Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 58

1.

Probing the RNA-Binding Proteome from Yeast to Man: Major Advances and Challenges.

Beckmann BM, Granneman S.

Methods Mol Biol. 2019;2049:213-231. doi: 10.1007/978-1-4939-9736-7_13.

PMID:
31602614
2.

Fast and unbiased purification of RNA-protein complexes after UV cross-linking.

Urdaneta EC, Beckmann BM.

Methods. 2019 Oct 3. pii: S1046-2023(18)30486-9. doi: 10.1016/j.ymeth.2019.09.013. [Epub ahead of print]

3.

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry.

Crotti L, Spazzolini C, Tester DJ, Ghidoni A, Baruteau AE, Beckmann BM, Behr ER, Bennett JS, Bezzina CR, Bhuiyan ZA, Celiker A, Cerrone M, Dagradi F, De Ferrari GM, Etheridge SP, Fatah M, Garcia-Pavia P, Al-Ghamdi S, Hamilton RM, Al-Hassnan ZN, Horie M, Jimenez-Jaimez J, Kanter RJ, Kaski JP, Kotta MC, Lahrouchi N, Makita N, Norrish G, Odland HH, Ohno S, Papagiannis J, Parati G, Sekarski N, Tveten K, Vatta M, Webster G, Wilde AAM, Wojciak J, George AL, Ackerman MJ, Schwartz PJ.

Eur Heart J. 2019 Sep 14;40(35):2964-2975. doi: 10.1093/eurheartj/ehz311.

PMID:
31170290
4.

TriPepSVM: de novo prediction of RNA-binding proteins based on short amino acid motifs.

Bressin A, Schulte-Sasse R, Figini D, Urdaneta EC, Beckmann BM, Marsico A.

Nucleic Acids Res. 2019 May 21;47(9):4406-4417. doi: 10.1093/nar/gkz203.

5.

Purification of cross-linked RNA-protein complexes by phenol-toluol extraction.

Urdaneta EC, Vieira-Vieira CH, Hick T, Wessels HH, Figini D, Moschall R, Medenbach J, Ohler U, Granneman S, Selbach M, Beckmann BM.

Nat Commun. 2019 Mar 1;10(1):990. doi: 10.1038/s41467-019-08942-3.

6.

Sudden unexpected death in the young - Value of massive parallel sequencing in postmortem genetic analyses.

Scheiper S, Ramos-Luis E, Blanco-Verea A, Niess C, Beckmann BM, Schmidt U, Kettner M, Geisen C, Verhoff MA, Brion M, Kauferstein S.

Forensic Sci Int. 2018 Dec;293:70-76. doi: 10.1016/j.forsciint.2018.09.034. Epub 2018 Oct 26.

PMID:
30415094
7.

Characterization of a novel KCNJ2 sequence variant detected in Andersen-Tawil syndrome patients.

Scheiper S, Hertel B, Beckmann BM, Kääb S, Thiel G, Kauferstein S.

BMC Med Genet. 2017 Oct 10;18(1):113. doi: 10.1186/s12881-017-0472-x.

8.

Relevance of molecular testing in patients with a family history of sudden death.

Kauferstein S, Herz N, Scheiper S, Biel S, Jenewein T, Kunis M, Erkapic D, Beckmann BM, Neumann T.

Forensic Sci Int. 2017 Jul;276:18-23. doi: 10.1016/j.forsciint.2017.04.001. Epub 2017 Apr 13.

PMID:
28472724
9.

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene.

Jenewein T, Beckmann BM, Rose S, Osterhues HH, Schmidt U, Wolpert C, Miny P, Marschall C, Alders M, Bezzina CR, Wilde AAM, Kääb S, Kauferstein S.

Forensic Sci Int. 2017 Jun;275:187-194. doi: 10.1016/j.forsciint.2017.02.038. Epub 2017 Mar 20.

PMID:
28391114
10.

RNA interactome capture in yeast.

Beckmann BM.

Methods. 2017 Apr 15;118-119:82-92. doi: 10.1016/j.ymeth.2016.12.008. Epub 2016 Dec 16.

11.

Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations.

