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Effect of Differences in the Microbiome of Cyp17a1-Deficient Mice on Atherosclerotic Background.
Künstner A, Aherrahrou R, Hirose M, Bruse P, Ibrahim SM, Busch H, Erdmann J, Aherrahrou Z
Cells, 10(6):1292, 23 May 2021
Cited by: 2 articles | PMID: 34070975 | PMCID: PMC8224745
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Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism.
Kessler T, Erdmann J, Vilne B, Bruse P, Kurowski V, Diemert P, Schunkert H, Sager HB
J Transl Med, 14(1):120, 05 May 2016
Cited by: 22 articles | PMID: 27150028 | PMCID: PMC4858885
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Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Pattaro C, Teumer A, Gorski M, Chu AY, Li M, Mijatovic V, Garnaas M, Tin A, Sorice R, Li Y, Taliun D, Olden M, Foster M, Yang Q, Chen MH, Pers TH, Johnson AD, Ko YA, Fuchsberger C, [...] Fox CS
Nat Commun, 7:10023, 21 Jan 2016
Cited by: 323 articles | PMID: 26831199 | PMCID: PMC4735748
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Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community.
Kaess BM, Preis SR, Lieb W, Beiser AS, Yang Q, Chen TC, Hengstenberg C, Erdmann J, Schunkert H, Seshadri S, Vasan RS, CARDIoGRAM, Assimes TL, Deloukas P, Holm H, Kathiresan S, König IR, McPherson R, Reilly MP, [...] Stewart AF
J Am Heart Assoc, 4(3):e001544, 11 Mar 2015
Cited by: 81 articles | PMID: 25762803 | PMCID: PMC4392437
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Genetic predisposition to higher blood pressure increases coronary artery disease risk.
Lieb W, Jansen H, Loley C, Pencina MJ, Nelson CP, Newton-Cheh C, Kathiresan S, Reilly MP, Assimes TL, Boerwinkle E, Hall AS, Hengstenberg C, Laaksonen R, McPherson R, Thorsteinsdottir U, Ziegler A, Peters A, Thompson JR, König IR, [...] CARDIoGRAM
Hypertension, 61(5):995-1001, 11 Mar 2013
Cited by: 53 articles | PMID: 23478099 | PMCID: PMC3855241
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Dysfunctional nitric oxide signalling increases risk of myocardial infarction.
Erdmann J, Stark K, Esslinger UB, Rumpf PM, Koesling D, de Wit C, Kaiser FJ, Braunholz D, Medack A, Fischer M, Zimmermann ME, Tennstedt S, Graf E, Eck S, Aherrahrou Z, Nahrstaedt J, Willenborg C, Bruse P, Brænne I, [...] Schunkert H
Nature, 504(7480):432-436, 10 Nov 2013
Cited by: 160 articles | PMID: 24213632
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Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels.
Holmes MV, Exeter HJ, Folkersen L, Nelson CP, Guardiola M, Cooper JA, Sofat R, Boekholdt SM, Khaw KT, Li KW, Smith AJ, Van't Hooft F, Eriksson P, Franco-Cereceda A, Asselbergs FW, Boer JM, Onland-Moret NC, Hofker M, Erdmann J, [...] CARDIoGRAM Consortium
Circ Cardiovasc Genet, 7(2):144-150, 21 Feb 2014
Cited by: 17 articles | PMID: 24563418 | PMCID: PMC4212409
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Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.
Ho JE, Chen WY, Chen MH, Larson MG, McCabe EL, Cheng S, Ghorbani A, Coglianese E, Emilsson V, Johnson AD, Walter S, Franceschini N, O'Donnell CJ, CARDIoGRAM Consortium, CHARGE Inflammation Working Group, Dehghan A, Lu C, Levy D, Newton-Cheh C, [...] Wang TJ
J Clin Invest, 123(10):4208-4218, 03 Sep 2013
Cited by: 67 articles | PMID: 23999434 | PMCID: PMC3784527
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Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Sabater-Lleal M, Huang J, Chasman D, Naitza S, Dehghan A, Johnson AD, Teumer A, Reiner AP, Folkersen L, Basu S, Rudnicka AR, Trompet S, Mälarstig A, Baumert J, Bis JC, Guo X, Hottenga JJ, Shin SY, Lopez LM, [...] O'Donnell CJ
Circulation, 128(12):1310-1324, 22 Aug 2013
Cited by: 101 articles | PMID: 23969696 | PMCID: PMC3842025
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Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.
Reiner AP, Hartiala J, Zeller T, Bis JC, Dupuis J, Fornage M, Baumert J, Kleber ME, Wild PS, Baldus S, Bielinski SJ, Fontes JD, Illig T, Keating BJ, Lange LA, Ojeda F, Müller-Nurasyid M, Munzel TF, Psaty BM, [...] Allayee H
