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by Traylor, Matthew, MSc and Farrall, Martin, FRCPath and Holliday, Elizabeth G, PhD and Sudlow, Cathie, FRCP and Hopewell, Jemma C, PhD and Cheng, Yu-Ching, PhD and Fornage, Myriam, PhD and Ikram, M Arfan, MD and Malik, Rainer, PhD and Bevan, Steve, PhD and Thorsteinsdottir, Unnur, PhD and Nalls, Mike A, PhD and Longstreth, WT, MD and Wiggins, Kerri L, MS and Yadav, Sunaina, MSc and Parati, Eugenio A, MD and DeStefano, Anita L, PhD and Worrall, Bradford B, MD and Kittner, Steven J, MD and Khan, Muhammad Saleem, MSc and Reiner, Alex P, MD and Helgadottir, Anna, MD and Achterberg, Sefanja, PhD and Fernandez-Cadenas, Israel, PhD and Abboud, Sherine, MD and Schmidt, Reinhold, MD and Walters, Matthew, MD and Chen, Wei-Min, PhD and Ringelstein, E Bernd, MD and O'Donnell, Martin, MD and Ho, Weang Kee, PhD and Pera, Joanna, MD and Lemmens, Robin, MD and Norrving, Bo, MD and Higgins, Peter, MRCP and Benn, Marianne, MD and Sale, Michele, PhD and Kuhlenbäumer, Gregor, MD and Doney, Alexander S F, PhD and Vicente, Astrid M, PhD and Delavaran, Hossein, MD and Algra, Ale, MD and Davies, Gail, PhD and Oliveira, Sofia A, PhD and Palmer, Colin N A, PhD and Deary, Ian, PhD and Schmidt, Helena, MD and Pandolfo, Massimo, MD and Montaner, Joan, MD and Carty, Cara, PhD and de Bakker, Paul I W, PhD and Kostulas, Konstantinos, MD and Ferro, Jose M, MD and van Zuydam, Natalie R, MSc and Valdimarsson, Einar, MD and Nordestgaard, Børge G, MD and Lindgren, Arne, MD and Thijs, Vincent, MD and Slowik, Agnieszka, MD and Saleheen, Danish, MD and Paré, Guillaume, MD and Berger, Klaus, MD and Thorleifsson, Gudmar, PhD and Hofman, Albert, MD and Mosley, Thomas H, PhD and Mitchell, Braxton D, PhD and Furie, Karen, MD and Clarke, Robert, FRCP and Levi, Christopher, MD and Seshadri, Sudha, MD and Gschwendtner, Andreas, MD and Boncoraglio, Giorgio B, MD and Sharma, Pankaj, PhD and Bis, Joshua C, PhD and Gretarsdottir, Solveig, PhD and Psaty, Bruce M and Rothwell, Peter M, FMedSci and Rosand, Jonathan, MD and Meschia, James F, MD and Stefansson, Kari, MD and Dichgans, Martin, MD and Markus, Hugh S, Dr and WTCCC 2 and Australian Stroke Genetics Collabo and Int Stroke Genetics Consortium and International Stroke Genetics Consortium and Australian Stroke Genetics Collaborative, Wellcome Trust Case Control Consortium 2 (WTCCC2) and EpiHealth: Epidemiology for Health and Lund University and Neurologi, Lund and Lunds universitet and Neurology, Lund
The Lancet Neurology, ISSN 1474-4422, 2012, Volume 11, Issue 11, pp. 951 - 962
Journal Article
by Helgadottir, Anna, MD, PhD and Gretarsdottir, Solveig, PhD and Thorleifsson, Gudmar, PhD and Holm, Hilma, MD and Patel, Riyaz S., MD and Gudnason, Thorarinn, MD, PhD and Jones, Gregory T., PhD and van Rij, Andre M., MD and Eapen, Danny J., MD and Baas, Annette F., PhD and Tregouet, David-Alexandre, PhD and Morange, Pierre-Emmanuel, MD and Emmerich, Joseph, MD, PhD and Lindblad, Bengt, MD, PhD and Gottsäter, Anders, MD, PhD and Kiemeny, Lambertus A., PhD and Lindholt, Jes S., MD, PhD and Sakalihasan, Natzi, MD, PhD and Ferrell, Robert E., PhD and Carey, David J., PhD and Elmore, James R., MD and Tsao, Philip S., PhD and Grarup, Niels, MD, PhD and Jørgensen, Torben, MD, DMSci and Witte, Daniel R., MD, PhD and Hansen, Torben, MD, PhD and Pedersen, Oluf, MD, DMSci and Pola, Roberto, MD, PhD and Gaetani, Eleonora, MD and Magnadottir, Hulda B., MD and Wijmenga, Cisca, PhD and Tromp, Gerard, PhD and Ronkainen, Antti, MD, PhD and Ruigrok, Ynte M., MD and Blankensteijn, Jan D and Mueller, Thomas, MD and Wells, Philip S., MD and Corral, Javier, PhD and Soria, Jose Manuel, PhD and Souto, Juan Carlos, MD, PhD and Peden, John F., PhD and Jalilzadeh, Shapour, MD, PhD and Mayosi, Bongani M., DPhil and Keavney, Bernard, MD and Strawbridge, Rona J., PhD and