المؤلفون: Wilson, Amanda, Chiorean, Alexandra, Aguiar, Mario, Sekulic, Davorka, Pavlick, Patrick, Shah, Neha, Sniderman King, Lisa, Génin, Marie, Rollot, Mélissa, Blanchon, Margot, Gosset, Simon, Montmerle, Martin, Molony, Cliona, Dumitriu, Alexandra^{Aff7, IDs13023023028682_cor14}

المصدر: Orphanet Journal of Rare Diseases. 18(1)

المؤلفون: Fathzadeh, Mohsen, Li, Jiehan, Rao, Abhiram, Cook, Naomi, Chennamsetty, Indumathi, Seldin, Marcus, Zhou, Xiang, Sangwung, Panjamaporn, Gloudemans, Michael J, Keller, Mark, Attie, Allan, Yang, Jing, Wabitsch, Martin, Carcamo-Orive, Ivan, Tada, Yuko, Lusis, Aldons J, Shin, Myung Kyun, Molony, Cliona M, McLaughlin, Tracey, Reaven, Gerald, Montgomery, Stephen B, Reilly, Dermot, Quertermous, Thomas, Ingelsson, Erik, Knowles, Joshua W

المصدر: Nature communications. 11(1)

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/03r3v8g2

المؤلفون: Dumitriu, Alexandra^Aff15, Molony, Cliona^Aff15, Daluwatte, Chathuri^Aff15

المساهمون: Jain, Lakhmi C., Editor-in-Chief^Aff1, Wu, Xindong, Editor-in-Chief^Aff2, Brahnam, Sheryl, Series Editor^Aff3, Cook, Diane J, Series Editor^Aff4, Domingo-Ferrer, Josep, Series Editor^Aff5, Gabrys, Bogdan, Series Editor^Aff6, Herrera, Francisco, Series Editor^Aff7, Mamitsuka, Hiroshi, Series Editor^Aff8, Phoha, Vir V., Series Editor^Aff9, Siebes, Arno, Series Editor^Aff10, de Wilde, Philippe, Series Editor^Aff11, Sikos, Leslie F., editor^Aff12, Seneviratne, Oshani W., editor^Aff13, McGuinness, Deborah L., editor^Aff14

المصدر: Provenance in Data Science : From Data Models to Context-Aware Knowledge Graphs. :75-110

المؤلفون: Luizon, Marcelo R, Eckalbar, Walter L, Wang, Yao, Jones, Stacy L, Smith, Robin P, Laurance, Megan, Lin, Lawrence, Gallins, Paul J, Etheridge, Amy S, Wright, Fred, Zhou, Yihui, Molony, Cliona, Innocenti, Federico, Yee, Sook Wah, Giacomini, Kathleen M, Ahituv, Nadav

المصدر: PLoS genetics. 12(11)

مصطلحات موضوعية: Liver, Hepatocytes, Humans, Diabetes Mellitus, Type 2, Metformin, Adaptor Proteins, Signal Transducing, Gluconeogenesis, Haplotypes, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Activating Transcription Factor 3, DEAD-box RNA Helicases, Enhancer Elements, Genetic, AMP-Activated Protein Kinases, Gene Knockdown Techniques, Ataxia Telangiectasia Mutated Proteins, Diabetes Mellitus, Type 2, Adaptor Proteins, Signal Transducing, Polymorphism, Single Nucleotide, Enhancer Elements, Genetic, Genetics, Digestive Diseases, Liver Disease, Human Genome, Biotechnology, Metabolic and Endocrine, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/5gp2361c

المؤلفون: Knowles, Joshua W, Xie, Weijia, Zhang, Zhongyang, Chennamsetty, Indumathi, Assimes, Themistocles L, Paananen, Jussi, Hansson, Ola, Pankow, James, Goodarzi, Mark O, Carcamo-Orive, Ivan, Morris, Andrew P, Chen, Yii-Der I, Mäkinen, Ville-Petteri, Ganna, Andrea, Mahajan, Anubha, Guo, Xiuqing, Abbasi, Fahim, Greenawalt, Danielle M, Lum, Pek, Molony, Cliona, Lind, Lars, Lindgren, Cecilia, Raffel, Leslie J, Tsao, Philip S, RISC (Relationship between Insulin Sensitivity and Cardiovascular Disease) Consortium, EUGENE (European Network on Functional Genomics of Type Diabetes) Study, GUARDIAN (Genetics UndeRlying DIAbetes in HispaNics) Consortium, SAPPHIRe (Stanford Asian and Pacific Program for Hypertension and Insulin Resistance) Study, Schadt, Eric E, Rotter, Jerome I, Sinaiko, Alan, Reaven, Gerald, Yang, Xia, Hsiung, Chao A, Groop, Leif, Cordell, Heather J, Laakso, Markku, Hao, Ke, Ingelsson, Erik, Frayling, Timothy M, Weedon, Michael N, Walker, Mark, Quertermous, Thomas

