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

Year Number of Results
2005 2
2006 3
2007 1
2008 1
2009 1
2010 2
2011 1
2012 5
2013 2
2014 1
2015 3
2016 5
2017 3
2018 2
2019 3
2020 3
2021 11
2022 6
2023 14
2024 5

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61 results

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Page 1
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: gallagher km. 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.
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: gallagher km. Genet Med. 2023 Sep;25(9):100880. doi: 10.1016/j.gim.2023.100880. Epub 2023 May 6. Genet Med. 2023. PMID: 37158195
Hope versus reality: Parent expectations of genomic testing.
Donohue KE, Dolan SM, Watnick D, Gallagher KM, Odgis JA, Suckiel SA, Teitelman N, Gelb BD, Kenny EE, Wasserstein MP, Horowitz CR, Bauman LJ. Donohue KE, et al. Among authors: gallagher km. Patient Educ Couns. 2021 Aug;104(8):2073-2079. doi: 10.1016/j.pec.2021.01.030. Epub 2021 Jan 29. Patient Educ Couns. 2021. PMID: 33640235 Free PMC article.
Parental involvement in neonatal critical care decision-making.
Shaw C, Stokoe E, Gallagher K, Aladangady N, Marlow N. Shaw C, et al. Among authors: gallagher k. Sociol Health Illn. 2016 Nov;38(8):1217-1242. doi: 10.1111/1467-9566.12455. Epub 2016 Sep 25. Sociol Health Illn. 2016. PMID: 27666147
Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.
Bonini KE, Thomas-Wilson A, Marathe PN, Sebastin M, Odgis JA, Di Biase M, Kelly NR, Ramos MA, Insel BJ, Scarimbolo L, Rehman AU, Guha S, Okur V, Abhyankar A, Phadke S, Nava C, Gallagher KM, Elkhoury L, Edelmann L, Zinberg RE, Abul-Husn NS, Diaz GA, Greally JM, Suckiel SA, Horowitz CR, Kenny EE, Wasserstein M, Gelb BD, Jobanputra V. Bonini KE, et al. Among authors: gallagher km. Clin Genet. 2023 Aug;104(2):210-225. doi: 10.1111/cge.14365. Epub 2023 Jun 19. Clin Genet. 2023. PMID: 37334874
End-of-life decisions in neonatal care: a conversation analytical study.
Marlow N, Shaw C, Connabeer K, Aladangady N, Gallagher K, Drew P. Marlow N, et al. Among authors: gallagher k. Arch Dis Child Fetal Neonatal Ed. 2021 Mar;106(2):184-188. doi: 10.1136/archdischild-2020-319544. Epub 2020 Sep 17. Arch Dis Child Fetal Neonatal Ed. 2021. PMID: 32943530
61 results