المؤلفون: Nathan Pankratz, Peng Wei, Jennifer A Brody, Ming-Huei Chen, Paul S de Vries, Jennifer E Huffman, Mary Rachel Stimson, Paul L Auer, Eric Boerwinkle, Mary Cushman, Moniek P M de Maat, Aaron R Folsom, Oscar H Franco, Richard A Gibbs, Kelly K Haagenson, Albert Hofman, Jill M Johnsen, Christie L Kovar, Robert Kraaij, Barbara McKnight, Ginger A Metcalf, Donna Muzny, Bruce M Psaty, Weihong Tang, André G Uitterlinden, Jeroen G J van Rooij, Abbas Dehghan, Christopher J O'Donnell, Alex P Reiner, Alanna C Morrison, Nicholas L Smith

المصدر: Hum Mol Genet

مصطلحات موضوعية: Factor VIII, Exome Sequencing, von Willebrand Factor, Genetics, Fibrinogen, Humans, Original Article, General Medicine, Factor VII, Polymorphism, Single Nucleotide, Molecular Biology, Hemostatics, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02a7d75c79ba75f31f58b4ffc1eb8bf6Test
https://doi.org/10.1093/hmg/ddac100Test

المؤلفون: Nicholas L. Smith, James A. Perry, Cecelia A. Laurie, Nancy J. Cox, Gonçalo R. Abecasis, Jerome I. Rotter, Laura Almasy, Zhe Wang, Michelle Daya, Yun Li, Eric Jorgenson, Adolfo Correa, Jai G. Broome, Nancy Min, Lisa R. Yanek, Alanna C. Morrison, Lynette Ekunwe, Debby Ngo, Victor E. Ortega, Klaudia Walter, John Blangero, Laura M. Raffield, Corey Cox, Terri H. Beaty, Deborah A. Meyers, Hua Tang, Marsha M. Wheeler, Kari E. North, Xue Zhong, Yann Ilboudo, Andrew D. Johnson, Caitlin P. McHugh, Jeffrey R. O'Connell, Ming-Huei Chen, Russell P. Tracy, Ramachandran S. Vasan, Nathan Pankratz, Joshua P. Lewis, Dawn L. DeMeo, Linda M. Polfus, Leslie A. Lange, Nancy L. Heard-Costa, Robert C. Kaplan, Meher Preethi Boorgula, Robert E. Gerszten, Albert V. Smith, Paul L. Auer, Sameer Chavan, Jennifer A. Brody, Charles Kooperberg, Michael Preuss, David C. Glahn, Rasika A. Mathias, Paul S. de Vries, Jonathon Rosen, Anna V. Mikhaylova, Joe Zein, Eric Boerwinkle, Nathalie Chami, Kathleen C. Barnes, Joanne E. Curran, Edwin K. Silverman, Matthew P. Conomos, Stephen S. Rich, Nicole Soranzo, Heather M. Highland, Michael H. Cho, Donald M. Lloyd-Jones, Myriam Fornage, Guillaume Lettre, Tyne W Miller-Fleming, Kathleen A. Ryan, Thomas W. Blackwell, Bruce M. Psaty, Lewis C. Becker, Nauder Faraday, Hélène Choquet, Alexander P. Reiner, Adam S. Butterworth, Kousik Kundu, Deepti Jain, Timothy A. Thornton, Brian D. Hobbs, Braxton D. Mitchell, Jee-Young Moon, Lifang Hou, Ani Manichaikul, Praveen Surendran, Suraj S. Nongmaithem, Quan Sun, Bingshan Li, Deborah A. Nickerson, Ruth J. F. Loos

المصدر: Am J Hum Genet

مصطلحات موضوعية: Proteome, Quantitative Trait Loci, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Article, Dermatitis, Atopic, Pulmonary Disease, Chronic Obstructive, Leukocytes, Genetics, medicine, Humans, Genetic Predisposition to Disease, Gene, Genetics (clinical), X chromosome, Genetic association, Whole genome sequencing, Autosome, Whole Genome Sequencing, Genome, Human, Monocyte, Prognosis, Asthma, United Kingdom, United States, Phenotype, medicine.anatomical_structure, National Heart, Lung, and Blood Institute (U.S.), Biomarkers, Imputation (genetics), Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51cbe1c35e5654539a7823886e9881b7Test
https://doi.org/10.1016/j.ajhg.2021.08.007Test

المؤلفون: Nauder Faraday, Brian D. Hobbs, Quan Sun, Michael Preuss, Ani Manichaikul, Eric Jorgenson, Ming-Huei Chen, Eric Boerwinkle, Florian Thibord, Arunoday Bhan, Alanna C. Morrison, Ramachandran S. Vasan, Nathan Pankratz, Charles Kooperberg, Deborah A. Nickerson, Joshua P. Lewis, Hélène Choquet, Jee-Young Moon, Jeffrey R. O'Connell, Marsha M. Wheeler, Albert V. Smith, Russell P. Tracy, Nathalie Chami, Ruth J. F. Loos, Alexander P. Reiner, Nicholas L. Smith, Gonçalo R. Abecasis, Laura M. Raffield, Amarise Little, Nancy L. Heard-Costa, Andrew D. Johnson, David C. Glahn, Rasika A. Mathias, Adam S. Butterworth, John Blangero, Joanne E. Curran, Timothy A. Thornton, Laura Almasy, Jerome I. Rotter, Nancy Min, Lisa R. Yanek, Donald M. Lloyd-Jones, Zhe Wang, Matthew P. Conomos, Myriam Fornage, Hua Tang, Lewis C. Becker, Lynette Ekunwe, Cecelia A. Laurie, Adolfo Correa, Jai G. Broome, Terri H. Beaty, Jennifer A. Brody, Caitlin P. McHugh, Yao Hu, Braxton D. Mitchell, Lifang Hou, Yun Li, Kathleen A. Ryan, Paul L. Auer, Stephen S. Rich, Kari E. North, Thomas W. Blackwell, Bruce M. Psaty, Deepti Jain, Paul S Vries, Praveen Surendran

