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

Year Number of Results
1994 2
1995 1
1996 9
1997 6
1998 3
2000 1
2001 1
2004 1
2006 3
2007 5
2008 8
2009 9
2010 9
2012 2
2013 2
2014 1
2015 3
2016 2
2017 1
2018 1
2020 3
2021 1
2022 2
2024 0

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68 results

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Page 1
Progressive multifocal leukoencephalopathy genetic risk variants for pharmacovigilance of immunosuppressant therapies.
Hatchwell E, Smith EB 3rd, Jalilzadeh S, Bruno CD, Taoufik Y, Hendel-Chavez H, Liblau R, Brassat D, Martin-Blondel G, Wiendl H, Schwab N, Cortese I, Monaco MC, Imberti L, Capra R, Oksenberg JR, Gasnault J, Stankoff B, Richmond TA, Rancour DM, Koralnik IJ, Hanson BA, Major EO, Chow CR, Eis PS. Hatchwell E, et al. Front Neurol. 2022 Dec 14;13:1016377. doi: 10.3389/fneur.2022.1016377. eCollection 2022. Front Neurol. 2022. PMID: 36588876 Free PMC article.
Autism and environmental genomics.
Herbert MR, Russo JP, Yang S, Roohi J, Blaxill M, Kahler SG, Cremer L, Hatchwell E. Herbert MR, et al. Among authors: hatchwell e. Neurotoxicology. 2006 Sep;27(5):671-84. doi: 10.1016/j.neuro.2006.03.017. Epub 2006 Mar 28. Neurotoxicology. 2006. PMID: 16644012 Review.
NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum.
Kimonis V, Al Dubaisi R, Maclean AE, Hall K, Weiss L, Stover AE, Schwartz PH, Berg B, Cheng C, Parikh S, Conner BR, Wu S, Hasso AN, Scott DA, Koenig MK, Karam R, Tang S, Smith M, Chao E, Balk J, Hatchwell E, Eis PS. Kimonis V, et al. Among authors: hatchwell e. J Med Genet. 2021 May;58(5):314-325. doi: 10.1136/jmedgenet-2020-106846. Epub 2020 Jun 9. J Med Genet. 2021. PMID: 32518176 Review.
Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice.
Cheng C, Cleak J, Weiss L, Cater H, Stewart M, Wells S, Columbres RC, Shmara A, Morato Torres CA, Zafar F, Schüle B, Neumann J, Hatchwell E, Kimonis V. Cheng C, et al. Among authors: hatchwell e. Orphanet J Rare Dis. 2022 Oct 24;17(1):386. doi: 10.1186/s13023-022-02446-y. Orphanet J Rare Dis. 2022. PMID: 36280881 Free PMC article.
Germline Genetic Risk Variants for Progressive Multifocal Leukoencephalopathy.
Eis PS, Bruno CD, Richmond TA, Koralnik IJ, Hanson BA, Major EO, Chow CR, Hendel-Chavez H, Stankoff B, Gasnault J, Taoufik Y, Hatchwell E. Eis PS, et al. Among authors: hatchwell e. Front Neurol. 2020 Mar 17;11:186. doi: 10.3389/fneur.2020.00186. eCollection 2020. Front Neurol. 2020. PMID: 32256442 Free PMC article.
Toriello-Carey syndrome phenotype and chromosome anomalies.
Toriello HV, Hatchwell E. Toriello HV, et al. Among authors: hatchwell e. Am J Med Genet A. 2008 Jan 1;146A(1):116. doi: 10.1002/ajmg.a.32057. Am J Med Genet A. 2008. PMID: 18074373 No abstract available.
Unstable mutation in incontinentia pigmenti?
Hatchwell E. Hatchwell E. J Med Genet. 1996 Apr;33(4):349-50. doi: 10.1136/jmg.33.4.349-a. J Med Genet. 1996. PMID: 8730298 Free PMC article. No abstract available.
68 results