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GENE ONTOLOGY ENRICHMENT ANALYSIS OF PARKIN INTERACTANTS
A., Zanon; I., Pichler; A., Rakovic; Schwienbacher, Christine; A. A., Hicks; A., Alexa; F. S., Domingues; C., Klein; P. P., Pramstaller
Atto di Convegno (Proceedings) |
The Movements Disorders Society,
The Movements Disorders Societies 15th INTERNATIONAL CONGRESS OF PARKINSON’S DISEASE AND MOVEMENT DISORDERS
pp: abstract 1047-abstract 1047, Anno: 2011 |
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Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels
Oexle, K.; Ried, J. S.; Hicks, A. A.; Tanaka, T.; Hayward, C.; Bruegel, M.; Gögele, M.; Lichtner, P.; Müller Myhsok, B.; Döring, A.; Illig, T.; Schwienbacher, Christine; Minelli, C.; Pichler, I.; Fiedler, G. M.; Thiery, J.; Rudan, I.; Wright, A. F.; Campbell, H.; Ferrucci, L.; Bandinelli, S.; Pramstaller, P. P.; Wichmann, H. E.; Gieger, C.; Winkelmann, J.; Meitinger, T.
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Contributo in rivista (Pubblicazione in Rivista) |
HUMAN MOLECULAR GENETICS
Vol. 20, No. 5, pp: 1042-1047, Anno: 2011 |
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Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels
Pichler, I.; Minelli, C.; Sanna, S.; Tanaka, T.; Schwienbacher, Christine; Naitza, S.; Porcu, E.; Pattaro, C.; Busonero, F.; Zanon, A.; Maschio, A.; Melville, S. A.; Grazia Piras, M.; Longo, D. L.; Guralnik, J.; Hernandez, D.; Bandinelli, S.; Aigner, E.; Murphy, A. T.; Wroblewski, V.; Marroni, F.; Theurl, I.; Gnewuch, C.; Schadt, E.; Mitterer, M.; Schlessinger, D.; Ferrucci, L.; Witcher, D. R.; Hicks, A. A.; Weiss, G.; Uda, M.; Pramstaller, P. P.
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Contributo in rivista (Pubblicazione in Rivista) |
HUMAN MOLECULAR GENETICS
Vol. 20, No. 6, pp: 1232-1240, Anno: 2011 |
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META-ANALYSIS ON IRON TRAITS REVEALS NOVEL GENETIC LOCI FOR IRON AND FERRITIN LEVELS AND A COMMON VARIANT IN TMPRSS6 THAT INFLUENCES HEPCIDIN LEVELS
Irene, Pichler; Cosetta, Minelli; Serena, Sanna; Toshiko, Tanaka; Schwienbacher, Christine; Silvia, Naitza; Eleonora, Porcu; Cristian, Pattaro; Fabio, Busonero; Alessandra, Zanon; Andrea, Maschio; Scott A., Melville; Maria Grazia, Piras; Dan L., Longo; Jack, Guralnik; Dena, Hernandez; Stefania, Bandinelli; Anthony, Murphy; Victor, Wroblewski; Fabio, Marroni; Igor, Theurl; Carsten, Gnewuch; Manfred, Mitterer; David, Schlessinger; Luigi, Ferrucci; Derrick R., Witcher; Andrew A., Hicks; Günter, Weiss; Manuela, Uda; Peter P., Pramstaller
Atto di Convegno (Proceedings) |
"EuroMediterranean University Center” of Ronzano,
Course in Genetics and Molecular Pathology of Age Related Neurodegenerative Diseases
pp: 25-25, Anno: 2010 |
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Copy number variation and association over T-cell receptor genes-influence of DNA source
Schwienbacher, Christine; De Grandi, A.; Fuchsberger, C.; Facheris, M. F.; Svaldi, M.; Wjst, M.; Pramstaller, P. P.; Hicks, A. A.
