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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Mary C Whitman

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Ophthalmology Science|August 21, 2025

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the <i>All of Us</i> Research ProgramKyoung A Viola Lee, Corey Tesdahl, Inas F Aboobakar, et al.

Cell Reports|October 10, 2019

Etv1 Controls the Establishment of Non-overlapping Motor Innervation of Neighboring Facial Muscles during DevelopmentAlan P Tenney, Jean Livet, Timothy Belton, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 28, 2002

Disulfide bond-mediated dimerization of HLA-G on the cell surfaceJonathan E Boyson, Robert Erskine, Mary C Whitman, et al.

American Journal of Medical Genetics. Part A|December 8, 2015

Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical developmentMary C Whitman, Caroline Andrews, Wai-Man Chan, et al.

Human Molecular Genetics|June 19, 2019

Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humansMary C Whitman, Noriko Miyake, Elaine H Nguyen, et al.

Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019

Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task ForceArlene V Drack, Virginia Miraldi Utz, Kai Wang, et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 16, 2007

Dynamic contribution of nestin-expressing stem cells to adult neurogenesisDiane C Lagace, Mary C Whitman, Michele A Noonan, et al.

European Journal of Human Genetics : EJHG|March 2, 2021

Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain developmentJulie A Jurgens, Brenda J Barry, Gabrielle Lemire, et al.

Investigative Ophthalmology & Visual Science|August 12, 2018

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin EffectSherin Shaaban, Sarah MacKinnon, Caroline Andrews, et al.

Cell Reports|August 16, 2018

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon RegenerationAlban Latremoliere, Long Cheng, Michelle DeLisle, et al.

Pageof 6

Search research articles

Showing results (41-50 of 59) with videos related to

Sort By:

Pageof 6

Ophthalmology Science|August 21, 2025

Genome-Wide Association Study and Rare Variant Association Studies of Strabismus in the <i>All of Us</i> Research ProgramKyoung A Viola Lee, Corey Tesdahl, Inas F Aboobakar, et al.

Cell Reports|October 10, 2019

Etv1 Controls the Establishment of Non-overlapping Motor Innervation of Neighboring Facial Muscles during DevelopmentAlan P Tenney, Jean Livet, Timothy Belton, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 28, 2002

Disulfide bond-mediated dimerization of HLA-G on the cell surfaceJonathan E Boyson, Robert Erskine, Mary C Whitman, et al.

American Journal of Medical Genetics. Part A|December 8, 2015

Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical developmentMary C Whitman, Caroline Andrews, Wai-Man Chan, et al.

Human Molecular Genetics|June 19, 2019

Decreased ACKR3 (CXCR7) function causes oculomotor synkinesis in mice and humansMary C Whitman, Noriko Miyake, Elaine H Nguyen, et al.

Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 25, 2019

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 16, 2007

Dynamic contribution of nestin-expressing stem cells to adult neurogenesisDiane C Lagace, Mary C Whitman, Michele A Noonan, et al.

European Journal of Human Genetics : EJHG|March 2, 2021

Novel variants in TUBA1A cause congenital fibrosis of the extraocular muscles with or without malformations of cortical brain developmentJulie A Jurgens, Brenda J Barry, Gabrielle Lemire, et al.

Investigative Ophthalmology & Visual Science|August 12, 2018

Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin EffectSherin Shaaban, Sarah MacKinnon, Caroline Andrews, et al.

Cell Reports|August 16, 2018

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon RegenerationAlban Latremoliere, Long Cheng, Michelle DeLisle, et al.

Pageof 6