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Material Type: Artigo
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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysisSmoller, JW ; Ripke, S ; Lee, PH ; Neale, B ; Nurnberger, JI ; Santangelo, S ; Sullivan, PF ; Perlis, RH ; Purcell, SM ; Fanous, A ; Landén, MikaelThe Lancet (British edition), 2013-04, Vol.381 (9875), p.1371-1379 [Periódico revisado por pares]Kidlington: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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Competitive activation cross amplification combined with smartphone-based quantification for point-of-care detection of single nucleotide polymorphismWen, Junping ; Gou, Hongchao ; Wang, Siyuan ; Lin, Qijie ; Chen, Kaifeng ; Wu, Yuqian ; Huang, Xuehuan ; Shen, Haiyan ; Qu, Xiaoyun ; Lin, Jianhan ; Liao, Ming ; Zhang, JianminBiosensors & bioelectronics, 2021-07, Vol.183, p.113200-113200, Article 113200 [Periódico revisado por pares]England: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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A multi-layer functional genomic analysis to understand noncoding genetic variation in lipidsJudd, Jonathan ; Kanoni, Stavroula ; Clarke, Shoa L. ; Klarin, Derek ; Hwang, Mi Yeong ; Akiyama, Masato ; Rasheed, Humaira ; Havulinna, Aki S. ; Feng, QiPing ; Martin, Hilary C. ; Hunt, Karen A. ; Trivedi, Bhavi ; Giulianini, Franco ; Miller, Jason E. ; Zhao, Wei ; Turman, Constance ; Yin, Xianyong ; Pitsillides, Achilleas ; Lee, Wen-Jane ; Zeng, Lingyao ; Poveda, Alaitz ; Kurbasic, Azra ; Galesloot, Tessel E. ; Ruotsalainen, Sanni E. ; Hemerich, Daiane ; Demirkan, Ayşe ; Arbeeva, Liubov ; Pauper, Marc ; Long, Jirong ; Bollepalli, Sailalitha ; Warner, Sophie C. ; Smith, Jennifer A. ; Lin, Maoxuan ; Vaccargiu, Simona ; Bentley, Amy R. ; Nethander, Maria ; Freitag-Wolf, Sandra ; Nikus, Kjell ; Martin, Lisa Warsinger ; Nabika, Toru ; Niinikoski, Harri ; Braund, Peter S. ; de Kleijn, Dominique ; Hansen, Torben ; Pennell, Craig E. ; Mori, Trevor A. ; Franke, Andre ; Ohlsson, Claes ; Stark, Klaus J. ; Evans, Michele K. ; Zonderman, Alan B. ; Snieder, Harold ; Schmidt, Reinhold ; Dedoussis, George ; Caulfield, Mark J. ; Guo, Xiuqing ; Kaprio, Jaakko ; Wu, Jer-Yuarn ; Arnett, Donna K. ; Chandak, Giriraj R. ; Mercader, Josep M. ; Orozco, Lorena ; Lehtimäki, Terho ; Liu, Jianjun ; Reilly, Dermot F. ; McCarthy, Mark I. ; Cruz, Miguel ; Rotimi, Charles N. ; Widén, Elisabeth ; Grant, Struan F.A. ; de Graaf, Jacqueline ; Erdmann, Jeanette ; Jukema, J. Wouter ; Francesco, Cucca ; Willems van Dijk, Ko ; Sabanayagam, Charumathi ; Pedersen, Nancy L. ; de Geus, Eco J.C. ; Langenberg, Claudia ; Zeggini, Eleftheria ; Laakso, Markku ; Abecasis, Goncalo ; Hazelhurst, Scott ; Ramsay, Michèle ; Walters, Robin G. ; Holmes, Michael V. ; Black, Corri ; van Heel, David A. ; Jarvik, Gail P. ; Ritchie, Marylyn D. ; Jousilahti, Pekka ; Kubo, Michiaki ; Thorsteinsdottir, Unnur ; Mohlke, Karen L. ; Hirschhorn, Joel N. ; Kathiresan, Sekar ; Natarajan, Pradeep ; Sun, Yan V. ; Peloso, Gina ; Brown, Christopher D.American journal of human genetics, 2022-08, Vol.109 (8), p.1366-1387 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Hypertension and hypertensive left ventricular hypertrophy are associated with ACE2 genetic polymorphismFan, Zhimin ; Wu, Guihai ; Yue, Minghui ; Ye, Jianfeng ; Chen, Yequn ; Xu, Bayi ; Shu, Zhouwu ; Zhu, Jinxiu ; Lu, Nan ; Tan, XueruiLife Sciences, 2019-05, Vol.225, p.39-45 [Periódico revisado por pares]Netherlands: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasetsSinghal, 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.American journal of human genetics, 2023-04, Vol.110 (4), p.575-591 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genesHaan, H. G. ; Hylckama Vlieg, A. ; Lotta, L. A. ; Gorski, M. M. ; Bucciarelli, P. ; Martinelli, I. ; Baglin, T. P. ; Peyvandi, F. ; Rosendaal, F. R. ; Amouyel, P. ; Andrade, M. ; Basu, S. ; Berr, C. ; Brody, J. A. ; Chasman, D. I ; Dartigues, J.