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المؤلفون: Anna O. Basile, Robert J. Carroll, Ky’Era Actkins, Joshua C. Denny, Ian B. Stanaway, Bahram Namjou, Rex L. Chisholm, Yoonjung Yoonie Joo, Kevin Ho, Maureen E. Smith, Jennifer A. Pacheco, Cindy Meun, Tugce Karderi, Margrit Urbanek, Gail P. Jarvik, David R. Crosslin, John B. Harley, Frank D. Mentch, Matthew Jones, Sarah A. Pendergrass, M. Geoffrey Hayes, Abel N. Kho, Felix R. Day, Lea K. Davis, Hakon Hakonarson, Digna R. Velez Edwards, Scott J. Hebbring, Theresa L. Walunas, Marylyn D. Ritchie
المساهمون: Obstetrics & Gynecology, Internal Medicine
المصدر: J Clin Endocrinol Metab
The Journal of clinical endocrinology and metabolism, 105(6), 1918-1936. Endocrine Societyمصطلحات موضوعية: 0301 basic medicine, Multifactorial Inheritance, Endocrinology, Diabetes and Metabolism, Clinical Biochemistry, Type 2 diabetes, Bioinformatics, Biochemistry, 0302 clinical medicine, Endocrinology, Risk Factors, Electronic Health Records, Phenomics, Child, 0303 health sciences, Framingham Risk Score, Sleep apnea, Middle Aged, Prognosis, Polycystic ovary, 3. Good health, Phenotype, Female, Algorithms, Polycystic Ovary Syndrome, medicine.medical_specialty, Adolescent, 030209 endocrinology & metabolism, Context (language use), Phenome, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Diabetes mellitus, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Clinical Research Articles, 030304 developmental biology, Aged, Genetic association, business.industry, Biochemistry (medical), medicine.disease, Comorbidity, Obesity, 030104 developmental biology, Case-Control Studies, business, Follow-Up Studies, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33f404b526c20f81fe1437d5d2146c17Test
https://doi.org/10.1210/clinem/dgz326Test -
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المؤلفون: Eric B. Larson, Atlas Khan, David Carrell, Murray H. Brilliant, George Hripcsak, Peggy L. Peissig, Iuliana Ionita-Laza, Shefali S. Verma, Vivian S. Gainer, David R. Crosslin, Gail P. Jarvik, Joshua C. Denny, Richard A. Dart, Nicholas P. Tatonetti, Karla Mehl, Robert J. Carrol, Sumit Mohan, Ning Shang, Fernanda Polubriaginof, Francesca Zanoni, Chunhua Weng, Marylyn D. Ritchie, Ian B. Stanaway, Matthew A. Hathcock, Krzysztof Kiryluk, Elizabeth W. Karlson, Sarah A. Pendergrass, David Fasel, Ali G. Gharavi, Paul E. Drawz, Adelaide M. Arruda-Olson, Adam S. Gordon, Barbara Benoit
المصدر: NPJ Digital Medicine
npj Digital Medicine, Vol 4, Iss 1, Pp 1-13 (2021)مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Epidemiology, Computer applications to medicine. Medical informatics, R858-859.7, MEDLINE, Medicine (miscellaneous), Renal function, Health Informatics, Pedigree chart, Article, 03 medical and health sciences, 0302 clinical medicine, Health Information Management, Internal medicine, Chronic kidney disease, Genetics research, medicine, 030212 general & internal medicine, Genetic association, business.industry, Medical record, medicine.disease, Computer Science Applications, 030104 developmental biology, Albuminuria, Observational study, medicine.symptom, business, Kidney disease
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1353c1328d6b6f6737738807f4bdc1aTest
http://europepmc.org/articles/PMC8044136Test -
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المؤلفون: David J. Carey, Yanfei Zhang, Lisa Bang, Marta Byrska-Bishop, Ming Ta Michael Lee, Anurag Verma, Yu Zhang, Sarah A. Pendergrass, Marylyn D. Ritchie, Dokyoon Kim, Jason E. Miller
المصدر: American Journal of Human Genetics
مصطلحات موضوعية: 0301 basic medicine, Epigenomics, Single-nucleotide polymorphism, Computational biology, Disease, Biology, Polymorphism, Single Nucleotide, Article, Autoimmune Diseases, 03 medical and health sciences, 0302 clinical medicine, Pleiotropy, Genetic variation, Genetics, Electronic Health Records, Humans, DiscovEHR study, Genetics (clinical), Genetic Association Studies, Genetic association, PheWAS, electronic health record, Biobank, Genetic architecture, 030104 developmental biology, Phenotype, Cardiovascular Diseases, 030220 oncology & carcinogenesis, human disease network, Diagnosis code, EHR-based population study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24380b6f02bf466199da0c8e95637057Test
http://europepmc.org/articles/PMC6323551Test -
