Shiwani Sharma

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Microbial Diversity, Interventions and Scope

Shiwani Guleria, Sharma., N. Sharma, 2020 .

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1

M. Brown, P. Mitchell, N. Martin, 2011, Nature Genetics.

blood Rapid inexpensive genome-wide association using pooled whole Material

P. Visscher, G. Montgomery, S. MacGregor, 2009 .

Rapid inexpensive genome-wide association using pooled whole blood.

P. Visscher, G. Montgomery, S. MacGregor, 2009, Genome research.

Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

M. Shaw, J. Gécz, L. FitzGerald, 2003, American journal of human genetics.

Identification of novel bovine RPE and retinal genes by subtractive hybridization.

P. Campochiaro, D. Zack, J. Chang, 2002, Molecular vision.

1. Awadalla MS, Thapa SS, Burdon KP, Hewitt AW, Craig JE. The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population. Mol Vis 2011;17:2248-54.

T. Haritunians, A. Hewitt, Y. Bykhovskaya, 2011 .

Measurement of Systemic Mitochondrial Function in Advanced Primary Open-Angle Glaucoma and Leber Hereditary Optic Neuropathy

Jonathan G. Crowston, Ian A. Trounce, David A. Mackey, 2015, PloS one.

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy

Nathan J Morris, Xuejun Qin, Joan E Bailey-Wilson, 2017, Nature Communications.

Association of TCF4 and CLU polymorphisms with Fuchs’ endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process

A. Hewitt, R. Mills, J. Craig, 2012, European Journal of Human Genetics.

Identification of LOXL1 protein and Apolipoprotein E as components of surgically isolated pseudoexfoliation material by direct mass spectrometry.

A. Hewitt, R. Mills, J. Craig, 2009, Experimental eye research.

Genotype, Age, Genetic Background, and Sex Influence Epha2-Related Cataract Development in Mice

J. Craig, K. Burdon, Shiwani Sharma, 2021, Investigative ophthalmology & visual science.

Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epithelium.

S. Bröer, Shiwani Sharma, D. Dimasi, 2007, Experimental cell research.

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

J. Haines, P. Mitchell, L. Pasquale, 2018, Scientific Reports.

Microbes Supporting Life Off-Planet

M. Sharma, Shiwani Sharma, 2020 .

Differential Gene Expression Profiling of Orbital Adipose Tissue in Thyroid Orbitopathy.

B. Llamas, J. Craig, K. Burdon, 2015, Investigative ophthalmology & visual science.

Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye.

P. Mitchell, D. Mackey, A. Hewitt, 2012, Investigative ophthalmology & visual science.

Microbial ACC-Deaminase Attributes: Perspectives and Applications in Stress Agriculture

P. Verma, Shiwani Sharma, M. Kaur, 2020 .

MALDI MS imaging analysis of apolipoprotein E and lysyl oxidase-like 1 in human lens capsules affected by pseudoexfoliation syndrome.

N. Voelcker, J. Craig, Shiwani Sharma, 2013, Journal of proteomics.

High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia

D. Mackey, A. Hewitt, E. Souzeau, 2017, G3: Genes, Genomes, Genetics.

Glaucoma Association of Genetic Variants in the TMCO 1 Gene with Clinical Parameters Related to Glaucoma and Characterization of the Protein in the Eye

P. Mitchell, D. Mackey, A. Hewitt, 2012 .

Reduced expression of apolipoprotein E and immunoglobulin heavy constant gamma 1 proteins in Fuchs endothelial corneal dystrophy

A. Urbani, R. Mills, J. Craig, 2019, Clinical & experimental ophthalmology.

Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus.

D. Siscovick, G. Montgomery, K. Taylor, 2011, Investigative ophthalmology & visual science.

Screening of the COL8A2 gene in an Australian family with early‐onset Fuchs’ endothelial corneal dystrophy

R. Mills, J. Craig, K. Burdon, 2014, Clinical & experimental ophthalmology.

Contribution of Mutations in Known Mendelian Glaucoma Genes to Advanced Early-Onset Primary Open-Angle Glaucoma.

M. Brown, D. Mackey, S. Graham, 2017, Investigative ophthalmology & visual science.

RNA Sequencing of Lens Capsular Epithelium Implicates Novel Pathways in Pseudoexfoliation Syndrome

R. Mills, E. Souzeau, J. Craig, 2022, Investigative ophthalmology & visual science.

RZF, a zinc-finger protein in the photoreceptors of human retina.

Shiwani Sharma, D. Dimasi, N. Della, 2004, Gene.

Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma

N. Martin, G. Montgomery, J. Beesley, 2018, Nature Genetics.

Role of small RNA in regulating plant viral pathogenesis

Lovepreet Kaur, M. Sharma, Shiwani Sharma, 2020, Plant Small RNA.

Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma

J. Haines, P. Mitchell, L. Pasquale, 2018, Scientific Reports.

Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma

Janey L. Wiggs, Paul Mitchell, Jonathan L. Haines, 2014, Nature Genetics.

Mutation in TMEM98 in a large white kindred with autosomal dominant nanophthalmos linked to 17p12-q12.

A. Hewitt, E. Souzeau, J. Craig, 2014, JAMA ophthalmology.

Association of Age-Related Cataract With Skin Cancer in an Australian Population

Shiwani Sharma, J. Khadka, M. Inacio, 2020, Investigative ophthalmology & visual science.

