Mortaza Bonyadi

Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice

Mortaza Bonyadi, Stephen D. Waldman, Danmei Liu et al. · Proceedings of the National Academy of Sciences · 2003 · 245 citations · Full text

Mapping of a major genetic modifier of embryonic lethality in TGFβ1 knockout mice

Mortaza Bonyadi, Sarah Anne Buchanan Rusholme, Frances Cousins et al. · Nature Genetics · 1997 · 170 citations

Knockout Mouse, Developmental Biology, Major Genetic Modifier +10

Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort

Güney Bademci, Joseph Foster, Nejat Mahdieh et al. · Genetics in Medicine · 2015 · 158 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +11

Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss

Oscar Diaz‐Horta, Duygu Duman, Joseph Foster et al. · PLoS ONE · 2012 · 155 citations · Full text

Genetics, Pathology, Arnshl Genes +16

Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss

Güney Bademci, Filiz Başak Cengiz, Joseph Foster et al. · Scientific Reports · 2016 · 56 citations · Full text