المؤلفون: Patel, Roshni A, Musharoff, Shaila A, Spence, Jeffrey P, Pimentel, Harold, Tcheandjieu, Catherine, Mostafavi, Hakhamanesh, Sinnott-Armstrong, Nasa, Clarke, Shoa L, Smith, Courtney J, Program, VA Million Veteran, Durda, Peter P, Taylor, Kent D, Tracy, Russell, Liu, Yongmei, Johnson, W Craig, Aguet, Francois, Ardlie, Kristin G, Gabriel, Stacey, Smith, Josh, Nickerson, Deborah A, Rich, Stephen S, Rotter, Jerome I, Tsao, Philip S, Assimes, Themistocles L, Pritchard, Jonathan K

المصدر: American Journal of Human Genetics. 109(7)

مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Atherosclerosis, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Cholesterol, LDL, Gene Expression, Genome-Wide Association Study, Humans, Multifactorial Inheritance, Polymorphism, Single Nucleotide, White People, V.A. Million Veteran Program, complex traits, genetic correlation, genome-wide association, population genetics, statistical genetics, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/11p81474Test

المؤلفون: Spracklen, Cassandra N, Karaderi, Tugce, Yaghootkar, Hanieh, Schurmann, Claudia, Fine, Rebecca S, Kutalik, Zoltan, Preuss, Michael H, Lu, Yingchang, Wittemans, Laura BL, Adair, Linda S, Allison, Matthew, Amin, Najaf, Auer, Paul L, Bartz, Traci M, Blüher, Matthias, Boehnke, Michael, Borja, Judith B, Bork-Jensen, Jette, Broer, Linda, Chasman, Daniel I, Chen, Yii-Der Ida, Chirstofidou, Paraskevi, Demirkan, Ayse, van Duijn, Cornelia M, Feitosa, Mary F, Garcia, Melissa E, Graff, Mariaelisa, Grallert, Harald, Grarup, Niels, Guo, Xiuqing, Haesser, Jeffrey, Hansen, Torben, Harris, Tamara B, Highland, Heather M, Hong, Jaeyoung, Ikram, M Arfan, Ingelsson, Erik, Jackson, Rebecca, Jousilahti, Pekka, Kähönen, Mika, Kizer, Jorge R, Kovacs, Peter, Kriebel, Jennifer, Laakso, Markku, Lange, Leslie A, Lehtimäki, Terho, Li, Jin, Li-Gao, Ruifang, Lind, Lars, Luan, Jian'an, Lyytikäinen, Leo-Pekka, MacGregor, Stuart, Mackey, David A, Mahajan, Anubha, Mangino, Massimo, Männistö, Satu, McCarthy, Mark I, McKnight, Barbara, Medina-Gomez, Carolina, Meigs, James B, Molnos, Sophie, Mook-Kanamori, Dennis, Morris, Andrew P, de Mutsert, Renee, Nalls, Mike A, Nedeljkovic, Ivana, North, Kari E, Pennell, Craig E, Pradhan, Aruna D, Province, Michael A, Raitakari, Olli T, Raulerson, Chelsea K, Reiner, Alex P, Ridker, Paul M, Ripatti, Samuli, Roberston, Neil, Rotter, Jerome I, Salomaa, Veikko, Sandoval-Zárate, America A, Sitlani, Colleen M, Spector, Tim D, Strauch, Konstantin, Stumvoll, Michael, Taylor, Kent D, Thuesen, Betina, Tönjes, Anke, Uitterlinden, Andre G, Venturini, Cristina, Walker, Mark, Wang, Carol A, Wang, Shuai, Wareham, Nicholas J, Willems, Sara M, Willems van Dijk, Ko, Wilson, James G, Wu, Ying, Yao, Jie, Young, Kristin L, Langenberg, Claudia, Frayling, Timothy M

المصدر: American Journal of Human Genetics. 105(1)

مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Human Genome, Nutrition, Obesity, 2.1 Biological and endogenous factors, Aetiology, Metabolic and endocrine, Cardiovascular, Adiponectin, Adipose Tissue, Adolescent, Adult, Black or African American, Aged, Aged, 80 and over, Exome, Female, Genetic Predisposition to Disease, Hispanic or Latino, Humans, Lipids, Male, Middle Aged, Phenotype, Polymorphism, Single Nucleotide, Quantitative Trait Loci, White People, Young Adult, adiponectin, cardio metabolic traits, exome, genetics, genome-wide association study, lipids, obesity, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/12167122Test

المؤلفون: Tajuddin, Salman M, Schick, Ursula M, Eicher, John D, Chami, Nathalie, Giri, Ayush, Brody, Jennifer A, Hill, W David, Kacprowski, Tim, Li, Jin, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Mihailov, Evelin, O’Donoghue, Michelle L, Pankratz, Nathan, Pazoki, Raha, Polfus, Linda M, Smith, Albert Vernon, Schurmann, Claudia, Vacchi-Suzzi, Caterina, Waterworth, Dawn M, Evangelou, Evangelos, Yanek, Lisa R, Burt, Amber, Chen, Ming-Huei, van Rooij, Frank JA, Floyd, James S, Greinacher, Andreas, Harris, Tamara B, Highland, Heather M, Lange, Leslie A, Liu, Yongmei, Mägi, Reedik, Nalls, Mike A, Mathias, Rasika A, Nickerson, Deborah A, Nikus, Kjell, Starr, John M, Tardif, Jean-Claude, Tzoulaki, Ioanna, Edwards, Digna R Velez, Wallentin, Lars, Bartz, Traci M, Becker, Lewis C, Denny, Joshua C, Raffield, Laura M, Rioux, John D, Friedrich, Nele, Fornage, Myriam, Gao, He, Hirschhorn, Joel N, Liewald, David CM, Rich, Stephen S, Uitterlinden, Andre, Bastarache, Lisa, Becker, Diane M, Boerwinkle, Eric, de Denus, Simon, Bottinger, Erwin P, Hayward, Caroline, Hofman, Albert, Homuth, Georg, Lange, Ethan, Launer, Lenore J, Lehtimäki, Terho, Lu, Yingchang, Metspalu, Andres, O’Donnell, Chris J, Quarells, Rakale C, Richard, Melissa, Torstenson, Eric S, Taylor, Kent D, Vergnaud, Anne-Claire, Zonderman, Alan B, Crosslin, David R, Deary, Ian J, Dörr, Marcus, Elliott, Paul, Evans, Michele K, Gudnason, Vilmundur, Kähönen, Mika, Psaty, Bruce M, Rotter, Jerome I, Slater, Andrew J, Dehghan, Abbas, White, Harvey D, Ganesh, Santhi K, Loos, Ruth JF, Esko, Tõnu, Faraday, Nauder, Wilson, James G, Cushman, Mary, Johnson, Andrew D, Edwards, Todd L, Zakai, Neil A, Lettre, Guillaume, Reiner, Alex P, Auer, Paul L

المصدر: American Journal of Human Genetics. 99(1)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Immunology, Stem Cell Research, Human Genome, Stem Cell Research - Nonembryonic - Non-Human, Autoimmune Disease, Hematology, 2.1 Biological and endogenous factors, 1.1 Normal biological development and functioning, Underpinning research, Aetiology, Inflammatory and immune system, Blood Cell Count, Exome, Genetic Loci, Genetic Pleiotropy, Genome-Wide Association Study, Humans, Immune System Diseases, Leukocytes, Quality Control, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/77z9z6drTest

