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ARVO Annual Meeting Abstract June 2024

Cross-sectional and longitudinal changes in the gut microbiota in non-infectious uveitis

Shilpa Kodati; Carra Simpson; Jung W Lee; Mary Maclean; Pulak Nath; Jonathan Jacobs; H Nida Sen

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):1443.

ARVO Annual Meeting Abstract June 2023

Enhancement of intravitreal gene transduction with a magnetic microsphere-mediated gene delivery system in mouse eyes

Jinghua Chen; Chiab Simpson; Seok Hong Min; W. Clay Smith

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):5087.

ARVO Annual Meeting Abstract June 2022

A modified arrestin1 increases lactate production in the retina and slows retinal degeneration

W. Clay Smith; Tiffany S Nelson; Chiab Simpson; Frank M Dyka; Astra Dinculescu

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):51 – A0024.

ARVO Annual Meeting Abstract June 2022

The Gut Microbiome in Ocular Inflammatory Diseases

Shilpa Kodati; Carra Simpson; Jung Lee; Mary Maclean; Patti Sherry; Pulak Ranjan Nath; Henry Lin; Jonathan Jacobs; H Nida Sen

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2217 – A0513.

Genetics July 2021

Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2

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Claire L. Simpson; Anthony M. Musolf; Roberto Y. Cordero; Jennifer B. Cordero; Laura Portas; Federico Murgia; Deyana D. Lewis; Candace D. Middlebrooks; Elise B. Ciner; Joan E. Bailey-Wilson; Dwight Stambolian
TAGS: african american, genes, myopia, chromosomes, family, body tissue
Invest. Ophthalmol. Vis. Sci.. 2021; 62(9):16. https://doi.org/10.1167/iovs.62.9.16

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2020

A novel epitope-tagged Clarin-1 knock-in mouse with retinal dysfunction and profound congenital deafness

Astra Dinculescu; Omar Akil; Susan Bolch; Frank M Dyka; William N Ruddick; Chiab Simpson; Lei Xu

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2446.

ARVO Annual Meeting Abstract July 2019

Myopia is Significantly Linked to Chromosomes 7p14.3 and 17p13.2 Across Five Discrete Populations

Anthony Musolf; Claire L. Simpson; Laura Portas; Federico Murgia; Qing Li; Elise Ciner; Dwight Stambolian; Joan E Bailey-Wilson

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):3146.

ARVO Annual Meeting Abstract July 2019

A novel locus identified in chromosome 14 modulates lens weight on mouse using Genome-wide Efficient Mixed Model Association

Jennifer Buenaventura Cordero; Robert W. Williams; Lu Lu; Claire L. Simpson

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5876.

ARVO Annual Meeting Abstract July 2019

QTL remapping of murine eye weight reveals novel candidate gene s for ocular growth

Roberto Yu Cordero; Robert W. Williams; Lu Lu; Claire L. Simpson

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):5888.

ARVO Annual Meeting Abstract July 2018

Phenotypic consequences of amino acid substitutions at the S163 position in C1QTNF5 protein following expression in murine RPE

Astra Dinculescu; Susan Bolch; Frank M Dyka; Manoj Kulkarni; Chiab Simpson; W Clay Smith; William W Hauswirth

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3052.

ARVO Annual Meeting Abstract July 2018

The expression pattern and pathological effects of CLRN1 mutant proteins in the mouse retina

Susan Bolch; Frank M Dyka; Manoj Kulkarni; Rachel Stupay; Chiab Simpson; W Clay Smith; William W Hauswirth; Astra Dinculescu

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3053.

ARVO Annual Meeting Abstract July 2018

Family-Based Association Tests of Myopia reveal a potentially hidden association signal upstream of two GABA receptor genes

Candace Middlebrooks; Claire L. Simpson; Anthony Musolf; Laura Portas; Federico Murgia; Elise B. Ciner; Dwight Stambolian; Joan E Bailey-Wilson

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):702.

ARVO Annual Meeting Abstract July 2018

Statistical approaches to the analysis of whole-genome sequencing in autosomal-dominant macular dystrophy

Roberto Y Cordero; Robert W. Williams; Michael B. Petersen; Haris Kokotas; Maria Grigoriadou; George Kitsos; Nawajes A Mandal; Claire L. Simpson

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):780.

