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Hani Bagheri

University of British Columbia

4

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46

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Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication

2019 European Journal of Medical Genetics
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Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis

2016 JCI insight
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MG-123 Genomics of early pregnancy loss

2015 Journal of Medical Genetics
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Genomic characteristics of miscarriage copy number variants

2015 Molecular Human Reproduction
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