Sfoglia per Autore
Molecular genetics of Hirschsprung disease.
2008-01-01 Lantieri, Francesca; P., Griseri; J., Amiel; Martucciello, Giuseppe; I., Ceccherini; G., Romeo; S., Lyonnet
Hirschsprung disease, associated syndromes and genetics: a review
2008-01-01 J., Amiel; E., SPROAT EMISON; M., GARCIA BARCELO; Lantieri, Francesca; G., Burzynski; S., Borrego; A., Pelet; S., Arnold; X., Miao; P., Griseri; A. S., Brooks; G., Antinolo; L., DE PONTUAL; M., CLEMENT ZIZA; A., Munnich; C., Kashuk; K., West; K. K., Wong; S., Lyonnet; A., Chakravarti; P. K., Tam; I., CECCHERINI I; R. M., Hofstra; R., Fernandez
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study
2009-01-01 Lantieri, Francesca; M. A., Jhun; J., Park; T., Park; M., Devoto
Inclusion of a priori information in genome-wide association analysis
2009-01-01 N., Tintle; Lantieri, Francesca; J., Lebrec; M., Sohns; D., Ballard; H., Bickeböller
Behavior of non-classical soluble HLA class G antigens in human immunodeficiency virus 1-infected patients before and after HAART: comparison with classical soluble HLA-A, -B, -C antigens and potential role in immune-reconstitution.
2009-01-01 Murdaca, Giuseppe; Contini, Paola; Setti, M.; Cagnati, P.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco
The impact of stapled transanal rectal resection on anorectal function in patients with obstructed defecation syndrome
2009-01-01 G., Reboa; M., Gipponi; M., Ligorio; P., Marino; Lantieri, Francesca
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A
2009-01-01 J., Elia; M., Capasso; Z., Zaheer; Lantieri, Francesca; P., Ambrosini; W., Berrettini; M., Devoto; H., Hakonarson
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder
2009-01-01 J., Elia; T., Takeda; ., Deberardinis; J., Burke; J., Accardo; P. J., Ambrosini; N. J., Blum; L. W., Brown; Lantieri, Francesca; W., Berrettini; M., Devoto; H., Hakonarson
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum
2010-01-01 Lantieri, Francesca; J. T., Glessner; H., Hakonarson; J., Elia; M., Devoto
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities
2010-01-01 Bachetti, T; DI ZANNI, E; Lantieri, Francesca; Caroli, F; Regis, S; Filocamo, M; Rainero, I; Gallone, S; Cilia, R; Romano, S; Savoiardo, M; Pareyson, D; Biancheri, R; Ravazzolo, Roberto; Ceccherini, I.
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes
2010-01-01 J., Elia; X., Gai; H. M., Xie; J. C., Perin; E., Geiger; J. T., Glessner; M., D'Arcy; R., Deberardinis; E., Frackelton; C., Kim; Lantieri, Francesca; B. M., Muganga; L., Wang; T., Takeda; E. F., Rappaport; S. F., Grant; W., Berrettini; M., Devoto; T. H., Shaikh; H., Hakonarson; P. S., White
Relevance of CD38 expression on CD8 T cells to evaluate antiretroviral therapy response in HIV-1-infected youths
2010-01-01 Rosso, Raffaella; Fenoglio, Daniela; Terranova, Mp; Lantieri, Francesca; Risso, Domenico; Pontali, E; Setti, M; Cossarizza, A; Ravetti, Jl; Viscoli, Claudio; Kunkl, A.
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability
2010-01-01 E. S., Emison; M., GARCIA BARCELO; E. A., Grice; Lantieri, Francesca; J., Amiel; G., Burzynski; R. M., Fernandez; L., Hao; C., Kashuk; K., West; X., Miao; P. K., Tam; P., Griseri; I., Ceccherini; A., Pelet; A. S., Jannot; L., DE PONTUAL; A., HENRION CAUDE; S., Lyonnet; J. B., Verheij; R. M., Hofstra; G., Antiñolo; S., Borrego; A. S., Mccallion; A., Chakravarti
Technological improvements in the treatment of haemorrhoids and obstructed defaecation syndrome
2011-01-01 Reboa, Giuliano; M., Gipponi; T., Testa; Lantieri, Francesca
Soluble HLA-G serum levels in patients with the Acquired Immunodeficiency Syndrome affected by different AIDS-defining conditions before and after anti-retroviral treatment
2011-01-01 Murdaca, Giuseppe; Contini, P.; Setti, S.; Cagnati, P.; Spanò, F.; Lantieri, Francesca; Puppo, Francesco
Attention-deficit hyperactivity disorder
2012-01-01 Elia, J; Lantieri, Francesca; Takeda, T; Gai, X; White, Ps; Devoto, M; Hakonarson, H.