Ortiz-Bonnin B, Rinné S, Moss R, Streit AK, Scharf M, Richter K, Stöber A, Pfeufer A, Seemann G, Kääb S, Beckmann BM, Decher N.

Pflugers Arch. 2016 Aug;468(8):1375-87. doi: 10.1007/s00424-016-1844-3. Epub 2016 Jun 11.

PMID:
27287068
12.

The expanding universe of ribonucleoproteins: of novel RNA-binding proteins and unconventional interactions.

Beckmann BM, Castello A, Medenbach J.

Pflugers Arch. 2016 Jun;468(6):1029-40. doi: 10.1007/s00424-016-1819-4. Epub 2016 May 10. Review.

13.

Early repolarization pattern is the strongest predictor of arrhythmia recurrence in patients with idiopathic ventricular fibrillation: results from a single centre long-term follow-up over 20 years.

Siebermair J, Sinner MF, Beckmann BM, Laubender RP, Martens E, Sattler S, Fichtner S, Estner HL, Kääb S, Wakili R.

Europace. 2016 May;18(5):718-25. doi: 10.1093/europace/euv301. Epub 2016 Jan 11.

PMID:
26759124
14.

Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia.

Tülümen E, Schulze-Bahr E, Zumhagen S, Stallmeyer B, Seebohm G, Beckmann BM, Kääb S, Rudic B, Liebe V, Wolpert C, Herrera-Siklody C, Veltmann C, Schimpf R, Borggrefe M.

Europace. 2016 Oct;18(10):1587-1592. Epub 2015 Dec 23.

PMID:
26705564
15.

The RNA-binding proteomes from yeast to man harbour conserved enigmRBPs.

Beckmann BM, Horos R, Fischer B, Castello A, Eichelbaum K, Alleaume AM, Schwarzl T, Curk T, Foehr S, Huber W, Krijgsveld J, Hentze MW.

Nat Commun. 2015 Dec 3;6:10127. doi: 10.1038/ncomms10127.

16.

Purkinje-related ventricular fibrillation associated with a homozygous H558R polymorphism in the sodium channel SCN5A gene.

Reithmann C, Beckmann BM, Kääb S.

Europace. 2016 Jun;18(6):896. doi: 10.1093/europace/euv134. Epub 2015 Jun 17. No abstract available.

PMID:
26084969
17.

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.

Kolder ICRM, Tanck MWT, Postema PG, Barc J, Sinner MF, Zumhagen S, Husemann A, Stallmeyer B, Koopmann TT, Hofman N, Pfeufer A, Lichtner P, Meitinger T, Beckmann BM, Myerburg RJ, Bishopric NH, Roden DM, Kääb S, Wilde AAM, Schott JJ, Schulze-Bahr E, Bezzina CR.

Circ Cardiovasc Genet. 2015 Jun;8(3):447-456. doi: 10.1161/CIRCGENETICS.114.000785. Epub 2015 Mar 3.

18.

Photo-cross-linking and high-resolution mass spectrometry for assignment of RNA-binding sites in RNA-binding proteins.

Kramer K, Sachsenberg T, Beckmann BM, Qamar S, Boon KL, Hentze MW, Kohlbacher O, Urlaub H.

Nat Methods. 2014 Oct;11(10):1064-70. doi: 10.1038/nmeth.3092. Epub 2014 Aug 31.

19.

Incidence of sudden cardiac death in Germany: results from an emergency medical service registry in Lower Saxony.

Martens E, Sinner MF, Siebermair J, Raufhake C, Beckmann BM, Veith S, Düvel D, Steinbeck G, Kääb S.

Europace. 2014 Dec;16(12):1752-8. doi: 10.1093/europace/euu153. Epub 2014 Jul 24.

20.

Genomewide comparison and novel ncRNAs of Aquificales.

Lechner M, Nickel AI, Wehner S, Riege K, Wieseke N, Beckmann BM, Hartmann RK, Marz M.

BMC Genomics. 2014 Jun 25;15:522. doi: 10.1186/1471-2164-15-522.

21.

