A. Drack

M. Repka, J. Edmond, R. Siatkowski, 2010, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Congenital Cataracts and Genetic Anomalies of the Lens

Y. Rabinowitz, A. Drack, E. Cotlier, 2013 .

The effect of ascorbic acid on galactose-induced cataracts

A. Drack, J. Vinson, C. Possanza, 1986 .

Endothelial BBSome is essential for vascular, metabolic, and retinal functions

Michael G. Anderson, E. Taylor, D. Morgan, 2021, Molecular metabolism.

Improved ocular alignment with adjustable sutures in adults undergoing strabismus surgery.

A. Hutchinson, A. Drack, S. Lambert, 2012, Ophthalmology.

Whats new and important in pediatric ophthalmology and strabismus

J. Zobal-Ratner, A. Drack, K. Arnoldi, 2010, Journal of American Association for Pediatric Ophthalmology and Strabismus.

Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy

J. Slakter, M. Larsen, L. Yannuzzi, 2014, Human mutation.

Ophthalmologic Complications in Children With Chronic Hepatitis C Treated With Pegylated Interferon

M. Repka, P. Rosenthal, A. Drack, 2010, Journal of pediatric gastroenterology and nutrition.

Visual acuity changes in patients with leber congenital amaurosis and mutations in CEP290.

J. J. McAnany, S. Jacobson, G. Fishman, 2013, JAMA ophthalmology.

Ophthalmic manifestations of Danon disease.

L. Mestroni, Matthew R. G. Taylor, A. Drack, 2006, Ophthalmology.

Strabismus surgery in patients receiving warfarin anticoagulation.

A. Drack, S. Larson, P. Kemp, 2014, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Patterns of Retinal Disease in Children

A. Drack, 2006 .

A Novel c.1135_1138delCTGT Mutation in CLN3 Leads to Juvenile Neuronal Ceroid Lipofuscinosis

A. Drack, D. Pearce, Jake N. Miller, 2013, Journal of child neurology.

Different Fate of Antibodies to Surface IgM and IgD in Germinal Centre Cell‐Associated Lymphomas

H. Steen, K. Beiske, A. Drack, 1984, Scandinavian journal of immunology.

Induction of maturation of human B-cell lymphomas in vitro. Morphologic changes in relation to immunoglobulin and DNA synthesis.

K. Beiske, P. Marton, A. Drack, 1984, The American journal of pathology.

Genotype–phenotype analysis of the branchio‐oculo‐facial syndrome

W. Reardon, G. Mortier, O. Klein, 2011, American journal of medical genetics. Part A.

A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene

A. Dumitrescu, J. Milunsky, A. Drack, 2012, Ophthalmic genetics.

Ectopic Expression of Human BBS4 Can Rescue Bardet-Biedl Syndrome Phenotypes in Bbs4 Null Mice

V. Sheffield, Xitiz Chamling, K. Rahmouni, 2013, PloS one.

Intravitreal Sepofarsen for Leber Congenital Amaurosis Type 10 (LCA10)

A. J. Roman, Ian C. Han, A. Cideciyan, 2020 .

Using Patient-Specific Induced Pluripotent Stem Cells and Wild-Type Mice to Develop a Gene Augmentation-Based Strategy to Treat CLN3-Associated Retinal Degeneration.

E. Stone, B. Tucker, E. Burnight, 2016, Human gene therapy.

The evolving role of genetics in ophthalmology

B. Brooks, A. Drack, S. Shankar, 2021, Ophthalmic genetics.

Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task Force.

I. C. Lloyd, Deborah M. Costakos, E. Héon, 2019, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Vitritis in pediatric genetic retinal disorders.

E. Stone, R. Mullins, A. Drack, 2015, Ophthalmology.

Electroretinogram abnormalities in FKRP-related limb–girdle muscular dystrophy (LGMDR9)

K. Mathews, A. Drack, W. Pfeifer, 2022, Documenta Ophthalmologica.

Heritable Disorders of RPE, Bruch’s Membrane, and the Choriocapillaris

A. Drack, 2006 .

Unilateral retinal hemorrhages in documented cases of child abuse.

