PubMed

Effect of gas flow rates on the anatase-rutile transformation temperature of nanocrystalline TiO2 synthesised by chemical vapour synthesis.

Ahmad MI, Bhattacharya SS, Fasel C, Hahn H.

J Nanosci Nanotechnol. 2009 Sep;9(9):5572-7.PMID: 19928267 [PubMed - in process]Related articles

TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.

Audo I, Kohl S, Leroy BP, Munier FL, Guillonneau X, Mohand-Saïd S, Bujakowska K, Nandrot EF, Lorenz B, Preising M, Kellner U, Renner AB, Bernd A, Antonio A, Moskova-Doumanova V, Lancelot ME, Poloschek CM, Drumare I, Defoort-Dhellemmes S, Wissinger B, Léveillard T, Hamel CP, Schorderet DF, De Baere E, Berger W, Jacobson SG, Zrenner E, Sahel JA, Bhattacharya SS, Zeitz C.

Am J Hum Genet. 2009 Nov;85(5):720-9. Epub 2009 Nov 5.PMID: 19896113 [PubMed - in process]Related articles

Study of Gene-Targeted Mouse Models of Splicing Factor Gene Prpf31 Implicated in Human Autosomal Dominant Retinitis Pigmentosa (RP).

Bujakowska K, Maubaret C, Chakarova CF, Tanimoto N, Beck SC, Fahl E, Humphries MM, Kenna PF, Makarov E, Makarova O, Paquet-Durand F, Ekström PA, van Veen T, Leveillard T, Humphries P, Seeliger MW, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2009 Dec;50(12):5927-33. Epub 2009 Jul 2.PMID: 19578015 [PubMed - in process]Related articles

Optimization of laccase mediated biodegradation of 2,4-dichlorophenol using genetic algorithm.

Bhattacharya SS, Karmakar S, Banerjee R.

Water Res. 2009 Aug;43(14):3503-10. Epub 2009 May 20.PMID: 19539342 [PubMed - indexed for MEDLINE]Related articles

Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.

Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Gränse L, Khanna R, Trager EH, Gieser LM, Hughbanks-Wheaton D, Cojocaru RI, Ghiasvand NM, Chakarova CF, Abrahamson M, Göring HH, Webster AR, Birch DG, Abecasis GR, Fann Y, Bhattacharya SS, Daiger SP, Heckenlively JR, Andréasson S, Swaroop A.

Am J Hum Genet. 2009 Jun;84(6):792-800.PMID: 19520207 [PubMed - indexed for MEDLINE]Related articles

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.

Khanna H, Davis EE, Murga-Zamalloa CA, Estrada-Cuzcano A, Lopez I, den Hollander AI, Zonneveld MN, Othman MI, Waseem N, Chakarova CF, Maubaret C, Diaz-Font A, Macdonald I, Muzny DM, Wheeler DA, Morgan M, Lewis LR, Logan CV, Tan PL, Beer MA, Inglehearn CF, Lewis RA, Jacobson SG, Bergmann C, Beales PL, Attié-Bitach T, Johnson CA, Otto EA, Bhattacharya SS, Hildebrandt F, Gibbs RA, Koenekoop RK, Swaroop A, Katsanis N.

Nat Genet. 2009 Jun;41(6):739-45. Epub 2009 May 10.PMID: 19430481 [PubMed - in process]Related articlesFree article

Mutations in TOPORS: a rare cause of autosomal dominant retinitis pigmentosa in continental Europe?

Schob C, Orth U, Gal A, Kindler S, Chakarova CF, Bhattacharya SS, Rüther K.

Ophthalmic Genet. 2009 Jun;30(2):96-8.PMID: 19373681 [PubMed - indexed for MEDLINE]Related articles

Mutations of the EPHA2 receptor tyrosine kinase gene cause autosomal dominant congenital cataract.

Zhang T, Hua R, Xiao W, Burdon KP, Bhattacharya SS, Craig JE, Shang D, Zhao X, Mackey DA, Moore AT, Luo Y, Zhang J, Zhang X.