المؤلفون: Liu, Ching-Ti, Raghavan, Sridharan, Maruthur, Nisa, Kabagambe, Edmond Kato, Hong, Jaeyoung, Ng, Maggie CY, Hivert, Marie-France, Lu, Yingchang, An, Ping, Bentley, Amy R, Drolet, Anne M, Gaulton, Kyle J, Guo, Xiuqing, Armstrong, Loren L, Irvin, Marguerite R, Li, Man, Lipovich, Leonard, Rybin, Denis V, Taylor, Kent D, Agyemang, Charles, Palmer, Nicholette D, Cade, Brian E, Chen, Wei-Min, Dauriz, Marco, Delaney, Joseph AC, Edwards, Todd L, Evans, Daniel S, Evans, Michele K, Lange, Leslie A, Leong, Aaron, Liu, Jingmin, Liu, Yongmei, Nayak, Uma, Patel, Sanjay R, Porneala, Bianca C, Rasmussen-Torvik, Laura J, Snijder, Marieke B, Stallings, Sarah C, Tanaka, Toshiko, Yanek, Lisa R, Zhao, Wei, Becker, Diane M, Bielak, Lawrence F, Biggs, Mary L, Bottinger, Erwin P, Bowden, Donald W, Chen, Guanjie, Correa, Adolfo, Couper, David J, Crawford, Dana C, Cushman, Mary, Eicher, John D, Fornage, Myriam, Franceschini, Nora, Fu, Yi-Ping, Goodarzi, Mark O, Gottesman, Omri, Hara, Kazuo, Harris, Tamara B, Jensen, Richard A, Johnson, Andrew D, Jhun, Min A, Karter, Andrew J, Keller, Margaux F, Kho, Abel N, Kizer, Jorge R, Krauss, Ronald M, Langefeld, Carl D, Li, Xiaohui, Liang, Jingling, Liu, Simin, Lowe, William L, Mosley, Thomas H, North, Kari E, Pacheco, Jennifer A, Peyser, Patricia A, Patrick, Alan L, Rice, Kenneth M, Selvin, Elizabeth, Sims, Mario, Smith, Jennifer A, Tajuddin, Salman M, Vaidya, Dhananjay, Wren, Mary P, Yao, Jie, Zhu, Xiaofeng, Ziegler, Julie T, Zmuda, Joseph M, Zonderman, Alan B, Zwinderman, Aeilko H, Consortium, AAAG, Consortium, CARe, Consortium, COGENT-BP, Consortium, eMERGE, Consortium, MEDIA, Adeyemo, Adebowale, Boerwinkle, Eric, Ferrucci, Luigi, Hayes, M Geoffrey, Kardia, Sharon LR

المصدر: American Journal of Human Genetics. 99(1)

مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Health Disparities, Human Genome, Diabetes, Minority Health, Metabolic and endocrine, Asian People, Black People, Blood Glucose, Diabetes Mellitus, Type 2, Enhancer Elements, Genetic, Ethnicity, Fasting, Female, Gene Frequency, Genome-Wide Association Study, Humans, Insulin, Insulin Resistance, Introns, Islets of Langerhans, Male, Molecular Sequence Annotation, Polymorphism, Single Nucleotide, Quantitative Trait Loci, Racial Groups, Transcription Factors, White People, AAAG Consortium, CARe Consortium, COGENT-BP Consortium, eMERGE Consortium, MEDIA Consortium, MAGIC Consortium, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/5wj692mgTest
https://escholarship.org/content/qt5wj692mg/qt5wj692mg.pdfTest