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المؤلفون: Lukas Habegger, Charumathi Sabanayagam, Michael Preuss, Laura M. Raffield, Mary F. Feitosa, Bamidele O. Tayo, Kevin Ho, Leo-Pekka Lyytikäinen, Florian Kronenberg, Valencia Hui Xian Foo, Adrienne Tin, Michael Cantor, Nisha Bansal, Tarunveer S. Ahluwalia, Melanie Waldenberger, Sarah A. Pendergrass, Behrooz Z. Alizadeh, Wolfgang Koenig, Qiong Yang, Xiaodong Bai, Christoph Wanner, Ben Schöttker, Giovanni Coppola, A. R. Shuldiner, Leslie A. Lange, Piyush Gampawar, Markus Scholz, Tien Yin Wong, Mary L. Biggs, Morris Swertz, Alicia Hawes, Girish N. Nadkarni, Christina-Alexandra Schulz, Chiea Chuen Khor, Ricardo H. Ulloa, Jeffrey C. Staples, Miao-Li Chee, Laura M. Yerges-Armstrong, Andrew Blumenfeld, Karlhans Endlich, Bernhard Banas, Bruce H.R. Wolffenbuttel, Kai-Uwe Eckardt, Pavel Hamet, Carsten A. Böger, Harold Snieder, Marcus B. Jones, Judy Wang, Shih-Jen Hwang, Mathias Gorski, Anselm Hoppmann, Josyf C. Mychaleckyj, Bernd Holleczek, Pamela R. Matias-Garcia, Rainer Rettig, Karsten B. Sieber, Manasi Pradhan, Pashupati P. Mishra, Peter Rossing, Matthias Wuttke, Miao-Ling Chee, H. Marike Boezen, Yong Li, M. Arfan Ikram, Jeffrey G. Reid, Teresa Nutile, Maria Sotiropoulos Padilla, Lude Franke, Robert J. Carroll, Luca A. Lotta, Bernhard K. Krämer, Kjell Nikus, Jerome I. Rotter, Thomas Meitinger, Lars Wallentin, Cisca Wijmenga, Kent D. Taylor, Holly Kramer, Louis Widom, Olli T. Raitakari, Marcus E. Kleber, Man Li, Nina Hutri-Kähönen, Massimiliano Cocca, Reinhold Schmidt, John D. Overton, Cristian Pattaro, Michael Lattari, Sarah E. Wolf, Jin-Fang Chai, Karina Toledo, Brigitte Kühnel, Zhenhua Gu, Peter Almgren, Caitlin Forsythe, Yuri Milaneschi, Stephan J. L. Bakker, Layal Chaker, Dawn M. Waterworth, Silke Szymczak, James G. Wilson, Peter J. van der Most, Michelle L. O'Donoghue, William Salerno, Masayuki Yasuda, Sahar Ghasemi, Eric Boerwinkle, Josef Coresh, Ilja M. Nolte, Kia Manoochehri, Konstantin Strauch, Thomas D. Schleicher, Myriam Rheinberger, Audrey Y. Chu, Sanaz Sedaghat, Sandra Freitag-Wolf, Boting Ning, Matthias Nauck, Christina Beechert, Helena Schmidt, Harvey D. White, Nina Mononen, Johanne Tremblay, Navya Shilpa Josyula, Mika Kähönen, Katrin Horn, Andre Franke, Marianne Rots, Bettina Jung, Alexander R. Rosenkranz, Christian M. Shaffer, Mary Ann Lukas, Gerjan Navis, Christian Gieger, John Chalmers, Shareef Khalid, Uwe Völker, Marju Orho-Melander, Iris M. Heid, Brenda W.J.H. Penninx, A. Baras, Alexander Lopez, Evan Maxwell, Ruth J. F. Loos, Erin D. Fuller, Christa Meisinger, Gonçalo R. Abecasis, Suganthi Balasubramanian, Chris H. L. Thio, Martin H. de Borst, Stefan Coassin, Ching-Yu Cheng, Wolfgang Lieb, Kenneth Rice, Alexander Teumer, Mark Woodward, Gisu Eom, Hermann Brenner, Thomas W. Winkler, Anna Köttgen, Edith Hofer, Aris Economides, Ron T. Gansevoort, Pim van der Harst, Lyndon J. Mitnaul, Bruce M. Psaty, Erwin P. Bottinger, Olle Melander, Niek Verweij, Frauke Degenhardt, Yan Zhang, Mohsen Ghanbari, Veronika Wanner, Terho Lehtimäki, Leland Barnard
المساهمون: Tampere University, Primary Health Care, Department of Paediatrics, Clinical Medicine, Department of Clinical Physiology and Nuclear Medicine, Department of Clinical Chemistry, TAYS Heart Centre, Groningen Institute for Organ Transplantation (GIOT), Groningen Kidney Center (GKC), Cardiovascular Centre (CVC), Life Course Epidemiology (LCE), Department of Marketing Management, Epidemiology, Internal Medicine, Psychiatry, Amsterdam Neuroscience - Complex Trait Genetics, Amsterdam Neuroscience - Mood, Anxiety, Psychosis, Stress & Sleep, APH - Mental Health, APH - Digital Health
المصدر: Gorski, M, Jung, B, Li, Y, Matias-Garcia, P R, Wuttke, M, Coassin, S, Thio, C H L, Kleber, M E, Winkler, T W, Wanner, V, Chai, J-F, Chu, A Y, Cocca, M, Feitosa, M F, Ghasemi, S, Hoppmann, A, Horn, K, Li, M, Nutile, T, Scholz, M, Sieber, K B, Teumer, A, Tin, A, Wang, J, Tayo, B O, Ahluwalia, T S, Almgren, P, Bakker, S J L, Banas, B, Bansal, N, Biggs, M L, Boerwinkle, E, Bottinger, E P, Brenner, H, Carroll, R J, Chalmers, J, Chee, M-L, Chee, M-L, Cheng, C-Y, Coresh, J, de Borst, M H, Degenhardt, F, Eckardt, K-U, Endlich, K, Franke, A, Freitag-Wolf, S, Gampawar, P, Gansevoort, R T, Loos, R J F, Rossing, P & LifeLines Cohort Study 2021, ' Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ', Kidney International, vol. 99, no. 4, pp. 926-939 . https://doi.org/10.1016/j.kint.2020.09.030Test
Kidney international (2020). doi:10.1016/j.kint.2020.09.030
info:cnr-pdr/source/autori:Mathias Gorski et al/titolo:Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline/doi:10.1016%2Fj.kint.2020.09.030/rivista:Kidney international/anno:2020/pagina_da:/pagina_a:/intervallo_pagine:/volume
Kidney International
Lifelines Cohort Study & Regeneron Genetics Center 2021, ' Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline ', Kidney International, vol. 99, no. 4, pp. 926-939 . https://doi.org/10.1016/j.kint.2020.09.030Test
Kidney International, 99(4), 926-939. ELSEVIER SCIENCE INC
Kidney International, 99(4), 926-939. Elsevier Inc.
