المؤلفون: Adolfo Correa, Jai G. Broome, Chunyan Ren, Kari E. North, Nancy L. Heard-Costa, Yao Yao, Brian D. Hobbs, Mary Cushman, Leslie A. Lange, Daniel E. Bauer, Xiuwen Zheng, Braxton D. Mitchell, Yun Li, Quan Sun, Sébastian Méric de Bellefon, Terri H. Beaty, Paul S. de Vries, Ruth J. F. Loos, Adrienne M. Stilp, Albert V. Smith, Paul L. Auer, Deepti Jain, Lifang Hou, Robert C. Kaplan, Jee-Young Moon, Michael Preuss, Stephen S. Rich, Guillaume Lettre, Nicole Soranzo, Eric Boerwinkle, Kousik Kundu, Laura Almasy, Marsha M. Wheeler, Thomas W. Blackwell, Nancy Min, Nicholas L. Smith, Bruce M. Psaty, Lisa R. Yanek, Joanne E. Curran, Stacey Gabriel, Kathleen A. Ryan, Alanna C. Morrison, Lynette Ekunwe, Caitlin P. McHugh, Laura M. Raffield, Adam S. Butterworth, Deborah A. Nickerson, Ravindranath Duggirala, Gonçalo R. Abecasis, John Lane, Hélène Choquet, Andrew D. Johnson, Nauder Faraday, Russell T. Walton, Praveen Surendran, Jennifer A. Brody, Yao Hu, Alexander P. Reiner, Jerome I. Rotter, Donald M. Lloyd-Jones, Cathy C. Laurie, Zhe Wang, Hua Tang, Charles Kooperberg, Eric Jorgenson, Jeffrey R. O'Connell, Shuquan Rao, Nathalie Chami, Rasika A. Mathias, Matthew P. Conomos, Myriam Fornage, Ramachandran S. Vasan, Nathan Pankratz, Joshua P. Lewis, Lewis C. Becker, Benjamin P. Kleinstiver, Cecelia A. Laurie, Ming-Huei Chen, John Blangero

المصدر: Am J Hum Genet

مصطلحات موضوعية: Adult, Male, Quality Control, 0301 basic medicine, Erythrocytes, Population, Datasets as Topic, Genome-wide association study, Biology, Quantitative trait locus, Article, 03 medical and health sciences, 0302 clinical medicine, Genetics, Humans, Indel, education, Gene, Genetics (clinical), Aged, Genetic association, Gene Editing, Whole genome sequencing, education.field_of_study, Genetic Variation, Reproducibility of Results, Correction, Middle Aged, United States, Genetic architecture, HEK293 Cells, Phenotype, 030104 developmental biology, 030220 oncology & carcinogenesis, Female, National Heart, Lung, and Blood Institute (U.S.), Chromosomes, Human, Pair 16, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b87edb710dac1b94b0361a1b7107d06Test
https://doi.org/10.1016/j.ajhg.2021.04.003Test

المؤلفون: Saonli Basu, Lu-Chen Weng, Weihua Guan, Mary Cushman, Lyn M. Steffen, James S. Pankow, Aaron R. Folsom, Weihong Tang, Ming-Huei Chen, Nathan Pankratz

المصدر: Thrombosis Research. 168:53-59

مصطلحات موضوعية: Male, 0301 basic medicine, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Biology, Fibrinogen, Hemostatics, Article, 03 medical and health sciences, Fatty Acids, Omega-3, medicine, Humans, Genetic association, chemistry.chemical_classification, Genetics, Genetic Variation, Fatty acid, Genetic Pleiotropy, Hematology, Middle Aged, 030104 developmental biology, chemistry, Fatty Acids, Unsaturated, Female, Protein C, Polyunsaturated fatty acid, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c76d838735e51c979cfa7220235bb02Test
https://doi.org/10.1016/j.thromres.2018.05.032Test

