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المؤلفون: Mary Cushman, John M. Starr, Min-Lee Yang, Wei Zhou, Ursula M. Schick, Vinna Clavo, Bella Hu, Oluf Pedersen, Tarunveer S. Ahluwalia, John D. Eicher, Santhi K. Ganesh, Albert V. Smith, Abbas Dehghan, Rebecca D. Jackson, Ian J. Deary, Mika Kähönen, Megan L. Grove, Jennifer A. Brody, Judy Wang, Amanda M Rosa Di Sant, Lenore J. Launer, Stephen S. Rich, Jiansong Wang, David C. Liewald, Paul I.W. de Bakker, Jerome I. Rotter, Leo-Pekka Lyytikäinen, Ruth J. F. Loos, Leonard I. Zon, Bruce M. Psaty, Nora Franceschini, Erwin P. Bottinger, Ming-Huei Chen, Paul L. Auer, James G. Wilson, Raha Pazoki, Nathan Pankratz, Russell P. Tracy, Vilmundur Gudnason, André G. Uitterlinden, Mike A. Nalls, Kristina L. Hunker, Frank J. A. van Rooij, Eric Boerwinkle, Kent D. Taylor, Albert Hofman, Yan Zhang, Mattijs E. Numans, Yong Huo, Yi Zhou, Folkert W. Asselbergs, James S. Floyd, Richard L. Proia, Yingchang Lu, Terho Lehtimäki, Liguang Dong, Riccardo E. Marioni, Jette Bork-Jensen, Jia Jia, Tamara B. Harris, Vy M. Nguyen, Fernando Rivadeneira, Oscar H. Franco, Yongmei Liu, Niels Grarup, Andrew D. Johnson, L. Adrienne Cupples, Ani Manichaikul, Elliott J. Hagedorn, Xiaoling Zhang, Maarten Leusink, Torben Hansen, Ingrid B. Borecki, Maria L. Allende, Betina Heinsbek Thuesen, Allan Linneberg, Olli T. Raitakari, Christopher J. O'Donnell, Mary F. Feitosa, Melissa E. Garcia, Alexander P. Reiner
المساهمون: Epidemiology, Internal Medicine
المصدر: Nature genetics
Pankratz, N, Schick, U M, Zhou, Y, Zhou, W, Ahluwalia, T S, Allende, M L, Auer, P L, Bork-Jensen, J, Brody, J A, Chen, M H, Clavo, V, Eicher, J D, Grarup, N, Hagedorn, E J, Hu, B, Hunker, K, Johnson, A D, Leusink, M, Lu, Y, Lyytikainen, L P, Manichaikul, A, Marioni, R, Nalls, M A, Pazoki, R, Smith, A V, Van Rooij, F J A, Yang, M L, Zhang, X, Zhang, Y, Asselbergs, F W, Boerwinkle, E, Borecki, I B, Bottinger, E P, Cushman, M, De Bakker, P I W, Deary, I, Dong, L, Feitosa, M F, Floyd, J S, Franceschini, N, Franco, O H, Garcia, M E, Grove, M L, Gudnason, V, Hansen, T, Harris, T B, Hofman, A, Jackson, R D, Jia, J, Kahonen, M, Launer, L J, Lehtimaki, T, Liewald, D, Linneberg, A, Liu, Y, Loos, R J F, Nguyen, V M, Numans, M E, Pedersen, O, Psaty, B M, Raitakari, O T, Rich, S S, Rivadeneira, F, Di Sant, A M R, Rotter, J I, Starr, J, Taylor, K D, Thuesen, B H, Tracy, R P, Uitterlinden, A G, Wang, J, Wang, J, Dehghan, A, Huo, Y, Adrienne Cupples, L, Wilson, J G, Proia, R L, Zon, L I, O'Donnell, C J, Reiner, A P & Ganesh, S K 2016, ' Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits ', Nature Genetics, vol. 48, no. 8, pp. 867-876 . https://doi.org/10.1038/ng.3607Test
Nature Genetics, 48(8), 867. Nature Publishing Group
Nature Genetics, 48(8), 867-876. Nature Publishing Group
Nature Genetics, 48(8), 867مصطلحات موضوعية: Male, 0301 basic medicine, Erythrocytes, Quantitative Trait Loci, Population, Genome-wide association study, Quantitative trait locus, Hematocrit, Biology, Article, Mice, 03 medical and health sciences, White blood cell, Genotype, Ethnicity, Journal Article, Genetics, medicine, Animals, Humans, Exome, education, Zebrafish, Medicine(all), education.field_of_study, medicine.diagnostic_test, ta1184, ta3121, 3. Good health, Receptors, Lysosphingolipid, 030104 developmental biology, medicine.anatomical_structure, Genetic Loci, Immunology, Erythrocyte Count, Absolute neutrophil count, Female, Genome-Wide Association Study
