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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 1
1999 1
2001 1
2003 2
2004 2
2005 1
2006 1
2007 2
2009 2
2010 2
2011 1
2012 2
2013 1
2014 4
2015 3
2016 3
2017 3
2018 2
2019 3
2020 4
2021 2
2022 1
2023 5
2024 0

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43 results

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Page 1
Polyethylene Glycol 20k. Does It Fluoresce?
Laatsch BF, Brandt M, Finke B, Fossum CJ, Wackett MJ, Lowater HR, Narkiewicz-Jodko A, Le CN, Yang T, Glogowski EM, Bailey-Hartsel SC, Bhattacharyya S, Hati S. Laatsch BF, et al. Among authors: glogowski em. ACS Omega. 2023 Apr 6;8(15):14208-14218. doi: 10.1021/acsomega.3c01124. eCollection 2023 Apr 18. ACS Omega. 2023. PMID: 37180871 Free PMC article.
A model for the return and referral of all clinically significant secondary findings of genomic sequencing.
Kodida R, Reble E, Clausen M, Shickh S, Mighton C, Sam J, Forster N, Panchal S, Aronson M, Semotiuk K, Graham T, Silberman Y, Randall Armel S, McCuaig JM, Cohn I, Morel CF, Elser C, Eisen A, Carroll JC, Glogowski E, Schrader KA, Di Gioacchino V, Lerner-Ellis J, Kim RH, Bombard Y; Incidental Genomics Study Team. Kodida R, et al. Among authors: glogowski e. J Med Genet. 2023 Aug;60(8):733-739. doi: 10.1136/jmg-2022-109091. Epub 2023 May 22. J Med Genet. 2023. PMID: 37217257 Review.
Great expectations: patients' preferences for clinically significant results from genomic sequencing.
Shickh S, Sebastian A, Clausen M, Mighton C, Elser C, Eisen A, Waldman L, Panchal S, Ward T, Carroll JC, Glogowski E, Schrader KA, Lerner-Ellis J, Kim RH, Thorpe KE, Bombard Y; Incidental Genomics Team members to be indexed in PubMed. Shickh S, et al. Among authors: glogowski e. Hum Genet. 2023 Apr;142(4):553-562. doi: 10.1007/s00439-023-02543-3. Epub 2023 Mar 21. Hum Genet. 2023. PMID: 36943453
PARC report: a perspective on the state of clinical pharmacogenomics testing.
Eichmeyer J, Rogers S, Formea CM, Giri J, Jones JS, Schnettler E, Schmidlen T, Glogowski E, Kurz RN. Eichmeyer J, et al. Among authors: glogowski e. Pharmacogenomics. 2020 Jul;21(11):809-820. doi: 10.2217/pgs-2019-0193. Epub 2020 Jul 8. Pharmacogenomics. 2020. PMID: 32635876 Review.
A636P testing in Ashkenazi Jews.
Guillem JG, Moore HG, Palmer C, Glogowski E, Finch R, Nafa K, Markowitz AJ, Offit K, Ellis NA. Guillem JG, et al. Among authors: glogowski e. Fam Cancer. 2004;3(3-4):223-7. doi: 10.1007/s10689-004-0899-z. Fam Cancer. 2004. PMID: 15516845 Review.
"I don't need any more unknowns hanging over my head": Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing.
Shickh S, Mighton C, Clausen M, Kodida R, Adi-Wauran E, Hirjikaka D, Krishnapillai S, Reble E, Sam J, Baxter NN, Laupacis A, Bombard Y; Incidental Genomics Study Team. Shickh S, et al. Genet Med. 2023 Dec;25(12):100960. doi: 10.1016/j.gim.2023.100960. Epub 2023 Aug 11. Genet Med. 2023. PMID: 37577963
Clinical correlation and molecular evaluation confirm that the MLH1 p.Arg182Gly (c.544A>G) mutation is pathogenic and causes Lynch syndrome.
Farrell MP, Hughes DJ, Berry IR, Gallagher DJ, Glogowski EA, Payne SJ, Kennedy MJ, Clarke RM, White SA, Muldoon CB, Macdonald F, Rehal P, Crompton D, Roring S, Duke ST, McDevitt T, Barton DE, Hodgson SV, Green AJ, Daly PA. Farrell MP, et al. Among authors: glogowski ea. Fam Cancer. 2012 Sep;11(3):509-18. doi: 10.1007/s10689-012-9544-4. Fam Cancer. 2012. PMID: 22773173 Review.
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care.
Shickh S, Rafferty SA, Clausen M, Kodida R, Mighton C, Panchal S, Lorentz J, Ward T, Watkins N, Elser C, Eisen A, Carroll JC, Glogowski E, Schrader KA, Lerner-Ellis J, Kim RH, Chitayat D, Shuman C, Bombard Y; Incidental Genomics Study Team. Shickh S, et al. Among authors: glogowski e. Genet Med. 2021 Jun;23(6):1086-1094. doi: 10.1038/s41436-021-01112-1. Epub 2021 Mar 2. Genet Med. 2021. PMID: 33654192 Free PMC article. Clinical Trial.
43 results