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Publications

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

Export 28 results:
Author Title Type [ Year(Asc)]
Filters: Keyword is Genome-Wide Association Study  [Clear All Filters]
2019
Malousi, A., Kouidou S., Tsagiopoulou M., Papakonstantinou N., Bouras E., Georgiou E., et al. (2019).  MeinteR: A framework to prioritize DNA methylation aberrations based on conformational and cis-regulatory element enrichment.. Sci Rep. 9(1), 19148.
Hadjigeorgiou, G. M., Kountra P-M., Koutsis G., Tsimourtou V., Siokas V., Dardioti M., et al. (2019).  Replication study of GWAS risk loci in Greek multiple sclerosis patients.. Neurol Sci. 40(2), 253-260.
2017
Aung, T., Ozaki M., Lee M. Chin, Schlötzer-Schrehardt U., Thorleifsson G., Mizoguchi T., et al. (2017).  Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.. Nat Genet. 49(7), 993-1004.
Wollstein, A., Walsh S., Liu F., Chakravarthy U., Rahu M., Seland J. H., et al. (2017).  Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour.. Sci Rep. 7, 43359.
2016
Bailey, J. N. Cooke, Loomis S. J., Kang J. H., R Allingham R., Gharahkhani P., Khor C. Chuen, et al. (2016).  Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.. Nat Genet. 48(2), 189-94.
2015
Aung, T., Ozaki M., Mizoguchi T., R Allingham R., Li Z., Haripriya A., et al. (2015).  A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.. Nat Genet. 47(4), 387-92.
2014
Kara, E., Xiromerisiou G., Spanaki C., Bozi M., Koutsis G., Panas M., et al. (2014).  Assessment of Parkinson's disease risk loci in Greece.. Neurobiol Aging. 35(2), 442.e9-442.e16.
Panoutsopoulou, K., Hatzikotoulas K., Xifara D. Kiara, Colonna V., Farmaki A-E., Ritchie G. R. S., et al. (2014).  Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants.. Nat Commun. 5, 5345.
Purrington, K. S., Slager S., Eccles D., Yannoukakos D., Fasching P. A., Miron P., et al. (2014).  Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.. Carcinogenesis. 35(5), 1012-9.
Kontakioti, E., Domvri K., Papakosta D., & Daniilidis M. (2014).  HLA and asthma phenotypes/endotypes: a review.. Hum Immunol. 75(8), 930-9.
Calero-Nieto, F. J., Ng F. S., Wilson N. K., Hannah R., Moignard V., Leal-Cervantes A. I., et al. (2014).  Key regulators control distinct transcriptional programmes in blood progenitor and mast cells.. EMBO J. 33(11), 1212-26.
2013
Blue Mountains Eye Study (BMES), Wellcome Trust Case Control Consortium 2 (WTCCC2) (2013).  Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.. Hum Mol Genet. 22(22), 4653-60.
Nho, K., Corneveaux J. J., Kim S., Lin H., Risacher S. L., Shen L., et al. (2013).  Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics.. Mol Psychiatry. 18(7), 739.
Stambolian, D., Wojciechowski R., Oexle K., Pirastu M., Li X., Raffel L. J., et al. (2013).  Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.. Hum Mol Genet. 22(13), 2754-64.
Bojesen, S. E., Pooley K. A., Johnatty S. E., Beesley J., Michailidou K., Tyrer J. P., et al. (2013).  Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.. Nat Genet. 45(4), 371-84, 384e1-2.
Fritsche, L. G., Chen W., Schu M., Yaspan B. L., Yu Y., Thorleifsson G., et al. (2013).  Seven new loci associated with age-related macular degeneration.. Nat Genet. 45(4), 433-9, 439e1-2.
Nho, K., Corneveaux J. J., Kim S., Lin H., Risacher S. L., Shen L., et al. (2013).  Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment.. Mol Psychiatry. 18(7), 781-7.
Yu, Y. P., Ding Y., Chen R., Liao S. G., Ren B-G., Michalopoulos A., et al. (2013).  Whole-genome methylation sequencing reveals distinct impact of differential methylations on gene transcription in prostate cancer.. Am J Pathol. 183(6), 1960-70.
2012
van Koolwijk, L. M. E., Ramdas W. D., M Ikram K., Jansonius N. M., Pasutto F., Hysi P. G., et al. (2012).  Common genetic determinants of intraocular pressure and primary open-angle glaucoma.. PLoS Genet. 8(5), e1002611.
Rouskas, K., Kouvatsi A., Paletas K., Papazoglou D., Tsapas A., Lobbens S., et al. (2012).  Common variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 show evidence of association with adult obesity in the Greek population.. Obesity (Silver Spring). 20(2), 389-95.
Gerrish, A., Russo G., Richards A., Moskvina V., Ivanov D., Harold D., et al. (2012).  The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.. J Alzheimers Dis. 28(2), 377-87.
2011
Ross, O. A., Soto-Ortolaza A. I., Heckman M. G., Aasly J. O., Abahuni N., Annesi G., et al. (2011).  Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.. Lancet Neurol. 10(10), 898-908.
Haiman, C. A., Chen G. K., Vachon C. M., Canzian F., Dunning A., Millikan R. C., et al. (2011).  A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.. Nat Genet. 43(12), 1210-4.
Furney, S. J., Simmons A., Breen G., Pedroso I., Lunnon K., Proitsi P., et al. (2011).  Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.. Mol Psychiatry. 16(11), 1130-8.
Kalinderi, K., Fidani L., Katsarou Z., Clarimón J., Bostantjopoulou S., & Kotsis A. (2011).  GSK3β polymorphisms, MAPT H1 haplotype and Parkinson's disease in a Greek cohort.. Neurobiol Aging. 32(3), 546.e1-5.

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