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المؤلفون: David C. Whiteman, Thomas L. Vaughan, Bradley J. Kendall, Puya Gharahkhani, Stuart MacGregor, Jue-Sheng Ong
المصدر: Human Molecular Genetics
مصطلحات موضوعية: AcademicSubjects/SCI01140, Male, medicine.medical_specialty, Coronary Artery Disease, Disease, Biology, Polymorphism, Single Nucleotide, Severity of Illness Index, Body Mass Index, Coronary artery disease, Risk Factors, Diabetes mellitus, Internal medicine, Mendelian randomization, Genetics, medicine, Humans, Genetic Predisposition to Disease, Obesity, Risk factor, Association Studies Article, Molecular Biology, Genetics (clinical), Genetic association, SARS-CoV-2, Smoking, COVID-19, General Medicine, Mendelian Randomization Analysis, medicine.disease, humanities, digestive system diseases, Hospitalization, Diabetes Mellitus, Type 2, Gastroesophageal Reflux, GERD, Female, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::386bd4a1e404d075ee3b04d054e98c46Test
https://doi.org/10.1093/hmg/ddab253Test -
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المؤلفون: Stuart MacGregor, Kiarash Khosrotehrani, Nicholas K. Hayward, Richard A. Scolyer, David L. Duffy, Casey Rowe, Gemma Cadby, Sarah V. Ward, Mark M. Iles, Lisa Bowdler, Jennifer H. Barrett, Matthew Law, Ernest Mangantig, Anne E. Cust, John F. Thompson, David C. Whiteman, Grant W. Montgomery, Georgina V. Long, Graham J. Mann, Anjali K. Henders
المصدر: Human Molecular Genetics
مصطلحات موضوعية: AcademicSubjects/SCI01140, 0301 basic medicine, Oncology, medicine.medical_specialty, Skin Neoplasms, Population, Genome-wide association study, Locus (genetics), Biology, Germline, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Genetic variation, Biomarkers, Tumor, Genetics, medicine, Humans, Genetic Predisposition to Disease, Association Studies Article, education, Melanoma, Molecular Biology, Germ-Line Mutation, Genetics (clinical), education.field_of_study, General Medicine, Heritability, Prognosis, medicine.disease, Survival Rate, Phenotype, 030104 developmental biology, 030220 oncology & carcinogenesis, Cutaneous melanoma, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1404356709eef562b7c7515cb9f278Test
https://doi.org/10.1093/hmg/ddaa222Test -
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المؤلفون: Nicholas K. Hayward, Robyn P. M. Saw, Jonathan R. Stretch, Kerwin F. Shannon, Grant W. Montgomery, Matthew Law, Antonia L. Pritchard, Jane M. Palmer, Kiarash Khosrotehrani, David L. Duffy, Graham J. Mann, Anne E. Cust, Peter Johansson, Nicholas G. Martin, Richard A. Scolyer, John F. Thompson, Georgina V. Long, Lauren G. Aoude, Andrew J. Spillane, Mark M. Iles, Stuart MacGregor
المصدر: Human Molecular Genetics
مصطلحات موضوعية: AcademicSubjects/SCI01140, Male, Multifactorial Inheritance, Skin Neoplasms, Ultraviolet Rays, Penetrance, Biology, medicine.disease_cause, Germline, 03 medical and health sciences, 0302 clinical medicine, CDKN2A, Genetics, medicine, Humans, Genetic Predisposition to Disease, Allele, Association Studies Article, Molecular Biology, neoplasms, Melanoma, Genetics (clinical), Alleles, Cyclin-Dependent Kinase Inhibitor p16, Germ-Line Mutation, 030304 developmental biology, Whole genome sequencing, 0303 health sciences, Mutation, General Medicine, medicine.disease, 030220 oncology & carcinogenesis, Cutaneous melanoma, Etiology, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c26eb2702a938ee4d5606f15869cab6Test
http://europepmc.org/articles/PMC7566496Test -
