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Concordance, disease progression, and heritability of coeliac disease in Italian twins

Gut, 2006-06, Vol.55 (6), p.803-808

2006

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HLA-class I markers and multiple sclerosis susceptibility in the Italian population

Genes and immunity, 2010-03, Vol.11 (2), p.173-180

2010

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MicroRNA in Cervical Cancer: OncomiRs and Tumor Suppressor miRs in Diagnosis and Treatment

TheScientificWorld, 2014-01, Vol.2014, p.178075-8

2014

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Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

Clinical genetics, 2003-08, Vol.64 (2), p.142-147

2003

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Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

Annals of human genetics, 2001-01, Vol.65 (1), p.35-41

2001

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SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)

Neuromuscular disorders : NMD, 2006-11, Vol.16 (11), p.800-804

2006

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A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population

Genes and immunity, 2006-10, Vol.7 (7), p.606-608

2006

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New polymorphisms in the IL-10 promoter region

Genes and immunity, 2000-02, Vol.1 (3), p.231-233

2000

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Genetic defects in GH synthesis and secretion

European journal of endocrinology, 2004-08, Vol.151 Suppl 1, p.S3-S9

2004

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A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency

Journal of endocrinological investigation, 2009-09, Vol.32 (8), p.653-658

2009

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A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy

Genes and immunity, 2008-01, Vol.9 (1), p.7-15

2008

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Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease

Gastroenterology (New York, N.Y. 1943), 2007-09, Vol.133 (3), p.808-817

2007

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Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5′ regulatory region

Genes and immunity, 2002-12, Vol.3 (8), p.454-463

2002

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Evidence for gene conversion in the generation of extensive polymorphism in the promoter of the growth hormone gene

Human genetics, 1997-08, Vol.100 (2), p.249-255

1997

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Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease

Annals of human genetics, 1999-05, Vol.63 (3), p.207-215

1999

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Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus

Arthritis and rheumatism, 2005-02, Vol.52 (2), p.539-547

2005

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Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

Journal of neuroimmunology, 2005-06, Vol.163 (1), p.172-178

2005

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Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects

Journal of medical genetics, 2011-07, Vol.48 (7), p.485-492

2011

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HLA–multiple sclerosis association in Continental Italy and correlation with disease prevalence in Europe

Journal of neuroimmunology, 2004-05, Vol.150 (1), p.178-185

2004

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A Novel Deletion in the GH1 Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency

The journal of clinical endocrinology and metabolism, 2006-03, Vol.91 (3), p.980-986

2006

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Maternal effect in multiple sclerosis

The Lancet (British edition), 2004-05, Vol.363 (9423), p.1748-1749

2004

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HLA class I in acute promyelocytic leukemia (APL) : possible correlation with clinical outcome

Leukemia, 2000-03, Vol.14 (3), p.393-398

2000

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Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients

Annals of neurology, 2003-07, Vol.54 (1), p.119-122

2003

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Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

Journal of neuroimmunology, 2006-10, Vol.179 (1), p.108-116

2006

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Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease

Tissue antigens, 2003-04, Vol.61 (4), p.308-316

2003

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Concordance, disease progression, and heritability of coeliac disease in Italian twins

HLA-class I markers and multiple sclerosis susceptibility in the Italian population

MicroRNA in Cervical Cancer: OncomiRs and Tumor Suppressor miRs in Diagnosis and Treatment

Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families

SOD1 gene mutations in Italian patients with Sporadic Amyotrophic Lateral Sclerosis (ALS)

A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population

New polymorphisms in the IL-10 promoter region

Genetic defects in GH synthesis and secretion

A novel recessive splicing mutation in the POU1F1 gene causing combined pituitary hormone deficiency

A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy

Neuropeptide S Receptor 1 Gene Polymorphism Is Associated With Susceptibility to Inflammatory Bowel Disease

Association tests with systemic lupus erythematosus (SLE) of IL10 markers indicate a direct involvement of a CA repeat in the 5′ regulatory region

Evidence for gene conversion in the generation of extensive polymorphism in the promoter of the growth hormone gene

Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease

Two single‐nucleotide polymorphisms in the 5′ and 3′ ends of the osteopontin gene contribute to susceptibility to systemic lupus erythematosus

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

Association of HLA class I markers with multiple sclerosis in the Italian and UK population: evidence of two independent protective effects

HLA–multiple sclerosis association in Continental Italy and correlation with disease prevalence in Europe

A Novel Deletion in the GH1 Gene Including the IVS3 Branch Site Responsible for Autosomal Dominant Isolated Growth Hormone Deficiency

Maternal effect in multiple sclerosis

HLA class I in acute promyelocytic leukemia (APL) : possible correlation with clinical outcome

Genetic interaction of CTLA-4 with HLA-DR15 in multiple sclerosis patients

Linkage disequilibrium screening for multiple sclerosis implicates JAG1 and POU2AF1 as susceptibility genes in Europeans

Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease

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