A dyadic approach to the delineation of diagnostic entities in clinical genomicsLeslie G. Biesecker, Yuri A. Zárate, Cynthia J. Curry et al.|The American Journal of Human Genetics|2021Cited by 116
Further delineation of the clinical spectrum of KAT6B disorders and allelic series of pathogenic variantsLi Xin Zhang, Yuri A. Zárate, Gabrielle Lemire et al.|Genetics in Medicine|2020Cited by 62
Genotype and phenotype in 12 additional individuals with <i><scp>SATB2</scp></i>‐associated syndromeYuri A. Zárate, David B. Everman, Louisa Kalsner et al.|Clinical Genetics|2017Cited by 42
Bi-allelic variants in INTS11 are associated with a complex neurological disorderBurak Tepe, Michael J. Bamshad, Erica L. Macke et al.|The American Journal of Human Genetics|2023Cited by 38
Activating variants in <scp><i>PDGFRB</i></scp> result in a spectrum of disorders responsive to imatinib monotherapyTara Wenger, William B. Dobyns, Randall A. Bly et al.|American Journal of Medical Genetics Part A|2020Cited by 34