المؤلفون: Umer, Muhammad J, Lu, Qing, Huang, Lu, Batool, Raufa, Liu, Hao, Li, Haifen, Wang, Runfeng, Qianxia, Yu, Varshney, Rajeev K, Pandey, Manish K, Hong, Yanbin, Chen, Xiaoping

مصطلحات موضوعية: Amino Acids - metabolism, Arachis - genetics, Arachis - metabolism, Genome-Wide Association Study, Polymorphism, Single Nucleotide - genetics, Seeds - genetics, Seeds - metabolism

وصف الملف: pdf

Relation: ispartof: Physiologia plantarum issue 5 vol 176; WOS:001328474800001; 991005707261707891; https://researchportal.murdoch.edu.au/view/delivery/61MUN_INST/12168332100007891/13168332090007891; alma:61MUN_INST/bibs/991005707261707891

الاتاحة: https://doi.org/10.1111/ppl.14542
https://researchportal.murdoch.edu.au/esploro/outputs/journalArticle/Genome-wide-association-study-reveals-the-genetic/991005707261707891
https://researchportal.murdoch.edu.au/view/delivery/61MUN_INST/12168332100007891/13168332090007891

المؤلفون: Li, Yanni, van den Berg, Eline H, Kurilshikov, Alexander, Zhernakova, Dasha V, Gacesa, Ranko, Hu, Shixian, Lopera-Maya, Esteban A, Zhernakova, Alexandra, de Meijer, Vincent E, Sanna, Serena, Dullaart, Robin P F, Blokzijl, Hans, Festen, Eleonora A M, Fu, Jingyuan, Weersma, Rinse K

المصدر: Lifelines Cohort Study , Li , Y , van den Berg , E H , Kurilshikov , A , Zhernakova , D V , Gacesa , R , Hu , S , Lopera-Maya , E A , Zhernakova , A , de Meijer , V E , Sanna , S , Dullaart , R P F , Blokzijl , H , Festen , E A M , Fu , J & Weersma , R K 2024 , ' Genome-wide Studies Reveal Genetic Risk Factors for Hepatic Fat Content ' , Genomics, Proteomics & Bioinformatics , vol. 22 , no. ....

مصطلحات موضوعية: Humans, Genome-Wide Association Study, Female, Male, Risk Factors, Genetic Predisposition to Disease/genetics, Liver/diagnostic imaging, Middle Aged, Polymorphism, Single Nucleotide/genetics, Magnetic Resonance Imaging, Non-alcoholic Fatty Liver Disease/genetics, Adult, Aged, Fatty Liver/genetics

وصف الملف: application/pdf

الاتاحة: https://hdl.handle.net/11370/6bb38271-0df2-4ec5-a98d-fc3d5fa906e3
https://research.rug.nl/en/publications/6bb38271-0df2-4ec5-a98d-fc3d5fa906e3
https://doi.org/10.1093/gpbjnl/qzae031
https://pure.rug.nl/ws/files/1080676554/qzae031.pdf

المؤلفون: Epi25 Collaborative, KRAUSE, Roland, FERREIRA DA SILVA, Izabela, ZIZOVIC, Milena, MAY, Patrick

المساهمون: Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group)

المصدر: Nature Neuroscience, 27 (10), 1864 - 1879 (2024-10)

مصطلحات موضوعية: Humans, DNA Copy Number Variations/genetics, Female, Male, Polymorphism, Single Nucleotide/genetics, Risk Factors, Epilepsy/genetics, Genetic Predisposition to Disease/genetics, Exome Sequencing, Exome/genetics, Life sciences, Genetics & genetic processes, Human health sciences, Neurology, Sciences du vivant, Génétique & processus génétiques, Sciences de la santé humaine, Neurologie

Relation: https://www.nature.com/articles/s41593-024-01747-8.pdf; FNR16394868 - Epileptogenesis Of Genetic Epilepsies, 2021 (01/10/2021-.) - Alexander Skupin; urn:issn:1097-6256; urn:issn:1546-1726; https://orbilu.uni.lu/handle/10993/62172; info:hdl:10993/62172; info:pmid:39363051

الاتاحة: https://orbilu.uni.lu/handle/10993/62172
https://orbilu.uni.lu/bitstream/10993/62172/1/Epi25-3.NatNeuro2024.pdf
https://doi.org/10.1038/s41593-024-01747-8

