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1. Full Text Prediction of ankylosing spondylitis in the population-based HUNT study by a genetic risk score combining 110 SNPs of genome-wide significance
by Rostami, Sina and Hoff, Mari and Brown, Matthew A and Hveem, Kristian and Holmen, Oddgeir L and Fritsche, Lars G and Videm, Vibeke
The Journal of rheumatology, ISSN 0315-162X, 04/2019
The genetic component of ankylosing spondylitis (AS) development is ~90%. Of the known heritability, ~20% is explained by HLA-B27, and 113 identified... 
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2. Full Text Prediction of Ankylosing Spondylitis in the HUNT Study by a Genetic Risk Score Combining 110 Single-nucleotide Polymorphisms of Genome-wide Significance
by Rostami, Sina and Hoff, Mari and Brown, Matthew A and Hveem, Kristian and Holmen, Oddgeir L and Fritsche, Lars G and Videm, Vibeke
The Journal of Rheumatology, ISSN 0315-162X, 04/2019, p. jrheum.181209
Objective The genetic component of ankylosing spondylitis (AS) development is ~90%. Of the known heritability, ~20% is explained by HLA-B27, and 113 identified... 
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3. Full Text A reference panel of 64,976 haplotypes for genotype imputation
by McCarthy, Shane and Das, Sayantan and Kretzschmar, Warren and Delaneau, Olivier and Wood, Anew R and Teumer, Alexander and Kang, Hyun Min and Fuchsberger, Christian and Danecek, Petr and Sharp, Kevin and Luo, Yang and Sidorel, Carlo and Kwong, Alan and Timpson, Nicholas and Koskinen, Seppo and Vrieze, Scott and Scott, Laura J and Zhang, He and Mahajan, Anubha and Veldink, Jan and Peters, Ulrike and Pato, Carlos and van Duijn, Cornelia M and Gillies, Christopher E and Gandin, Ilaria and Mezzavilla, Massimo and Gilly, Arthur and Cocca, Massimiliano and Traglia, Michela and Angius, Anea and Barrett, Jeffrey C and Boomsma, Dorrett and Branham, Kari and Breen, Gerome and Brummett, Chad M and Busonero, Fabio and Campbell, Harry and Chan, Anew and Che, Sai and Chew, Emily and Collins, Francis S and Corbin, Laura J and Smith, George Davey and Dedoussis, George and Dorr, Marcus and Farmaki, Aliki-Eleni and Ferrucci, Luigi and Forer, Lukas and Fraser, Ross M and Gabriel, Stacey and Levy, Shawn and Groop, Leif and Harrison, Tabitha and Hattersley, Anew and Holmen, Oddgeir L and Hveem, Kristian and Kretzler, Matthias and Lee, James C and McGue, Matt and Meitinger, Thomas and Melzer, David and Min, Josine L and Mohlke, Karen L and Vincent, John B and Nauck, Matthias and Nickerson, Deborah and Palotie, Aarno and Pato, Michele and Pirastu, Nicola and McInnis, Melvin and Richards, J. Brent and Sala, Cinzia and Salomaa, Veikko and Schlessinger, David and Schoenherr, Sebastian and Slagboom, P. Eline and Small, Kerrin and Spector, Timothy and Stambolian, Dwight and Tuke, Marcus and Tuomilehto, Jaakko and van den Berg, Leonard H and Van Rheenen, Wouter and Volker, Uwe and Wijmenga, Cisca and Toniolo, Daniela and Zeggini, Eleftheria and Gasparini, Paolo and Sampson, Matthew G and Wilson, James F and Frayling, Timothy and de Bakker, Paul I. W and Swertz, Morris A and McCarroll, Steven and Kooperberg, Charles and Dekker, Annelot and Altshuler, David and Willer, Cristen and Iacono, William and Ripatti, Samuli and ... and the Haplotype Reference Consortium and Genomik, diabetes och endokrinologi and Lund University and Genomics, Diabetes and Endocrinology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1279 - 1283
We describe a reference panel of 64,976 human haplotypes at 39,235,157 SNPs constructed using whole-genome sequence data from 20 studies of predominantly... 
