Jacqueline M. Ogier

CHD7 Deficiency in “Looper”, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment

Jacqueline M. Ogier, Marina R. Carpinelli, Benedicta D. Arhatari et al. · PLoS ONE · 2014 · 32 citations · Full text

Medicine, Genetics, Molecular Genetics +15

Organotypic Culture of Neonatal Murine Inner Ear Explants

Jacqueline M. Ogier, Rachel Burt, Hannah R. Drury et al. · Frontiers in Cellular Neuroscience · 2019 · 27 citations · Full text

Health Professions, Cell Biology, Neuroscience +17

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome

Marina R. Carpinelli, Elizabeth Kruse, Benedicta D. Arhatari et al. · American Journal Of Pathology · 2015 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Intravenously delivered aminoglycoside antibiotics, tobramycin and amikacin, are not ototoxic in mice

Jacqueline M. Ogier, Paul J. Lockhart, Rachel Burt · Hearing Research · 2019 · 17 citations · Full text

Medicine, Otolaryngology, Pharmacology +15

An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome

Jacqueline M. Ogier, Benedicta D. Arhatari, Marina R. Carpinelli et al. · Scientific Reports · 2018 · 10 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14