ARVO Annual Meeting Abstract July 2018

African-American families show genome-wide significant linkage to myopia at 7p15.2-14.2

Joan E Bailey-Wilson; Anthony Musolf; Claire L. Simpson; Laura Portas; Federico Murgia; Qing Li; Elise B. Ciner; Dwight Stambolian

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1823.

ARVO Annual Meeting Abstract July 2018

Myopia in Amish Families Linked to Five Chromosomes

Anthony Musolf; Claire L. Simpson; Laura Portas; Federico Murgia; Qing Li; Elise B. Ciner; Dwight Stambolian; Joan E Bailey-Wilson

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1824.

ARVO Annual Meeting Abstract July 2018

Rare Variant TDT Association Study of Familial Myopia in Caucasian Families

Deyana Lewis; Claire L. Simpson; Anthony Musolf; Kyle Long; Laura Portas; Federico Murgia; Elise B. Ciner; Dwight Stambolian; Joan E Bailey-Wilson

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1825.

ARVO Annual Meeting Abstract July 2018

In silico functional analysis of genetic variants in chromosome 19 to identify disease-causing gene in a large Greek family with autosomal dominant macular dystrophy

Jennifer Buenaventura Cordero; Robert W. Williams; Michael B. Petersen; Haris Kokotas; Maria Grigoriadou; George Kitsos; Nawajes A Mandal; Claire L. Simpson

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):3141.

Genetics July 2017

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p

PDF

Anthony M. Musolf; Claire L. Simpson; Bilal A. Moiz; Kyle A. Long; Laura Portas; Federico Murgia; Elise B. Ciner; Dwight Stambolian; Joan E. Bailey-Wilson
TAGS: chromosomes, european continental ancestry group, family, myopia, single nucleotide polymorphism, genome
Invest. Ophthalmol. Vis. Sci.. 2017; 58(9):3547-3554. https://doi.org/10.1167/iovs.16-21271

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2017

Han Chinese families show significant linkage for myopia on 10q26 and suggestive linkage on 9q33.

Joan E Bailey-Wilson; Anthony Musolf; Claire L Simpson; Bilal A. Moiz; Kyle A. Long; Deyana D. Lewis; Candace D. Middlebrooks; Laura Portas; Federico Murgia; Dwight Stambolian

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):1223.

ARVO Annual Meeting Abstract June 2017

Chromosome 11p is Significantly Linked to Myopia in Caucasian Families

Anthony Musolf; Claire L Simpson; Bilal A. Moiz; Kyle A. Long; Deyana D. Lewis; Candace D. Middlebrooks; Laura Portas; Federico Murgia; Elise B Ciner; Dwight Stambolian; Joan E Bailey-Wilson

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):182.

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Cross-sectional and longitudinal changes in the gut microbiota in non-infectious uveitis

Enhancement of intravitreal gene transduction with a magnetic microsphere-mediated gene delivery system in mouse eyes

A modified arrestin1 increases lactate production in the retina and slows retinal degeneration

The Gut Microbiome in Ocular Inflammatory Diseases

Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2

A novel epitope-tagged Clarin-1 knock-in mouse with retinal dysfunction and profound congenital deafness

Myopia is Significantly Linked to Chromosomes 7p14.3 and 17p13.2 Across Five Discrete Populations

A novel locus identified in chromosome 14 modulates lens weight on mouse using Genome-wide Efficient Mixed Model Association

QTL remapping of murine eye weight reveals novel candidate gene s for ocular growth

Phenotypic consequences of amino acid substitutions at the S163 position in C1QTNF5 protein following expression in murine RPE

The expression pattern and pathological effects of CLRN1 mutant proteins in the mouse retina

Family-Based Association Tests of Myopia reveal a potentially hidden association signal upstream of two GABA receptor genes

Statistical approaches to the analysis of whole-genome sequencing in autosomal-dominant macular dystrophy

African-American families show genome-wide significant linkage to myopia at 7p15.2-14.2

Myopia in Amish Families Linked to Five Chromosomes

Rare Variant TDT Association Study of Familial Myopia in Caucasian Families

In silico functional analysis of genetic variants in chromosome 19 to identify disease-causing gene in a large Greek family with autosomal dominant macular dystrophy

Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p

Han Chinese families show significant linkage for myopia on 10q26 and suggestive linkage on 9q33.

Chromosome 11p is Significantly Linked to Myopia in Caucasian Families

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