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1. Full Text Genetic characterization of Greek population isolates reveals strong genetic drift at missense and trait-associated variants
by Panoutsopoulou, Kalliope and Hatzikotoulas, Konstantinos and Xifara, Dionysia Kiara and Colonna, Vincenza and Farmaki, Aliki-Eleni and Ritchie, Graham R. S and Southam, Lorraine and Gilly, Arthur and Tachmazidou, Ioanna and Fatumo, Segun and Matchan, Angela and Rayner, Nigel W and Ntalla, Ioanna and Mezzavilla, Massimo and Chen, Yuan and Kiagiadaki, Chrysoula and Zengini, Eleni and Mamakou, Vasiliki and Athanasiadis, Antonis and Giannakopoulou, Margarita and Kariakli, Vassiliki-Eirini and Nsubuga, Rebecca N and Karabarinde, Alex and Sandhu, Manjinder and McVean, Gil and Tyler-Smith, Chris and Tsafantakis, Emmanouil and Karaleftheri, Maria and Xue, Yali and Dedoussis, George and Zeggini, Eleftheria
Nature communications, ISSN 2041-1723, 2014, Volume 5, Issue 1, pp. 5345 - 5345
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetics, Population | Gene Frequency - genetics | Genetic Drift | Genome-Wide Association Study | Humans | Cell Size | Genotype | Mutation, Missense - genetics | Greece | Haplotypes - genetics | Phenotype | Blood Cells - cytology | Adolescent | Genetic Variation - genetics | Social Isolation | Population - genetics | Cohort Studies | Index Medicus
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2. Full Text Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk (vol 49, pg 403, 2017)
by Warren, Helen R and Evangelou, Evangelos and Cabrera, Claudia P and Gao, He and Ren, Meixia and Mifsud, Borbala and Ntalla, Ioanna and Surendran, Praveen and Liu, Chunyu and Cook, James P and Kraja, Aldi T and Drenos, Fotios and Loh, Marie and Verweij, Niek and Marten, Jonathan and Karaman, Ibrahim and Lepe, Marcelo P. Segura and O'Reilly, Paul F and Knight, Joanne and Snieder, Harold and Kato, Norihiro and He, Jiang and Tai, E. Shyong and Said, M. Abdullah and Porteous, David and Alver, Maris and Poulter, Neil and Farrall, Martin and Gansevoort, Ron T and Padmanabhan, Sandosh and Magi, Reedik and Stanton, Alice and Connell, John and Bakker, Stephan J. L and Metspalu, Andres and Shields, Denis C and Thom, Simon and Brown, Morris and Sever, Peter and Esko, Tonu and Hayward, Caroline and van der Harst, Pim and Saleheen, Danish and Chowdhury, Rajiv and Chambers, John C and Chasman, Daniel I and Chakravarti, Aravinda and Newton-Cheh, Christopher and Lindgren, Cecilia M and Levy, Daniel and Kooner, Jaspal S and Keavney, Bernard and Tomaszewski, Maciej and Samani, Nilesh J and Howson, Joanna M. M and Tobin, Martin D and Munroe, Patricia B and Ehret, Georg B and Wain, Louise V and Barnes, Michael R and Tzoulaki, Ioanna and Caulfield, Mark J and Elliott, Paul and Uk Biobank CardioMetab Consortium and Int Consortium Blood Pressure ICBP and Cohorts Heart Ageing Res Genome and ExomeBP Consortium and GoT2DGenes Consortium and CHD Exome Consortium and T2D-GENES Consortium and Int Genomics Blood Pressure
Nature genetics, ISSN 1061-4036, 10/2017, Volume 49, Issue 10, pp. 1558 - 1558
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology
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3. Genetic Risk Score for Coronary Disease Identifies Predispositions to Cardiovascular and Noncardiovascular Diseases
by Ntalla, Ioanna and Kanoni, Stavroula and Zeng, Lingyao and Giannakopoulou, Olga and Danesh, John and Watkins, Hugh and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and UK Biobank CardioMetab Consort and UK Biobank CardioMetabolic Consortium CHD Working Group
Journal of the American College of Cardiology, ISSN 0735-1097, 06/2019, Volume 73, Issue 23, pp. 2932 - 2942
coronary artery disease | heart failure | genetic risk score | migraine | cardiovascular diseases | UK Biobank | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Risk Assessment - methods | Prospective Studies | Humans | Kidney Diseases - diagnosis | Middle Aged | Male | Kidney Diseases - genetics | Kidney Diseases - epidemiology | Adult | Female | Hypertension - epidemiology | Hypertension - genetics | Genetic Predisposition to Disease - epidemiology | Hypertension - diagnosis | Arthritis, Rheumatoid - diagnosis | Hypercholesterolemia - epidemiology | Genetic Predisposition to Disease - genetics | Risk Factors | Arthritis, Rheumatoid - epidemiology | Biological Specimen Banks - trends | Arthritis, Rheumatoid - genetics | Coronary Artery Disease - diagnosis | Coronary Artery Disease - genetics | Hypercholesterolemia - diagnosis | Aged | Coronary Artery Disease - epidemiology | Hypercholesterolemia - genetics | Longitudinal Studies | United Kingdom - epidemiology | Cohort Studies | Heart | Headache | Cardiac arrhythmia | Taxonomy | Embolisms | Cardiomyopathy | Health services | Aneurysms | Cardiovascular disease | Genomes | Angina | Risk factors | Genetic relationship | Fibrillation | Atherosclerosis | Genetic analysis | Aorta | Heart diseases | Heart failure | Hypertension | Stroke | Sensitivity analysis | Congenital diseases | Comorbidity | Migraine | Coronary artery | Health risks | Risk analysis | Coronary artery disease | Thrombosis | Diseases | Abdomen | Studies | Sensitivity | Ethnicity | Hospitals | Hypercholesterolemia | Rheumatoid arthritis | Quality control | Gene loci | Kidney diseases | Diabetes | Health risk assessment
