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1. Full Text Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J. Michael and Wilson, Peter W. F and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Lin, Wei-Yu and Luan, Jian’an and Mangino, Massimo and Oldmeadow, Christopher and Prins, Bram Peter and Qian, Yong and Sargurupremraj, Muralidharan and Shah, Nabi and Surendran, Praveen and Thériault, Sébastien and Verweij, Niek and Willems, Sara M and Zhao, Jing-Hua and Amouyel, Philippe and Connell, John and de Mutsert, Renée and Doney, Alex S. F and Farrall, Martin and Menni, Cristina and Morris, Andrew D and Noordam, Raymond and Paré, Guillaume and Poulter, Neil R and Shields, Denis C and Stanton, Alice and Thom, Simon and Abecasis, Gonçalo and Amin, Najaf and Arking, Dan E and Ayers, Kristin L and Barbieri, Caterina M and Batini, Chiara and Bis, Joshua C and Blake, Tineka and Bochud, Murielle and Boehnke, Michael and Boerwinkle, Eric and Boomsma, Dorret I and Bottinger, Erwin P and Braund, Peter S and Brumat, Marco and Campbell, Archie and Campbell, Harry and Chakravarti, Aravinda and Chambers, John C and Chauhan, Ganesh and Ciullo, Marina and Cocca, Massimiliano and Collins, Francis and Cordell, Heather J and Davies, Gail and Borst, Martin H. de and Geus, Eco J. de and Deary, Ian J and Deelen, Joris and Del Greco M, Fabiola and Demirkale, Cumhur Yusuf and Dörr, Marcus and Ehret, Georg B and Elosua, Roberto and Enroth, Stefan and Erzurumluoglu, A. Mesut and Ferreira, Teresa and Frånberg, Mattias and Franco, Oscar H and Gandin, Ilaria and ... and Million Vet Program and Million Veteran Program and the Million Veteran Program and Stockholms universitet and Matematiska institutionen and Naturvetenskapliga fakulteten
Nature Genetics, ISSN 1061-4036, 10/2018, Volume 50, Issue 10, pp. 1412 - 1425
High blood pressure is a highly heritable and modifiable risk factor for cardiovascular disease. We report the largest genetic association study of blood... 
CARDIOVASCULAR-DISEASE RISK | UK BIOBANK | METAANALYSIS | VARIANTS | RARE | HYPERALDOSTERONISM | GENETICS & HEREDITY | COMMON | HEALTH | HYPERTENSION | GENOME-WIDE ASSOCIATION | Hypertension | Health risks | Cardiovascular disease | Genomes | Risk analysis | Loci | Blood | Risk factors | Meta-analysis | Studies | Consortia | Genetic analysis | Blood pressure | Gene loci | Lifestyles | Cardiovascular diseases | Health risk assessment | Biological Sciences | Naturvetenskap | Natural Sciences | Biologiska vetenskaper
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2. Full Text Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
by Mahajan, Anubha and Taliun, Daniel and Thurner, Matthias and Robertson, Neil R and Torres, Jason M and Rayner, N. William and Payne, Anthony J and Steinthorsdottir, Valgerdur and Scott, Robert A and Grarup, Niels and Cook, James P and Schmidt, Ellen M and Wuttke, Matthias and Sarnowski, Chloé and Mägi, Reedik and Nano, Jana and Gieger, Christian and Trompet, Stella and Lecoeur, Cécile and Preuss, Michael H and Prins, Bram Peter and Guo, Xiuqing and Bielak, Lawrence F and Below, Jennifer E and Bowden, Donald W and Chambers, John Campbell and Kim, Young Jin and Ng, Maggie C. Y and Petty, Lauren E and Sim, Xueling and Zhang, Weihua and Bennett, Amanda J and Bork-Jensen, Jette and Brummett, Chad M and Canouil, Mickaël and Ec kardt, Kai-Uwe and Fischer, Krista and Kardia, Sharon L. R and Kronenberg, Florian and Läll, Kristi and Liu, Ching-Ti and Locke, Adam E and Luan, Jian’an and Ntalla, Ioanna and Nylander, Vibe and Schönherr, Sebastian and Schurmann, Claudia and Yengo, Loïc and Bottinger, Erwin P and Brandslund, Ivan and Christensen, Cramer and Dedoussis, George and Florez, Jose C and Ford, Ian and Franco, Oscar H and Frayling, Timothy M and Giedraitis, Vilmantas and Hackinger, Sophie and Hattersley, Andrew T and Herder, Christian and Ikram, M. Arfan and Ingelsson, Martin and Jørgensen, Marit E and Jørgensen, Torben and Kriebel, Jennifer and Kuusisto, Johanna and Ligthart, Symen and Lindgren, Cecilia M and Linneberg, Allan and Lyssenko, Valeriya and Mamakou, Vasiliki and Meitinger, Thomas and Mohlke, Karen L and Morris, Andrew D and Nadkarni, Girish and Pankow, James S and Peters, Annette and Sattar, Naveed and Stančáková, Alena and Strauch, Konstantin and Taylor, Kent D and Thorand, Barbara and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and Tuomilehto, Jaakko and Witte, Daniel R and Dupuis, Josée and Peyser, Patricia A and Zeggini, Eleftheria and Loos, Ruth J. F and Froguel, Philippe and Ingelsson, Erik and Lind, Lars and Groop, Leif and Laakso, Markku and Collins, Francis S and Jukema, J. Wouter and Palmer, Colin N. A and Grallert, Harald and Metspalu, Andres and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Klinisk epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 11/2018, Volume 50, Issue 11, pp. 1505 - 1513
