Betts DR - Search Results

1

Early Bilateral Gonadoblastoma in a Young Child with Mosaicism for Turner Syndrome and Trisomy 18 with Y Chromosome.

MacMahon JM, O'Sullivan MJ, McDermott M, Quinn F, Morris T, Green AJ, Betts DR, O'Connell SM. MacMahon JM, et al. Among authors: betts dr. Horm Res Paediatr. 2017;87(2):130-135. doi: 10.1159/000448172. Epub 2016 Sep 10. Horm Res Paediatr. 2017. PMID: 27614983

2

Ectomesenchymoma with t(1;12)(p32;p13) evolving from embryonal rhabdomyosarcoma shows no rearrangement of ETV6.

Howley S, Stack D, Morris T, McDermott M, Capra M, Betts D, O'Sullivan MJ. Howley S, et al. Hum Pathol. 2012 Feb;43(2):299-302. doi: 10.1016/j.humpath.2011.03.010. Epub 2011 Jul 30. Hum Pathol. 2012. PMID: 21803398

3

High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcoma.

Lynn M, Wang Y, Slater J, Shah N, Conroy J, Ennis S, Morris T, Betts DR, Fletcher JA, O'Sullivan MJ. Lynn M, et al. Among authors: betts dr. Diagn Mol Pathol. 2013 Jun;22(2):76-84. doi: 10.1097/PDM.0b013e31827a47f9. Diagn Mol Pathol. 2013. PMID: 23628818

4

A study of alveolar rhabdomyosarcoma copy number alterations by single nucleotide polymorphism analysis.

Lynn M, Shah N, Conroy J, Ennis S, Morris T, Betts D, O'Sullivan M. Lynn M, et al. Appl Immunohistochem Mol Morphol. 2014 Mar;22(3):213-21. doi: 10.1097/PDM.0000000000000030. Appl Immunohistochem Mol Morphol. 2014. PMID: 24614150

5

Rhabdomyosarcoma-associated renal cell carcinoma: a link with constitutional Tp53 mutation.

Curry S, Ibrahim F, Grehan D, McDermott M, Capra M, Betts D, O'Sullivan M. Curry S, et al. Pediatr Dev Pathol. 2011 May-Jun;14(3):248-51. doi: 10.2350/10-07-0871-CR.1. Epub 2010 Nov 5. Pediatr Dev Pathol. 2011. PMID: 21054160

6

Congenital sacrococcygeal PNET and chemotherapy.

Hawkes CP, Betts DR, O'Brien J, O'Sullivan MJ, Capra M. Hawkes CP, et al. Among authors: betts dr. Indian J Med Paediatr Oncol. 2012 Jul;33(3):182-4. doi: 10.4103/0971-5851.103151. Indian J Med Paediatr Oncol. 2012. PMID: 23248428 Free PMC article.

7

Ongoing excellent outcomes with reduced toxicities following integration of molecular targeted therapies in pediatric anaplastic large cell lymphoma.

McCarthy P, Harford J, O'Marcaigh A, Malone A, Evans P, Sills A, Storey L, Rooney S, Betts D, O'Sullivan MJ, McDermott M, Bond J, Trinquand A, Smith OP. McCarthy P, et al. Leuk Lymphoma. 2021 Aug;62(8):1995-1999. doi: 10.1080/10428194.2021.1894644. Epub 2021 Mar 8. Leuk Lymphoma. 2021. PMID: 33685326 No abstract available.

8

Nicolaides-Baraitser syndrome in a patient with hypertrophic cardiomyopathy and SMARCA2 gene deletion.

Foley R, Duignan S, McArdle L, Betts DR, Green A, McMahon CJ. Foley R, et al. Among authors: betts dr. Cardiol Young. 2022 May;32(5):821-823. doi: 10.1017/S1047951121003826. Epub 2021 Sep 15. Cardiol Young. 2022. PMID: 34521483

9

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.

Al Shehhi M, Forman EB, Fitzgerald JE, McInerney V, Krawczyk J, Shen S, Betts DR, Ardle LM, Gorman KM, King MD, Green A, Gallagher L, Lynch SA. Al Shehhi M, et al. Among authors: betts dr. Eur J Med Genet. 2019 Mar;62(3):204-209. doi: 10.1016/j.ejmg.2018.07.015. Epub 2018 Jul 18. Eur J Med Genet. 2019. PMID: 30031152

10

Epidemiology of chromosomal trisomies in the East of Ireland.

McDonnell R, Monteith C, Kennelly M, Martin A, Betts D, Delany V, Lynch SA, Coulter-Smith S, Sheehan S, Mahony R. McDonnell R, et al. J Public Health (Oxf). 2017 Dec 1;39(4):e145-e151. doi: 10.1093/pubmed/fdw087. J Public Health (Oxf). 2017. PMID: 27591300

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