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 TitleAuthors / EditorsDate
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Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. Vinuela Rodriguez, Ana; McCarthy, Mark I 2020
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Genetic Predisposition to Developmental Dysplasia of the Hip Kenanidis, Eustathios; Gkekas, Nifon K; Karasmani, Areti; Anagnostis, Panagiotis; ... Tsiridis, Eleftherios 2020
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Association of NUDT15*3 and FPGS 2572C>T Variants with the Risk of Early Hematologic Toxicity During 6-MP and Low-Dose Methotrexate-Based Maintenance Therapy in Indian Patients with Acute Lymphoblastic Leukemia Kodidela, Sunitha; Dorababu, Patchava; Thakkar, Dimpal N; Dubashi, Biswajit; ... Uppugunduri Satyanarayana, Chakradhara Rao 2020
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Identification of regulatory variants associated with genetic susceptibility to meningococcal disease Borghini, Lisa; Png, Eileen; Binder, Alexander; Wright, Victoria J; ... Davila, Sonia 2019
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Combined linkage and association analysis identifies rare and low frequency variants for blood pressure at 1q31 Wang, Heming; Nandakumar, Priyanka; Tekola-Ayele, Fasil; Tayo, Bamidele O; ... Zhu, Xiaofeng 2019
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Exome sequencing identifies a de novo FOXA2 variant in a patient with syndromic diabetes Stekelenburg, Caroline; Gerster, Karine; Blouin, Jean-Louis; Lang-Muritano, Mariarosaria; ... Schwitzgebel Luscher, Valérie 2019
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Accurate, scalable and integrative haplotype estimation Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil 2019
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An integrated systems genetics and omics toolkit to probe gene function Li, Hao; Wang, Xu; Rukina, Daria; Huang, Qingyao; ... Auwerx, Johan 2018
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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Evangelou, Evangelos; Warren, Helen R; Mosen-Ansorena, David; Mifsud, Borbala; ... Caulfield, Mark J 2018
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Colistin Heteroresistance and Involvement of the PmrAB Regulatory System in Acinetobacter baumannii Charretier, Yannick; Diene, Seydina Mouhamadou; Baud, Damien; Chatellier, Sonia; ... Schrenzel, Jacques 2018
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Incorporation of GSTA1 genetic variations into a population pharmacokinetic model for IV busulfan in paediatric hematopoietic stem cell transplantation Nava, Tiago; Kassir, Nastya; Rezgui, Mohamed Aziz; Uppugunduri Satyanarayana, Chakradhara Rao; ... Bittencourt, Henrique 2018
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A comprehensive evaluation of the genetic architecture of sudden cardiac arrest SCD working group of the CHARGE Consortium 2018
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Genetic polymorphisms associated with smoking behaviour predict the risk of surgery in patients with Crohn's disease Lang, B M; Biedermann, L; van Haaften, W T; de Vallière, C; ... Misselwitz, B 2018
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Molecular characterization of Treponema pallidum subsp. pallidum in Switzerland and France with a new multilocus sequence typing scheme Grillová, Linda; Bawa, Tanika; Mikalová, Lenka; Gayet-Ageron, Angèle; ... Bosshard, Philipp P 2018
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Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries Collaboration 2018
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A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure Sung, Yun J.; Winkler, Thomas W.; de las Fuentes, Lisa; Bentley, Amy R.; ... Chasman, Daniel I. 2018
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Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI Gong, J; Nishimura, K K; Fernandez-Rhodes, L; Haessler, J; ... Peters, U 2018
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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation Hoffmann, Thomas J; Ehret, Georg Benedikt; Nandakumar, Priyanka; Ranatunga, Dilrini; ... Risch, Neil 2017
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Mapping genetic variations to three-dimensional protein structures to enhance variant interpretation: a proposed framework Glusman, Gustavo; Rose, Peter W; Prlić, Andreas; Dougherty, Jennifer; ... Deutsch, Eric W 2017
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Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles EPIC-CVD consortium and the CHD Exome+ consortium 2017
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