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المؤلفون: Upekha E Liyanage, Jiyuan An, David C. Whiteman, Matthew Law, Stuart MacGregor, Scott D. Gordon, Xikun Han, Catherine M. Olsen, Puya Gharahkhani, Jue-Sheng Ong, Rachel E. Neale
المصدر: Human Molecular Genetics
مصطلحات موضوعية: Keratinocytes, Linkage disequilibrium, Skin Neoplasms, Quantitative Trait Loci, Single-nucleotide polymorphism, Genome-wide association study, Quantitative trait locus, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Quantitative Trait, Heritable, Genetic variation, Genetics, medicine, Odds Ratio, Humans, Genetic Predisposition to Disease, Association Studies Article, Molecular Biology, Genetics (clinical), Alleles, 030304 developmental biology, Genetic association, 0303 health sciences, Gene Expression Profiling, Cancer, Computational Biology, Molecular Sequence Annotation, General Medicine, medicine.disease, Genetic architecture, 3. Good health, Carcinoma, Basal Cell, 030220 oncology & carcinogenesis, Case-Control Studies, Carcinoma, Squamous Cell, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004f10d7b23a88a3e18df5533d560aefTest
http://europepmc.org/articles/PMC6737293Test -
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المؤلفون: Alex W. Hewitt, Yukihiro Shiga, Yukihide Momozawa, Adeyinka O. Ashaye, Koichi Matsuda, Shoichiro Tsugane, Haruo Mikami, Koh Hei Sonoda, Koji M. Nishiguchi, Makoto Araie, Kenji Kashiwagi, Yoichiro Kamatani, Mamoru Satoh, Tetsuya Yamamoto, Chiea Chuen Khor, Janey L. Wiggs, Toru Nakazawa, Takeshi Iwata, Puya Gharahkhani, Shamira A. Perera, Kazuhide Kawase, Mariko Naito, Masahiro Miyake, Taiki Yamaji, Koji Nitta, Nobuo Fuse, Micheal Hauser, Susan Williams, Nobuhiro Shimozawa, Kota Sato, Ching-Yu Cheng, Atsushi Takahashi, Masato Akiyama, Tin Aung, Makoto Aihara, Tatsuro Ishibashi, Aiko Iwase, Eranga N. Vithana, Mitsuko Takamoto, R. Rand Allingham, Kenji Wakai, Mineo Ozaki, Mani Baskaran, Makoto Sasaki, Munemitsu Yoshikawa, Yasuhiro Ikeda, Louis R. Pasquale, Motoki Iwasaki, Donald L. Budenz, Jamie E Craig, Kathryn P. Burdon, Yoshitaka Oka, Stuart MacGregor, Fumihiko Mabuchi, Kenji Yamashiro, Stephan Akafo, David A. Mackey, Jae H. Kang, Yoshiaki Kiuchi, Michiaki Kubo, Makoto Nakamura, Yoichi Suzuki, Isao Oze, Shiroaki Shirato, Jessica N. Cooke Bailey, Makoto Hirata, Jonathan L. Haines
المصدر: Human Molecular Genetics. 27:1486-1496
مصطلحات موضوعية: Male, 0301 basic medicine, Candidate gene, genetic structures, Black People, Gene Expression, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, White People, 03 medical and health sciences, 0302 clinical medicine, Asian People, Polymorphism (computer science), Genetics, Humans, Genetic Predisposition to Disease, Eye Proteins, Association Studies Article, Molecular Biology, Genetics (clinical), Genetic association, Case-control study, General Medicine, eye diseases, Genetic architecture, ErbB Receptors, 030104 developmental biology, Diabetes Mellitus, Type 2, Cardiovascular Diseases, Genetic Loci, Case-Control Studies, Mutation, 030221 ophthalmology & optometry, Female, sense organs, Candidate Disease Gene, Glaucoma, Open-Angle, Genome-Wide Association Study, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298869a72354e1a0ffbbd8fec9552469Test
https://doi.org/10.1093/hmg/ddy053Test -