Hum Mutat. 2009 May;30(5):E603-11.PMID: 19306328 [PubMed - indexed for MEDLINE]Related articles

Dominant cataract formation in association with a vimentin assembly disrupting mutation.

Müller M, Bhattacharya SS, Moore T, Prescott Q, Wedig T, Herrmann H, Magin TM.

Hum Mol Genet. 2009 Mar 15;18(6):1052-7. Epub 2009 Jan 6.PMID: 19126778 [PubMed - indexed for MEDLINE]Related articles

EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, Barragan I, O'Driscoll CA, Goodstadt L, Prigmore E, Borrego S, Mena M, Pieras JI, El-Ashry MF, Safieh LA, Shah A, Cheetham ME, Carter NP, Chakarova C, Ponting CP, Bhattacharya SS, Antinolo G.

Nat Genet. 2008 Nov;40(11):1285-7. Epub 2008 Oct 5.PMID: 18836446 [PubMed - indexed for MEDLINE]Related articlesFree article

Laccase mediated biodegradation of 2,4-dichlorophenol using response surface methodology.

Bhattacharya SS, Banerjee R.

Chemosphere. 2008 Aug;73(1):81-5. Epub 2008 Jun 30. Erratum in: Chemosphere. 2009 Jan;74(3):479. PMID: 18590926 [PubMed - indexed for MEDLINE]Related articles

Linkage validation of RP25 Using the 10K genechip array and further refinement of the locus by new linked families.

Barragán I, Abd El-Aziz MM, Borrego S, El-Ashry MF, O'Driscoll C, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jul;72(Pt 4):454-62. Epub 2007 May 29.PMID: 18510647 [PubMed - indexed for MEDLINE]Related articles

Large-scale molecular analysis of a 34 Mb interval on chromosome 6q: major refinement of the RP25 interval.

Abd El-Aziz MM, Barragan I, O'Driscoll C, Borrego S, Abu-Safieh L, Pieras JI, El-Ashry MF, Prigmore E, Carter N, Antinolo G, Bhattacharya SS.

Ann Hum Genet. 2008 Jul;72(Pt 4):463-77. Epub 2007 May 29.PMID: 18510646 [PubMed - indexed for MEDLINE]Related articlesFree article

Effect of gene therapy on visual function in Leber's congenital amaurosis.

Bainbridge JW, Smith AJ, Barker SS, Robbie S, Henderson R, Balaggan K, Viswanathan A, Holder GE, Stockman A, Tyler N, Petersen-Jones S, Bhattacharya SS, Thrasher AJ, Fitzke FW, Carter BJ, Rubin GS, Moore AT, Ali RR.

N Engl J Med. 2008 May 22;358(21):2231-9. Epub 2008 Apr 27.PMID: 18441371 [PubMed - indexed for MEDLINE]Related articlesFree article

Disease mechanism for retinitis pigmentosa (RP11) caused by missense mutations in the splicing factor gene PRPF31.

Wilkie SE, Vaclavik V, Wu H, Bujakowska K, Chakarova CF, Bhattacharya SS, Warren MJ, Hunt DM.

Mol Vis. 2008 Apr 18;14:683-90.PMID: 18431455 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotype associated with the H626P mutation and other changes in the TGFBI gene in Czech families.

Liskova P, Klintworth GK, Bowling BL, Filipec M, Jirsova K, Tuft SJ, Bhattacharya SS, Hardcastle AJ, Ebenezer ND.

Ophthalmic Res. 2008;40(2):105-8. Epub 2008 Feb 6.PMID: 18259096 [PubMed - indexed for MEDLINE]Related articles

Bilateral giant macular schisis in a patient with enhanced S-cone syndrome from a family showing pseudo-dominant inheritance.

Vaclavik V, Chakarova C, Bhattacharya SS, Robson AG, Holder GE, Bird AC, Webster AR.

