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1. Full Text Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
by Wain, Louise V and Shrine, Nick R. G and Artigas, Maria Soler and Erzurumluoglu, A Mesut and Noyvert, Boris and Bossini-Castillo, Lara and Obeidat, Ma'en and Henrys, Amanda P and Portelli, Michael A and Hall, Robert J and Billington, Charlotte K and Rimington, Tracy L and Fenech, Anthony G and John, Catherine and Blake, Tineka and Jackson, Victoria E and Allen, Richard J and Prins, Bram P and Campbell, Archie and Porteous, David J and Jarvelin, Marjo-Riitta and Wielscher, Matthias and Jamess, Alan L and Hui, Jennie and Wareham, Nicholas J and Zhao, Jing Hua and Wilson, James F and Joshi, Peter K and Stubbe, Beate and Rawal, Rajesh and Schulz, Holger and Imboden, Medea and Probst-Hensch, Nicole M and Karrasch, Stefan and Gieger, Christian and Deary, Ian J and Harris, Sarah E and Marten, Jonathan and Rudan, Igor and Enroth, Stefan and Gyllensten, Ulf and Kerr, Shona M and Polasek, Ozren and Kahonen, Mika and Surakka, Ida and Vitart, Veronique and Hayward, Caroline and van den Berge, Maarten and Brandsma, Corry-Anke and Trynka, Gosia and Geisinger-Regeneron DiscovEHR and Understanding Soc Sci Grp and Understanding Society Scientific Group and Geisinger-Regeneron DiscovEHR Collaboration
Nature genetics, ISSN 1061-4036, 03/2017, Volume 49, Issue 3, pp. 416 - 425
POPULATION | VARIANTS | GENETICS | SUSCEPTIBILITY | FAM13A | HEALTH | EPIDEMIOLOGY | AIR-FLOW OBSTRUCTION | COPD | HISTORY | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease - genetics | Humans | Middle Aged | Risk Factors | Genetic Loci - genetics | Male | Lung - physiopathology | Asthma - genetics | Epigenesis, Genetic - genetics | Alleles | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | Genome-Wide Association Study - methods | Pulmonary Disease, Chronic Obstructive - genetics | Quantitative trait loci | Molecular targeted therapy | Lung diseases, Obstructive | Care and treatment | Innovations | Development and progression | Genetic aspects | Health aspects | Studies | Chronic obstructive pulmonary disease | Genomes | Health risk assessment | Index Medicus
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2. Full Text Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study
by Behr, Elijah R and Savio-Galimberti, Eleonora and Barc, Julien and Holst, Anders G and Petropoulou, Evmorfia and Prins, Bram P and Jabbari, Javad and Torchio, Margherita and Berthet, Myriam and Mizusawa, Yuka and Yang, Tao and Nannenberg, Eline A and Dagradi, Federica and Weeke, Peter and Bastiaenan, Rachel and Ackerman, Michael J and Haunso, Stig and Leenhardt, Antoine and Kääb, Stefan and Probst, Vincent and Redon, Richard and Sharma, Sanjay and Wilde, Arthur and Tfelt-Hansen, Jacob and Schwartz, Peter and Roden, Dan M and Bezzina, Connie R and Olesen, Morten and Darbar, Dawood and Guicheney, Pascale and Crotti, Lia and Jamshidi, Yalda and UK10K Consortium
Cardiovascular research, ISSN 0008-6363, 2015, Volume 106, Issue 3, pp. 520 - 529
Genetics | SCN10A | QRS duration | Brugada syndrome | Rare variants | Brugada Syndrome - genetics | Brugada Syndrome - diagnosis | United States | Brugada Syndrome - physiopathology | Humans | Middle Aged | Databases, Genetic | Male | Case-Control Studies | Action Potentials | Saudi Arabia | Transfection | DNA Mutational Analysis | Adult | Female | Odds Ratio | Cell Line | Genetic Predisposition to Disease | Genetic Association Studies | Europe | Gene Frequency | Risk Factors | Computational Biology | Heredity | Phenotype | Pedigree | NAV1.8 Voltage-Gated Sodium Channel - metabolism | Aged | Polymorphism, Single Nucleotide | NAV1.8 Voltage-Gated Sodium Channel - genetics | Index Medicus | Life Sciences | Original