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المؤلفون: Louis R. Pasquale, Jia Yu Koh, Aniket Mishra, Ananth C. Viswanathan, Mani Baskaran, Jie Jin Wang, Jonathan L. Haines, Angela J. Cree, Henriët Springelkamp, Puya Gharahkhani, Seyhan Yazar, Gabriel Cuellar-Partida, Herma C. van der Linde, Hans G Lemij, Thibaud Boutin, Yik Ying Teo, Stuart MacGregor, Jae H. Kang, Li Zheng, Leonieke M E van Koolwijk, Janey L. Wiggs, Qiao Fan, Cornelia M. van Duijn, Rob Willemsen, René Höhn, Stefan Nickels, Tien Yin Wong, Najaf Amin, Shamira A. Perera, Lisa S. Kearns, Pirro G. Hysi, Roger C. W. Wolfs, Jost B. Jonas, Robert Luben, Tiger Zhou, André G. Uitterlinden, Wanting Zhao, Elisabeth M. van Leeuwen, Wishal D. Ramdas, Cristina Venturini, Caroline C W Klaver, Xueling Sim, Sven J. van der Lee, Tin Aung, Jiemin Liao, Karl J. Lackner, Andrew J. Lotery, Adriana I Iglesias, Albert Hofman, Ben A. Oostra, Fernando Rivadeneira, Paul J. Foster, Eranga N. Vithana, Nomdo M. Jansonius, Jamie E Craig, E. Shyong Tai, Veronique Vitart, Ching-Yu Cheng, Ekaterina Yonova-Doing, Robert Wojciechowski, Chiea Chuen Khor, Kathryn P. Burdon, Anthony P Khawaja, Christopher J Hammond, Jane Gibson, Norbert Pfeiffer, Tanja Zeller, Johannes R. Vingerling, Emmanuelle Souzeau, Ya Xing Wang, Grant W. Montgomery, David A. Mackey, Philipp S. Wild, Paul Mitchell, Terri L. Young, Alex W. Hewitt, Paulus T. V. M. de Jong, Paul G. Sanfilippo, Abhishek Nag, Yih Chung Tham, Christian P. Müller, Jessica N. Cooke Bailey, James F. Wilson
المساهمون: Perceptual and Cognitive Neuroscience (PCN), Complex Trait Genetics, Amsterdam Neuroscience - Complex Trait Genetics, Culture, Organization and Management, Epidemiology, Ophthalmology, Internal Medicine, Clinical Genetics, Neurology, MUMC+: MA UECM Oogartsen ZL (9), MUMC+: MA UECM Oogartsen MUMC (9), RS: FHML non-thematic output, Netherlands Institute for Neuroscience (NIN)
المصدر: Springelkamp, H, Iglesias, A I, Mishra, A, Höhn, R, Wojciechowski, R, Khawaja, A P, Nag, A, Wang, Y X, Wang, J J, Cuellar-Partida, G, Gibson, J, Cooke Bailey, J N, Vithana, E N, Gharahkhani, P, Boutin, T, Ramdas, W D, Zeller, T, Luben, R N, Yonova-Doing, E, Viswanathan, A C, Yazar, S, Cree, A J, Haines, J L, Koh, J Y, Souzeau, E, Wilson, J F, Amin, N, Müller, C, Venturini, C, Kearns, L S, Kang, J H, Tham, Y C, Zhou, T, van Leeuwen, E M, Nickels, S, Sanfilippo, P, Liao, J, van der Linde, H, Zhao, W, van Koolwijk, L M E, Zheng, L, Rivadeneira, F, Baskaran, M, van der Lee, S J, Perera, S, de Jong, P T V M, Oostra, B A, Uitterlinden, A G, Fan, Q, Hofman, A & NEIGHBORHOOD Consortium 2017, ' New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics ', Human Molecular Genetics, vol. 26, no. 2, pp. 438-453 . https://doi.org/10.1093/hmg/ddw399Test
Human Molecular Genetics, 26(2), 438-453
Human Molecular Genetics, 26(2), 438-453. Oxford University Press
Human Molecular Genetics, 26, 2, pp. 438-453
Human Molecular Genetics
Human Molecular Genetics, 26, 438-453
Springelkamp, H, Iglesias, A I, Mishra, A, Höhn, R, Wojciechowski, R, Khawaja, A P, Nag, A, Wang, Y X, Wang, J J, Cuellar-partida, G, Gibson, J, Cooke Bailey, J N, Vithana, E N, Gharahkhani, P, Boutin, T, Ramdas, W D, Zeller, T, Luben, R N, Yonova-doing, E, Viswanathan, A C, Yazar, S, Cree, A J, Haines, J L, Koh, J Y, Souzeau, E, Wilson, J F, Amin, N, Müller, C, Venturini, C, Kearns, L S, Hee Kang, J, Consortium, N, Tham, Y C, Zhou, T, Van Leeuwen, E M, Nickels, S, Sanfilippo, P, Liao, J, Linde, H V D, Zhao, W, Van Koolwijk, L M E, Zheng, L, Rivadeneira, F, Baskaran, M, Van Der Lee, S J, Perera, S, De Jong, P T V M, Oostra, B A, Uitterlinden, A G, Fan, Q, Hofman, A, Shyong Tai, E, Vingerling, J R, Sim, X, Wolfs, R C W, Teo, Y Y, Lemij, H G, Khor, C C, Willemsen, R, Lackner, K J, Aung, T, Jansonius, N M, Montgomery, G, Wild, P S, Young, T L, Burdon, K P, Hysi, P G, Pasquale, L R, Wong, T Y, Klaver, C C W, Hewitt, A W, Jonas, J B, Mitchell, P, Lotery, A J, Foster, P J, Vitart, V, Pfeiffer, N, Craig, J E, Mackey, D A, Hammond, C J, Wiggs, J L, Cheng, C, Van Duijn, C M & Macgregor, S 2017, ' New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics ', Human Molecular Genetics, pp. ddw399 . https://doi.org/10.1093/hmg/ddw399Test