Integration of Linkage Analysis and Next-Generation Sequencing Data
2012-01-01 Devoto, M.; Lantieri, Francesca; L. e. v. e. n. s. t. i. e. n., . M. A.
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease.
2012-01-01 Jannot, As; Amiel, J; Pelet, A; Lantieri, Francesca; Fernandez, Rm; Verheij, Jb; Garcia Barcelo, M; Arnold, S; Ceccherini, I; Borrego, S; Hofstra, Rm; Tam, Pk; Munnich, A; Chakravarti, A; Clerget Darpoux, F; Lyonnet, S.
The involvement of the RET variant G691S in medullary thyroid carcinoma: Conflicting results of meta-analyses need to be reconciled
2013-01-01 Lantieri, Francesca; Caroli, F; Ceccherini, I; Griseri, P.
Pathways systematically associated to Hirschsprung's disease.
2013-01-01 R. M., Fernández; M., Bleda; B., Luzón Toro; L., García Alonso; S., Arnold; Y., Sribudiani; C., Besmond; Lantieri, Francesca; B., Doan; I., Ceccherini; S., Lyonnet; R. M., Hofstra; A., Chakravarti; G., Antiñolo; J., Dopazo; S., Borrego
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
Molecular genetics of Hirschsprung disease. | 1-gen-2008 | Lantieri, Francesca; P., Griseri; J., Amiel; Martucciello, Giuseppe; I., Ceccherini; G., Romeo; S., Lyonnet | |
Hirschsprung disease, associated syndromes and genetics: a review | 1-gen-2008 | J., Amiel; E., SPROAT EMISON; M., GARCIA BARCELO; Lantieri, Francesca; G., Burzynski; S., Borrego; A., Pelet; S., Arnold; X., Miao; P., Griseri; A. S., Brooks; G., Antinolo; L., DE PONTUAL; M., CLEMENT ZIZA; A., Munnich; C., Kashuk; K., West; K. K., Wong; S., Lyonnet; A., Chakravarti; P. K., Tam; I., CECCHERINI I; R. M., Hofstra; R., Fernandez | |
Comparative analysis of different approaches for dealing with candidate regions in the context of a genome-wide association study | 1-gen-2009 | Lantieri, Francesca; M. A., Jhun; J., Park; T., Park; M., Devoto | |
Inclusion of a priori information in genome-wide association analysis | 1-gen-2009 | N., Tintle; Lantieri, Francesca; J., Lebrec; M., Sohns; D., Ballard; H., Bickeböller | |
Behavior of non-classical soluble HLA class G antigens in human immunodeficiency virus 1-infected patients before and after HAART: comparison with classical soluble HLA-A, -B, -C antigens and potential role in immune-reconstitution. | 1-gen-2009 | Murdaca, Giuseppe; Contini, Paola; Setti, M.; Cagnati, P.; Lantieri, Francesca; Indiveri, Francesco; Puppo, Francesco | |
The impact of stapled transanal rectal resection on anorectal function in patients with obstructed defecation syndrome | 1-gen-2009 | G., Reboa; M., Gipponi; M., Ligorio; P., Marino; Lantieri, Francesca | |
Candidate gene analysis in an on-going genome-wide association study of attention-deficit hyperactivity disorder: suggestive association signals in ADRA1A | 1-gen-2009 | J., Elia; M., Capasso; Z., Zaheer; Lantieri, Francesca; P., Ambrosini; W., Berrettini; M., Devoto; H., Hakonarson | |
Nocturnal enuresis: a suggestive endophenotype marker for a subgroup of inattentive attention-deficit/hyperactivity disorder | 1-gen-2009 | J., Elia; T., Takeda; ., Deberardinis; J., Burke; J., Accardo; P. J., Ambrosini; N. J., Blum; L. W., Brown; Lantieri, Francesca; W., Berrettini; M., Devoto; H., Hakonarson | |