Hum Mol Genet, 22(16):3381-3393, 24 Apr 2013
Cited by: 17 articles | PMID: 23620142 | PMCID: PMC3723315
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The shared allelic architecture of adiponectin levels and coronary artery disease.
Dastani Z, Johnson T, Kronenberg F, Nelson CP, Assimes TL, März W, CARDIoGRAM Consortium, ADIPOGen Consortium, Richards JB
Atherosclerosis, 229(1):145-148, 22 Apr 2013
Cited by: 25 articles | PMID: 23664276 | PMCID: PMC6139652
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RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.
Herder C, Peeters W, Illig T, Baumert J, de Kleijn DP, Moll FL, Poschen U, Klopp N, Müller-Nurasyid M, Roden M, Preuss M, CARDIoGRAM Consortium, Karakas M, Meisinger C, Thorand B, Pasterkamp G, Koenig W, Assimes TL, Deloukas P, [...] Stewart AF
PLoS One, 6(12):e25734, 06 Dec 2011
Cited by: 29 articles | PMID: 22162987 | PMCID: PMC3232218
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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, [...] Gu D
Nat Genet, 44(8):890-894, 01 Jul 2012
Cited by: 217 articles | PMID: 22751097 | PMCID: PMC3927410
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Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.
O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, Hwang SJ, Sun YV, Province MA, Aspelund T, Dehghan A, Hoffmann U, Bielak LF, Zhang Q, Eiriksdottir G, van Duijn CM, Fox CS, de Andrade M, Kraja AT, Sigurdsson S, [...] Witteman JC
Circulation, 124(25):2855-2864, 05 Dec 2011
Cited by: 196 articles | PMID: 22144573 | PMCID: PMC3397173
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Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.
Demirkan A, van Duijn CM, Ugocsai P, Isaacs A, Pramstaller PP, Liebisch G, Wilson JF, Johansson Å, Rudan I, Aulchenko YS, Kirichenko AV, Janssens AC, Jansen RC, Gnewuch C, Domingues FS, Pattaro C, Wild SH, Jonasson I, Polasek O, [...] EUROSPAN consortium
PLoS Genet, 8(2):e1002490, 16 Feb 2012
Cited by: 141 articles | PMID: 22359512 | PMCID: PMC3280968
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Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Wain LV, Verwoert GC, O'Reilly PF, Shi G, Johnson T, Johnson AD, Bochud M, Rice KM, Henneman P, Smith AV, Ehret GB, Amin N, Larson MG, Mooser V, Hadley D, Dörr M, Bis JC, Aspelund T, Esko T, [...] van Duijn CM
Nat Genet, 43(10):1005-1011, 11 Sep 2011
Cited by: 300 articles | PMID: 21909110 | PMCID: PMC3445021
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Human metabolic individuality in biomedical and pharmaceutical research.
Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E, CARDIoGRAM, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, [...] Gieger C
Nature, 477(7362):54-60, 31 Aug 2011
Cited by: 649 articles | PMID: 21886157 | PMCID: PMC3832838
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Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.
Erdmann J, Willenborg C, Nahrstaedt J, Preuss M, König IR, Baumert J, Linsel-Nitschke P, Gieger C, Tennstedt S, Belcredi P, Aherrahrou Z, Klopp N, Loley C, Stark K, Hengstenberg C, Bruse P, Freyer J, Wagner AK, Medack A, [...] Schunkert H
Eur Heart J, 32(2):158-168, 18 Nov 2010
Cited by: 83 articles | PMID: 21088011
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Post-genomic update on a classical candidate gene for coronary artery disease: ESR1.
Lucas G, Lluís-Ganella C, Subirana I, Sentí M, Willenborg C, Musameh MD, Schwartz SM, O'Donnell CJ, Melander O, Salomaa V, Elosua R, CARDIoGRAM Consortium
Circ Cardiovasc Genet, 4(6):647-654, 09 Oct 2011
Cited by: 4 articles | PMID: 21984528 | PMCID: PMC3260440
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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, [...] Johnson T
Nature, 478(7367):103-109, 11 Sep 2011
Cited by: 1304 articles | PMID: 21909115 | PMCID: PMC3340926
