Feurstein S - Search Results

1

Functional genomics for curation of variants in telomere biology disorder associated genes: A systematic review.

Nelson N, Feurstein S, Niaz A, Truong J, Holien JK, Lucas S, Fairfax K, Dickinson J, Bryan TM. Nelson N, et al. Among authors: feurstein s. Genet Med. 2023 Mar;25(3):100354. doi: 10.1016/j.gim.2022.11.021. Epub 2022 Dec 7. Genet Med. 2023. PMID: 36496180 Free article. Review.

2

How I diagnose and manage individuals at risk for inherited myeloid malignancies.

University of Chicago Hematopoietic Malignancies Cancer Risk Team. University of Chicago Hematopoietic Malignancies Cancer Risk Team. Blood. 2016 Oct 6;128(14):1800-1813. doi: 10.1182/blood-2016-05-670240. Epub 2016 Jul 28. Blood. 2016. PMID: 27471235 Free PMC article.

3

Genetic predisposition to leukemia and other hematologic malignancies.

Feurstein S, Drazer MW, Godley LA. Feurstein S, et al. Semin Oncol. 2016 Oct;43(5):598-608. doi: 10.1053/j.seminoncol.2016.10.003. Epub 2016 Oct 25. Semin Oncol. 2016. PMID: 27899193 Review.

4

Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q Deletion.

Feurstein S, Thomay K, Hofmann W, Buesche G, Kreipe H, Thol F, Heuser M, Ganser A, Schlegelberger B, Göhring G. Feurstein S, et al. Int J Mol Sci. 2018 Oct 21;19(10):3269. doi: 10.3390/ijms19103269. Int J Mol Sci. 2018. PMID: 30347879 Free PMC article.

5

Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotype.

Feurstein S, Rücker FG, Bullinger L, Hofmann W, Manukjan G, Göhring G, Lehmann U, Heuser M, Ganser A, Döhner K, Schlegelberger B, Steinemann D. Feurstein S, et al. BMC Genomics. 2014 Sep 11;15(1):784. doi: 10.1186/1471-2164-15-784. BMC Genomics. 2014. PMID: 25213837 Free PMC article.

6

Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.

Praulich I, Tauscher M, Göhring G, Glaser S, Hofmann W, Feurstein S, Flotho C, Lichter P, Niemeyer CM, Schlegelberger B, Steinemann D. Praulich I, et al. Among authors: feurstein s. Genes Chromosomes Cancer. 2010 Oct;49(10):885-900. doi: 10.1002/gcc.20797. Genes Chromosomes Cancer. 2010. PMID: 20589934

7

Accurate germline RUNX1 variant interpretation and its clinical significance.

Feurstein S, Zhang L, DiNardo CD. Feurstein S, et al. Blood Adv. 2020 Dec 22;4(24):6199-6203. doi: 10.1182/bloodadvances.2020003304. Blood Adv. 2020. PMID: 33351114 Free PMC article. No abstract available.

8

A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias.

Feurstein S, Hahn CN, Mehta N, Godley LA. Feurstein S, et al. Genet Med. 2022 Apr;24(4):931-954. doi: 10.1016/j.gim.2021.12.008. Epub 2022 Jan 19. Genet Med. 2022. PMID: 35063349 Free article.

9

Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations.

Feurstein S, Adegunsoye A, Mojsilovic D, Vij R, West DePersia AH, Rajagopal PS, Osman A, Collins RH, Kim RH, Gore SD, Greenberg P, Godley LA, Li Z, Del Gaudio D, Subramanian HP, Das S, Walsh T, Gulsuner S, Segal JP, Husain AN, Gurbuxani S, King MC, Strek ME, Churpek JE. Feurstein S, et al. Blood Adv. 2020 Oct 13;4(19):4873-4886. doi: 10.1182/bloodadvances.2020001721. Blood Adv. 2020. PMID: 33035329 Free PMC article.

10

Revision of RUNX1 variant curation rules.

Feurstein S, Luo X, Shah M, Walker T, Mehta N, Wu D, Godley LA. Feurstein S, et al. Blood Adv. 2022 Aug 23;6(16):4726-4730. doi: 10.1182/bloodadvances.2022008017. Blood Adv. 2022. PMID: 35764482 Free PMC article. No abstract available.

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