المؤلفون: Yang, Xin, Mooij, Thea M, Leslie, Goska, Ficorella, Lorenzo, Andrieu, Nadine, Kast, Karin, Singer, Christian F, Jakubowska, Anna, van Gils, Carla H, Tan, Yen Y, Engel, Christoph, Adank, Muriel A, van Asperen, Christi J, Ausems, Margreet G E M, Berthet, Pascaline, Collee, Margriet J, Cook, Jackie A, Eason, Jacqueline, Spaendonck-Zwarts, Karin Y van, Evans, D Gareth, Gómez García, Encarna B, Hanson, Helen, Izatt, Louise, Kemp, Zoe, Lalloo, Fiona, Lasset, Christine, Lesueur, Fabienne, Musgrave, Hannah, Nambot, Sophie, Noguès, Catherine, Oosterwijk, Jan C, Stoppa-Lyonnet, Dominique, Tischkowitz, Marc, Tripathi, Vishakha, Wevers, Marijke R, Zhao, Emily, van Leeuwen, Flora E, Schmidt, Marjanka K, Easton, Douglas F, Rookus, Matti A, Antoniou, Antonis C

المصدر: EMBRACE Collaborators , Yang , X , Mooij , T M , Leslie , G , Ficorella , L , Andrieu , N , Kast , K , Singer , C F , Jakubowska , A , van Gils , C H , Tan , Y Y , Engel , C , Adank , M A , van Asperen , C J , Ausems , M G E M , Berthet , P , Collee , M J , Cook , J A , Eason , J , Spaendonck-Zwarts , K Y V , Evans , D G , ....

مصطلحات موضوعية: Humans, Female, Breast Neoplasms/genetics, BRCA2 Protein/genetics, BRCA1 Protein/genetics, Middle Aged, Adult, Prospective Studies, Heterozygote, Genetic Predisposition to Disease, Risk Factors, Risk Assessment, Polymorphism, Single Nucleotide/genetics

وصف الملف: application/pdf

الاتاحة: https://hdl.handle.net/11370/734c0554-5e3b-43ee-b7d7-74b363130169
https://research.rug.nl/en/publications/734c0554-5e3b-43ee-b7d7-74b363130169
https://doi.org/10.1136/jmg-2024-109943
https://pure.rug.nl/ws/files/1082038863/803.full.pdf

المؤلفون: Hewett, A.M., Johnston, S.E., Morris, A., Morris, S., Pemberton, J.M.

المصدر: Molecular ecology, vol. 33, no. 9, pp. e17335

مصطلحات موضوعية: Animals, Deer/genetics, Inbreeding Depression/genetics, Genetic Fitness, Genetics, Population, Polymorphism, Single Nucleotide/genetics, Models, Genetic, Inbreeding, Homozygote, Genotype, Male, Female, inbreeding depression, quantitative genetics, runs of homozygosity

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38549143; info:eu-repo/semantics/altIdentifier/eissn/1365-294X; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_1EAC9FD75BF30; https://serval.unil.ch/notice/serval:BIB_1EAC9FD75BF3; https://serval.unil.ch/resource/serval:BIB_1EAC9FD75BF3.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_1EAC9FD75BF3
https://doi.org/10.1111/mec.17335
https://serval.unil.ch/resource/serval:BIB_1EAC9FD75BF3.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_1EAC9FD75BF30

المؤلفون: Cavinato, T., Rubinacci, S., Malaspinas, A.S., Delaneau, O.

المصدر: Nature computational science, vol. 4, no. 5, pp. 360-366

مصطلحات موضوعية: Humans, Genome-Wide Association Study/methods, Genotype, Linkage Disequilibrium, Haplotypes/genetics, Polymorphism, Single Nucleotide/genetics, Information Dissemination/methods, Computer Simulation, Models, Genetic, Algorithms, Genome, Human/genetics, Poisson Distribution

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38745108; info:eu-repo/semantics/altIdentifier/eissn/2662-8457; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_981E899095A47; https://serval.unil.ch/notice/serval:BIB_981E899095A4; https://serval.unil.ch/resource/serval:BIB_981E899095A4.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_981E899095A4
https://doi.org/10.1038/s43588-024-00630-7
https://serval.unil.ch/resource/serval:BIB_981E899095A4.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_981E899095A47

المؤلفون: Constantinescu, Andrei-Emil, Hughes, David A, Bull, Caroline J, Fleming, Kathryn, Mitchell, Ruth E, Zheng, Jie, Kar, Siddhartha, Timpson, Nicholas J, Amulic, Borko, Vincent, Emma E