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

Arking DE, Pulit SL, Crotti L, van der Harst P, Munroe PB, Koopmann TT, Sotoodehnia N, Rossin EJ, Morley M, Wang X, Johnson AD, Lundby A, Gudbjartsson DF, Noseworthy PA, Eijgelsheim M, Bradford Y, Tarasov KV, Dörr M, Müller-Nurasyid M, Lahtinen AM, Nolte IM, Smith AV, Bis JC, Isaacs A, Newhouse SJ, Evans DS, Post WS, Waggott D, Lyytikäinen LP, Hicks AA, Eisele L, Ellinghaus D, Hayward C, Navarro P, Ulivi S, Tanaka T, Tester DJ, Chatel S, Gustafsson S, Kumari M, Morris RW, Naluai ÅT, Padmanabhan S, Kluttig A, Strohmer B, Panayiotou AG, Torres M, Knoflach M, Hubacek JA, Slowikowski K, Raychaudhuri S, Kumar RD, Harris TB, Launer LJ, Shuldiner AR, Alonso A, Bader JS, Ehret G, Huang H, Kao WH, Strait JB, Macfarlane PW, Brown M, Caulfield MJ, Samani NJ, Kronenberg F, Willeit J; CARe Consortium; COGENT Consortium, Smith JG, Greiser KH, Meyer Zu Schwabedissen H, Werdan K, Carella M, Zelante L, Heckbert SR, Psaty BM, Rotter JI, Kolcic I, Polašek O, Wright AF, Griffin M, Daly MJ; DCCT/EDIC, Arnar DO, Hólm H, Thorsteinsdottir U; eMERGE Consortium, Denny JC, Roden DM, Zuvich RL, Emilsson V, Plump AS, Larson MG, O'Donnell CJ, Yin X, Bobbo M, D'Adamo AP, Iorio A, Sinagra G, Carracedo A, Cummings SR, Nalls MA, Jula A, Kontula KK, Marjamaa A, Oikarinen L, Perola M, Porthan K, Erbel R, Hoffmann P, Jöckel KH, Kälsch H, Nöthen MM; HRGEN Consortium, den Hoed M, Loos RJ, Thelle DS, Gieger C, Meitinger T, Perz S, Peters A, Prucha H, Sinner MF, Waldenberger M, de Boer RA, Franke L, van der Vleuten PA, Beckmann BM, Martens E, Bardai A, Hofman N, Wilde AA, Behr ER, Dalageorgou C, Giudicessi JR, Medeiros-Domingo A, Barc J, Kyndt F, Probst V, Ghidoni A, Insolia R, Hamilton RM, Scherer SW, Brandimarto J, Margulies K, Moravec CE, del Greco M F, Fuchsberger C, O'Connell JR, Lee WK, Watt GC, Campbell H, Wild SH, El Mokhtari NE, Frey N, Asselbergs FW, Mateo Leach I, Navis G, van den Berg MP, van Veldhuisen DJ, Kellis M, Krijthe BP, Franco OH, Hofman A, Kors JA, Uitterlinden AG, Witteman JC, Kedenko L, Lamina C, Oostra BA, Abecasis GR, Lakatta EG, Mulas A, Orrú M, Schlessinger D, Uda M, Markus MR, Völker U, Snieder H, Spector TD, Ärnlöv J, Lind L, Sundström J, Syvänen AC, Kivimaki M, Kähönen M, Mononen N, Raitakari OT, Viikari JS, Adamkova V, Kiechl S, Brion M, Nicolaides AN, Paulweber B, Haerting J, Dominiczak AF, Nyberg F, Whincup PH, Hingorani AD, Schott JJ, Bezzina CR, Ingelsson E, Ferrucci L, Gasparini P, Wilson JF, Rudan I, Franke A, Mühleisen TW, Pramstaller PP, Lehtimäki TJ, Paterson AD, Parsa A, Liu Y, van Duijn CM, Siscovick DS, Gudnason V, Jamshidi Y, Salomaa V, Felix SB, Sanna S, Ritchie MD, Stricker BH, Stefansson K, Boyer LA, Cappola TP, Olsen JV, Lage K, Schwartz PJ, Kääb S, Chakravarti A, Ackerman MJ, Pfeufer A, de Bakker PI, Newton-Cheh C.

Nat Genet. 2014 Aug;46(8):826-36. doi: 10.1038/ng.3014. Epub 2014 Jun 22.

22.

