Emily C. Lisi

3q29 interstitial microduplication: A new syndrome in a three‐generation family

Emily C. Lisi, Ada Hamosh, Kimberly F. Doheny et al. · American Journal of Medical Genetics Part A · 2008 · 153 citations

Cytogenetics, Genetics, Pathology +16

Genomic analysis of partial 21q monosomies with variable phenotypes

Elisha Roberson, Elizabeth Wohler, Julie Hoover‐Fong et al. · European Journal of Human Genetics · 2010 · 100 citations · Full text

Genetic Disorder, Genetics, Statistical Genetics +4

3q29 interstitial microdeletion syndrome: An inherited case associated with cardiac defect and normal cognition

Feng Li, Emily C. Lisi, Elizabeth Wohler et al. · European Journal of Medical Genetics · 2009 · 69 citations

Cardiomyopathy, Heart Failure, Inherited Case +9

Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: Evidence for <i>HMX2</i> and <i>HMX3</i> as candidate genes in hearing and vestibular function

Nathaniel D. Miller, Melonie A. Nance, Elizabeth Wohler et al. · American Journal of Medical Genetics Part A · 2009 · 46 citations · Full text

Genetics, Pathology, Molecular Genetics +18

Identification of Genetic Causes of Focal Segmental Glomerulosclerosis Increases With Proper Patient Selection

Jing Miao, Filippo Pinto e Vairo, Marie C. Hogan et al. · Mayo Clinic Proceedings · 2021 · 44 citations · Full text