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المؤلفون: Anne-Claire Vergnaud, Nauder Faraday, Tim Kacprowski, Lisa R. Yanek, Oscar H. Franco, Yongmei Liu, Andreas Greinacher, Gina M. Peloso, Cristen J. Willer, Leslie A. Lange, Eric S. Torstenson, Reedik Mägi, Jeanette Erdmann, Ethan M. Lange, Deborah A. Nickerson, Henry Völzke, David R. Crosslin, Gunnar Engström, Albert V. Smith, André G. Uitterlinden, Salman M. Tajuddin, W. David Hill, Diane M. Becker, Paul Elliot, Caterina Vacchi-Suzzi, Linda M. Polfus, Traci M. Bartz, Nathalie Chami, Abbas Dehghan, Mike A. Nalls, John D. Eicher, Leo-Pekka Lyytikäinen, Evelin Mihailov, Uwe Völker, Caroline Hayward, Ioanna Tzoulaki, Myriam Fornage, Marju Orho-Melander, Mary Cushman, Lars Wallentin, Terho Lehtimäki, Ayush Giri, Laura M. Raffield, Lewis C. Becker, Yingchang Lu, Emma Raitoharju, Sekar Kathiresan, Simon de Denus, Ruth J. F. Loos, James S. Floyd, Dawn M. Waterworth, James G. Wilson, Nathan Pankratz, Lenore J. Launer, Andrew D. Johnson, Andrew J. Slater, Jean-Claude Tardif, Raha Pazoki, Evangelos Evangelou, Kenneth Rice, Harvey D. White, Marie-Pierre Dubé, Frank J. A. van Rooij, Akihiro Nomura, Tamara B. Harris, Vilmundur Gudnason, Gonçalo R. Abecasis, Alan B. Zonderman, Guillaume Lettre, Todd L. Edwards, Amber A. Burt, Ani Manichaikul, Heribert Schunkert, Ming-Huei Chen, Ian J. Deary, Michelle L. O'Donoghue, Jennifer A. Brody, Russell P. Tracy, Tõnu Esko, Mika Kähönen, Panos Deloukas, Eric Boerwinkle, Rasika A. Mathias, Dajiang J. Liu, Jin Li, Santhi K. Ganesh, David C. Liewald, Paul L. Auer, Digna R. Velez Edwards, Erwin P. Bottinger, Nina Mononen, Claudia Schurmann, Michele K. Evans, John M. Starr, Thomas Thiele, Jussi Hernesniemi, Jerome I. Rotter, Rakale C. Quarells, He Gao, Kjell Nikus, Stephen S. Rich, Heather M. Highland, Bruce M. Psaty, Ursula M. Schick, Andres Metspalu, Melissa A. Richard, Neil A. Zakai, Olle Melander, John D. Rioux, Olli T. Raitakari, Alexander P. Reiner, Joel N. Hirschhorn, Nilesh J. Samani
المساهمون: Epidemiology, Internal Medicine, Home Office, National Institute for Health Research, Medical Research Council (MRC)
المصدر: American Journal of Human Genetics, 99(1), 40-55. Cell Press
Eicher, J D, Chami, N, Kacprowski, T, Nomura, A, Chen, M-H, Yanek, L R, Tajuddin, S M, Schick, U M, Slater, A J, Pankratz, N, Polfus, L, Schurmann, C, Giri, A, Brody, J A, Lange, L A, Manichaikul, A, Hill, W D, Pazoki, R, Elliot, P, Evangelou, E, Tzoulaki, I, Gao, H, Vergnaud, A-C, Mathias, R A, Becker, D M, Becker, L C, Burt, A, Crosslin, D R, Lyytikäinen, L-P, Nikus, K, Hernesniemi, J, Kähönen, M, Raitoharju, E, Mononen, N, Raitakari, O T, Lehtimäki, T, Cushman, M, Zakai, N A, Nickerson, D A, Raffield, L M, Quarells, R, Willer, C J, Peloso, G M, Abecasis, G R, Liu, D J, Deloukas, P, Starr, J M, Liewald, D C M & Hayward, C & Deary, I J 2016, ' Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals ', American Journal of Human Genetics, vol. 99, no. 1, pp. 40-55 . https://doi.org/10.1016/j.ajhg.2016.05.005Test
