnitaZagonel, Vittorina + CLINICAL CANCER RESEARCH - -