Ganguly A - Search Results

1

Chromosome rearrangement with no apparent gene mutation in familial adenomatous polyposis and hepatocellular neoplasia.

de Chadarévian JP, Dunn S, Malatack JJ, Ganguly A, Blecker U, Punnett HH. de Chadarévian JP, et al. Among authors: ganguly a. Pediatr Dev Pathol. 2002 Jan-Feb;5(1):69-75. doi: 10.1007/s10024-001-0121-3. Pediatr Dev Pathol. 2002. PMID: 11815870

2

Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations.

Suchi M, MacMullen C, Thornton PS, Ganguly A, Stanley CA, Ruchelli ED. Suchi M, et al. Among authors: ganguly a. Pediatr Dev Pathol. 2003 Jul-Aug;6(4):322-33. doi: 10.1007/s10024-002-0026-9. Pediatr Dev Pathol. 2003. PMID: 14692646

3

TP53, BRCA1, and BRCA2 tumor suppressor genes are not commonly mutated in survivors of Hodgkin's disease with second primary neoplasms.

Nichols KE, Heath JA, Friedman D, Biegel JA, Ganguly A, Mauch P, Diller L. Nichols KE, et al. Among authors: ganguly a. J Clin Oncol. 2003 Dec 15;21(24):4505-9. doi: 10.1200/JCO.2003.12.042. J Clin Oncol. 2003. PMID: 14673037

4

Dominant form of congenital hyperinsulinism maps to HK1 region on 10q.

Pinney SE, Ganapathy K, Bradfield J, Stokes D, Sasson A, Mackiewicz K, Boodhansingh K, Hughes N, Becker S, Givler S, Macmullen C, Monos D, Ganguly A, Hakonarson H, Stanley CA. Pinney SE, et al. Among authors: ganguly a. Horm Res Paediatr. 2013;80(1):18-27. doi: 10.1159/000351943. Epub 2013 Jul 13. Horm Res Paediatr. 2013. PMID: 23859901 Free PMC article.

5

ACMG technical standards and guidelines for genetic testing for inherited colorectal cancer (Lynch syndrome, familial adenomatous polyposis, and MYH-associated polyposis).

Hegde M, Ferber M, Mao R, Samowitz W, Ganguly A; Working Group of the American College of Medical Genetics and Genomics (ACMG) Laboratory Quality Assurance Committee. Hegde M, et al. Among authors: ganguly a. Genet Med. 2014 Jan;16(1):101-16. doi: 10.1038/gim.2013.166. Epub 2013 Dec 5. Genet Med. 2014. PMID: 24310308 Free article.

6

Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene.

Nichols KE, Houseknecht MD, Godmilow L, Bunin G, Shields C, Meadows A, Ganguly A. Nichols KE, et al. Among authors: ganguly a. Hum Mutat. 2005 Jun;25(6):566-74. doi: 10.1002/humu.20184. Hum Mutat. 2005. PMID: 15884040

7

High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation.

Citron M, Godmilow L, Ganguly T, Ganguly A. Citron M, et al. Among authors: ganguly t, ganguly a. Hum Mutat. 2002 Oct;20(4):267-74. doi: 10.1002/humu.10119. Hum Mutat. 2002. PMID: 12325022

8

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. Bossler AD, et al. Among authors: ganguly a. Hum Mutat. 2006 Jul;27(7):667-75. doi: 10.1002/humu.20342. Hum Mutat. 2006. PMID: 16752392

9

Clinical and molecular characterization of a dominant form of congenital hyperinsulinism caused by a mutation in the high-affinity sulfonylurea receptor.

Thornton PS, MacMullen C, Ganguly A, Ruchelli E, Steinkrauss L, Crane A, Aguilar-Bryan L, Stanley CA. Thornton PS, et al. Among authors: ganguly a. Diabetes. 2003 Sep;52(9):2403-10. doi: 10.2337/diabetes.52.9.2403. Diabetes. 2003. PMID: 12941782

10

Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).

Mao R, Krautscheid P, Graham RP, Ganguly A, Shankar S, Ferber M, Hegde M; ACMG Laboratory Quality Assurance Committee. Mao R, et al. Among authors: ganguly a. Genet Med. 2021 Oct;23(10):1807-1817. doi: 10.1038/s41436-021-01207-9. Epub 2021 Jun 17. Genet Med. 2021. PMID: 34140662 Free article.

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