CRTR-1, a Developmentally Regulated Transcriptional Repressor Related to the CP2 Family of Transcription Factors*

P. Rathjen, G. Chapman, Shiwani Sharma, 2001, The Journal of Biological Chemistry.

Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.

P. Mitchell, Jie-Jin Wang, D. Mackey, 2007, Human molecular genetics.

Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a review

J. Craig, R. Casson, Shiwani Sharma, 2016, Clinical & experimental ophthalmology.

Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome.

N. Voelcker, A. Hewitt, J. Craig, 2016, Experimental eye research.

Novel protein constituents of pathological ocular pseudoexfoliation syndrome deposits identified with mass spectrometry

N. Voelcker, R. Mills, J. Craig, 2018, Molecular vision.

Ocular Expression and Distribution of Products of the POAG-Associated Chromosome 9p21 Gene Region

J. Craig, K. Burdon, R. Casson, 2013, PloS one.

Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka

J. Craig, K. Burdon, R. Casson, 2018, Molecular genetics & genomic medicine.

Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform

J. Gécz, B. Lorenz, J. Craig, 2008, Molecular vision.

Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions.

M. Shaw, J. Gécz, D. Mackey, 2006, Human molecular genetics.

Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene

M. Brown, N. Petrovsky, A. Jenkins, 2015, Diabetologia.

TGC repeat expansion in the TCF4 gene increases the risk of Fuchs’ endothelial corneal dystrophy in Australian cases

A. Hewitt, R. Mills, E. Souzeau, 2017, PloS one.

Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO 1 and CDKN 2 BAS 1

M. Brown, P. Mitchell, N. Martin, 2011 .

A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start site

D. Mackey, J. Craig, K. Burdon, 2007, Human mutation.

Rare variants in optic disc area gene CARD10 enriched in primary open‐angle glaucoma

M. Brown, D. Mackey, S. Graham, 2016, Molecular genetics & genomic medicine.

DNA methylation at the 9p21 glaucoma susceptibility locus is associated with normal-tension glaucoma

P. Mitchell, Jie-Jin Wang, S. Graham, 2018, Ophthalmic genetics.

Atomic force microscopy-based antibody recognition imaging of proteins in the pathological deposits in pseudoexfoliation syndrome.

N. Voelcker, C. Gibson, J. Craig, 2011, Ultramicroscopy.

Partial duplication of the CRYBB1-CRYBA4 locus is associated with autosomal dominant congenital cataract

E. Souzeau, J. Craig, K. Burdon, 2016, European Journal of Human Genetics.

MALDI-MS-imaging of whole human lens capsule.

N. Voelcker, J. Craig, K. Burdon, 2011, Journal of proteome research.

Identification of a Novel Oligomerization Disrupting Mutation in CRYΑA Associated with Congenital Cataract in a South Australian Family

E. Souzeau, J. Craig, K. Burdon, 2013, Human mutation.

Detecting protein aggregates on untreated human tissue samples by atomic force microscopy recognition imaging.

N. Voelcker, C. Gibson, J. Craig, 2010, Biophysical journal.

Variation in pathogenicity of some Indian isolates of Xanthomonas campestris pv. oryzae

Anuj Gupta, Shiwani Sharma, R. Saini, 1986 .

Genes Lr48 and Lr49 for hypersensitive adult plant leaf rust resistance in wheat (Triticum aestivum L.)

M. Kaur, G. S. Nanda, Shiwani Sharma, 2002, Euphytica.

Epha2 genotype influences ultraviolet radiation induced cataract in mice.

D. Mackey, J. Craig, K. Burdon, 2019, Experimental eye research.

Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)

Kathryn P. Burdon, Theresa Casey, Jamie E. Craig, 2017, BMC Medical Genetics.

Virus-mediated secretion gene therapy--a potential treatment for ocular neovascularization.

I. Constable, P. Rakoczy, C. Lai, 2003, Advances in experimental medicine and biology.

Genetic analysis of the clusterin gene in pseudoexfoliation syndrome

P. Mitchell, Jie-Jin Wang, D. Mackey, 2008, Molecular vision.

Microbes in Food and Beverage Industry

Shiwani Sharma, Neegam Nain, K. Kumari, 2020 .

Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract

E. Souzeau, J. Craig, K. Burdon, 2016, BMC Research Notes.

Mutations in the EPHA2 Gene Are a Major Contributor to Inherited Cataracts in South-Eastern Australia

P. Mitchell, Jie-Jin Wang, D. Mackey, 2013, PloS one.

Whole exome sequencing implicates eye development, the unfolded protein response and plasma membrane homeostasis in primary open-angle glaucoma

Tiger Zhou, Stuart MacGregor, Stuart Graham, 2017, PloS one.

Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouse

J. Craig, S. Klebe, Shiwani Sharma, 2023, Scientific reports.

The status of intercellular junctions in established lens epithelial cell lines

J. Craig, Shiwani Sharma, Alpana Dave, 2012, Molecular vision.

Role of the nucleolus in neurodegenerative diseases with particular reference to the retina: a review

J. Craig, R. Casson, Shiwani Sharma, 2016, Clinical & experimental ophthalmology.

EPHA2 MUTATIONS CONTRIBUTE TO CONGENITAL CATARACT THROUGH DIVERSE MECHANISMS

J. Craig, K. Burdon, Shiwani Sharma, 2016, Molecular vision.