A. Capone, A. Drack, J. Petronio, 1999, American journal of ophthalmology.

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.

V. Sheffield, E. Stone, B. Nichols, 1993, Human molecular genetics.

BBS mutations modify phenotypic expression of CEP290-related ciliopathies.

V. Sheffield, E. Stone, A. Drack, 2014, Human molecular genetics.

Alström syndrome caused by maternal uniparental disomy

M. Brodsky, H. Kearney, L. Schimmenti, 2022, American journal of ophthalmology case reports.

Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.

V. Sheffield, A. Dumitrescu, E. Stone, 2013, Investigative ophthalmology & visual science.

Translational Subretinal Gene Therapy of Mice With Bardet-Biedl Syndrome Type 1

V. Sheffield, A. Dumitrescu, E. Stone, 2013 .

Strabismus and mitochondrial defects in chronic progressive external ophthalmoplegia.

H. Grossniklaus, J. Shoffner, A. Drack, 1997, American journal of ophthalmology.

Expanded Retinal Disease Spectrum Associated With Autosomal Recessive Mutations in GUCY2D.

A. V. Cideciyan, S. Brodie, A. Cideciyan, 2018, American journal of ophthalmology.

Durability of Voretigene Neparvovec for Biallelic RPE65-Mediated Inherited Retinal Disease: Phase 3 Results at 3 Years and 4 Years.

S. Russell, J. Bennett, D. Chung, 2021, Ophthalmology.

Neuroretinitis in cat scratch disease.

G. Chrousos, J. Kattah, A. Drack, 1990, Journal of clinical neuro-ophthalmology.

Longitudinal changes in the refractive errors of children with tears in Descemet's membrane following forceps injuries.

A. Hutchinson, A. Drack, S. Lambert, 2004, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Long-term surgical and visual outcomes in primary congenital glaucoma: 360° trabeculotomy versus goniotomy

M. Lynn, A. Beck, A. Drack, 2000 .

A comparison of grating visual acuity, strabismus, and reoperation outcomes among children with aphakia and pseudophakia after unilateral cataract surgery during the first six months of life.

M. E. Wilson, E. Buckley, M. Lynn, 2001, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Infantile cataracts.

A. Drack, S. Lambert, 1996, Survey of ophthalmology.

Visual acuity in patients with Leber's congenital amaurosis and early childhood-onset retinitis pigmentosa.

T. Aleman, S. Jacobson, G. Fishman, 2010, Ophthalmology.

Heterochromia after pediatric cataract surgery.

R. Tarnuzzer, A. Drack, A. Fernandes, 2000, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

MD Consult - REFRACTIVE SURGERY IN CHILDREN - Ophthalmology Clinics of North America - Medical Journal

P. Nucci, A. Drack, 2012 .

Refractive surgery in children.

P. Nucci, A. Drack, 2001, Ophthalmology clinics of North America.

Prevalence and characteristics of abnormal head posture in children with Down syndrome: a 20-year retrospective, descriptive review.

A. Dumitrescu, D. Moga, A. Drack, 2011, Ophthalmology.

Retinopathy of prematurity.

A. Drack, 2006, Advances in pediatrics.

Refractive surgery for unilateral high myopia in children.

P. Nucci, A. Drack, 2001, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Clinical albinism score, presence of nystagmus and optic nerves defects are correlated with visual outcome in patients with oculocutaneous albinism

T. Scheetz, A. Dumitrescu, A. Drack, 2021, Ophthalmic genetics.

The clinical evaluation of infantile nystagmus: What to do first and why

A. Drack, W. Pfeifer, M. Bertsch, 2017, Ophthalmic genetics.

Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)

R. Giorda, I. Maumenee, A. Drack, 2001, Ophthalmic genetics.

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

S. Jacobson, B. Koop, D. Birch, 2000, Nature Genetics.

Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial

Kathleen A. Marshall, V. Mahajan, S. Russell, 2017, The Lancet.

Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseases

Allison E. Songstad, E. Stone, B. Tucker, 2015, Progress in Retinal and Eye Research.

CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype

E. Stone, B. Tucker, E. Burnight, 2014, Gene Therapy.

Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa

T. Braun, E. Stone, B. Tucker, 2013, eLife.

Optic nerve hypoplasia: absence of posterior pituitary bright signal on magnetic resonance imaging correlates with diabetes insipidus.

L. Meacham, P. Davis, J. Parks, 1996, American journal of ophthalmology.

Retinitis Pigmentosa and Associated Disorders

A. Drack, A. Kimura, 2006 .

Efficacy of phosphodiesterase‐4 inhibitors in juvenile Batten disease (CLN3)

J. Cooper, Megan E Bosch, A. Aldrich, 2016, Annals of neurology.

Characterization of a novel porcine model of CLN3-Batten disease

Tyler B. Johnson, J. Cooper, A. Drack, 2019, Molecular Genetics and Metabolism.

Bilateral visual loss, behavioral changes, and overlooking in a young child with stargardt disease: Neurodiagnostic considerations

M. Brodsky, A. Drack, 2022, American journal of ophthalmology case reports.

Immunosuppressive Treatment for Retinal Degeneration in Juvenile Neuronal Ceroid Lipofuscinosis (Juvenile Batten Disease)

S. Stasheff, R. Mullins, E. Augustine, 2015, Ophthalmic genetics.

Cataract and Glaucoma Development in Juvenile Neuronal Ceroid Lipofuscinosis (Batten Disease)

A. Drack, J. Ostergaard, Anders K Nielsen, 2015, Ophthalmic genetics.

CRISPR-Cas9 genome engineering: Treating inherited retinal degeneration

E. Stone, B. Tucker, E. Burnight, 2018, Progress in Retinal and Eye Research.

α2δ-4 Is Required for the Molecular and Structural Organization of Rod and Cone Photoreceptor Synapses

Joseph G. Laird, R. Wong, S. Baker, 2018, The Journal of Neuroscience.

Mutations in the RNA Granule Component TDRD7 Cause Cataract and Glaucoma

Fowzan S Alkuraya, Martha L Bulyk, Anton Aboukhalil, 2011, Science.

Long-term surgical and visual outcomes in primary congenital glaucoma: 360 degrees trabeculotomy versus goniotomy.

A. Beck, A. Drack, M. Lynn, 2000, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

William E. Byrd, Gabor T. Marth, David R. Murdock, 2020, Genetics in Medicine.

A novel mutation in ACTG1 causing Baraitser-Winter syndrome with extremely variable expressivity in three generations

Christina M. Sloan, C. Sloan, A. Drack, 2017, Ophthalmic genetics.

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.

V. Sheffield, E. Stone, T. Weingeist, 1994, Archives of ophthalmology.

Gene Therapy for Blinding Pediatric Eye Disorders.

A. Dumitrescu, A. Drack, 2015, Advances in pediatrics.

Progression of retinopathy in olivopontocerebellar atrophy with retinal degeneration.

E. Traboulsi, I. Maumenee, A. Drack, 1992, Archives of ophthalmology.

Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-Seq.

Adam P. DeLuca, T. Scheetz, T. Braun, 2014, Experimental eye research.

Balloon dilatation for treatment of resistant nasolacrimal duct obstruction.

A. Drack, S. Lambert, K. Hutcheson, 1997, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Wide-Field Swept-Source OCT and Angiography in X-Linked Retinoschisis.

Adam P. DeLuca, Ian C. Han, S. Lee, 2019, Ophthalmology. Retina.

AAV2/4-RS1 gene therapy in the retinoschisin knockout mouse model of X-linked retinoschisis

Joseph G. Laird, A. Drack, Megan Helms, 2022, PloS one.

Efficacy of topical brinzolamide in children with retinal dystrophies

A. Drack, W. Pfeifer, Kai Wang, 2019, Ophthalmic genetics.

Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma.

A. Kwitek, E. Stone, R. L. Cannon, 1993, Ophthalmology.

Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet–Biedl syndrome

V. Sheffield, C. Allamargot, A. Drack, 2015, Proceedings of the National Academy of Sciences.

The two-stage mutation model in retinal hemangioblastoma.

