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PPARG2 Pro12Ala and ADAMTS9 rs4607103 as “insulin resistance loci” and “insulin secretion loci” in Italian individuals. The GENFIEV study and the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 4

Acta diabetologica, 2013-06, Vol.50 (3), p.401-408

2013

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Recommendations for the classification of diseases as CFTR-related disorders

Journal of cystic fibrosis, 2011-06, Vol.10, p.S86-S102

2011

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Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma

Clinical and experimental allergy, 2007-01, Vol.37 (1), p.83-89

2007

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Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

Journal of cystic fibrosis, 2008-05, Vol.7 (3), p.179-196

2008

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Tumour necrosis factor family genes in a phenotype of COPD associated with emphysema

The European respiratory journal, 2003-03, Vol.21 (3), p.444-449

2003

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X-linked alport syndrome : an SSCP-based mutation survey over all 51 exons of the COL4A5 gene

American journal of human genetics, 1996-06, Vol.58 (6), p.1192-1204

1996

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Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

Human molecular genetics, 1995-04, Vol.4 (4), p.635-639

1995

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Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma

Clinical and experimental allergy, 2001-08, Vol.31 (8), p.1220-1224

2001

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Upregulated Expression of Toll-like Receptor 4 in Peripheral Blood of Ischaemic Stroke Patients Correlates with Cyclooxygenase 2 Expression

European journal of vascular and endovascular surgery, 2011-03, Vol.41 (3), p.358-363

2011

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A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism

Clinical and experimental medicine, 2002-05, Vol.2 (1), p.7-12

2002

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Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

Journal of cystic fibrosis, 2008-09, Vol.7 (5), p.347-351

2008

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Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease

Human genetics, 1998-12, Vol.103 (6), p.718-722

1998

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Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic Fibrosis

European journal of human genetics : EJHG, 2000-09, Vol.8 Suppl 2 (S2), p.S2-S12

2000

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Methylenetetrahydrofolate Reductase C677T Mutation, Plasma Homocysteine, and Folate in Subjects From Northern Italy With or Without Angiographically Documented Severe Coronary Atherosclerotic Disease: Evidence for an Important Genetic-Environmental Interaction

Blood, 1998-06, Vol.91 (11), p.4158-4163

1998

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Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children

American journal of respiratory and critical care medicine, 2000-10, Vol.162 (4), p.1587-1590

2000

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High Frequency of Cystic Fibrosis Transmembrane Regulator Mutation L997F in Patients with Recurrent Idiopathic Pancreatitis and in Newborns with Hypertrypsinemia

American journal of human genetics, 2000-06, Vol.66 (6), p.2013-2014

2000

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Association of a lymphotoxin α gene polymorphism and atopy in Italian families

Journal of medical genetics, 1999-04, Vol.36 (4), p.323-325

1999

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The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelated

British journal of haematology, 1998-12, Vol.103 (3), p.813-816

1998

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A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

Human genetics, 2000-02, Vol.106 (2), p.172-178

2000

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Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery disease

Clinical and experimental medicine, 2005-05, Vol.5 (1), p.20-30

2005

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Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis

Journal of neuroimmunology, 2002-12, Vol.133 (1), p.241-243

2002

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CFTR gene variant IVS8-5T in disseminated bronchiectasis

American journal of human genetics, 1996-04, Vol.58 (4), p.889-892

1996

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An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene

American journal of kidney diseases, 1996-11, Vol.28 (5), p.759-761

1996

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Interaction between smoking and PON2 Ser311Cys polymorphism as a determinant of the risk of myocardial infarction

European journal of clinical investigation, 2004-01, Vol.34 (1), p.14-20

2004

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Homocysteine and atheromatous renal artery stenosis

Clinical and experimental medicine, 2001-12, Vol.1 (4), p.211-218

2001

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PPARG2 Pro12Ala and ADAMTS9 rs4607103 as “insulin resistance loci” and “insulin secretion loci” in Italian individuals. The GENFIEV study and the Verona Newly Diagnosed Type 2 Diabetes Study (VNDS) 4

Recommendations for the classification of diseases as CFTR-related disorders

Chromosome 7p linkage and GPR154 gene association in Italian families with allergic asthma

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice

Tumour necrosis factor family genes in a phenotype of COPD associated with emphysema

X-linked alport syndrome : an SSCP-based mutation survey over all 51 exons of the COL4A5 gene

Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma

Upregulated Expression of Toll-like Receptor 4 in Peripheral Blood of Ischaemic Stroke Patients Correlates with Cyclooxygenase 2 Expression

A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism

Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study

Complete mutational screening of the CFTR gene in 120 patients with pulmonary disease

Recommendations for quality improvement in genetic testing for cystic fibrosis. European Concerted Action on Cystic Fibrosis

Methylenetetrahydrofolate Reductase C677T Mutation, Plasma Homocysteine, and Folate in Subjects From Northern Italy With or Without Angiographically Documented Severe Coronary Atherosclerotic Disease: Evidence for an Important Genetic-Environmental Interaction

Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children

High Frequency of Cystic Fibrosis Transmembrane Regulator Mutation L997F in Patients with Recurrent Idiopathic Pancreatitis and in Newborns with Hypertrypsinemia

Association of a lymphotoxin α gene polymorphism and atopy in Italian families

The haemochromatosis mutations do not modify the clinical picture of thalassaemia major in patients regularly transfused and chelated

A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

Interaction between metabolic syndrome and PON1 polymorphisms as a determinant of the risk of coronary artery disease

Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis

CFTR gene variant IVS8-5T in disseminated bronchiectasis

An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 gene

Interaction between smoking and PON2 Ser311Cys polymorphism as a determinant of the risk of myocardial infarction

Homocysteine and atheromatous renal artery stenosis

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