‐F. ; Folsom, A. R. ; Germain, M. ; Heit, J. ; Houwing‐Duitermaat, J. ; Kabrhel, C. ; Kraft, P. ; Le Gal, G. ; Lindström, S. ; Monajemi, R. ; Morange, P.‐E. ; Psaty, B. M. ; Reitsma, P. H. ; Ridker, P. M. ; Rose, L. M. ; Saut, N. ; Slagboom, E. ; Smadja, D. ; Smith, N. L. ; Suchon, P. ; Tang, W. ; Taylor, K. D. ; Trégouët, D.‐A. ; Tzourio, C. ; Visser, M. C. H. ; Weng, L.‐C. ; Wiggins, K. L.Journal of thrombosis and haemostasis, 2018-12, Vol.16 (12), p.2432-2441 [Periódico revisado por pares]England: Wiley Subscription Services, IncTexto completo disponível |
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Material Type: Artigo
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A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkersWhitfield, John B. ; Schwantes-An, Tae-Hwi ; Darlay, Rebecca ; Aithal, Guruprasad P. ; Atkinson, Stephen R. ; Bataller, Ramon ; Botwin, Greg ; Chalasani, Naga P. ; Cordell, Heather J. ; Daly, Ann K. ; Day, Christopher P. ; Eyer, Florian ; Foroud, Tatiana ; Gleeson, Dermot ; Goldman, David ; Haber, Paul S. ; Jacquet, Jean-Marc ; Liang, Tiebing ; Liangpunsakul, Suthat ; Masson, Steven ; Mathurin, Philippe ; Moirand, Romain ; McQuillin, Andrew ; Moreno, Christophe ; Morgan, Marsha Y. ; Mueller, Sebastian ; Müllhaupt, Beat ; Nagy, Laura E. ; Nahon, Pierre ; Nalpas, Bertrand ; Naveau, Sylvie ; Perney, Pascal ; Pirmohamed, Munir ; Seitz, Helmut K. ; Soyka, Michael ; Stickel, Felix ; Thompson, Andrew ; Thursz, Mark R. ; Trépo, Eric ; Morgan, Timothy R. ; Seth, DevanshiJournal of hepatology, 2022-02, Vol.76 (2), p.275-282 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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Material Type: Artigo
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Shared genetic variants suggest common pathways in allergy and autoimmune diseasesKreiner, Eskil, MD, PhD ; Waage, Johannes, PhD ; Standl, Marie, PhD ; Brix, Susanne, PhD ; Pers, Tune H., PhD ; Couto Alves, Alexessander, PhD ; Warrington, Nicole M., PhD ; Tiesler, Carla M.T., MSc ; Fuertes, Elaine, PhD ; Franke, Lude, PhD ; Hirschhorn, Joel N., MD, PhD ; James, Alan, MD ; Simpson, Angela, MD, PhD ; Tung, Joyce Y., PhD ; Koppelman, Gerard H., MD, PhD ; Postma, Dirkje S., MD, PhD ; Pennell, Craig E., MD, PhD ; Jarvelin, Marjo-Riitta, MD ; Custovic, Adnan, MD, PhD ; Timpson, Nicholas, PhD ; Ferreira, Manuel A., PhD ; Strachan, David P., MD ; Henderson, John, MD ; Hinds, David, PhD ; Bisgaard, Hans, MD, DMSc ; Bønnelykke, Klaus, MD, PhDJournal of allergy and clinical immunology, 2017-09, Vol.140 (3), p.771-781 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Association between the genetic polymorphisms of the pharmacokinetics of anthracycline drug and myelosuppression in a patient with breast cancer with anthracycline-based chemotherapyCui, Lulu ; Huang, Jia ; Zhan, Yongtao ; Qiu, Ni ; Jin, Huan ; Li, Jia ; Huang, Huiqi ; Li, HongshengLife Sciences, 2021-07, Vol.276, p.119392, Article 119392 [Periódico revisado por pares]Netherlands: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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MMP3 single‐nucleotide polymorphisms are associated with noncontact ACL injuries in competing high‐level athletesSimunic‐Briski, Nina ; Vrgoc, Goran ; Knjaz, Damir ; Jankovic, Sasa ; Dembic, Zlatko ; Lauc, GordanJournal of orthopaedic research, 2024-01, Vol.42 (1), p.109-114 [Periódico revisado por pares]United StatesTexto completo disponível |