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Journal of Alzheimer's Disease, ISSN 1387-2877, 11/2018, Volume 66, Issue 3, pp. 1275 - 1282
Journal Article
by Do, Ron and Stitziel, Nathan O and Won, Hong-Hee and Jørgensen, Anders Berg and Duga, Stefano and Angelica Merlini, Pier and Kiezun, Adam and Farrall, Martin and Goel, Anuj and Zuk, Or and Guella, Illaria and Asselta, Rosanna and Lange, Leslie A and Peloso, Gina M and Auer, Paul L and Girelli, Domenico and Martinelli, Nicola and Farlow, Deborah N and DePristo, Mark A and Roberts, Robert and Stewart, Alexander F. R and Saleheen, Danish and Danesh, John and Epstein, Stephen E and Sivapalaratnam, Suthesh and Hovingh, G. Kees and Kastelein, John J and Samani, Nilesh J and Schunkert, Heribert and Erdmann, Jeanette and Shah, Svati H and Kraus, William E and Davies, Robert and Nikpay, Majid and Johansen, Christopher T and Wang, Jian and Hegele, Robert A and Hechter, Eliana and Marz, Winfried and Kleber, Marcus E and Huang, Jie and Johnson, Anew D and Li, Mingyao and Burke, Greg L and Gross, Myron and Liu, Yongmei and Assimes, Themistocles L and Heiss, Gerardo and Lange, Ethan M and Folsom, Aaron R and Taylor, Herman A and Olivieri, Oliviero and Hamsten, Anders and Clarke, Robert and Reilly, Dermot F and Yin, Wu and Rivas, Manuel A and Donnelly, Peter and Rossouw, Jacques E and Psaty, Bruce M and Herrington, David M and Wilson, James G and Rich, Stephen S and Bamshad, Michael J and Tracy, Russell P and Cupples, L. Aienne and Rader, Daniel J and Reilly, Muredach P and Spertus, John A and Cresci, Sharon and Hartiala, Jaana and Tang, W. H. Wilson and Hazen, Stanley L and Allayee, Hooman and Reiner, Alex P and Carlson, Christopher S and Kooperberg, Charles and Jackson, Rebecca D and Boerwinkle, Eric and Lander, Eric S and Schwartz, Stephen M and Siscovick, David S and McPherson, Ruth and Tybjaerg-Hansen, Anne and Abecasis, Goncalo R and Watkins, Hugh and Nickerson, Deborah A and Ardissino, Diego and Sunyaev, Shamil R and O'Donnell, Christopher J and Altshuler, David and Gabriel, Stacey and Kathiresan, Sekar and Gabriel, Stacey B and Altshuler, David M and Abecasis, Gonçalo R and Daly, Mark J and de Bakker, Paul I. W and Fennell, Tim and Garimella, Kiran and ... and NHLBI Exome Sequencing Project
Nature, ISSN 0028-0836, 2015, Volume 518, Issue 7537, pp. 102 - +
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
BMC Proceedings, 09/2018, Volume 12
Journal Article
Nature, ISSN 0028-0836, 2016, Volume 536, Issue 7616, pp. 285 - 291
Large-scale reference data sets of human genetic variation are critical for the medical and functional interpretation of DNA sequence changes. Here we describe... 
