Widmeyer K - Search Results

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RMND1 and PLN variants are the underlying cause of Perrault-like syndrome and cardiac anomalies in a patient.

Du X, Barnett CL, Widmeyer KM, Wang X, Brightman DS, Noonan CW, Weaver KN, Hopkin RJ, Wu Y. Du X, et al. Among authors: widmeyer km. Clin Case Rep. 2024 Oct 31;12(11):e9537. doi: 10.1002/ccr3.9537. eCollection 2024 Nov. Clin Case Rep. 2024. PMID: 39493792 Free PMC article.

14q22.3 duplication including OTX2 in a girl with medulloblastoma: A case report with literature review.

Blake C, Widmeyer K, DAquila K, Mochizuki A, Smolarek TA, Pillay-Smiley N, Kim SY. Blake C, et al. Among authors: widmeyer k. Am J Med Genet A. 2024 Jul;194(7):e63604. doi: 10.1002/ajmg.a.63604. Epub 2024 Mar 21. Am J Med Genet A. 2024. PMID: 38511879 Review.

Preparedness and training of genetic counselors practicing in inpatient settings.

Mancl N, Myers MF, Miller EM, Jackson F, Widmeyer K. Mancl N, et al. Among authors: widmeyer k. J Genet Couns. 2024 Jun;33(3):539-553. doi: 10.1002/jgc4.1754. Epub 2023 Aug 1. J Genet Couns. 2024. PMID: 37528675

Factors that influence the management recommendations breast surgeons provide to women with pathogenic variants in moderate penetrance breast cancer susceptibility genes.

Vanderwal A, Lewis J, Basil J, Atzinger C, Widmeyer K. Vanderwal A, et al. Among authors: widmeyer k. J Genet Couns. 2023 Jun;32(3):674-684. doi: 10.1002/jgc4.1674. Epub 2023 Jan 15. J Genet Couns. 2023. PMID: 36642783

Factors that impact risk management decisions among women with pathogenic variants in moderate penetrance genes associated with hereditary breast cancer.

Napoli M, Lewis J, Hopper J, Widmeyer K. Napoli M, et al. Among authors: widmeyer k. J Genet Couns. 2020 Dec;29(6):960-970. doi: 10.1002/jgc4.1220. Epub 2020 Feb 3. J Genet Couns. 2020. PMID: 32012395

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