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

Year Number of Results
1982 2
1983 2
1984 2
1985 3
1986 1
1987 1
1988 1
1989 1
1990 8
1991 7
1992 4
1993 6
1994 9
1995 5
1996 6
1997 5
1998 7
1999 5
2000 11
2001 7
2002 9
2003 3
2004 5
2005 4
2006 3
2007 2
2008 2
2009 1
2010 1
2011 3
2012 3
2013 4
2014 2
2015 3
2016 2
2017 5
2018 3
2019 1
2020 1
2021 4
2022 5
2023 8
2024 4

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164 results

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Page 1
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Lahm H, Jia M, Dreßen M, Wirth F, Puluca N, Gilsbach R, Keavney BD, Cleuziou J, Beck N, Bondareva O, Dzilic E, Burri M, König KC, Ziegelmüller JA, Abou-Ajram C, Neb I, Zhang Z, Doppler SA, Mastantuono E, Lichtner P, Eckstein G, Hörer J, Ewert P, Priest JR, Hein L, Lange R, Meitinger T, Cordell HJ, Müller-Myhsok B, Krane M. Lahm H, et al. J Clin Invest. 2021 Jan 19;131(2):e141837. doi: 10.1172/JCI141837. J Clin Invest. 2021. PMID: 33201861 Free PMC article. Clinical Trial.
Cardiac fibroblasts: more than mechanical support.
Doppler SA, Carvalho C, Lahm H, Deutsch MA, Dreßen M, Puluca N, Lange R, Krane M. Doppler SA, et al. Among authors: lahm h. J Thorac Dis. 2017 Mar;9(Suppl 1):S36-S51. doi: 10.21037/jtd.2017.03.122. J Thorac Dis. 2017. PMID: 28446967 Free PMC article. Review.
Elucidation of the genetic causes of bicuspid aortic valve disease.
Gehlen J, Stundl A, Debiec R, Fontana F, Krane M, Sharipova D, Nelson CP, Al-Kassou B, Giel AS, Sinning JM, Bruenger CMH, Zelck CF, Koebbe LL, Braund PS, Webb TR, Hetherington S, Ensminger S, Fujita B, Mohamed SA, Shrestha M, Krueger H, Siepe M, Kari FA, Nordbeck P, Buravezky L, Kelm M, Veulemans V, Adam M, Baldus S, Laugwitz KL, Haas Y, Karck M, Mehlhorn U, Conzelmann LO, Breitenbach I, Lebherz C, Urbanski P, Kim WK, Kandels J, Ellinghaus D, Nowak-Goettl U, Hoffmann P, Wirth F, Doppler S, Lahm H, Dreßen M, von Scheidt M, Knoll K, Kessler T, Hengstenberg C, Schunkert H, Nickenig G, Nöthen MM, Bolger AP, Abdelilah-Seyfried S, Samani NJ, Erdmann J, Trenkwalder T, Schumacher J. Gehlen J, et al. Among authors: lahm h. Cardiovasc Res. 2023 May 2;119(3):857-866. doi: 10.1093/cvr/cvac099. Cardiovasc Res. 2023. PMID: 35727948 Free PMC article.
Distinct Genetic Risk Profile in Aortic Stenosis Compared With Coronary Artery Disease.
Trenkwalder T, Maj C, Al-Kassou B, Debiec R, Doppler SA, Musameh MD, Nelson CP, Dasmeh P, Grover S, Knoll K, Naamanka J, Mordi IR, Braund PS, Dreßen M, Lahm H, Wirth F, Baldus S, Kelm M, von Scheidt M, Krefting J, Ellinghaus D, Small AM, Peloso GM, Natarajan P, Thanassoulis G, Engert JC, Dufresne L, Franke A, Görg S, Laudes M, Nowak-Göttl U, Vaht M, Metspalu A, Stoll M, Berger K, Pellegrini C, Kastrati A, Hengstenberg C, Lang CC, Kessler T, Hovatta I, Nickenig G, Nöthen MM, Krane M, Schunkert H, Samani NJ, Schumacher J, Kals M, Reigo A, Teder-Laving M, Gehlen J, Webb TR, Giel AS, Koebbe LL, Feirer N, Billmann M, Srinivasan S, Zimmer S, Palmer CNA, Li L, Yang C, Borisov O, Adam M, Veulemans V, Joner M, Xhepa E; TARGET Consortium; Estonian Biobank; and the European Consortium for Genetics of Aortic Stenosis (EGAS). Trenkwalder T, et al. Among authors: lahm h. JAMA Cardiol. 2024 Nov 6:e243738. doi: 10.1001/jamacardio.2024.3738. Online ahead of print. JAMA Cardiol. 2024. PMID: 39504041
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes.
Yu M, Aguirre M, Jia M, Gjoni K, Cordova-Palomera A, Munger C, Amgalan D, Rosa Ma X, Pereira A, Tcheandjieu C, Seidman C, Seidman J, Tristani-Firouzi M, Chung W, Goldmuntz E, Srivastava D, Loos RJF, Chami N, Cordell H, Dreßen M, Mueller-Myhsok B, Lahm H, Krane M, Pollard KS, Engreitz JM, Gagliano Taliun SA, Gelb BD, Priest JR. Yu M, et al. Among authors: lahm h. Circ Genom Precis Med. 2023 Jun;16(3):258-266. doi: 10.1161/CIRCGEN.122.003968. Epub 2023 Apr 7. Circ Genom Precis Med. 2023. PMID: 37026454 Free PMC article.
Myosin binding protein H-like (MYBPHL): a promising biomarker to predict atrial damage.
Lahm H, Dreßen M, Beck N, Doppler S, Deutsch MA, Matsushima S, Neb I, König KC, Sideris K, Voss S, Eschenbach L, Puluca N, Deisenhofer I, Doll S, Holdenrieder S, Mann M, Lange R, Krane M. Lahm H, et al. Sci Rep. 2019 Jul 10;9(1):9986. doi: 10.1038/s41598-019-46123-w. Sci Rep. 2019. PMID: 31292467 Free PMC article.
Region and cell-type resolved quantitative proteomic map of the human heart.
Doll S, Dreßen M, Geyer PE, Itzhak DN, Braun C, Doppler SA, Meier F, Deutsch MA, Lahm H, Lange R, Krane M, Mann M. Doll S, et al. Among authors: lahm h. Nat Commun. 2017 Nov 13;8(1):1469. doi: 10.1038/s41467-017-01747-2. Nat Commun. 2017. PMID: 29133944 Free PMC article.
Sequential Defects in Cardiac Lineage Commitment and Maturation Cause Hypoplastic Left Heart Syndrome.
Krane M, Dreßen M, Santamaria G, My I, Schneider CM, Dorn T, Laue S, Mastantuono E, Berutti R, Rawat H, Gilsbach R, Schneider P, Lahm H, Schwarz S, Doppler SA, Paige S, Puluca N, Doll S, Neb I, Brade T, Zhang Z, Abou-Ajram C, Northoff B, Holdt LM, Sudhop S, Sahara M, Goedel A, Dendorfer A, Tjong FVY, Rijlaarsdam ME, Cleuziou J, Lang N, Kupatt C, Bezzina C, Lange R, Bowles NE, Mann M, Gelb BD, Crotti L, Hein L, Meitinger T, Wu S, Sinnecker D, Gruber PJ, Laugwitz KL, Moretti A. Krane M, et al. Among authors: lahm h. Circulation. 2021 Oct 26;144(17):1409-1428. doi: 10.1161/CIRCULATIONAHA.121.056198. Epub 2021 Oct 25. Circulation. 2021. PMID: 34694888 Free PMC article.
164 results