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Contributo in rivista (Pubblicazione in Rivista) |
IMMUNOGENETICS
Vol. 62, No. 8, pp: 561-567, Anno: 2010 |
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Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction
Sotoodehnia, N.; Isaacs, A.; de Bakker, P. I.; Dörr, M.; Newton Cheh, C.; Nolte, I. M.; van der Harst, P.; Müller, M.; Eijgelsheim, M.; Alonso, A.; Hicks, A. A.; Padmanabhan, S.; Hayward, C.; Smith, A. V.; Polasek, O.; Giovannone, S.; Fu, J.; Magnani, J. W.; Marciante, K. D.; Pfeufer, A.; Gharib, S. A.; Teumer, A.; Li, M.; Bis, J. C.; Rivadeneira, F.; Aspelund, T.; Köttgen, A.; Johnson, T.; Rice, K.; Sie, M. P.; Wang, Y. A.; Klopp, N.; Fuchsberger, C.; Wild, S. H.; Mateo Leach, I.; Estrada, K.; Völker, U.; Wright, A. F.; Asselbergs, F. W.; Qu, J.; Chakravarti, A.; Sinner, M. F.; Kors, J. A.; Petersmann, A.; Harris, T. B.; Soliman, E. Z.; Munroe, P. B.; Psaty, B. M.; Oostra, B. A.; Cupples, L. A.; Perz, S.; de Boer, R. A.; Uitterlinden, A. G.; Völzke, H.; Spector, T. D.; Liu, F. Y.; Boerwinkle, E.; Dominiczak, A. F.; Rotter, J. I.; van Herpen, G.; Levy, D.; Wichmann, H. E.; van Gilst, W. H.; Witteman, J. C.; Kroemer, H. K.; Kao, W. H.; Heckbert, S. R.; Meitinger, T.; Hofman, A.; Campbell, H.; Folsom, A. R.; van Veldhuisen, D. J.; Schwienbacher, Christine; O'Donnell, C. J.; Volpato, C. B.; Caulfield, M. J.; Connell, J. M.; Launer, L.; Lu, X.; Franke, L.; Fehrmann, R. S.; te Meerman, G.; Groen, H. J.; Weersma, R. K.; van den Berg, L. H.; Wijmenga, C.; Ophoff, R. A.; Navis, G.; Rudan, I.; Snieder, H.; Wilson, J. F.; Pramstaller, P. P.; Siscovick, D. S.; Wang, T. J.; Gudnason, V.; van Duijn, C. M.; Felix, S. B.; Fishman, G. I.; Jamshidi, Y.; Stricker, B. H.; Samani, N. J.; Kääb, S.; Arking, D. E.
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Contributo in rivista (Pubblicazione in Rivista) |
NATURE GENETICS
Vol. 42, No. 12, pp: 1068-1076, Anno: 2010 |
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GENOME-WIDE ASSOCIATION STUDY IDENTIFIES MULTIPLE GENETIC LOCI FOR ACTIVATED PARTIAL THROMBOPLASTIN TIME AND PROTHROMBIN TIME
W., Tang; M., Cushman; Schwienbacher, Christine; L. M., López; Y., Ben Shlomo; S., Basu; M., Gögele; G. Davies G., Lowe; J. S., Pankow; A., Tenesa; C., Volpato; A., Rumley; A., Gow; C., Minelli; J. W. G., Yarnell; D., Porteous; J. M., Starr; E., Boerwinkle; P. M., Visscher; P. P., Pramstaller; I. J., Deary; A. A., Hicks; A. R., Folsom
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Atto di Convegno (Proceedings) |
BLOOD
Vol. 116, No. 1, pp: 1-2, Anno: 2010 |
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TANDEM AFFINITY PURIFICATION AND MASS SPECTROMETRY FOR THE ISOLATION OF PROTEIN COMPLEXDES FROM CYTOSOLIC AND MITOCHONDRIAL FRACTIONS OF MAMMALIAN CELLS
A., Zanon; Schwienbacher, Christine; A. A., Hicks; C., Klein; P. P., Pramstaller; I., Pichler; A., Rakovic
Atto di Convegno (Proceedings) |
11th Conference of Junior Neuroscientists of Tübingen,
11th Conference of Junior Neuroscientists of Tübingen- Pioneering Neuroscience FROM PAST TO THE FUTURE
pp: 26-27, Anno: 2010 |
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NOVEL ASSOCIATION TO THE PROPROTEIN CONVERTASE PCSK7 ALONGSIDE HFE AND TMPRSS6 GENE LOCI REVEALED BY ANALYSING SOLUBLE TRANSFERRIN RECEPTOR LEVELS.