H. Grossniklaus, A. Drack, M. Lynn, 1998, Ophthalmic genetics.

Transient punctate lenticular opacities as a complication of argon laser photoablation in an infant with retinopathy of prematurity.

J. Pulido, R. Keech, A. Drack, 1992, American journal of ophthalmology-glaucoma.

Infantile Cataracts: Indications for Systemic and Genetic Workup

A. Drack, 1997 .

Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure

Deborah M. Costakos, W. Hauswirth, C. Summers, 2021, Translational vision science & technology.

Lipid peroxidation and diabetic complications: effect of antioxidant vitamins C and E.

A. Drack, J. Vinson, C. Possanza, 1994, Advances in experimental medicine and biology.

From the laboratory to the clinic: molecular genetic testing in pediatric ophthalmology.

E. Stone, A. Drack, S. Lambert, 2010, American journal of ophthalmology.

TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl syndrome type 1 mice.

V. Sheffield, A. Dumitrescu, E. Stone, 2012, Investigative ophthalmology & visual science.

Cataract and phthisis bulbi after laser photoablation for threshold retinopathy of prematurity.

A. Capone, A. Drack, S. Lambert, 2000, American journal of ophthalmology.

Anterior hyaloid face opacification after pediatric Nd:YAG laser capsulotomy.

A. Drack, S. Lambert, K. Hutcheson, 1999, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

How Often Are Our Patients’ Spectacle Lenses Dispensed as Prescribed?

A. Drack, Colleen Smith, R. Sands, 2006 .

Is it Usher syndrome? Collaborative diagnosis and molecular genetics of patients with visual impairment and hearing loss

Amy E. Weaver, D. Kolbe, J. Kamholz, 2020, Ophthalmic genetics.

Refractive Errors in Childhood

A. Drack, M. Simon, 2020, Albert and Jakobiec's Principles and Practice of Ophthalmology.

Refractive Errors in Children

A. Drack, 2008 .

Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10

T. Aleman, S. Jacobson, J. Duncan, 2021, Investigative ophthalmology & visual science.

Prism Adaptation in Decompensated Monofixation Syndrome

A. Drack, Cameile N. Moore, 2000 .

Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

V. Sheffield, E. Stone, B. Nichols, 1993, Nature Genetics.

Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect

A. J. Roman, Ian C. Han, A. Cideciyan, 2018, Nature Medicine.

RNA Interference-Based Therapy for Spinocerebellar Ataxia Type 7 Retinal Degeneration

B. Davidson, A. Drack, R. Boudreau, 2014, PloS one.

Subretinal gene therapy delays vision loss in a Bardet-Biedl Syndrome type 10 mouse model

V. Sheffield, L. Vandenberghe, A. Drack, 2022, Molecular therapy. Nucleic acids.

How long does gene therapy last? 4-year follow-up of phase 3 voretigene neparvovec trial in RPE65-associated LCA/inherited retinal disease

S. Russell, J. Bennett, D. Chung, 2019, Journal of American Association for Pediatric Ophthalmology and Strabismus.

Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model

V. Sheffield, A. Drack, Seongjin Seo, 2022, Disease models & mechanisms.

Knockout of Bbs10 results in lack of cone electrical function and progressive retinal degeneration of rods and cones

V. Sheffield, A. Drack, Seongjin Seo, 2022, bioRxiv.

Overcoming the overexpression toxicity of gene replacement therapy for Bardet Biedl Syndrome type 1

V. Sheffield, E. Stone, B. Tucker, 2014 .

A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea.

V. Sheffield, E. Stone, B. Nichols, 1993, Human molecular genetics.

Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31

V. Sheffield, E. Stone, W. Alward, 1993, Nature Genetics.

Transient lens changes after diode laser retinal photoablation for retinopathy of prematurity.

