Publications

Enhanced Sensitivity for Detection of Low-level Germline Mosaic RB1 Mutations in Sporadic Retinoblastoma Cases Using Deep Semi–conductor Sequencing. Chen Z, Moran K, Richards–Yutz J, Toorens E, Gerhart D, Ganguly T, Shields CL, Ganguly A. Hum Mutat. 2013 Nov 26. doi: 10.1002/humu.22488.

Molecular Karyotyping for Detection of Prognostic Markers in Fine Needle Aspiration Biopsy Samples of Uveal Melanoma. Arupa Ganguly, Jennifer Richards–Yutz, Kathryn G. Ewens. Methods Mol Biol. 2014;1102:441–58. doi: 10.1007/978–1–62703–727–3_23.

Genomic profile of 320 uveal melanoma cases: chromosome 8p–loss and metastatic outcome. Ewens KG, Kanetsky PA, Richards–Yutz J, Al–Dahmash S, De Luca MC, Bianciotto CG, Shields CL, Ganguly A. Invest Ophthalmol Vis Sci. 2013 Aug 23;54(8):5721–9. doi: 10.1167/iovs.13–12195.

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. Snider KE, Becker S, Boyajian L, Shyng SL, MacMullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A. J Clin Endocrinol Metab. 2013 Feb;98(2):E355–63. doi: 10.1210/jc.2012–2169.

Parental nutrient intake and risk of retinoblastoma resulting from new germline RB1 mutation. Bunin GR, Li Y, Ganguly A, Meadows AT, Tseng M. Cancer Causes Control. 2013 Feb;24(2):343–55. doi: 10.1007/s10552–012–0120–x

Uveal melanoma trapped in the temple of doom. Shields CL, Ganguly A, O'Brien J, Sato T, Shields JA. Am J Ophthalmol. 2012 Aug;154(2):219–21. doi: 10.1016/j.ajo.2012.03.009.

Cytogenetic testing of iris melanoma using fine needle aspiration biopsy in 17 patients. Shields CL, Ramasubramanian A, Ganguly A, Mohan D, Shields JA. Retina. 2011 Mar;31(3):574–80. doi: 10.1097/IAE.0b013e3181f57e62.

Prognosis of uveal melanoma in 500 cases using genetic testing of fine–needle aspiration biopsy specimens. Shields CL, Ganguly A, Bianciotto CG, Turaka K, Tavallali A, Shields JA. Ophthalmology. 2011 Feb;118(2):396–401. doi: 10.1016/j.ophtha.2010.05.023.

Differential gene expression profile of retinoblastoma compared to normal retina. Ganguly A, Shields CL. Mol Vis. 2010 Jul 13;16:1292–303.

Medical radiation exposure and risk of retinoblastoma resulting from new germline RB1 mutation. Bunin GR, Felice MA, Davidson W, Friedman DL, Shields CL, Maidment A, O'Shea M, Nichols KE, Leahey A, Dunkel IJ, Jubran R, Rodriguez–Galindo C, Schmidt ML, Weinstein JL, Goldman S, Abramson DH, Wilson MW, Gallie BL, Chan HS, Shapiro M, Cnaan A, Ganguly A, Meadows AT. Int J Cancer. 2011 May 15;128(10):2393–404. doi: 10.1002/ijc.25565.

Update on molecular diagnosis of hereditary hemorrhagic telangiectasia. Richards–Yutz J, Grant K, Chao EC, Walther SE, Ganguly A. Hum Genet. 2010 Jul;128(1):61–77. doi: 10.1007/s00439–010–0825–4.

Recent advances in retinoblastoma genetic research. Nichols KE, Walther S, Chao E, Shields C, Ganguly A. Curr Opin Ophthalmol. 2009 Sep;20(5):351–5. doi: 10.1097/ICU.0b013e32832f7f25.

Molecular karyotype of sporadic unilateral retinoblastoma tumors. Ganguly A, Nichols KE, Grant G, Rappaport E, Shields C. Retina. 2009 Jul–Aug;29(7):1002–12. doi: 10.1097/IAE.0b013e3181a0be05.

Regression of uveal melanoma after plaque radiotherapy and thermotherapy based on chromosome 3 status. Shields CL, Bianciotto C, Rudich D, Materin MA, Ganguly A, Shields JA. Retina. 2008 Oct;28(9):1289–95. doi: 10.1097/IAE.0b013e31817f7b3e.

Altered chromosome expression of uveal melanoma in the setting of melanocytosis. Horgan N, Shields CL, Swanson L, Teixeira LF, Eagle RC Jr, Ganguly A, Shields JA. Acta Ophthalmol. 2009 Aug;87(5):578–80. doi: 10.1111/j.1755–3768.2008.01235.x.

Early diagnosis of fibrodysplasia ossificans progressiva. Kaplan FS, Xu M, Glaser DL, Collins F, Connor M, Kitterman J, Sillence D, Zackai E, Ravitsky V, Zasloff M, Ganguly A, Shore EM. Pediatrics. 2008 May;121(5):e1295–300. doi: 10.1542/peds.2007–1980.

Chromosome 3 analysis of uveal melanoma using fine–needle aspiration biopsy at the time of plaque radiotherapy in 140 consecutive cases. Shields CL, Ganguly A, Materin MA, Teixeira L, Mashayekhi A, Swanson LA, Marr BP, Shields JA. Trans Am Ophthalmol Soc. 2007;105:43–52; discussion 52–3.

Role of cytogenetics in management of uveal melanoma. Shields JA, Shields CL, Materin M, Sato T, Ganguly A. Arch Ophthalmol. 2008 Mar;126(3):416–9. doi: 10.1001/archopht.126.3.416.

Chromosome 3 analysis of uveal melanoma using fine–needle aspiration biopsy at the time of plaque radiotherapy in 140 consecutive cases: the Deborah Iverson, MD, Lectureship. Shields CL, Ganguly A, Materin MA, Teixeira L, Mashayekhi A, Swanson LA, Marr BP, Shields JA. Arch Ophthalmol. 2007 Aug;125(8):1017–24. Small choroidal melanoma with chromosome 3 monosomy on fine–needle aspiration biopsy. Shields CL, Materin MA, Teixeira L, Mashayekhi A, Ganguly A, Shields JA. Ophthalmology. 2007 Oct;114(10):1919–24.

Human embryonic and neuronal stem cell markers in retinoblastoma. Seigel GM, Hackam AS, Ganguly A, Mandell LM, Gonzalez–Fernandez F. Mol Vis. 2007 Jun 8;13:823–32.

Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP–sensitive K+ channels: identification and rescue. Yan FF, Lin YW, MacMullen C, Ganguly A, Stanley CA, Shyng SL. Diabetes. 2007 Sep;56(9):2339–48.

Prenatal diagnosis and postnatal management of diffuse congenital hyperinsulinism: a case report. Peranteau WH, Ganguly A, Steinmuller L, Thornton P, Johnson MP, Howell LJ, Stanley CA, Adzick NS. Fetal Diagn Ther. 2006;21(6):515–8. Epub 2006 Sep 12.

Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype. Bossler AD, Richards J, George C, Godmilow L, Ganguly A. Hum Mutat. 2006 Jul;27(7):667–75.

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