Sabater-Lleal, Maria, PhD and Gertow, Karl, PhD and Baldassarre, Damiano, PhD and Nyyssönen, Kristiina, PhD and Rauramaa, Rainer, MD, PhD and Smit, Andries J., MD, PhD and Mannarino, Elmo, MD and Giral, Philippe, MD and Tremoli, Elena, PhD and de Faire, Ulf, MD, PhD and Humphries, Steve E., PhD and Hamsten, Anders, MD, PhD and Haraldsdottir, Vilhelmina, MD and Olafsson, Isleifur, MD, PhD and Magnusson, Magnus K., MD and Samani, Nilesh J., MD and Levey, Allan I., MD, PhD and Markus, Hugh S., MD and Kostulas, Konstantinos, MD, PhD and Dichgans, Martin, MD and Berger, Klaus, MD and Kuhlenbäumer, Gregor, MD and Ringelstein, E. Bernd, MD and Stoll, Monika, PhD and Seedorf, Udo, PhD and Rothwell, Peter M., MD, PhD and Powell, Janet T., MD and Kuivaniemi, Helena, MD, PhD and Onundarson, Pall T., MD and Valdimarsson, Einar, MD and Matthiasson, Stefan E., MD, PhD and Gudbjartsson, Daniel F., PhD and Thorgeirsson, Guðmundur, MD, PhD and Quyyumi, Arshed A., MD and Watkins, Hugh, MD, PhD and Farrall, Martin, MD and Thorsteinsdottir, Unnur, PhD and Stefansson, Kari, MD, PhD and Lund University and Vascular Diseases - Clinical Research and Vaskulära sjukdomar - kliniska studier and Lunds universitet
Journal of the American College of Cardiology, ISSN 0735-1097, 08/2012, Volume 60, Issue 8, pp. 722 - 729
Objectives The purpose of this study is investigate the effects of variants in the apolipoprotein(a) gene ( LPA ) on vascular diseases with different... 
Cardiovascular | Internal Medicine | atherosclerosis | genetic | association | thrombosis | lipoprotein(a) | INTIMA-MEDIA THICKNESS | CARDIAC & CARDIOVASCULAR SYSTEMS | RISK-FACTORS | METAANALYSIS | MYOCARDIAL-INFARCTION | VASCULAR-DISEASE | WOMEN | PERIPHERAL ARTERIAL-DISEASE | ISCHEMIC-STROKE | SEVERITY | Severity of Illness Index | Myocardial Infarction - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Apolipoproteins A - genetics | Angiography | Carotid Intima-Media Thickness | Intracranial Aneurysm - genetics | Atherosclerosis - genetics | Humans | Risk Factors | Brain Ischemia - genetics | African Americans - genetics | Linear Models | Logistic Models | Aortic Aneurysm, Abdominal - genetics | Stroke - genetics | Venous Thromboembolism - genetics | Peripheral Arterial Disease - genetics | Age of Onset | Coronary Artery Disease - genetics | Polymorphism, Single Nucleotide | Odds Ratio | Medical colleges | Neurosciences | Stock options | Genes | Aneurysms | Coronary heart disease | Biometry | Lipoprotein A | Anopheles | Atherosclerosis | Medical genetics | Genetic research | Genetic aspects | Diabetes | Thromboembolism | Cardiology | Public health | Dementia | Stroke | Medical imaging | Values | Cardiovascular disease | Apolipoproteins | Thrombosis | Studies | Confidence intervals | Coronary vessels | Blood pressure | Drug therapy | Age | Methods | Kardiologi | Clinical Medicine | Cardiac and Cardiovascular Systems | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin
Journal Article
Journal Article
by Peden, John F and Hopewell, Jemma C and Saleheen, Danish and Chambers, John C and Hager, Jorg and Soranzo, Nicole and Collins, Rory and Danesh, John and Elliott, Paul and Farrall, Martin and Stirrups, Kathy and Zhang, Weihua and Hamsten, Anders and Parish, Sarah and Lathrop, Mark and Watkins, Hugh and Clarke, Robert and Deloukas, Panos and Kooner, Jaspal S and Goel, Anuj and Ongen, Halit and Strawbridge, Rona J and Heath, Simon and Mälarstig, Anders and Helgadottir, Anna and Öhrvik, John and Murtaza, Muhammed and Potter, Simon and Hunt, Sarah E and Delepine, Marc and Jalilzadeh, Shapour and Axelsson, Tomas and Syvanen, Ann-Christine and Gwilliam, Rhian and Bumpstead, Suzannah and Gray, Emma and Edkins, Sarah and Folkersen, Lasse and Kyriakou, Theodosios and Franco-Cereceda, Anders and Gabrielsen, Anders and Seedorf, Udo and Eriksson, Per and Offer, Alison