المصدر: Constantinescu , A-E , Hughes , D A , Bull , C J , Fleming , K , Mitchell , R E , Zheng , J , Kar , S , Timpson , N J , Amulic , B & Vincent , E E 2024 , ' A genome-wide association study of neutrophil count in individuals associated to an African continental ancestry group facilitates studies of malaria pathogenesis ' , Human Genomics , vol. 18 , no. 1 , 26 , pp. 26 . https://doi.org/10.1186/s40246-024-00585-w

مصطلحات موضوعية: /dk/atira/pure/core/keywords/icep, name=ICEP, Humans, Genome-Wide Association Study/methods, Neutrophils, Black People/genetics, Malaria/epidemiology, Gene Frequency, Polymorphism, Single Nucleotide/genetics, Genetic Predisposition to Disease

الاتاحة: https://hdl.handle.net/1983/e8979da3-6223-4ddb-8da0-7e63cdf0631d
https://research-information.bris.ac.uk/en/publications/e8979da3-6223-4ddb-8da0-7e63cdf0631d
https://doi.org/10.1186/s40246-024-00585-w

المصدر: 2024 , ' Genetic variants for head size share genes and pathways with cancer ' , Cell reports. Medicine , vol. 5 , no. 5 , 101529 , pp. 101529 . https://doi.org/10.1016/j.xcrm.2024.101529

مصطلحات موضوعية: Humans, Genome-Wide Association Study, Head/anatomy & histology, Neoplasms/genetics, Female, Male, Polymorphism, Single Nucleotide/genetics, Genetic Variation, Organ Size/genetics, Signal Transduction/genetics, Adult, Genetic Predisposition to Disease

الاتاحة: https://hdl.handle.net/1983/22e9ca6a-b623-402d-b33b-f02d1bea8707
https://research-information.bris.ac.uk/en/publications/22e9ca6a-b623-402d-b33b-f02d1bea8707
https://doi.org/10.1016/j.xcrm.2024.101529

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

Relation: https://www.nature.com/articles/s41588-023-01384-0; urn:issn:1061-4036; urn:issn:1546-1718

URL الوصول: https://orbi.uliege.be/handle/2268/309996

المؤلفون: Singhal, Pankhuri, Veturi, Yogasudha, Dudek, Scott M, Lucas, Anastasia, Frase, Alex, Van Steen, Kristel, Schrodi, Steven J, Fasel, David, Weng, Chunhua, Pendergrass, Rion, Schaid, Daniel J, Kullo, Iftikhar J, Dikilitas, Ozan, Sleiman, Patrick M A, Hakonarson, Hakon, Moore, Jason H, Williams, Scott M, Ritchie, Marylyn D, Verma, Shefali S

المصدر: American Journal of Human Genetics, 110 (4), 575 - 591 (2023-04-06)

مصطلحات موضوعية: complex human disease, epistasis, essential genes, evolution, interchromosomal, linkage disequilibrium, long-range, pleiotropy, variable expressivity, Linkage Disequilibrium/genetics, Genotype, Biological Specimen Banks, United Kingdom, Polymorphism, Single Nucleotide/genetics, Genome-Wide Association Study, Epistasis, Genetic, Polymorphism, Single Nucleotide, Genetics, Genetics (clinical), Life sciences, Sciences du vivant

Relation: https://api.elsevier.com/content/article/PII:S0002929723000915?httpAccept=text/xml; urn:issn:0002-9297; urn:issn:1537-6605

URL الوصول: https://orbi.uliege.be/handle/2268/304724

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

Relation: NATURE GENETICS; J02294; OAK-2023-02622; OAK-2023-02623; https://ir.ymlib.yonsei.ac.kr/handle/22282913/196118; T202302780; NATURE GENETICS, Vol.55(1) : 89-99, 2023-01

الاتاحة: https://ir.ymlib.yonsei.ac.kr/handle/22282913/196118
https://doi.org/10.1038/s41588-022-01222-9

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

Relation: https://dspace.library.uu.nl/handle/1874/447289

الاتاحة: https://dspace.library.uu.nl/handle/1874/447289

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/ehad101

مصطلحات موضوعية: Humans, Blood Pressure, Hypertension/complications, Cognitive Dysfunction/genetics, Brain, Mendelian Randomization Analysis/methods, Genome-Wide Association Study, Polymorphism, Single Nucleotide/genetics

Relation: https://research.manchester.ac.uk/en/publications/c67a94e1-d53d-43c3-ac99-0efe8d03f6b0

الاتاحة: https://research.manchester.ac.uk/en/publications/c67a94e1-d53d-43c3-ac99-0efe8d03f6b0
https://doi.org/10.1093/eurheartj/ehad101
http://www.scopus.com/inward/record.url?scp=85163892242&partnerID=8YFLogxK
https://www.mendeley.com/catalogue/3cfd4945-f251-3228-b88d-94efe3391660/

المؤلفون: Rubinacci, S., Hofmeister, R.J., Sousa da Mota, B., Delaneau, O.

