Gupta RM. Hippo Pathway Looms Large for the Function of the JCAD (Junctional Protein Associated With Coronary Artery Disease) on Endothelial Cells. Arterioscler Thromb Vasc Biol. 2018;38(11):2546-2547. doi:10.1161/ATVBAHA.118.311342
Publications
Brabetz S, Leary SES, Gröbner SN, et al. A biobank of patient-derived pediatric brain tumor models. Nat Med. 2018;24(11):1752-1761. doi:10.1038/s41591-018-0207-3
D’Gama AM, Walsh CA. Somatic mosaicism and neurodevelopmental disease. Nat Neurosci. 2018;21(11):1504-1514. doi:10.1038/s41593-018-0257-3
Saha M, Reddy HM, Salih MA, et al. Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan. Physiol Genomics. 2018;50(11):929-939. doi:10.1152/physiolgenomics.00036.2018
Galván-FemenÃa I, Obón-Santacana M, Piñeyro D, et al. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. J Med Genet. 2018;55(11):765-778. doi:10.1136/jmedgenet-2018-105437
Rohdin C, Häggström J, Ljungvall I, et al. Presence of thoracic and lumbar vertebral malformations in pugs with and without chronic neurological deficits. Vet J. 2018;241:24-30. doi:10.1016/j.tvjl.2018.09.008
Perraki A, DeFalco TA, Derbyshire P, et al. Author Correction: Phosphocode-dependent functional dichotomy of a common co-receptor in plant signalling. Nature. 2018;563(7733):E30. doi:10.1038/s41586-018-0663-4
Savatt JM, Azzariti DR, Faucett A, et al. ClinGen’s GenomeConnect registry enables patient-centered data sharing. Hum Mutat. 2018;39(11):1668-1676. doi:10.1002/humu.23633
Harrison SM, Dolinksy JS, Chen W, et al. Scaling resolution of variant classification differences in ClinVar between 41 clinical laboratories through an outlier approach. Hum Mutat. 2018;39(11):1641-1649. doi:10.1002/humu.23643
Dolman L, Page A, Babb L, et al. ClinGen advancing genomic data-sharing standards as a GA4GH driver project. Hum Mutat. 2018;39(11):1686-1689. doi:10.1002/humu.23625