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Journal of Virology|May 14, 2010
Counteraction of HLA-C-mediated immune control of HIV-1 by NefAnke Specht, Amalio Telenti, Raquel Martinez, et al.
Nature Genetics|September 11, 2024
Disease prediction with multi-omics and biomarkers empowers case-control genetic discoveries in the UK BiobankManik Garg, Marcin Karpinski, Dorota Matelska, et al.
The Lancet. Neurology|November 15, 2016
MicroRNAs in epilepsy: pathophysiology and clinical utilityDavid C Henshall, Hajo M Hamer, R Jeroen Pasterkamp, et al.
Ebiomedicine|February 9, 2017
Whole Exome Sequencing Reveals Severe Thrombophilia in Acute Unprovoked Idiopathic Fatal Pulmonary EmbolismMatt Halvorsen, Ying Lin, Barbara A Sampson, et al.
The Journal of Infectious Diseases|August 8, 2008
The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavirSara Colombo, Andri Rauch, Margalida Rotger, et al.
Gastroenterology|January 5, 2011
Inosine triphosphate protects against ribavirin-induced adenosine triphosphate loss by adenylosuccinate synthase functionYuki Hitomi, Elizabeth T Cirulli, Jacques Fellay, et al.
Pharmacogenetics and Genomics|September 27, 2006
A common polymorphism in the SCN1A gene associates with phenytoin serum levels at maintenance doseSarah K Tate, Rinki Singh, Chin-Chuan Hung, et al.
Genome Biology|July 6, 2010
Screening the human exome: a comparison of whole genome and whole transcriptome sequencingElizabeth T Cirulli, Abanish Singh, Kevin V Shianna, et al.
Nature|August 10, 2021
Rare variant contribution to human disease in 281,104 UK Biobank exomesQuanli Wang, Ryan S Dhindsa, Keren Carss, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnosesKelly Schoch, Queenie K-G Tan, Nicholas Stong, et al.
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