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1دورية أكاديمية
المؤلفون: Liu, Zhanju, Liu, Ruize, Gao, Han, Jung, Seulgi, Gao, Xiang, Sun, Ruicong, Liu, Xiaoming, Kim, Yongjae, Lee, Ho-Su, Kawai, Yosuke, Nagasaki, Masao, Umeno, Junji, Tokunaga, Katsushi, Kinouchi, Yoshitaka, Masamune, Atsushi, Shi, Wenzhao, Shen, Chengguo, Guo, Zhenglin, Yuan, Kai, FinnGen, International Inflammatory Bowel Disease Genetics, Chinese Inflammatory Bowel Disease Genetics, Zhu, Shu, Li, Dalin, Liu, Jianjun, Ge, Tian, Cho, Judy, Daly, Mark J, McGovern, Dermot P B, Ye, Byong Duk, Song, Kyuyoung, Kakuta, Yoichi, Li, Mingsong, Huang, Hailiang
المساهمون: Abreu, Maria, Achkar, Jean-Paul, Andersen, Vibeke, Bernstein, Charles, Brant, Steven R, Bujanda, Luis, Ng, Siew Chien, Denson, Lee A, Duerr, Richard H, Ferguson, Lynnette R, Franchimont, Denis, Franke, Andre, Gearry, Richard, Hakonarson, Hakon, Halfvarson, Jonas, Heller, Caren, Julià, Antonio, Kelsen, Judith, Khalili, Hamed, Kugathasan, Subramaniam, Kupcinskas, Juozas, Latiano, Anna, Louis, Edouard, Malekzadeh, Reza, McCauley, Jacob L, Moran, Christopher, Okou, David, Orchard, Tim, Palotie, Aarno, Parkes, Miles, Pekow, Joel, Potočnik, Uroš, Radford-Smith, Graham, Rioux, John D, Rogler, Gerhard, Sands, Bruce, Silverberg, Mark, Sokol, Harry, Vermeire, Séverine, Weersma, Rinse K, Xavier, Ramnik J, Hu, Naizhong, Cao, Qian, Wang, Yufang, Miao, Yinglei, Zhang, Hongjie, Lv, Xiaoping, Gao, Xiang, Zhang, Hu, Su, Jingling, Feng, Baisui, Zhao, Ye, Zhu, Liangru, Chen, Yan, Zhu, Lanxiang, Chen, Chunxiao, Wang, Yali, Wang, Yingde, Pang, Zhi, Chen, Yingxuan, Zhang, Xiaolan, Li, Hui, Yu, Qin, Ye, Mei, Zhang, Sumin, Tang, Wen, Wang, Mei, Cao, Xiaocang, Zhu, Ruixin, Zhou, Guangxi, Bian, Zhaolian, Guo, Xiaofeng, Wu, Xiaoli, Liu, Jinchun, Xu, Wei, Li, Yuqin, Guo, Qin, Guo, Zhiguo
المصدر: Nature Genetics, 55 (5), 796-806 (2023-05)
مصطلحات موضوعية: ADAP1 protein, human, GIT2 protein, human, NOD2 protein, human, TNFSF15 protein, human, Tumor Necrosis Factor Ligand Superfamily Member 15, Humans, Colitis, Ulcerative/genetics, Crohn Disease/genetics, East Asian People, European People, Genetic Predisposition to Disease, Genome-Wide Association Study, Inflammatory Bowel Diseases/genetics, Polymorphism, Single Nucleotide/genetics, Tumor Necrosis Factor Ligand Superfamily Member 15/genetics, Human health sciences, Gastroenterology & hepatology, Sciences de la santé humaine, Gastroentérologie & hépatologie
العلاقة: https://www.nature.com/articles/s41588-023-01384-0Test; 10.1038/s41588-023-01384-0; urn:issn:1061-4036; urn:issn:1546-1718
الوصول الحر: https://orbi.uliege.be/handle/2268/309996Test
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2دورية أكاديمية
المساهمون: Ceres Fernandez-Rozadilla, Maria Timofeeva, Zhishan Chen, Philip Law, Minta Thomas, Stephanie Schmit, Virginia Díez-Obrero, Li Hsu, Juan Fernandez-Tajes, Claire Palles, Kitty Sherwood, Sarah Briggs, Victoria Svinti, Kevin Donnelly, Susan Farrington, James Blackmur, Peter Vaughan-Shaw, Xiao-Ou Shu, Jirong Long, Qiuyin Cai, Xingyi Guo, Yingchang Lu, Peter Broderick, James Studd, Jeroen Huyghe, Tabitha Harrison, David Conti, Christopher Dampier, Mathew Devall, Fredrick Schumacher, Marilena