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Results by year

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

Year Number of Results
1959 1
1961 1
1962 1
1963 1
1968 2
1970 2
1971 4
1972 2
1973 2
1974 1
1976 1
1977 2
1978 2
1979 5
1980 4
1981 2
1983 2
1984 3
1985 3
1986 9
1987 12
1988 8
1989 13
1990 21
1991 34
1992 27
1993 25
1994 36
1995 32
1996 45
1997 46
1998 65
1999 61
2000 102
2001 121
2002 122
2003 171
2004 226
2005 274
2006 341
2007 364
2008 417
2009 506
2010 614
2011 668
2012 828
2013 809
2014 918
2015 984
2016 969
2017 979
2018 1102
2019 1173
2020 1284
2021 1450
2022 1373
2023 670

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14,996 results

Results by year

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Page 1
Common and rare variant associations with clonal haematopoiesis phenotypes.
Kessler MD, Damask A, O'Keeffe S, Banerjee N, Li D, Watanabe K, Marketta A, Van Meter M, Semrau S, Horowitz J, Tang J, Kosmicki JA, Rajagopal VM, Zou Y, Houvras Y, Ghosh A, Gillies C, Mbatchou J, White RR, Verweij N, Bovijn J, Parikshak NN, LeBlanc MG, Jones M; Regeneron Genetics Center; GHS-RGC DiscovEHR Collaboration; Glass DJ, Lotta LA, Cantor MN, Atwal GS, Locke AE, Ferreira MAR, Deering R, Paulding C, Shuldiner AR, Thurston G, Ferrando AA, Salerno W, Reid JG, Overton JD, Marchini J, Kang HM, Baras A, Abecasis GR, Jorgenson E. Kessler MD, et al. Among authors: kang hm. Nature. 2022 Dec;612(7939):301-309. doi: 10.1038/s41586-022-05448-9. Epub 2022 Nov 30. Nature. 2022. PMID: 36450978 Free PMC article.
Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development.
Chung C, Yang X, Bae T, Vong KI, Mittal S, Donkels C, Westley Phillips H, Li Z, Marsh APL, Breuss MW, Ball LL, Garcia CAB, George RD, Gu J, Xu M, Barrows C, James KN, Stanley V, Nidhiry AS, Khoury S, Howe G, Riley E, Xu X, Copeland B, Wang Y, Kim SH, Kang HC, Schulze-Bonhage A, Haas CA, Urbach H, Prinz M, Limbrick DD Jr, Gurnett CA, Smyth MD, Sattar S, Nespeca M, Gonda DD, Imai K, Takahashi Y, Chen HH, Tsai JW, Conti V, Guerrini R, Devinsky O, Silva WA Jr, Machado HR, Mathern GW, Abyzov A, Baldassari S, Baulac S; Focal Cortical Dysplasia Neurogenetics Consortium; Brain Somatic Mosaicism Network; Gleeson JG. Chung C, et al. Among authors: kang hc. Nat Genet. 2023 Feb;55(2):209-220. doi: 10.1038/s41588-022-01276-9. Epub 2023 Jan 12. Nat Genet. 2023. PMID: 36635388
Response.
Park SW, Lee KJ, Chung MJ, Jo JH, Lee HS, Park JY, Park SW, Song SY, Kang H, Kim EJ, Kim YS, Cho JH, Bang S. Park SW, et al. Among authors: kang h. Gastrointest Endosc. 2023 Mar;97(3):603-604. doi: 10.1016/j.gie.2022.11.007. Gastrointest Endosc. 2023. PMID: 36801022 No abstract available.
[No title available]