Kidney International, 99(4), 926-939. Nature Publishing Groupمصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Genome-wide association study, 030232 urology & nephrology, Protein Disulfide-Isomerases, Hasso-Plattner-Institut für Digital Engineering GmbH, Renal function, Locus (genetics), Biology, AMP-Activated Protein Kinases, Kidney, 3121 Internal medicine, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, end-stage kidney disease, rapid eGFRcrea decline, Urologi och njurmedicin, medicine, Humans, Urology and Nephrology, ddc:610, Allele, Genetic association, Genetics, Creatinine, genome-wide association study, Acute kidney injury, acute kidney injury, medicine.disease, United Kingdom, ddc, 030104 developmental biology, chemistry, Nephrology, Medical genetics, 3111 Biomedicine, 610 Medizin und Gesundheit, Glomerular Filtration Rate
وصف الملف: application/pdf; fulltext
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfe030174e9e300043a2bda6960bc9c1Test
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-430992Test -
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المؤلفون: Peter Kraft, Adriana Iglesias, Steffen Uebe, Alberta A H J Thiadens, Jessica N. Cooke Bailey, Paul Mitchell, Olusola Olawoye, Michele Ramsay, Caroline C.W. Klaver, Eranga N. Vithana, Ayub Qassim, Mark James Simcoe, Pirro G. Hysi, Xin Wang, Angela J. Cree, Juha Karjalainen, René Höhn, Cornelia van Duijn, Andrew J. Lotery, Veronique Vitart, Anthony P Khawaja, Terri L. Young, James E. Morgan, UK Biobank Eye, Yukihiro Shiga, Owen M. Siggs, Yukihide Momozawa, Stephen Akafo, Puya Gharahkhani, Robert P. Igo, Masato Akiama, Gen Tamiya, Sarah A. Pendergrass, Navya Shilpa Josyula, Chris Hammond, David A. Mackey, FinnGen study, Chiea Chuen Khor, Francesca Pasutto, Ewan Birney, Pieter W.M. Bonnemaijer, Aarno Palotie, Susan E. Williams, John Rouhana, Nishani Amersinghe, Peng T. Khaw, Stuart MacGregor, Ching-Yu Cheng, Yoichito Kamatani, Calvin Chi Pui Pang, Xikun Han, Alex W. Hewitt, Louis R. Pasquale, Jae Hee Kang, Eric Jorgenson, Ronald B. Melles, Michael Hauser, Li Jia Chen, Jonathan Haines, Masayuki Yamamoto, Alicia Poplawski, Ayellet V. Segrè, Jue-Sheng Ong, Kazuki Hashimoto, Hélène Choquet, Hannah Currant, Jamie E. Craig, Robert Luben, Adam Auton, Tin Aung, Paul J. Foster, Toru Nakazawa, Nicholas G. Strouthidis, Michiaki Kubo, K. Saidas Nair, Janey L. Wiggs, Adeyinka O. Ashaye
مصطلحات موضوعية: Genetics, 0303 health sciences, genetic structures, Open angle glaucoma, Glaucoma, Genome-wide association study, Disease, Biology, medicine.disease, eye diseases, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Meta-analysis, medicine, sense organs, Gene, 030217 neurology & neurosurgery, 030304 developmental biology, Genetic association
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c722c6c7f99a49eed99cfe006e4a86a9Test
https://doi.org/10.1101/2020.01.30.927822Test -
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المؤلفون: Diego R. Mazzotti, Allan I. Pack, Sarah A. Pendergrass, Navya Shilpa Josyula, Brendan T. Keenan, Christopher R. Bauer, Beth A. Malow, Janet D. Robishaw, Olivia J. Veatch, Kanika Bagai
المصدر: BMC Medical Genomics
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-14 (2020)مصطلحات موضوعية: Male, 0301 basic medicine, lcsh:Internal medicine, Candidate gene, lcsh:QH426-470, Genotype, Single-nucleotide polymorphism, Disease, Health records, Bioinformatics, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Diabetes mellitus, Ethnicity, Genetics, medicine, Humans, Electronic health records, SNP, Genetic Predisposition to Disease, lcsh:RC31-1245, Genetics (clinical), Genetic association, Pleiotropy, Sleep Apnea, Obstructive, Genetic heterogeneity, business.industry, Sleep disorders, Middle Aged, medicine.disease, Obstructive sleep apnea, Human genetics, nervous system diseases, 3. Good health, respiratory tract diseases, lcsh:Genetics, Phenotype, 030104 developmental biology, Systematic review, 030228 respiratory system, Case-Control Studies, Female, business, 030217 neurology & neurosurgery, Genome-Wide Association Study, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd9599d928809239d82a2ecc223e101Test
