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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 36
2010 40
2011 55
2012 44
2013 52
2014 60
2015 54
2016 63
2017 63
2018 77
2019 51
2020 73
2021 82
2022 91
2023 87
2024 91
2025 77

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1,263 results

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Page 1
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 Sep-Oct;24(5):v. doi: 10.7224/1537-2073-24.5.v. Epub 2022 Sep 8. Int J MS Care. 2022. PMID: 36090240 Free PMC article. No abstract available.
Editorial.
Willis MA. Willis MA. Int J MS Care. 2021 Mar-Apr;23(2):iv. doi: 10.7224/1537-2073-23.2.iv. Epub 2021 Apr 14. Int J MS Care. 2021. PMID: 33880086 Free PMC article. No abstract available.
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.
Imaging of Sarcopenia.
Boutin RD, Houston DK, Chaudhari AS, Willis MH, Fausett CL, Lenchik L. Boutin RD, et al. Among authors: willis mh. Radiol Clin North Am. 2022 Jul;60(4):575-582. doi: 10.1016/j.rcl.2022.03.001. Radiol Clin North Am. 2022. PMID: 35672090 Review.
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.
Tessadori F, Duran K, Knapp K, Fellner M; Deciphering Developmental Disorders Study; Smithson S, Beleza Meireles A, Elting MW, Waisfisz Q, O'Donnell-Luria A, Nowak C, Douglas J, Ronan A, Brunet T, Kotzaeridou U, Svihovec S, Saenz MS, Thiffault I, Del Viso F, Devine P, Rego S, Tenney J, van Haeringen A, Ruivenkamp CAL, Koene S, Robertson SP, Deshpande C, Pfundt R, Verbeek N, van de Kamp JM, Weiss JMM, Ruiz A, Gabau E, Banne E, Pepler A, Bottani A, Laurent S, Guipponi M, Bijlsma E, Bruel AL, Sorlin A, Willis M, Powis Z, Smol T, Vincent-Delorme C, Baralle D, Colin E, Revencu N, Calpena E, Wilkie AOM, Chopra M, Cormier-Daire V, Keren B, Afenjar A, Niceta M, Terracciano A, Specchio N, Tartaglia M, Rio M, Barcia G, Rondeau S, Colson C, Bakkers J, Mace PD, Bicknell LS, van Haaften G. Tessadori F, et al. Among authors: willis m. Am J Hum Genet. 2022 Apr 7;109(4):750-758. doi: 10.1016/j.ajhg.2022.02.003. Epub 2022 Feb 23. Am J Hum Genet. 2022. PMID: 35202563 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.
Editorial.
Willis MA. Willis MA. Int J MS Care. 2021 Jul-Aug;23(4):iv. doi: 10.7224/1537-2073-23.4.iv. Epub 2021 Aug 27. Int J MS Care. 2021. PMID: 34483759 Free PMC article. 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.
1,263 results