Studies | Datasets | Haplotypes | Consortia | Accuracy | Genealogy | Researchers | Genomics | Collaboration | Genomes | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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4. Full Text Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
by Crosby, Jacy and Peloso, Gina M and Auer, Paul L and Crosslin, David R and Stitziel, Nathan O and Lange, Leslie A and Lu, Yingchang and Tang, Zheng-Zheng and Zhang, He and Hindy, George and Masca, Nicholas and Stirrups, Kathleen and Kanoni, Stavroula and Do, Ron and Jun, Goo and Hu, Youna and Kang, Hyun Min and Xue, Chenyi and Goel, Anuj and Farrall, Martin and Duga, Stefano and Merlini, Pier Angelica and Asselta, Rosanna and Girelli, Domenico and Olivieri, Oliviero and Martinelli, Nicola and Yin, Wu and Reilly, Dermot and Speliotes, Elizabeth and Fox, Caroline S and Hveem, Kristian and Holmen, Oddgeir L and Nikpay, Majid and Farlow, Deborah N and Assimes, Themistocles L and Franceschini, Nora and Robinson, Jennifer and North, Kari E and Martin, Lisa W and DePristo, Mark and Gupta, Namrata and Escher, Stefan A and Jansson, Jan-Håkan and Van Zuydam, Natalie and Palmer, Colin N. A and Wareham, Nicholas and Koch, Werner and Meitinger, Thomas and Peters, Annette and Lieb, Wolfgang and Erbel, Raimund and Konig, Inke R and Kruppa, Jochen and Degenhardt, Franziska and Gottesman, Omri and Bottinger, Erwin P and O'Donnell, Christopher J and Psaty, Bruce M and Ballantyne, Christie M and Abecasis, Goncalo and Ordovas, Jose M and Melander, Olle and Watkins, Hugh and Orho-Melander, Marju and Ardissino, Diego and Loos, Ruth J. F and McPherson, Ruth and Willer, Cristen J and Erdmann, Jeanette and Hall, Alistair S and Samani, Nilesh J and Deloukas, Panos and Schunkert, Heribert and Wilson, James G and Kooperberg, Charles and Rich, Stephen S and Tracy, Russell P and Lin, Dan-Yu and Altshuler, David and Gabriel, Stacey and Nickerson, Deborah A and Jarvik, Gail P and Cupples, L. Adrienne and Reiner, Alex P and Boerwinkle, Eric and Kathiresan, Sekar and The TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Natl Heart Lung Blood Inst and Exome Sequencing Project and TG and HDL Working Group of the Exome Sequencing Project, National Heart, Lung, and Blood Institute and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 07/2014, Volume 371, Issue 1, pp. 22 - 31
Whole-exome sequencing revealed an association between four rare loss-of-function mutations in the apoliprotein C3 gene ( APOC3 ) and low plasma triglyceride... 