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3. Full Text Poor replication of candidate genes for major depressive disorder using genome-wide association data
by Bosker, F. J and Hartman, C. A and Nolte, I. M and Prins, B. P and Terpstra, P and Posthuma, D and van Veen, T and Willemsen, G and DeRijk, R. H and de Geus, E. J and Hoogendijk, W. J and Sullivan, P. F and Penninx, B. W and Boomsma, D. I and Snieder, H and Nolen, W. A
Molecular psychiatry, ISSN 1359-4184, 05/2011, Volume 16, Issue 5, pp. 516 - 532
replication | FUNCTIONAL POLYMORPHISM | ALZHEIMERS-DISEASE | GLUCOCORTICOID-RECEPTOR GENE | ANTIDEPRESSANT TREATMENT | PROMOTER POLYMORPHISM | SEROTONIN TRANSPORTER GENE | UMCG Approved | major depressive disorder | candidate genes | MOOD DISORDERS | INCREASED RISK | KOREAN POPULATION | genome-wide association study | single-nucleotide polymorphisms | ALPHA-GENE | Biochemistry & Molecular Biology | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Psychology. Psychoanalysis. Psychiatry | Adult and adolescent clinical studies | Psychopathology. Psychiatry | Mood disorders | Biological and medical sciences | Depression | Medical sciences | Genetic Predisposition to Disease | Genome-Wide Association Study | Gene Frequency | Humans | Tumor Necrosis Factor-alpha - genetics | Computational Biology | Genotype | Neuropeptide Y - genetics | Nerve Tissue Proteins - genetics | Linkage Disequilibrium | Peptidyl-Dipeptidase A - genetics | PubMed - statistics & numerical data | Depressive Disorder, Major - genetics | Norepinephrine Plasma Membrane Transport Proteins - genetics | Polymorphism, Single Nucleotide - genetics | Odds Ratio | Genetic aspects | Research | Single nucleotide polymorphisms | Major depressive disorder | Risk factors | Index Medicus
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4. Full Text lodGWAS: a software package for genome-wide association analysis of biomarkers with a limit of detection
by Vaez, Ahmad and van der Most, Peter J and Prins, Bram P and Snieder, Harold and van den Heuvel, Edwin and Alizadeh, Behrooz Z and Nolte, Ilja M
Bioinformatics (Oxford, England), ISSN 1367-4803, 05/2016, Volume 32, Issue 10, pp. 1552 - 1554
REGRESSION | Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Biomarkers | Limit of Detection | Software | Genome-Wide Association Study - methods | Humans | Index Medicus | Software packages | Packages | Falling | Summaries | Online | Survival | Bioinformatics
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5. Full Text QCGWAS: A flexible R package for automated quality control of genome-wide association results
by van der Most, Peter J and Vaez, Ahmad and Prins, Bram P and Muñoz Venegas, Loretto and Snieder, Harold and Alizadeh, Behrooz Z and Nolte, Ilja M
Bioinformatics (Oxford, England), ISSN 1367-4803, 04/2014, Volume 30, Issue 8, pp. 1185 - 1186
Qaulity Control | META ANALYSIS | GWAS | Genome-Wide Assocation Study | Statistics & Probability | Biochemistry & Molecular Biology | Physical Sciences | Computer Science, Interdisciplinary Applications | Life Sciences & Biomedicine | Technology | Biochemical Research Methods | Computer Science | Mathematics | Biotechnology & Applied Microbiology | Science & Technology | Mathematical & Computational Biology | Computational Biology - methods | Genome-Wide Association Study | Software | Humans | Quality Control | Automated | Packages | Quality control | Automatic control | Summaries | Online | Bioinformatics | Index Medicus
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6. Full Text Evidence for large-scale gene-by-smoking interaction effects on pulmonary function
