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

Year Number of Results
1943 1
1950 3
1951 2
1970 1
1973 1
1975 7
1976 3
1977 1
1978 9
1979 3
1980 7
1981 2
1982 9
1983 9
1984 10
1985 16
1986 19
1987 11
1988 15
1989 16
1990 15
1991 16
1992 18
1993 17
1994 27
1995 23
1996 21
1997 19
1998 16
1999 12
2000 10
2001 28
2002 22
2003 33
2004 25
2005 13
2006 26
2007 28
2008 25
2009 28
2010 24
2011 18
2012 26
2013 22
2014 13
2015 14
2016 22
2017 17
2018 16
2019 21
2020 14
2021 10
2022 7
2023 17
2024 7
2025 8

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779 results

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Page 1
Alternating hemiplegia of childhood associated mutations in Atp1a3 reveal diverse neurological alterations in mice.
Terrey M, Krivoshein G, Adamson SI, Arystarkhova E, Anderson L, Szwec J, McKee S, Jones H, Perkins S, Selvam V, Piec PA, Chhaya D, Dehn A, Zuberi A, Murray SA, Morsci NS, Sweadner KJ, Knowles DA, Tolner EA, van den Maagdenberg AMJM, Lutz CM. Terrey M, et al. Among authors: knowles da. Neurobiol Dis. 2025 Aug;212:106954. doi: 10.1016/j.nbd.2025.106954. Epub 2025 May 15. Neurobiol Dis. 2025. PMID: 40381892 Free article.
Phenotypic complexities of rare heterozygous neurexin-1 deletions.
Fernando MB, Fan Y, Zhang Y, Tokolyi A, Murphy AN, Kammourh S, Deans PJM, Ghorbani S, Onatzevitch R, Pero A, Padilla C, Williams SE, Flaherty EK, Prytkova IA, Cao L, Knowles DA, Fang G, Slesinger PA, Brennand KJ. Fernando MB, et al. Among authors: knowles da. Nature. 2025 Apr 9. doi: 10.1038/s41586-025-08864-9. Online ahead of print. Nature. 2025. PMID: 40205044
SingleBrain: A Meta-Analysis of Single-Nucleus eQTLs Linking Genetic Risk to Brain Disorders.
Jang B, Bp K, Tokolyi A, Cuddleston WH, Ravi A, Jung SH, Naito T, Kim B, Seo Kim M, Cho M, Park MS, Rosen M, Blanchard J, Humphrey J, Knowles DA, Won HH, Raj T. Jang B, et al. Among authors: knowles da. medRxiv [Preprint]. 2025 Mar 7:2025.03.06.25323424. doi: 10.1101/2025.03.06.25323424. medRxiv. 2025. PMID: 40093234 Free PMC article. Preprint.
779 results