We expanded GWAS discovery for type 2 diabetes (T2D) by combining data from 898,130 European-descent individuals (9% cases), after imputation to high-density... 
METAANALYSIS | SCORE | DISEASE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | GENETIC ARCHITECTURE | PHENOTYPES | IDENTIFICATION | TRAITS | EXPRESSION | GENOME-WIDE ASSOCIATION | Type 2 diabetes | Medical colleges | Research | Genetic translation | Analysis | Genomics | Haplotypes | Obesity | Therapeutic applications | Diabetes mellitus | Risk | Genomes | Mapping | Conditional probability | Gene expression | Density | Loci | Annotations | Maps | Gene frequency | Alleles | Heritability | Diabetes | Islets of Langerhans | Gene mapping | Pancreas | Females | Diabetes mellitus (non-insulin dependent) | Bioinformatics | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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3. Full Text Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes article
by Mahajan, Anubha and Wessel, Jennifer and Willems, Sara M and Zhao, Wei and Robertson, Neil R and Chu, Audrey Y and Gan, Wei and Kitajima, Hidetoshi and Taliun, Daniel and Rayner, N. William and Guo, Xiuqing and Lu, Yingchang and Li, Man and Jensen, Richard A and Hu, Yao and Huo, Shaofeng and Lohman, Kurt K and Zhang, Weihua and Cook, James P and Prins, Bram Peter and Flannick, Jason and Grarup, Niels and Trubetskoy, Vassily Vladimirovich and Kravic, Jasmina and Kim, Young Jin and Rybin, Denis V and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Meidtner, Karina and Li-Gao, Ruifang and Varga, Tibor V and Marten, Jonathan and Li, Jin and Smith, Albert Vernon and An, Ping and Ligthart, Symen and Gustafsson, Stefan and Malerba, Giovanni and Demirkan, Ayse and Tajes, Juan Fernandez and Steinthorsdottir, Valgerdur and Wuttke, Matthias and Lecoeur, Cécile and Preuss, Michael and Bielak, Lawrence F and Graff, Marielisa and Highland, Heather M and Justice, Anne E and Liu, Dajiang J and Marouli, Eirini and Peloso, Gina Marie and Warren, Helen R and Afaq, Saima and Afzal, Shoaib and Ahlqvist, Emma and Bang, Lia B and Bertoni, Alain G and Bombieri, Cristina and Bork-Jensen, Jette and Brandslund, Ivan and Brody, Jennifer A and Burtt, Noël P and Canouil, Mickaël and Chen, Yii-Der Ida and Cho, Yoon Shin and Christensen, Cramer and Eastwood, Sophie V and Eckardt, Kai-Uwe and Fischer, Krista and Gambaro, Giovanni and Giedraitis, Vilmantas and Grove, Megan L and De Haan, Hugoline G and Hackinger, Sophie and Hai, Yang and Han, Sohee and Tybjærg-Hansen, Anne and Hivert, Marie-France and Isomaa, Bo and Jäger, Susanne and Jørgensen, Marit E and Jørgensen, Torben and Käräjämäki, Annemari and Kim, Bong-Jo and Kim, Sung Soo and Koistinen, Heikki A and Kovacs, Peter and Kriebel, Jennifer and Kronenberg, Florian and Läll, Kristi and Lange, Leslie A and Lee, Jung-Jin and Lehne, Benjamin and Li, Huaixing and Lin, Keng-Hung and Linneberg, Allan and Liu, Ching-Ti and Liu, Jun and Loh, Marie and Mägi, Reedik and ... and Diabetes - kardiovaskulär sjukdom and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Genomics, Diabetes and Endocrinology and Diabetes - Islet Patophysiology and EpiHealth: Epidemiology for Health and Genomik, diabetes och endokrinologi and Genetisk och molekylär epidemiologi and Lunds universitet and Diabetes - Cardiovascular Disease and Lund University and Diabetes - öpatofysiologi and Genetic and Molecular Epidemiology
Nature Genetics, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 559 - 571
We aggregated coding variant data for 81,412 type 2 diabetes cases and 370,832 controls of diverse ancestry, identifying 40 coding variant association signals... 