by Aschard, Hugues and Tobin, Martin and Hancock, Dana and Skurnik, D and Sood, A and James, Alan and Smith, Albert Vernon and Manichaikul, Ani and Campbell, Archie and Prins, B.P and Hayward, Caroline and Loth, Daan and Porteous, David J and Strachan, David and Zeggini, Eleftheria and O'Connor, George and Brusselle, Guy and Boezen, Marike and Schulz, Holger and Deary, Ian and Hall, Ian and Rudan, Igor and Kaprio, Jaakko and Wilson, James and Wilk, Jemma and Huffman, Jennifer and Zhao, J.H and Jong, Kim and Lyytikäinen, Leo-Pekka and Wain, L.V and Jarvelin, Marjo-Riitta and Kähönen, Mika and Fornage, Myriam and Polasek, Ozren and Cassano, Patricia and Barr, Graham and Rawal, Rajesh and Harris, Sarah and Gharib, Sina and Enroth, Stefan and Heckbert, Susan and Lehtimäki, Terho and Gyllensten, Ulf and Jackson, V.E and Gudnason, Vilmundur and Tang, Wenbo and Dupuis, Josée and Artigas, M.S and Joshi, A.D and London, Stephanie J and Kraft, Peter and Understanding Soc Sci Grp and Understanding Society Scientific Group
International journal of epidemiology, ISSN 0300-5771, 06/2017, Volume 46, Issue 3, pp. 894 - 904
Genetic risk score | FEV1/FVC | Gene-environment interaction | Smoking | FVC | FEV | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Forced Expiratory Volume - genetics | Multivariate Analysis | Spirometry | Risk Assessment | Europe | Humans | Middle Aged | Vital Capacity - genetics | Linear Models | Male | Smoking - genetics | Gene-Environment Interaction | Smoking - epidemiology | Female | Polymorphism, Single Nucleotide | Index Medicus | gene–environment interaction | genetic risk score | Tobacco | FEV1 | smoking
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7. Full Text Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
by Tin, Aienne and Marten, Jonathan and Halperin Kuhns, Victoria L and Li, Yong and Wuttke, Matthias and Kirsten, Holger and Sieber, Karsten B and Qiu, Chengxiang and Gorski, Mathias and Yu, Zhi and Giri, Ayush and Sveinbjornsson, Gardar and Li, Man and Chu, Auey Y and Hoppmann, Anselm and O’Connor, Luke J and Prins, Bram and Nutile, Teresa and Noce, Damia and Akiyama, Masato and Cocca, Massimiliano and Ghasemi, Sahar and van der Most, Peter J and Horn, Katrin and Xu, Yizhe and Fuchsberger, Christian and Sedaghat, Sanaz and Afaq, Saima and Amin, Najaf and Ärnlöv, Johan and Bakker, Stephan J.L and Bansal, Nisha and Baptista, Daniela and Bergmann, Sven and Biggs, Mary L and Biino, Ginevra and Boerwinkle, Eric and Bottinger, Erwin P and Boutin, Thibaud S and Brumat, Marco and Burkhardt, Ralph and Campana, Eric and Campbell, Archie and Campbell, Harry and Carroll, Robert J and Catamo, Eulalia and Chambers, John C and Ciullo, Marina and Concas, Maria Pina and Penninx, Brenda W.J.H and Pattaro, Cristian and Woodward, O.M and Vitart, Veronique and Köttgen, Anna
Nature genetics, ISSN 1061-4036, 10/2019, Volume 51, Issue 10, pp. 1459 - 1474
yes | Genetics | d_article_not_yet_freely_accessible
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8. Full Text Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
by Ligthart, Symen and Vaez, Ahmad and Võsa, Urmo and Stathopoulou, Maria G and de Vries, Paul S and Prins, Bram P and Van der Most, Peter J and Tanaka, Toshiko and Naderi, Elnaz and Rose, Lynda M and Wu, Ying and Karlsson, Robert and Barbalic, Maja and Lin, Honghuang and Pool, René and Zhu, Gu and Macé, Aurélien and Sidore, Carlo and Trompet, Stella and Mangino, Massimo and Sabater-Lleal, Maria and Kemp, John P and Abbasi, Ali and Kacprowski, Tim and Verweij, Niek and Smith, Albert V and Huang, Tao and Marzi, Carola and Feitosa, Mary F and Lohman, Kurt K and Kleber, Marcus E and Milaneschi, Yuri and Huq, Mahmudul and Zhao, Jing Hua and Amini, Marzyeh