المصدر: The Journal of clinical investigation. 126(1)

مصطلحات موضوعية: RISC (Relationship between Insulin Sensitivity and Cardiovascular Disease) Consortium, EUGENE (European Network on Functional Genomics of Type Diabetes) Study, GUARDIAN (Genetics UndeRlying DIAbetes in HispaNics) Consortium, SAPPHIRe (Stanford Asian and Pacific Program for Hypertension and Insulin Resistance) Study, Immunology, Medical and Health Sciences

URL الوصول: https://escholarship.org/uc/item/5qj1p0tf

المؤلفون: Nalls, Mike A, McLean, Cory Y, Rick, Jacqueline, Eberly, Shirley, Hutten, Samantha J, Gwinn, Katrina, Sutherland, Margaret, Martinez, Maria, Heutink, Peter, Williams, Nigel M, Hardy, John, Gasser, Thomas, Brice, Alexis, Price, T Ryan, Nicolas, Aude, Keller, Margaux F, Molony, Cliona, Gibbs, J Raphael, Chen-Plotkin, Alice, Suh, Eunran, Letson, Christopher, Fiandaca, Massimo S, Mapstone, Mark, Federoff, Howard J, Noyce, Alastair J, Morris, Huw, Van Deerlin, Vivianna M, Weintraub, Daniel, Zabetian, Cyrus, Hernandez, Dena G, Lesage, Suzanne, Mullins, Meghan, Conley, Emily Drabant, Northover, Carrie AM, Frasier, Mark, Marek, Ken, Day-Williams, Aaron G, Stone, David J, Ioannidis, John PA, Singleton, Andrew B, investigators*, Parkinson's Disease Biomarkers Program and Parkinson's Progression Marker Initiative

المصدر: The Lancet Neurology. 14(10)

مصطلحات موضوعية: Aging, Prevention, Neurodegenerative, Brain Disorders, Neurosciences, Parkinson's Disease, Clinical Research, 2.1 Biological and endogenous factors, 4.2 Evaluation of markers and technologies, Detection, screening and diagnosis, Aetiology, 4.1 Discovery and preclinical testing of markers and technologies, Neurological, Good Health and Well Being, Aged, Cohort Studies, Disease Progression, Female, Humans, Male, Middle Aged, Models, Statistical, Parkinson Disease, Prodromal Symptoms, Parkinson's Disease Biomarkers Program and Parkinson's Progression Marker Initiative investigators, Clinical Sciences, Neurology & Neurosurgery

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/9nf852rq

المؤلفون: Knowles, Joshua W, Xie, Weijia, Zhang, Zhongyang, Chennemsetty, Indumathi, Assimes, Themistocles L, Paananen, Jussi, Hansson, Ola, Pankow, James, Goodarzi, Mark O, Carcamo-Orive, Ivan, Morris, Andrew P, Chen, Yii-Der I, Maekinen, Ville-Petteri, Ganna, Andrea, Mahajan, Anubha, Guo, Xiuqing, Abbasi, Fahim, Greenawalt, Danielle M, Lum, Pek, Molony, Cliona, Lind, Lars, Lindgren, Cecilia, Raffel, Leslie J, Tsao, Philip S, Schadt, Eric E, Rotter, Jerome I, Sinaiko, Alan, Reaven, Gerald, Yang, Xia, Hsiung, Chao A, Groop, Leif, Cordell, Heather J, Laakso, Markku, Hao, Ke, Ingelsson, Erik, Frayling, Timothy M, Weedon, Michael N, Walker, Mark, Quertermous, Thomas, Insulin, RISC Relationship, Functional, EUGENE European Network, UndeRlying, GUARDIAN Genetics, Pacific, SAPPHIRE Stanford Asian

المصدر: JOURNAL OF CLINICAL INVESTIGATION. 125(4)

مصطلحات موضوعية: Immunology, Medical and Health Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/0423w1kd

المؤلفون: Narayanan, Manikandan, Huynh, Jimmy L, Wang, Kai, Yang, Xia, Yoo, Seungyeul, McElwee, Joshua, Zhang, Bin, Zhang, Chunsheng, Lamb, John R, Xie, Tao, Suver, Christine, Molony, Cliona, Melquist, Stacey, Johnson, Andrew D, Fan, Guoping, Stone, David J, Schadt, Eric E, Casaccia, Patrizia, Emilsson, Valur, Zhu, Jun

المصدر: Molecular systems biology. 10(7)