ancestry group | Medical and Health Sciences | Medicin och hälsovetenskap | major clinical study | Article | genetic association | odds ratio | Klinisk medicin | genetic code | Medicinsk genetik | Medical Genetics | Endokrinologi och diabetes | gene mapping | priority journal | human | Endocrinology and Diabetes | Basic Medicine | gene sequence | disease predisposition | genetic variability | non insulin dependent diabetes mellitus | gene locus | genome | Clinical Medicine | Medicinska och farmaceutiska grundvetenskaper
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4. Full Text Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
by Mahajan, A and Wessel, J and Willems, SM and Zhao, W and Robertson, NR and Chu, AY and Gan, W and Kitajima, H and Taliun, D and Rayner, NW and Guo, XQ and Lu, YC and Li, M and Jensen, RA and Hu, Y and Huo, SF and Lohman, KK and Zhang, WH and Cook, JP and Prins, BP and Flannick, J and Grarup, N and Trubetskoy, VV and Kravic, J and Kim, YJ and Rybin, DV and Yaghootkar, H and Muuller-Nurasyid, M and Meidtner, K and Li-Gao, RF and Varga, TV and Marten, J and Li, J and Smith, AV and An, P and Ligthart, S and Gustafsson, S and Malerba, G and Demirkan, A and Tajes, JF and Steinthorsdottir, V and Wuttke, M and Lecoeur, C and Preuss, M and Bielak, LF and Graff, M and Highland, HM and Justice, AE and Liu, DJ and Marouli, E and Peloso, GM and Warren, HR and Afaq, S and Afzal, S and Ahlqvist, E and Almgren, P and Amin, N and Bang, LB and Bertoni, AG and Bombieri, C and Bork-Jensen, J and Brandslund, I and Brody, JA and Burtt, NP and Canouil, M and Chen, YDI and Cho, YS and Christensen, C and Eastwood, SV and Eckardt, KU and Fischer, K and Gambaro, G and Giedraitis, V and Grove, ML and de Haan, HG and Hackinger, S and Hai, Y and Han, S and Tybjaerg-Hansen, A and Hivert, MF and Isomaa, B and Jager, S and Jorgensen, ME and Jorgensen, T and Karajamaki, A and Kim, BJ and Kim, SS and Koistinen, HA and Kovacs, P and Kriebel, J and Kronenberg, F and Lall, K and Lange, LA and Lee, JJ and Lehne, B and Li, HX and Lin, KH and Linneberg, A and Liu, CT and Liu, J and ... and MAGIC Consortium and ExomeBP Consortium and GIANT Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet
NATURE GENETICS, ISSN 1061-4036, 04/2018, Volume 50, Issue 4, pp. 559 - 559
We aggregated coding variant data for 81,412 type 2 diabetes cases and 370,832 controls of diverse ancestry, identifying 40 coding variant association signals... 