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المؤلفون: Sarah A. Pendergrass, Yuki Bradford, Marylyn D. Ritchie, Anurag Verma, Scott M. Dudek, Anastasia Lucas, Shefali S. Verma
المصدر: BMC Bioinformatics, Vol 19, Iss 1, Pp 1-8 (2018)
BMC Bioinformaticsمصطلحات موضوعية: 0301 basic medicine, Simulation study, EHR, Computer science, Quantitative Trait Loci, Phenome, Biology, Quantitative trait locus, Bioinformatics, lcsh:Computer applications to medicine. Medical informatics, Polymorphism, Single Nucleotide, Biochemistry, Statistical power, 03 medical and health sciences, 0302 clinical medicine, Structural Biology, Statistics, Range (statistics), Humans, Computer Simulation, Disease, Molecular Biology, lcsh:QH301-705.5, Genetic Association Studies, ICD-9 codes, 030304 developmental biology, Genetic association, 0303 health sciences, Applied Mathematics, PheWAS, Penetrance, Power (physics), Computer Science Applications, Minor allele frequency, Power analysis, Phenotype, 030104 developmental biology, lcsh:Biology (General), Sample size determination, 030221 ophthalmology & optometry, lcsh:R858-859.7, Algorithms, Genome-Wide Association Study, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff1b9f9f0241dcad009e2a40cfb83d52Test
http://link.springer.com/article/10.1186/s12859-018-2135-0Test -
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المؤلفون: Joseph B. Leader, Marylyn D. Ritchie, Sarah A. Pendergrass, Yu Zhang, Anastasia Lucas, Anqa Khan, Dustin N. Hartzel, Shefali S. Verma, Daniel R. Lavage, Anurag Verma, Navya Shilpa Josyula
المصدر: The American Journal of Human Genetics. 102:592-608
مصطلحات موضوعية: 0301 basic medicine, Context (language use), Genome-wide association study, Single-nucleotide polymorphism, Disease, Biology, Article, Open Reading Frames, 03 medical and health sciences, International Classification of Diseases, Genetics, Electronic Health Records, Humans, Medical diagnosis, Genetics (clinical), Genetic association, Clinical Laboratory Techniques, Genome, Human, Sequence Analysis, RNA, Reproducibility of Results, Molecular Sequence Annotation, Chromatin, Minor allele frequency, Phenotype, 030104 developmental biology, Gene Expression Regulation, Haplotypes, Genetic epidemiology, DNA, Intergenic, Genome-Wide Association Study, Demography
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02c785761e829bca4b1242823e513500Test
https://doi.org/10.1016/j.ajhg.2018.02.017Test -
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المؤلفون: Tobias Hermle, Holger Kirsten, Karsten B. Sieber, Aiko P. J. de Vries, Su Chi Lim, Peter Kovacs, Charumathi Sabanayagam, Carl D. Langefeld, Bernhard K. Krämer, Kent D. Taylor, Janine F. Felix, Belen Ponte, Markus Loeffler, Mary F. Feitosa, Kai-Uwe Eckardt, Jianjun Liu, Katalin Dittrich, Charlene A. Wong, Uwe Völker, Adriana M. Hung, Thomas Meitinger, Anubha Mahajan, Anselm Hoppmann, Erik Ingelsson, Martin H. de Borst, Oscar H. Franco, Niek Verweij, Kai-Uwe Saum, Vilmundur Gudnason, Bram P. Prins, Carsten A. Böger, Terho Lehtimäki, Andrew A. Hicks, Todd L. Edwards, Olivier Devuyst, Peter P. Pramstaller, Katrin Horn, Leslie A. Lange, Johanne Tremblay, Jin-Fang Chai, Sahar Ghasemi, Kjell Nikus, Tanja Poulain, Massimiliano Cocca, Anna Köttgen, Eric Boerwinkle, Barry I. Freedman, Miao-Ling Chee, Man Li, Stephan J. L. Bakker, Tamara B. Harris, Albert V. Smith, Ton J. Rabelink, Dennis O. Mook-Kanamori, Iris