المساهمون: Butterworth, Adam [0000-0002-6915-9015], Apollo - University of Cambridge Repository

المصدر: Human molecular genetics, vol 31, iss 3
Hum Mol Genet

مصطلحات موضوعية: Blood Platelets, Platelet disorder, Population, Genome-wide association study, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, Medical and Health Sciences, Genome, 03 medical and health sciences, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, 0302 clinical medicine, Clinical Research, and Blood Institute (U.S.), Genetics, Humans, 2.1 Biological and endogenous factors, Polymorphism, Precision Medicine, Aetiology, Mean platelet volume, education, Hemostatic function, Lung, Molecular Biology, Genetics (clinical), 030304 developmental biology, Blood Platelet Disorders, Genetics & Heredity, 0303 health sciences, education.field_of_study, Human Genome, Single Nucleotide, National Heart, Hematology, General Medicine, Biological Sciences, United States, 3. Good health, Phenotype, Good Health and Well Being, 030220 oncology & carcinogenesis, General Article, National Heart, Lung, and Blood Institute (U.S.), Genome-Wide Association Study, Biotechnology

وصف الملف: application/pdf; application/octet-stream

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc9557e325812482460ef4586ad1a77Test
https://doi.org/10.1093/hmg/ddab252Test

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: Florian Thibord, Melissa V. Chan, Ming-Huei Chen, Andrew D. Johnson

المصدر: HGG advances. 3(2)

مصطلحات موضوعية: Molecular Medicine, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cbdfd4b7c973f03150e1eb323ff6743Test
https://pubmed.ncbi.nlm.nih.gov/35224516Test

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: 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

المؤلفون: Raha Pazoki, Nora Franceschini, James S. Floyd, Guillaume Lettre, Fernando Rivadeneira, Abbas Dehghan, Leo-Pekka Lyytikäinen, Albert Hofman, Ming-Huei Chen, Eric Boerwinkle, Jill M. Johnsen, Mart Kals, Xiaoling Zhang, Lewis C. Becker, Jennifer A. Brody, Dennis O. Mook-Kanamori, Lu Chen, James G. Wilson, Rajiv K. Khajuria, Vijay G. Sankaran, Nathan Pankratz, Lisa R. Yanek, Leslie A. Lange, Mika Kähönen, Linda M. Polfus, Traci M. Bartz, Nena Matijevic, Oscar H. Franco, Donna M. Muzny, Keolu Fox, Richard A. Gibbs, Narayanan Veeraraghavan, Tõnu Esko, Aoi Wakabayashi, Gina M. Peloso, André G. Uitterlinden, Paul L. Auer, Frank J. A. van Rooij, Kenneth Rice, Santhi K. Ganesh, Terho Lehtimäki, Klaudia Walter, Ruifang Li-Gao, Ginger A. Metcalf, Jie Huang, Stephen S. Rich, Cornelia M. van Duijn, Nicole Soranzo, Bruce M. Psaty, Robert B. Wallace, Ursula M. Schick, Andres Metspalu, Olli T. Raitakari, Christopher J. O'Donnell, Alexander P. Reiner, Andrew D. Johnson

المساهمون: Epidemiology, Internal Medicine

المصدر: The American Journal of Human Genetics
American Journal of Human Genetics, 99(2), 481-488
American Journal of Human Genetics, 99(2), 481-488. Cell Press

مصطلحات موضوعية: 0301 basic medicine, Blood Platelets, Megakaryocyte differentiation, DNA Mutational Analysis, 030204 cardiovascular system & hematology, Biology, Blood cell, 03 medical and health sciences, 0302 clinical medicine, Proto-Oncogene Proteins, Report, medicine, Genetics, CRISPR, Humans, splice, Exome, Genetics(clinical), Progenitor cell, Genetics (clinical), Exome sequencing, Gene Editing, Platelet Count, Alternative splicing, Correction, ta3121, Hematopoietic Stem Cells, Human genetics, 3. Good health, Hematopoiesis, Repressor Proteins, Haematopoiesis, Alternative Splicing, 030104 developmental biology, medicine.anatomical_structure, Genetic Loci, CRISPR-Cas Systems, Megakaryocytes

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4f6d80589b1a4bd405fc06eccbc542Test
http://juuli.fi/Record/0252259916Test

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 Press

مصطلحات 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

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353c5b69e7bcc0868f5061124262a3d4Test
https://pure.eur.nl/en/publications/ef09e5cb-1bbc-4be2-9236-e4b21d7864c7Test