Human molecular genetics, 26(2), 438-453. Oxford University Press
Springelkamp, Henriët; Iglesias, Adriana I; Mishra, Aniket; Höhn, René; Wojciechowski, Robert; Khawaja, Anthony P; Nag, Abhishek; Wang, Ya Xing; Wang, Jie Jin; Cuellar-Partida, Gabriel; Gibson, Jane; Bailey, Jessica N Cooke; Vithana, Eranga N; Gharahkhani, Puya; Boutin, Thibaud; Ramdas, Wishal D; Zeller, Tanja; Luben, Robert N; Yonova-Doing, Ekaterina; Viswanathan, Ananth C; ... (2017). New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Human molecular genetics, 26(2), pp. 438-453. Oxford University Press 10.1093/hmg/ddw399 <http://dx.doi.org/10.1093/hmg/ddw399Test>
Human Molecular Genetics, 26, 438-453. Oxford University Pressمصطلحات موضوعية: 0301 basic medicine, Male, Intraocular pressure, genetic structures, Optic disk, Glaucoma, PROTEIN, Genome-wide association study, IDENTIFIES 5, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Optic neuropathy, Optic Nerve Diseases, PROSTATE, Genetics (clinical), RISK, Association Studies Articles, COMMON VARIANTS, General Medicine, Middle Aged, CANCER, 3. Good health, medicine.anatomical_structure, Optic nerve, Female, Glaucoma, Open-Angle, Optic disc, Cyclin-Dependent Kinase Inhibitor p21, medicine.medical_specialty, Open angle glaucoma, SUSCEPTIBILITY LOCI, Optic Disk, 610 Medicine & health, Biology, 03 medical and health sciences, Tonometry, Ocular, Ophthalmology, Genetics, medicine, Humans, GENOME-WIDE ASSOCIATION, Molecular Biology, Intraocular Pressure, Homeodomain Proteins, P53, Genome, Human, POPULATION-BASED EPIDEMIOLOGY, Zebrafish Proteins, medicine.disease, eye diseases, 030104 developmental biology, sense organs, Genome-Wide Association Study
وصف الملف: application/pdf; text
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d9396fd5e09b693625d429c267b9157Test
https://doi.org/10.1093/hmg/ddw399Test -
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المؤلفون: Pirro G. Hysi, Xikun Han, Alex W. Hewitt, Puya Gharahkhani, Mark M. Hassall, Anthony P Khawaja, Tiger Zhou, Stuart MacGregor, Paul J. Foster, Peng T. Khaw, David A. Mackey, Jue-Sheng Ong, Jiyuan An, Jamie E Craig, Ayub Qassim, Henry Marshall
المصدر: Human molecular genetics. 28(21)
مصطلحات موضوعية: Adult, Male, Intraocular pressure, genetic structures, Databases, Factual, Optic Disk, Optic disk, Glaucoma, Gene Expression, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, 0302 clinical medicine, Genetics, medicine, Humans, Prospective Studies, Molecular Biology, Genetics (clinical), 030304 developmental biology, Aged, 0303 health sciences, Anophthalmia, General Medicine, Middle Aged, medicine.disease, eye diseases, medicine.anatomical_structure, Optic nerve, Female, sense organs, 030217 neurology & neurosurgery, Optic disc, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27715e6c863f7dd3a4f9557ac7b66e5bTest
https://pubmed.ncbi.nlm.nih.gov/31809533Test -
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المؤلفون: Stuart MacGregor, Rachel E. Neale, Puya Gharahkhani, Jiyuan An, David C. Whiteman, Jue-Sheng Ong, Matthew Law
المصدر: Human Molecular Genetics.
