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

Year Number of Results
1987 1
1990 4
1991 1
1992 4
1993 1
1994 3
1995 2
1996 4
1997 3
1998 9
1999 6
2000 11
2001 15
2002 15
2003 11
2004 6
2005 8
2006 7
2007 9
2008 6
2009 5
2010 6
2011 7
2012 14
2013 4
2014 9
2015 7
2016 4
2017 7
2018 7
2019 2
2020 13
2021 4
2022 5
2023 4
2024 0

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PubMed for id: 815

214 results

Results by year

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Page 1
Genome sequencing demonstrates high diagnostic yield in children with undiagnosed global developmental delay/intellectual disability: A prospective study.
Sun Y, Peng J, Liang D, Ye X, Xu N, Chen L, Yan D, Zhang H, Xiao B, Qiu W, Shen Y, Pang N, Liu Y, Liang C, Qin Z, Luo J, Chen F, Wang J, Zhang Z, Wei H, Du J, Yan H, Duan R, Wang J, Zhang Y, Liao S, Sun K, Wu L, Yu Y. Sun Y, et al. Hum Mutat. 2022 May;43(5):568-581. doi: 10.1002/humu.24347. Epub 2022 Mar 1. Hum Mutat. 2022. PMID: 35143101
Association of a CAMK2A genetic variant with logical memory performance and hippocampal volume in the elderly.
Rhein C, Mühle C, Lenz B, Richter-Schmidinger T, Kogias G, Boix F, Lourdusamy A, Dörfler A, Peters O, Ramirez A, Jessen F, Maier W, Hüll M, Frölich L, Teipel S, Wiltfang J, Kornhuber J, Müller CP. Rhein C, et al. Brain Res Bull. 2020 Aug;161:13-20. doi: 10.1016/j.brainresbull.2020.05.001. Epub 2020 May 11. Brain Res Bull. 2020. PMID: 32418901
De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders.
Akita T, Aoto K, Kato M, Shiina M, Mutoh H, Nakashima M, Kuki I, Okazaki S, Magara S, Shiihara T, Yokochi K, Aiba K, Tohyama J, Ohba C, Miyatake S, Miyake N, Ogata K, Fukuda A, Matsumoto N, Saitsu H. Akita T, et al. Ann Clin Transl Neurol. 2018 Jan 29;5(3):280-296. doi: 10.1002/acn3.528. eCollection 2018 Mar. Ann Clin Transl Neurol. 2018. PMID: 29560374 Free PMC article.
214 results