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by Peloso, Gina M and Auer, Paul L and Bis, Joshua C and Voorman, Arend and Morrison, Alanna C and Stitziel, Nathan O and Brody, Jennifer A and Khetarpal, Sumeet A and Crosby, Jacy R and Fornage, Myriam and Isaacs, Aaron and Jakobsdottir, Johanna and Feitosa, Mary F and Davies, Gail and Huffman, Jennifer E and Manichaikul, Ani and Davis, Brian and Lohman, Kurt and Joon, Aron Y and Smith, Albert V and Grove, Megan L and Zanoni, Paolo and Redon, Valeska and Demissie, Serkalem and Lawson, Kim and Peters, Ulrike and Carlson, Christopher and Jackson, Rebecca D and Ryckman, Kelli K and Mackey, Rachel H and Robinson, Jennifer G and Siscovick, David S and Schreiner, Pamela J and Mychaleckyj, Josyf C and Pankow, James S and Hofman, Albert and Uitterlinden, Andre G and Harris, Tamara B and Taylor, Herman A and Taylor, Kent D and Stafford, Jeanette M and Reynolds, Lindsay M and Marioni, Riccardo E and Dehghan, Abbas and Franco, Oscar H and Patel, Aniruddh P and Lu, Yingchang and Hindy, George and Gottesman, Omri and Bottinger, Erwin P and Melander, Olle and Orho-Melander, Marju and Loos, Ruth J.F and Duga, Stefano and Merlini, Piera Angelica and Farrall, Martin and Goel, Anuj and Asselta, Rosanna and Girelli, Domenico and Martinelli, Nicola and Shah, Svati H and Kraus, William E and Li, Mingyao and Rader, Daniel J and Reilly, Muredach P and McPherson, Ruth and Watkins, Hugh and Ardissino, Diego and Zhang, Qunyuan and Wang, Judy and Tsai, Michael Y and Correa, Adolfo and Griswold, Michael E and Lange, Leslie A and Starr, John M and Rudan, Igor and Eiriksdottir, Gudny and Launer, Lenore J and Ordovas, Jose M and Levy, Daniel and Chen, Y.-D. Ida and Reiner, Alexander P and Hayward, Caroline and Polasek, Ozren and Deary, Ian J and Borecki, Ingrid B and Liu, Yongmei and Gudnason, Vilmundur and Wilson, James G and van Duijn, Cornelia M and Kooperberg, Charles and Rich, Stephen S and Psaty, Bruce M and Rotter, Jerome I and O’Donnell, Christopher J and Rice, Kenneth and Boerwinkle, Eric and Kathiresan, Sekar and Cupples, L. Adrienne and NHLBI GO Exome Sequencing Project 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
The American Journal of Human Genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 223 - 232
Low-frequency coding DNA sequence variants in the proprotein convertase subtilisin/kexin type 9 gene ( ) lower plasma low-density lipoprotein cholesterol... 
DENSITY-LIPOPROTEIN CHOLESTEROL | FACTOR ACETYLHYDROLASES | PROTEIN | LDL | GENETICS & HEREDITY | PCSK9 | PLATELET-ACTIVATING-FACTOR | TRAITS | Genetic Code | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | Middle Aged | Male | Genetic Variation | 1-Alkyl-2-acetylglycerophosphocholine Esterase - genetics | Adult | Cholesterol, LDL - blood | Female | Subtilisins - metabolism | African Continental Ancestry Group - genetics | Coronary Disease - blood | European Continental Ancestry Group - genetics | Genetic Association Studies | Gene Frequency | Mice, Inbred C57BL | Linear Models | Cholesterol, HDL - genetics | Sequence Analysis, DNA | 1-Alkyl-2-acetylglycerophosphocholine Esterase - metabolism | Cholesterol, LDL - genetics | Phenotype | Animals | Coronary Disease - genetics | Alleles | Triglycerides - blood | Cholesterol, HDL - blood | Subtilisins - genetics | Aged | Mice | Cohort Studies | Genetic code | Genetic variation | Physiological aspects | Genetic research | Genetic aspects | Research | Coronary heart disease | Population genetics | Lipids | Cardiovascular disease | Low density lipoprotein | Risk assessment | Deoxyribonucleic acid--DNA | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
JACC (Journal of the American College of Cardiology), ISSN 0735-1097, 2016, Volume 67, Issue 22, pp. 2578 - 2589
Abstract Background Approximately 7% of American adults have severe hypercholesterolemia (untreated low-density lipoprotein [LDL] cholesterol ≥190 mg/dl),... 