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4. Full Text Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system
by Ramírez, Julia and Duijvenboden, Stefan Van and Ntalla, Ioanna and Mifsud, Borbala and Warren, Helen R and Tzanis, Evan and Orini, Michele and Tinker, Andrew and Lambiase, Pier D and Munroe, Patricia B
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 1947 - 10
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Cardiovascular Diseases - physiopathology | Genetic Predisposition to Disease - genetics | Heart Rate - genetics | Humans | Risk Factors | Male | Autonomic Nervous System - physiopathology | Cardiovascular Diseases - genetics | Exercise | Heart Rate - physiology | Female | Autonomic Nervous System - metabolism | Polymorphism, Single Nucleotide | Genome-Wide Association Study - methods | Heart rate | Phenotypes | Physical training | Autonomic nervous system | Health risks | Nervous system | Genomes | Single-nucleotide polymorphism | Cardiovascular diseases | Recovery | Loci | Index Medicus
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5. Full Text An Overweight Preventive Score associates with obesity and glycemic traits
by Ntalla, Ioanna and Yannakoulia, Mary and Dedoussis, George V
Metabolism, clinical and experimental, ISSN 0026-0495, 2016, Volume 65, Issue 1, pp. 81 - 88
Endocrinology & Metabolism | Glycemic control | Obesity | Children | Adolescents | Dietary index | Life Sciences & Biomedicine | Science & Technology | Body Mass Index | Blood Glucose - analysis | Humans | Obesity - prevention & control | Adolescent | Insulin Resistance | Female | Male | Child | Overweight - prevention & control | Prevention | Obesity in adolescence | Index Medicus
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6. Full Text Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
by Gilly, Arthur and Suveges, Daniel and Kuchenbaecker, Karoline and Pollard, Martin and Southam, Lorraine and Hatzikotoulas, Konstantinos and Farmaki, Aliki-Eleni and Bjornland, Thea and Waples, Ryan and Appel, Emil V. R and Casalone, Elisabetta and Melloni, Giorgio and Kilian, Britt and Rayner, Nigel W and Ntalla, Ioanna and Kundu, Kousik and Walter, Klaudia and Danesh, John and Butterworth, Adam and Barroso, Inês and Tsafantakis, Emmanouil and Dedoussis, George and Moltke, Ida and Zeggini, Eleftheria
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 4674 - 9
Genetic Variation | Gene Frequency - genetics | Quantitative Trait, Heritable | Humans | Alleles | Cohort Studies | Whole Genome Sequencing | Replicating | Lipids | Genomes | Lipid metabolism | Metabolism | Adiponectin | Gene sequencing | Index Medicus
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7. Full Text Population‐wide copy number variation calling using variant call format files from 6,898 individuals
by Png, Grace and Suveges, Daniel and Park, Young‐Chan and Walter, Klaudia and Kundu, Kousik and Ntalla, Ioanna and Tsafantakis, Emmanouil and Karaleftheri, Maria and Dedoussis, George and Zeggini, Eleftheria and Gilly, Arthur
Genetic epidemiology, ISSN 0741-0395, 01/2020, Volume 44, Issue 1, pp. 79 - 89
whole‐genome sequencing | copy‐number variant | association study | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Mathematical & Computational Biology | Genome-Wide Association Study | Genetics, Population - methods | Glutathione Transferase - genetics | Nodal Protein - genetics | Chemokine CCL3 - genetics | Gene Deletion | Genomics | Humans | Recombinant Fusion Proteins - genetics | DNA Copy Number Variations - genetics | Genome, Human - genetics | Whole Genome Sequencing | Proteins | Genetic variance | Copy number | Computer applications | CCL3 protein | Population studies | Genomes | GSTM1 protein | Gene deletion | Index Medicus
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8. Full Text Genetically modulated educational attainment and coronary disease risk
