Van Renne N, Wei R, Pochet N, Nauwynck HJ. Dissecting clinical outcome of porcine circovirus type 2 with in vivo derived transcriptomic signatures of host tissue responses. BMC Genomics. 2018;19(1):831. doi:10.1186/s12864-018-5217-5DOIGoogle ScholarPubMed
Galinsky KJ, Reshef YA, Finucane HK, et al. Estimating cross-population genetic correlations of causal effect sizes. Genet Epidemiol. 2019;43(2):180-188. doi:10.1002/gepi.22173DOIGoogle ScholarPubMed
Rivera-Munoz EA, Milko LV, Harrison SM, et al. ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation. Hum Mutat. 2018;39(11):1614-1622. doi:10.1002/humu.23645DOIGoogle ScholarPubMed
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.23625DOIGoogle ScholarPubMed
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.23643DOIGoogle ScholarPubMed
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.23633DOIGoogle ScholarPubMed
Frankish A, Diekhans M, Ferreira AM, et al. GENCODE reference annotation for the human and mouse genomes. Nucleic Acids Res. 2019;47(D1):D766-D773. doi:10.1093/nar/gky955DOIGoogle ScholarPubMed
Guo MH, Plummer L, Chan YM, Hirschhorn JN, Lippincott MF. Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data. Am J Hum Genet. 2018;103(4):522-534. doi:10.1016/j.ajhg.2018.08.016DOIGoogle ScholarPubMed
Rehm H. Rapid communication of efforts to resolve differences or update variant interpretations in ClinVar through case-level data sharing. Cold Spring Harb Mol Case Stud. 2018;4(5). doi:10.1101/mcs.a003467DOIGoogle ScholarPubMed
Milko LV, Funke BH, Hershberger RE, et al. Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future. Genet Med. 2019;21(4):987-993. doi:10.1038/s41436-018-0267-2DOIGoogle ScholarPubMed