Cardiovascular | Internal Medicine | coronary artery disease | gene sequencing | genetics | low-density lipoprotein cholesterol | POPULATION | CARDIAC & CARDIOVASCULAR SYSTEMS | METAANALYSIS | MYOCARDIAL-INFARCTION | RANDOMIZED-TRIALS | AUTOSOMAL-DOMINANT HYPERCHOLESTEROLEMIA | RISK | MUTATION DETECTION RATE | CORONARY-HEART-DISEASE | ASSOCIATION | PARTICIPANTS | Receptors, LDL - genetics | Humans | Middle Aged | Hyperlipoproteinemia Type II - diagnosis | Male | Proprotein Convertase 9 - genetics | Apolipoprotein B-100 - genetics | Case-Control Studies | Genetic Variation | Cholesterol, LDL - blood | Female | Heterozygote | Coronary Artery Disease - epidemiology | Sequence Analysis | Cohort Studies | Hypercholesterolemia - epidemiology | Hyperlipoproteinemia Type II - genetics | Medical colleges | Care and treatment | Low density lipoproteins | Genes | Coronary heart disease | Population genetics | Epidemiology | Blood | Hypercholesterolemia | Analysis and chemistry | Atherosclerosis | Genetic research | Genetic aspects | Diagnosis | Research institutes | Cardiology | Trans fatty acids | Heart attacks | Cardiovascular disease | Lipids | Apolipoproteins | Low density lipoprotein | Cholesterol | Proteins | Studies | Confidence intervals | Consortia | Algorithms | Coronary vessels | Population | Mutation | Deoxyribonucleic acid--DNA | Index Medicus | Abridged Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 01/2010, Volume 42, Issue 1, pp. 45 - 52
Journal Article
by Liang, Jingjing and Le, Thu H and Edwards, Digna R. Velez and Tayo, Bamidele O and Gaulton, Kyle J and Smith, Jennifer A and Lu, Yingchang and Jensen, Richard A and Chen, Guanjie and Yanek, Lisa R and Schwander, Karen and Tajuddin, Salman M and Sofer, Tamar and Kim, Wonji and Kayima, James and McKenzie, Colin A and Fox, Ervin and Nalls, Michael A and Young, J. Hunter and Sun, Yan V and Lane, Jacqueline M and Cechova, Sylvia and Zhou, Jie and Tang, Hua and Fornage, Myriam and Musani, Solomon K and Wang, Heming and Lee, Juyoung and Adeyemo, Adebowale and Dreisbach, Albert W and Forrester, Terrence and Chu, Pei-Lun and Cappola, Anne and Evans, Michele K and Morrison, Alanna C and Martin, Lisa W and Wiggins, Kerri L and Hui, Qin and Zhao, Wei and Jackson, Rebecca D and Ware, Erin B and Faul, Jessica D and Reiner, Alex P and Bray, Michael and Denny, Joshua C and Mosley, Thomas H and Palmas, Walter and Guo, Xiuqing and Papanicolaou, George J and Penman, Alan D and Polak, Joseph F and Rice, Kenneth and Taylor, Ken D and Boerwinkle, Eric and Bottinger, Erwin P and Liu, Kiang and Risch, Neil and Hunt, Steven C and Kooperberg, Charles and Zonderman, Alan B and Laurie, Cathy C and Becker, Diane M and Cai, Jianwen and Loos, Ruth J. F and Psaty, Bruce M and Weir, David R and Kardia, Sharon L. R and Arnett, Donna K and Won, Sungho and Edwards, Todd L and Redline, Susan and Cooper, Richard S and Rao, D.C and Rotter, Jerome I and Rotimi, Charles and Levy, Daniel and Chakravarti, Aravinda and Zhu, Xiaofeng and Franceschini, Nora
PLoS Genetics, ISSN 1553-7390, 05/2017, Volume 13, Issue 5, pp. e1006728 - e1006728
Journal Article
by Wain, Louise and Verwoert, Germaine and O'Reilly, Paul and Shi, Gang and Johnson, Toby and Bochud, Murielle and Rice, Kenneth and Henneman, Peter and Smith, Albert Vernon and Ehret, Georg and Amin, Najaf and Larson, Martin and Mooser, Vincent and Hadley, David and Dörr, Marcus and Bis, Joshua and Aspelund, Thor and Esko, Tõnu and Janssens, Cécile and Zhao, Jing Hua and Heath, Simon and Laan, Maris and Fu, Jingyuan and Pistis, Giorgio and Luan, J and Lucas, Gavin and Pirastu, Nicola and Pichler, Irene and Jackson, Anne and Webster, Rebecca J and Zhang, F.F and Peden, John and Schmidt, Reinhold and Tanaka, Toshiko and Campbell, Harry and Igl, Wilmar and Milaneschi, Yuri and Hottenga, Jouke Jan and