CONFERS SUSCEPTIBILITY | RARE VARIANTS | GENOTYPE IMPUTATION | FATTY LIVER-DISEASE | LOW-FREQUENCY | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | BODY-MASS INDEX | GENETIC ARCHITECTURE | QUALITY-CONTROL | GENOME-WIDE ASSOCIATION | Type 2 diabetes | Genome-wide association studies | Usage | Genetic aspects | Risk factors | Exome sequencing | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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5. Full Text Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations
by Prins, Bram Peter and Kuchenbaecker, Karoline B and Bao, Yanchun and Smart, Melissa and Zabaneh, Delilah and Fatemifar, Ghazaleh and Luan, Jian'an and Wareham, Nicholas John and Scott, Robert A and Perry, John Richard and Langenberg, Claudia and Benzeval, Michaela and Kumari, Meena and Zeggini, Eleftheria
ISSN 2045-2322, 2017
Serum biomarker levels are associated with the risk of complex diseases. Here, we aimed to gain insights into the genetic architecture of biomarker traits... 
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6. Full Text Blood Eosinophil Count and Metabolic, Cardiac and Pulmonary Outcomes: A Mendelian Randomization Study
by Amini, Marzyeh and Vonk, Judith M and Abbasi, Ali and Prins, Bram Peter and Bruinenberg, Marcel and Franke, Lude and van der Harst, Pim and Navis, Gerjan and Koppelman, Gerard H and Wolffenbuttel, Bruce HR and Boezen, H Marike and Snieder, Harold and Chasman, Daniel I and Alizadeh, Behrooz Z
ISSN 1832-4274, 2018
Blood eosinophil count is associated with a variety of common complex outcomes in epidemiological observation. The aim of this study was to explore the causal... 
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7. Full Text Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6
by Prins, Bram Peter and Mead, Timothy J and Brody, Jennifer A and Sveinbjornsson, Gardar and Ntalla, Ioanna and Bihlmeyer, Nathan A and van den Berg, Marten and Bork-Jensen, Jette and Cappellani, Stefania and Van Duijvenboden, Stefan and Klena, Nikolai T and Gabriel, George C and Liu, Xiaoqin and Gulec, Cagri and Grarup, Niels and Haessler, Jeffrey and Hall, Leanne M and Iorio, Annamaria and Isaacs, Aaron and Li-Gao, Ruifang and Lin, Honghuang and Liu, Ching-Ti and Lyytikäinen, Leo-Pekka and Marten, Jonathan and Mei, Hao and Müller-Nurasyid, Martina and Orini, Michele and Padmanabhan, Sandosh and Radmanesh, Farid and Ramirez, Julia and Robino, Antonietta and Schwartz, Molly and van Setten, Jessica and Smith, Albert V and Verweij, Niek and Warren, Helen R and Weiss, Stefan and Alonso, Alvaro and Arnar, David O and Bots, Michiel L and de Boer, Rudolf A and Dominiczak, Anna F and Eijgelsheim, Mark and Ellinor, Patrick T and Guo, Xiuqing and Felix, Stephan B and Harris, Tamara B and Hayward, Caroline and Heckbert, Susan R and Huang, Paul L and Jukema, JW and Kähönen, Mika and Kors, Jan A and Lambiase, Pier D and Launer, Lenore J and Li, Man and Linneberg, Allan and Nelson, Christopher P and Pedersen, Oluf and Perez, Marco and Peters, Annette and Polasek, Ozren and Psaty, Bruce M and Raitakari, Olli T and Rice, Kenneth M and Rotter, Jerome I and Sinner, Moritz F and Soliman, Elsayed Z and Spector, Tim D and Strauch, Konstantin and Thorsteinsdottir, Unnur and Tinker, Andrew and Trompet, Stella and Uitterlinden, André and Vaartjes, Ilonca and van der Meer, Peter and Völker, Uwe and Völzke, Henry and Waldenberger, Melanie and Wilson, James G and Xie, Zhijun and Asselbergs, Folkert W and Dörr, Marcus and van Duijn, Cornelia M and Gasparini, Paolo and Gudbjartsson, Daniel F and Gudnason, Vilmundur and Hansen, Torben and Kääb, Stefan and Kanters, Jørgen K and Kooperberg, Charles and Lehtimäki, Terho and Lin, Henry J and Lubitz, Steven A and Mook-Kanamori, Dennis O and Conti, Francesco J and Newton-Cheh, Christopher H and Rosand, Jonathan and Rudan, Igor and Samani, Nilesh J and ...
ISSN 1474-7596, 2018
Background: Genome-wide association studies conducted on QRS duration, an electrocardiographic measurement associated with heart failure and sudden cardiac... 