Novel calmodulin mutations associated with congenital arrhythmia susceptibility.

Makita N, Yagihara N, Crotti L, Johnson CN, Beckmann BM, Roh MS, Shigemizu D, Lichtner P, Ishikawa T, Aiba T, Homfray T, Behr ER, Klug D, Denjoy I, Mastantuono E, Theisen D, Tsunoda T, Satake W, Toda T, Nakagawa H, Tsuji Y, Tsuchiya T, Yamamoto H, Miyamoto Y, Endo N, Kimura A, Ozaki K, Motomura H, Suda K, Tanaka T, Schwartz PJ, Meitinger T, Kääb S, Guicheney P, Shimizu W, Bhuiyan ZA, Watanabe H, Chazin WJ, George AL Jr.

Circ Cardiovasc Genet. 2014 Aug;7(4):466-74. doi: 10.1161/CIRCGENETICS.113.000459. Epub 2014 Jun 10.

23.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

Bezzina CR, Barc J, Mizusawa Y, Remme CA, Gourraud JB, Simonet F, Verkerk AO, Schwartz PJ, Crotti L, Dagradi F, Guicheney P, Fressart V, Leenhardt A, Antzelevitch C, Bartkowiak S, Borggrefe M, Schimpf R, Schulze-Bahr E, Zumhagen S, Behr ER, Bastiaenen R, Tfelt-Hansen J, Olesen MS, Kääb S, Beckmann BM, Weeke P, Watanabe H, Endo N, Minamino T, Horie M, Ohno S, Hasegawa K, Makita N, Nogami A, Shimizu W, Aiba T, Froguel P, Balkau B, Lantieri O, Torchio M, Wiese C, Weber D, Wolswinkel R, Coronel R, Boukens BJ, Bézieau S, Charpentier E, Chatel S, Despres A, Gros F, Kyndt F, Lecointe S, Lindenbaum P, Portero V, Violleau J, Gessler M, Tan HL, Roden DM, Christoffels VM, Le Marec H, Wilde AA, Probst V, Schott JJ, Dina C, Redon R.

Nat Genet. 2013 Sep;45(9):1044-9. doi: 10.1038/ng.2712. Epub 2013 Jul 21. Erratum in: Nat Genet. 2013 Nov;45(11):1409. Borggrefe, Martin [added]; Schimpf, Rainer [added].

24.

Clinical utility gene card for: long-QT syndrome (types 1-13).

Beckmann BM, Wilde AA, Kääb S.

Eur J Hum Genet. 2013 Oct;21(10). doi: 10.1038/ejhg.2013.28. Epub 2013 Mar 20. No abstract available.

25.

Calmodulin mutations associated with recurrent cardiac arrest in infants.

Crotti L, Johnson CN, Graf E, De Ferrari GM, Cuneo BF, Ovadia M, Papagiannis J, Feldkamp MD, Rathi SG, Kunic JD, Pedrazzini M, Wieland T, Lichtner P, Beckmann BM, Clark T, Shaffer C, Benson DW, Kääb S, Meitinger T, Strom TM, Chazin WJ, Schwartz PJ, George AL Jr.

Circulation. 2013 Mar 5;127(9):1009-17. doi: 10.1161/CIRCULATIONAHA.112.001216. Epub 2013 Feb 6.

26.

[Magnetic resonance imaging of hypertrophic cardiomyopathy : evaluation of diastolic function].

Schwarz F, Schwab F, Beckmann BM, Schuessler F, Zinsser D, Gölz T, Kääb S, Reiser MF, Theisen D.

Radiologe. 2013 Jan;53(1):15-23. doi: 10.1007/s00117-012-2381-5. German.

PMID:
23338245
27.

Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: higher recurrence of events under metoprolol.

Chockalingam P, Crotti L, Girardengo G, Johnson JN, Harris KM, van der Heijden JF, Hauer RN, Beckmann BM, Spazzolini C, Rordorf R, Rydberg A, Clur SA, Fischer M, van den Heuvel F, Kääb S, Blom NA, Ackerman MJ, Schwartz PJ, Wilde AA.

J Am Coll Cardiol. 2012 Nov 13;60(20):2092-9. doi: 10.1016/j.jacc.2012.07.046. Epub 2012 Oct 17.