Melas, Gad Rennert, Mireia Obón-Santacana, Vicente Martín-Sánchez, Ferran Moratalla-Navarro, Jae Hwan Oh, Jeongseon Kim, Sun Ha Jee, Keum Ji Jung, Sun-Seog Kweon, Min-Ho Shin, Aesun Shin, Yoon-Ok Ahn, Dong-Hyun Kim, Isao Oze, Wanqing Wen, Keitaro Matsuo, Koichi Matsuda, Chizu Tanikawa, Zefang Ren, Yu-Tang Gao, Wei-Hua Jia, John Hopper, Mark Jenkins, Aung Ko Win, Rish Pai, Jane Figueiredo, Robert Haile, Steven Gallinger, Michael Woods, Polly Newcomb, David Duggan, Jeremy Cheadle, Richard Kaplan, Timothy Maughan, Rachel Kerr, David Kerr, Iva Kirac, Jan Böhm, Lukka-Pekka Mecklin, Pekka Jousilahti, Paul Knekt, Lauri Aaltonen, Harri Rissanen, Eero Pukkala, Johan Eriksson, Tatiana Cajuso, Ulrika Hänninen, Johanna Kondelin, Kimmo Palin, Tomas Tanskanen, Laura Renkonen-Sinisalo, Brent Zanke, Satu Männistö, Demetrius Albanes, Stephanie Weinstein, Edward Ruiz-Narvaez, Julie Palmer, Daniel Buchanan, Elizabeth Platz, Kala Visvanathan, Cornelia Ulrich, Erin Siegel, Stefanie Brezina, Andrea Gsur, Peter Campbell, Jenny Chang-Claude, Michael Hoffmeister, Hermann Brenner, Martha Slattery
مصطلحات موضوعية: Colorectal Neoplasms* / genetics, East Asian People* / genetics, European People* / genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Multiomics, Polymorphism, Single Nucleotide / genetics
العلاقة: NATURE GENETICS; J02294; OAK-2023-02622; OAK-2023-02623; https://ir.ymlib.yonsei.ac.kr/handle/22282913/196118Test; T202302780; NATURE GENETICS, Vol.55(1) : 89-99, 2023-01
الإتاحة: https://doi.org/10.1038/s41588-022-01222-9Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/196118Test -
3دورية أكاديميةGenetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage
المؤلفون: Gaastra, Ben, Duncan, Poppy, Bakker, Mark K., Hostettler, Isabel C., Alg, Varinder S., Houlden, Henry, Ruigrok, Ynte M., Galea, Ian, Tapper, Will, Werring, David, Bulters, Diederik
المساهمون: Neurogenetica, Neurologen, Brain, Circulatory Health
مصطلحات موضوعية: NF-E2-related factor 2, polymorphism, single nucleotide, subarachnoid haemorrhage, Single Nucleotide/genetics, Subarachnoid Hemorrhage/genetics, Humans, Alleles, Genotype, NF-E2-Related Factor 2/genetics, Clinical Neurology, Neurology, Journal Article, Meta-Analysis
وصف الملف: application/pdf
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4دورية أكاديمية
المؤلفون: Siedlinski, Mateusz, Carnevale, Lorenzo, Xu, Xiaoguang, Carnevale, Daniela, Evangelou, Evangelos, Caulfield, Mark J, Maffia, Pasquale, Wardlaw, Joanna, Samani, Nilesh J, Tomaszewski, Maciej, Lembo, Giuseppe, Holmes, Michael V, Guzik, Tomasz J
المصدر: Siedlinski , M , Carnevale , L , Xu , X , Carnevale , D , Evangelou , E , Caulfield , M J , Maffia , P , Wardlaw , J , Samani , N J , Tomaszewski , M , Lembo , G , Holmes , M V & Guzik , T J 2023 , ' Genetic analyses identify brain structures related to cognitive impairment associated with elevated blood pressure ' , European Heart Journal , vol. 44 , no. 23 , pp. 2114-2125 . https://doi.org/10.1093/eurheartj/ehad101Test
مصطلحات موضوعية: Humans, Blood Pressure, Hypertension/complications, Cognitive Dysfunction/genetics, Brain, Mendelian Randomization Analysis/methods, Genome-Wide Association Study, Polymorphism, Single Nucleotide/genetics