Gene Expression | Genome-Wide Association Study | Heart Conduction System | Humans | Open Reading Frames | Middle Aged | European Continental Ancestry Group | Male | Gene Expression Profiling | Connexin 43 | Genetic Loci | Whole Exome Sequencing | Exome | Animals | Myocardium | Electrocardiography | Female | ADAMTS Proteins | Mice | Polymorphism, Single Nucleotide | African Continental Ancestry Group
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8. Full Text Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J.Michael and Wilson, Peter WF and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Lin, Wei-Yu and Luan, Jian'an and Mangino, Massimo and Oldmeadow, Christopher and Prins, Bram Peter and Qian, Yong and Sargurupremraj, Muralidharan and Shah, Nabi and Surendran, Praveen and Thériault, Sébastien and Verweij, Niek and Willems, Sara M and Zhao, Jing-Hua and Amouyel, Philippe and Connell, John and de Mutsert, Renée and Doney, Alex SF and Farrall, Martin and Menni, Cristina and Morris, Andrew D and Noordam, Raymond and Paré, Guillaume and Poulter, Neil R and Shields, Denis C and Stanton, Alice and Thom, Simon and Abecasis, Gonçalo and Amin, Najaf and Arking, Dan E and Ayers, Kristin L and Barbieri, Caterina M and Batini, Chiara and Bis, Joshua C and Blake, Tineka and Bochud, Murielle and Boehnke, Michael and Boerwinkle, Eric and Boomsma, Dorret I and Bottinger, Erwin P and Braund, Peter S and Brumat, Marco and Campbell, Archie and Campbell, Harry and Chakravarti, Aravinda and Chambers, John C and Chauhan, Ganesh and Ciullo, Marina and Cocca, Massimiliano and Collins, Francis and Cordell, Heather J and Davies, Gail and de Borst, Martin H and de Geus, Eco J and Deary, Ian J and Deelen, Joris and Del Greco, M Fabiola and Demirkale, Cumhur Yusuf and Dörr, Marcus and Ehret, Georg B and Elosua, Roberto and Enroth, Stefan and Erzurumluoglu, A Mesut and Ferreira, Teresa and Frånberg, Mattias and Franco, Oscar H and Gandin, Ilaria and ...
Nature genetics, ISSN 1061-4036, 10/2018, Volume 50, Issue 10, pp. 1412 - 1425
High blood pressure is a highly heritable and modifiable risk factor for cardiovascular disease. We report the largest genetic association study of blood... 
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9. Full Text Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J Michael and Wilson, Peter W F and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Lin, Wei-Yu and Luan, Jian'an and Mangino, Massimo and Oldmeadow, Christopher and Prins, Bram Peter and Qian, Yong and Sargurupremraj, Muralidharan and Shah, Nabi and Surendran, Praveen and Thériault, Sébastien and Verweij, Niek and Willems, Sara M and Zhao, Jing-Hua and Amouyel, Philippe and Connell, John and de Mutsert, Renée and Doney, Alex S F and Farrall, Martin and Menni, Cristina and Morris, Andrew D and Noordam, Raymond and Paré, Guillaume and Poulter, Neil R and Shields, Denis C and Stanton, Alice and Thom, Simon and Abecasis, Gonçalo and Amin, Najaf and Arking, Dan E and Ayers, Kristin L and Barbieri, Caterina M and Batini, Chiara and Bis, Joshua C and Blake, Tineka and Bochud, Murielle and Boehnke, Michael and Boerwinkle, Eric and Boomsma, Dorret I and Bottinger, Erwin P and Braund, Peter S and Brumat, Marco and Campbell, Archie and Campbell, Harry and Chakravarti, Aravinda and Chambers, John C and Chauhan, Ganesh and Ciullo, Marina and Cocca, Massimiliano and Collins, Francis and Cordell, Heather J and Davies, Gail and de Borst, Martin H and de Geus, Eco J and Deary, Ian J and Deelen, Joris and Del Greco M, Fabiola and Demirkale, Cumhur Yusuf and Dörr, Marcus and Ehret, Georg B and Elosua, Roberto and Enroth, Stefan and Erzurumluoglu, A Mesut and Ferreira, Teresa and Frånberg, Mattias and Franco, Oscar H and Gandin, Ilaria and ... and Million Veteran Program and the Million Veteran Program
Nature genetics, ISSN 1061-4036, 12/2018, Volume 50, Issue 12, pp. 1755 - 1755
In the version of this article originally published, the name of author Martin H. de Borst was coded incorrectly in the XML. The error has now been corrected... 
