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

Year Number of Results
1886 1
1890 1
1891 5
1893 1
1895 1
1900 1
1902 1
1905 1
1910 1
1947 1
1949 2
1950 1
1951 5
1953 2
1954 1
1956 1
1959 1
1960 1
1961 2
1963 1
1964 1
1965 1
1972 2
1973 1
1974 2
1976 1
1977 2
1979 5
1980 1
1981 2
1982 2
1983 3
1985 1
1987 2
1988 1
1989 4
1990 1
1991 1
1992 1
1993 1
1995 2
1996 2
1997 2
1998 2
1999 1
2000 10
2001 13
2002 12
2003 13
2004 18
2005 14
2006 16
2007 18
2008 22
2009 23
2010 16
2011 19
2012 10
2013 21
2014 13
2015 10
2016 7
2017 8
2018 6
2019 3
2020 11
2021 6
2022 6
2023 6
2024 5
2025 0

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345 results

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Page 1
Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.
Auer-Grumbach M, Toegel S, Schabhüttl M, Weinmann D, Chiari C, Bennett DLH, Beetz C, Klein D, Andersen PM, Böhme I, Fink-Puches R, Gonzalez M, Harms MB, Motley W, Reilly MM, Renner W, Rudnik-Schöneborn S, Schlotter-Weigel B, Themistocleous AC, Weishaupt JH, Ludolph AC, Wieland T, Tao F, Abreu L, Windhager R, Zitzelsberger M, Strom TM, Walther T, Scherer SS, Züchner S, Martini R, Senderek J. Auer-Grumbach M, et al. Among authors: renner w. Am J Hum Genet. 2016 Sep 1;99(3):607-623. doi: 10.1016/j.ajhg.2016.07.008. Am J Hum Genet. 2016. PMID: 27588448 Free PMC article.
Telomeres and Age-Related Diseases.
Gruber HJ, Semeraro MD, Renner W, Herrmann M. Gruber HJ, et al. Among authors: renner w. Biomedicines. 2021 Sep 27;9(10):1335. doi: 10.3390/biomedicines9101335. Biomedicines. 2021. PMID: 34680452 Free PMC article. Review.
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
International Consortium for Blood Pressure Genome-Wide Association Studies; Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND; CARDIoGRAM consortium; CKDGen Consortium; KidneyGen Consortium; EchoGen consortium; CHARGE-HF consortium; Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hi… See abstract for full author list ➔ International Consortium for Blood Pressure Genome-Wide Association Studies, et al. Nature. 2011 Sep 11;478(7367):103-9. doi: 10.1038/nature10405. Nature. 2011. PMID: 21909115 Free PMC article.
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.
Lu X, Wang L, Chen S, He L, Yang X, Shi Y, Cheng J, Zhang L, Gu CC, Huang J, Wu T, Ma Y, Li J, Cao J, Chen J, Ge D, Fan Z, Li Y, Zhao L, Li H, Zhou X, Chen L, Liu D, Chen J, Duan X, Hao Y, Wang L, Lu F, Liu Z, Yao C, Shen C, Pu X, Yu L, Fang X, Xu L, Mu J, Wu X, Zheng R, Wu N, Zhao Q, Li Y, Liu X, Wang M, Yu D, Hu D, Ji X, Guo D, Sun D, Wang Q, Yang Y, Liu F, Mao Q, Liang X, Ji J, Chen P, Mo X, Li D, Chai G, Tang Y, Li X, Du Z, Liu X, Dou C, Yang Z, Meng Q, Wang D, Wang R, Yang J, Schunkert H, Samani NJ, Kathiresan S, Reilly MP, Erdmann J; Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Consortium; Peng X, Wu X, Liu D, Yang Y, Chen R, Qiang B, Gu D. Lu X, et al. Nat Genet. 2012 Jul 1;44(8):890-4. doi: 10.1038/ng.2337. Nat Genet. 2012. PMID: 22751097 Free PMC article.
Immune Aging and Immunotherapy in Cancer.
Kaiser M, Semeraro MD, Herrmann M, Absenger G, Gerger A, Renner W. Kaiser M, et al. Among authors: renner w. Int J Mol Sci. 2021 Jun 29;22(13):7016. doi: 10.3390/ijms22137016. Int J Mol Sci. 2021. PMID: 34209842 Free PMC article. Review.
Thrombophilic gene variants.
Steinbrugger I, Haas A, Maier R, Renner W, Mattes D, El-Shabrawi Y, Wedrich A, Schmut O, Weger M. Steinbrugger I, et al. Among authors: renner w. Ophthalmology. 2010 Apr;117(4):856-856.e1. doi: 10.1016/j.ophtha.2009.10.013. Ophthalmology. 2010. PMID: 20346836 No abstract available.
Paroxysmal Sneezing.
Renner WS. Renner WS. Buffalo Med J. 1895 Aug;35(1):31-37. Buffalo Med J. 1895. PMID: 36887504 Free PMC article. No abstract available.
[Bis(1,1'-(2-piperidyl)2,2'-hydroxyethyl)-amine].
Winterfeld K, Renner W. Winterfeld K, et al. Among authors: renner w. Arch Pharm (Weinheim). 1972 Oct;305(10):766-71. doi: 10.1002/ardp.19723051010. Arch Pharm (Weinheim). 1972. PMID: 5085533 German. No abstract available.
Haptoglobin polymorphism and prostate cancer mortality.
Kaiser M, Thurner EM, Mangge H, Herrmann M, Semeraro MD, Renner W, Langsenlehner T. Kaiser M, et al. Among authors: renner w. Sci Rep. 2020 Aug 4;10(1):13117. doi: 10.1038/s41598-020-69333-z. Sci Rep. 2020. PMID: 32753660 Free PMC article.
Review of high-resolution CT of the lung.
Corcoran HL, Renner WR, Milstein MJ. Corcoran HL, et al. Among authors: renner wr. Radiographics. 1992 Sep;12(5):917-39; discussion 940-1. doi: 10.1148/radiographics.12.5.1529134. Radiographics. 1992. PMID: 1529134 Review.
345 results