المؤلفون: Chami, Nathalie, Chen, Ming-Huei, Slater, Andrew J, Eicher, John D, Evangelou, Evangelos, Tajuddin, Salman M, Love-Gregory, Latisha, Kacprowski, Tim, Schick, Ursula M, Nomura, Akihiro, Giri, Ayush, Lessard, Samuel, Brody, Jennifer A, Schurmann, Claudia, Pankratz, Nathan, Yanek, Lisa R, Manichaikul, Ani, Pazoki, Raha, Mihailov, Evelin, Hill, W David, Raffield, Laura M, Burt, Amber, Bartz, Traci M, Becker, Diane M, Becker, Lewis C, Boerwinkle, Eric, Bork-Jensen, Jette, Bottinger, Erwin P, O’Donoghue, Michelle L, Crosslin, David R, de Denus, Simon, Dubé, Marie-Pierre, Elliott, Paul, Engström, Gunnar, Evans, Michele K, Floyd, James S, Fornage, Myriam, Gao, He, Greinacher, Andreas, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hayward, Caroline, Hernesniemi, Jussi, Highland, Heather M, Hirschhorn, Joel N, Hofman, Albert, Irvin, Marguerite R, Kähönen, Mika, Lange, Ethan, Launer, Lenore J, Lehtimäki, Terho, Li, Jin, Liewald, David CM, Linneberg, Allan, Liu, Yongmei, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Mägi, Reedik, Mathias, Rasika A, Melander, Olle, Metspalu, Andres, Mononen, Nina, Nalls, Mike A, Nickerson, Deborah A, Nikus, Kjell, O’Donnell, Chris J, Orho-Melander, Marju, Pedersen, Oluf, Petersmann, Astrid, Polfus, Linda, Psaty, Bruce M, Raitakari, Olli T, Raitoharju, Emma, Richard, Melissa, Rice, Kenneth M, Rivadeneira, Fernando, Rotter, Jerome I, Schmidt, Frank, Smith, Albert Vernon, Starr, John M, Taylor, Kent D, Teumer, Alexander, Thuesen, Betina H, Torstenson, Eric S, Tracy, Russell P, Tzoulaki, Ioanna, Zakai, Neil A, Vacchi-Suzzi, Caterina, van Duijn, Cornelia M, van Rooij, Frank JA, Cushman, Mary, Deary, Ian J, Edwards, Digna R Velez, Vergnaud, Anne-Claire, Wallentin, Lars, Waterworth, Dawn M, White, Harvey D, Wilson, James G, Zonderman, Alan B

المصدر: American Journal of Human Genetics. 99(1)

مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Rare Diseases, Hematology, Human Genome, Clinical Research, 2.1 Biological and endogenous factors, Aetiology, Black or African American, Allelic Imbalance, Erythrocyte Indices, Erythrocytes, Erythropoiesis, Exome, Gene Frequency, Genetic Pleiotropy, Genetic Variation, Genotype, Hematocrit, Hemoglobins, Humans, Quantitative Trait Loci, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3207t3drTest

المؤلفون: Schick, Ursula M, Jain, Deepti, Hodonsky, Chani J, Morrison, Jean V, Davis, James P, Brown, Lisa, Sofer, Tamar, Conomos, Matthew P, Schurmann, Claudia, McHugh, Caitlin P, Nelson, Sarah C, Vadlamudi, Swarooparani, Stilp, Adrienne, Plantinga, Anna, Baier, Leslie, Bien, Stephanie A, Gogarten, Stephanie M, Laurie, Cecelia A, Taylor, Kent D, Liu, Yongmei, Auer, Paul L, Franceschini, Nora, Szpiro, Adam, Rice, Ken, Kerr, Kathleen F, Rotter, Jerome I, Hanson, Robert L, Papanicolaou, George, Rich, Stephen S, Loos, Ruth JF, Browning, Brian L, Browning, Sharon R, Weir, Bruce S, Laurie, Cathy C, Mohlke, Karen L, North, Kari E, Thornton, Timothy A, Reiner, Alex P

المصدر: American Journal of Human Genetics. 98(2)

مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Clinical Research, Hematology, Underpinning research, 1.1 Normal biological development and functioning, Blood, Actinin, Adolescent, Adult, Aged, Alleles, Gene Frequency, Genetic Association Studies, Genetic Loci, Genotype, Genotyping Techniques, Hispanic or Latino, Humans, MEF2 Transcription Factors, Membrane Proteins, Middle Aged, Phenotype, Platelet Count, Polymorphism, Single Nucleotide, Receptors, GABA-B, Young Adult, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/35t0h7p6Test