Ried, J. S.; Oexle, K.; Hicks, A. A.; Tanaka, T.; Hayward, C.; Bruegel, M.; Gögele, M.; Lichtner, P.; Müller Myhsok, B.; Döring, A.; Illig, T.; Schwienbacher, Christine; Minelli, C.; Pichler, I.; Fiedler, G. M.; Thiery, J.; Rudan, I.; Ferrucci, L.; Bandinelli, S.; Pramstaller, P. P.; Wichmann, H. E.; Gieger, C.; Winkelmann, J.; Meitinger, T.
Atto di Convegno (Proceedings) |
The American Society of Human Genetics,
THE AMERICAN SOCIETY OF HUMAN GENETICS. 60th ANNUAL MEETING
pp: 140 poster session-140 poster session, Anno: 2010 |
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Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations
Hicks, Aa; Pramstaller, Pp; Johansson, A; Vitart, V; Rudan, I; Ugocsai, P; Aulchenko, Y; Franklin, Cs; Liebisch, G; Erdmann, J; Jonasson, I; Zorkoltseva, I. V.; Pattaro, C; Hayward, C.; Isaacs, A.; Hengstenberg, C.; Campbell, S.; Gnewuch, C.; Janssens, A. C.; Kirichenko, A. V.; König, I. R.; Marroni, F.; Polasek, O.; Demirkan, A.; Kolcic, I.; Schwienbacher, Christine; Igl, W.; Biloglav, Z.; Witteman, J. C.; Pichler, I.; Zaboli, G.; Axenovich, T. I.; Peters, A.; Schreiber, S.; Wichmann, H. E.; Schunkert, H.; Hastie, N.; Oostra, B. A.; Wild, S. H.; Meitinger, T.; Gyllensten, U.; van Duijn, C. M.; Wilson, J. F.; Wright, A.; Schmitz, G.; Campbell, H.
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Contributo in rivista (Pubblicazione in Rivista) |
PLOS GENETICS
Vol. 5, No. 10, pp: e1000672-1-e1000672-11, Anno: 2009 |
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Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour
Sparago, A; Russo, S; Cerrato, F; Ferraiuolo, S; Castorina, P; Selicorni, A; Schwienbacher, Christine; Negrini, Massimo; Ferrero, G. B.; Silengo, M. C.; Anichini, C; Larizza, L; Riccio, A.
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Contributo in rivista (Pubblicazione in Rivista) |
Oxford University Press:Journals Department, Great Clarendon Street, Oxford OX2 6DP United Kingdom:011 44 1865 556767, EMAIL: jnlorders@oup.co.uk, INTERNET: http://www.oup.co.uk, Fax: 011 44 1865 267485,
HUMAN MOLECULAR GENETICS
Vol. 16, No. 3, pp: 254-264, Anno: 2007 |
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KVDMR1, A LOCUS FREQUENTLY HYPOMETHYLATED IN HUMAN CANCER, IS A STRONG ENHANCER-PROMOTER ELEMENT FOR THE EXPRESSION OF LIT1, AN UNTRANSLATED IMPRINTOR GENE AT CHROMOSOME 11p15.5.
