No April fools in clinical genomics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-022-01084-z.pdf
Reference12 articles.
1. Bertonazzi B, Turchetti D, Godino L. Outcomes of support groups for carriers of BRCA 1/2 pathogenic variants and their relatives: a systematic review. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-022-01044-7
2. Woodward ER, Green K, Burghel GJ, Bulman M, Clancy T, Lalloo F, et al. 30 year experience of index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-01011-8
3. Canzian F, Piredda C, Macauda A, Zawirska D, Andersen NF, Nagler A, et al. A polygenic risk score for multiple myeloma risk prediction. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00986-8
4. Mendoza-Fandiño G, Lyra PCM Jr., Nepomuceno TC, Harro CM, Woods NT, Li X, et al. Two distinct mechanisms underlie estrogen-receptor-negative breast cancer susceptibility at the 2p23.2 locus. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-01005-6
5. Moualed D, Wong J, Thomas O, Heal C, Saqib R, Choi C, et al. Prevalence and natural history of schwannomas in neurofibromatosis type 2 (NF2): the influence of pathogenic variants. Eur J Hum Genet. 2022. https://doi.org/10.1038/s41431-021-01029-y
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