المؤلفون: Peloso, Gina M, Auer, Paul L, Bis, Joshua C, Voorman, Arend, Morrison, Alanna C, Stitziel, Nathan O, Brody, Jennifer A, Khetarpal, Sumeet A, Crosby, Jacy R, Fornage, Myriam, Isaacs, Aaron, Jakobsdottir, Johanna, Feitosa, Mary F, Davies, Gail, Huffman, Jennifer E, Manichaikul, Ani, Davis, Brian, Lohman, Kurt, Joon, Aron Y, Smith, Albert V, Grove, Megan L, Zanoni, Paolo, Redon, Valeska, Demissie, Serkalem, Lawson, Kim, Peters, Ulrike, Carlson, Christopher, Jackson, Rebecca D, Ryckman, Kelli K, Mackey, Rachel H, Robinson, Jennifer G, Siscovick, David S, Schreiner, Pamela J, Mychaleckyj, Josyf C, Pankow, James S, Hofman, Albert, Uitterlinden, Andre G, Harris, Tamara B, Taylor, Kent D, Stafford, Jeanette M, Reynolds, Lindsay M, Marioni, Riccardo E, Dehghan, Abbas, Franco, Oscar H, Patel, Aniruddh P, Lu, Yingchang, Hindy, George, Gottesman, Omri, Bottinger, Erwin P, Melander, Olle, Orho-Melander, Marju, Loos, Ruth JF, Duga, Stefano, Merlini, Piera Angelica, Farrall, Martin, Goel, Anuj, Asselta, Rosanna, Girelli, Domenico, Martinelli, Nicola, Shah, Svati H, Kraus, William E, Li, Mingyao, Rader, Daniel J, Reilly, Muredach P, McPherson, Ruth, Watkins, Hugh, Ardissino, Diego, Project, NHLBI GO Exome Sequencing, Zhang, Qunyuan, Wang, Judy, Tsai, Michael Y, Taylor, Herman A, Correa, Adolfo, Griswold, Michael E, Lange, Leslie A, Starr, John M, Rudan, Igor, Eiriksdottir, Gudny, Launer, Lenore J, Ordovas, Jose M, Levy, Daniel, Chen, Y-D Ida, Reiner, Alexander P, Hayward, Caroline, Polasek, Ozren, Deary, Ian J, Borecki, Ingrid B, Liu, Yongmei, Gudnason, Vilmundur, Wilson, James G, van Duijn, Cornelia M, Kooperberg, Charles, Rich, Stephen S, Psaty, Bruce M, Rotter, Jerome I, O’Donnell, Christopher J, Rice, Kenneth, Boerwinkle, Eric, Kathiresan, Sekar, Cupples, L Adrienne

المصدر: American Journal of Human Genetics. 94(2)

مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Heart Disease - Coronary Heart Disease, Human Genome, Cardiovascular, Heart Disease, Atherosclerosis, Aetiology, 2.1 Biological and endogenous factors, 1-Alkyl-2-acetylglycerophosphocholine Esterase, Adult, Aged, Alleles, Animals, Black People, Cholesterol, HDL, Cholesterol, LDL, Cohort Studies, Coronary Disease, Female, Gene Frequency, Genetic Association Studies, Genetic Code, Genetic Variation, Humans, Linear Models, Male, Mice, Mice, Inbred C57BL, Microtubule-Associated Proteins, Middle Aged, Phenotype, Sequence Analysis, DNA, Subtilisins, Triglycerides, White People, NHLBI GO Exome Sequencing Project, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7tn5d4hfTest

