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Items: 36


Concealed Wolff-Parkinson-White Syndrome revealed by acute coronary syndrome.

de Castro RL Jr, de Alcantara Lima N, da Costa Lino DO, Bannon SF.

Ann Noninvasive Electrocardiol. 2019 Dec 19:e12735. doi: 10.1111/anec.12735. [Epub ahead of print]


Successful lenalidomide treatment in high risk myelodysplastic syndrome with germline DDX41 mutation.

Abou Dalle I, Kantarjian H, Bannon SA, Kanagal-Shamanna R, Routbort M, Patel KP, Hu S, Bhalla K, Garcia-Manero G, DiNardo CD.

Am J Hematol. 2020 Feb;95(2):227-229. doi: 10.1002/ajh.25610. Epub 2019 Aug 29. No abstract available.


Clinical applicability of proposed algorithm for identifying individuals at risk for hereditary hematologic malignancies.

Clifford M, Bannon S, Bednar EM, Czerwinski J, Davis J, Dunnington L, Shahrukh Hashmi S, DiNardo CD.

Leuk Lymphoma. 2019 Dec;60(12):3020-3027. doi: 10.1080/10428194.2019.1630618. Epub 2019 Jul 5.


Outcomes of disease-specific next-generation sequencing gene panel testing in adolescents and young adults with colorectal cancer.

Mork ME, Rodriguez A, Bannon SA, Lynch PM, Rodriguez-Bigas MA, Thirumurthi S, You YN, Vilar E.

Cancer Genet. 2019 Jun;235-236:77-83. doi: 10.1016/j.cancergen.2019.04.064. Epub 2019 Apr 26.


Takayasu arteritis with multiple coronary involvement and early graft relapse.

Macedo LM, Lima NA, de Castro Junior RL, Bannon SF.

BMJ Case Rep. 2019 Apr 30;12(4). pii: e229383. doi: 10.1136/bcr-2019-229383.


Pancreatic Cancer Early Detection and Interception in an Atypical Case of Peutz-Jeghers Syndrome.

Mork M, Quesada PR, Bannon S, Montiel MF, Fleming JB, Lynch PM, Bhutani MS, Lee JH, McAllister F.

Pancreas. 2019 Apr;48(4):e29-e30. doi: 10.1097/MPA.0000000000001293. No abstract available.


DDX41 mutations in myeloid neoplasms are associated with male gender, TP53 mutations and high-risk disease.

Quesada AE, Routbort MJ, DiNardo CD, Bueso-Ramos CE, Kanagal-Shamanna R, Khoury JD, Thakral B, Zuo Z, Yin CC, Loghavi S, Ok CY, Wang SA, Tang Z, Bannon SA, Benton CB, Garcia-Manero G, Kantarjian H, Luthra R, Medeiros LJ, Patel KP.

Am J Hematol. 2019 Jul;94(7):757-766. doi: 10.1002/ajh.25486. Epub 2019 May 7.


Hematologic malignancies and Li-Fraumeni syndrome.

Swaminathan M, Bannon SA, Routbort M, Naqvi K, Kadia TM, Takahashi K, Alvarado Y, Ravandi-Kashani F, Patel KP, Champlin R, Kantarjian H, Strong L, DiNardo CD.

Cold Spring Harb Mol Case Stud. 2019 Feb 1;5(1). pii: a003210. doi: 10.1101/mcs.a003210. Print 2019 Feb.


Myeloid malignancies with somatic GATA2 mutations can be associated with an immunodeficiency phenotype.

Alfayez M, Wang SA, Bannon SA, Kontoyiannis DP, Kornblau SM, Orange JS, Mace EM, DiNardo CD.

Leuk Lymphoma. 2019 Aug;60(8):2025-2033. doi: 10.1080/10428194.2018.1551535. Epub 2019 Jan 16.


High Prevalence of Hereditary Cancer Syndromes and Outcomes in Adults with Early-Onset Pancreatic Cancer.

Bannon SA, Montiel MF, Goldstein JB, Dong W, Mork ME, Borras E, Hasanov M, Varadhachary GR, Maitra A, Katz MH, Feng L, Futreal A, Fogelman DR, Vilar E, McAllister F.

Cancer Prev Res (Phila). 2018 Nov;11(11):679-686. doi: 10.1158/1940-6207.CAPR-18-0014. Epub 2018 Oct 1.


Demographic Patterns Associated With Compliance in Pain Contract Patients: A Residency Clinic Experience.

Aggarwal S, Papani R, Roumia M, Bannon S.