APOLIPOPROTEIN C-III | RICH LIPOPROTEINS | MEDICINE, GENERAL & INTERNAL | DESIGN | ASSOCIATIONS | INHIBITION | RARE VARIANTS | CARDIOVASCULAR-DISEASE | PCSK9 | CAPTURE | PLASMA TRIGLYCERIDES | Coronary Disease - blood | European Continental Ancestry Group - genetics | Liver - pathology | Humans | Risk Factors | Apolipoprotein C-III - blood | Genotype | Apolipoprotein C-III - genetics | Sequence Analysis, DNA | Exome | Coronary Disease - genetics | Triglycerides - blood | Heterozygote | African Continental Ancestry Group - genetics | Mutation | Usage | Phenotype | Analysis and chemistry | Gene mutations | Analysis | Nucleotide sequencing | Research | Coronary heart disease | Risk factors | Blood | DNA sequencing | Phenotypes | Missense mutation | Nonsense mutation | Genes | Cardiovascular disease | Triglycerides | Genomes | Apolipoproteins | Heart diseases | Coronary artery disease | Medical and Health Sciences | Medicin och hälsovetenskap
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5. Full Text Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
by Morris, Andrew P and Voight, Benjamin F and Teslovich, Tanya M and Ferreira, Teresa and Segrè, Ayellet V and Steinthorsdottir, Valgerdur and Strawbridge, Rona J and Khan, Hassan and Grallert, Harald and Mahajan, Anubha and Prokopenko, Inga and Kang, Hyun Min and Dina, Christian and Esko, Tonu and Fraser, Ross M and Kanoni, Stavroula and Kumar, Ashish and Lagou, Vasiliki and Langenberg, Claudia and Luan, Jian'An and Lindgren, Cecilia M and Müller-Nurasyid, Martina and Pechlivanis, Sonali and Rayner, N. William and Scott, Laura J and Wiltshire, Steven and Yengo, Loic and Kinnunen, Leena and Rossin, Elizabeth J and Raychaudhuri, Soumya and Johnson, Andrew D and Dimas, Antigone S and Loos, Ruth J.F and Vedantam, Sailaja and Chen, Han and Florez, Jose C and Fox, Caroline and Liu, Ching-Ti and Rybin, Denis and Couper, David J and Kao, Wen Hong L and Li, Man and Cornelis, Marilyn C and Kraft, Peter and Sun, Qi and Van Dam, Rob M and Stringham, Heather M and Chines, Peter S and Fischer, Krista and Fontanillas, Pierre and Holmen, Oddgeir L and Hunt, Sarah E and Jackson, Anne U and Kong, Augustine and Lawrence, Robert and Meyer, Julia and Perry, John R.B and Platou, Carl G.P and Potter, Simon and Rehnberg, Emil and Robertson, Neil and Sivapalaratnam, Suthesh and Stančáková, Alena and Stirrups, Kathleen and Thorleifsson, Gudmar and Tikkanen, Emmi and Wood, Andrew R and Almgren, Peter and Atalay, Mustafa and Benediktsson, Rafn and Bonnycastle, Lori L and Burtt, Noël and Carey, Jason and Charpentier, Guillaume and Crenshaw, Andrew T and Doney, Alex S.F and Dorkhan, Mozhgan and Edkins, Sarah and Emilsson, Valur and Eury, Elodie and Forsen, Tom and Gertow, Karl and Gigante, Bruna and Grant, George B and Groves, Christopher J and Guiducci, Candace and Herder, Christian and Hreidarsson, Astradur B and Hui, Jennie and James, Alan and Jonsson, Anna and Rathmann, Wolfgang and Klopp, Norman and Kravic, Jasmina and Krjutškov, Kaarel and Langford, Cordelia and Leander, Karin and Lindholm, Eero and Lobbens, Stéphane and MäNnistö, Satu and ... and Meta-Anal Glucose Insulin-Related and Genetic Invest ANthropometric and Wellcome Trust Case Control and Asian Genetic Epidemiology and S Asian Type 2 Diabet SAT2D and DIAbet Genetics Replication and the DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and Genomics, Diabetes and Endocrinology and Internmedicin - epidemiologi and EpiHealth: Epidemiology for Health and Genomik, diabetes och endokrinologi and Internal Medicine - Epidemiology and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 9, pp. 981 - 990
To extend understanding of the genetic architecture and molecular basis of type 2 diabetes (T2D), we conducted a meta-analysis of genetic variants on the... 