M. Heid, Jasmin Divers, Chaolong Wang, Kathleen A. Ryan, Pavel Hamet, Silke Szymczak, Shih-Jen Hwang, Hauke Thomsen, Rainer Rettig, Ayush Giri, Fernando Rivadeneira, Leo-Pekka Lyytikäinen, Cristian Pattaro, Andrej Teren, Valencia Hui Xian Foo, Myriam Rheinberger, Audrey Y. Chu, Barbara McMullen, Franziska Grundner-Culemann, Masayuki Yasuda, Murielle Bochud, Martin Gögele, Anke Tönjes, Jeannette Lee, Adrienne Tin, Kevin Ho, Konstantin Strauch, Josef Coresh, Renée de Mutsert, Sandra Freitag-Wolf, Gardar Sveinbjornsson, Yizhe Xu, Katalin Susztak, Tien Yin Wong, Mary L. Biggs, Isleifur Olafsson, Qiong Yang, Antje Körner, Chengxiang Qiu, E-Shyong Tai, Martina Müller-Nurasyid, Ben Schöttker, Jeffrey O' Connell, Mengmeng Chen, Daniel F. Gudbjartsson, Dermot F. Reilly, Vincent W. V. Jaddoe, Damia Noce, Pim van der Harst, Sanaz Sedaghat, Chiea Chuen Khor, Adam S. Butterworth, Mathias Gorski, Robert J. Carroll, James G. Wilson, Johan Ärnlöv, Christa Meisinger, Kenneth Rice, Bettina Jung, Christian M. Shaffer, Unnur Thorsteinsdottir, Matthias Nauck, Shreeram Akilesh, Mika Kähönen, Johanna Jakobsdottir, Melanie Waldenberger, Ralph Burkhardt, Daniela Baptista, John Danesh, Benjamin B. Sun, Karlhans Endlich, Holly Kramer, Frauke Degenhardt, Wolfgang Lieb, Kari Stefansson, Joachim Thiery, Lars Lind, Nicholette D. Palmer, Sarah A. Pendergrass, Suzanne Vogelezang, Peter J. van der Most, Afshin Parsa, Markus Scholz, Florian Kronenberg, Joseph C. Maranville, Laura M. Raffield, Hermann Brenner, Wieland Kiess, Anna I. Podgornaia, Yuan Shi, Tanguy Corre, Miao-Li Chee, Deborah Mascalzoni, Bamidele O. Tayo, Navya Shilpa Josyula, Ching-Yu Cheng, Lea Gerstner, Nisha Bansal, Jerome I. Rotter, Alexander Teumer, Vilmantas Giedraitis, Raymond Noordam, Ron T. Gansevoort, Lihua Wang, Andrew P. Morris, Bruce M. Psaty, Boting Ning, Zhi Yu, Christian Fuchsberger, Matthias Wuttke, Heiko Runz, Annette Peters, Yih Chung Tham, James P. Cook, Yong Li, Chris H. L. Thio, Hilma Holm, Alessandro De Grandi, Jonathan Marten, André G. Uitterlinden, Andre Franke, Nicholas Y. Q. Tan, Otis D. Wilson, Georg Ehret, Cecilia M. Lindgren, Josyf C. Mychaleckyj, Wolfgang Koenig, Harold Snieder, Michael Stumvoll, Kozeta Miliku, M. Arfan Ikram, Teresa Nutile
المساهمون: Læknadeild (HÍ), Faculty of Medicine (UI), School of Health Sciences (UI), Heilbrigðisvísindasvið (HÍ), Háskóli Íslands, University of Iceland, Teumer, Alexander [0000-0002-8309-094X], Li, Yong [0000-0003-2651-8791], Wuttke, Matthias [0000-0003-3420-5082], Giri, Ayush [0000-0002-7786-4670], Qiu, Chengxiang [0000-0002-6346-8669], Kirsten, Holger [0000-0002-3126-7950], Tin, Adrienne [0000-0002-4207-5866], Feitosa, Mary F. [0000-0002-0933-2410], Chai, Jin-Fang [0000-0003-3770-1137], Cocca, Massimiliano [0000-0002-1127-7596], Gorski, Mathias [0000-0002-9103-5860], Horn, Katrin [0000-0002-5307-6936], Li, Man [0000-0002-3839-0281], Marten, Jonathan [0000-0001-6916-2014], van der Most, Peter J. [0000-0001-8450-3518], Burkhardt, Ralph [0000-0003-1924-1202], Coresh, Josef [0000-0002-4598-0669], de Borst, Martin H. [0000-0002-4127-8733], Ehret, Georg [0000-0002-5730-0675], Endlich, Karlhans [0000-0001-6052-6061], Felix, Janine F. [0000-0002-9801-5774], Franke, Andre [0000-0003-1530-5811], Freedman, Barry I. [0000-0003-0275-5530], Freitag-Wolf, Sandra [0000-0002-1069-7740], Giedraitis, Vilmantas [0000-0003-3423-2021], Grundner-Culemann, Franziska [0000-0001-9649-281X], Gudnason, Vilmundur [0000-0001-5696-0084], Hicks, Andrew A. [0000-0001-6320-0411], Ikram, M. Arfan [0000-0003-0372-8585], Ingelsson, Erik [0000-0003-2256-6972], Jaddoe, Vincent W. V. [0000-0003-2939-0041], Josyula, Navya Shilpa [0000-0003-2782-8812], Khor, Chiea-Chuen [0000-0002-1128-4729], Koenig, Wolfgang [0000-0002-2064-9603], Kovacs, Peter [0000-0002-0290-5423], Kronenberg, Florian [0000-0003-2229-1120], Lindgren, Cecilia M. [0000-0002-4903-9374], Liu, Jianjun [0000-0002-3255-3019], Lyytikäinen, Leo-Pekka [0000-0002-7200-5455], Mahajan, Anubha [0000-0001-5585-3420], Mascalzoni, Deborah [0000-0003-4156-1464], Miliku, Kozeta [0000-0002-9614-7191], Müller-Nurasyid, Martina [0000-0003-3793-5910], Mychaleckyj, Josyf C. [0000-0003-2595-0005], Palmer, Nicholette D. [0000-0001-8883-2511], Poulain, Tanja [0000-0003-3825-5829], Raffield, Laura M. [0000-0002-7892-193X], Rice, Kenneth M. [0000-0002-3071-7278], Rivadeneira, Fernando [0000-0001-9435-9441], Sabanayagam, Charumathi [0000-0002-4042-4719], Smith, Albert V. [0000-0003-1942-5845], Sun, Benjamin B. [0000-0001-6347-2281], Szymczak, Silke [0000-0002-8897-9035], Taylor, Kent D. [0000-0002-2756-4370], Thio, Chris H. L. [0000-0003-2623-7172], Uitterlinden, André G. [0000-0002-7276-3387], van der Harst, Pim [0000-0002-2713-686X], Verweij, Niek [0000-0002-4303-7685], Völker, Uwe [0000-0002-5689-3448], Wang, Chaolong [0000-0003-3945-1012], Yang, Qiong [0000-0002-3658-1375], Devuyst, Olivier [0000-0003-3744-4767], Edwards, Todd L. [0000-0003-4318-6119], Ho, Kevin [0000-0002-3054-8697], Morris, Andrew P. [0000-0002-6805-6014], Pendergrass, Sarah A. [0000-0002-0565-6522], Rotter, Jerome I. [0000-0001-7191-1723], Stefansson, Kari [0000-0003-1676-864X], Susztak, Katalin [0000-0002-1005-3726], Scholz, Markus [0000-0002-4059-1779], Butterworth, Adam S. [0000-0002-6915-9015], Hung, Adriana M. [0000-0002-3203-1608], Pattaro, Cristian [0000-0002-4119-0109], Köttgen, Anna [0000-0002-4671-3714], Apollo - University of Cambridge Repository, Groningen Institute for Organ Transplantation (GIOT), Lifestyle Medicine (LM), Groningen Kidney Center (GKC), Cardiovascular Centre (CVC), Life Course Epidemiology (LCE), Epidemiology, Erasmus MC other, Pediatrics, Internal Medicine, Feitosa, Mary F [0000-0002-0933-2410], van der Most, Peter J [0000-0001-8450-3518], de Borst, Martin H [0000-0002-4127-8733], Felix, Janine F [0000-0002-9801-5774], Freedman, Barry I [0000-0003-0275-5530], Hicks, Andrew A [0000-0001-6320-0411], Ikram, M Arfan [0000-0003-0372-8585], Jaddoe, Vincent WV [0000-0003-2939-0041], Lindgren, Cecilia M [0000-0002-4903-9374], Mychaleckyj, Josyf C [0000-0003-2595-0005], Palmer, Nicholette D [0000-0001-8883-2511], Raffield, Laura M [0000-0002-7892-193X], Rice, Kenneth M [0000-0002-3071-7278], Smith, Albert V [0000-0003-1942-5845], Sun, Benjamin B [0000-0001-6347-2281], Taylor, Kent D [0000-0002-2756-4370], Thio, Chris HL [0000-0003-2623-7172], Uitterlinden, André G [0000-0002-7276-3387], Edwards, Todd L [0000-0003-4318-6119], Morris, Andrew P [0000-0002-6805-6014], Pendergrass, Sarah A [0000-0002-0565-6522], Rotter, Jerome I [0000-0001-7191-1723], Butterworth, Adam S [0000-0002-6915-9015], Hung, Adriana M [0000-0002-3203-1608]
المصدر: Nature Communications
Nature Communications, 10. NATURE PUBLISHING GROUP
Nature Communications, 10(1):4130. Nature Publishing Group
Nature Communications, 10:4130. Nature Publishing Group
Nature Communications, Vol 10, Iss 1, Pp 1-19 (2019)
Nature Communications, Vol. 10, No 1 (2019) P. 4130
NATURE COMMUNICATIONS
Nat. Commun. 10:4130 (2019)
Teumer, A, Li, Y, Ghasemi, S, Prins, B P, Wuttke, M, Hermle, T, Giri, A, Sieber, K B, Qiu, C, Kirsten, H, Tin, A, Chu, A Y, Bansal, N, Feitosa, M F, Wang, L, Chai, J-F, Cocca, M, Fuchsberger, C, Gorski, M, Hoppmann, A, Horn, K, Li, M, Marten, J, Noce, D, Nutile, T, Sedaghat, S, Sveinbjornsson, G, Tayo, B O, van der Most, P J, Xu, Y, Yu, Z, Gerstner, L, Ärnlöv, J, Bakker, S J L, Baptista, D, Biggs, M L, Boerwinkle, E, Brenner, H, Burkhardt, R, Carroll, R J, Chee, M-L, Chee, M-L, Chen, M, Cheng, C-Y, Cook, J P, Coresh, J, Corre, T, Danesh, J, de Borst, M H, De Grandi, A, de Mutsert, R, de