Mayo Clin Proc Innov Qual Outcomes. 2017 Dec 1;1(3):248-249. doi: 10.1016/j.mayocpiqo.2017.10.001. eCollection 2017 Dec. No abstract available.


Improving the detection of patients with inherited predispositions to hematologic malignancies using next-generation sequencing-based leukemia prognostication panels.

DiNardo CD, Routbort MJ, Bannon SA, Benton CB, Takahashi K, Kornblau SM, Luthra R, Kanagal-Shamanna R, Medeiros LJ, Garcia-Manero G, M Kantarjian H, Futreal PA, Meric-Bernstam F, Patel KP.

Cancer. 2018 Jul 1;124(13):2704-2713. doi: 10.1002/cncr.31331. Epub 2018 Apr 6. Review.


In Silico Systems Biology Analysis of Variants of Uncertain Significance in Lynch Syndrome Supports the Prioritization of Functional Molecular Validation.

Borras E, Chang K, Pande M, Cuddy A, Bosch JL, Bannon SA, Mork ME, Rodriguez-Bigas MA, Taggart MW, Lynch PM, You YN, Vilar E.

Cancer Prev Res (Phila). 2017 Oct;10(10):580-587. doi: 10.1158/1940-6207.CAPR-17-0058. Epub 2017 Aug 1.


Can Microsatellite Status of Colorectal Cancer Be Reliably Assessed after Neoadjuvant Therapy?

Goldstein JB, Wu W, Borras E, Masand G, Cuddy A, Mork ME, Bannon SA, Lynch PM, Rodriguez-Bigas M, Taggart MW, Wu J, Scheet P, Kopetz S, You YN, Vilar E.

Clin Cancer Res. 2017 Sep 1;23(17):5246-5254. doi: 10.1158/1078-0432.CCR-16-2994. Epub 2017 May 18.


Frequency of Germline BRCA1/2 Mutations in Unselected Patients With Colorectal Cancer.

Daniels MS, Bannon SA, Mork ME.

J Clin Oncol. 2017 Aug 1;35(22):2588. doi: 10.1200/JCO.2017.72.7222. Epub 2017 May 16. No abstract available.


Spectrum of mismatch repair gene mutations and clinical presentation of Hispanic individuals with Lynch syndrome.

Sunga AY, Ricker C, Espenschied CR, Castillo D, Melas M, Herzog J, Bannon S, Cruz-Correa M, Lynch P, Solomon I, Gruber SB, Weitzel JN.

Cancer Genet. 2017 Apr;212-213:1-7. doi: 10.1016/j.cancergen.2017.01.003. Epub 2017 Feb 9.


Identification of MSH2 inversion of exons 1-7 in clinical evaluation of families with suspected Lynch syndrome.

Mork ME, Rodriguez A, Taggart MW, Rodriguez-Bigas MA, Lynch PM, Bannon SA, You YN, Vilar E.

Fam Cancer. 2017 Jul;16(3):357-361. doi: 10.1007/s10689-016-9960-y.


Hyponatremic Seizures With Severe Tongue Contusion After Initial Use of Intranasal DDAVP.

Patri S, Agrawal Y, Bannon SF.

Am J Ther. 2017 May;24(3):e371-e372. doi: 10.1097/MJT.0000000000000487. No abstract available.


Hereditary Predispositions to Myelodysplastic Syndrome.

Bannon SA, DiNardo CD.

Int J Mol Sci. 2016 May 30;17(6). pii: E838. doi: 10.3390/ijms17060838. Review.


Evaluation of Patients and Families With Concern for Predispositions to Hematologic Malignancies Within the Hereditary Hematologic Malignancy Clinic (HHMC).

DiNardo CD, Bannon SA, Routbort M, Franklin A, Mork M, Armanios M, Mace EM, Orange JS, Jeff-Eke M, Churpek JE, Takahashi K, Jorgensen JL, Garcia-Manero G, Kornblau S, Bertuch A, Cheung H, Bhalla K, Futreal A, Godley LA, Patel KP.

Clin Lymphoma Myeloma Leuk. 2016 Jul;16(7):417-428.e2. doi: 10.1016/j.clml.2016.04.001. Epub 2016 Apr 27.


Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency.

Mork ME, Borras E, Taggart MW, Cuddy A, Bannon SA, You YN, Lynch PM, Ramirez PT, Rodriguez-Bigas MA, Vilar E.

Fam Cancer. 2016 Oct;15(4):587-91. doi: 10.1007/s10689-016-9902-8.


High Prevalence of Hereditary Cancer Syndromes in Adolescents and Young Adults With Colorectal Cancer.