28.

[Genetic testing in hereditary arrythmia syndromes today and in the future].

Beckmann BM, Kääb S.

Herzschrittmacherther Elektrophysiol. 2012 Sep;23(3):161-6. doi: 10.1007/s00399-012-0230-x. Epub 2012 Sep 20. German.

PMID:
22993117
29.

A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.

Sinner MF, Porthan K, Noseworthy PA, Havulinna AS, Tikkanen JT, Müller-Nurasyid M, Peloso G, Ulivi S, Beckmann BM, Brockhaus AC, Cooper RR, Gasparini P, Hengstenberg C, Hwang SJ, Iorio A, Junttila MJ, Klopp N, Kähönen M, Laaksonen MA, Lehtimäki T, Lichtner P, Lyytikäinen LP, Martens E, Meisinger C, Meitinger T, Merchant FM, Nieminen MS, Peters A, Pietilä A, Perz S, Oikarinen L, Raitakari O, Reinhard W, Silander K, Thorand B, Wichmann HE, Sinagra G, Viikari J, O'Donnell CJ, Ellinor PT, Huikuri HV, Kääb S, Newton-Cheh C, Salomaa V.

Heart Rhythm. 2012 Oct;9(10):1627-34. doi: 10.1016/j.hrthm.2012.06.008. Epub 2012 Jun 6.

30.

Insights into RNA biology from an atlas of mammalian mRNA-binding proteins.

Castello A, Fischer B, Eichelbaum K, Horos R, Beckmann BM, Strein C, Davey NE, Humphreys DT, Preiss T, Steinmetz LM, Krijgsveld J, Hentze MW.

Cell. 2012 Jun 8;149(6):1393-406. doi: 10.1016/j.cell.2012.04.031. Epub 2012 May 31.

31.

A pRNA-induced structural rearrangement triggers 6S-1 RNA release from RNA polymerase in Bacillus subtilis.

Beckmann BM, Hoch PG, Marz M, Willkomm DK, Salas M, Hartmann RK.

EMBO J. 2012 Apr 4;31(7):1727-38. doi: 10.1038/emboj.2012.23. Epub 2012 Feb 14.

32.

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes.

Kääb S, Crawford DC, Sinner MF, Behr ER, Kannankeril PJ, Wilde AA, Bezzina CR, Schulze-Bahr E, Guicheney P, Bishopric NH, Myerburg RJ, Schott JJ, Pfeufer A, Beckmann BM, Martens E, Zhang T, Stallmeyer B, Zumhagen S, Denjoy I, Bardai A, Van Gelder IC, Jamshidi Y, Dalageorgou C, Marshall V, Jeffery S, Shakir S, Camm AJ, Steinbeck G, Perz S, Lichtner P, Meitinger T, Peters A, Wichmann HE, Ingram C, Bradford Y, Carter S, Norris K, Ritchie MD, George AL Jr, Roden DM.

Circ Cardiovasc Genet. 2012 Feb 1;5(1):91-9. doi: 10.1161/CIRCGENETICS.111.960930. Epub 2011 Nov 18.

33.

[A rest or arrest--asystolic episodes of 7 seconds in a 22-year-old athlete].

Siebermair J, Pohl T, Wakili R, Schüssler F, Lange P, Martens E, Beckmann BM, Sinner MF, Steinbigler P, Steinbeck G, Kääb S.

Internist (Berl). 2012 Feb;53(2):218-22. doi: 10.1007/s00108-011-2948-7. German.

PMID:
22002765
34.

Inherited cardiac arrhythmias: diagnosis, treatment, and prevention.

Beckmann BM, Pfeufer A, Kääb S.

Dtsch Arztebl Int. 2011 Sep;108(37):623-33; quiz 634. doi: 10.3238/arztebl.2011.0623. Epub 2011 Sep 16. Review.

35.

Recurrent torsades de pointes after catheter ablation of incessant ventricular bigeminy in combination with QT prolongation.

Reithmann C, Fiek M, Beckmann BM, Kääb S.

Europace. 2012 Feb;14(2):299-300. doi: 10.1093/europace/eur278. Epub 2011 Sep 8.

