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المؤلفون: Josh C. Denny, Yong Chen, Ruowang Li, Xinyuan Zhang, Patrick M. A. Sleiman, Rui Duan, Thomas Lumley, Marylyn D. Ritchie, David Carrell, Christopher R. Bauer, Jason H. Moore, Wei-Qi Wei, Jonathan D. Mosley, Georgia L. Wiesner, Robert J. Carroll, Hakon Hakonarson, Digna R. Velez Edwards, Jordan W. Smoller, Sarah A. Pendergrass
المصدر: Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Nature Communicationsمصطلحات موضوعية: 0301 basic medicine, Databases, Factual, Statistical methods, Computer science, Science, General Physics and Astronomy, Health records, Models, Biological, Polymorphism, Single Nucleotide, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Genetic Pleiotropy, Electronic Health Records, Humans, Generalizability theory, Statistical hypothesis testing, Lossless compression, Multidisciplinary, Communication, Genetic data, General Chemistry, Data science, Summary statistics, Phenotype, 030104 developmental biology, Pleiotropy (drugs), Privacy, Data integration, 030217 neurology & neurosurgery, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f29830d863f88144ed6590b83466d23bTest
https://doaj.org/article/f563b6a1c3d34087b48dd7004f4f0993Test -
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المؤلفون: Ian B. Stanaway, David Fasel, Sarah A. Pendergrass, Yatong K. Li, Melody R. Palmer, Hakon Hakonarson, Chunhua Weng, Sunghwan Sohn, David Cronkite, Eric B. Larson, Gail P. Jarvik, David R. Crosslin, Rongling Li, Iftikhar J. Kullo, Adam S. Gordon, David Carrell, Daniel Seung Kim, Xiaomeng Du, QiPing Feng, Samuel K. Handelman, Patrick M. A. Sleiman, Marc S. Williams, Elisabeth A. Rosenthal, Elizabeth K. Speliotes
المصدر: Genetic Epidemiology
مصطلحات موضوعية: medicine.medical_specialty, Epidemiology, Carotid arteries, Bilateral carotid artery stenosis, Locus (genetics), Genome-wide association study, Polymorphism, Single Nucleotide, Gastroenterology, 03 medical and health sciences, Internal medicine, carotid artery atherosclerosis, medicine, Humans, Carotid Stenosis, Genetic Predisposition to Disease, Research Articles, Genetics (clinical), genome‐wide association study, 030304 developmental biology, 0303 health sciences, Models, Genetic, business.industry, 030305 genetics & heredity, Atherosclerotic disease, Genomics, Odds ratio, medicine.disease, Confidence interval, Stenosis, electronic health records, business, Genome-Wide Association Study, Lipoprotein(a), Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68ec6ab9cbd68d69ae19ae8d44180244Test
https://doi.org/10.1002/gepi.22360Test -
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المؤلفون: Jacqueline A, Piekos, Jacklyn N, Hellwege, Yanfei, Zhang, Eric S, Torstenson, Gail P, Jarvik, Ozan, Dikilitas, Iftikhar J, Kullo, Daniel J, Schaid, David R, Crosslin, Sarah A, Pendergrass, Ming Ta Michael, Lee, Dan, Roden, Josh C, Denny, Todd L, Edwards, Digna R, Velez Edwards
المصدر: Human genetics. 141(11)
مصطلحات موضوعية: Leiomyoma, Risk Factors, Humans, Female, Genetic Predisposition to Disease, Genomics, Linkage Disequilibrium, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::0d9267c3027986170877633508a91ad3Test
https://pubmed.ncbi.nlm.nih.gov/35226188Test -
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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: Bertram Müller-Myhsok, John B. Harley, Patrick M. A. Sleiman, Anastasia Lucas, Murray H. Brilliant, Beibei Jiang, Jiayan Zhou, Molly A. Hall, John M. Wallace, Jason H. Moore, John McGuigan, Shefali S. Verma, Yuki Bradford, Hakon Hakonarson, Kristel Van Steen, Yanfei Zhang, Krzysztof Kiryluk, Sarah A. Pendergrass, Kristin Passero, Marylyn D. Ritchie, Peggy L. Peissig
المصدر: PLoS Genetics, Vol 17, Iss 6, p e1009534 (2021)