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Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.
Linsel-Nitschke P, Heeren J, Aherrahrou Z, Bruse P, Gieger C, Illig T, Prokisch H, Heim K, Doering A, Peters A, Meitinger T, Wichmann HE, Hinney A, Reinehr T, Roth C, Ortlepp JR, Soufi M, Sattler AM, Schaefer J, [...] Erdmann J
Atherosclerosis, 208(1):183-189, 08 Jul 2009
Cited by: 97 articles | PMID: 19660754
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Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.
Linsel-Nitschke P, Götz A, Medack A, König IR, Bruse P, Lieb W, Mayer B, Stark K, Hengstenberg C, Fischer M, Baessler A, Ziegler A, Schunkert H, Erdmann J
Clin Sci (Lond), 115(10):309-315, 01 Nov 2008
Cited by: 22 articles | PMID: 18318662
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New susceptibility locus for coronary artery disease on chromosome 3q22.3.
Erdmann J, Grosshennig A, Braund PS, König IR, Hengstenberg C, Hall AS, Linsel-Nitschke P, Kathiresan S, Wright B, Trégouët DA, Cambien F, Bruse P, Aherrahrou Z, Wagner AK, Stark K, Schwartz SM, Salomaa V, Elosua R, Melander O, [...] Schunkert H
Nat Genet, 41(3):280-282, 08 Feb 2009
Cited by: 321 articles | PMID: 19198612 | PMCID: PMC2695543
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The 4977 bp deletion of mitochondrial DNA in human skeletal muscle, heart and different areas of the brain: a useful biomarker or more?
Meissner C, Bruse P, Mohamed SA, Schulz A, Warnk H, Storm T, Oehmichen M
Exp Gerontol, 43(7):645-652, 20 Mar 2008
Cited by: 93 articles | PMID: 18439778
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Large scale association analysis of novel genetic loci for coronary artery disease.
Coronary Artery Disease Consortium, Samani NJ, Deloukas P, Erdmann J, Hengstenberg C, Kuulasmaa K, McGinnis R, Schunkert H, Soranzo N, Thompson J, Tiret L, Ziegler A
Arterioscler Thromb Vasc Biol, 29(5):774-780, 22 Jan 2009
Cited by: 98 articles | PMID: 19164808 | PMCID: PMC3315048
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1-25 of 32 results

1 2

Search life-sciences literature (45,100,050 articles, preprints and more)

Search results

Effect of Differences in the Microbiome of Cyp17a1-Deficient Mice on Atherosclerotic Background.

Serum microRNA-1233 is a specific biomarker for diagnosing acute pulmonary embolism.

Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.

Circulating brain-derived neurotrophic factor concentrations and the risk of cardiovascular disease in the community.

Genetic predisposition to higher blood pressure increases coronary artery disease risk.

Dysfunctional nitric oxide signalling increases risk of myocardial infarction.

Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels.

Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.

Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.

Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.

The shared allelic architecture of adiponectin levels and coronary artery disease.

RANTES/CCL5 and risk for coronary events: results from the MONICA/KORA Augsburg case-cohort, Athero-Express and CARDIoGRAM studies.

Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.

Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.

Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.

Human metabolic individuality in biomedical and pharmaceutical research.

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.

Post-genomic update on a classical candidate gene for coronary artery disease: ESR1.

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.

Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.

Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population.

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

The 4977 bp deletion of mitochondrial DNA in human skeletal muscle, heart and different areas of the brain: a useful biomarker or more?

Large scale association analysis of novel genetic loci for coronary artery disease.

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