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المؤلفون: Jue-Sheng Ong, René Thieme, Janusz Jankowski, Jiyuan An, Anne C. Böhmer, Stuart MacGregor, David C. Whiteman, Johannes Schumacher, Claire Palles, Rachel E. Neale, Matthew Law, Puya Gharahkhani, Ines Gockel, John Lai, Catherine M. Olsen, Xikun Han, Beacon, Rebecca C. Fitzgerald, Tom L. Vaughan
المساهمون: Gharahkhani, Puya [0000-0002-4203-5952], Law, Matthew H [0000-0002-4303-8821], Ong, Jue-Sheng [0000-0002-6062-710X], Han, Xikun [0000-0002-3823-7308], Olsen, Catherine M [0000-0003-4483-1888], Böhmer, Anne C [0000-0002-5716-786X], Fitzgerald, Rebecca C [0000-0002-3434-3568], MacGregor, Stuart [0000-0001-6731-8142], Apollo - University of Cambridge Repository
المصدر: Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Nature Communicationsمصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Science, General Physics and Astronomy, Genome-wide association study, Disease, Esophageal Diseases, Genome-wide association studies, Polymorphism, Single Nucleotide, Gastroenterology, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Gastro-oesophageal reflux disease, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Allele, Esophagus, Risk factor, lcsh:Science, Cancer genetics, Multidisciplinary, business.industry, Esophageal disease, Oesophageal cancer, General Chemistry, medicine.disease, humanities, digestive system diseases, 3. Good health, 030104 developmental biology, medicine.anatomical_structure, Genetic Loci, 030220 oncology & carcinogenesis, Gastroesophageal Reflux, GERD, Adenocarcinoma, lcsh:Q, Female, business, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a530542f0d7f586e929d882bc728eb4dTest
https://doaj.org/article/69989b38dc994e248ea97c1493de2f41Test -
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المؤلفون: Ines Gockel, Janusz Jankowski, Puya Gharahkhani, Claire Palles, Johannes Schumacher, Anne C. Böhmer, Tom L. Vaughan, Jue-Sheng Ong, John Lai, Xikun Han, Rebecca C. Fitzgerald, Jiyuan An, Rachel E. Neale, David C. Whiteman, Catherine M. Olsen, Matthew Law, Stuart MacGregor, René Thieme
المصدر: Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)مصطلحات موضوعية: Male, medicine.medical_specialty, Science, General Physics and Astronomy, Genome-wide association study, Esophageal Diseases, Gastroenterology, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, lcsh:Science, Author Correction, Multidisciplinary, Esophageal disease, business.industry, Reflux, General Chemistry, medicine.disease, Genetic Loci, Gastroesophageal Reflux, lcsh:Q, Female, business, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::315024ced1096294f972d171ad01f510Test
http://europepmc.org/articles/PMC6890747Test -
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المؤلفون: S.E. Moroi, Christopher J Hammond, Peter Kraft, Terri L. Young, Tin Aung, Unnar Thorsteinsdottir, R. Rand Allingham, Francesca Pasutto, Murray H. Brilliant, Robert P. Igo, Joel S. Schuman, Paul R. Lichter, Adriana I. Iglesias Gonzalez, Jessica N. Cooke Bailey, Jonathan L. Haines, Chiea Chuen Khor, Robert Ritch, René Hoehn, John H. Fingert, Puya Gharahkhani, Terry Gaasterland, Calvin C P Pang, Cheng Yu Cheng, Louis R. Pasquale, Lisa A Hark, Andrew J. Lotery, Douglas Vollrath, Yutao Liu, David A. Mackey, Stuart MacGregor, William K. Scott, Pirro G. Hysi, Alex W. Hewitt, Jae H. Kang, Cornelia M. van Duijn, Arthur J. Sit, Margaret A. Pericak-Vance, Michael A. Hauser, Peter Bonnemaijer, Veronique Vitart, Kuldev Singh, D. L. Budenz, Doaa Nabih Maria, Gudmar Thorleifsson, Julia R. Richards, Kari Stefansson, Sumana R Chintalapudi, Doug Rhee, Richard K. Lee, Anthony P Khawaja, Anthony Realini, Robert W. Williams, Eranga N. Vithana, Gadi Wollstein, Fridbert Jonansson, Jamie E Craig, Xiang Di Wang, Tanja Zeller, Douglas E. Gaasterland, Donald J. Zack, Caroline C W Klaver, Janey L. Wiggs, Monica M. Jablonski
المساهمون: Psychiatry, Epidemiology, Clinical Genetics, Ophthalmology