by Zeng, Lingyao and Ntalla, Ioanna and Kessler, Thorsten and Kastrati, Adnan and Erdmann, Jeanette and Danesh, John and Watkins, Hugh and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and UK Biobank CardioMetab Consortium and UK Biobank CardioMetabolic Consortium CHD Working Group and The UK Biobank CardioMetabolic Consortium CHD Working Group
European heart journal, ISSN 0195-668X, 08/2019, Volume 40, Issue 29, pp. 2413 - U53
Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Index Medicus | Genome-wide association studies | Editor's Choice | School education | Atherosclerosis | Basic Science | Genetics | Coronary artery disease
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9. Full Text Global real‐world evidence of sofosbuvir/velpatasvir as simple, effective HCV treatment: Analysis of 5552 patients from 12 cohorts
by Mangia, Alessandra and Milligan, Scott and Khalili, Mandana and Fagiuoli, Stefano and Shafran, Stephen D and Carrat, Fabrice and Ouzan, Denis and Papatheodoridis, George and Ramji, Alnoor and Borgia, Sergio M and Wedemeyer, Heiner and Losappio, Ruggero and Pérez‐Hernandez, Francisco and Wick, Nicole and Brown, Robert S and Lampertico, Pietro and Doucette, Karen and Ntalla, Ioanna and Ramroth, Heribert and Mertens, Michael and Vanstraelen, Kim and Turnes, Juan
Liver international, ISSN 1478-3223, 08/2020, Volume 40, Issue 8, pp. 1841 - 1852
sofosbuvir/velpatasvir | real‐world | HCV elimination | heterogenous | Hepatitis C | sustained virological response | real-world | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Drug abuse | Evaluation | Intravenous administration | Regression analysis | Patients | Ribavirin | Risk factors | Cirrhosis | Hepatitis | Genotype & phenotype | Human immunodeficiency virus--HIV | Hepatitis C virus | Genotypes | Index Medicus
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10. Full Text Metabolic syndrome in a Mediterranean pediatric cohort: prevalence using International Diabetes Federation–derived criteria and associations with adiponectin and leptin
by Papoutsakis, Constantina and Yannakoulia, Mary and Ntalla, Ioanna and Dedoussis, George V
Metabolism, clinical and experimental, ISSN 0026-0495, 2012, Volume 61, Issue 2, pp. 140 - 145
Endocrinology & Metabolism | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Feeding. Feeding behavior | Diabetes. Impaired glucose tolerance | Miscellaneous | Vertebrates: anatomy and physiology, studies on body, several organs or systems | Other metabolic disorders | Biological and medical sciences | Endocrinopathies | Etiopathogenesis. Screening. Investigations. Target tissue resistance | Metabolic diseases | Medical sciences | Endocrine pancreas. Apud cells (diseases) | Body Mass Index | Prevalence | Cross-Sectional Studies | Diagnostic Techniques, Endocrine | Humans | Male | Endocrinology - organization & administration | Adiponectin - blood | Metabolic Syndrome - blood | Leptin - blood | International Agencies | Insulin Resistance - physiology | Metabolic Syndrome - diagnosis | Adolescent | Female | Mediterranean Region - epidemiology | Child | Research Design | Metabolic Syndrome - epidemiology | Cohort Studies | Pediatrics | Analysis | Low density lipoproteins | Leptin | Body weight | Insulin resistance | Triglycerides | Glucose | Dextrose | Cholesterol | Prevalence studies (Epidemiology) | Index Medicus
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11. Full Text Issue Cover
by Mangia, Alessandra and Milligan, Scott and Khalili, Mandana and Fagiuoli, Stefano and Shafran, Stephen D and Carrat, Fabrice and Ouzan, Denis and Papatheodoridis, George and Ramji, Alnoor and Borgia, Sergio M and Wedemeyer, Heiner and Losappio, Ruggero and Pérez‐Hernandez, Francisco and Wick, Nicole and Brown, Robert S and Lampertico, Pietro and Doucette, Karen and Ntalla, Ioanna and Ramroth, Heribert and Mertens, Michael and Vanstraelen, Kim and Turnes, Juan
Liver international, ISSN 1478-3223, 08/2020, Volume 40, Issue 8, pp. i - i
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12. Full Text Author Correction: Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits
by Gilly, Arthur and Suveges, Daniel and Kuchenbaecker, Karoline and Pollard, Martin and Southam, Lorraine and Hatzikotoulas, Konstantinos and Farmaki, Aliki-Eleni and Bjornland, Thea and Waples, Ryan and Appel, Emil V R and Casalone, Elisabetta and Melloni, Giorgio and Kilian, Britt and Rayner, Nigel W and Ntalla, Ioanna and Kundu, Kousik and Walter, Klaudia and Danesh, John and Butterworth, Adam and Barroso, Inês and Tsafantakis, Emmanouil and Dedoussis, George and Moltke, Ida and Zeggini, Eleftheria
Nature communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 5460 - 1
Genomes | Gene sequencing
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