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

Year Number of Results
1987 1
1988 2
1990 3
1993 1
1994 2
1995 1
1996 1
2001 2
2008 1
2009 1
2010 1
2011 1
2012 4
2013 3
2014 1
2015 2
2016 1
2017 1
2019 2
2020 2
2021 7
2022 8
2023 4

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47 results

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Page 1
Clinical application of whole-exome sequencing across clinical indications.
Retterer K, Juusola J, Cho MT, Vitazka P, Millan F, Gibellini F, Vertino-Bell A, Smaoui N, Neidich J, Monaghan KG, McKnight D, Bai R, Suchy S, Friedman B, Tahiliani J, Pineda-Alvarez D, Richard G, Brandt T, Haverfield E, Chung WK, Bale S. Retterer K, et al. Among authors: neidich j. Genet Med. 2016 Jul;18(7):696-704. doi: 10.1038/gim.2015.148. Epub 2015 Dec 3. Genet Med. 2016. PMID: 26633542 Free article.
Clinical whole-genome sequencing in cancer diagnosis.
Hou YC, Neidich JA, Duncavage EJ, Spencer DH, Schroeder MC. Hou YC, et al. Among authors: neidich ja. Hum Mutat. 2022 Nov;43(11):1519-1530. doi: 10.1002/humu.24381. Epub 2022 Apr 26. Hum Mutat. 2022. PMID: 35471774 Review.
Genome Sequencing as an Alternative to Cytogenetic Analysis in Myeloid Cancers.
Duncavage EJ, Schroeder MC, O'Laughlin M, Wilson R, MacMillan S, Bohannon A, Kruchowski S, Garza J, Du F, Hughes AEO, Robinson J, Hughes E, Heath SE, Baty JD, Neidich J, Christopher MJ, Jacoby MA, Uy GL, Fulton RS, Miller CA, Payton JE, Link DC, Walter MJ, Westervelt P, DiPersio JF, Ley TJ, Spencer DH. Duncavage EJ, et al. Among authors: neidich j. N Engl J Med. 2021 Mar 11;384(10):924-935. doi: 10.1056/NEJMoa2024534. N Engl J Med. 2021. PMID: 33704937 Free PMC article.
The childless man.
Scheuerle AE, Picconi JL, Neidich J, Panny S, Plecher BA, Randolph LM, Trapane P, Trotter TL. Scheuerle AE, et al. Among authors: neidich j. Am J Med Genet A. 2014 Feb;164A(2):561. doi: 10.1002/ajmg.a.36290. Epub 2013 Dec 5. Am J Med Genet A. 2014. PMID: 24311465 No abstract available.
Comparing Gene Panels for Non-Retinal Indications: A Systematic Review.
Procopio R, Pulido JS, Gunton KB, Syed ZA, Lee D, Moster ML, Sergott R, Neidich JA, Reynolds MM. Procopio R, et al. Among authors: neidich ja. Genes (Basel). 2023 Mar 17;14(3):738. doi: 10.3390/genes14030738. Genes (Basel). 2023. PMID: 36981008 Free PMC article.
From karyotypes to precision genomics in 9p deletion and duplication syndromes.
Sams EI, Ng JK, Tate V, Claire Hou YC, Cao Y, Antonacci-Fulton L, Belhassan K, Neidich J, Mitra RD, Cole FS, Dickson P, Milbrandt J, Turner TN. Sams EI, et al. Among authors: neidich j. HGG Adv. 2021 Dec 24;3(1):100081. doi: 10.1016/j.xhgg.2021.100081. eCollection 2022 Jan 13. HGG Adv. 2021. PMID: 35047865 Free PMC article.
Acceptance of Saliva-Based Specimen Collection for SARS-CoV-2 Testing Among K-12 Students, Teachers, and Staff.
McLaughlin HP, Worrell MC, Malone S, Dawson P, Maricque B, Halpin JL, Lee S, Fritz SA, Tinker SC, Neidich JA, Towns K, Lee JS, Barrios LC, Neatherlin JC, Newland JG, Salzer JS; SARS-CoV-2 Specimen Collection Field Team. McLaughlin HP, et al. Among authors: neidich ja. Public Health Rep. 2022 May-Jun;137(3):557-563. doi: 10.1177/00333549221074395. Epub 2022 Feb 9. Public Health Rep. 2022. PMID: 35137643 Free PMC article.
A comparative analysis of RAS variants in patients with disorders of somatic mosaicism.
Claire Hou YC, Evenson MJ, Corliss MM, Mahapatra L, Aldawood A, Carpentieri DF, Chamlin SL, Kulungowski AM, Madan-Khetarpal S, Sebastian J, Pet MA, Coughlin CC, Willing MC, Pearson GD, Setty BA, El-Haffaf Z, Cottrell CE, Parikh BA, Krysiak K, Schroeder MC, Heusel JW, Neidich JA, Cao Y. Claire Hou YC, et al. Among authors: neidich ja. Genet Med. 2023 Mar;25(3):100348. doi: 10.1016/j.gim.2022.11.016. Epub 2022 Dec 7. Genet Med. 2023. PMID: 36571464
47 results