Scelfo, R. A. M.; Zagatti, Barbara; Veronese, Angelo; Barbanti Brodano, G.; Schwienbacher, Christine; Negrini, Massimo
Atto di Convegno (Proceedings) |
TUMORI
Vol. 3, No. 1, pp: 68-68, Anno: 2004 |
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NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15)
Rosati, R.; LA STARZA, R.; Veronese, Angelo; Aventin, A.; Schwienbacher, Christine; Vallespi, T.; Negrini, Massimo; Martelli, M. F.; Mecucci, C.
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Contributo in rivista (Pubblicazione in Rivista) |
BLOOD
Vol. 99, No. 10, pp: 3857-3860, Anno: 2002 |
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Loss of methylation at chromosome 11p15.5 is common in human adult tumors
Scelfo, R. A. M.; Schwienbacher, Christine; Veronese, Angelo; Gramantieri, L.; Bolondi, L.; Querzoli, Patrizia; Nenci, Italo; Calin, G. A.; Angioni, A.; BARBANTI BRODANO, Giuseppe; Negrini, Massimo
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Contributo in rivista (Pubblicazione in Rivista) |
ONCOGENE
Vol. 21, No. 16, pp: 2564-2572, Anno: 2002 |
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EPIGENETIC CHANGES AT CHROMOSOME REGION 11p15.5 IN HUMAN CANCER
M. R., Scelfo; Schwienbacher, Christine; Sabbioni, Silvia; Veronese, Angelo; Zagatti, Barbara; Biscuolo, Giorgia; Miotto, Elena; Negrini, Massimo
Atto di Convegno (Proceedings) |
TUMORI
Vol. 87, No. 1, pp: 62-63, Anno: 2001 |
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Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumor
Schwienbacher, Christine; Angioni, A.; Scelfo, R.; Veronese, Angelo; Calin, G.; Massazza, G.; Hatada, I.; BARBANTI BRODANO, Giuseppe; Negrini, Massimo
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Contributo in rivista (Pubblicazione in Rivista) |
CANCER RESEARCH
Vol. 60, No. 1, pp: 1521-1525, Anno: 2000 |
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Gain of imprinting at chromosome 11p15: a pathogenetic mechanism identified in human hepatocarcinomas
Schwienbacher, Christine; Gramantieri, L.; Scelfo, R.; Veronese, Angelo; Calin, Ga; Bolondi, L.; Croce, Carlo Maria; BARBANTI BRODANO, Giuseppe; Negrini, Massimo
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Contributo in rivista (Pubblicazione in Rivista) |
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Vol. 97, No. 10, pp: 5445-5449, Anno: 2000 |
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CLONING AND CHARACTERIZATION OF A CLUSTER OF IMPRINRTED GENES AT 11p15.5 AND THEIR INVOLVEMENT IN TUMORIGENESIS.
Schwienbacher, Christine; Sabbioni, Silvia; Scelfo, R.; Veronese, Angelo; BARBANTI BRODANO, G.; Negrini, Massimo
Atto di Convegno (Proceedings) |
IV Meeting of Molecular Oncology,
IV Meeting of Molecular Oncology
pp: 113-113, Anno: 1999 |
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CHARACTERIZATION OF CHROMOSOMAL REGION 11p15 FOR THE IDENTIFICATION GENES INVOLVED IN BECKWITH-WIEDEMANN SYNDROME.
Negrini, Massimo; Schwienbacher, Christine; Scelfo, R.; Sabbioni, Silvia
Atto di Convegno (Proceedings) |
VIII Telethon scientific convention,
VIII Telethon scientific convention
pp: 446-446, Anno: 1999 |
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CHARACTERIZATION OF CHROMOSOMAL REGION 11p15 FOR THE IDENTIFICATION OF GENES INVOLVED IN BECKWITH-WIEDEMANN SYNDROME
Schwienbacher, Christine; Scelfo, R.; Sabbioni, Silvia; Negrini, Massimo
Atto di Convegno (Proceedings) |
VII Telethon scientific convention,
VII Telethon scientific convention
pp: 514-514, Anno: 1998 |
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