Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

975 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene.
Davison LJ, Wallace C, Cooper JD, Cope NF, Wilson NK, Smyth DJ, Howson JM, Saleh N, Al-Jeffery A, Angus KL, Stevens HE, Nutland S, Duley S, Coulson RM, Walker NM, Burren OS, Rice CM, Cambien F, Zeller T, Munzel T, Lackner K, Blakenberg S; Cardiogenics Consortium; Fraser P, Gottgens B, Todd JA, Attwood T, Belz S, Braund P, Cambien F, Cooper J, Crisp-Hihn A, Diemert P, Deloukas P, Foad N, Erdmann J, Goodall AH, Gracey J, Gray E, Williams RG, Heimerl S, Hengstenberg C, Jolley J, Krishnan U, Lloyd-Jones H, Lugauer I, Lundmark P, Maouche S, Moore JS, Muir D, Murray E, Nelson CP, Neudert J, Niblett D, O'Leary K, Ouwehand WH, Pollard H, Rankin A, Rice CM, Sager H, Samani NJ, Sambrook J, Schmitz G, Scholz M, Schroeder L, Schunkert H, Syvannen AC, Tennstedt S, Wallace C. Davison LJ, et al. Among authors: schunkert h. Hum Mol Genet. 2012 Jan 15;21(2):322-33. doi: 10.1093/hmg/ddr468. Epub 2011 Oct 11. Hum Mol Genet. 2012. PMID: 21989056 Free PMC article.
Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease.
Baessler A, Fischer M, Mayer B, Koehler M, Wiedmann S, Stark K, Doering A, Erdmann J, Riegger G, Schunkert H, Kwitek AE, Hengstenberg C. Baessler A, et al. Among authors: schunkert h. Hum Mol Genet. 2007 Apr 15;16(8):887-99. doi: 10.1093/hmg/ddm033. Epub 2007 Feb 26. Hum Mol Genet. 2007. PMID: 17324965
Lymphotoxin-alpha and galectin-2 SNPs are not associated with myocardial infarction in two different German populations.
Sedlacek K, Neureuther K, Mueller JC, Stark K, Fischer M, Baessler A, Reinhard W, Broeckel U, Lieb W, Erdmann J, Schunkert H, Riegger G, Illig T, Meitinger T, Hengstenberg C. Sedlacek K, et al. Among authors: schunkert h. J Mol Med (Berl). 2007 Sep;85(9):997-1004. doi: 10.1007/s00109-007-0211-4. Epub 2007 May 12. J Mol Med (Berl). 2007. PMID: 17497114
A locus on chromosome 10 influences C-reactive protein levels in two independent populations.
Broeckel U, Hengstenberg C, Mayer B, Maresso K, Gaudet D, Seda O, Tremblay J, Holmer S, Erdmann J, Glöckner C, Harrison M, Martin LJ, Williams JT, Schmitz G, Riegger GA, Jacob HJ, Hamet P, Schunkert H. Broeckel U, et al. Among authors: schunkert h. Hum Genet. 2007 Aug;122(1):95-102. doi: 10.1007/s00439-007-0380-9. Epub 2007 May 26. Hum Genet. 2007. PMID: 17530289
Genomewide association analysis of coronary artery disease.
Samani NJ, Erdmann J, Hall AS, Hengstenberg C, Mangino M, Mayer B, Dixon RJ, Meitinger T, Braund P, Wichmann HE, Barrett JH, König IR, Stevens SE, Szymczak S, Tregouet DA, Iles MM, Pahlke F, Pollard H, Lieb W, Cambien F, Fischer M, Ouwehand W, Blankenberg S, Balmforth AJ, Baessler A, Ball SG, Strom TM, Braenne I, Gieger C, Deloukas P, Tobin MD, Ziegler A, Thompson JR, Schunkert H; WTCCC and the Cardiogenics Consortium. Samani NJ, et al. Among authors: schunkert h. N Engl J Med. 2007 Aug 2;357(5):443-53. doi: 10.1056/NEJMoa072366. Epub 2007 Jul 18. N Engl J Med. 2007. PMID: 17634449 Free PMC article.
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
Schunkert H, Götz A, Braund P, McGinnis R, Tregouet DA, Mangino M, Linsel-Nitschke P, Cambien F, Hengstenberg C, Stark K, Blankenberg S, Tiret L, Ducimetiere P, Keniry A, Ghori MJ, Schreiber S, El Mokhtari NE, Hall AS, Dixon RJ, Goodall AH, Liptau H, Pollard H, Schwarz DF, Hothorn LA, Wichmann HE, König IR, Fischer M, Meisinger C, Ouwehand W, Deloukas P, Thompson JR, Erdmann J, Ziegler A, Samani NJ; Cardiogenics Consortium. Schunkert H, et al. Circulation. 2008 Apr 1;117(13):1675-84. doi: 10.1161/CIRCULATIONAHA.107.730614. Epub 2008 Mar 24. Circulation. 2008. PMID: 18362232 Free PMC article.
Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction.
Lieb W, Zeller T, Mangino M, Götz A, Braund P, Wenzel JJ, Horn C, Proust C, Linsel-Nitschke P, Amouyel P, Bruse P, Arveiler D, König IR, Ferrières J, Ziegler A, Balmforth AJ, Evans A, Ducimetière P, Cambien F, Hengstenberg C, Stark K, Hall AS, Schunkert H, Blankenberg S, Samani NJ, Erdmann J, Tiret L. Lieb W, et al. Among authors: schunkert h. J Mol Med (Berl). 2008 Oct;86(10):1163-70. doi: 10.1007/s00109-008-0376-5. Epub 2008 Jul 1. J Mol Med (Berl). 2008. PMID: 18592168
975 results