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Genome‐wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA‐A*03:01 allele.
- Published in:
- HLA: Immune Response Genetics, 2023, v. 102, n. 6, p. 707, doi. 10.1111/tan.15157
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- Article
50 shades of lockdown: sex workers' hidden world during COVID pandemic.
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- Journal of Public Health, 2023, v. 45, n. 4, p. 964, doi. 10.1093/pubmed/fdad159
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- Publication type:
- Article
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.
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- Audiology Research, 2023, v. 13, n. 3, p. 341, doi. 10.3390/audiolres13030029
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- Article
Regulator of G-Protein Signalling 9: A New Candidate Gene for Sweet Food Liking?
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- Foods, 2023, v. 12, n. 9, p. 1739, doi. 10.3390/foods12091739
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- Article
Whole‐exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 5, p. 1, doi. 10.1002/mgg3.2143
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- Article
Circular RNAs Could Encode Unique Proteins and Affect Cancer Pathways.
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- Biology (2079-7737), 2023, v. 12, n. 4, p. 493, doi. 10.3390/biology12040493
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- Article
Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population.
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- BMC Genomic Data, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12863-022-01087-1
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- Article
Genetic characterization of two North Italian villages: A story of isolation, ancient admixture, and genetic drift.
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- American Journal of Biological Anthropology, 2022, v. 179, n. 3, p. 460, doi. 10.1002/ajpa.24620
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- Article
High Throughput Genetic Characterisation of Caucasian Patients Affected by Multi-Drug Resistant Rheumatoid or Psoriatic Arthritis.
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- Journal of Personalized Medicine, 2022, v. 12, n. 10, p. 1618, doi. 10.3390/jpm12101618
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- Article
Ancestry-related distribution of Runs of homozygosity and functional variants in Qatari population.
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- BMC Genomic Data, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12863-022-01087-1
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- Publication type:
- Article
TTC5 syndrome: Clinical and molecular spectrum of a severe and recognizable condition.
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- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 9, p. 2652, doi. 10.1002/ajmg.a.62852
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- Article
Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30187-w
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- Article
Sensory Capacities and Eating Behavior: Intriguing Results from a Large Cohort of Italian Individuals.
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- Foods, 2022, v. 11, n. 5, p. 735, doi. 10.3390/foods11050735
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- Article
The Genetic Diagnosis of Ultrarare DEEs: An Ongoing Challenge.
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- Genes, 2022, v. 13, n. 3, p. 500, doi. 10.3390/genes13030500
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- Article
There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss.
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- Biomedicines, 2022, v. 10, n. 1, p. 12, doi. 10.3390/biomedicines10010012
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- Article
Genetic Dissection of Temperament Personality Traits in Italian Isolates.
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- Genes, 2022, v. 13, n. 1, p. 4, doi. 10.3390/genes13010004
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- Article
Hearing Function: Identification of New Candidate Genes Further Explaining the Complexity of This Sensory Ability.
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- Genes, 2021, v. 12, n. 8, p. 1228, doi. 10.3390/genes12081228
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- Article
Runs of homozygosity are associated with staging of periodontitis in isolated populations.
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- Human Molecular Genetics, 2021, v. 30, n. 12, p. 1154, doi. 10.1093/hmg/ddab085
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- Article
The Role of Knockout Olfactory Receptor Genes in Odor Discrimination.
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- Genes, 2021, v. 12, n. 5, p. 631, doi. 10.3390/genes12050631
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- Article
Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique.
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- PLoS ONE, 2021, v. 16, n. 3, p. 1, doi. 10.1371/journal.pone.0247603
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- Article
Primary Ciliary Dyskinesia: The Impact of Taste Receptor (TAS2R38) Gene Polymorphisms on Disease Outcome and Severity.
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- International Archives of Allergy & Immunology, 2020, v. 181, n. 9, p. 727, doi. 10.1159/000508938
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- Publication type:
- Article
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-15706-x
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- Article
A population-based approach for gene prioritization in understanding complex traits.
- Published in:
- Human Genetics, 2020, v. 139, n. 5, p. 647, doi. 10.1007/s00439-020-02152-4
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- Article
From flood risk mapping toward reducing vulnerability: the case of Addis Ababa.
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- Natural Hazards, 2020, v. 100, n. 1, p. 387, doi. 10.1007/s11069-019-03817-8
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- Article
Mutations in PLS1, encoding fimbrin, cause autosomal dominant nonsyndromic hearing loss.