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10. Full Text Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
by Mahajan, Anubha and Wessel, Jennifer and Willems, Sara M and Zhao, Wei and Robertson, Neil R and Chu, Audrey Y and Gan, Wei and Kitajima, Hidetoshi and Taliun, Daniel and Rayner, N William and Guo, Xiuqing and Lu, Yingchang and Li, Man and Jensen, Richard A and Hu, Yao and Huo, Shaofeng and Lohman, Kurt K and Zhang, Weihua and Cook, James P and Prins, Bram Peter and Flannick, Jason and Grarup, Niels and Trubetskoy, Vassily Vladimirovich and Kravic, Jasmina and Kim, Young Jin and Rybin, Denis V and Yaghootkar, Hanieh and Müller-Nurasyid, Martina and Meidtner, Karina and Li-Gao, Ruifang and Varga, Tibor V and Marten, Jonathan and Li, Jin and Smith, Albert Vernon and An, Ping and Ligthart, Symen and Gustafsson, Stefan and Malerba, Giovanni and Demirkan, Ayse and Tajes, Juan Fernandez and Steinthorsdottir, Valgerdur and Wuttke, Matthias and Lecoeur, Cécile and Preuss, Michael and Bielak, Lawrence F and Graff, Marielisa and Highland, Heather M and Justice, Anne E and Liu, Dajiang J and Marouli, Eirini and Peloso, Gina Marie and Warren, Helen R and ExomeBP Consortium and MAGIC Consortium and GIANT Consortium and Afaq, Saima and Afzal, Shoaib and Ahlqvist, Emma and Almgren, Peter and Amin, Najaf and Bang, Lia B and Bertoni, Alain G and Bombieri, Cristina and Bork-Jensen, Jette and Brandslund, Ivan and Brody, Jennifer A and Burtt, Noël P and Canouil, Mickaël and Chen, Yii-Der Ida and Cho, Yoon Shin and Christensen, Cramer and Eastwood, Sophie V and Eckardt, Kai-Uwe and Fischer, Krista and Gambaro, Giovanni and Giedraitis, Vilmantas and Grove, Megan L and de Haan, Hugoline G and Hackinger, Sophie and Hai, Yang and Han, Sohee and Tybjærg-Hansen, Anne and Hivert, Marie-France and Isomaa, Bo and Jäger, Susanne and Jørgensen, Marit E and Jørgensen, Torben and Käräjämäki, Annemari and Kim, Bong-Jo and Kim, Sung Soo and Koistinen, Heikki A and Kovacs, Peter and Kriebel, Jennifer and Kronenberg, Florian and Läll, Kristi and Lange, Leslie A and Lee, Jung-Jin and Lehne, Benjamin and Li, Huaixing and Lin, Keng-Hung and ... and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 2018, Volume 50, Issue 4, p. 559
Identification of coding variant associations for complex diseases offers a direct route to biological insight, but is dependent on appropriate inference... 
ExomeBP Consortium | MAGIC Consortium | GIANT Consortium | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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11. Full Text Investigating the Causal Relationship of C-Reactive Protein with 32 Complex Somatic and Psychiatric Outcomes: A Large-Scale Cross-Consortium Mendelian Randomization Study
by Prins, Bram. P and Abbasi, Ali and Wong, Anson and Vaez, Ahmad and Nolte, Ilja and Franceschini, Nora and Stuart, Philip E and Gutierrez Achury, Javier and Mistry, Vanisha and Bradfield, Jonathan P and Valdes, Ana M and Bras, Jose and Shatunov, Aleksey and Lu, Chen and Han, Buhm and Raychaudhuri, Soumya and Bevan, Steve and Mayes, Maureen D and Tsoi, Lam C and Evangelou, Evangelos and Nair, Rajan P and Grant, Struan F. A and Polychronakos, Constantin and Radstake, Timothy R. D and van Heel, David A and Dunstan, Melanie L and Wood, Nicholas W and Al-Chalabi, Ammar and Dehghan, Abbas and Hakonarson, Hakon and Markus, Hugh S and Elder, James T and Knight, Jo and Arking, Dan E and Spector, Timothy D and Koeleman, Bobby P. C and van Duijn, Cornelia M and Martin, Javier and Morris, Anew P and Weersma, Rinse K and Wijmenga, Cisca and Munroe, Patricia B and Perry, John R. B and Pouget, Jennie G and Jamshidi, Yalda and Snieder, Harold and Alizadeh, Behrooz Z
PLOS MEDICINE, ISSN 1549-1277, 06/2016, Volume 13, Issue 6
Background C-reactive protein (CRP) is associated with immune, cardiometabolic, and psychiatric traits and diseases. Yet it is inconclusive whether these... 
