Factors determining the band gap of a nanocrystalline multicomponent equimolar transition metal based high entropy oxide (Co,Cu,Mg,Ni,Zn)O
Usharani, Nandhini J., Arivazhagan, P., Thomas, Tiju, Bhattacharya, S.S.
Published in Materials science & engineering. B, Solid-state materials for advanced technology (01.09.2022)
Published in Materials science & engineering. B, Solid-state materials for advanced technology (01.09.2022)
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Journal Article
Single Jersey Modal Fabrics-Better Choice for Sportswear Applications
Ajmeri, Jitendra R, Bhattacharya, SS
Published in Journal of Textile Engineering & Fashion Technology (19.09.2017)
Published in Journal of Textile Engineering & Fashion Technology (19.09.2017)
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Journal Article
Fox's in development and disease
Lehmann, Ordan J, Sowden, Jane C, Carlsson, Peter, Jordan, Tim, Bhattacharya, Shomi S
Published in Trends in genetics (01.06.2003)
Published in Trends in genetics (01.06.2003)
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Journal Article
OPA1 , encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28
Wissinger, Bernd, Votruba, Marcela, Bhattacharya, Shomi S, Moore, Anthony, Leo-Kottler, Beate, Mayer, Simone, Pesch, Ulrike E.A, Alexander, Christiane, Thiselton, Dawn L, Kellner, Ulrich, Rodriguez, Miguel, Auburger, Georg
Published in Nature genetics (01.10.2000)
Published in Nature genetics (01.10.2000)
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Journal Article
Molecular genetic basis of inherited cataract and associated phenotypes
Reddy, M.Ashwin, Francis, Peter J, Berry, Vanita, Bhattacharya, Shomi S, Moore, Anthony T
Published in Survey of ophthalmology (01.05.2004)
Published in Survey of ophthalmology (01.05.2004)
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Journal Article
Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC)
Yardley, Jill, Leroy, Bart P, Hart-Holden, Niki, Lafaut, Bart A, Loeys, Bart, Messiaen, Ludwine M, Perveen, Rahat, Reddy, M. Ashwin, Bhattacharya, Shomi S, Traboulsi, Elias, Baralle, Diana, De Laey, Jean-Jacques, Puech, Bernard, Kestelyn, Philippe, Moore, Anthony T, Manson, Forbes D. C, Black, Graeme C. M
Published in Investigative ophthalmology & visual science (01.10.2004)
Published in Investigative ophthalmology & visual science (01.10.2004)
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Journal Article
Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene
Aung, Tin, Rezaie, Tayebeh, Okada, Koji, Viswanathan, Ananth C, Child, Anne H, Brice, Glen, Bhattacharya, Shomi S, Lehmann, Ordan J, Sarfarazi, Mansoor, Hitchings, Roger A
Published in Investigative ophthalmology & visual science (01.08.2005)
Published in Investigative ophthalmology & visual science (01.08.2005)
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Journal Article
Alpha-B Crystallin Gene ( CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans
Berry, Vanita, Francis, Peter, Reddy, M. Ashwin, Collyer, Dean, Vithana, Eranga, MacKay, Ian, Dawson, Gary, Carey, Alisoun H., Moore, Anthony, Bhattacharya, Shomi S., Quinlan, Roy A.
Published in American journal of human genetics (01.11.2001)
Published in American journal of human genetics (01.11.2001)
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Journal Article
A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 ( RP11)
Vithana, Eranga N., Abu-Safieh, Leen, Allen, Maxine J., Carey, Alisoun, Papaioannou, Myrto, Chakarova, Christina, Al-Maghtheh, Mai, Ebenezer, Neil D., Willis, Catherine, Moore, Anthony T., Bird, Alan C., Hunt, David M., Bhattacharya, Shomi S.
Published in Molecular cell (01.08.2001)
Published in Molecular cell (01.08.2001)
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Journal Article
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)
Cremers, Frans P.M, den Hollander, Anneke I, ten Brink, Jacoline B, de Kok, Yvette J.M, van Soest, Simone, van den Born, L. Ingeborgh, van Driel, Marc A, van de Pol, Dorien J.R, Payne, Annette M, Bhattacharya, Shomi S, Kellner, Ulrich, Hoyng, Carel B, Westerveld, Andries, Brunner, Han G, Bleeker-Wagemakers, Elisabeth M, Deutman, August F, Heckenlively, John R, Bergen, Arthur A.B
Published in Nature genetics (01.10.1999)
Published in Nature genetics (01.10.1999)
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Journal Article
Expression of PRPF31 mRNA in Patients with Autosomal Dominant Retinitis Pigmentosa: A Molecular Clue for Incomplete Penetrance?
Vithana, Eranga N, Abu-Safieh, Leen, Pelosini, Lucia, Winchester, Elizabeth, Hornan, Dan, Bird, Alan C, Hunt, David M, Bustin, Stephen A, Bhattacharya, Shomi S
Published in Investigative ophthalmology & visual science (01.10.2003)
Published in Investigative ophthalmology & visual science (01.10.2003)
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Journal Article
Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy
Votruba, M, Thiselton, D, Bhattacharya, S S
Published in British journal of ophthalmology (01.01.2003)
Published in British journal of ophthalmology (01.01.2003)
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Journal Article
Mutations in the pre-mRNA splicing factor gene PRPC8 in autosomal dominant retinitis pigmentosa (RP13)
MCKIE, Arthur B, MCHALE, John C, MACKEY, David A, BHATTACHARYA, Shomi S, BIRD, Alan C, MARKHAM, Alexander F, INGLEHEARN, Chris F, KEEN, T. Jeffrey, TARTTELIN, Emma E, GOLIATH, Rene, VAN LITH-VERHOEVEN, Janneke J. C, GREENBERG, Jacquie, RAMESAR, Rajkumar S, HOYNG, Carel B, CREMERS, Frans P. M
Published in Human molecular genetics (15.07.2001)
Published in Human molecular genetics (15.07.2001)
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Journal Article
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
CHAKAROVA, Christina F, HIMS, Matthew M, ROSENBERG, Thomas, WEBSTER, Andrew R, BIRD, Alan C, GAL, Andreas, HUNT, David, VITHANA, Eranga N, BHATTACHARYA, Shomi S, BOLZ, Hanno, ABU-SAFIEH, Leen, PATEL, Reshma J, PAPAIOANNOU, Myrto G, INGLEHEARN, Chris F, KEEN, T. Jeffrey, WILLIS, Catherine, MOORE, Anthony T
Published in Human molecular genetics (2002)
Published in Human molecular genetics (2002)
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Journal Article
The genetics of childhood cataract
Francis, P J, Berry, V, Bhattacharya, S S, Moore, A T
Published in Journal of Medical Genetics (01.07.2000)
Published in Journal of Medical Genetics (01.07.2000)
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Journal Article
Book Review
Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy
Ali, Robin R, Sarra, Gian-Marco, Stephens, Clare, Alwis, Mahesh de, Bainbridge, James W.B, Munro, Peter M, Fauser, Sascha, Reichel, Martin B, Kinnon, Christine, Hunt, David M, Bhattacharya, Shomi S, Thrasher, Adrian J
Published in Nature genetics (01.07.2000)
Published in Nature genetics (01.07.2000)
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Journal Article
A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
Arora, A, Minogue, P J, Liu, X, Reddy, M A, Ainsworth, J R, Bhattacharya, S S, Webster, A R, Hunt, D M, Ebihara, L, Moore, A T, Beyer, E C, Berthoud, V M
Published in Journal of medical genetics (01.01.2006)
Published in Journal of medical genetics (01.01.2006)
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