المؤلفون: Tanika N. Kelly, May E Montasser, Alyna T. Khan, Laura M. Raffield, Carla Wilson, Elizabeth C. Oelsner, Kerri L. Wiggins, Ming-Huei Chen, Gina M. Peloso, Adolfo Correa, Andrew D. Johnson, Donna K. Arnett, Xiuqing Guo, Jai G. Broome, Daniel E. Weeks, Rebecca D. Jackson, Lucia Juarez, Stephen T. McGarvey, Pradeep Natarajan, Braxton D. Mitchell, Kent D. Taylor, Bruce M. Psaty, Santhi K Ganesh, Cathy C. Laurie, Nicola L. Hawley, Leslie S. Emery, Adrienne M. Stilp, Alanna C. Morrison, Jennifer A Smith, Charles Kooperberg, Catherine M. D’Augustine, Jan Graffelman, Paul S. de Vries, Chancellor Hohensee, Sharon L R Kardia, Patricia A Peyser, Wan-Ling Hsu, Erin J Buth, Kathleen C. Barnes, Susan R. Heckbert, Ramachandran S. Vasan, Nathan Pankratz, Karen M. Mutalik, Quenna Wong, Brian E. Cade, Jingmin Liu, Joshua C. Bis, Cecelia A. Laurie, Kari E. North, Fei Fei Wang, Mariza de Andrade, Nancy L. Heard-Costa, William Craig Johnson, L. Adrienne Cupples, Scott T. Weiss, Seyed Mehdi Nouraie, Patrick T. Ellinor, Jerome I. Rotter, Weiniu Gan, Shannon Kelly, Stephen S. Rich, Cashell E. Jaquish, Dongquan Chen, Nora Franceschini, Lisa R. Yanek, Jiwon Lee, Alexander P. Reiner, Megan L. Grove, Stella Aslibekyan, Myriam Fornage, Lawrence F Bielak, Rasika A. Mathias

المساهمون: Universitat Politècnica de Catalunya. Departament d'Estadística i Investigació Operativa, Universitat Politècnica de Catalunya. COSDA-UPC - COmpositional and Spatial Data Analysis

المصدر: UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
American Journal of Epidemiology
American journal of epidemiology, vol 190, iss 10

مصطلحات موضوعية: 0301 basic medicine, Program evaluation, Computer science, Epidemiology, common data elements, hematologic disease, Matemàtiques i estadística::Matemàtica aplicada a les ciències [Àrees temàtiques de la UPC], Medical and Health Sciences, Mathematical Sciences, 0302 clinical medicine, Documentation, cardiovascular disease, and Blood Institute (U.S.), 030212 general & internal medicine, Phenomics, Precision Medicine, Lung, lung diseases, Sleep-wake disorders, phenotypes, 92 Biology and other natural sciences::92B Mathematical biology in general [Classificació AMS], Common data elements, Cardiovascular disease, Phenotype, Phenotypes, Biomatemàtica, Information Dissemination, Harmonization, 62 Statistics::62D05 Sampling theory, sample surveys [Classificació AMS], Hematologic disease, 03 medical and health sciences, Data Aggregation, Clinical Research, Controlled vocabulary, Genetics, Humans, AcademicSubjects/MED00860, sleep-wake disorders, Sampling (Statistics), Genetic Association Studies, Lung diseases, Biomathematics, Data collection, Study Design, Matemàtiques i estadística::Estadística aplicada::Estadística biosanitària [Àrees temàtiques de la UPC], Information dissemination, Human Genome, National Heart, Precision medicine, Data science, United States, 030104 developmental biology, Good Health and Well Being, National Heart, Lung, and Blood Institute (U.S.), Mostreig (Estadística), Program Evaluation

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0380088474cfe1cc5218a3fad8da984aTest
http://hdl.handle.net/2117/359840Test

المؤلفون: Yoav Ben-Shlomo, Ming-Huei Chen, Peter Creighton Elwood, Arunoday Bhan, Mete Civelek, FinnGen Study, David-Alexandre Trégouët, Veikko Salomaa, Benjamin Rodriguez, Teemu J. Niiranen, Thorsten M. Schlaeger, Andrew D. Johnson, Andrew D Beswick, Pierre-Emmanuel Morange

المساهمون: Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

المصدر: American Journal of Human Genetics
American Journal of Human Genetics, Elsevier (Cell Press), In press, 107 (2), pp.211-221. ⟨10.1016/j.ajhg.2020.06.008⟩
American Journal of Human Genetics, In press, 107 (2), pp.211-221. ⟨10.1016/j.ajhg.2020.06.008⟩
Am J Hum Genet
Rodriguez, B A T, Bhan, A, Beswick, A, Elwood, P C, Niiranen, T J, Salomaa, V, Trégouët, D-A, Morange, P-E, Civelek, M, Ben-Shlomo, Y, Schlaeger, T, Chen, M-H & Johnson, A D 2020, ' A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2020.06.008Test