The American Journal of Human Geneticsمصطلحات موضوعية: 0301 basic medicine, Blood Platelets, Male, CARDIoGRAM Exome Consortium, Genome-wide association study, 030204 cardiovascular system & hematology, Biology, Myocardial Infarction Genetics Consortium, Article, 03 medical and health sciences, 0302 clinical medicine, Genetics, Humans, Platelet, Exome, Genetics(clinical), Mean platelet volume, Allele frequency, Genotyping, Genetics (clinical), Genetics & Heredity, Platelet Count, ta1184, Genetic Variation, Global Lipids Genetics Consortium, 11 Medical And Health Sciences, 06 Biological Sciences, FCER1A, Genetic architecture, 030104 developmental biology, Hemostasis, Immunology, Female, Mean Platelet Volume, Genome-Wide Association Study
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https://pure.eur.nl/en/publications/1465b06f-411f-49c0-a589-3e97bc2a5f08Test -
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المؤلفون: Yingchang Lu, Lisa R. Yanek, Evangelos Evangelou, Andreas Greinacher, Leslie A. Lange, Albert Hofman, Rakale C. Quarells, Christopher J. O'Donnell, Simon de Denus, Marcus Dörr, Tamara B. Harris, Mary Cushman, Lars Wallentin, Digna R. Velez Edwards, Michelle L. O'Donoghue, Deborah A. Nickerson, Lisa Bastarache, Caterina Vacchi-Suzzi, Harvey D. White, Rasika A. Mathias, Jin Li, Santhi K. Ganesh, Leo-Pekka Lyytikäinen, Kjell Nikus, Ayush Giri, Paul Elliott, John M. Starr, Ruth J. F. Loos, Vilmundur Gudnason, Ioanna Tzoulaki, Myriam Fornage, Joshua C. Denny, Alan B. Zonderman, Caroline Hayward, Lewis C. Becker, Raha Pazoki, Guillaume Lettre, Lenore J. Launer, Ursula M. Schick, Michele K. Evans, Andrew J. Slater, Diane M. Becker, Jean-Claude Tardif, Ethan M. Lange, John D. Eicher, He Gao, James S. Floyd, Eric Boerwinkle, Paul L. Auer, Nathalie Chami, Frank J. A. van Rooij, Claudia Schurmann, Nele Friedrich, Kent D. Taylor, Andres Metspalu, Todd L. Edwards, Anne-Claire Vergnaud, Yongmei Liu, W. David Hill, Nauder Faraday, Terho Lehtimäki, Amber A. Burt, Jerome I. Rotter, Albert V. Smith, Tõnu Esko, Traci M. Bartz, Tim Kacprowski, Mike A. Nalls, Alexander P. Reiner, Ani Manichaikul, Ian J. Deary, Eric S. Torstenson, Laura M. Raffield, David C. Liewald, Ming-Huei Chen, Erwin P. Bottinger, Reedik Mägi, Andrew D. Johnson, Melissa A. Richard, Neil A. Zakai, John D. Rioux, Mika Kähönen, Stephen S. Rich, Heather M. Highland, Bruce M. Psaty, Joel N. Hirschhorn, Salman M. Tajuddin, Linda M. Polfus, Dawn M. Waterworth, James G. Wilson, Nathan Pankratz, Abbas Dehghan, Evelin Mihailov, David R. Crosslin, André G. Uitterlinden, Georg Homuth, Jennifer A. Brody
المساهمون: Gastroenterology & Hepatology, Epidemiology, Internal Medicine
المصدر: The American Journal of Human Genetics
Tajuddin, S M, Schick, U M, Eicher, J D, Chami, N, Giri, A, Brody, J A, Hill, W D, Kacprowski, T, Li, J, Lyytikäinen, L-P, Manichaikul, A, Mihailov, E, O'Donoghue, M L, Pankratz, N, Pazoki, R, Polfus, L M, Smith, A V, Schurmann, C, Vacchi-Suzzi, C, Waterworth, D M, Evangelou, E, Yanek, L R, Burt, A, Chen, M-H, van Rooij, F J A, Floyd, J S, Greinacher, A, Harris, T B, Highland, H M, Lange, L A, Liu, Y, Mägi, R, Nalls, M A, Mathias, R A, Nickerson, D A, Nikus, K, Starr, J M, Tardif, J-C, Tzoulaki, I, Velez Edwards, D R, Wallentin, L, Bartz, T M, Becker, L C, Denny, J C, Raffield, L M, Rioux, J D, Friedrich, N, Fornage, M, Gao, H, Hirschhorn, J