| | Title | Authors / Editors | Date |
|
unige:132661 |
Genetic Predisposition to Developmental Dysplasia of the Hip |
Kenanidis, Eustathios; Gkekas, Nifon K; Karasmani, Areti; Anagnostis, Panagiotis; ... Tsiridis, Eleftherios |
2020 |
|
unige:150583 |
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 |
|
unige:144670 |
Genetic variant effects on gene expression in human pancreatic islets and their implications for T2D. |
Vinuela Rodriguez, Ana; McCarthy, Mark I |
2020 |
|
unige:135503 |
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 |
|
unige:145129 |
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease |
Borghini, Lisa; Png, Eileen; Binder, Alexander; Wright, Victoria J; ... Davila, Sonia |
2019 |
|
unige:144668 |
Accurate, scalable and integrative haplotype estimation |
Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil |
2019 |
|
unige:127542 |
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 |
|
unige:128978 |
Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries |
Collaboration |
2018 |
|
unige:128980 |
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 |
|
unige:128497 |
A comprehensive evaluation of the genetic architecture of sudden cardiac arrest |
SCD working group of the CHARGE Consortium |
2018 |
|
unige:127888 |
Colistin Heteroresistance and Involvement of the PmrAB Regulatory System in Acinetobacter baumannii |
Charretier, Yannick; Diene, Seydina Mouhamadou; Baud, Damien; Chatellier, Sonia; ... Schrenzel, Jacques |
2018 |
|
unige:128688 |
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 |
|
unige:128086 |
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 |
|
unige:143012 |
An integrated systems genetics and omics toolkit to probe gene function |
Li, Hao; Wang, Xu; Rukina, Daria; Huang, Qingyao; ... Auwerx, Johan |
2018 |
|
unige:128591 |
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 |
|
unige:128631 |
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 |
|
unige:124464 |
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 |
|
unige:112335 |
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 |
|
unige:128976 |
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 |
|
unige:124369 |
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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