Dyer L - Search Results

1

Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients.

Lesmana H, Dyer L, Li X, Denton J, Griffiths J, Chonat S, Seu KG, Heeney MM, Zhang K, Hopkin RJ, Kalfa TA. Lesmana H, et al. Among authors: dyer l. Hum Mutat. 2018 Mar;39(3):389-393. doi: 10.1002/humu.23392. Epub 2018 Jan 11. Hum Mutat. 2018. PMID: 29288557 Free PMC article.

2

Confirmatory testing illustrates additional risks for structural sex chromosome abnormalities in fetuses with a non-invasive prenatal screen positive for monosomy X.

Sund KL, Khattar D, Boomer T, Caldwell S, Dyer L, Hopkin RJ, Smolarek TA. Sund KL, et al. Among authors: dyer l. Am J Med Genet C Semin Med Genet. 2020 Jun;184(2):294-301. doi: 10.1002/ajmg.c.31783. Epub 2020 Jun 1. Am J Med Genet C Semin Med Genet. 2020. PMID: 32476283

3

A rare case of postnatal mosaic trisomy 12 with severe congenital heart disease and literature review.

Hu X, Ayala SS, Dyer L, Guan Q, Pena L. Hu X, et al. Among authors: dyer l. Am J Med Genet A. 2021 Jun;185(6):1864-1869. doi: 10.1002/ajmg.a.62166. Epub 2021 Mar 24. Am J Med Genet A. 2021. PMID: 33759348

4

Genetic Testing in Patients with Neurodevelopmental Disorders: Experience of 511 Patients at Cincinnati Children's Hospital Medical Center.

Du X, Glass JE, Balow S, Dyer LM, Rathbun PA, Guan Q, Liu J, Wu Y, Dawson DB, Walters-Sen L, Smolarek TA, Zhang W. Du X, et al. Among authors: dyer lm. J Autism Dev Disord. 2022 Nov;52(11):4828-4842. doi: 10.1007/s10803-021-05337-6. Epub 2021 Nov 13. J Autism Dev Disord. 2022. PMID: 34773222 Free PMC article.

5

3q29 microduplication syndrome: Clinical and molecular description of eleven new cases.

Coyan AG, Dyer LM. Coyan AG, et al. Eur J Med Genet. 2020 Dec;63(12):104083. doi: 10.1016/j.ejmg.2020.104083. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33039685 Review.

6

Assessing Genomic Copy Number Alterations as Best Practice for Renal Cell Neoplasia: An Evidence-Based Review from the Cancer Genomics Consortium Workgroup.

Liu YJ, Houldsworth J, Emmadi R, Dyer L, Wolff DJ. Liu YJ, et al. Among authors: dyer l. Cancer Genet. 2020 Jun;244:40-54. doi: 10.1016/j.cancergen.2020.04.004. Epub 2020 May 1. Cancer Genet. 2020. PMID: 32434132 Review.

7

The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing.

Cajaiba MM, Dyer LM, Geller JI, Jennings LJ, George D, Kirschmann D, Rohan SM, Cost NG, Khanna G, Mullen EA, Dome JS, Fernandez CV, Perlman EJ. Cajaiba MM, et al. Cancer. 2018 Aug;124(16):3381-3389. doi: 10.1002/cncr.31578. Epub 2018 Jun 15. Cancer. 2018. PMID: 29905933 Free PMC article.

8

Diffuse Intrinsic Pontine Glioma Cells Are Vulnerable to Mitotic Abnormalities Associated with BMI-1 Modulation.

Senthil Kumar S, Sengupta S, Zhu X, Mishra DK, Phoenix T, Dyer L, Fuller C, Stevenson CB, DeWire M, Fouladi M, Drissi R. Senthil Kumar S, et al. Among authors: dyer l. Mol Cancer Res. 2020 Nov;18(11):1711-1723. doi: 10.1158/1541-7786.MCR-20-0099. Epub 2020 Aug 14. Mol Cancer Res. 2020. PMID: 32801164

9

Placental Histomorphology in a Case of Double Trisomy 48,XXX,+18.

Shah SI, Dyer L, Stanek J. Shah SI, et al. Among authors: dyer l. Case Rep Pathol. 2018 Mar 8;2018:2839765. doi: 10.1155/2018/2839765. eCollection 2018. Case Rep Pathol. 2018. PMID: 29707399 Free PMC article.

10

ATM is required for SOD2 expression and homeostasis within the mammary gland.

Dyer LM, Kepple JD, Ai L, Kim WJ, Stanton VL, Reinhard MK, Backman LRF, Streitfeld WS, Babu NR, Treiber N, Scharffetter-Kochanek K, McKinnon PJ, Brown KD. Dyer LM, et al. Breast Cancer Res Treat. 2017 Dec;166(3):725-741. doi: 10.1007/s10549-017-4424-0. Epub 2017 Aug 28. Breast Cancer Res Treat. 2017. PMID: 28849346 Free PMC article.

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