Vries, A P J, Degenhardt, F, Dittrich, K, Divers, J, Eckardt, K-U, Ehret, G, Endlich, K, Felix, J F, Franco, O H, Franke, A, Freedman, B I, Freitag-Wolf, S, Gansevoort, R T, Giedraitis, V, Gögele, M, Grundner-Culemann, F, Gudbjartsson, D F, Gudnason, V, Hamet, P, Harris, T B, Hicks, A A, Holm, H, Foo, V H X, Hwang, S-J, Ikram, M A, Ingelsson, E, Jaddoe, V W V, Jakobsdottir, J, Josyula, N S, Jung, B, Kähönen, M, Khor, C-C, Kiess, W, Koenig, W, Körner, A, Kovacs, P, Kramer, H, Krämer, B K, Kronenberg, F, Lange, L A, Langefeld, C D, Lee, J J-M, Lehtimäki, T, Lieb, W, Lim, S-C, Lind, L, Lindgren, C M, Liu, J, Loeffler, M, Lyytikäinen, L-P, Mahajan, A, Maranville, J C, Mascalzoni, D, McMullen, B, Meisinger, C, Meitinger, T, Miliku, K, Mook-Kanamori, D O, Müller-Nurasyid, M, Mychaleckyj, J C, Nauck, M, Nikus, K, Ning, B, Noordam, R, Connell, J O, Olafsson, I, Palmer, N D, Peters, A, Podgornaia, A I, Ponte, B, Poulain, T, Pramstaller, P P, Rabelink, T J, Raffield, L M, Reilly, D F, Rettig, R, Rheinberger, M, Rice, K M, Rivadeneira, F, Runz, H, Ryan, K A, Sabanayagam, C, Saum, K-U, Schöttker, B, Shaffer, C M, Shi, Y, Smith, A V, Strauch, K, Stumvoll, M, Sun, B B, Szymczak, S, Tai, E-S, Tan, N Y Q, Taylor, K D, Teren, A, Tham, Y-C, Thiery, J, Thio, C H L, Thomsen, H, Thorsteinsdottir, U, Tönjes, A, Tremblay, J, Uitterlinden, A G, van der Harst, P, Verweij, N, Vogelezang, S, Völker, U, Waldenberger, M, Wang, C, Wilson, O D, Wong, C, Wong, T-Y, Yang, Q, Yasuda, M, Akilesh, S, Bochud, M, Böger, C A, Devuyst, O, Edwards, T L, Ho, K, Morris, A P, Parsa, A, Pendergrass, S A, Psaty, B M, Rotter, J I, Stefansson, K, Wilson, J G, Susztak, K, Snieder, H, Heid, I M, Scholz, M, Butterworth, A S, Hung, A M, Pattaro, C & Köttgen, A 2019, ' Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria ', Nature Communications, vol. 10, no. 1, pp. 4130 . https://doi.org/10.1038/s41467-019-11576-0Test
Teumer, Alexander; Li, Yong; Ghasemi, Sahar; Prins, Bram P; Wuttke, Matthias; Hermle, Tobias; Giri, Ayush; Sieber, Karsten B; Qiu, Chengxiang; Kirsten, Holger; Tin, Adrienne; Chu, Audrey Y; Bansal, Nisha; Feitosa, Mary F; Wang, Lihua; Chai, Jin-Fang; Cocca, Massimiliano; Fuchsberger, Christian; Gorski, Mathias; Hoppmann, Anselm; ... (2019). Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Nature communications, 10(1), p. 4130. Nature Publishing Group 10.1038/s41467-019-11576-0 <http://dx.doi.org/10.1038/s41467-019-11576-0Test>
Nature communications 10 (2019). doi:10.1038/s41467-019-11576-0
info:cnr-pdr/source/autori:Teumer A.; Li Y.; Ghasemi S.; Prins B.P.; Wuttke M.; Hermle T.; Giri A.; Sieber K.B.; Qiu C.; Kirsten H.; Tin A.; Chu A.Y.; Bansal N.; Feitosa M.F.; Wang L.; Chai J.-F.; Cocca M.; Fuchsberger C.; Gorski M.; Hoppmann A.; Horn K.; Li M.; Marten J.; Noce D.; Nutile T.; Sedaghat S.; Sveinbjornsson G.; Tayo B.O.; van der Most P.J.; Xu Y.; Yu Z.; Gerstner L.; Arnlov J.; Bakker S.J.L.; Baptista D.; Biggs M.L.; Boerwinkle E.; Brenner H.; Burkhardt R.; Carroll R.J.; Chee M.-L.; Chee M.-L.; Chen M.; Cheng C.-Y.; Cook J.P.; Coresh J.; Corre T.; Danesh J.; de Borst M.H.; De Grandi A.; de Mutsert R.; de Vries A.P.J.; Degenhardt F.; Dittrich K.; Divers J.; Eckardt K.-U.; Ehret G.; Endlich K.; Felix J.F.; Franco O.H.; Franke A.; Freedman B.I.; Freitag-Wolf S.; Gansevoort R.T.; Giedraitis V.; Gogele M.; Grundner-Culemann F.; Gudbjartsson D.F.; Gudnason V.; Hamet P.; Harris T.B.; Hicks A.A.; Holm H.; Foo V.H.X.; Hwang S.-J.; Ikram M.A.; Ingelsson E.; Jaddoe V.W.V.; Jakobsdottir J.; Josyula N.S.; Jung B.; Kahonen M.; Khor C.-C.; Kiess W.; Koenig W.; Korner A.; Kovacs P.; Kramer H.; Kramer B.K.; Kronenberg F.; Lange L.A.; Langefeld C.D.; Lee J.J.-M.; Lehtimaki T.; Lieb W.; Lim S.-C.; Lind L.; Lindgren C.M.; Liu J.; Loeffler M.; Lyytikainen L.