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Results by year

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

Year Number of Results
1946 1
1947 1
1950 7
1951 3
1952 5
1953 3
1954 3
1955 4
1956 5
1957 6
1958 2
1959 3
1960 9
1961 9
1962 11
1963 5
1964 4
1965 1
1966 6
1967 11
1968 18
1969 18
1970 31
1971 38
1972 26
1973 15
1974 15
1975 19
1976 27
1977 11
1978 19
1979 7
1980 7
1981 6
1982 3
1983 1
1985 2
1986 1
1987 2
1988 1
1989 6
1990 7
1991 5
1992 5
1993 1
1995 1
1996 1
1997 2
2005 1
2008 3
2009 3
2010 2
2011 3
2012 5
2013 5
2014 4
2015 8
2016 6
2017 6
2018 6
2019 2
2020 6
2021 14
2022 10
2023 8
2024 1

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Search Results

472 results

Results by year

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Page 1
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients.
Stranneheim H, Lagerstedt-Robinson K, Magnusson M, Kvarnung M, Nilsson D, Lesko N, Engvall M, Anderlid BM, Arnell H, Johansson CB, Barbaro M, Björck E, Bruhn H, Eisfeldt J, Freyer C, Grigelioniene G, Gustavsson P, Hammarsjö A, Hellström-Pigg M, Iwarsson E, Jemt A, Laaksonen M, Enoksson SL, Malmgren H, Naess K, Nordenskjöld M, Oscarson M, Pettersson M, Rasi C, Rosenbaum A, Sahlin E, Sardh E, Stödberg T, Tesi B, Tham E, Thonberg H, Töhönen V, von Döbeln U, Vassiliou D, Vonlanthen S, Wikström AC, Wincent J, Winqvist O, Wredenberg A, Ygberg S, Zetterström RH, Marits P, Soller MJ, Nordgren A, Wirta V, Lindstrand A, Wedell A. Stranneheim H, et al. Among authors: naess k. Genome Med. 2021 Mar 17;13(1):40. doi: 10.1186/s13073-021-00855-5. Genome Med. 2021. PMID: 33726816 Free PMC article.
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsy.
Mattison KA, Tossing G, Mulroe F, Simmons C, Butler KM, Schreiber A, Alsadah A, Neilson DE, Naess K, Wedell A, Wredenberg A, Sorlin A, McCann E, Burghel GJ, Menendez B, Hoganson GE, Botto LD, Filloux FM, Aledo-Serrano Á, Gil-Nagel A, Tatton-Brown K, Verbeek NE, van der Zwaag B, Aleck KA, Fazenbaker AC, Balciuniene J, Dubbs HA, Marsh ED, Garber K, Ek J, Duno M, Hoei-Hansen CE, Deardorff MA, Raca G, Quindipan C, van Hirtum-Das M, Breckpot J, Hammer TB, Møller RS, Whitney A, Douglas AGL, Kharbanda M, Brunetti-Pierri N, Morleo M, Nigro V, May HJ, Tao JX, Argilli E, Sherr EH, Dobyns WB; Genomics England Research Consortium; Baines RA, Warwicker J, Parker JA, Banka S, Campeau PM, Escayg A. Mattison KA, et al. Among authors: naess k. Brain. 2023 Apr 19;146(4):1357-1372. doi: 10.1093/brain/awac330. Brain. 2023. PMID: 36074901 Free PMC article.
[Analeptics].
Naess K. Naess K. Tidsskr Nor Laegeforen. 1967 Dec 15;87(24):2055-7. Tidsskr Nor Laegeforen. 1967. PMID: 4385472 Norwegian. No abstract available.
[Dextropropoxyphene].
Lunde I, Naess K. Lunde I, et al. Among authors: naess k. Tidsskr Nor Laegeforen. 1971 Jan 10;91(1):31-2. Tidsskr Nor Laegeforen. 1971. PMID: 5538882 Norwegian. No abstract available.
[Placebo--nocebo].
Naess K. Naess K. Tidsskr Nor Laegeforen. 1989 Mar 10;109(7-8):802-4. Tidsskr Nor Laegeforen. 1989. PMID: 2650013 Clinical Trial. Norwegian. No abstract available.
[Analgesics].
Naess K. Naess K. Tidsskr Nor Laegeforen. 1977 Aug 10;97(22):1095-8. Tidsskr Nor Laegeforen. 1977. PMID: 905987 Norwegian. No abstract available.
Renal Phenotype in Mitochondrial Diseases: A Multicenter Study.
Parasyri M, Brandström P, Uusimaa J, Ostergaard E, Hikmat O, Isohanni P, Naess K, de Coo IFM, Nascimento Osorio A, Nuutinen M, Lindberg C, Bindoff LA, Tulinius M, Darin N, Sofou K. Parasyri M, et al. Among authors: naess k. Kidney Dis (Basel). 2022 Jan 24;8(2):148-159. doi: 10.1159/000521148. eCollection 2022 Mar. Kidney Dis (Basel). 2022. PMID: 35527992 Free PMC article.
472 results