Chintagumpala MM - Search Results

1

Circulating tumor DNA sequencing of pediatric solid and brain tumor patients: An institutional feasibility study.

Mangum R, Reuther J, Sen Baksi K, Gandhi I, Zabriskie RC, Recinos A, Raesz-Martinez R, Lin FY, Potter SL, Sher AC, Kralik SF, Mohila CA, Chintagumpala MM, Muzny D, Hu J, Gibbs RA, Fisher KE, Bernini JC, Gill J, Griffin TC, Tomlinson GE, Vallance KL, Plon SE, Roy A, Parsons DW. Mangum R, et al. Among authors: chintagumpala mm. Pediatr Hematol Oncol. 2023;40(8):719-738. doi: 10.1080/08880018.2023.2228837. Epub 2023 Jun 27. Pediatr Hematol Oncol. 2023. PMID: 37366551 Free PMC article.

2

Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer.

Airewele GE, Sigurdson AJ, Wiley KJ, Frieden BE, Caldarera LW, Riccardi VM, Lewis RA, Chintagumpala MM, Ater JL, Plon SE, Bondy ML. Airewele GE, et al. Among authors: chintagumpala mm. Genet Epidemiol. 2001 Jan;20(1):75-86. doi: 10.1002/1098-2272(200101)20:1<75::AID-GEPI7>3.0.CO;2-Z. Genet Epidemiol. 2001. PMID: 11119298

3

Clinical manifestations in a cohort of 41 Rothmund-Thomson syndrome patients.

Wang LL, Levy ML, Lewis RA, Chintagumpala MM, Lev D, Rogers M, Plon SE. Wang LL, et al. Among authors: chintagumpala mm. Am J Med Genet. 2001 Jul 22;102(1):11-7. doi: 10.1002/1096-8628(20010722)102:1<11::aid-ajmg1413>3.0.co;2-a. Am J Med Genet. 2001. PMID: 11471165

4

Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome.

Wang LL, Worley K, Gannavarapu A, Chintagumpala MM, Levy ML, Plon SE. Wang LL, et al. Among authors: chintagumpala mm. Am J Hum Genet. 2002 Jul;71(1):165-7. doi: 10.1086/341234. Epub 2002 May 9. Am J Hum Genet. 2002. PMID: 12016592 Free PMC article.

5

Association between osteosarcoma and deleterious mutations in the RECQL4 gene in Rothmund-Thomson syndrome.

Wang LL, Gannavarapu A, Kozinetz CA, Levy ML, Lewis RA, Chintagumpala MM, Ruiz-Maldanado R, Contreras-Ruiz J, Cunniff C, Erickson RP, Lev D, Rogers M, Zackai EH, Plon SE. Wang LL, et al. Among authors: chintagumpala mm. J Natl Cancer Inst. 2003 May 7;95(9):669-74. doi: 10.1093/jnci/95.9.669. J Natl Cancer Inst. 2003. PMID: 12734318

6

Outcomes of systematic screening for optic pathway tumors in children with Neurofibromatosis Type 1.

Blazo MA, Lewis RA, Chintagumpala MM, Frazier M, McCluggage C, Plon SE. Blazo MA, et al. Among authors: chintagumpala mm. Am J Med Genet A. 2004 Jun 15;127A(3):224-9. doi: 10.1002/ajmg.a.20650. Am J Med Genet A. 2004. PMID: 15150770

7

A homozygous mutation in MSH6 causes Turcot syndrome.

Hegde MR, Chong B, Blazo ME, Chin LH, Ward PA, Chintagumpala MM, Kim JY, Plon SE, Richards CS. Hegde MR, et al. Among authors: chintagumpala mm. Clin Cancer Res. 2005 Jul 1;11(13):4689-93. doi: 10.1158/1078-0432.CCR-04-2025. Clin Cancer Res. 2005. PMID: 16000562

8

Retinoblastoma: review of current management.

Chintagumpala M, Chevez-Barrios P, Paysse EA, Plon SE, Hurwitz R. Chintagumpala M, et al. Oncologist. 2007 Oct;12(10):1237-46. doi: 10.1634/theoncologist.12-10-1237. Oncologist. 2007. PMID: 17962617 Free article. Review.

9

Outcomes of integrating genetics in management of patients with retinoblastoma.

Dhar SU, Chintagumpala M, Noll C, Chévez-Barrios P, Paysse EA, Plon SE. Dhar SU, et al. Arch Ophthalmol. 2011 Nov;129(11):1428-34. doi: 10.1001/archophthalmol.2011.292. Arch Ophthalmol. 2011. PMID: 22084214

10

Maternal variation in EPHX1, a xenobiotic metabolism gene, is associated with childhood medulloblastoma: an exploratory case-parent triad study.

Lupo PJ, Nousome D, Okcu MF, Chintagumpala M, Scheurer ME. Lupo PJ, et al. Pediatr Hematol Oncol. 2012 Nov;29(8):679-85. doi: 10.3109/08880018.2012.722747. Epub 2012 Sep 20. Pediatr Hematol Oncol. 2012. PMID: 22994552 Free PMC article. Clinical Trial.

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