-P.; Mahajan A.; Maranville J.C.; Mascalzoni D.; McMullen B.; Meisinger C.; Meitinger T.; Miliku K.; Mook-Kanamori D.O.; Muller-Nurasyid M.; Mychaleckyj J.C.; Nauck M.; Nikus K.; Ning B.; Noordam R.; Connell J.O.; Olafsson I.; Palmer N.D.; Peters A.; Podgornaia A.I.; Ponte B.; Poulain T.; Pramstaller P.P.; Rabelink T.J.; Raffield L.M.; Reilly D.F.; Rettig R.; Rheinberger M.; Rice K.M.; Rivadeneira F.; Runz H.; Ryan K.A.; Sabanayagam C.; Saum K.-U.; Schottker B.; Shaffer C.M.; Shi Y.; Smith A.V.; Strauch K.; Stumvoll M.; Sun B.B.; Szymczak S.; Tai E.-S.; Tan N.Y.Q.; Taylor K.D.; Teren A.; Tham Y.-C.; Thiery J.; Thio C.H.L.; Thomsen H.; Thorsteinsdottir U.; Tonjes A.; Tremblay J.; Uitterlinden A.G.; van der Harst P.; Verweij N.; Vogelezang S.; Volker U.; Waldenberger M.; Wang C.; Wilson O.D.; Wong C.; Wong T.-Y.; Yang Q.; Yasuda M.; Akilesh S.; Bochud M.; Boger C.A.; Devuyst O.; Edwards T.L.; Ho K.; Morris A.P.; Parsa A.; Pendergrass S.A.; Psaty B.M.; Rotter J.I.; Stefansson K.; Wilson J.G.; Susztak K.; Snieder H.; Heid I.M.; Scholz M.; Butterworth A.S.; Hung A.M.; Pattaro C.; Kottgen A./titolo:Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria/doi:10.1038%2Fs41467-019-11576-0/rivista:Nature communications/anno:2019/pagina_da:/pagina_a:/intervallo_pagine:/volume:10مصطلحات موضوعية: 0301 basic medicine, Drosophila melanogaster/genetics, Diabetes Mellitus/genetics, LD SCORE REGRESSION, 030232 urology & nephrology, 45/43, General Physics and Astronomy, Genome-wide association study, BLOOD-PRESSURE, Bioinformatics, GLOMERULAR-FILTRATION-RATE, Genome-wide association studies, Diabetes mellitus genetics, 0302 clinical medicine, Creatinine/urine, Risk Factors, Genome-wide, Phenomics, lcsh:Science, ddc:616, Regulation of gene expression, RISK, Gene knockdown, Kidney diseases, Multidisciplinary, HERITABILITY, Albuminuria/genetics, article, Chromosome Mapping, Kidney disease, ddc, 3. Good health, Drosophila melanogaster, Creatinine, Nýrnasjúkdómar, 692/4022/1585, Slit diaphragm, Medical genetics, medicine.symptom, Erfðarannsóknir, Medical Genetics, medicine.medical_specialty, Science, 631/208/205/2138, 610 Medicine & health, Biology, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Meta-Analysis as Topic, 360 Social problems & social services, Diabetes Mellitus, medicine, Animals, Humans, Albuminuria, Genetic Predisposition to Disease, ddc:610, EXCRETION RATE, CARDIOVASCULAR EVENTS, Genetic association, Medicinsk genetik, TRANS-EQTLS, KIDNEY-DISEASE, General Chemistry, 030104 developmental biology, Gene Expression Regulation, Genetic Loci, COLLABORATIVE METAANALYSIS, lcsh:Q, Genome-Wide Association Study
وصف الملف: application/pdf; application/zip; text/xml
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb733a69b246c6a1b99c26277821ed0dTest
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المؤلفون: Xinyuan Zhang, Frederick E. Dewey, Navya Shilpa Josyula, Dustin N. Hartzel, Shefali S. Verma, Daniel R. Lavage, Sarah A. Pendergrass, Joe Leader, Anurag Verma, Yogasudha Veturi, Marylyn D. Ritchie
المصدر: Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-16 (2018)مصطلحات موضوعية: 0301 basic medicine, Genotype, Databases, Pharmaceutical, lcsh:Medicine, Computational biology, Phenome, Biology, Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, 0302 clinical medicine, Genetic variation, Humans, Disease, lcsh:Science, Author Correction, Gene, Exome sequencing, Loss function, Genetic Association Studies, Genetic association, Multidisciplinary, Genome, Human, lcsh:R, Computational Biology, Phenotype, 030104 developmental biology, Pharmaceutical Preparations, lcsh:Q, DrugBank, 030217 neurology & neurosurgery, Algorithms, Biomarkers, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1568fdf1840c539e19eb72f7d510f7fTest
https://pubmed.ncbi.nlm.nih.gov/30353015Test