A. Capone, A. Drack, 1994, American journal of ophthalmology.

TRIP8b Is Required for Maximal Expression of HCN1 in the Mouse Retina

S. Baker, D. Chetkovich, M. Modestou, 2014, PloS one.

Neurodevelopmental outcome of preterm infants enrolled in myo-inositol randomized controlled trial

David L. Rogers, Margaret M. Crawford, W. R. Lucas, 2021, Journal of Perinatology.

Cortical Evoked Potentials Preceding Voluntary Saccadic Eye Movements

C. Balaban, A. Drack, J. Weinstein, 1984 .

Recommendations of the American Academy of Ophthalmology Task Force on Genetic Testing

V. Sheffield, E. Stone, E. Traboulsi, 2012 .

GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery.

Mallory R. Tollefson, T. Scheetz, E. Stone, 2023, JAMA ophthalmology.

Nanophthalmos patient with a THR518MET mutation in MYRF, a case report

Young H. Kwon, M. Schnieders, J. Fingert, 2020, BMC Ophthalmology.

Homocystinuria Ocular Manifestations in Homocystinuria

A. Drack, Heather A. Stiff, 2020 .

Long-term functional and structural outcomes in X-linked retinoschisis: implications for clinical trials

Ian C. Han, S. Russell, A. Dumitrescu, 2023, Frontiers in Medicine.

Neurodevelopmental outcome of preterm infants enrolled in myo-inositol randomized controlled trial.

David L. Rogers, Margaret M. Crawford, W. R. Lucas, 2021, Journal of Perinatology.

Which Leber congenital amaurosis patients are eligible for gene therapy trials?

E. Stone, A. Drack, Rebecca M. Johnston, 2009, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Avoidance and treatment of retinopathy of prematurity.

A. Drack, C. Whitfill, 2000, Seminars in pediatric surgery.

Progressive retinal degeneration of rods and cones in a Bardet-Biedl syndrome type 10 mouse model

V. Sheffield, A. Drack, Seongjin Seo, 2022, Disease Models & Mechanisms.

Patient-specific induced pluripotent stem cells (iPSCs) for the study and treatment of retinal degenerative diseases

Allison E. Songstad, E. Stone, B. Tucker, 2015, Progress in Retinal and Eye Research.

Results of phase III clinical trial subretinal gene therapy for RPE65-mediated Leber congenital amaurosis (LCA)

E. Stone, J. Bennett, D. Chung, 2016 .

Restoration of Cone Sensitivity to Individuals with Congenital Photoreceptor Blindness within the Phase 1/2 Sepofarsen Trial

A. J. Roman, A. Cideciyan, S. Jacobson, 2022, Ophthalmology science.

A Novel c.1135_1138delCTGT Mutation in CLN3 Leads to Juvenile Neuronal Ceroid Lipofuscinosis

A. Drack, D. Pearce, Jake N. Miller, 2013, Journal of child neurology.

Ophthalmologic Complications in Children With Chronic Hepatitis C Treated With Pegylated Interferon

M. Repka, P. Rosenthal, A. Drack, 2010, Journal of pediatric gastroenterology and nutrition.

Recommendations for genetic testing of inherited eye diseases: report of the American Academy of Ophthalmology task force on genetic testing.

V. Sheffield, E. Stone, E. Traboulsi, 2012, Ophthalmology.

Prevalence of Cerebrotendinous Xanthomatosis (CTX) Among Patients Diagnosed With Early-Onset Idiopathic Bilateral Cataracts: Final Analysis.

D. Vanderveen, S. Freedman, A. Drack, 2023, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Optic nerve abnormalities in children: a practical approach.

M. Repka, J. Edmond, A. Drack, 2010, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Genotype–phenotype analysis of the branchio‐oculo‐facial syndrome

W. Reardon, G. Mortier, O. Klein, 2011, American journal of medical genetics. Part A.

A visually guided swim assay for mouse models of human retinal disease recapitulates the multi-luminance mobility test in humans

Joseph G. Laird, A. Drack, Megan Helms, 2023, Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society.

Pediatric golf-related ophthalmic injuries.

S. Oliver, A. Drack, V. Durairaj, 2008, Archives of ophthalmology.