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Genome Biology|November 25, 2014
Whole genome sequencing of SIV-infected macaques identifies candidate loci that may contribute to host control of virus replicationAdam J Ericsen, Gabriel J Starrett, Justin M Greene, et al.
Circulation. Cardiovascular Genetics|August 12, 2017
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular NoncompactionKarol Miszalski-Jamka, John L Jefferies, Wojciech Mazur, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyStephanie J London, Wei Gao, Sina A Gharib, et al.
Science Advances|February 4, 2026
Overcoming host restrictions to enable continuous passaging of GII.3 human norovirus in human intestinal enteroidsGurpreet Kaur, Sue E Crawford, Sara Javornik Cregeen, et al.
American Journal of Human Genetics|December 29, 2015
Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual DisabilityAsbjørg Stray-Pedersen, Jan-Maarten Cobben, Trine E Prescott, et al.
Cancer Genetics|February 22, 2025
Anaplastic meningioma in a 6-year-old with somatic YAP1::MAML2 fusion and multiple endocrine neoplasia type 4 (MEN4) syndromeLauren R Desrosiers-Battu, John H Lee, Izabela Tarasiewicz, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2026
Multi-Omics Characterization of Human Molecular Responses to Spaceflight Across Two Independent MissionsAbirami Santhanam, Zeineen Momin, Xiang Qin, et al.
Genome Research|July 11, 2008
Mouse let-7 miRNA populations exhibit RNA editing that is constrained in the 5'-seed/ cleavage/anchor regions and stabilize predicted mmu-let-7a:mRNA duplexesJeffrey G Reid, Ankur K Nagaraja, Francis C Lynn, et al.
Molecular Psychiatry|February 11, 2015
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsyG McMichael, M N Bainbridge, E Haan, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Constellation illuminates rare disease geneticsSiyuan Cheng, Qing Zhang, Xinchang Zheng, et al.
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