PMID:
21908450
36.

In vivo and in vitro analysis of 6S RNA-templated short transcripts in Bacillus subtilis.

Beckmann BM, Burenina OY, Hoch PG, Kubareva EA, Sharma CM, Hartmann RK.

RNA Biol. 2011 Sep-Oct;8(5):839-49. doi: 10.4161/rna.8.5.16151. Epub 2011 Sep 1.

PMID:
21881410
37.

Polymer-related off-target effects in non-viral siRNA delivery.

Merkel OM, Beyerle A, Beckmann BM, Zheng M, Hartmann RK, Stöger T, Kissel TH.

Biomaterials. 2011 Mar;32(9):2388-98. doi: 10.1016/j.biomaterials.2010.11.081. Epub 2010 Dec 22.

PMID:
21183213
38.

Lack of replication in polymorphisms reported to be associated with atrial fibrillation.

Sinner MF, Lubitz SA, Pfeufer A, Makino S, Beckmann BM, Lunetta KL, Steinbeck G, Perz S, Rahman R, Sonni A, Greenberg SM, Furie KL, Wichmann HE, Meitinger T, Peters A, Benjamin EJ, Rosand J, Ellinor PT, Kääb S.

Heart Rhythm. 2011 Mar;8(3):403-9. doi: 10.1016/j.hrthm.2010.11.003. Epub 2010 Nov 4.

39.

Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: a population-based prospective cohort study (MONICA/KORA).

Sinner MF, Reinhard W, Müller M, Beckmann BM, Martens E, Perz S, Pfeufer A, Winogradow J, Stark K, Meisinger C, Wichmann HE, Peters A, Riegger GA, Steinbeck G, Hengstenberg C, Kääb S.

PLoS Med. 2010 Jul 27;7(7):e1000314. doi: 10.1371/journal.pmed.1000314.

40.

Usefulness of short-term variability of QT intervals as a predictor for electrical remodeling and proarrhythmia in patients with nonischemic heart failure.

Hinterseer M, Beckmann BM, Thomsen MB, Pfeufer A, Ulbrich M, Sinner MF, Perz S, Wichmann HE, Lengyel C, Schimpf R, Maier SK, Varró A, Vos MA, Steinbeck G, Kääb S.

Am J Cardiol. 2010 Jul 15;106(2):216-20. doi: 10.1016/j.amjcard.2010.02.033.

PMID:
20599006
41.

Northern blot detection of endogenous small RNAs (approximately14 nt) in bacterial total RNA extracts.

Beckmann BM, Grünweller A, Weber MH, Hartmann RK.

Nucleic Acids Res. 2010 Aug;38(14):e147. doi: 10.1093/nar/gkq437. Epub 2010 May 26.

42.

Laminopathy presenting as familial atrial fibrillation.

Beckmann BM, Holinski-Feder E, Walter MC, Haserück N, Reithmann C, Hinterseer M, Wilde AA, Kääb S.

Int J Cardiol. 2010 Nov 19;145(2):394-396. doi: 10.1016/j.ijcard.2010.04.024. Epub 2010 May 15. No abstract available.

PMID:
20472316
43.

Common variants in KCNN3 are associated with lone atrial fibrillation.

Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, de Bakker PI, Mueller M, Lubitz SA, Fox E, Darbar D, Smith NL, Smith JD, Schnabel RB, Soliman EZ, Rice KM, Van Wagoner DR, Beckmann BM, van Noord C, Wang K, Ehret GB, Rotter JI, Hazen SL, Steinbeck G, Smith AV, Launer LJ, Harris TB, Makino S, Nelis M, Milan DJ, Perz S, Esko T, Köttgen A, Moebus S, Newton-Cheh C, Li M, Möhlenkamp S, Wang TJ, Kao WH, Vasan RS, Nöthen MM, MacRae CA, Stricker BH, Hofman A, Uitterlinden AG, Levy D, Boerwinkle E, Metspalu A, Topol EJ, Chakravarti A, Gudnason V, Psaty BM, Roden DM, Meitinger T, Wichmann HE, Witteman JC, Barnard J, Arking DE, Benjamin EJ, Heckbert SR, Kääb S.

