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Your search keyword '"Blaveri, Ekaterina"' showing total 12 results
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12 results on '"Blaveri, Ekaterina"'

1. Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia

Author

Gurling, Hugh M.D., Critchley, Hugo, Datta, Susmita R., Mcquillin, Andrew, Blaveri, Ekaterina, Thirumalai, Srinivasa, Pimm, Jonathan, Krasucki, Robert, Kalsi, Gursharan, Quested, Digby, Lawrence, Jacob, Bass, Nicholas, Choudhury, Khalid, Puri, Vinay, O'Daly, Owen, Curtis, David, Blackwood, Douglas, Muir, Walter, Malhotra, Anil K., Buchanan, Robert W., Good, Catriona D., Frackowiak, Richard S.J., and Dolan, Raymond J.

Subjects
Schizophrenia -- Genetic aspects, Schizophrenia -- Causes of, Genetic susceptibility -- Research, Genetic markers -- Research, Health, Psychology and mental health
Published
2006

3. Gene–Brain Structure Relationships: Arbitrary Assumptions of Heterogeneity Generate Unfalsifiable Claims

Author

Gurling, Hugh M. D., Critchley, Hugo, Datta, Susmita R., McQuillin, Andrew, Blaveri, Ekaterina, Thirumalai, Srinivasa, Pimm, Jonathan, Krasucki, Robert, Kalsi, Gursharan, Quested, Digby, Lawrence, Jacob, Bass, Nicholas, Choudhury, Khalid, Puri, Vinay, OʼDaly, Owen, Curtis, David, Blackwood, Douglas, Muir, Walter, Malhotra, Anil K., Buchanan, Robert W., Good, Catriona D., Frackowiak, Richard S. J., and Dolan, Raymond J.

Published
2007

4. Gene-brain structure relationships: arbitrary assumptions of heterogeneity generate unfalsifiable claims

Author

Crow, Tim J., DeLisi, Lynn, Gurling, Hugh M.D., Critchley, Hugo, Datta, Susmita R., McQuillin, Andrew, Blaveri, Ekaterina, Thirumalai, Srinivasa, Pimm, Jonathan, Krasucki, Robert, Kalsi, Gursharan, Quested, Digby, Lawrence, Jacob, Bass, Nicholas, Choudhury, Khalid, Puri, Vinay, OEDaly, Owen, Curtis, David, Blackwood, Douglas, Muir, Walter, Malhotra, Anil K., Buchanan, Robert W., Good, Catriona D., Frackowiak, Richard, and Dolan, Raymond J.

Subjects
Brain -- Structure, Schizophrenia -- Genetic aspects, Schizophrenia -- Research, Genes -- Identification and classification, Chromosome deletion -- Psychological aspects, Health, Psychology and mental health
Published
2007

6. Identification of a robust gene signature that predicts breast cancer outcome in independent data sets

Author

Estep Anne LH, Chen Yunn-Yi, Hwang E Shelley, Moore Dan H, DeVries Sandy, Blaveri Ekaterina, Korkola James E, Chew Karen L, Jensen Ronald H, and Waldman Frederic M

Subjects
Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
Abstract

Abstract Background Breast cancer is a heterogeneous disease, presenting with a wide range of histologic, clinical, and genetic features. Microarray technology has shown promise in predicting outcome in these patients. Methods We profiled 162 breast tumors using expression microarrays to stratify tumors based on gene expression. A subset of 55 tumors with extensive follow-up was used to identify gene sets that predicted outcome. The predictive gene set was further tested in previously published data sets. Results We used different statistical methods to identify three gene sets associated with disease free survival. A fourth gene set, consisting of 21 genes in common to all three sets, also had the ability to predict patient outcome. To validate the predictive utility of this derived gene set, it was tested in two published data sets from other groups. This gene set resulted in significant separation of patients on the basis of survival in these data sets, correctly predicting outcome in 62–65% of patients. By comparing outcome prediction within subgroups based on ER status, grade, and nodal status, we found that our gene set was most effective in predicting outcome in ER positive and node negative tumors. Conclusion This robust gene selection with extensive validation has identified a predictive gene set that may have clinical utility for outcome prediction in breast cancer patients.

Published
2007
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7. Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

Author

Gurling, Hugh M.D., Kalsi, Gursharan, Brynjolfson, Jon, Sigmundsson, Thordur, Sherrington, Robin, Mankoo, Baljinder S., Read, Timothy, Murphy, Patrice, Blaveri, Ekaterina, McQuillin, Andrew, Petursson, Hannes, and Curtis, David

Published
2001
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12. In reply.

Author

Gurling, Hugh M. D., Critchley, Hugo, Datta, Susmita R., Mcquillin, Andrew, Blaveri, Ekaterina, Thirumalai, Srinivasa, Pimm, Jonathan, Krasucki, Robert, Kalsi, Gursharan, Quested, Digby, Lawrence, Jacob, Bass, Nicholas, Choudhury, Khalid, Pun, Vinay, O'daly, Owen, Curtis, David, Blackwood, Douglas, Muir, Walter, Maihotra, Anil K., and Buchanan, Robert W.

Subjects
LETTERS to the editor, GENETICS
Abstract

A response by Hugh M. D. Gurling and colleagues to a letter to the editor about their article "Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia" is presented.

Published
2007
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