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), 867

مصطلحات 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

وصف الملف: image/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5aecb861e80d29ff2a272e87236da408Test
https://doi.org/10.1038/ng.3607Test

المؤلفون: Nauder Faraday, Lewis C. Becker, Lisa R. Yanek, Shiow J. Lin, Diane M. Becker, Michael A. Province, Qiong Yang, Ming-Huei Chen, Geoffrey H. Tofler, Christopher J. O'Donnell, Andrew D. Johnson, Martin G. Larson, Aldi T. Kraja

المصدر: Nature Genetics. 42:608-613

مصطلحات موضوعية: 0303 health sciences, medicine.medical_specialty, Sticky platelet syndrome, Locus (genetics), Genome-wide association study, Single-nucleotide polymorphism, 030204 cardiovascular system & hematology, Biology, medicine.disease, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Framingham Heart Study, Internal medicine, Genotype, Genetics, medicine, Platelet, Prospective cohort study, 030304 developmental biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5f78f6bf363beb4d3b1b7d1619acf686Test
https://doi.org/10.1038/ng.604Test

المؤلفون: Jerome I. Rotter, Abbas Dehghan, Gang Zheng, Willem H. Ouwehand, Caroline S. Fox, Jack M. Guralnik, Tamara B. Harris, Toshiko Tanaka, Andrew E. Jaffe, Albert Hofman, Andrew B. Singleton, Jing-Ping Lin, Joshua C. Bis, Santhi K. Ganesh, Christian Gieger, Christa Meisinger, Jaap Jan Zwaginga, Mary Cushman, Matthias Nauck, Aravinda Chakravarti, Gudny Eiriksdottir, Daniel Levy, Kenneth Rice, Swee Lay Thein, Augusto Rendon, Vilmundur Gudnason, Luigi Ferrucci, Frank J. A. van Rooij, Jennifer G. Sambrook, Andreas Greinacher, Dena G. Hernandez, Jacqueline C.M. Witteman, Lenore J. Launer, Qiong Yang, Thor Aspelund, Panos Deloukas, Eric Boerwinkle, Ben A. Oostra, Germaine C. Verwoert, Cornelia M. van Duijn, Albert V. Smith, Thomas Lumley, Anna Köttgen, Nicole L. Glazer, André G. Uitterlinden, Janine M. Vangils, Ming-Huei Chen, Georg Ehret, Janine F. Felix, Mike A. Nalls, Kushang V. Patel, Alexander Teumer, L. Adrienne Cupples, Susan L. Furth, Christopher J. O'Donnell, Josef Coresh, Tim D. Spector, Brigitte Kühnel, Stefania Bandinelli, Neil A. Zakai, Nicole Soranzo, Bruce M. Psaty

المساهمون: Ehret, Georg Benedikt, Epidemiology, Internal Medicine, Clinical Genetics

المصدر: Nature genetics
Nature Genetics, Vol. 41, No 11 (2009) pp. 1191-1198
Nature Genetics, 41(11), 1191-U48. Nature Publishing Group

مصطلحات موضوعية: Quantitative Trait Loci, Gene Expression, Mean corpuscular hemoglobin, Genome-wide association study, Endothelial Cells/metabolism, Biology, Quantitative trait locus, Hematocrit, Polymorphism, Single Nucleotide, Article, Cell Line, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Genome-Wide Association Study, Erythrocytes/metabolism, Mean corpuscular volume, 030304 developmental biology, Genetic association, ddc:616, 0303 health sciences, medicine.diagnostic_test, Mean corpuscular hemoglobin concentration, Genome, Human, 3. Good health, Blood Pressure/*genetics, Phenotype, 030220 oncology & carcinogenesis, Hypertension/*genetics, Hemoglobin

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c19e41e06d50b5bfeecad06fdaab1beTest
https://doi.org/10.1038/ng.466Test

المؤلفون: Ganesh, Santhi K., Zakai, Neil A., van Rooij, Frank J. A., Soranzo, Nicole, Smith, Albert V., Nalls, Michael A., Ming-Huei Chen, Kottgen, Anna, Glazer, Nicole L., Dehghan, Abbas, Kuhnel, Brigitte, Aspelund, Thor, Qiong Yang, Tanaka, Toshiko, Jaffe, Andrew, Bis, Joshua C. M., Verwoert, Germaine C., Teumer, Alexander, Fox, Caroline S., Guralnik, Jack M.

المصدر: Nature Genetics; Nov2009, Vol. 41 Issue 11, p1191-1198, 8p, 1 Diagram, 3 Charts, 2 Graphs

مصطلحات موضوعية: ERYTHROCYTES, PHENOTYPES, BLOOD proteins, BLOOD cells, HEMOGLOBINS