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OPERATIONAL EARTHQUAKE FORECASTING. State of Knowledge and Guidelines for Utilization

Annals of geophysics, 2011-01, Vol.54 (4)

2011

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A general approach for haplotype phasing across the full spectrum of relatedness

PLoS genetics, 2014-04, Vol.10 (4), p.e1004234-e1004234

2014

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Coarse-grained/molecular mechanics of the TAS2R38 bitter taste receptor: experimentally-validated detailed structural prediction of agonist binding

PloS one, 2013-05, Vol.8 (5), p.e64675

2013

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Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique

PloS one, 2021-03, Vol.16 (3), p.e0247603-e0247603

2021

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Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset

Cancers, 2019-04, Vol.11 (4), p.483

2019

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Seismic reflections reveal a massive melt layer feeding Campi Flegrei caldera

Geophysical research letters, 2008-06, Vol.35 (12), p.L12306-n/a

2008

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Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies

Journal of the American College of Cardiology, 2022-11, Vol.80 (21), p.1981-1994

2022

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Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal

Scientific reports, 2016-05, Vol.6 (1), p.25506, Article 25506

2016

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Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase

American journal of human genetics, 2008-06, Vol.82 (6), p.1281-1289

2008

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A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions

Nutrients, 2019-07, Vol.11 (8), p.1735

2019

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Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits

Nature communications, 2022-05, Vol.13 (1), p.2743-2743, Article 2743

2022

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SDHAF1 , encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy

Nature genetics, 2009-06, Vol.41 (6), p.654-656

2009

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Factors Influencing the Phenotypic Characterization of the Oral Marker, PROP

Nutrients, 2017-11, Vol.9 (12), p.1275

2017

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Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

Nature communications, 2017-06, Vol.8 (1), p.15927-15927, Article 15927

2017

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The thermal regime of the Campi Flegrei magmatic system reconstructed through 3D numerical simulations

Journal of volcanology and geothermal research, 2016-12, Vol.328, p.210-221

2016

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Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss

European journal of human genetics : EJHG, 2019-01, Vol.27 (1), p.70-79

2019

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Variation in the Bitter‐taste Receptor Gene TAS2R38, and Adiposity in a Genetically Isolated Population in Southern Italy

Obesity (Silver Spring, Md.), 2008-10, Vol.16 (10), p.2289-2295

2008

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MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

Nature genetics, 2006-05, Vol.38 (5), p.570-575

2006

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Quantifying probabilities of volcanic events: The example of volcanic hazard at Mount Vesuvius

Journal of Geophysical Research - Solid Earth, 2004-11, Vol.109 (B11), p.B11201-n/a

2004

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A genome‐wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population

Journal of periodontal research, 2018-12, Vol.53 (6), p.992-998

2018

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A population-based approach to study the impact of PROP perception on food liking in populations along the Silk Road

PloS one, 2014-03, Vol.9 (3), p.e91716

2014

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Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss

PloS one, 2013-12, Vol.8 (12), p.e80323-e80323

2013

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Autosomal recessive stickler syndrome due to a loss of function mutation in the COL9A3 gene

American journal of medical genetics. Part A, 2014-01, Vol.164A (1), p.42-47

2014

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OPERATIONAL EARTHQUAKE FORECASTING. State of Knowledge and Guidelines for Utilization

A general approach for haplotype phasing across the full spectrum of relatedness

Coarse-grained/molecular mechanics of the TAS2R38 bitter taste receptor: experimentally-validated detailed structural prediction of agonist binding

Systematic analysis of factors that improve homologous direct repair (HDR) efficiency in CRISPR/Cas9 technique

Heterogeneity in Circulating Tumor Cells: The Relevance of the Stem-Cell Subset

Seismic reflections reveal a massive melt layer feeding Campi Flegrei caldera

Prognostic Prediction of Genotype vs Phenotype in Genetic Cardiomyopathies

Global diversity in the TAS2R38 bitter taste receptor: revisiting a classic evolutionary PROPosal

Age- and sex-related variations in platelet count in Italy: a proposal of reference ranges based on 40987 subjects' data

Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase

A Brief Review of Genetic Approaches to the Study of Food Preferences: Current Knowledge and Future Directions

Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits

SDHAF1 , encoding a LYR complex-II specific assembly factor, is mutated in SDH-defective infantile leukoencephalopathy

Factors Influencing the Phenotypic Characterization of the Oral Marker, PROP

Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

The thermal regime of the Campi Flegrei magmatic system reconstructed through 3D numerical simulations

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss

Variation in the Bitter‐taste Receptor Gene TAS2R38, and Adiposity in a Genetically Isolated Population in Southern Italy

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

Quantifying probabilities of volcanic events: The example of volcanic hazard at Mount Vesuvius

A genome‐wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population

A population-based approach to study the impact of PROP perception on food liking in populations along the Silk Road

Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss

Cx26 partial loss causes accelerated presbycusis by redox imbalance and dysregulation of Nfr2 pathway

Autosomal recessive stickler syndrome due to a loss of function mutation in the COL9A3 gene

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