HUMAN-DISEASE | EVOLUTION | MULTIDISCIPLINARY SCIENCES | MUTATION | GUIDELINES | FRAMEWORK | SEQUENCE VARIANTS | NETWORKS | DISCOVERY | HUMAN-POPULATION HISTORY | Genetic aspects | Research | Man | Human beings | Genetic variation | Analysis | Datasets | Proteins | Disease | Genes | Principal components analysis | Genetics | Genomes | Data bases | Index Medicus
Journal Article
by Voight, Benjamin F, PhD|Peloso, Gina M, PhD|Orho-Melander, Marju, PhD|Frikke-Schmidt, Ruth, DMSc|Barbalic, Maja, PhD|Jensen, Majken K, PhD|Hindy, George, MD|Hólm, Hilma, MD|Ding, Eric L, ScD|Johnson, Toby, PhD|Schunkert, Heribert, Prof|Samani, Nilesh J, Prof|Clarke, Robert, MD|Hopewell, Jemma C, PhD|Thompson, John F, Prof|Li, Mingyao, PhD|Thorleifsson, Gudmar, PhD|Newton-Cheh, Christopher, MD|Musunuru, Kiran, MD|Pirruccello, James P, BS|Saleheen, Danish, MBBS|Chen, Li, MSc|Stewart, Alexandre FR, PhD|Schillert, Arne, PhD|Thorsteinsdottir, Unnur, PhD|Thorgeirsson, Gudmundur, MD|Anand, Sonia, Prof|Engert, James C, PhD|Morgan, Thomas, MD|Spertus, John, Prof|Stoll, Monika, Prof|Berger, Klaus, Prof|Martinelli, Nicola, MD|Girelli, Domenico, Prof|McKeown, Pascal P, Prof|Patterson, Christopher C, PhD|Epstein, Stephen E, MD|Devaney, Joseph, PhD|Burnett, Mary-Susan, PhD|Mooser, Vincent, MD|Ripatti, Samuli, PhD|Surakka, Ida, BSci|Nieminen, Markku S, Prof|Sinisalo, Juha, MD|Lokki, Marja-Liisa, PhD|Perola, Markus, Prof|Havulinna, Aki, PhD|de Faire, Ulf, Prof|Gigante, Bruna, MD|Ingelsson, Erik, PhD|Zeller, Tanja, PhD|Wild, Philipp, MD|de Bakker, Paul I W, Prof|Klungel, Olaf H, PhD|Maitland-van der Zee, Anke-Hilse, PhD|Peters, Bas J M, PhD|de Boer, Anthonius, Prof|Grobbee, Diederick E, Prof|Kamphuisen, Pieter W, PhD|Deneer, Vera H M, PhD|Elbers, Clara C, PhD|Onland-Moret, N Charlotte, PhD|Hofker, Marten H, Prof|Wijmenga, Cisca, Prof|Verschuren, WM Monique, PhD|Boer, Jolanda MA, PhD|van der Schouw, Yvonne T, Prof|Rasheed, Asif|Frossard, Philippe|Demissie, Serkalem, PhD|Willer, Cristen, PhD|Do, Ron, PhD|Ordovas, Jose M, Prof|Abecasis, Gonçalo R, Prof|Boehnke, Michael, Prof|Mohlke, Karen L, PhD|Daly, Mark J, PhD|Guiducci, Candace, BS|Burtt, Noël P, BS|Surti, Aarti, BS|Gonzalez, Elena, BS|Purcell, Shaun, PhD|Gabriel, Stacey, PhD|Marrugat, Jaume, PhD|Peden, John, PhD|Erdmann, Jeanette, PhD|Diemert, Patrick, MD|Willenborg, Christina, MSc|König, Inke R, PhD|Fischer, Marcus, MD|Hengstenberg, Christian, MD|Ziegler, Andreas, PhD|Buysschaert, Ian, MD|Lambrechts, Diether, PhD|Van de Werf, Frans, Prof|Fox, Keith A, Prof|El Mokhtari, Nour Eddine, MD|Rubin, Diana, MD|Schrezenmeir, Jürgen, PhD|Schreiber, Stefan, Prof|Schäfer, Arne, PhD|Danesh, John, Prof|Blankenberg, Stefan, Prof|Roberts, Robert, Prof|McPherson, Ruth, Prof|Watkins, Hugh, Prof|Hall, Alistair S, Prof|Overvad, Kim, Prof|Rimm, Eric, ScD|Boerwinkle, Eric, PhD|Tybjaerg-Hansen, Anne, Prof|Cupples, L Adrienne, Prof|Reilly, Muredach P, MD|Melander, Olle, Prof|Mannucci, Pier M, Prof|Ardissino, Diego, Prof|Siscovick, David, Prof|Elosua, Roberto, PhD|Stefansson, Kari, MD|O'Donnell, Christopher J, MD|Salomaa, Veikko, Prof|Rader, Daniel J, Prof|Peltonen, Leena, Prof|Schwartz, Stephen M, Prof|Altshuler, David, Prof|Kathiresan, Sekar, Dr MD
Lancet, The, ISSN 0140-6736, 08/2012, Volume 380, Issue 9841, pp. 572 - 580
Journal Article
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, ISSN 1552-5260, 07/2018, Volume 14, Issue 7, pp. P711 - P711
Journal Article
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