المؤلفون: Franceschini, Nora, Fox, Ervin, Zhang, Zhaogong, Edwards, Todd L, Nalls, Michael A, Sung, Yun Ju, Tayo, Bamidele O, Sun, Yan V, Gottesman, Omri, Adeyemo, Adebawole, Johnson, Andrew D, Young, J Hunter, Rice, Ken, Duan, Qing, Chen, Fang, Li, Yun, Tang, Hua, Fornage, Myriam, Keene, Keith L, Andrews, Jeanette S, Smith, Jennifer A, Faul, Jessica D, Guangfa, Zhang, Guo, Wei, Liu, Yu, Murray, Sarah S, Musani, Solomon K, Srinivasan, Sathanur, Edwards, Digna R Velez, Wang, Heming, Becker, Lewis C, Bovet, Pascal, Bochud, Murielle, Broeckel, Ulrich, Burnier, Michel, Carty, Cara, Chasman, Daniel I, Ehret, Georg, Chen, Wei-Min, Chen, Guanjie, Chen, Wei, Ding, Jingzhong, Dreisbach, Albert W, Evans, Michele K, Guo, Xiuqing, Garcia, Melissa E, Jensen, Rich, Keller, Margaux F, Lettre, Guillaume, Lotay, Vaneet, Martin, Lisa W, Moore, Jason H, Morrison, Alanna C, Mosley, Thomas H, Ogunniyi, Adesola, Palmas, Walter, Papanicolaou, George, Penman, Alan, Polak, Joseph F, Ridker, Paul M, Salako, Babatunde, Singleton, Andrew B, Shriner, Daniel, Taylor, Kent D, Vasan, Ramachandran, Wiggins, Kerri, Williams, Scott M, Yanek, Lisa R, Zhao, Wei, Zonderman, Alan B, Becker, Diane M, Berenson, Gerald, Boerwinkle, Eric, Bottinger, Erwin, Cushman, Mary, Eaton, Charles, Nyberg, Fredrik, Heiss, Gerardo, Hirschhron, Joel N, Howard, Virginia J, Karczewsk, Konrad J, Lanktree, Matthew B, Liu, Kiang, Liu, Yongmei, Loos, Ruth, Margolis, Karen, Snyder, Michael, Consortium, the Asian Genetic Epidemiology Network, Go, Min Jin, Kim, Young Jin, Lee, Jong-Young, Jeon, Jae-Pil, Kim, Sung Soo, Han, Bok-Ghee, Cho, Yoon Shin, Sim, Xueling, Tay, Wan Ting, Ong, Rick Twee Hee, Seielstad, Mark, Liu, Jian Jun

المصدر: American Journal of Human Genetics. 93(3)

مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Cardiovascular, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Africa, Black People, Blood Pressure, Cohort Studies, Databases, Genetic, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide, Quantitative Trait, Heritable, Reproducibility of Results, Asian Genetic Epidemiology Network Consortium, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7sp4s4hcTest
https://escholarship.org/content/qt7sp4s4hc/qt7sp4s4hc.pdfTest

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

المؤلفون: Dai Wang, Nathan Fischel-Ghodsian, Huiying Yang, Stephan R. Targan, Ying-Chao Lin, Kazuhito Sugimura, Tieu Hang, Jerome I. Rotter, Kent D. Taylor, Yong-Ming Tang

المصدر: American journal of human genetics. 72(3)

مصطلحات موضوعية: Nod2 Signaling Adaptor Protein, Single-nucleotide polymorphism, Locus (genetics), Biology, Polymorphism, Single Nucleotide, Genetic determinism, White People, 03 medical and health sciences, 0302 clinical medicine, Crohn Disease, Genetic linkage, Risk Factors, Genetics, Humans, Genetics(clinical), Genetic Predisposition to Disease, Genetics (clinical), Phylogeny, 030304 developmental biology, DNA Primers, 0303 health sciences, Base Sequence, Haplotype, Case-control study, Intracellular Signaling Peptides and Proteins, Chromosome Mapping, Articles, Ashkenazi jews, digestive system diseases, Europe, Amino Acid Substitution, Haplotypes, Case-Control Studies, Jews, Microsatellite, 030211 gastroenterology & hepatology, Carrier Proteins, Microsatellite Repeats

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d58806509e2172cadaf756b0b2f835Test
https://pubmed.ncbi.nlm.nih.gov/14765395Test