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Nature Genetics|October 9, 2012
LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppressionJan J Molenaar, Raquel Domingo-Fernández, Marli E Ebus, et al.Nature Genetics|September 1, 1997
A candidate gene for familial Mediterranean feverNature Genetics|September 1, 1997
A mouse model for Zellweger syndromeM Baes, P Gressens, E Baumgart, et al.Nature Genetics|September 1, 1997
Epilepsy and mental retardation limited to females: an X-linked dominant disorder with male sparingS G Ryan, P F Chance, C H Zou, et al.Nature Genetics|August 11, 2022
Substantial somatic genomic variation and selection for BCOR mutations in human induced pluripotent stem cellsFoad J Rouhani, Xueqing Zou, Petr Danecek, et al.Nature Genetics|November 5, 2022
DNA sequence and chromatin modifiers cooperate to confer epigenetic bistability at imprinting control regionsStefan Butz, Nina Schmolka, Ino D Karemaker, et al.Nature Genetics|November 5, 2022
Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical featuresPauline Robbe, Kate E Ridout, Dimitrios V Vavoulis, et al.Nature Genetics|November 5, 2022
Non-coding variants disrupting a tissue-specific regulatory element in HK1 cause congenital hyperinsulinismMatthew N Wakeling, Nick D L Owens, Jessica R Hopkinson, et al.Nature Genetics|August 18, 2022
Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genesXueya Zhou, Pamela Feliciano, Chang Shu, et al.Nature Genetics|March 21, 2023
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individualsKangcheng Hou, Yi Ding, Ziqi Xu, et al.Pageof 745