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum | 1-gen-2010 | Lantieri, Francesca; J. T., Glessner; H., Hakonarson; J., Elia; M., Devoto | |
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activities | 1-gen-2010 | Bachetti, T; DI ZANNI, E; Lantieri, Francesca; Caroli, F; Regis, S; Filocamo, M; Rainero, I; Gallone, S; Cilia, R; Romano, S; Savoiardo, M; Pareyson, D; Biancheri, R; Ravazzolo, Roberto; Ceccherini, I. | |
Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes | 1-gen-2010 | J., Elia; X., Gai; H. M., Xie; J. C., Perin; E., Geiger; J. T., Glessner; M., D'Arcy; R., Deberardinis; E., Frackelton; C., Kim; Lantieri, Francesca; B. M., Muganga; L., Wang; T., Takeda; E. F., Rappaport; S. F., Grant; W., Berrettini; M., Devoto; T. H., Shaikh; H., Hakonarson; P. S., White | |
Relevance of CD38 expression on CD8 T cells to evaluate antiretroviral therapy response in HIV-1-infected youths | 1-gen-2010 | Rosso, Raffaella; Fenoglio, Daniela; Terranova, Mp; Lantieri, Francesca; Risso, Domenico; Pontali, E; Setti, M; Cossarizza, A; Ravetti, Jl; Viscoli, Claudio; Kunkl, A. | |
Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability | 1-gen-2010 | E. S., Emison; M., GARCIA BARCELO; E. A., Grice; Lantieri, Francesca; J., Amiel; G., Burzynski; R. M., Fernandez; L., Hao; C., Kashuk; K., West; X., Miao; P. K., Tam; P., Griseri; I., Ceccherini; A., Pelet; A. S., Jannot; L., DE PONTUAL; A., HENRION CAUDE; S., Lyonnet; J. B., Verheij; R. M., Hofstra; G., Antiñolo; S., Borrego; A. S., Mccallion; A., Chakravarti | |
Technological improvements in the treatment of haemorrhoids and obstructed defaecation syndrome | 1-gen-2011 | Reboa, Giuliano; M., Gipponi; T., Testa; Lantieri, Francesca | |
Soluble HLA-G serum levels in patients with the Acquired Immunodeficiency Syndrome affected by different AIDS-defining conditions before and after anti-retroviral treatment | 1-gen-2011 | Murdaca, Giuseppe; Contini, P.; Setti, S.; Cagnati, P.; Spanò, F.; Lantieri, Francesca; Puppo, Francesco | |
Attention-deficit hyperactivity disorder | 1-gen-2012 | Elia, J; Lantieri, Francesca; Takeda, T; Gai, X; White, Ps; Devoto, M; Hakonarson, H. | |
Integration of Linkage Analysis and Next-Generation Sequencing Data | 1-gen-2012 | Devoto, M.; Lantieri, Francesca; L. e. v. e. n. s. t. i. e. n., . M. A. | |
Male and female differential reproductive rate could explain parental transmission asymmetry of mutation origin in Hirschsprung disease. | 1-gen-2012 | Jannot, As; Amiel, J; Pelet, A; Lantieri, Francesca; Fernandez, Rm; Verheij, Jb; Garcia Barcelo, M; Arnold, S; Ceccherini, I; Borrego, S; Hofstra, Rm; Tam, Pk; Munnich, A; Chakravarti, A; Clerget Darpoux, F; Lyonnet, S. | |
The involvement of the RET variant G691S in medullary thyroid carcinoma: Conflicting results of meta-analyses need to be reconciled | 1-gen-2013 | Lantieri, Francesca; Caroli, F; Ceccherini, I; Griseri, P. | |
Pathways systematically associated to Hirschsprung's disease. | 1-gen-2013 | R. M., Fernández; M., Bleda; B., Luzón Toro; L., García Alonso; S., Arnold; Y., Sribudiani; C., Besmond; Lantieri, Francesca; B., Doan; I., Ceccherini; S., Lyonnet; R. M., Hofstra; A., Chakravarti; G., Antiñolo; J., Dopazo; S., Borrego |
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