Mork ME, You YN, Ying J, Bannon SA, Lynch PM, Rodriguez-Bigas MA, Vilar E.

J Clin Oncol. 2015 Nov 1;33(31):3544-9. doi: 10.1200/JCO.2015.61.4503. Epub 2015 Jul 20.


A Prospective Six Sigma Quality Improvement Trial to Optimize Universal Screening for Genetic Syndrome Among Patients With Young-Onset Colorectal Cancer.

Dineen S, Lynch PM, Rodriguez-Bigas MA, Bannon S, Taggart M, Reeves C, Modaro C, Overman M, Chang GJ, Skibber JM, You YN.

J Natl Compr Canc Netw. 2015 Jul;13(7):865-72.


Displacement of impella post chest compressions.

Aggarwal S, Bannon S.

Heart Views. 2014 Oct-Dec;15(4):127-8. doi: 10.4103/1995-705X.151090.


Weight-related abuse: Perceived emotional impact and the effect on disordered eating.

Salwen JK, Hymowitz GF, Bannon SM, O'Leary KD.

Child Abuse Negl. 2015 Jul;45:163-71. doi: 10.1016/j.chiabu.2014.12.005. Epub 2015 Jan 28. Erratum in: Child Abuse Negl. 2015 Dec;50:267.


Role of microsatellite instability-low as a diagnostic biomarker of Lynch syndrome in colorectal cancer.

Vilar E, Mork ME, Cuddy A, Borras E, Bannon SA, Taggart MW, Ying J, Broaddus RR, Luthra R, Rodriguez-Bigas MA, Lynch PM, You YQ.

Cancer Genet. 2014 Oct-Dec;207(10-12):495-502. doi: 10.1016/j.cancergen.2014.10.002. Epub 2014 Oct 13.



Aggarwal S, Bannon S.

J Glob Infect Dis. 2014 Jan;6(1):47-8. doi: 10.4103/0974-777X.127958. No abstract available.


Patient-reported disease knowledge and educational needs in Lynch syndrome: findings of an interactive multidisciplinary patient conference.

Bannon SA, Mork M, Vilar E, Peterson SK, Lu K, Lynch PM, Rodriguez-Bigas MA, You YN.

Hered Cancer Clin Pract. 2014 Feb 5;12(1):1. doi: 10.1186/1897-4287-12-1.


Comparison of attitudes regarding preimplantation genetic diagnosis among patients with hereditary cancer syndromes.

Rich TA, Liu M, Etzel CJ, Bannon SA, Mork ME, Ready K, Saraiya DS, Grubbs EG, Perrier ND, Lu KH, Arun BK, Woodard TL, Schover LR, Litton JK.

Fam Cancer. 2014 Jun;13(2):291-9. doi: 10.1007/s10689-013-9685-0.


Cancer spectrum in DNA mismatch repair gene mutation carriers: results from a hospital based Lynch syndrome registry.

Pande M, Wei C, Chen J, Amos CI, Lynch PM, Lu KH, Lucio LA, Boyd-Rogers SG, Bannon SA, Mork ME, Frazier ML.

Fam Cancer. 2012 Sep;11(3):441-7. doi: 10.1007/s10689-012-9534-6.


Processing impairments in OCD: it is more than inhibition!

Bannon S, Gonsalvez CJ, Croft RJ.

Behav Res Ther. 2008 Jun;46(6):689-700. doi: 10.1016/j.brat.2008.02.006. Epub 2008 Feb 29.


QT prolongation with methadone.

Dhamija R, Bannon S.

Indian J Crit Care Med. 2008 Jan;12(1):46-7. doi: 10.4103/0972-5229.40954. No abstract available.


Executive functions in obsessive-compulsive disorder: state or trait deficits?

Bannon S, Gonsalvez CJ, Croft RJ, Boyce PM.

Aust N Z J Psychiatry. 2006 Nov-Dec;40(11-12):1031-8.


Response inhibition deficits in obsessive-compulsive disorder.

Bannon S, Gonsalvez CJ, Croft RJ, Boyce PM.

Psychiatry Res. 2002 Jun 1;110(2):165-74.


Needs analysis of a cancer education program in south western Sydney.

Patterson P, Moylan E, Bannon S, Salih F.

Cancer Nurs. 2000 Jun;23(3):186-92.


The normal diameter of the fetal aorta and pulmonary artery: echocardiographic evaluation in utero.

Cartier MS, Davidoff A, Warneke LA, Hirsh MP, Bannon S, Sutton MS, Doubilet PM.

AJR Am J Roentgenol. 1987 Nov;149(5):1003-7.


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