Br J Ophthalmol. 2008 Feb;92(2):299-300. No abstract available. PMID: 18227217 [PubMed - indexed for MEDLINE]Related articles

An assessment of the apex microarray technology in genotyping patients with Leber congenital amaurosis and early-onset severe retinal dystrophy.

Henderson RH, Waseem N, Searle R, van der Spuy J, Russell-Eggitt I, Bhattacharya SS, Thompson DA, Holder GE, Cheetham ME, Webster AR, Moore AT.

Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5684-9.PMID: 18055820 [PubMed - indexed for MEDLINE]Related articlesFree article

British family with early-onset Fuchs' endothelial corneal dystrophy associated with p.L450W mutation in the COL8A2 gene.

Liskova P, Prescott Q, Bhattacharya SS, Tuft SJ.

Br J Ophthalmol. 2007 Dec;91(12):1717-8. No abstract available. PMID: 18024822 [PubMed - indexed for MEDLINE]Related articles

Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation.

Liskova P, Veraitch B, Jirsova K, Filipec M, Neuwirth A, Ebenezer ND, Hysi PG, Hardcastle AJ, Tuft SJ, Bhattacharya SS.

Br J Ophthalmol. 2008 Feb;92(2):265-7. Epub 2007 Oct 25.PMID: 17962390 [PubMed - indexed for MEDLINE]Related articles

Mutations in TOPORS cause autosomal dominant retinitis pigmentosa with perivascular retinal pigment epithelium atrophy.

Chakarova CF, Papaioannou MG, Khanna H, Lopez I, Waseem N, Shah A, Theis T, Friedman J, Maubaret C, Bujakowska K, Veraitch B, Abd El-Aziz MM, Prescott de Q, Parapuram SK, Bickmore WA, Munro PM, Gal A, Hamel CP, Marigo V, Ponting CP, Wissinger B, Zrenner E, Matter K, Swaroop A, Koenekoop RK, Bhattacharya SS.

Am J Hum Genet. 2007 Nov;81(5):1098-103. Epub 2007 Sep 26.PMID: 17924349 [PubMed - indexed for MEDLINE]Related articlesFree article

The Roles of PAX6 and SOX2 in Myopia: lessons from the 1958 British Birth Cohort.

Simpson CL, Hysi P, Bhattacharya SS, Hammond CJ, Webster A, Peckham CS, Sham PC, Rahi JS.

Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4421-5.PMID: 17898260 [PubMed - indexed for MEDLINE]Related articlesFree article

Genetic analysis of FAM46A in Spanish families with autosomal recessive retinitis pigmentosa: characterisation of novel VNTRs.

Barragán I, Borrego S, Abd El-Aziz MM, El-Ashry MF, Abu-Safieh L, Bhattacharya SS, Antiñolo G.

Ann Hum Genet. 2008 Jan;72(Pt 1):26-34. Epub 2007 Sep 5.PMID: 17803723 [PubMed - indexed for MEDLINE]Related articles

Study of p.N247S KERA mutation in a British family with cornea plana.

Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, Tuft SJ, Bhattacharya SS.

Mol Vis. 2007 Jul 27;13:1339-47.PMID: 17679937 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in splicing factor PRPF3, causing retinal degeneration, form detrimental aggregates in photoreceptor cells.

Comitato A, Spampanato C, Chakarova C, Sanges D, Bhattacharya SS, Marigo V.

Hum Mol Genet. 2007 Jul 15;16(14):1699-707. Epub 2007 May 20.PMID: 17517693 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy.

Liskova P, Tuft SJ, Gwilliam R, Ebenezer ND, Jirsova K, Prescott Q, Martincova R, Pretorius M, Sinclair N, Boase DL, Jeffrey MJ, Deloukas P, Hardcastle AJ, Filipec M, Bhattacharya SS.

Hum Mutat. 2007 Jun;28(6):638.PMID: 17437275 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN.

