Impact of COVID-19 on Water Quality Index of river Yamuna in Himalayan and upper segment: analysis of monsoon and post-monsoon season

por Sharma, Shiwani, Gupta, AnuShri
Publicado 2022

The status of intercellular junctions in established lens epithelial cell lines

por Dave, Alpana, Craig, Jamie E., Sharma, Shiwani
Publicado 2012

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

por Sharma, Shiwani, Lang, Catherine, Khadka, Jyoti, Inacio, Maria C.
Publicado 2020

Bacteriological Surveillance of Ambulance Vehicles from a Tertiary Care Hospital of North India

por Sharma, Shiwani, Datta, Priya, Gupta, Varsha, Vasesi, Dipanshu, Chander, Jagdish
Publicado 2021

EPHA2 MUTATIONS CONTRIBUTE TO CONGENITAL CATARACT THROUGH DIVERSE MECHANISMS

por Dave, Alpana, Martin, Sarah, Kumar, Raman, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
Publicado 2016

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

por Javadiyan, Shari, Craig, Jamie E., Sharma, Shiwani, Lower, Karen M., Casey, Theresa, Haan, Eric, Souzeau, Emmanuelle, Burdon, Kathryn P.
Publicado 2017

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

por Chidlow, Glyn, Wood, John P. M., Sharma, Shiwani, Dimasi, David P., Burdon, Kathryn P., Casson, Robert J., Craig, Jamie E.
Publicado 2013

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

por Kuot, Abraham, Hewitt, Alex W., Snibson, Grant R., Souzeau, Emmanuelle, Mills, Richard, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
Publicado 2017

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

por Javadiyan, Shari, Craig, Jamie E., Souzeau, Emmanuelle, Sharma, Shiwani, Lower, Karen M., Pater, John, Casey, Theresa, Hodson, Trevor, Burdon, Kathryn P.
Publicado 2016

Genetic analysis of the clusterin gene in pseudoexfoliation syndrome

por Burdon, Kathryn P., Sharma, Shiwani, Hewitt, Alex W., McMellon, Amy E., Wang, Jie Jin, Mackey, David A., Mitchell, Paul, Craig, Jamie E.
Publicado 2008

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

por Hassall, Mark M., Javadiyan, Shari, Klebe, Sonja, Awadalla, Mona S., Sharma, Shiwani, Qassim, Ayub, White, Melissa, Thomas, Paul Q., Craig, Jamie E., Siggs, Owen M.
Publicado 2023

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

por Sharma, Shiwani, Burdon, Kathryn P., Dave, Alpana, Jamieson, Robyn V., Yaron, Yuval, Billson, Frank, Van Maldergem, Lionel, Lorenz, Birgit, Gécz, Jozef, Craig, Jamie E.
Publicado 2008

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

por Dave, Alpana, Craig, Jamie E., Alamein, Mohammad, Skrzypiec, Karina, Beltz, Justin, Pfaff, Annalise, Burdon, Kathryn P., Ercal, Nuran, de Iongh, Robb U., Sharma, Shiwani
Publicado 2021

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

por Dave, Alpana, Laurie, Kate, Staffieri, Sandra E., Taranath, Deepa, Mackey, David A., Mitchell, Paul, Wang, Jie Jin, Craig, Jamie E., Burdon, Kathryn P., Sharma, Shiwani
Publicado 2013

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

por Van Bergen, Nicole J, Crowston, Jonathan G., Craig, Jamie E., Burdon, Kathryn P., Kearns, Lisa S., Sharma, Shiwani, Hewitt, Alex W., Mackey, David A., Trounce, Ian A.
Publicado 2015

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

por Sharma, Shiwani, Chataway, Tim, Klebe, Sonja, Griggs, Kim, Martin, Sarah, Chegeni, Nusha, Dave, Alpana, Zhou, Tiger, Ronci, Maurizio, Voelcker, Nicolas H., Mills, Richard A., Craig, Jamie E.
Publicado 2018

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

por Javadiyan, Shari, Lucas, Sionne E. M., Wangmo, Dechen, Ngy, Meng, Edussuriya, Kapila, Craig, Jamie E., Rudkin, Adam, Casson, Robert, Selva, Dinesh, Sharma, Shiwani, Lower, Karen M., Meucke, James, Burdon, Kathryn P.
Publicado 2018

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

por Javadiyan, Shari, Craig, Jamie E., Souzeau, Emmanuelle, Sharma, Shiwani, Lower, Karen M., Mackey, David A., Staffieri, Sandra E., Elder, James E., Taranath, Deepa, Straga, Tania, Black, Joanna, Pater, John, Casey, Theresa, Hewitt, Alex W., Burdon, Kathryn P.
Publicado 2017

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

por Zhou, Tiger, Souzeau, Emmanuelle, Sharma, Shiwani, Siggs, Owen M., Goldberg, Ivan, Healey, Paul R., Graham, Stuart, Hewitt, Alex W., Mackey, David A., Casson, Robert J., Landers, John, Mills, Richard, Ellis, Jonathan, Leo, Paul, Brown, Matthew A., MacGregor, Stuart, Burdon, Kathryn P., Craig, Jamie E.
Publicado 2016

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

por Zhou, Tiger, Souzeau, Emmanuelle, Sharma, Shiwani, Landers, John, Mills, Richard, Goldberg, Ivan, Healey, Paul R., Graham, Stuart, Hewitt, Alex W., Mackey, David A., Galanopoulos, Anna, Casson, Robert J., Ruddle, Jonathan B., Ellis, Jonathan, Leo, Paul, Brown, Matthew A., MacGregor, Stuart, Lynn, David J., Burdon, Kathryn P., Craig, Jamie E.
Publicado 2017