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, medicine.medical_specialty, Genotype, Colorectal cancer, Biology, Polymorphism, Single Nucleotide, White People, vitamin D deficiency, 03 medical and health sciences, Prostate cancer, 0302 clinical medicine, Breast cancer, Risk Factors, Neoplasms, Internal medicine, Mendelian randomization, Genetics, medicine, Humans, Genetic Predisposition to Disease, Vitamin D, Molecular Biology, Genetics (clinical), Aged, Cancer Death Rate, Cancer, General Medicine, Odds ratio, Mendelian Randomization Analysis, Middle Aged, medicine.disease, 030104 developmental biology, 030220 oncology & carcinogenesis, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84927cbb0f1b843a91d2633c81c6b1fTest
https://doi.org/10.1093/hmg/ddy307Test -
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المؤلفون: Stuart MacGregor, Thomas L. Vaughan, David A. Hinds, David C. Whiteman, Barrett's, Joyce Y. Tung, Aniket Mishra, Puya Gharahkhani
المصدر: Human Molecular Genetics. 25:828-835
مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Linkage disequilibrium, Esophageal Neoplasms, Single-nucleotide polymorphism, Adenocarcinoma, Biology, Bioinformatics, Polymorphism, Single Nucleotide, Risk Assessment, Gastroenterology, Linkage Disequilibrium, White People, Barrett Esophagus, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Esophagus, Molecular Biology, Genetic Association Studies, Genetics (clinical), Incidence, Case-control study, Genetic Variation, General Medicine, medicine.disease, humanities, digestive system diseases, 3. Good health, Editorial, 030104 developmental biology, medicine.anatomical_structure, Case-Control Studies, Meta-analysis, Barrett's esophagus, Gastroesophageal Reflux, GERD, Female, 030211 gastroenterology & hepatology, Genetic Background
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ddb463ba76c6f79e347099c5f080448Test
https://doi.org/10.1093/hmg/ddv512Test -
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المؤلفون: Gabriel Cuellar-Partida, Nicholas G. Martin, Johannes R. Vingerling, Alex W. Hewitt, André G. Uitterlinden, Grant W. Montgomery, Richard A. Mills, Matthew A. Brown, Stuart MacGregor, Kathryn P. Burdon, Cornelia M. van Duijn, Roger C. W. Wolfs, Wishal D. Ramdas, David A. Mackey, Albert Hofman, Jamie E Craig, Seyhan Yazar, Virginie J. M. Verhoeven, Adriana I Iglesias, Elisabeth M. van Leeuwen, Craig E. Pennell, Henriët Springelkamp, Sionne E. M. Lucas, Caroline C W Klaver
المساهمون: MUMC+: MA UECM Oogartsen ZL (9), MUMC+: MA UECM Oogartsen MUMC (9), RS: FHML non-thematic output, Ophthalmology, Epidemiology, Internal Medicine
المصدر: Human Molecular Genetics, 24(17), 5060-5068. Oxford University Press
مصطلحات موضوعية: Adult, Male, Risk, Keratoconus, medicine.medical_specialty, Genotype, genetic structures, Population, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Cornea, Young Adult, Ophthalmology, Genetics, medicine, Humans, Genetic Predisposition to Disease, education, Molecular Biology, Allele frequency, Genetics (clinical), Aged, education.field_of_study, Australia, Genetic Variation, Exons, General Medicine, Odds ratio, Middle Aged, medicine.disease, Twin study, eye diseases, Wnt Proteins, Minor allele frequency, Phenotype, Female, sense organs, Follow-Up Studies
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56ba4fb42d147fe0f7a0cff500022a48Test
https://doi.org/10.1093/hmg/ddv211Test