مصطلحات موضوعية: 0301 basic medicine, Male, Platelet Aggregation, Embolism, Genome-wide association study, 030204 cardiovascular system & hematology, Pharmacology, 0302 clinical medicine, Megakaryocyte, Cardiovascular Disease, Neoplasms, Medicine, Platelet, Receptor, Lung, Genetics (clinical), Thrombin, Middle Aged, thrombin, stroke, 3. Good health, Stroke, medicine.anatomical_structure, VINTAGE, Cardiovascular Diseases, Female, medicine.drug, Signal Transduction, Platelets, Blood Platelets, venous thromboembolism, eQTL, GWA, Article, 03 medical and health sciences, Downregulation and upregulation, Mendelian randomization, Genetics, Humans, Receptor, PAR-1, Platelet activation, thrombosis, Alleles, Heart Failure, business.industry, Platelet Activation, 030104 developmental biology, Receptors, Thrombin, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, business, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ed6f4d72d2a9d16e1e20ed0efb7eff0Test
https://hal.archives-ouvertes.fr/hal-03141739Test

المؤلفون: Melissa E. Garcia, Majken K. Jensen, Margaux F. Keller, Joachim H. Ix, Richard A. Jensen, Vasan S. Ramachandran, Jie Yao, Kenneth J. Mukamal, Anne B. Newman, Tamara B. Harris, Frank B. Hu, Ming-Huei Chen, Jorge R. Kizer, Bruce M. Psaty, Alice M. Arnold, James S. Pankow, Jerome I. Rotter, Ronit Katz, Luc Djoussé, David S. Siscovick, Xiuqing Guo, Mike A. Nalls, Ida Chen, Yongmei Liu, Ron C. Hoogeveen, Qi Sun, Eric B. Rimm, Mark O. Goodarzi, Marilyn C. Cornelis, Joseph M. Zmuda, Kathryn M. Rexrode

المصدر: Human molecular genetics, vol 26, iss 11

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Genotype, alpha-2-HS-Glycoprotein, Population, 030209 endocrinology & metabolism, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Medical and Health Sciences, White People, 03 medical and health sciences, Exon, 0302 clinical medicine, Diabetes Mellitus, Genetics, Humans, 2.1 Biological and endogenous factors, SNP, Polymorphism, Aetiology, education, Molecular Biology, Gene, Metabolic and endocrine, Genetics (clinical), Aged, Metabolic Syndrome, Genetics & Heredity, education.field_of_study, Association Studies Articles, Human Genome, Single Nucleotide, General Medicine, Middle Aged, Biological Sciences, Black or African American, 030104 developmental biology, Diabetes Mellitus, Type 2, Genetic Loci, Female, Type 2, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fb5b598bf38b9e518ce5be416e1c53fTest
https://doi.org/10.1093/hmg/ddx091Test

المؤلفون: Kyung Ae Ko, Craig N. Morrell, Christopher J. O'Donnell, Sara Ture, Joseph M. Miano, Qiuyu Martin Zhu, Andrew D. Johnson, Michael A. Mastrangelo, Ming-Huei Chen, Charles J. Lowenstein

المصدر: Arteriosclerosis, Thrombosis, and Vascular Biology. 37:264-270

مصطلحات موضوعية: Blood Platelets, 0301 basic medicine, Genotype, CRISPR-Associated Proteins, Down-Regulation, Mice, Transgenic, Nerve Tissue Proteins, Locus (genetics), Single-nucleotide polymorphism, Genome-wide association study, 030204 cardiovascular system & hematology, Polymorphism, Single Nucleotide, Exocytosis, Article, R-SNARE Proteins, 03 medical and health sciences, 0302 clinical medicine, Von Willebrand factor, von Willebrand Factor, Animals, Humans, SNP, CRISPR, Clustered Regularly Interspaced Short Palindromic Repeats, Platelet activation, Blood Coagulation, Gene Editing, Genetics, biology, Thrombosis, Platelet Activation, Minor allele frequency, Disease Models, Animal, Phenotype, 030104 developmental biology, biology.protein, CRISPR-Cas Systems, Cardiology and Cardiovascular Medicine, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8119394b5318104d43798d132610da0eTest
https://doi.org/10.1161/atvbaha.116.308614Test

المؤلفون: Nauder Faraday, Lisa R. Yanek, Richard A. Gibbs, Narayanan Veeraraghavan, Rasika A. Mathias, John D. Eicher, Lewis C. Becker, Eric Boerwinkle, Jennifer A. Brody, Honghuang Lin, Donna M. Muzny, L. Adrienne Cupples, Ginger A. Metcalf, Andrew D. Johnson, Diane M. Becker, Achilleas N. Pitsillides, Ming-Huei Chen