N, Liewald, D C M, Rich, S S, Uitterlinden, A, Bastarache, L, Becker, D M, Boerwinkle, E, de Denus, S, Bottinger, E P, Hayward, C, Hofman, A, Homuth, G, Lange, E, Launer, L J, Lehtimäki, T, Lu, Y, Metspalu, A, O'Donnell, C J, Quarells, R C, Richard, M, Torstenson, E S, Taylor, K D, Vergnaud, A-C, Zonderman, A B, Crosslin, D R, Deary, I J, Dörr, M, Elliott, P, Evans, M K, Gudnason, V, Kähönen, M, Psaty, B M, Rotter, J I, Slater, A J, Dehghan, A, White, H D, Ganesh, S K, Loos, R J F, Esko, T, Faraday, N, Wilson, J G, Cushman, M, Johnson, A D, Edwards, T L, Zakai, N A, Lettre, G, Reiner, A P & Auer, P L 2016, ' Large-scale exome-wide association analysis identifies loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases ', American Journal of Human Genetics, vol. 99, no. 1, pp. 22-39 . https://doi.org/10.1016/j.ajhg.2016.05.003Test
American journal of human genetics, vol 99, iss 1
American Journal of Human Genetics, 99(1), 22-39. Cell Pressمصطلحات موضوعية: 0301 basic medicine, Quality Control, Myeloid, 1.1 Normal biological development and functioning, Genome-wide association study, Biology, Autoimmune Disease, Medical and Health Sciences, Article, 03 medical and health sciences, Underpinning research, White blood cell, medicine, Leukocytes, Genetics, Humans, 2.1 Biological and endogenous factors, Genetics(clinical), Exome, Aetiology, Genetics (clinical), Genetic association, Genetics & Heredity, Medical And Health Sciences, Neutrophil clearance, Hematopoietic stem cell differentiation, Inflammatory and immune system, Human Genome, Genetic Pleiotropy, Hematology, Biological Sciences, Acquired immune system, Stem Cell Research, 3. Good health, Blood Cell Count, 030104 developmental biology, medicine.anatomical_structure, Immune System Diseases, Genetic Loci, Immunology, Stem Cell Research - Nonembryonic - Non-Human, Genome-Wide Association Study
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المؤلفون: Wolfgang Koenig, Lynda M. Rose, Konstantin Strauch, Charles Kooperberg, Kent D. Taylor, Aaron R. Folsom, Nathan Pankratz, Daniel I. Chasman, Jie Yao, Sarah E. Harris, Caroline Hayward, Albert Hofman, Bruce M. Psaty, Kerri L. Wiggins, Megan L. Grove, Ming-Huei Chen, Alan F. Wright, Lihong Qi, Jennifer A. Brody, Paul M. Ridker, Ozren Polasek, Mary Cushman, Maria Sabater-Lleal, Eric Boerwinkle, Christopher J. O'Donnell, Tim Kacprowski, Myriam Fornage, Riccardo E. Marioni, Alexander P. Reiner, Franco Giulianini, Alanna C. Morrison, Alexander Teumer, Fernando Rivadeneira, Xiuqing Guo, Hugh Watkins, Oscar H. Franco, Abbas Dehghan, Helene Riess, Melanie Waldenberger, Barbara McKnight, André G. Uitterlinden, Neil A. Zakai, Anders Hamsten, Bengt Sennblad, Jennifer E. Huffman, Paul L. Auer, Uwe Völker, Rasika A. Mathias, Rona J. Strawbridge, Angela Silveira, Moniek P.M. de Maat, Geoffrey H. Tofler, Chiang Ching Huang, Lisa R. Yanek, Andreas Greinacher, Paul S. de Vries, Anuj Goel, Dhananjay Vaidya, Daniel Levy, Jerome I. Rotter, Martina Müller-Nurasyid, Nicholas L. Smith, John M. Starr, Weihong Tang, Li-An Lin, Ian J. Deary, Diane M. Becker
المساهمون: Epidemiology, Hematology, Internal Medicine
المصدر: Blood, vol 126, iss 11
