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

Year Number of Results
1897 1
1908 1
1947 3
1952 2
1953 2
1954 1
1956 1
1958 2
1960 1
1961 2
1962 1
1964 3
1965 1
1966 3
1967 1
1968 2
1969 1
1970 1
1972 1
1973 2
1974 2
1975 2
1976 1
1977 1
1978 6
1979 3
1980 2
1981 2
1982 3
1983 6
1984 9
1985 5
1986 6
1987 6
1988 3
1989 1
1991 4
1992 3
1993 4
1994 7
1995 3
1996 7
1997 10
1998 5
1999 11
2000 13
2001 7
2002 18
2003 11
2004 16
2005 30
2006 14
2007 27
2008 37
2009 33
2010 40
2011 54
2012 44
2013 51
2014 52
2015 50
2016 61
2017 62
2018 70
2019 51
2020 71
2021 81
2022 88
2023 83
2024 88
2025 20

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1,170 results

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Page 1
A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.
Kingsmore SF, Smith LD, Kunard CM, Bainbridge M, Batalov S, Benson W, Blincow E, Caylor S, Chambers C, Del Angel G, Dimmock DP, Ding Y, Ellsworth K, Feigenbaum A, Frise E, Green RC, Guidugli L, Hall KP, Hansen C, Hobbs CA, Kahn SD, Kiel M, Van Der Kraan L, Krilow C, Kwon YH, Madhavrao L, Le J, Lefebvre S, Mardach R, Mowrey WR, Oh D, Owen MJ, Powley G, Scharer G, Shelnutt S, Tokita M, Mehtalia SS, Oriol A, Papadopoulos S, Perry J, Rosales E, Sanford E, Schwartz S, Tran D, Reese MG, Wright M, Veeraraghavan N, Wigby K, Willis MJ, Wolen AR, Defay T. Kingsmore SF, et al. Among authors: willis mj. Am J Hum Genet. 2022 Sep 1;109(9):1605-1619. doi: 10.1016/j.ajhg.2022.08.003. Epub 2022 Aug 24. Am J Hum Genet. 2022. PMID: 36007526 Free PMC article. Review.
Oligoclonal bands.
Willis MD, Kreft KL, Dancey B. Willis MD, et al. Pract Neurol. 2024 Sep 13;24(5):400-406. doi: 10.1136/pn-2023-003814. Pract Neurol. 2024. PMID: 38937092 Review.
Editorial.
Willis MA. Willis MA. Int J MS Care. 2022 May-Jun;24(3):v. doi: 10.7224/1537-2073-24.3.iv. Epub 2022 May 24. Int J MS Care. 2022. PMID: 35645624 Free PMC article. No abstract available.
Editorial.
Willis MA. Willis MA. Int J MS Care. 2020 Sep-Oct;22(5):xii. doi: 10.7224/1537-2073-22.5.xii. Epub 2020 Oct 27. Int J MS Care. 2020. PMID: 33177962 Free PMC article. No abstract available.
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders.
Di Donato N, Guerrini R, Billington CJ, Barkovich AJ, Dinkel P, Freri E, Heide M, Gershon ES, Gertler TS, Hopkin RJ, Jacob S, Keedy SK, Kooshavar D, Lockhart PJ, Lohmann DR, Mahmoud IG, Parrini E, Schrock E, Severi G, Timms AE, Webster RI, Willis MJH, Zaki MS, Gleeson JG, Leventer RJ, Dobyns WB. Di Donato N, et al. Among authors: willis mjh. Brain. 2022 Sep 14;145(9):3274-3287. doi: 10.1093/brain/awac164. Brain. 2022. PMID: 35769015 Free PMC article.
Association of Initial Disease-Modifying Therapy With Later Conversion to Secondary Progressive Multiple Sclerosis.
Brown JWL, Coles A, Horakova D, Havrdova E, Izquierdo G, Prat A, Girard M, Duquette P, Trojano M, Lugaresi A, Bergamaschi R, Grammond P, Alroughani R, Hupperts R, McCombe P, Van Pesch V, Sola P, Ferraro D, Grand'Maison F, Terzi M, Lechner-Scott J, Flechter S, Slee M, Shaygannejad V, Pucci E, Granella F, Jokubaitis V, Willis M, Rice C, Scolding N, Wilkins A, Pearson OR, Ziemssen T, Hutchinson M, Harding K, Jones J, McGuigan C, Butzkueven H, Kalincik T, Robertson N; MSBase Study Group. Brown JWL, et al. Among authors: willis m. JAMA. 2019 Jan 15;321(2):175-187. doi: 10.1001/jama.2018.20588. JAMA. 2019. PMID: 30644981 Free PMC article.
Cwilted.
Willis MA. Willis MA. Emerg Nurse. 2001 Feb;8(9):18-22. doi: 10.7748/en2001.02.8.9.18.c1348. Emerg Nurse. 2001. PMID: 11935723 No abstract available.
Letter From the Editor.
Willis MA. Willis MA. Int J MS Care. 2023 Jul-Aug;25(4):xi. doi: 10.7224/1537-2073-25.4.xi. Epub 2023 Jul 11. Int J MS Care. 2023. PMID: 37469333 Free PMC article. No abstract available.
Editorial.
Willis MA. Willis MA. Int J MS Care. 2020 May-Jun;22(3):vi. doi: 10.7224/1537-2073-22.3.vi. Epub 2020 Jun 13. Int J MS Care. 2020. PMID: 32607078 Free PMC article. No abstract available.
1,170 results