Maurer M, Magerl M, Betschel S, Aberer W, Ansotegui IJ, Aygören-Pürsün E, Banerji A, Bara NA, Boccon-Gibod I, Bork K, Bouillet L, Boysen HB, Brodszki N, Busse PJ, Bygum A, Caballero T, Cancian M, Castaldo A, Cohn DM, Csuka D, Farkas H, Gompels M, Gower R, Grumach AS, Guidos-Fogelbach G, Hide M, Kang HR, Kaplan AP, Katelaris C, Kiani-Alikhan S, Lei WT, Lockey R, Longhurst H, Lumry WR, MacGinnitie A, Malbran A, Saguer IM, Matta JJ, Nast A, Nguyen D, Nieto-Martinez SA, Pawankar R, Peter J, Porebski G, Prior N, Reshef A, Riedl M, Ritchie B, Sheikh FR, Smith WB, Spaeth PJ, Stobiecki M, Toubi E, Varga LA, Weller K, Zanichelli A, Zhi Y, Zuraw B, Craig T. Maurer M, et al. Among authors: kang hr. Arerugi. 2023;72(3):237-272. doi: 10.15036/arerugi.72.237. Arerugi. 2023. PMID: 37225467 Japanese. No abstract available.
Message From the New Editor-in-Chief.
Kang H. Kang H. J Lipid Atheroscler. 2023 Jan;12(1):1. doi: 10.12997/jla.2023.12.1.1. Epub 2023 Jan 18. J Lipid Atheroscler. 2023. PMID: 36761058 Free PMC article. No abstract available.
Mechanical stimuli-driven cancer therapeutics.
An J, Hong H, Won M, Rha H, Ding Q, Kang N, Kang H, Kim JS. An J, et al. Among authors: kang h. Chem Soc Rev. 2023 Jan 3;52(1):30-46. doi: 10.1039/d2cs00546h. Chem Soc Rev. 2023. PMID: 36511945 Review.
Journal Metrics and Statistics.
Kang H. Kang H. J Lipid Atheroscler. 2023 Jan;12(1):87. doi: 10.12997/jla.2023.12.1.87. Epub 2023 Jan 18. J Lipid Atheroscler. 2023. PMID: 36761065 Free PMC article. No abstract available.
Bartter Syndrome: Perspectives of a Pediatric Nephrologist.
Choi N, Kang HG. Choi N, et al. Among authors: kang hg. Electrolyte Blood Press. 2022 Dec;20(2):49-56. doi: 10.5049/EBP.2022.20.2.49. Epub 2022 Dec 30. Electrolyte Blood Press. 2022. PMID: 36688207 Free PMC article. Review.
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Weinstock JS, Gopakumar J, Burugula BB, Uddin MM, Jahn N, Belk JA, Bouzid H, Daniel B, Miao Z, Ly N, Mack TM, Luna SE, Prothro KP, Mitchell SR, Laurie CA, Broome JG, Taylor KD, Guo X, Sinner MF, von Falkenhausen AS, Kääb S, Shuldiner AR, O'Connell JR, Lewis JP, Boerwinkle E, Barnes KC, Chami N, Kenny EE, Loos RJF, Fornage M, Hou L, Lloyd-Jones DM, Redline S, Cade BE, Psaty BM, Bis JC, Brody JA, Silverman EK, Yun JH, Qiao D, Palmer ND, Freedman BI, Bowden DW, Cho MH, DeMeo DL, Vasan RS, Yanek LR, Becker LC, Kardia SLR, Peyser PA, He J, Rienstra M, Van der Harst P, Kaplan R, Heckbert SR, Smith NL, Wiggins KL, Arnett DK, Irvin MR, Tiwari H, Cutler MJ, Knight S, Muhlestein JB, Correa A, Raffield LM, Gao Y, de Andrade M, Rotter JI, Rich SS, Tracy RP, Konkle BA, Johnsen JM, Wheeler MM, Smith JG, Melander O, Nilsson PM, Custer BS, Duggirala R, Curran JE, Blangero J, McGarvey S, Williams LK, Xiao S, Yang M, Gu CC, Chen YI, Lee WJ, Marcus GM, Kane JP, Pullinger CR, Shoemaker MB, Darbar D, Roden DM, Albert C, Kooperberg C, Zhou Y, Manson JE, Desai P, Johnson AD, Mathias RA; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium; Blackwell TW, Abecasis GR, Smith AV, Kang HM, Sat… See abstract for full author list ➔ Weinstock JS, et al. Among authors: kang hm. Nature. 2023 Apr;616(7958):755-763. doi: 10.1038/s41586-023-05806-1. Epub 2023 Apr 12. Nature. 2023. PMID: 37046083
14,996 results
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