Huffman, J E, de Vries, P, Morrison, A C, Sabater-Lleal, M, Kacprowski, T, Auer, P L, Brody, J A, Chasman, D I, Chen, M-H, Guo, X, Lin, L-A, Marioni, R, muller-nurasyid, M, Yanek, L R, Pankratz, N, Grove, M L, de Maat, M P M, Cushman, M, Wiggins, K L, Qi, L, Sennblad, B, Harris, S, Polašek, O, Riess, H, Rivadeneira, F, Rose, L M, Goel, A, Taylor, K D, Teumer, A, Uitterlinden, A G, Vaidya, D, Yao, J, Tang, W, Levy, D, Waldenberger, M, Becker, D M, Folsom, A R, Giulianini, F, Greinacher, A, Hofman, A, Huang, C-C, Kooperberg, C, Silveira, A, Starr, J M, Strauch, K, Strawbridge, R J, Wright, A F, McKnight, B, Franco, O H, Zakai, N, Mathias, R A, Psaty, B M, Ridker, P M, Tofler, G H, Voelker, U, Watkins, H, Fornage, M, Hamsten, A, Deary, I, Boerwinkle, E, Koenig, W, Rotter, J I, Hayward, C, Dehghan, A, Reiner, A P, O'Donnell, C J & Smith, N L 2015, ' Rare and low-frequency variants and their association with plasma levels of fibrinogen, FVII, FVIII, and vWF ', Blood . https://doi.org/10.1182/blood-2015-02-624551Test
Blood, 126(11), E19-E29. American Society of Hematologyمصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Candidate gene, Potassium Channels, Clinical Sciences, Immunology, Nerve Tissue Proteins, Genome-wide association study, Potassium Channels, Sodium-Activated, Cardiorespiratory Medicine and Haematology, Fibrinogen, Polymorphism, Single Nucleotide, Biochemistry, Thrombosis and Hemostasis, Cohort Studies, Paediatrics and Reproductive Medicine, chemistry.chemical_compound, Gene Frequency, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, medicine, Humans, Polymorphism, Allele frequency, Genetic Association Studies, Genetics, Factor VIII, biology, Factor VII, Genetic Variation, Single Nucleotide, Cell Biology, Hematology, Minor allele frequency, chemistry, Hemostasis, biology.protein, medicine.drug
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https://doi.org/10.1182/blood-2015-02-624551Test -
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المؤلفون: Jens Baumert, Gerjan Navis, Shelly G. Smith, Peter J. Grant, Anders Hamsten, Frances M K Williams, Russell P. Tracy, James B. Meigs, Maria Grazia Franzosi, Angela M. Carter, François Cambien, Wiek H. van Gilst, Kent D. Taylor, Folkert W. Asselbergs, Marcus E. Kleber, Kurt Lohman, Scott M. Williams, Saonli Basu, Martina Müller-Nurasyid, Angela Silveira, Pim van der Harst, Rory Collins, Geoffrey H. Tofler, Lasse Folkersen, Wolfgang Koenig, Christa Meisinger, Christopher J. O'Donnell, Qiong Yang, Aaron R. Folsom, John C. Chambers, Muredach P. Reilly, Norman Klopp, Weihong Tang, Ming-Huei Chen, Mahir Karakas, Bernhard R. Winkelmann, John Danesh, Sekar Kathiresan, Tamara B. Harris, Tim D. Spector, Pierre-Emmanuel Morange, John F. Peden, Danish Saleheen, Jaspal S. Kooner, Ann-Christine Syvänen, David-Alexandre Trégouët, Winfried März, Bernhard O. Boehm, Robert Clarke, Tiphaine Oudot-Mellakh, Nicholas L. Smith, Vinh Truong, Mary Cushman, André G. Uitterlinden, Lewis C. Becker, Joshua C. Bis, Udo Seedorf, Bengt Sennblad, Anders Franco-Cereceda, Yongmei Liu, Elisabeth M. C. Schrijvers, Hugh Watkins, Barbara McKnight, Diane M. Becker, Jingzhong Ding, Nicole Soranzo, Bruce M. Psaty, Anuj Goel, Per Eriksson, Mohammad Arfan Ikram, Annette Peters, So-Youn Shin, Abbas Dehghan, Lisa R. Yanek, Albert Hofman, Jason H. Moore, Hans L. Hillege, Per Lundmark, Jie Huang, Günther Silbernagel, Jemma C. Hopewell, John Öhrvik, Nena Matijevic, Alison H. Goodall, Maria Sabater-Lleal, Josyf C. Mychaleckyj, Rona J. Strawbridge, Andrew D. Johnson