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12. Full Text Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets
by Wain, LV and Shrine, N and Artigas, MS and Erzurumluoglu, AM and Noyvert, B and Bossini-Castillo, L and Obeidat, M and Henry, AP and Portelli, MA and Hall, RJ and Billington, CK and Rimington, TL and Fenech, AG and John, C and Blake, T and Jackson, VE and Allen, RJ and Prins, Bram Peter and Understanding Society Scientific Group and Campbell, A and Porteous, DJ and Jarvelin, M-R and Wielscher, M and James, AL and Hui, J and Wareham, Nicholas John and Zhao, Jing Hua and Wilson, JF and Joshi, PK and Stubbe, B and Rawal, R and Schulz, H and Imboden, M and Probst-Hensch, NM and Karrasch, S and Gieger, C and Deary, IJ and Harris, SE and Marten, J and Rudan, I and Enroth, S and Gyllensten, U and Kerr, SM and Polasek, O and Kähönen, M and Surakka, I and Vitart, V and Hayward, C and Lehtimäki, T and Raitakari, OT and Evans, DM and Henderson, AJ and Pennell, CE and Wang, CA and Sly, PD and Wan, ES and Busch, R and Hobbs, BD and Litonjua, AA and Sparrow, DW and Gulsvik, A and Bakke, PS and Crapo, JD and Beaty, TH and Hansel, NN and Mathias, RA and Ruczinski, I and Barnes, KC and Bossé, Y and Joubert, P and van den Berge, M and Brandsma, C-A and Paré, PD and Sin, DD and Nickle, DC and Hao, K and Gottesman, O and Dewey, FE and Bruse, SE and Carey, DJ and Kirchner, HL and Geisinger-Regeneron DiscovEHR Collaboration and Jonsson, S and Thorleifsson, G and Jonsdottir, I and Gislason, T and Stefansson, K and Schurmann, C and Nadkarni, G and Bottinger, EP and Loos, RJF and Walters, RG and Chen, Z and Millwood, IY and Vaucher, J and Kurmi, OP and Li, L and Hansell, AL and Brightling, C and Zeggini, E and ...
ISSN 1061-4036, 2017
Chronic obstructive pulmonary disease (COPD) is characterized by reduced lung function and is the third leading cause of death globally. Through genome-wide... 
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13. Full Text Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
by Evangelou, Evangelos and Warren, Helen R and Mosen-Ansorena, David and Mifsud, Borbala and Pazoki, Raha and Gao, He and Ntritsos, Georgios and Dimou, Niki and Cabrera, Claudia P and Karaman, Ibrahim and Ng, Fu Liang and Evangelou, Marina and Witkowska, Katarzyna and Tzanis, Evan and Hellwege, Jacklyn N and Giri, Ayush and Velez Edwards, Digna R and Sun, Yan V and Cho, Kelly and Gaziano, J Michael and Wilson, Peter W F and Tsao, Philip S and Kovesdy, Csaba P and Esko, Tonu and Mägi, Reedik and Milani, Lili and Almgren, Peter and Boutin, Thibaud and Debette, Stéphanie and Ding, Jun and Giulianini, Franco and Holliday, Elizabeth G and Jackson, Anne U and Li-Gao, Ruifang and Lin, Wei-Yu and Luan, Jian'an and Mangino, Massimo and Oldmeadow, Christopher and Prins, Bram Peter and Qian, Yong and Sargurupremraj, Muralidharan and Shah, Nabi and Surendran, Praveen and Thériault, Sébastien and Verweij, Niek and Willems, Sara M and Zhao, Jing-Hua and Amouyel, Philippe and Connell, John and de Mutsert, Renée and Doney, Alex S F and Farrall, Martin and Menni, Cristina and Morris, Andrew D and Noordam, Raymond and Paré, Guillaume and Poulter, Neil R and Shields, Denis C and Stanton, Alice and Thom, Simon and Abecasis, Gonçalo and Amin, Najaf and Arking, Dan E and Ayers, Kristin L and Barbieri, Caterina M and Batini, Chiara and Bis, Joshua C and Blake, Tineka and Bochud, Murielle and Boehnke, Michael and Boerwinkle, Eric and Boomsma, Dorret I and Bottinger, Erwin P and Braund, Peter S and Brumat, Marco