المصدر: Chintalapudi, S R, Maria, D, Di Wang, X, Bailey, J N C, Allingham, R, Brilliant, M, Budenz, D, Fingert, J, Gaasterland, D, Gaasterland, T, Haines, J L, Hark, L, Hauser, M, Igo, R, Hee Kang, J, Kraft, P, Lee, R, Lichter, P, Liu, Y, Moroi, S, Pasquale, L R, Pericak-Vance, M, Realini, A, Rhee, D, Richards, J R, Ritch, R, Schuman, J, Scott, W K, Singh, K, Sit, A, Vollrath, D, Wollstein, G, Zack, D, Aung, T, Bonnemaijer, P, Cheng, C Y, Craig, J, Van Duijn, C, Gharahkhani, P, Iglesias Gonzalez, A, Hammond, C J, Hewitt, A, Hoehn, R, Jonansson, F, Khawaja, A, Chuen Khor, C, Klaver, C C W, Lotery, A, MacKey, D, MacGregor, S, Pang, C, Pasutto, F, Stefansson, K, Thorleifsson, G, Thorsteinsdottir, U, Vitart, V, Vithana, E, Young, T, Zeller, T, Hysi, P G, Wiggs, J L, Williams, R W & Jablonski, M M 2017, ' Systems genetics identifies a role for Cacna2d1 regulation in elevated intraocular pressure and glaucoma susceptibility ', Nature Communications, vol. 8, no. 1, 1755 . https://doi.org/10.1038/s41467-017-00837-5Test
Nature Communications, Vol 8, Iss 1, Pp 1-12 (2017)
Nature Communications
Nature Communications, 8(1):1755. Nature Publishing Groupمصطلحات موضوعية: 0301 basic medicine, Male, Intraocular pressure, Candidate gene, genetic structures, General Physics and Astronomy, Glaucoma, Genome-wide association study, Disease, Bioinformatics, Cohort Studies, Mice, 0302 clinical medicine, lcsh:Science, Multidisciplinary, biology, 3. Good health, Mice, Inbred DBA, CACNA2D1, Female, Glaucoma, Open-Angle, Open angle glaucoma, Science, Polymorphism, Single Nucleotide, General Biochemistry, Genetics and Molecular Biology, Article, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Genetic variation, medicine, Animals, Humans, Genetic Predisposition to Disease, Intraocular Pressure, Aged, business.industry, General Chemistry, medicine.disease, eye diseases, Mice, Inbred C57BL, Disease Models, Animal, 030104 developmental biology, 030221 ophthalmology & optometry, biology.protein, lcsh:Q, Calcium Channels, sense organs, business, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b10ace24e0c92bcd94cc63b53e0738fTest
http://www.scopus.com/inward/record.url?scp=85035018930&partnerID=8YFLogxKTest -
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المؤلفون: Shea Ping Yip, Patrick Y. P. Kao, Fumihiko Matsuda, Hideo Nakanishi, Maria Schache, Tien Yin Wong, Satoshi Morooka, Kyoko Ohno-Matsui, Ozen Polasek, Kenji Yamashiro, Akitaka Tsujikawa, Zhenglin Yang, Chiea Chuen Khor, E-Shyong Tai, Norimoto Gotoh, Yumiko Akagi-Kurashige, Peng Chen, Stuart MacGregor, David A. Mackey, Isao Nakata, Alan F. Wright, Akira Meguro, Seang-Mei Saw, Maurice Yap, Fan Qiao, Yasuharu Tabara, Paul N. Baird, Muka Moriyama, Caroline Hayward, Ching-Yu Cheng, Luling Huang, Andrea J. Richardson, Nobuhisa Mizuki, Veronique Vitart, Yi Shi, Alex W. Hewitt, Sentaro Kusuhara, Tin Aung, Harry Campbell, Kim Hung Leung, Masaki Takeuchi, Gabriel Cuellar, Kenji Suda, Masahiro Miyake, Ryo Yamada, Nagahisa Yoshimura
المصدر: Miyake, M, Yamashiro, K, Tabara, Y, Suda, K, Morooka, S, Nakanishi, H, Khor, C-C, Chen, P, Qiao, F, Nakata, I, Akagi-Kurashige, Y, Gotoh, N, Tsujikawa, A, Meguro, A, Kusuhara, S, Polasek, O, Hayward, C, Wright, A F, Campbell, H, Richardson, A J, Schache, M, Takeuchi, M, Mackey, D A, Hewitt, A W, Cuellar, G, Shi, Y, Huang, L, Yang, Z, Leung, K H, Kao, P Y P, Yap, M K H, Yip, S P, Moriyama, M, Ohno-Matsui, K, Mizuki, N, MacGregor, S, Vitart, V, Aung, T, Saw, S-M, Tai, E-S, Wong, T Y, Cheng, C-Y, Baird, P N, Yamada, R & Matsuda, F & Yoshimura, N 2015, ' Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia ', Nature Communications, vol. 6, 6689 . https://doi.org/10.1038/ncomms7689Test
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic structures, Adolescent, Genotype, General Physics and Astronomy, Animals, Asian Continental Ancestry Group, Cohort Studies, Cornea, Disease Models, Animal, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Humans, Immunohistochemistry, Mice, Middle Aged, Myopia, Polymorphism, Single Nucleotide, Proto-Oncogene Proteins, Retina, RNA, Messenger, Severity of Illness Index, Wnt Proteins, Young Adult, Genome-wide association study, General Biochemistry, Genetics and Molecular Biology, White People, Asian People, Polymorphism (computer science), Ophthalmology, Severity of illness, medicine, Young adult, Multidisciplinary, business.industry, General Chemistry, Odds ratio, eye diseases, medicine.anatomical_structure, Choroidal neovascularization, sense organs, medicine.symptom, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c98516bbd4611cfefdd1d755849650Test
https://pubmed.ncbi.nlm.nih.gov/25823570Test