الإتاحة: https://doi.org/10.1093/eurheartj/ehad101Test
https://research.manchester.ac.uk/en/publications/c67a94e1-d53d-43c3-ac99-0efe8d03f6b0Test
http://www.scopus.com/inward/record.url?scp=85163892242&partnerID=8YFLogxKTest
https://www.mendeley.com/catalogue/3cfd4945-f251-3228-b88d-94efe3391660Test/ -
5دورية أكاديمية
المصدر: 2023 , ' A multivariate genome-wide association study of psycho-cardiometabolic multimorbidity ' , Plos Genetics , vol. 19 , no. 6 , e1010508 . https://doi.org/10.1371/journal.pgen.1010508Test
مصطلحات موضوعية: Humans, Diabetes Mellitus, Type 2/epidemiology, Genome-Wide Association Study, Multimorbidity, Risk Factors, Coronary Artery Disease/epidemiology, Mendelian Randomization Analysis, Polymorphism, Single Nucleotide/genetics, /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being
الإتاحة: https://doi.org/10.1371/journal.pgen.1010508Test
https://researchportal.bath.ac.uk/en/publications/f7cc15a4-8e34-44d0-91c3-88909dcc45c5Test
http://www.scopus.com/inward/record.url?scp=85164715294&partnerID=8YFLogxKTest -
6دورية أكاديمية
المصدر: The PRACTICAL Consortium 2023 , ' Genetically proxied glucose-lowering drug target perturbation and risk of cancer : a Mendelian randomisation analysis ' , Diabetologia , vol. 66 , no. 8 , pp. 1481-1500 . https://doi.org/10.1007/s00125-023-05925-4Test
مصطلحات موضوعية: ABCC8, Breast cancer, Colorectal cancer, GLP1R, Glucose-lowering drug targets, Mendelian randomisation, PPARG, Prostate cancer, Genome-Wide Association Study, Humans, Risk Factors, Colorectal Neoplasms/genetics, Male, Glucose, Polymorphism, Single Nucleotide/genetics, Diabetes Mellitus, Type 2/drug therapy, Prostatic Neoplasms/complications, Mendelian Randomization Analysis, Breast Neoplasms/genetics, PPAR gamma/genetics
الإتاحة: https://doi.org/10.1007/s00125-023-05925-4Test
https://pure.au.dk/portal/en/publications/ccc37670-0dee-479b-bd77-1f542cb4bd93Test
http://www.scopus.com/inward/record.url?scp=85164210817&partnerID=8YFLogxKTest -
7دورية أكاديمية
المصدر: Privé , F , Albiñana , C , Arbel , J , Pasaniuc , B & Vilhjálmsson , B J 2023 , ' Inferring disease architecture and predictive ability with LDpred2-auto ' , American Journal of Human Genetics , vol. 110 , no. 12 , pp. 2042-2055 . https://doi.org/10.1016/j.ajhg.2023.10.010Test
مصطلحات موضوعية: LDpred2, inference, Polymorphism, Single Nucleotide/genetics, Genome-Wide Association Study/methods, Humans, Bayes Theorem, Multifactorial Inheritance/genetics
الإتاحة: https://doi.org/10.1016/j.ajhg.2023.10.010Test
https://pure.au.dk/portal/en/publications/5c98c8f3-2487-4851-bda2-0e241ecebea1Test
http://www.scopus.com/inward/record.url?scp=85177768550&partnerID=8YFLogxKTest -
8دورية أكاديمية
المؤلفون: Wang, Xiaotong, Hivert, Valentin, Groot, Shiane, Wang, Ying, Yengo, Loic, McGrath, John J, Kemper, Kathryn E, Visscher, Peter M, Wray, Naomi R, Revez, Joana A
المصدر: Wang , X , Hivert , V , Groot , S , Wang , Y , Yengo , L , McGrath , J J , Kemper , K E , Visscher , P M , Wray , N R & Revez , J A 2023 , ' Cross-ancestry analyses identify new genetic loci associated with 25-hydroxyvitamin D ' , PLOS Genetics , vol. 19 , no. 11 , e1011033 . https://doi.org/10.1371/journal.pgen.1011033Test