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- Human Mutation, 2019, v. 40, n. 12, p. 2286, doi. 10.1002/humu.23891
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- Article
A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions.
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- Nutrients, 2019, v. 11, n. 8, p. 1735, doi. 10.3390/nu11081735
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- Publication type:
- Article
TAS2R38 bitter taste genotype is associated with complementary feeding behavior in infants.
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- Genes & Nutrition, 2019, v. 14, n. 1, p. N.PAG, doi. 10.1186/s12263-019-0640-z
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- Publication type:
- Article
Two further patients with Warsaw breakage syndrome. Is a mild phenotype possible?
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 5, p. N.PAG, doi. 10.1002/mgg3.639
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- Publication type:
- Article
Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset.
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- Cancers, 2019, v. 11, n. 4, p. 483, doi. 10.3390/cancers11040483
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- Article
Association of LTA gene haploblock with periodontal disease in Italian adults.
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- Journal of Periodontal Research, 2019, v. 54, n. 2, p. 128, doi. 10.1111/jre.12609
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- Article
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00142
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- Publication type:
- Article
A probabilistic tool for multi-hazard risk analysis using a bow-tie approach: application to environmental risk assessments for geo-resource development projects.
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- Acta Geophysica, 2019, v. 67, n. 1, p. 385, doi. 10.1007/s11600-018-0201-7
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- Publication type:
- Article
A genome‐wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population.
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- Journal of Periodontal Research, 2018, v. 53, n. 6, p. 992, doi. 10.1111/jre.12598
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- Publication type:
- Article
Genetic Landscape of Slovenians: Past Admixture and Natural Selection Pattern.
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- Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00551
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- Article
Mutations in L-type amino acid transporter-2 support SLC7A8 as a novel gene involved in age-related hearing loss.
- Published in:
- eLife, 2018, p. 1, doi. 10.7554/eLife.31511
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- Publication type:
- Article
Factors Influencing the Phenotypic Characterization of the Oral Marker, PROP.
- Published in:
- Nutrients, 2017, v. 9, n. 12, p. 1275, doi. 10.3390/nu9121275
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- Publication type:
- Article
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 15927, doi. 10.1038/ncomms15927
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- Article
Genetic structure in the Sherpa and neighboring Nepalese populations.
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- BMC Genomics, 2017, v. 18, p. 1, doi. 10.1186/s12864-016-3469-5
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- Publication type:
- Article
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.
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- Pflügers Archiv: European Journal of Physiology, 2017, v. 469, n. 1, p. 91, doi. 10.1007/s00424-016-1913-7
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- Publication type:
- Article
Caries and Innate Immunity: DEFB1 Gene Polymorphisms and Caries Susceptibility in Genetic Isolates from North-Eastern Italy.
- Published in:
- 2016
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- Publication type:
- journal article
Preface to the special issue 'Strategic applications of real-time risk mitigation strategies and tools: case studies and lessons learned in REAKT'.
- Published in:
- 2016
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- Publication type:
- Editorial
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption.
- Published in:
- Scientific Reports, 2016, p. 31590, doi. 10.1038/srep31590
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- Publication type:
- Article
Corrigendum: Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal.
- Published in:
- Scientific Reports, 2016, p. 28406, doi. 10.1038/srep28406
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- Publication type:
- Article
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings.
- Published in:
- Reviews in Endocrine & Metabolic Disorders, 2016, v. 17, n. 2, p. 209, doi. 10.1007/s11154-016-9354-3
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- Publication type:
- Article
Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal.
- Published in:
- Scientific Reports, 2016, p. 25506, doi. 10.1038/srep25506
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- Publication type:
- Article
Genetic analysis of Italian patients with congenital tufting enteropathy.
- Published in:
- World Journal of Pediatrics, 2016, v. 12, n. 2, p. 219, doi. 10.1007/s12519-015-0070-y
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- Publication type:
- Article
Pharmacogenetics driving personalized medicine: analysis of genetic polymorphisms related to breast cancer medications in Italian isolated populations.
- Published in:
- 2016
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- Publication type:
- journal article
PSIP1/LEDGF: a new gene likely involved in sensorineural progressive hearing loss.
- Published in:
- Scientific Reports, 2015, p. 18568, doi. 10.1038/srep18568
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- Publication type:
- Article
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1717, doi. 10.1038/ejhg.2015.34
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- Publication type:
- Article
Genetic testing and genomic analysis: a debate on ethical, social and legal issues in the Arab world with a focus on Qatar.
- Published in:
- 2015
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- Publication type:
- journal article