المصدر: Nature genetics, vol. 55, no. 7, pp. 1088-1090

مصطلحات موضوعية: Gene Frequency, Biological Specimen Banks, Polymorphism, Single Nucleotide/genetics, Genome, United Kingdom, Genotype

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/37386250; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_11B2963EE6A65; https://serval.unil.ch/notice/serval:BIB_11B2963EE6A6; https://serval.unil.ch/resource/serval:BIB_11B2963EE6A6.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_11B2963EE6A6
https://doi.org/10.1038/s41588-023-01438-3
https://serval.unil.ch/resource/serval:BIB_11B2963EE6A6.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_11B2963EE6A65

المؤلفون: Hofmeister, R.J., Ribeiro, D.M., Rubinacci, S., Delaneau, O.

المصدر: Nature genetics, vol. 55, no. 7, pp. 1243-1249

مصطلحات موضوعية: Humans, Biological Specimen Banks, Exome Sequencing, Sequence Analysis, DNA/methods, Genotype, Haplotypes, Genome, Human/genetics, United Kingdom, Polymorphism, Single Nucleotide/genetics

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/37386248; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_EA0C8B7D22EF8; https://serval.unil.ch/notice/serval:BIB_EA0C8B7D22EF; https://serval.unil.ch/resource/serval:BIB_EA0C8B7D22EF.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_EA0C8B7D22EF
https://doi.org/10.1038/s41588-023-01415-w
https://serval.unil.ch/resource/serval:BIB_EA0C8B7D22EF.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_EA0C8B7D22EF8

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.1010508

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

Relation: https://researchportal.bath.ac.uk/en/publications/f7cc15a4-8e34-44d0-91c3-88909dcc45c5

الاتاحة: https://researchportal.bath.ac.uk/en/publications/f7cc15a4-8e34-44d0-91c3-88909dcc45c5
https://doi.org/10.1371/journal.pgen.1010508
http://www.scopus.com/inward/record.url?scp=85164715294&partnerID=8YFLogxK

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/s00125-023-05925-4

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

وصف الملف: application/pdf

الاتاحة: https://pure.au.dk/portal/en/publications/ccc37670-0dee-479b-bd77-1f542cb4bd93
https://doi.org/10.1007/s00125-023-05925-4
https://pure.au.dk/ws/files/401297701/s00125-023-05925-4.pdf
http://www.scopus.com/inward/record.url?scp=85164210817&partnerID=8YFLogxK

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.1011033

مصطلحات موضوعية: Genome-Wide Association Study, Humans, Polymorphism, Single Nucleotide/genetics, Vitamin D Deficiency/genetics, Vitamin D/genetics

وصف الملف: application/pdf

الاتاحة: https://pure.au.dk/portal/en/publications/6ad7bd83-50dd-4723-9864-c2f0d9a9bb9c
https://doi.org/10.1371/journal.pgen.1011033
https://pure.au.dk/ws/files/372729997/journal.pgen.1011033.pdf
http://www.scopus.com/inward/record.url?scp=85176756696&partnerID=8YFLogxK

المؤلفون: Privé, Florian, Albiñana, Clara, Arbel, Julyan, Pasaniuc, Bogdan, Vilhjálmsson, Bjarni J

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.2023.10.010

مصطلحات موضوعية: LDpred2, inference, Polymorphism, Single Nucleotide/genetics, Genome-Wide Association Study/methods, Humans, Bayes Theorem, Multifactorial Inheritance/genetics

الاتاحة: https://pure.au.dk/portal/en/publications/5c98c8f3-2487-4851-bda2-0e241ecebea1
https://doi.org/10.1016/j.ajhg.2023.10.010
http://www.scopus.com/inward/record.url?scp=85177768550&partnerID=8YFLogxK
https://www.biorxiv.org/content/10.1101/2022.10.10.511629v2

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.2023.01.003

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

Relation: https://portal.findresearcher.sdu.dk/da/publications/98cd3b12-3a75-4438-9571-d109e81f492b

الاتاحة: https://portal.findresearcher.sdu.dk/da/publications/98cd3b12-3a75-4438-9571-d109e81f492b
https://doi.org/10.1016/j.neurobiolaging.2023.01.003
https://findresearcher.sdu.dk/ws/files/252957430/1-s2.0-S0197458023000039-main.pdf