مصطلحات موضوعية: Prefrontal Cortex, Chromatin, Animals, Mice, Knockout, Humans, Mice, Huntington Disease, Dementia, Alzheimer Disease, Autopsy, Case-Control Studies, Reproducibility of Results, Gene Expression Profiling, Gene Expression Regulation, Gene Regulatory Networks, DNA (Cytosine-5-)-Methyltransferase 1, DNA (Cytosine-5-)-Methyltransferases, differential co‐expression, dysregulatory gene networks, epigenetic regulation of neural differentiation, network alignment, neurodegenerative diseases, differential co-expression, Knockout, DNA (Cytosine-5-)-Methyltransferase, Bioinformatics, Biochemistry and Cell Biology, Other Biological Sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/34p6n4pf

المؤلفون: Ganesh, Santhi K, Tragante, Vinicius, Guo, Wei, Guo, Yiran, Lanktree, Matthew B, Smith, Erin N, Johnson, Toby, Castillo, Berta Almoguera, Barnard, John, Baumert, Jens, Chang, Yen-Pei Christy, Elbers, Clara C, Farrall, Martin, Fischer, Mary E, Franceschini, Nora, Gaunt, Tom R, Gho, Johannes MIH, Gieger, Christian, Gong, Yan, Isaacs, Aaron, Kleber, Marcus E, Leach, Irene Mateo, McDonough, Caitrin W, Meijs, Matthijs FL, Mellander, Olle, Molony, Cliona M, Nolte, Ilja M, Padmanabhan, Sandosh, Price, Tom S, Rajagopalan, Ramakrishnan, Shaffer, Jonathan, Shah, Sonia, Shen, Haiqing, Soranzo, Nicole, van der Most, Peter J, Van Iperen, Erik PA, Van Setten, Jessic A, Vonk, Judith M, Zhang, Li, Beitelshees, Amber L, Berenson, Gerald S, Bhatt, Deepak L, Boer, Jolanda MA, Boerwinkle, Eric, Burkley, Ben, Burt, Amber, Chakravarti, Aravinda, Chen, Wei, Cooper-DeHoff, Rhonda M, Curtis, Sean P, Dreisbach, Albert, Duggan, David, Ehret, Georg B, Fabsitz, Richard R, Fornage, Myriam, Fox, Ervin, Furlong, Clement E, Gansevoort, Ron T, Hofker, Marten H, Hovingh, G Kees, Kirkland, Susan A, Kottke-Marchant, Kandice, Kutlar, Abdullah, LaCroix, Andrea Z, Langaee, Taimour Y, Li, Yun R, Lin, Honghuang, Liu, Kiang, Maiwald, Steffi, Malik, Rainer, Murugesan, Gurunathan, Newton-Cheh, Christopher, O'Connell, Jeffery R, Onland-Moret, N Charlotte, Ouwehand, Willem H, Palmas, Walter, Penninx, Brenda W, Pepine, Carl J, Pettinger, Mary, Polak, Joseph F, Ramachandran, Vasan S, Ranchalis, Jane, Redline, Susan, Ridker, Paul M, Rose, Lynda M, Scharnag, Hubert, Schork, Nicholas J, Shimbo, Daichi, Shuldiner, Alan R, Srinivasan, Sathanur R, Stolk, Ronald P, Taylor, Herman A, Thorand, Barbara, Trip, Mieke D, van Duijn, Cornelia M, Verschuren, W Monique, Wijmenga, Cisca, Winkelmann, Bernhard R, Wyatt, Sharon, Young, J Hunter

المصدر: Human Molecular Genetics. 22(8)

مصطلحات موضوعية: Hypertension, Heart Disease, Human Genome, Genetics, Clinical Research, Cardiovascular, Aetiology, 2.1 Biological and endogenous factors, Adult, Aged, Blood Pressure, Cardiovascular Diseases, Chromosome Mapping, Cohort Studies, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, White People, CARDIOGRAM, METASTROKE, LifeLines Cohort Study, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

URL الوصول: https://escholarship.org/uc/item/16d246b2

المؤلفون: Yang, Xia, Zhang, Bin, Molony, Cliona, Chudin, Eugene, Hao, Ke, Zhu, Jun, Gaedigk, Andrea, Suver, Christine, Zhong, Hua, Leeder, J Steven, Guengerich, F Peter, Strom, Stephen C, Schuetz, Erin, Rushmore, Thomas H, Ulrich, Roger G, Slatter, J Greg, Schadt, Eric E, Kasarskis, Andrew, Lum, Pek Yee

المصدر: Genome Research. 20(8)

مصطلحات موضوعية: Biotechnology, Genetics, Digestive Diseases, Liver Disease, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Adolescent, Adult, Aged, Aged, 80 and over, Animals, Child, Child, Preschool, Cytochrome P-450 Enzyme System, Female, Gene Expression, Gene Expression Regulation, Enzymologic, Genome-Wide Association Study, Genomics, Humans, Infant, Infant, Newborn, Liver, Male, Mice, Middle Aged, Pharmaceutical Preparations, Polymorphism, Single Nucleotide, Rats, Systems Biology, Transcription, Genetic, Young Adult, Biological Sciences, Medical and Health Sciences, Bioinformatics

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/7651r7tx