INDIVIDUALS | MC4R | COMMON VARIANTS | METAANALYSIS | REPLICATION | GLUCOSE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | RISK | EXPRESSION | GENOME-WIDE ASSOCIATION | Type 2 diabetes | Physiological aspects | Development and progression | Genetic aspects | Kardiologi | Clinical Medicine | Other Clinical Medicine | Cardiac and Cardiovascular Systems | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Annan klinisk medicin | Klinisk medicin | Endocrinology and Diabetes
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6. Full Text Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk
by Holmen, Oddgeir L and Zhang, He and Fan, Yanbo and Hovelson, Daniel H and Schmidt, Ellen M and Zhou, Wei and Guo, Yanhong and Zhang, Ji and Langhammer, Arnulf and Løchen, Maja-Lisa and Ganesh, Santhi K and Vatten, Lars and Skorpen, Frank and Dalen, Håvard and Zhang, Jifeng and Pennathur, Subramaniam and Chen, Jin and Platou, Carl and Mathiesen, Ellisiv B and Wilsgaard, Tom and Njølstad, Inger and Boehnke, Michael and Chen, Y Eugene and Abecasis, Gonçalo R and Hveem, Kristian and Willer, Cristen J
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 4, pp. 345 - 351
Blood lipid levels are heritable, treatable risk factors for cardiovascular disease. We systematically assessed genome-wide coding variation to identify new... 
COHORT PROFILE | DENSITY-LIPOPROTEIN CHOLESTEROL | HEART-DISEASE | RARE VARIANTS | GENETICS & HEREDITY | MISSING HERITABILITY | LOCI | ASSOCIATION | MAP | CORONARY-ARTERY-DISEASE | Myocardial Infarction - genetics | Genome-Wide Association Study | Lipids - genetics | Myocardial Infarction - epidemiology | Membrane Proteins - genetics | Humans | Mice, Inbred C57BL | Risk Factors | Genotype | Mutation, Missense - genetics | Gene Knockdown Techniques | Genetic Variation | Cholesterol, LDL - genetics | Exome - genetics | Animals | Lipids - blood | Norway - epidemiology | Cholesterol, LDL - blood | Mice | Genes | Physiological aspects | Genetic aspects | Blood lipids | Identification and classification | Health aspects | Heart attack | Risk factors | Cholesterol | Studies | Heart | Cardiovascular disease | Lipids | Genomes | Experiments | Epidemiology
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7. Full Text Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
by Mahajan, Anubha and Go, Min Jin and Zhang, Weihua and Below, Jennifer E and Gaulton, Kyle J and Ferreira, Teresa and Horikoshi, Momoko and Johnson, Anew D and Ng, Maggie C. Y and Prokopenko, Inga and Saleheen, Danish and Wang, Xu and Zeggini, Eleftheria and Abecasis, Goncalo R and Adair, Linda S and Almgren, Peter and Atalay, Mustafa and Aung, Tin and Baldassarre, Damiano and Balkau, Beverley and Bao, Yuqian and Barnett, Anthony H and Barroso, Ines and Basit, Abdul and Been, Latonya F and Beilby, John and Bell, Graeme I and Benediktsson, Rafn and Bergman, Richard N and Boehm, Bernhard O and Boerwinkle, Eric and Bonnycastle, Lori L and Burtt, Noël and Cai, Qiuyin and Campbell, Harry and Carey, Jason and Cauchi, Stephane and Caulfield, Mark and Chan, Juliana C. N and Chang, Li-Ching and Chang, Tien-Jyun and Chang, Yi-Cheng and Charpentier, Guillaume and Chen, Chien-Hsiun and Chen, Han and Chen, Yuan-Tsong and Chia, Kee-Seng and Chidambaram, Manickam and Chines, Peter S and Cho, Nam H and Cho, Young Min and Chuang, Lee-Ming and Collins, Francis S and Cornelis, Marilyn C and Couper, David J and Crenshaw, Anew T and van Dam, Rob M and Danesh, John and Das, Debashish and de Faire, Ulf and Dedoussis, George and Deloukas, Panos and