المساهمون: Radiology & Nuclear Medicine, Epidemiology, Neurology, Internal Medicine, Life Course Epidemiology (LCE), Cardiovascular Centre (CVC), Lifestyle Medicine (LM), Groningen Kidney Center (GKC), Vascular Ageing Programme (VAP)
المصدر: Blood
Blood, 120(24), 4873-4881. American Society of Hematology
Blood, 120(24), 4873-4881. AMER SOC HEMATOLOGY
Blood; Vol 120مصطلحات موضوعية: Candidate gene, Genome-wide association study, Coronary Artery Disease, 030204 cardiovascular system & hematology, CIRCADIAN CLOCK, PLASMINOGEN-ACTIVATOR INHIBITOR-1, Biochemistry, TYPE-1 EXPRESSION, Monocytes, Thrombosis and Hemostasis, Cohort Studies, 0302 clinical medicine, Gene Frequency, Genetics, RISK, 0303 health sciences, ARNTL Transcription Factors, GENETIC-VARIATION, Hematology, LIM Domain Proteins, 3. Good health, ARNTL, CORONARY-ARTERY-DISEASE, RNA Interference, Proteasome Endopeptidase Complex, SUSCEPTIBILITY LOCI, Genotype, Immunology, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Cell Line, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Meta-Analysis as Topic, Cell Line, Tumor, Plasminogen Activator Inhibitor 1, SNP, Humans, PLASMA-LEVELS, Allele frequency, 030304 developmental biology, Adaptor Proteins, Signal Transducing, Mucin-3, Gene Expression Profiling, Cell Biology, Molecular biology, Gene expression profiling, PPAR gamma, MYOCARDIAL-INFARCTION, Diabetes Mellitus, Type 2, Gene Expression Regulation, TISSUE, ATPases Associated with Diverse Cellular Activities, Genome-Wide Association Study, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b86409435b3e3ad600f075d3e1bb70Test
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المؤلفون: Geoffrey H. Tofler, Peter M. Visscher, Gail Davies, Brendan M. Buckley, Albert Tenesa, Ann Rumley, John M. Starr, Xiuqing Guo, Veronique Vitart, Nicole Soranzo, Ozren Polasek, Rudi G. J. Westendorp, Jennifer E. Huffman, André G. Uitterlinden, Barbara Thorand, Igor Rudan, Naveed Sattar, Bruce M. Psaty, Ming-Huei Chen, Jens Baumert, Mary Cushman, Qiong Yang, Ian J. Deary, Stella Trompet, Lorna M. Lopez, Mahir Karakas, Drazen Pulanic, Alicja R Rudnicka, Peter J. Grant, So-Youn Shin, Edwin G. Bovill, Thomas Illig, Sarah H. Wild, Abbas Dehghan, Gordon D.O. Lowe, Jacqueline C. M. Witteman, Anton J. M. de Craen, Christian Gieger, Nicholas D. Hastie, Ian Ford, J. Wouter Jukema, Nicholas L. Smith, Wendy L. McArdle, Thomas Lumley, David J. Stott, James F. Wilson, Harry Campbell, Jie Huang, Albert Hofman, Susan Campbell, Annette Peters, Wolfgang Koenig, Barbara McKnight, Michelle Luciano, Angela M. Carter, Christopher J. O'Donnell, Tim D. Spector, David P. Strachan, Alan F. Wright, P. Eline Slagboom, David J. Porteous, Sarah E. Harris, Alan J. Gow, Caroline Hayward, Joshua C. Bis, David C. Liewald
المساهمون: Epidemiology, Internal Medicine
المصدر: Circulation
