Olivia Wenger

Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies

Bo Yuan, Juanita Neira, Davut Pehli̇van et al. · Genetics in Medicine · 2018 · 87 citations · Full text

Bioinformatics, Mendelian Disorder, Genetic Disorder +10

Recessive nephrocerebellar syndrome on the Galloway-Mowat syndrome spectrum is caused by homozygous protein-truncating mutations of<i>WDR73</i>

Robert N. Jinks, Erik G. Puffenberger, Emma L. Baple et al. · Brain · 2015 · 65 citations · Full text

Underimmunization in Ohio's Amish: Parental Fears Are a Greater Obstacle Than Access to Care

Olivia Wenger, Mark D. McManus, John R. Bower et al. · PEDIATRICS · 2011 · 56 citations

Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier

Lauren E. Bowser, Millie Young, Olivia Wenger et al. · Molecular Genetics and Metabolism · 2019 · 53 citations

Developmental Biology, Genetic Disorder, Genetics +9

Biallelic <i>PI4KA</i> variants cause neurological, intestinal and immunological disease

Claire Salter, Yiying Cai, Bernice Lo et al. · Brain · 2021 · 44 citations · Full text