American journal of human genetics, ISSN 0002-9297, 11/2018, Volume 103, Issue 5, pp. 691 - 706
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9. Full Text Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
by Setten, Jessica and Verweij, Niek and Mbarek, H and Niemeijer, M.N and Trompet, Stella and Arking, Dan
European journal of human genetics : EJHG, ISSN 1018-4813, 01/2019, Volume 27, Issue 6, pp. 952 - 962
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | EKG | Heart rate | Gene frequency | Exons | Gene regulation | Electrocardiography | Genomes | Single-nucleotide polymorphism | Regulatory sequences | Genotypes | Index Medicus | Genome-wide association studies | Quantitative trait
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10. Full Text Genomic atlas of the human plasma proteome
by Sun, Benjamin B and Maranville, Joseph C and Peters, James E and Stacey, David and Staley, James R and Blackshaw, James and Burgess, Stephen and Jiang, Tao and Paige, Ellie and Surendran, Praveen and Oliver-Williams, Clare and Kamat, Mihir A and Prins, Bram P and Wilcox, Sheri K and Zimmerman, Erik S and Chi, An and Bansal, Narinder and Spain, Sarah L and Wood, Angela M and Morrell, Nicholas W and Bradley, John R and Janjic, Nebojsa and Roberts, David J and Ouwehand, Willem H and Todd, John A and Soranzo, Nicole and Suhre, Karsten and Paul, Dirk S and Fox, Caroline S and Plenge, Robert M and Danesh, John and Runz, Heiko and Butterworth, Adam S
Nature (London), ISSN 0028-0836, 06/2018, Volume 558, Issue 7708, pp. 73 - 79
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Physiological aspects | Methods | Proteomics | Blood plasma | Drugs | Integrated approach | Blood & organ donations | Architecture | Therapeutic applications | Cardiovascular disease | Genomes | Genetic diversity | Drug development | Gene expression | Loci | Blood donors | Biological activity | Quantitative trait loci | Proteins | Plasma proteins | Acids | Genetic analysis | Biomarkers | Genetic factors | Proteomes | Bioinformatics | Index Medicus
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11. Full Text Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits
by van Setten, Jessica and Verweij, Niek and Mbarek, Hamdi and Niemeijer, Maartje N and Trompet, Stella and Arking, Dan E and Brody, Jennifer A and Gandin, Ilaria and Grarup, Niels and Hall, Leanne M and Hemerich, Daiane and Lyytikäinen, Leo Pekka and Mei, Hao and Müller-Nurasyid, Martina and Prins, Bram P and Robino, Antonietta and Smith, Albert V and Warren, Helen R and Asselbergs, Folkert W and Boomsma, Dorret I and Caulfield, Mark J and Eijgelsheim, Mark and Ford, Ian and Hansen, Torben and Harris, Tamara B and Heckbert, Susan R and Hottenga, Jouke Jan and Iorio, Anita and Kors, Jan A and Linneberg, Allan and MacFarlane, Peter W and Meitinger, Thomas and Nelson, Christopher P and Raitakari, Olli T and Silva Aldana, Claudia T and Sinagra, Gianfranco and Sinner, Moritz and Soliman, Elsayed Z and Stoll, Monika and Uitterlinden, Ane and van Duijn, Cornelia M and Waldenberger, Melanie and Alonso, Alvaro and Gasparini, Paolo and Gudnason, Vilmundur and Jamshidi, Yalda and Kääb, Stefan and Kanters, Jørgen K and Lehtimäki, Terho and Munroe, Patricia B and Peters, Annette and Samani, Nilesh J and Sotoodehnia, Nona and Ulivi, Sheila and Wilson, James G and de Geus, Eco J.C and Jukema, J. Wouter and Stricker, Bruno and van der Harst, Pim and de Bakker, Paul I.W and Isaacs, Aaron
European journal of human genetics : EJHG, ISSN 1018-4813, 06/2019, Volume 27, Issue 6, pp. 952 - 962
Genetics(clinical) | Genetics
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