Dimas, Antigone S and Dina, Christian and Doney, Alex S. F and Donnelly, Peter J and Dorkhan, Mozhgan and van Duijn, Cornelia and Dupuis, Josée and Edkins, Sarah and Elliott, Paul and Emilsson, Valur and Erbel, Raimund and Eriksson, Johan G and Escobedo, Jorge and Esko, Tonu and Eury, Elodie and Florez, Jose C and Fontanillas, Pierre and Forouhi, Nita G and Forsen, Tom and Fox, Caroline and Fraser, Ross M and Frayling, Timothy M and Froguel, Philippe and Frossard, Philippe and Gao, Yutang and Gertow, Karl and Gieger, Christian and Gigante, Bruna and Grallert, Harald and Grant, George B and Groop, Leif C and Groves, Christopher J and Grundberg, Elin and Guiducci, Candace and Hamsten, Anders and Han, Bok-Ghee and Hara, Kazuo and Hassanali, Neelam and ... and South Asian Type Diabet SAT2D Cons and DIAbet Genetics Replication & Meta and Mexican Amer Type 2 Diabet MAT2D C and Asian Genetic Epidemiology Network and Type 2 Diabet Genetic Exploration and South Asian Type 2 Diabetes (SAT2D) Consortium and Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Mexican American Type 2 Diabetes (MAT2D) Consortium and Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 3, pp. 234 - 244
To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies... 
INDIVIDUALS | GLUCOSE-HOMEOSTASIS | IMPUTATION | VARIANTS | CHROMATIN | GENETICS & HEREDITY | POPULATIONS | TRANSETHNIC METAANALYSIS | LOCI | SCALE ASSOCIATION ANALYSIS | MAP | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Hispanic Americans - genetics | Diabetes Mellitus, Type 2 - genetics | Humans | Risk Factors | Alleles | Asian Continental Ancestry Group - genetics | Polymorphism, Single Nucleotide | Case-Control Studies | Type 2 diabetes | Genetic research | Genetic aspects | Research | Genetic susceptibility | Immigration | Genomes | Genealogy | Diabetes | Architecture | Meta-analysis | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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8. Full Text Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease
by Stitziel, Nathan O and Stirrups, Kathleen E and Masca, Nicholas G. D and Erdmann, Jeanette and Ferrario, Paola G and König, Inke R and Weeke, Peter E and Webb, Thomas R and Auer, Paul L and Schick, Ursula M and Lu, Yingchang and Zhang, He and Dube, Marie-Pierre and Goel, Anuj and Farrall, Martin and Peloso, Gina M and Won, Hong-Hee and Do, Ron and van Iperen, Erik and Kanoni, Stavroula and Kruppa, Jochen and Mahajan, Anubha and Scott, Robert A and Willenborg, Christina and Braund, Peter S and van Capelleveen, Julian C and Doney, Alex S. F and Donnelly, Louise A and Asselta, Rosanna and Merlini, Piera A and Duga, Stefano and Marziliano, Nicola and Denny, Josh C and Shaffer, Christian M and El-Mokhtari, Nour Eddine and Franke, Ane and Gottesman, Omri and Heilmann, Stefanie and Hengstenberg, Christian and Hoffmann, Per and Holmen, Oddgeir L and Hveem, Kristian and Jansson, Jan-Håkan and Jöckel, Karl-Heinz and Kessler, Thorsten and Kriebel, Jennifer and Laugwitz, Karl L and Marouli, Eirini and Martinelli, Nicola and McCarthy, Mark I and van Zuydam, Natalie R and Meisinger, Christa and Esko, Tõnu and Mihailov, Evelin and Escher, Stefan A and Alver, Maris and Moebus, Susanne and Morris, Anew D and Müller-Nurasyid, Martina and Nikpay, Majid and Olivieri, Oliviero and Perreault, Louis-Philippe Lemieux and AlQarawi, Alaa and Robertson, Neil R and Akinsanya, Karen O and Reilly, Dermot F and Vogt, Thomas F and Yin, Wu and Asselbergs, Folkert W and Kooperberg, Charles and Jackson, Rebecca D and Stahl, Eli and Strauch, Konstantin