Nat Genet. 2010 Mar;42(3):240-4. doi: 10.1038/ng.537. Epub 2010 Feb 21.

44.

Genome-wide association study of PR interval.

Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, Müller M, Sotoodehnia N, Sinner MF, Verwoert GC, Li M, Kao WH, Köttgen A, Coresh J, Bis JC, Psaty BM, Rice K, Rotter JI, Rivadeneira F, Hofman A, Kors JA, Stricker BH, Uitterlinden AG, van Duijn CM, Beckmann BM, Sauter W, Gieger C, Lubitz SA, Newton-Cheh C, Wang TJ, Magnani JW, Schnabel RB, Chung MK, Barnard J, Smith JD, Van Wagoner DR, Vasan RS, Aspelund T, Eiriksdottir G, Harris TB, Launer LJ, Najjar SS, Lakatta E, Schlessinger D, Uda M, Abecasis GR, Müller-Myhsok B, Ehret GB, Boerwinkle E, Chakravarti A, Soliman EZ, Lunetta KL, Perz S, Wichmann HE, Meitinger T, Levy D, Gudnason V, Ellinor PT, Sanna S, Kääb S, Witteman JC, Alonso A, Benjamin EJ, Heckbert SR.

Nat Genet. 2010 Feb;42(2):153-9. doi: 10.1038/ng.517. Epub 2010 Jan 10.

45.

Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study.

Sinner MF, Pfeufer A, Perz S, Schulze-Bahr E, Mönnig G, Eckardt L, Beckmann BM, Wichmann HE, Breithardt G, Steinbeck G, Fabritz L, Kääb S, Kirchhof P.

Europace. 2009 Oct;11(10):1338-44. doi: 10.1093/europace/eup205. Epub 2009 Aug 4.

PMID:
19654127
46.

Relation of increased short-term variability of QT interval to congenital long-QT syndrome.

Hinterseer M, Beckmann BM, Thomsen MB, Pfeufer A, Dalla Pozza R, Loeff M, Netz H, Steinbeck G, Vos MA, Kääb S.

Am J Cardiol. 2009 May 1;103(9):1244-8. doi: 10.1016/j.amjcard.2009.01.011. Epub 2009 Mar 18.

PMID:
19406266
47.

Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation.

Kääb S, Darbar D, van Noord C, Dupuis J, Pfeufer A, Newton-Cheh C, Schnabel R, Makino S, Sinner MF, Kannankeril PJ, Beckmann BM, Choudry S, Donahue BS, Heeringa J, Perz S, Lunetta KL, Larson MG, Levy D, MacRae CA, Ruskin JN, Wacker A, Schömig A, Wichmann HE, Steinbeck G, Meitinger T, Uitterlinden AG, Witteman JC, Roden DM, Benjamin EJ, Ellinor PT.

Eur Heart J. 2009 Apr;30(7):813-9. doi: 10.1093/eurheartj/ehn578. Epub 2009 Jan 13.

48.

Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study.

Zellerhoff S, Pistulli R, Mönnig G, Hinterseer M, Beckmann BM, Köbe J, Steinbeck G, Kääb S, Haverkamp W, Fabritz L, Gradaus R, Breithardt G, Schulze-Bahr E, Böcker D, Kirchhof P.

J Cardiovasc Electrophysiol. 2009 Apr;20(4):401-7. doi: 10.1111/j.1540-8167.2008.01339.x. Epub 2008 Oct 27.

PMID:
19017345
49.

Baseline values and sotalol-induced changes of ventricular repolarization duration, heterogeneity, and instability in patients with a history of drug-induced torsades de pointes.

Couderc JP, Kaab S, Hinterseer M, McNitt S, Xia X, Fossa A, Beckmann BM, Polonsky S, Zareba W.

J Clin Pharmacol. 2009 Jan;49(1):6-16. doi: 10.1177/0091270008325927. Epub 2008 Oct 28.

PMID:
18957528
50.

Dual inheritance of sudden death from cardiovascular causes.

Beckmann BM, Wilde AA, Kääb S.

N Engl J Med. 2008 May 8;358(19):2077-8. doi: 10.1056/NEJMc0708596. No abstract available.

PMID:
18463390

Supplemental Content

Loading ...
Support Center