A new impact factor for European Journal of Human Genetics
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-021-00941-7.pdf
Reference9 articles.
1. Savige J, Storey H, Watson E, Hertz JM, Deltas C, Renieri A, et al. Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00858-1.
2. Turbitt E, D’Amanda C, Hyman S, Weber JD, Bridges JFP, Peay HL, et al. Parent clinical trial priorities for fragile X syndrome: a best–worst scaling. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00922-w.
3. Wagener R, Taeubner J, Walter C, Yasin L, Alzoubi D, Bartenhagen C, et al. Comprehensive germline-genomic and clinical profiling in 160 unselected children and adolescents with cancer. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00878-x.
4. Gervais O, Ueno K, Kawai Y, Hitomi Y, Aiba Y, Ueta M, et al. Regional heritability mapping identifies several novel loci (STAT4, ULK4, and KCNH5) for primary biliary cholangitis in the Japanese population. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00854-5.
5. Luo H, Liu D, Liu W, Wang G, Chen L, Cao Y, et al. Germline variants in UNC13D and AP3B1 are enriched in COVID-19 patients experiencing severe cytokine storms. Eur J Hum Genet. 2021. https://doi.org/10.1038/s41431-021-00886-x.
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