Publications by authors named "Jefferson Doyle"

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Genetic influences on intergenerational refractive error shifts and extreme myopia.
Maria Ludovica Ruggeri, Jefferson James Doyle

Br J Ophthalmol· September 2025

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Ocular manifestations of SREBF1-associated hereditary mucoepithelial dysplasia.
Whitney Stuard Sambhariya, Jefferson Doyle, Courtney L Kraus

J AAPOS· February 2025

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Map2k6 is a potent genetic modifier of arterial rupture in vascular Ehlers-Danlos syndrome mice.
Caitlin J Bowen, Rebecca Sorber, Juan Francisco Calderón Giadrosic, Jefferson J Doyle, Graham Rykiel

JCI Insight· January 2025

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Accessory iris membranes: Removing the veil.
Oded Lagstein, Rachel R Milante, Kapil Mishra, Jefferson J Doyle

Am J Ophthalmol Case Rep· March 2022

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Survey of Ehlers-Danlos Patients' ophthalmic surgery experiences.
Anita Louie, Catherine Meyerle, Clair Francomano, Divya Srikumaran, Farhan Merali, Jefferson J Doyle

Mol Genet Genomic Med· April 2020

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Acquired reversible Brown syndrome caused by focal abscess of the superior oblique muscle.
Julius T Oatts, Jefferson J Doyle, Mary-Magdalene U Dodd, Iason S Mantagos, Linda R Dagi

J AAPOS· June 2019

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Angioid Streaks Are Not a Common Feature of Ehlers-Danlos Syndrome.
Eric Lowell Singman, Jefferson James Doyle

JAMA Ophthalmol· March 2019

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Transposition procedures in Duane retraction syndrome.
Jefferson J Doyle, David G Hunter

J AAPOS· February 2019

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Neonatal-Onset Chronic Diarrhea Caused by Homozygous Nonsense WNT2B Mutations.
Amy E O'Connell, Fanny Zhou, Manasvi S Shah, Quinn Murphy, Hannah Rickner, Jefferson J Doyle

Am J Hum Genet· July 2018

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Brown Syndrome Following Upper Eyelid Ptosis Repair.
Yao Wang, Timothy J McCulley, Jefferson J Doyle, Jessica Chang, Michael S Lee

Neuroophthalmology· February 2018

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Bilateral Persistent Pupillary Membranes.
Jefferson J Doyle, Ashvini K Reddy

JAMA Ophthalmol· July 2016

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A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndrome.
Jefferson J Doyle, Alexander J Doyle, Nicole K Wilson, Jennifer P Habashi, Djahida Bedja

Elife· October 2015

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Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm.
Alexander J Doyle, Jefferson J Doyle, Seneca L Bessling, Samantha Maragh, Mark E Lindsay

Nat Genet· November 2012

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Targeting collagen strands by photo-triggered triple-helix hybridization.
Yang Li, Catherine A Foss, Daniel D Summerfield, Jefferson J Doyle, Collin M Torok

Proc Natl Acad Sci U S A· September 2012

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Matrix-dependent perturbation of TGFβ signaling and disease.
Jefferson J Doyle, Elizabeth E Gerber, Harry C Dietz

FEBS Lett· July 2012

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Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm.
Mark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, Jefferson J Doyle, Elena Gallo

Nat Genet· July 2012

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Altered tissue behavior of a non-aneurysmal descending thoracic aorta in the mouse model of Marfan syndrome.
Darren Haskett, Jefferson J Doyle, Connie Gard, Hwudaurw Chen, Corbie Ball

Cell Tissue Res· January 2012

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Transforming growth factor-β signaling pathway activation in Keratoconus.
Christoph Engler, Shukti Chakravarti, Jefferson Doyle, Charles G Eberhart, Huan Meng

Am J Ophthalmol· May 2011

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Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
Tammy M Holm, Jennifer P Habashi, Jefferson J Doyle, Djahida Bedja, YiChun Chen

Science· April 2011

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Angiotensin II type 2 receptor signaling attenuates aortic aneurysm in mice through ERK antagonism.
Jennifer P Habashi, Jefferson J Doyle, Tammy M Holm, Hamza Aziz, Florian Schoenhoff

Science· April 2011

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Changing environments and alternative perspectives in evaluating the cost-effectiveness of new antipsychotic drugs.
Robert Rosenheck, Jefferson Doyle, Douglas Leslie, Alan Fontana

Schizophr Bull· December 2003

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