Hum Mutat. 2007 May;28(5):522-3.PMID: 17397048 [PubMed - indexed for MEDLINE]Related articles

A sudden rise in occurrence of Salmonella paratyphi a infection in Rourkela orissa.

Bhattacharya SS, Dash U.

Indian J Med Microbiol. 2007 Jan;25(1):78-9. No abstract available. PMID: 17377367 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosa.

Waseem NH, Vaclavik V, Webster A, Jenkins SA, Bird AC, Bhattacharya SS.

Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1330-4.PMID: 17325180 [PubMed - indexed for MEDLINE]Related articlesFree article

A clinical and molecular genetic study of Egyptian and Saudi Arabian patients with primary congenital glaucoma (PCG).

El-Ashry MF, Abd El-Aziz MM, Bhattacharya SS.

J Glaucoma. 2007 Jan;16(1):104-11.PMID: 17224759 [PubMed - indexed for MEDLINE]Related articles

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Friedman JS, Chang B, Kannabiran C, Chakarova C, Singh HP, Jalali S, Hawes NL, Branham K, Othman M, Filippova E, Thompson DA, Webster AR, Andréasson S, Jacobson SG, Bhattacharya SS, Heckenlively JR, Swaroop A.

Am J Hum Genet. 2006 Dec;79(6):1059-70. Epub 2006 Oct 23. Erratum in: Am J Hum Genet. 2007 Feb;80(2):388. PMID: 17186464 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel genetic study of Chinese families with autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, El-Ashry MF, Chan WM, Chong KL, Barragan I, Antiñolo G, Pang CP, Bhattacharya SS.

Ann Hum Genet. 2007 May;71(Pt 3):281-94. Epub 2006 Nov 29.PMID: 17156103 [PubMed - indexed for MEDLINE]Related articles

Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects.

Iannaccone A, Man D, Waseem N, Jennings BJ, Ganapathiraju M, Gallaher K, Reese E, Bhattacharya SS, Klein-Seetharaman J.

Vision Res. 2006 Dec;46(27):4556-67. Epub 2006 Oct 2.PMID: 17014888 [PubMed - indexed for MEDLINE]Related articles

Antibiogram, phage typing and biotyping of Salmonella Typhi and Salmonella Paratyphi A from Rourkela, Orissa.

Das U, Bhattacharya SS.

Indian J Med Res. 2006 Jul;124(1):109-11. No abstract available. PMID: 16926466 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular genetics of retinitis pigmentosa in two Romani (Gypsy) families.

Chakarova CF, Cherninkova S, Tournev I, Waseem N, Kaneva R, Jordanova A, Veraitch BK, Gill B, Colclough T, Nakova A, Oscar A, Mihaylova V, Nikolova-Hill A, Wright AF, Black GC, Ramsden S, Kremensky I, Bhattacharya SS.

Mol Vis. 2006 Aug 11;12:909-14.PMID: 16917484 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.

Addison PK, Berry V, Holden KR, Espinal D, Rivera B, Su H, Srivastava AK, Bhattacharya SS.

Mol Vis. 2006 Jul 20;12:791-5.PMID: 16885921 [PubMed - indexed for MEDLINE]Related articlesFree article

Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction.

Michaelides M, Jenkins SA, Brantley MA Jr, Andrews RM, Waseem N, Luong V, Gregory-Evans K, Bhattacharya SS, Fitzke FW, Webster AR.

Invest Ophthalmol Vis Sci. 2006 Jul;47(7):3085-97.PMID: 16799055 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.

Tschernutter M, Jenkins SA, Waseem NH, Saihan Z, Holder GE, Bird AC, Bhattacharya SS, Ali RR, Webster AR.

Br J Ophthalmol. 2006 Jun;90(6):718-23.PMID: 16714263 [PubMed - indexed for MEDLINE]Related articlesFree article

A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of disease.

Abu-Safieh L, Vithana EN, Mantel I, Holder GE, Pelosini L, Bird AC, Bhattacharya SS.