Smith, N L, Huffman, J E, Strachan, D P, Huang, J, Dehghan, A, Trompet, S, Lopez, L M, Shin, S-Y, Baumert, J, Vitart, V, Bis, J C, Wild, S H, Rumley, A, Yang, Q, Uitterlinden, A G, Stott, D J, Davies, G, Carter, A M, Thorand, B, Polašek, O, McKnight, B, Campbell, H, Rudnicka, A R, Chen, M-H, Buckley, B M, Harris, S E, Peters, A, Pulanic, D, Lumley, T, de Craen, A J M, Liewald, D C, Gieger, C, Campbell, S, Ford, I, Gow, A J, Luciano, M, Porteous, D J, Guo, X, Sattar, N, Tenesa, A, Cushman, M, Slagboom, P E, Visscher, P M, Spector, T D, Illig, T, Rudan, I, Bovill, E G, Wright, A F, McArdle, W L, Tofler, G, Hofman, A, Westendorp, R G J, Starr, J M, Grant, P J, Karakas, M, Hastie, N D, Psaty, B M, Wilson, J F, Lowe, G D O, O'Donnell, C J, Witteman, J C M, Jukema, J W, Deary, I J, Soranzo, N, Koenig, W & Hayward, C 2011, ' Genetic Predictors of Fibrin D-Dimer Levels in Healthy Adults ', Circulation, vol. 123, no. 17, pp. 1864-1872 . https://doi.org/10.1161/circulationaha.110.009480Test
Circulation; Vol 123
Circulation, 123(17), 1864
Circulation, 123(17), 1864-+. Lippincott Williams & Wilkinsمصطلحات موضوعية: Male, Plasmin, Genome-wide association study, 030204 cardiovascular system & hematology, Fibrinogen, polymorphism, 0302 clinical medicine, Reference Values, thr312ala, risk, Genetics, 0303 health sciences, biology, von-willebrand-factor, Factor V, cardiovascular health, Middle Aged, myocardial-infarction, epidemiology fibrin fragment D genome-wide association study hemostasis meta-analysis thrombosis genome-wide association tissue-plasminogen activator coronary heart-disease von-willebrand-factor venous thromboembolism thr312ala polymorphism cardiovascular health myocardial-infarction aging research risk, Female, epidemiology, Cardiology and Cardiovascular Medicine, medicine.drug, Adult, venous thromboembolism, Locus (genetics), Fibrin, White People, Article, Thromboplastin, Fibrin Fibrinogen Degradation Products, 03 medical and health sciences, Physiology (medical), Genetic model, D-dimer, medicine, Humans, Genetic Testing, Blood Coagulation, coronary, thrombosis, 030304 developmental biology, Aged, genome-wide association study, research, fibrin fragment D, business.industry, aging, heart-disease, tissue-plasminogen activator, meta-analysis, Immunology, biology.protein, hemostasis, genome-wide association, business, Genome-Wide Association Study
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المؤلفون: Man Li, Vilmundur Gudnason, Eric Boerwinkle, Christopher J. O'Donnell, Cornelia M. van Duijn, Thor Aspelund, Guo Li, Dan E. Arking, Paul M. Ridker, Talin Haritunians, Tamara B. Harris, W. H. Linda Kao, Abbas Dehghan, Alex Parker, Bruno H. Stricker, Thomas Lumley, David S. Siscovick, Daniel I. Chasman, Michael G. Shlipak, Bruce M. Psaty, Megan L. Grove, Albert Hofman, Lenore J. Launer, Ashish Upadhyay, Josef Coresh, Fernando Rivadeneira, Albert V. Smith, Gudny Eiriksdottir, Jacqueline C.M. Witteman, Martin G. Larson, Dena G. Hernandez, Anna Köttgen, Michel Chonchol, Nicole L. Glazer, André G. Uitterlinden, Ming-Huei Chen, Caroline S. Fox, Mike A. Nalls, Qiong Yang, Guillaume Paré, Shih-Jen Hwang
المساهمون: Epidemiology, Public Administration, Internal Medicine
المصدر: Circulation-cardiovascular genetics, 3(6), 523-530. Lippincott Williams & Wilkins
