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

Year Number of Results
1971 4
1973 3
1974 1
1977 2
1978 3
1979 2
1980 2
1982 1
1983 1
1984 3
1985 1
1986 1
1988 1
1989 2
1991 3
1992 2
1993 1
1994 4
1995 3
1996 2
1997 1
1998 2
1999 4
2000 1
2001 6
2002 4
2004 4
2005 2
2006 1
2007 5
2008 6
2009 3
2010 13
2011 1
2012 6
2013 7
2014 9
2015 6
2016 5
2017 6
2018 5
2019 7
2020 3
2021 2
2022 3
2023 5
2024 0

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142 results

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Page 1
Institutional profile: translational pharmacogenomics at the Icahn School of Medicine at Mount Sinai.
Scott SA, Owusu Obeng A, Botton MR, Yang Y, Scott ER, Ellis SB, Wallsten R, Kaszemacher T, Zhou X, Chen R, Nicoletti P, Naik H, Kenny EE, Vega A, Waite E, Diaz GA, Dudley J, Halperin JL, Edelmann L, Kasarskis A, Hulot JS, Peter I, Bottinger EP, Hirschhorn K, Sklar P, Cho JH, Desnick RJ, Schadt EE. Scott SA, et al. Among authors: edelmann l. Pharmacogenomics. 2017 Oct;18(15):1381-1386. doi: 10.2217/pgs-2017-0137. Epub 2017 Oct 6. Pharmacogenomics. 2017. PMID: 28982267 Free PMC article. Review.
Detection of mosaic variants using genome sequencing in a large pediatric cohort.
Odgis JA, Gallagher KM, Rehman AU, Marathe PN, Bonini KE, Sebastin M, Di Biase M, Brown K, Kelly NR, Ramos MA, Thomas-Wilson A, Guha S, Okur V, Ganapathi M, Elkhoury L, Edelmann L, Zinberg RE, Abul-Husn NS, Diaz GA, Greally JM, Suckiel SA, Jobanputra V, Horowitz CR, Kenny EE, Wasserstein MP, Gelb BD. Odgis JA, et al. Among authors: edelmann l. Am J Med Genet A. 2023 Mar;191(3):699-710. doi: 10.1002/ajmg.a.63062. Epub 2022 Dec 23. Am J Med Genet A. 2023. PMID: 36563179 Free PMC article.
Role of copy number variants in structural birth defects.
Southard AE, Edelmann LJ, Gelb BD. Southard AE, et al. Among authors: edelmann lj. Pediatrics. 2012 Apr;129(4):755-63. doi: 10.1542/peds.2011-2337. Epub 2012 Mar 19. Pediatrics. 2012. PMID: 22430448 Review.
Prenatal Diagnosis of Cystic Fibrosis.
Fedick AM, Zhang J, Edelmann L, Kornreich R. Fedick AM, et al. Among authors: edelmann l. Methods Mol Biol. 2019;1885:221-231. doi: 10.1007/978-1-4939-8889-1_15. Methods Mol Biol. 2019. PMID: 30506201
Prenatal genetic screening in the Ashkenazi Jewish population.
Zinberg RE, Kornreich R, Edelmann L, Desnick RJ. Zinberg RE, et al. Among authors: edelmann l. Clin Perinatol. 2001 Jun;28(2):367-82. doi: 10.1016/s0095-5108(05)70089-0. Clin Perinatol. 2001. PMID: 11499058 Review.
Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients.
Abul-Husn NS, Marathe PN, Kelly NR, Bonini KE, Sebastin M, Odgis JA, Abhyankar A, Brown K, Di Biase M, Gallagher KM, Guha S, Ioele N, Okur V, Ramos MA, Rodriguez JE, Rehman AU, Thomas-Wilson A, Edelmann L, Zinberg RE, Diaz GA, Greally JM, Jobanputra V, Suckiel SA, Horowitz CR, Wasserstein MP, Kenny EE, Gelb BD. Abul-Husn NS, et al. Among authors: edelmann l. Genet Med. 2023 Sep;25(9):100880. doi: 10.1016/j.gim.2023.100880. Epub 2023 May 6. Genet Med. 2023. PMID: 37158195
Characterization of Reference Materials for TPMT and NUDT15: A GeT-RM Collaborative Project.
Pratt VM, Wang WY, Boone EC, Broeckel U, Cody N, Edelmann L, Gaedigk A, Lynnes TC, Medeiros EB, Moyer AM, Mitchell MW, Scott SA, Starostik P, Turner A, Kalman LV. Pratt VM, et al. Among authors: edelmann l. J Mol Diagn. 2022 Oct;24(10):1079-1088. doi: 10.1016/j.jmoldx.2022.06.008. Epub 2022 Aug 2. J Mol Diagn. 2022. PMID: 35931342 Free PMC article.
142 results