PLoS Geneticsمصطلحات موضوعية: Cancer Research, Heredity, Eye Diseases, Single Nucleotide Polymorphisms, Datasets as Topic, Genome-wide association study, SUSCEPTIBILITY, QH426-470, DISEASE, Homozygosity, Macular Degeneration, 0302 clinical medicine, Medical Conditions, Gene Frequency, Medicine and Health Sciences, Genetics (clinical), Genetics & Heredity, 0303 health sciences, Heterozygosity, Genomics, BREAST-CANCER RISK, Genetic Mapping, ISCHEMIC-STROKE, Phenotype, Hypertension, symbols, Life Sciences & Biomedicine, Research Article, Single-nucleotide polymorphism, Variant Genotypes, Computational biology, Biology, Polymorphism, Single Nucleotide, Cataract, 03 medical and health sciences, symbols.namesake, Genetic model, LOCUS, Genome-Wide Association Studies, Genetics, Humans, Allele, GENOME-WIDE ASSOCIATION, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Alleles, 030304 developmental biology, TOOLS, Science & Technology, EMERGE NETWORK, Models, Genetic, Cataracts, ELECTRONIC MEDICAL-RECORDS, Biology and Life Sciences, Computational Biology, Human Genetics, Glaucoma, Genome Analysis, POLYMORPHISM, Minor allele frequency, Ophthalmology, Bonferroni correction, Diabetes Mellitus, Type 2, Genetic Loci, Lens Disorders, Multiple comparisons problem, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: Electronic-eCollection
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2417c0b12ab33679e6e18047153250dcTest
https://doaj.org/article/b37fdfc15813491fa1c98bc3372f6d22Test -
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المؤلفون: Mohammad R. Arbabshirani, Yogasudha Veturi, Sarah A. Pendergrass, Chirag Agarwal, Elliott D. K. Cha, Aalpen A. Patel
المصدر: Journal of Obesity, Vol 2018 (2018)
Journal of Obesityمصطلحات موضوعية: Adult, Male, 0301 basic medicine, lcsh:Internal medicine, medicine.medical_specialty, Article Subject, Adolescent, Health Personnel, Endocrinology, Diabetes and Metabolism, education, Adipose tissue, Genome-wide association study, Disease, Type 2 diabetes, Intra-Abdominal Fat, behavioral disciplines and activities, Body Mass Index, Young Adult, 03 medical and health sciences, Risk Factors, Internal medicine, Humans, Medicine, Obesity, lcsh:RC31-1245, Adiposity, Metabolic Syndrome, business.industry, Data Collection, Middle Aged, medicine.disease, Obstructive sleep apnea, 030104 developmental biology, Female, Metabolic syndrome, Tomography, X-Ray Computed, business, Body mass index, Genome-Wide Association Study, Research Article
وصف الملف: text/xhtml
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ce566a9febcb8acda20332e29b7f758Test
https://doi.org/10.1155/2018/3253096Test -
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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: Ky’Era Actkins, Kevin Ho, Gail P. Jarvik, Brody Holohan, Felix R. Day, Navya Shilpa Josyula, Yanfei Zhang, Hakon Hakonarson, Sarah A. Pendergrass, Digna R. Velez Edwards, Ming Ta Michael Lee, Jacob M. Keaton, Dustin N. Hartzel, David R. Crosslin, Patrick M. A. Sleiman, Lea K. Davis, Marc S. Williams, Anne E. Justice, Andrea H. Ramirez, Ian B. Stanaway
مصطلحات موضوعية: Adult, Infertility, Oncology, medicine.medical_specialty, Receptor, ErbB-4, Population, Single-nucleotide polymorphism, Genome-wide association study, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Electronic Health Records, Humans, 030212 general & internal medicine, education, ERBB4, Adaptor Proteins, Signal Transducing, 030304 developmental biology, education.field_of_study, 0303 health sciences, 030219 obstetrics & reproductive medicine, Superoxide Dismutase, business.industry, Hyperandrogenism, Obstetrics and Gynecology, YAP-Signaling Proteins, Middle Aged, medicine.disease, Phenotype, Polycystic ovary, Biobank, 3. Good health, Oligomenorrhea, Ovarian Cysts, Case-Control Studies, Transcriptional Coactivator with PDZ-Binding Motif Proteins, Trans-Activators, Etiology, Female, business, Infertility, Female, Genome-Wide Association Study, Polycystic Ovary Syndrome, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b5dbbd75a0b3144f975140a493278dTest
https://doi.org/10.1101/2019.12.12.19014761Test -
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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