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Christine Schwienbacher

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Anatomy

Physiology

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Irene Pichler; Maurizio Facheris; Christian Fuchsberger; James F Gusella; Ulf Gyllensten; Andrew A Hicks; Fabio Marroni; Cristian Pattaro; Christine Schwienbacher; Alice Serafin; Yiping Shen; Christian Tellgren-Roth; Alessandra Zanon; Peter P Pramstaller
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.
Cosetta Minelli; Mirko Modenese; Giovanni Parmigiani; Andrea Pastore; Cristian Pattaro; Arne Pfeufer; Peter P Pramstaller; Fabrizio Ruggeri; Christine Schwienbacher; Daniel Taliun; John Attia; Jennifer H Barrett; Michael Boehnke; Giuseppe Borsani; Giorgio Casari; Alessandro De Grandi; Francisco S Domingues; Caroline S Fox; Thomas Freina; Martin Gögele; Andrew A Hicks; Fabio Marroni; Christian X Weichenberger; John R Thompson
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
John R Thompson; Christian X Weichenberger; John Attia; Jennifer H Barrett; Michael Boehnke; Giuseppe Borsani; Giorgio Casari; Ckdgen Consortium; Alessandro De Grandi; Francisco S Domingues; Caroline S Fox; Martin Gögele; Andrew A Hicks; Fabio Marroni; Mirko Modenese; Giovanni Parmigiani; Andrea Pastore; Cristian Pattaro; Arne Pfeufer; Peter P Pramstaller; Fabrizio Ruggeri; Christine Schwienbacher; Daniel Taliun; Cosetta Minelli
SNP prioritization using a Bayesian probability of association.

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All Publications

2013: Irene Pichler; Maurizio Facheris; Christian Fuchsberger; James F Gusella; Ulf Gyllensten; Andrew A Hicks; Fabio Marroni; Cristian Pattaro; Christine Schwienbacher; Alice Serafin; Yiping Shen; Christian Tellgren-Roth; Alessandra Zanon; Peter P Pramstaller
Fine-mapping of restless legs locus 4 (RLS4) identifies a haplotype over the SPATS2L and KCTD18 genes.
Journal of molecular neuroscience : MN 2013;49(3):600-5.
2013: Cosetta Minelli; Mirko Modenese; Giovanni Parmigiani; Andrea Pastore; Cristian Pattaro; Arne Pfeufer; Peter P Pramstaller; Fabrizio Ruggeri; Christine Schwienbacher; Daniel Taliun; John Attia; Jennifer H Barrett; Michael Boehnke; Giuseppe Borsani; Giorgio Casari; Alessandro De Grandi; Francisco S Domingues; Caroline S Fox; Thomas Freina; Martin Gögele; Andrew A Hicks; Fabio Marroni; Christian X Weichenberger; John R Thompson
Importance of different types of prior knowledge in selecting genome-wide findings for follow-up.
Genetic epidemiology 2013;37(2):205-13.
2013: John R Thompson; Christian X Weichenberger; John Attia; Jennifer H Barrett; Michael Boehnke; Giuseppe Borsani; Giorgio Casari; Ckdgen Consortium; Alessandro De Grandi; Francisco S Domingues; Caroline S Fox; Martin Gögele; Andrew A Hicks; Fabio Marroni; Mirko Modenese; Giovanni Parmigiani; Andrea Pastore; Cristian Pattaro; Arne Pfeufer; Peter P Pramstaller; Fabrizio Ruggeri; Christine Schwienbacher; Daniel Taliun; Cosetta Minelli
SNP prioritization using a Bayesian probability of association.
Genetic epidemiology 2013;37(2):214-21.
2011: Konrad Oexle; Janina S Ried; Andrew A Hicks; Toshiko Tanaka; Caroline Hayward; Mathias Bruegel; Martin Gögele; Peter Lichtner; Bertram Müller-Myhsok; Angela Döring; Thomas Illig; Christine Schwienbacher; Cosetta Minelli; Irene Pichler; Georg Martin Fiedler; Joachim Thiery; Igor Rudan; Alan F Wright; Harry Campbell; Luigi Ferrucci; Stefania Bandinelli; Peter P Pramstaller; H-Erich Wichmann; Christian Gieger; Juliane Winkelmann; Thomas Meitinger
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.
Human molecular genetics 2011;20(5):1042-7.
2010: Christine Schwienbacher; Alessandro De Grandi; Christian Fuchsberger; Maurizio F Facheris; Mirija Svaldi; Matthias Wjst; Peter P Pramstaller; Andrew A Hicks
Copy number variation and association over T-cell receptor genes--influence of DNA source.
Immunogenetics 2010;62(8):561-7.
2007: Angela Sparago; Silvia Russo; Flavia Cerrato; Serena Ferraiuolo; Pierangela Castorina; Angelo Selicorni; Christine Schwienbacher; Massimo Negrini; Giovanni Battista Ferrero; Margherita Silengo; Cecilia Anichini; Lidia Larizza; Andrea Riccio
Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.
Human molecular genetics 2007;16(3):254-64.
2002: Roberto Rosati; Roberta La Starza; Angelo Veronese; Anna Aventin; Christine Schwienbacher; Teresa Vallespi; Massimo Negrini; Massimo F Martelli; Cristina Mecucci
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15).
Blood 2002;99(10):3857-60.
2002: Rosaria A M Scelfo; Christine Schwienbacher; Angelo Veronese; Laura Gramantieri; Luigi Bolondi; Patrizia Querzoli; italo nenci; George A Calin; Adriano Angioni; Giuseppe Barbanti-Brodano; Massimo Negrini
Loss of methylation at chromosome 11p15.5 is common in human adult tumors.
Oncogene 2002;21(16):2564-72.
2000: Christine Schwienbacher; Laura Gramantieri; Rosaria A M Scelfo; Angelo Veronese; George A Calin; Luigi Bolondi; Carlo M Croce; Giuseppe Barbanti-Brodano; Massimo Negrini
Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(10):5445-9.
2000: Christine Schwienbacher; A Angioni; Rosaria A M Scelfo; Angelo Veronese; George A Calin; G Massazza; I Hatada; Giuseppe Barbanti-Brodano; Massimo Negrini
Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumor.
Cancer research 2000;60(6):1521-5.
1998: Christine Schwienbacher; Silvia Sabbioni; M Campi; Angelo Veronese; G Bernardi; A Menegatti; I Hatada; T Mukai; H Ohashi; Giuseppe Barbanti-Brodano; Carlo M Croce; Massimo Negrini
Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(7):3873-8.
1997: Christine Schwienbacher; Silvia Sabbioni; Giuseppe Barbanti-Brodano; Massimo Negrini
Refined subchromosomal location of 21 expressed sequence tags from unknown genes at region 11p15.
European journal of human genetics : EJHG 1997;5(4):214-7.