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

Year Number of Results
2002 6
2003 4
2004 7
2005 2
2006 5
2007 4
2008 3
2009 3
2010 4
2011 5
2012 5
2013 3
2014 1
2015 6
2016 4
2017 7
2018 6
2019 2
2020 5
2021 2
2022 3
2023 6
2024 1

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83 results

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Page 1
Classical twin studies and beyond.
Boomsma D, Busjahn A, Peltonen L. Boomsma D, et al. Among authors: busjahn a. Nat Rev Genet. 2002 Nov;3(11):872-82. doi: 10.1038/nrg932. Nat Rev Genet. 2002. PMID: 12415317 Review.
Anti-ß1-Adrenoreceptor auto-Antibodies in elderly heart failure patients.
Trippel TD, Mueller DN, Obradovic D, Edelmann F, Tahirovic E, Wilck N, Riemekasten G, Dragun D, Busjahn A, Heidecke H, Junker J, Pieske B, Dungen HD, Dechend R. Trippel TD, et al. Among authors: busjahn a. Front Biosci (Landmark Ed). 2019 Mar 1;24(6):1037-1049. doi: 10.2741/4766. Front Biosci (Landmark Ed). 2019. PMID: 30844728 Free article. Clinical Trial.
Exercise blood-drop metabolic profiling links metabolism with perceived exertion.
Opialla T, Gollasch B, Kuich PHJL, Klug L, Rahn G, Busjahn A, Spuler S, Boschmann M, Kirwan JA, Luft FC, Kempa S. Opialla T, et al. Among authors: busjahn a. Front Mol Biosci. 2022 Dec 21;9:1042231. doi: 10.3389/fmolb.2022.1042231. eCollection 2022. Front Mol Biosci. 2022. PMID: 36619172 Free PMC article.
Normobaric hypoxic conditioning in men with metabolic syndrome.
Klug L, Mähler A, Rakova N, Mai K, Schulz-Menger J, Rahn G, Busjahn A, Jordan J, Boschmann M, Luft FC. Klug L, et al. Among authors: busjahn a. Physiol Rep. 2018 Dec;6(24):e13949. doi: 10.14814/phy2.13949. Physiol Rep. 2018. PMID: 30565412 Free PMC article. Clinical Trial.
Soluble (pro)renin receptor in elderly chronic heart failure patients.
Obradovic D, Loncar G, Radenovic S, Tahirovic E, Heidecke H, Schulze-Forster K, Muller D, Busjahn A, Buttner P, Veskovic J, Zdravkovic M, Li H, Li S, Savkovic V, Pieske B, Dungen HD, Dechend R. Obradovic D, et al. Among authors: busjahn a. Front Biosci (Landmark Ed). 2020 Jun 1;25(10):1839-1853. doi: 10.2741/4880. Front Biosci (Landmark Ed). 2020. PMID: 32472760 Free article.
PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, Wefeld-Neuenfeld Y, Bartels-Klein E, Mühl A, Kann M, Schuster H, Chitayat D, Bialer MG, Wienker TF, Ott J, Rittscher K, Liehr T, Jordan J, Plessis G, Tank J, Mai K, Naraghi R, Hodge R, Hopp M, Hattenbach LO, Busjahn A, Rauch A, Vandeput F, Gong M, Rüschendorf F, Hübner N, Haller H, Mundlos S, Bilginturan N, Movsesian MA, Klussmann E, Toka O, Bähring S. Maass PG, et al. Among authors: busjahn a. Nat Genet. 2015 Jun;47(6):647-53. doi: 10.1038/ng.3302. Epub 2015 May 11. Nat Genet. 2015. PMID: 25961942 Free article.
83 results