Show items per page
Elements: 50
Page 1 on 3
 TitleAuthors / EditorsDate
add to browser selection
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest SCD working group of the CHARGE Consortium 2018
add to browser selection
A frequent hypofunctional IRAK2 variant is associated with reduced spontaneous hepatitis C virus clearance Wang, Hui; El Maadidi, Souhayla; Fischer, Janett; Grabski, Elena; ... Weber, Alexander N R 2015
add to browser selection
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
add to browser selection
A novel recessive RPGRIP1 mutation causing leber congenital amaurosis Abouzeid, Hana; Othman, I S; Schorderet, D F 2016
add to browser selection
Accurate, scalable and integrative haplotype estimation Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil 2019
add to browser selection
An integrated systems genetics and omics toolkit to probe gene function Li, Hao; Wang, Xu; Rukina, Daria; Huang, Qingyao; ... Auwerx, Johan 2018
add to browser selection
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
add to browser selection
Causes and Consequences of Variability in Drug Transporter Activity in Pediatric Drug Therapy Rodieux, Frédérique; Gotta, Verena; Pfister, Marc; van den Anker, Johannes N 2016
add to browser selection
Colistin Heteroresistance and Involvement of the PmrAB Regulatory System in Acinetobacter baumannii Charretier, Yannick; Diene, Seydina Mouhamadou; Baud, Damien; Chatellier, Sonia; ... Schrenzel, Jacques 2018
add to browser selection
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
add to browser selection
Contribution of lipid components to the permeability barrier of oral mucosa Ganem-Quintanar, A.; Falson-Rieg, Françoise; Buri, Pierre 1997
add to browser selection
Defining the role of common variation in the genomic and biological architecture of adult human height Wood, Andrew R; Esko, Tonu; Yang, Jian; Vedantam, Sailaja; ... Goddard, Michael E 2014
add to browser selection
DNA analysis of the immunoglobulin IGHG loci in a Mandenka population from eastern Senegal : correlation with Gm haplotypes and hypotheses for the evolution of the Ig CH region Dard, Patricia Nathalie; Sanchez-Mazas, Alicia; Dugoujon, J. M.; De Lange, G.; ... Lefranc, G. 1996
add to browser selection
Effects of single genetic variants and polygenic obesity risk scores on disordered eating in adolescents - The HUNT study Sardahaee, Farzaneh Saeedzadeh; Holmen, Turid Lingaas; Micali, Nadia; Kvaløy, Kirsti 2017
add to browser selection
Emerging Roles for Connexins in Hypertension Carballo, Alfonso S.; Pfenniger, Daniel; Carballo, David; Perrier, Arnaud; ... Pfenniger, Anna 2008
add to browser selection
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
add to browser selection
Generalization and fine mapping of European ancestry-based central adiposity variants in African ancestry populations Yoneyama, S; Yao, J; Guo, X; Fernandez-Rhodes, L; ... North, K E 2017
add to browser selection
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
add to browser selection
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
add to browser selection
Genetic loci associated with heart rate variability and their effects on cardiac disease risk Nolte, Ilja M; Munoz, M Loretto; Tragante, Vinicius; Snieder, Harold; de Geus, Eco J C 2017
<< previous | 1 | 2 | 3 |