and Bowman, Louise and Sleight, Peter and Armitage, Jane and Peto, Richard and Abecasis, Goncalo and Ahmed, Nabeel and Caulfield, Mark and Donnelly, Peter and Froguel, Philippe and Kooner, Angad S and McCarthy, Mark I and Samani, Nilesh J and Scott, James and Sehmi, Joban and Silveira, Angela and Hellénius, Mai-Lus and van't Hooft, Ferdinand M and Olsson, Gunnar and Rust, Stephan and Assman, Gerd and Barlera, Simona and Tognoni, Gianni and Franzosi, Maria Grazia and Linksted, Pamela and Green, Fiona R and Rasheed, Asif and Zaidi, Moazzam and Shah, Nabi and Samuel, Maria and Mallick, Nadeem H and Azhar, Muhammad and Zaman, Khan S and Samad, Abdus and Ishaq, Mohammad and Gardezi, Ali R and Fazal-ur-Rehman, Memon and Frossard, Philippe M and Spector, Tim and Peltonen, Leena and Nieminen, Markku S and Sinisalo, Juha and Salomaa, Veikko and Ripatti, Samuli and Bennett, Derrick and Leander, Karin and Gigante, Bruna and de Faire, Ulf and Pietri, Silvia and Gori, Francesca and Marchioli, Roberto and Sivapalaratnam, Suthesh and Kastelein, John J. P and Trip, Mieke D and Theodoraki, Eirini V and Dedoussis, George V and Engert, Jamie C and ... and Coronary Artery Dis C4D Genetics C and MuTHER Consortium and Coronary Artery Disease (C4D) Genetics Consortium and The Coronary Artery Disease (C4D) Genetics Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature genetics, ISSN 1061-4036, 2011, Volume 43, Issue 4, pp. 339 - 344
Journal Article
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 2, pp. 221 - 227
Journal Article
by Bellenguez, Céline and Bevan, Steve and Gschwendtner, Andreas and Spencer, Chris C.A and Burgess, Annette I and Pirinen, Matti and Jackson, Caroline A and Traylor, Matthew and Strange, Amy and Su, Zhan and Band, Gavin and Syme, Paul D and Malik, Rainer and Pera, Joanna and Bo, Norrving and Lemmens, Robin and Freeman, Colin and Schanz, Renata and James, Tom and Poole, Deborah and Murphy, Lee and Segal, Helen and Cortellini, Lynelle and Cheng, Yu-Ching and Woo, Daniel and Nalls, Michael A and Müller-Myhsok, Bertram and Meisinger, Christa and Seedorf, Udo and Ross-Adams, Helen and Boonen, Steven and Wloch-Kopec, Dorota and Valant, Valerie and Slark, Julia and Furie, Karen and Delavaran, Hossein and Langford, Cordelia and Deloukas, Panos and Edkins, Sarah and Hunt, Sarah and Gray, Emma and Dronov, Serge and Peltonen, Leena and Gretarsdottir, Solveig and Thorleifsson, Gudmar and Thorsteinsdottir, Unnur and Stefansson, Kari and Boncoraglio, Giorgio B and Parati, Eugenio A and Attia, John and Holliday, Elizabeth and Levi, Chris and Franzosi, Maria-Grazia and Goel, Anuj and Helgadottir, Anna and Blackwell, Jenefer M and Bramon, Elvira and Brown, Matthew A and Casas, Juan P and Corvin, Aiden and Duncanson, Audrey and Jankowski, Janusz and Mathew, Christopher G and Palmer, Colin N.A and Plomin, Robert and Rautanen, Anna and Sawcer, Stephen J and Trembath, Richard C and Viswanathan, Ananth C and Wood, Nicholas W and Worrall, Bradford B and Kittner, Steven J and Mitchell, Braxton D and Kissela, Brett and Meschia, James F and Thijs, Vincent and Lindgren, Arne and MacLeod, Mary Joan and Slowik, Agnieszka and Walters, Matthew and Rosand, Jonathan and Sharma, Pankaj and Farrall, Martin and Sudlow, Cathie L.M and Rothwell, Peter M and Dichgans, Martin and Donnelly, Peter and Markus, Hugh S and ISGC and WTCCC2 and Wellcome Trust Case Control Consortium 2 (WTCCC2) and International Stroke Genetics Consortium (ISGC) and The International Stroke Genetics Consortium (ISGC) and the Wellcome Trust Case Control Consortium 2 (WTCCC2)
Nature Genetics, ISSN 1061-4036, 03/2012, Volume 44, Issue 3, pp. 328 - 333
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 3636 - 9
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Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 5101 - 11
Journal Article