and Varga, Tibor V and Waldenberger, Melanie and Zeng, Lingyao and Kraja, Aldi T and Liu, Chunyu and Ehret, Georg B and Newton-Cheh, Christopher and Chasman, Daniel I and Chowdhury, Rajiv and Ferrario, Marco and Ford, Ian and Jukema, J. Wouter and Kee, Frank and Kuulasmaa, Kari and Nordestgaard, Børge G and Perola, Markus and Saleheen, Danish and Sattar, Naveed and Surenan, Praveen and Tregouet, David and Young, Robin and Howson, Joanna M. M and Butterworth, Adam S and Danesh, John and Ardissino, Diego and Bottinger, Erwin P and Erbel, Raimund and ... and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia Investigators and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Umeå universitet and Medicin
The New England Journal of Medicine, ISSN 0028-4793, 03/2016, Volume 374, Issue 12, pp. 1134 - 1144
Searching for genes in which loss-of-function mutations confer protection against disease is a strategy to identity drug targets. This study reports an... 
MEDICINE, GENERAL & INTERNAL | PCSK9 | INHIBITION | MUTATIONS | LIPOPROTEIN-LIPASE | VARIANT | Cell Adhesion Molecules - genetics | Lipoprotein Lipase - antagonists & inhibitors | Lipoprotein Lipase - genetics | Humans | Middle Aged | Risk Factors | Male | Mutation, Missense | Genotyping Techniques | Sequence Analysis, DNA | Angiopoietin-like 4 Protein | Coronary Artery Disease - genetics | Triglycerides - blood | Female | Aged | Mutation | Triglycerides - genetics | Angiopoietins - genetics | Lipoprotein Lipase - metabolism | Genotype | Care and treatment | Research | Nucleotide sequence | Coronary heart disease | Myocardial infarction | Angiopoietin | Therapeutic applications | Genes | Coronary artery | Cardiovascular disease | Triglycerides | Lipoprotein lipase | Lipase | Cholesterol | Studies | Genotyping | Gene frequency | Coronary vessels | Alleles | Heart diseases | DNA sequencing | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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9. Full Text Meta-analysis of gene-level tests for rare variant association
by Liu, Dajiang J and Peloso, Gina M and Zhan, Xiaowei and Holmen, Oddgeir L and Zawistowski, Matthew and Feng, Shuang and Nikpay, Majid and Auer, Paul L and Goel, Anuj and Zhang, He and Peters, Ulrike and Farrall, Martin and Orho-Melander, Marju and Kooperberg, Charles and Mcpherson, Ruth and Watkins, Hugh and Willer, Cristen J and Hveem, Kristian and Melander, Olle and Kathiresan, Sekar and Abecasis, Gonçalo R and Diabetes - Cardiovascular Disease and Diabetes - kardiovaskulär sjukdom and Kardiovaskulär forskning - hypertoni and Cardiovascular Research - Hypertension and Lund University and EpiHealth: Epidemiology for Health and Lunds universitet and EXODIAB: Excellence in Diabetes Research in Sweden
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 2, pp. 200 - 204
The majority of reported complex disease associations for common genetic variants have been identified through metaanalysis, a powerful approach that enables... 
POLYMORPHISMS | DEEP | STATISTICS | SEQUENCE | DISEASE | GENETICS & HEREDITY | FRAMEWORK | MODEL | COMPLEX TRAITS | DISCOVERY | STRATEGIES | Physiological aspects | Genetic aspects | Blood lipids | Research | Genetic variation | Studies | Heart | Medical research | Genes | Population | Software | Genomes | Grants | Cholesterol | Methods | Meta-analysis | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Endokrinologi och diabetes | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Endocrinology and Diabetes
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