مصطلحات موضوعية: Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide/genetics, Vitamin D Deficiency/genetics, Vitamin D/genetics
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.1371/journal.pgen.1011033Test
https://pure.au.dk/portal/en/publications/6ad7bd83-50dd-4723-9864-c2f0d9a9bb9cTest
https://pure.au.dk/ws/files/372729997/journal.pgen.1011033.pdfTest
http://www.scopus.com/inward/record.url?scp=85176756696&partnerID=8YFLogxKTest -
9دورية أكاديمية
المؤلفون: Fernandez-Rozadilla, Ceres, Timofeeva, Maria, Chen, Zhishan, Law, Philip, Thomas, Minta, Schmit, Stephanie, Díez-Obrero, Virginia, Hsu, Li, Fernandez-Tajes, Juan, Palles, Claire, Sherwood, Kitty, Briggs, Sarah, Svinti, Victoria, Donnelly, Kevin, Farrington, Susan, Blackmur, James, Vaughan-Shaw, Peter, Shu, Xiao ou, Long, Jirong, Cai, Qiuyin, Guo, Xingyi, Lu, Yingchang, Broderick, Peter, Studd, James, Huyghe, Jeroen, Harrison, Tabitha, Conti, David, Dampier, Christopher, Devall, Mathew, Schumacher, Fredrick, Melas, Marilena, Rennert, Gad, Obón-Santacana, Mireia, Martín-Sánchez, Vicente, Moratalla-Navarro, Ferran, Oh, Jae Hwan, Kim, Jeongseon, Jee, Sun Ha, Jung, Keum Ji, Kweon, Sun Seog, Shin, Min Ho, Shin, Aesun, Ahn, Yoon Ok, Kim, Dong Hyun, Oze, Isao, Wen, Wanqing, Matsuo, Keitaro, Matsuda, Koichi, Tanikawa, Chizu, Ren, Zefang, Gao, Yu Tang, Jia, Wei Hua, Hopper, John, Jenkins, Mark, Win, Aung Ko, Pai, Rish, Figueiredo, Jane, Haile, Robert, Gallinger, Steven, Woods, Michael, Newcomb, Polly, Duggan, David, Cheadle, Jeremy, Kaplan, Richard, Maughan, Timothy, Kerr, Rachel, Kerr, David, Kirac, Iva, Böhm, Jan, Mecklin, Lukka Pekka, Jousilahti, Pekka, Knekt, Paul, Aaltonen, Lauri, Rissanen, Harri, Pukkala, Eero, Eriksson, Johan, Cajuso, Tatiana, Hänninen, Ulrika, Kondelin, Johanna, Palin, Kimmo, Tanskanen, Tomas, Renkonen-Sinisalo, Laura, Zanke, Brent, Männistö, Satu, Albanes, Demetrius, Weinstein, Stephanie, Ruiz-Narvaez, Edward, Palmer, Julie, Buchanan, Daniel, Platz, Elizabeth, Visvanathan, Kala, Ulrich, Cornelia, Siegel, Erin, Brezina, Stefanie, Gsur, Andrea, Campbell, Peter, Chang-Claude, Jenny, Hoffmeister, Michael, Brenner, Hermann, Slattery, Martha, Potter, John, Tsilidis, Konstantinos, Schulze, Matthias, Gunter, Marc, Murphy, Neil, Castells, Antoni, Castellví-Bel, Sergi, Moreira, Leticia, Arndt, Volker, Shcherbina, Anna, Stern, Mariana, Pardamean, Bens, Bishop, Timothy, Giles, Graham, Southey, Melissa, Idos, Gregory, McDonnell, Kevin, Abu-Ful, Zomoroda, Greenson, Joel, Shulman, Katerina, Lejbkowicz, Flavio, Offit, Kenneth, Su, Yu Ru, Steinfelder, Robert, Keku, Temitope, van Guelpen, Bethany, Hudson, Thomas, Hampel, Heather, Pearlman, Rachel, Berndt, Sonja, Hayes, Richard, Martinez, Marie Elena, Thomas, Sushma, Corley, Douglas, Pharoah, Paul, Larsson, Susanna, Yen, Yun, Lenz, Heinz Josef, White, Emily, Li, Li, Doheny, Kimberly, Pugh, Elizabeth, Shelford, Tameka, Chan, Andrew, Cruz-Correa, Marcia, Lindblom, Annika, Hunter, David, Joshi, Amit, Schafmayer, Clemens, Scacheri, Peter, Kundaje, Anshul, Nickerson, Deborah, Schoen, Robert, Hampe, Jochen, Stadler, Zsofia, Vodicka, Pavel, Vodickova, Ludmila, Vymetalkova, Veronika, Papadopoulos, Nickolas, Edlund, Chistopher, Gauderman, William, Thomas, Duncan, Shibata, David, Toland, Amanda, Markowitz, Sanford, Kim, Andre, Chanock, Stephen, van