مصطلحات موضوعية: Male, medicine.medical_specialty, Gout, Coronary Disease, Genome-wide association study, Article, chemistry.chemical_compound, SDG 3 - Good Health and Well-being, Risk Factors, Internal medicine, Genetics, Genetic predisposition, Humans, Medicine, Genetics (clinical), biology, business.industry, Mendelian Randomization Analysis, medicine.disease, Uric Acid, Endocrinology, chemistry, Cardiovascular Diseases, Genetic Loci, Meta-analysis, Immunology, biology.protein, Uric acid, Female, SLC22A12, Cardiology and Cardiovascular Medicine, business, Genome-Wide Association Study, SLC2A9
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd613c509ad3dde879a5e610f38aebcTest
https://doi.org/10.1161/circgenetics.109.934455Test -
8
المؤلفون: Qiong Yang, Wolfgang Lieb, Douglas B. Sawyer, Gary F. Mitchell, Holly M. Smith, Radwan Safa, Ming-Huei Chen, Ramachandran S. Vasan, Lisa M. Sullivan, Vanessa Xanthakis, Martin G. Larson, Justin P. Zachariah, Joseph A. Vita
المصدر: Circulation: Cardiovascular Genetics. 3:300-306
مصطلحات موضوعية: Adult, Male, Genetic Linkage, Angiogenesis, Blood Pressure, Article, Angiopoietin-2, Cohort Studies, Risk Factors, Genetics, Humans, Medicine, Obesity, Genetics (clinical), Dyslipidemias, Metabolic Syndrome, Endothelial Growth Factors, business.industry, Angiopoietin 2, Angiopoietins, Middle Aged, Receptor, TIE-2, Cardiovascular Diseases, Immunology, Female, Cardiology and Cardiovascular Medicine, business, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07de59528fcd203becd3ea2860e7455Test
https://doi.org/10.1161/circgenetics.109.914556Test -
9
المؤلفون: Martin G. Larson, Jian Rong, Tanja Zeller, Josée Dupuis, Emelia J. Benjamin, Renate B. Schnabel, Izabella Lipinska, Claire Perret, John F. Keaney, Zhenming Zhao, Jennifer F. Yamamoto, Viviane Nicaud, Stefan Blankenberg, Kathryn L. Lunetta, James B. Meigs, Ming-Huei Chen, Laurence Tiret, Ramachandran S. Vasan
المصدر: Circulation: Cardiovascular Genetics. 2:229-237
مصطلحات موضوعية: Community-Based Participatory Research, Candidate gene, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Article, Cohort Studies, Gene Frequency, Risk Factors, Genetics, Humans, Allele, Allele frequency, Alleles, Genetics (clinical), Inflammation, Heritability, Minor allele frequency, Phenotype, Multivariate Analysis, Immunology, Biomarker (medicine), Tumor necrosis factor alpha, Inflammation Mediators, Cardiology and Cardiovascular Medicine, Biomarkers
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::415627be68c214e6bb309971df79cb65Test
https://doi.org/10.1161/circgenetics.108.804245Test -
10
المؤلفون: Sun-Lung Tsai, Jyh-Hsiung Huang, Ming-Huei Chen, Chao-Yuan Huang, I-Shyan Sheen, Y. C. Chen, George Kuo, Chau-Ting Yeh, Yun-Fan Liaw
المصدر: Gastroenterology. 115:954-966
مصطلحات موضوعية: Adult, Male, Receptors, Antigen, T-Cell, alpha-beta, Hepatitis C virus, Molecular Sequence Data, Immunoglobulin Variable Region, chemical and pharmacologic phenomena, Hepacivirus, Biology, medicine.disease_cause, Major histocompatibility complex, Virus, Epitope, Cell Line, Viral Proteins, HLA-A2 Antigen, medicine, Humans, Cytotoxic T cell, Amino Acid Sequence, Base Sequence, Hepatology, T-cell receptor, Gastroenterology, Genetic Variation, hemic and immune systems, Hepatitis C, Chronic, Middle Aged, Virology, Peptide Fragments, Hypervariable region, CTL, Acute Disease, Immunology, biology.protein, Female, T-Lymphocytes, Cytotoxic
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27ae1285133d38e68e763ad5ce6da65aTest
https://doi.org/10.1016/s0016-5085Test(98)70268-9