Mol Vis. 2006 Apr 18;12:384-8.PMID: 16636657 [PubMed - indexed for MEDLINE]Related articlesFree article

A study of the nuclear trafficking of the splicing factor protein PRPF31 linked to autosomal dominant retinitis pigmentosa (ADRP).

Wilkie SE, Morris KJ, Bhattacharya SS, Warren MJ, Hunt DM.

Biochim Biophys Acta. 2006 Mar;1762(3):304-11. Epub 2006 Jan 4.PMID: 16427773 [PubMed - indexed for MEDLINE]Related articles

A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract.

Arora A, Minogue PJ, Liu X, Reddy MA, Ainsworth JR, Bhattacharya SS, Webster AR, Hunt DM, Ebihara L, Moore AT, Beyer EC, Berthoud VM.

J Med Genet. 2006 Jan;43(1):e2.PMID: 16397066 [PubMed - indexed for MEDLINE]Related articlesFree article

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus.

Abd El-Aziz MM, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS.

Curr Eye Res. 2005 Dec;30(12):1081-7.PMID: 16354621 [PubMed - indexed for MEDLINE]Related articles

Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene.

Gwilliam R, Liskova P, Filipec M, Kmoch S, Jirsova K, Huckle EJ, Stables CL, Bhattacharya SS, Hardcastle AJ, Deloukas P, Ebenezer ND.

Invest Ophthalmol Vis Sci. 2005 Dec;46(12):4480-4.PMID: 16303937 [PubMed - indexed for MEDLINE]Related articlesFree article

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

Abd El-Aziz MM, Patel RJ, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS.

Ophthalmic Res. 2006;38(1):19-23. Epub 2005 Sep 23.PMID: 16192744 [PubMed - indexed for MEDLINE]Related articles

A new locus (RP31) for autosomal dominant retinitis pigmentosa maps to chromosome 9p.

Papaioannou M, Chakarova CF, Prescott DC, Waseem N, Theis T, Lopez I, Gill B, Koenekoop RK, Bhattacharya SS.

Hum Genet. 2005 Dec;118(3-4):501-3. Epub 2005 Sep 28.PMID: 16189705 [PubMed - indexed for MEDLINE]Related articles

A clinical and molecular genetic study of autosomal-dominant stromal corneal dystrophy in British population.

El-Ashry MF, Abd El-Aziz MM, Hardcastle AJ, Bhattacharya SS, Ebenezer ND.

Ophthalmic Res. 2005 Nov-Dec;37(6):310-7. Epub 2005 Aug 23.PMID: 16118514 [PubMed - indexed for MEDLINE]Related articles

Clinical features and course of patients with glaucoma with the E50K mutation in the optineurin gene.

Aung T, Rezaie T, Okada K, Viswanathan AC, Child AH, Brice G, Bhattacharya SS, Lehmann OJ, Sarfarazi M, Hitchings RA.

Invest Ophthalmol Vis Sci. 2005 Aug;46(8):2816-22.PMID: 16043855 [PubMed - indexed for MEDLINE]Related articlesFree article

Transformation of nitrogen during vermicomposting of fly ash.

Bhattacharya SS, Chattopadhyay GN.

Waste Manag Res. 2004 Dec;22(6):488-91.PMID: 15666451 [PubMed - indexed for MEDLINE]Related articles

Posterior polar cataract is the predominant consequence of a recurrent mutation in the PITX3 gene.

Addison PK, Berry V, Ionides AC, Francis PJ, Bhattacharya SS, Moore AT.

Br J Ophthalmol. 2005 Feb;89(2):138-41.PMID: 15665340 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophy.

El-Ashry MF, Abd El-Aziz MM, Shalaby O, Wilkins S, Poopalasundaram S, Cheetham M, Tuft SJ, Hardcastle AJ, Bhattacharya SS, Ebenezer ND.

Am J Ophthalmol. 2005 Jan;139(1):192-3.PMID: 15652851 [PubMed - indexed for MEDLINE]Related articles