Duijnhoven, Franzel, Feskens, Edith, Sakoda, Lori, Gago-Dominguez, Manuela, Wolk, Alicja, Naccarati, Alessio, Pardini, Barbara, FitzGerald, Liesel, Lee, Soo Chin, Ogino, Shuji, Bien, Stephanie, Kooperberg, Charles, Li, Christopher, Lin, Yi, Prentice, Ross, Qu, Conghui, Bézieau, Stéphane, Tangen, Catherine, Mardis, Elaine, Yamaji, Taiki, Sawada, Norie, Iwasaki, Motoki, Haiman, Christopher, Le Marchand, Loic, Wu, Anna, Qu, Chenxu, McNeil, Caroline, Coetzee, Gerhard, Hayward, Caroline, Deary, Ian, Harris, Sarah, Theodoratou, Evropi, Reid, Stuart, Walker, Marion, Ooi, Li Yin, Moreno, Victor, Casey, Graham, Gruber, Stephen, Tomlinson, Ian, Zheng, Wei, Dunlop, Malcolm, Houlston, Richard, Peters, Ulrike
المصدر: Fernandez-Rozadilla , C , Timofeeva , M , Chen , Z , Law , P , Thomas , M , Schmit , S , Díez-Obrero , V , Hsu , L , Fernandez-Tajes , J , Palles , C , Sherwood , K , Briggs , S , Svinti , V , Donnelly , K , Farrington , S , Blackmur , J , Vaughan-Shaw , P , Shu , X O , Long , J , Cai , Q , Guo , X , Lu , Y , Broderick , P , Studd , J , Huyghe , ....
مصطلحات موضوعية: Colorectal Neoplasms/genetics, East Asian People/genetics, European People/genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Multiomics, Polymorphism, Single Nucleotide/genetics
وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.spreadsheetml.sheet
العلاقة: https://portal.findresearcher.sdu.dk/da/publications/6611e9c2-5392-4b94-bd23-1bcac0010cb4Test
الإتاحة: https://doi.org/10.1038/s41588-022-01222-9Test
https://doi.org/10.1038/s41588-023-01334-wTest
https://portal.findresearcher.sdu.dk/da/publications/6611e9c2-5392-4b94-bd23-1bcac0010cb4Test
https://findresearcher.sdu.dk/ws/files/226512438/62499_2_merged_1665683535.pdfTest
https://findresearcher.sdu.dk/ws/files/226512440/SuppTables_110422.xlsxTest
https://findresearcher.sdu.dk/ws/files/226512442/62499_2_supp_707822_rbznjt_convrt.pdfTest -
10دورية أكاديمية
المؤلفون: Wang, Chaoqun, Han, Xiaolei, Dong, Yi, Liu, Cuicui, Wang, Xiaojie, Hou, Tingting, Tan, Qihua, Wang, Yangxiang, Du, Yifeng, Qiu, Chengxuan
المصدر: Wang , C , Han , X , Dong , Y , Liu , C , Wang , X , Hou , T , Tan , Q , Wang , Y , Du , Y & Qiu , C 2023 , ' Associations of WWC1 variants with Alzheimer's disease and vascular dementia among rural older adults in China: A population-based study ' , Neurobiology of Aging , vol. 125 , pp. 109-114 . https://doi.org/10.1016/j.neurobiolaging.2023.01.003Test
مصطلحات موضوعية: Alzheimer's disease, Population-based study, Vascular dementia, WWC1 rs17070145, Stroke, Humans, Alzheimer Disease/epidemiology, Genotype, Male, Polymorphism, Single Nucleotide/genetics, Intracellular Signaling Peptides and Proteins/genetics, Female, Aged, China/epidemiology, Dementia, Vascular/genetics
وصف الملف: application/pdf
العلاقة: https://portal.findresearcher.sdu.dk/da/publications/98cd3b12-3a75-4438-9571-d109e81f492bTest
الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2023.01.003Test
https://portal.findresearcher.sdu.dk/da/publications/98cd3b12-3a75-4438-9571-d109e81f492bTest
https://findresearcher.sdu.dk/ws/files/252957430/1-s2.0-S0197458023000039-main.pdfTest