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

Year Number of Results
1962 2
1963 3
1964 1
1965 3
1966 6
1967 6
1968 1
1969 8
1970 3
1971 2
1972 9
1973 5
1974 5
1975 3
1976 4
1977 9
1978 2
1979 9
1981 6
1982 3
1983 7
1984 5
1985 9
1986 12
1987 9
1988 11
1989 16
1990 13
1991 11
1992 18
1993 24
1994 20
1995 19
1996 29
1997 33
1998 55
1999 45
2000 44
2001 51
2002 80
2003 102
2004 124
2005 150
2006 162
2007 172
2008 205
2009 196
2010 291
2011 270
2012 334
2013 406
2014 441
2015 475
2016 503
2017 535
2018 604
2019 640
2020 772
2021 271
Text availability
Article attribute
Article type
Publication date

Search Results

6,506 results
Results by year
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Page 1
Response.
Park SS, Han KS. Park SS, et al. Among authors: han ks. Gastrointest Endosc. 2020 Jul;92(1):231. doi: 10.1016/j.gie.2020.03.004. Gastrointest Endosc. 2020. PMID: 32586556 No abstract available.
Genomic surveillance of COVID-19 cases in Beijing.
Du P, Ding N, Li J, Zhang F, Wang Q, Chen Z, Song C, Han K, Xie W, Liu J, Wang L, Wei L, Ma S, Hua M, Yu F, Wang L, Wang W, An K, Chen J, Liu H, Gao G, Wang S, Huang Y, Wu AR, Wang J, Liu D, Zeng H, Chen C. Du P, et al. Among authors: han k. Nat Commun. 2020 Oct 30;11(1):5503. doi: 10.1038/s41467-020-19345-0. Nat Commun. 2020. PMID: 33127911 Free PMC article.
Circuit and molecular architecture of a ventral hippocampal network.
Gergues MM, Han KJ, Choi HS, Brown B, Clausing KJ, Turner VS, Vainchtein ID, Molofsky AV, Kheirbek MA. Gergues MM, et al. Among authors: han kj. Nat Neurosci. 2020 Nov;23(11):1444-1452. doi: 10.1038/s41593-020-0705-8. Epub 2020 Sep 14. Nat Neurosci. 2020. PMID: 32929245 Free PMC article.
Haploinsufficiency of Cyfip2 Causes Lithium-Responsive Prefrontal Dysfunction.
Lee SH, Zhang Y, Park J, Kim B, Kim Y, Lee SH, Kim GH, Huh YH, Lee B, Kim Y, Lee Y, Kim JY, Kang H, Choi SY, Jang S, Li Y, Kim S, Jin C, Pang K, Kim E, Lee Y, Kim H, Kim E, Choi JH, Kim J, Lee KJ, Choi SY, Han K. Lee SH, et al. Among authors: han k. Ann Neurol. 2020 Sep;88(3):526-543. doi: 10.1002/ana.25827. Epub 2020 Jul 27. Ann Neurol. 2020. PMID: 32562430
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
Jia X, Yamamura T, Gbadegesin R, McNulty MT, Song K, Nagano C, Hitomi Y, Lee D, Aiba Y, Khor SS, Ueno K, Kawai Y, Nagasaki M, Noiri E, Horinouchi T, Kaito H, Hamada R, Okamoto T, Kamei K, Kaku Y, Fujimaru R, Tanaka R, Shima Y; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan, Baek J, Kang HG, Ha IS, Han KH, Yang EM; Korean Consortium of Hereditary Renal Diseases in Children, Abeyagunawardena A, Lane B, Chryst-Stangl M, Esezobor C, Solarin A; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group), Dossier C, DeschĂȘnes G; NEPHROVIR, Vivarelli M, Debiec H, Ishikura K, Matsuo M, Nozu K, Ronco P, Cheong HI, Sampson MG, Tokunaga K, Iijima K. Jia X, et al. Among authors: han kh. Kidney Int. 2020 Nov;98(5):1308-1322. doi: 10.1016/j.kint.2020.05.029. Epub 2020 Jun 14. Kidney Int. 2020. PMID: 32554042 Free article.
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