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Bernardo Dalla Bernardina

Bernardo Dalla Bernardina

D-Index & Metrics

Neuroscience

D-Index
58
Citations
12726
World Ranking
4156
National Ranking
179

Overview

Bernardo Dalla Bernardina is affiliated with the University of Verona in Italy. Their research primarily focuses on medicine, with specific attention to pediatrics, perinatology, and child health, psychiatry and mental health, public health, environmental and occupational health, genetics, and molecular biology.

The scientist's main topics of work include:

  • Pharmacological Effects and Toxicity Studies
  • Epilepsy research and treatment
  • Pregnancy and Medication Impact
  • Genomics and Rare Diseases
  • Epigenetics and DNA Methylation
  • Neurogenetic and Muscular Disorders Research

Bernardo Dalla Bernardina has collaborated frequently with several coauthors. These include Torbjörn Tomson, Sanjeev V. Thomas, Frank Vajda, John Craig, and Emilio Perucca. Collaborations with these researchers have contributed to a breadth of publications mainly concerning epilepsy and related medical fields.

Frequent publication venues for Dalla Bernardina's work include:

  • Epilepsy & Behavior
  • JAMA Neurology
  • Epileptic Disorders
  • Epilepsia Open
  • Epilepsia

Among recent publications are:

  • "Risk of Major Congenital Malformations and Exposure to Antiseizure Medication Monotherapy" (2024), JAMA Neurology
  • "Breastfeeding while on treatment with antiseizure medications: a systematic review from the ILAE Women Task Force" (2022), Epileptic Disorders
  • "Global Survey of Guidelines for the Management of Epilepsy in Pregnancy: A report from the International League Against Epilepsy Task Force on Women and Pregnancy" (2020), Epilepsia Open
  • "Antiepileptic Drug Teratogenicity and De Novo Genetic Variation Load" (2020), Annals of Neurology
  • "Epilepsy-pregnancy registries: An update" (2024), Epilepsia

The research output of Bernardo Dalla Bernardina reflects a consistent focus on epilepsy, treatment impacts in pregnancy, and pharmacological safety, especially concerning antiseizure medications. Their work spans clinical and epidemiological perspectives as well as genetic studies relevant to maternal and child health.

Best Publications

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    F. Kyle Satterstrom;F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S. Breen

  • A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.

    Andrew J Sharp;Heather C Mefford;Kelly Li;Carl Baker

  • Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    F. Kyle Satterstrom;Jack A. Kosmicki;Jiebiao Wang;Michael S Breen;Michael S Breen

  • Oxidative stress-related biomarkers in autism: systematic review and meta-analyses.

    Alessandra Frustaci;Monica Neri;Alfredo Cesario;James B. Adams

  • Attention-Deficit/Hyperactivity Disorder (ADHD) and obesity: A systematic review of the literature

    Samuele Cortese;Marco Angriman;Claudio Maffeis;Pascale Isnard

  • Epilepsy and EEG findings in males with fragile X syndrome

    S. A. Musumeci;Randi J Hagerman;R. Ferri;P. Bosco

  • Epilepsy in tuberous sclerosis complex: Findings from the TOSCA Study.

    Rima Nabbout;Elena Belousova;Mirjana P. Benedik;Tom Carter

  • Attention-Deficit/Hyperactivity Disorder (Adhd) and Binge Eating

    Samuele Cortese;Bernardo Dalla Bernardina;Marie Christine Mouren

  • Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

    Tianyun Wang;Kendra Hoekzema;Davide Vecchio;Huidan Wu

  • TSC-associated neuropsychiatric disorders (TAND): findings from the TOSCA natural history study

    Petrus J de Vries;Elena Belousova;Mirjana P Benedik;Tom Carter

  • Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.

    Francesca Ragona;Tiziana Granata;Bernardo Dalla Bernardina;Francesca Offredi

  • Brain iron levels in attention-deficit/hyperactivity disorder: a pilot MRI study.

    Samuele Cortese;Robin Azoulay;F. Xavier Castellanos;François Chalard

  • Genetic testing in benign familial epilepsies of the first year of life : Clinical and diagnostic significance

    Federico Zara;Nicola Specchio;Pasquale Striano;Angela Robbiano

  • Association between symptoms of attention-deficit/hyperactivity disorder and bulimic behaviors in a clinical sample of severely obese adolescents.

    Samuele Cortese;P. Isnard;M.L. Frelut;G. Michel

  • Attention-deficit/hyperactivity disorder, Tourette's syndrome, and restless legs syndrome: the iron hypothesis.

    Samuele Cortese;Michel Lecendreux;Bernardo Dalla Bernardina;Marie Christine Mouren

  • PRRT2 Mutations are the major cause of benign familial infantile seizures

    Julian Schubert;Roberta Paravidino;Felicitas Becker;Andrea Berger;Andrea Berger

  • Startle disease: an avoidable cause of sudden infant death.

    Federico Vigevano;Matteo Di Capua;BernardoDalla Bernardina

  • Sleep disturbances and serum ferritin levels in children with attention-deficit/hyperactivity disorder

    Samuele Cortese;Eric Konofal;Bernardo Dalla Bernardina;Marie Christine Mouren

  • Recommendations of the Italian League Against Epilepsy Working Group on Generic Products of Antiepileptic Drugs

    Emilio Perucca;Fiorenzo Albani;Giuseppe Capovilla;Bernardo Dalla Bernardina

  • Electroencephalographic characteristics of Dravet syndrome

    Michelle Bureau;Bernardo Dalla Bernardina

  • Severe myoclonic epilepsy in infancy (Dravet syndrome) 30 years later

    Charlotte Dravet;Michelle Bureau;Bernardo Dalla Bernardina;Renzo Guerrini

  • Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations.

    Pasquale Striano;Maria Margherita Mancardi;Roberta Biancheri;Francesca Madia

  • Status epilepticus in benign rolandic epilepsy manifesting as anterior operculum syndrome

    Vito Colamaria;Vincenzo Sgro;Roberto Caraballo;Marina Simeone

  • Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern

    M P Canevini;V Sgro;O Zuffardi;R Canger

  • Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletion

    Claudia Torniero;Bernardo Dalla Bernardina;Francesca Novara;Roberto Cerini

Frequent Co-Authors

Renzo Guerrini
Renzo Guerrini University of Florence
Federico Vigevano
Federico Vigevano Bambino Gesù Children's Hospital
Tiziana Granata
Tiziana Granata Istituto Neurologico Carlo Besta
Orsetta Zuffardi
Orsetta Zuffardi University of Pavia
Maria Paola Canevini
Maria Paola Canevini University of Milan
Maurizio Elia
Maurizio Elia University of Southampton
Federico Zara
Federico Zara University of Genoa
Giuseppe Capovilla
Giuseppe Capovilla Boston Children's Hospital
Pierangelo Veggiotti
Pierangelo Veggiotti University of Milan
Corrado Romano
Corrado Romano I.R.C.C.S. Oasi Maria SS

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