Alessandro Vaisfeld

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Venues

NPJ genomic medicine

Genes

Epilepsia

Diagnostics (Basel, Switzerland)

Università Cattolica del Sacro Cuore Sede di Roma

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Università Cattolica del Sacro Cuore Sede di Roma

Italy

MD, junior post-doc :: Medicina Genomica

Publications

Marta Viggiano, Fabiola Ceroni, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Laura Sandoni, Irene Baravelli, Cinzia Cameli, Magali J Rochat, Alessandra Maresca, Alessandro Vaisfeld, Davide Gentilini, Luciano Calzari, Valerio Carelli, Michael C Zody, Elena Maestrini, Elena Bacchelli
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. NPJ genomic medicine 9 (1) (2024)
Marta Viggiano, Fabiola Ceroni, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Laura Sandoni, Irene Baravelli, Cinzia Cameli, Magali J Rochat, Alessandra Maresca, Alessandro Vaisfeld, Davide Gentilini, Luciano Calzari, Valerio Carelli, Michael C Zody, Elena Maestrini, Elena Bacchelli
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. NPJ genomic medicine 9 (1) (2024)
Alessandro Vaisfeld, Giovanni Neri
Simpson-Golabi-Behmel syndrome. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Marta Viggiano, Fabiola Ceroni, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Laura Sandoni, Irene Baravelli, Cinzia Cameli, Magali J Rochat, Alessandra Maresca, Alessandro Vaisfeld, Davide Gentilini, Luciano Calzari, Valerio Carelli, Michael C Zody, Elena Maestrini, Elena Bacchelli
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. NPJ genomic medicine 9 (1) (2024)
Marta Viggiano, Fabiola Ceroni, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Laura Sandoni, Irene Baravelli, Cinzia Cameli, Magali J Rochat, Alessandra Maresca, Alessandro Vaisfeld, Davide Gentilini, Luciano Calzari, Valerio Carelli, Michael C Zody, Elena Maestrini, Elena Bacchelli
Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. NPJ genomic medicine 9 (1) (2024)
Maria Grazia Giuffrida, Marina Goldoni, Maria Luce Genovesi, Giovanna Carpentieri, Barbara Torres, Anca Daniela Deac, Serena Cecchetti, Anna Martinelli, Alessandro Vaisfeld, Elisabetta Flex, Laura Bernardini
3'UTR Deletion of NONO Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein's Anomaly in a Male Fetus. Diagnostics (Basel, Switzerland) 12 (10) (2022)
Alessandro Vaisfeld, Sara Taormina, Alessandro Simonati, Giovanni Neri
Phenotypic Spectrum and Molecular Findings in 17 ATR-X Syndrome Italian Patients: Some New Insights. Genes 13 (10) (2022)
Alessandro Vaisfeld, Giorgia Bruno, Martina Petracca, Anna Rita Bentivoglio, Serenella Servidei, Maria Gabriella Vita, Francesco Bove, Giulia Straccia, Clemente Dato, Giuseppe Di Iorio, Simone Sampaolo, Silvio Peluso, Anna De Rosa, Giuseppe De Michele, Melissa Barghigiani, Daniele Galatolo, Alessandra Tessa, Filippo Santorelli, Pietro Chiurazzi, Mariarosa Anna Beatrice Melone
Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement. Genes 12 (3) (2021)
Alessandro Vaisfeld, Serena Spartano, Giuseppe Gobbi, Annamaria Vezzani, Giovanni Neri
Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma. Epilepsia 62 (1) (2020)
Alessandro Vaisfeld, Martina Calicchia, Maria Grazia Pomponi, Emanuela Lucci Cordisco, Luca Reggiani Bonetti, Maurizio Genuardi
Lynch syndrome with exclusive skin involvement: time to consider a molecular definition? Familial cancer 18 (4) (2020)

Alessandro Vaisfeld.css-eqlu8i{font-size:small;padding-left:4px;}

Publication Activity (10 Years)

Top Topics

Top Venues

Alessandro Vaisfeld