Vitart, Veronique and Chasman, Daniel and Trompet, Stella and Bragg-Gresham, Jennifer L and Alizadeh, Behrooz and Chambers, John and Guo, Xiuqing and Lehtimäki, Terho and Kuhnel, Brigitte and Lopez, L.M and Polasek, Ozren and Boban, Mladen and Nelson, Christopher P and Morrison, Alanna and Pihur, Vasyl and Ganesh, Santhi and Hofman, Albert and Kundu, Suman and Mattace Raso, Francesco and Rivadeneira Ramirez, Fernando and Sijbrands, Eric and Uitterlinden, Ané and Hwang, S.J and Vasan, Ramachanan Srini and Wang, Ying and Bergmann, Sven and Vollenweider, Peter and Waeber, Gérard and Laitinen, Jaana and Pouta, Anneli and Zitting, Paavo and McArdle, Wendy and Kroemer, Heyo and Völker, Uwe and Völzke, Henry and Glazer, Nicole and Taylor, Kent and Harris, Tamara and Alavere, Helene and Haller, Toomas and Keis, Aime and Tammesoo, M.L and Aulchenko, Yurii and Khaw, Kay-Tee and Galan, Pilar and Hercberg, Serge and Lathrop, Mark and Eyheramendy, Susana and Org, Elin and Sõber, Siim and Lu, Xiaowen and Nolte, Ilja and Penninx, Brenda and Corre, Tanguy and Masciullo, Corrado and Sala, Cinzia and Groop, Leif and Voight, Benjamin and Melander, Olle and O'Donnell, Christopher and Salomaa, Veikko and Adamo, Pio and ... and CHARGE Consortium Heart Failure and Cardiogenics Consortium and AortaGen Consortium and LifeLines Cohort Study and EchoGen Consortium and KidneyGen Consortium and CKDGen Consortium and CardioGram and Cardiogenics consortium and KidneyGen consortium and CHARGE Consortium Heart Failure Working Group and EchoGen consortium and CKDGen consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 10/2011, Volume 43, Issue 10, pp. 1005 - 1012
Journal Article
by Liu, C and Kraja, Aldi and Smith, Jennifer A and Brody, Jennifer and Franceschini, Nora and Bis, Joshua and Rice, Kenneth and Morrison, Alanna and Lu, Yingchang and Weiss, S and Guo, Xiuqing and Palmas, Walter and Martin, Lisa and Chen, Y and Surenan, P and nos, Fotios and Cook, J.P and Auer, Paul and Chu, Auey and Giri, A and Zhao, W and Jakobsdottir, Margret and Lin, L.-A and Stafford, Jeanette M and Amin, Najaf and Mei, H and Yao, Jiefen and Voorman, Jeanine and Larson, Martin and Grove, Megan and Smith, Albert Vernon and Hwang, S.J and Chen, Han and Huan, Tianxiao and Kosova, G and Stitziel, Nathan and Kathiresan, Sekar and Samani, Nilesh and Schunkert, Heribert and Deloukas, Panagiotis and Li, Man and Fuchsberger, Christian and Pattaro, Cristian and Gorski, Mathias and Kooperberg, Charles and Papanicolaou, George and Rossouw, J.E and Faul, Jessica D and Kardia, Sharon and Bouchard, Claude and Raffel, Leslie and Uitterlinden, A.G and Franco, Oscar and Vasan, Ramachanan and O'Donnell, Christopher and Taylor, Kent and Liu, K.Y and Bottinger, Erwin and Gottesman, Rebecca and Daw, E. Warwick and Giulianini, Franco and Ganesh, Santhi and Salfati, Elias and Harris, Tamara and Launer, L.J and Dörr, Marcus and Felix, Stephan and Rettig, Rainer and Völzke, Henry and Kim, Eric and Lee, Wen-Jane and Lee, I.T and Sheu, W.H.-H and Tsosie, K.S and Edwards, D.R.V and Liu, Yongmei and Correa, A and Weir, David and Völker, Uwe and Ridker, Paul and Boerwinkle, Eric and Gudnason, Vilmundur and Reiner, Alexander and Van Duijn, C.M and Borecki, Ingrid and Edwards, Todd L and Chakravarti, Aravinda and Rotter, J.I and Psaty, Bruce and Loos, Ruth and Fornage, Myriam and Ehret, Georg and Newton-Cheh, Christopher and Levy, Daniel and Chasman, Daniel and Myocardial Infarction Genetics CAR and GOT2Dgenes Consortium and ExomeBP Consortium and CHD Exome Consortium and T2D-Genes Consortium and CKDGen Consortium and Myocardial Infarction Genetics and CARDIoGRAM Exome Consortia and CHD Exome+ Consortium and GoT2DGenes Consortium and T2D-GENES Consortium
Nature Genetics, ISSN 1061-4036, 10/2016, Volume 48, Issue 10, pp. 1162 - 1170
Journal Article