Wen, J. G., Chang, Q. L., Lou, A. F., Li, Z. Z., Lu, S.
, Wang, Y., Wang, Y. L., Hu, J. H., Mao, S. P., Zhang, Y., Xue, R., Ren, C., Xing, L., Zhang, G. X., Zhang, S.
, Djurhuus, J. C. & Frøkiaer, J. (2011).
Melamine-Related Urinary Stones in 195 Infants and Young Children: Clinical Features within 2 Years of Follow-Up.
Urologia Internationalis.
https://doi.org/10.1159/000330795
Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A.
, Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S.
, Mortensen, P. B. ... iPSYCH-Broad Autism Group (2017).
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
Nature Genetics,
49(7), 978-985.
https://doi.org/10.1038/ng.3863
Weiner, D. J., Ling, E., Erdin, S., Tai, D. J. C., Yadav, R.
, Grove, J., Fu, J. M., Nadig, A., Carey, C. E., Baya, N., Bybjerg-Grauholm, J., iPSYCH Consortium, ASD Working Group of the Psychiatric Genomics Consortium, ADHD Working Group of the Psychiatric Genomics Consortium, Berretta, S., Macosko, E. Z., Sebat, J., O'Connor, L. J., Hougaard, D. M. ... Robinson, E. B. (2022).
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.
Nature Genetics,
54(11), 1630-1639.
https://doi.org/10.1038/s41588-022-01203-y