المصدر: Thrombosis and Haemostasis. 117:1083-1092

مصطلحات موضوعية: Adult, Blood Platelets, Male, 0301 basic medicine, Epinephrine, Genotype, Platelet Aggregation, Population, Hyaluronoglucosaminidase, Disease, Gene mutation, GSTZ1, Biology, GPI-Linked Proteins, Cohort Studies, 03 medical and health sciences, Framingham Heart Study, Population Groups, Exome Sequencing, Humans, Missense mutation, Exome, education, Gene, Alleles, Exome sequencing, Genetics, education.field_of_study, Polymorphism, Genetic, Membrane Proteins, Hematology, Middle Aged, Phosphoproteins, Adenosine Diphosphate, Protein Transport, 030104 developmental biology, Massachusetts, Cardiovascular Diseases, Mutation, Female, Cell Adhesion Molecules

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53a7304d7a29263b018de9266acd175cTest
https://doi.org/10.1160/th16-09-0677Test

المؤلفون: Robert Kraaij, Teresa Nutile, Peter Vollenweider, Cassianne Robinson-Cohen, Caroline S. Fox, André G. Uitterlinden, Sanaz Sedaghat, Cornelia M. van Duijn, Alanna C. Morrison, Meng Li, Bing Yu, Sahar Ghasemi, Zoltán Kutalik, Eric Boerwinkle, Alexanda Teumer, Jeroen van Rooij, Qiong Yang, Audrey Y. Chu, Jennifer E. Huffman, Bruce M. Psaty, Jun Liu, Najaf Amin, Jennifer A. Brody, Adrienne Tin, Rossella Sorice, Ming-Huei Chen, Marina Ciullo, Anna Köttgen, Yong Li, Ayse Demirkan, Owen M. Woodward, Melody Swen, Abbas Dehghan, Aurélien Macé, Barbara McKnight

المساهمون: Epidemiology, Internal Medicine

المصدر: Nature Communications
Nature communications 9 (2018). doi:10.1038/s41467-018-06620-4
info:cnr-pdr/source/autori:Tin A.; Li Y.; Brody J.A.; Nutile T.; Chu A.Y.; Huffman J.E.; Yang Q.; Chen M.-H.; Robinson-Cohen C.; Mace A.; Liu J.; Demirkan A.; Sorice R.; Sedaghat S.; Swen M.; Yu B.; Ghasemi S.; Teumer A.; Vollenweider P.; Ciullo M.; Li M.; Uitterlinden A.G.; Kraaij R.; Amin N.; van Rooij J.; Kutalik Z.; Dehghan A.; McKnight B.; van Duijn C.M.; Morrison A.; Psaty B.M.; Boerwinkle E.; Fox C.S.; Woodward O.M.; Kottgen A./titolo:Large-scale whole-exome sequencing association studies identify rare functional variants influencing serum urate levels/doi:10.1038%2Fs41467-018-06620-4/rivista:Nature communications/anno:2018/pagina_da:/pagina_a:/intervallo_pagine:/volume:9
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
Nature Communications, 9:4228. Nature Publishing Group
Nature communications, vol. 9, no. 1, pp. 4228

مصطلحات موضوعية: 0301 basic medicine, Organic Cation Transport Proteins, Science, Glucose Transport Proteins, Facilitative, General Physics and Astronomy, Organic Anion Transporters, Genome-wide association study, Disease, Bioinformatics, Kidney Function Tests, General Biochemistry, Genetics and Molecular Biology, Article, Protein Structure, Secondary, 03 medical and health sciences, chemistry.chemical_compound, Exome/genetics, Genetic Predisposition to Disease, Glucose Transport Proteins, Facilitative/chemistry, Glucose Transport Proteins, Facilitative/genetics, Glucose Transport Proteins, Facilitative/metabolism, Humans, Meta-Analysis as Topic, Organic Anion Transporters/chemistry, Organic Anion Transporters/genetics, Organic Anion Transporters/metabolism, Organic Cation Transport Proteins/chemistry, Organic Cation Transport Proteins/genetics, Organic Cation Transport Proteins/metabolism, Uric Acid/blood, MD Multidisciplinary, medicine, Exome, lcsh:Science, Exome sequencing, Genetic association, Multidisciplinary, biology, business.industry, Lesinurad, serum urate levels, General Chemistry, medicine.disease, 3. Good health, Gout, Uric Acid, 030104 developmental biology, chemistry, biology.protein, SLC22A12, lcsh:Q, business, SLC2A9

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09617704df3edc2b2becb350d2b1af49Test
https://doi.org/10.1038/s41467-018-06620-4Test

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: 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 Genetics

مصطلحات 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

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d29acca27b4a34b35a3f588b7f78da1Test
https://pure.eur.nl/en/publications/1465b06f-411f-49c0-a589-3e97bc2a5f08Test