1. Lionel, Anath C, Costain, Gregory, Monfared, Nasim, Scherer, Stephen W, Marshall, Christian R. 2017. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test. In Genetics in medicine : official journal of the American College of Medical Genetics, 20, 435-443. doi:10.1038/gim.2017.119. https://pubmed.ncbi.nlm.nih.gov/28771251/
2. Tremblay-Laganière, Camille, Maroofian, Reza, Nguyen, Thi Tuyet Mai, Campeau, Philippe M, Murakami, Yoshiko. 2021. PIGG variant pathogenicity assessment reveals characteristic features within 19 families. In Genetics in medicine : official journal of the American College of Medical Genetics, 23, 1873-1881. doi:10.1038/s41436-021-01215-9. https://pubmed.ncbi.nlm.nih.gov/34113002/
3. Makrythanasis, Periklis, Kato, Mitsuhiro, Zaki, Maha S, Antonarakis, Stylianos E, Murakami, Yoshiko. 2016. Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia. In American journal of human genetics, 98, 615-26. doi:10.1016/j.ajhg.2016.02.007. https://pubmed.ncbi.nlm.nih.gov/26996948/
4. Lane, William J, Aeschlimann, Judith, Vege, Sunitha, Joshi, Sanmukh R, Westhoff, Connie M. 2021. PIGG defines the Emm blood group system. In Scientific reports, 11, 18545. doi:10.1038/s41598-021-98090-w. https://pubmed.ncbi.nlm.nih.gov/34535746/
5. Long, Pinpin, Si, Jiahui, Zhu, Ziwei, Wang, Chaolong, Wu, Tangchun. 2024. Genome-wide DNA methylation profiling in blood reveals epigenetic signature of incident acute coronary syndrome. In Nature communications, 15, 7431. doi:10.1038/s41467-024-51751-6. https://pubmed.ncbi.nlm.nih.gov/39198424/