and Campbell, Archie and Campbell, Harry and Chakravarti, Aravinda and Chambers, John C and Chauhan, Ganesh and Ciullo, Marina and Cocca, Massimiliano and Collins, Francis and Cordell, Heather J and Davies, Gail and de Borst, Martin H and de Geus, Eco J and Deary, Ian J and Deelen, Joris and Del Greco M, Fabiola and Demirkale, Cumhur Yusuf and Dörr, Marcus and Ehret, Georg B and Elosua, Roberto and Enroth, Stefan and Erzurumluoglu, A Mesut and Ferreira, Teresa and Frånberg, Mattias and Franco, Oscar H and Gandin, Ilaria and ... and Science for Life Laboratory, SciLifeLab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Geriatrik and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi and Institutionen för folkhälso- och vårdvetenskap
Nature Genetics, ISSN 1061-4036, 2018, Volume 50, Issue 10, p. 1412
High blood pressure is a highly heritable and modifiable risk factor for cardiovascular disease. We report the largest genetic association study of blood... 
Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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14. Full Text Fine-mapping of an expanded set of type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps
by Mahajan, Anubha and Taliun, Daniel and Thurner, Matthias and Robertson, Neil R and Torres, Jason M and Rayner, N William and Steinthorsdottir, Valgerdur and Scott, Robert A and Grarup, Niels and Cook, James P and Schmidt, Ellen M and Wuttke, Matthias and Sarnowski, Chloé and Mägi, Reedik and Nano, Jana and Gieger, Christian and Trompet, Stella and Lecoeur, Cécile and Preuss, Michael and Prins, Bram Peter and Guo, Xiuqing and Bielak, Lawrence F and and Bennett, Amanda J and Bork-Jensen, Jette and Brummett, Chad M and Canouil, Mickaël and Eckardt, Kai-Uwe and Fischer, Krista and Kardia, Sharon LR and Kronenberg, Florian and Läll, Kristi and Liu, Ching-Ti and Locke, Adam E and Luan, Jian'an and Ntalla, Ioanna and Nylander, Vibe and Schönherr, Sebastian and Schurmann, Claudia and Yengo, Loïc and Bottinger, Erwin P and Brandslund, Ivan and Christensen, Cramer and Dedoussis, George and Florez, Jose C and ford, Ian and Franco, Oscar H and Frayling, Timothy M and Giedraitis, Vilmantas and Hackinger, Sophie and Hattersley, Andrew T and Herder, Christian and Ikram, M Arfan and Ingelsson, Martin and Jørgensen, Marit E and Jørgensen, Torben and Kriebel, Jennifer and Kuusisto, Johanna and Ligthart, Symen and Lindgren, Cecilia M and Linneberg, Allan and Lyssenko, Valeriya and Mamakou, Vasiliki and Meitinger, Thomas and Mohlke, Karen L and Morris, Andrew D and Nadkarni, Girish and Pankow, James S and Peters, Annette and Sattar, Naveed and Stančáková, Alena and Strauch, Konstantin and Taylor, Kent D and Thorand, Barbara and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and Tuomilehto, Jaakko and Witte, Daniel R and Dupuis, Josée and Peyser, Patricia A and Zeggini, Eleftheria and Loos, Ruth J F and Froguel, Philippe and Ingelsson, Erik and Lind, Lars and Groop, Leif and Laakso, Markku and Collins, Francis S and Jukema, J Wouter and Palmer, Colin N A and Grallert, Harald and Metspalu, Andres and Dehghan, Abbas and Köttgen, Anna and Abecasis, Goncalo and Meigs, James B and Rotter, Jerome I and Marchini, Jonathan and Pedersen, Oluf and Hansen, Torben and ...
Nature genetics, ISSN 1061-4036, 11/2018, Volume 50, Issue 11, pp. 1505 - 1513
We aggregated genome-wide genotyping data from 32 European-descent GWAS (74,124 T2D cases, 824,006 controls) imputed to high-density reference panels of... 
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