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Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.
Am J Hum Genet. 2016 Mar 3;98(3):592. doi: 10.1016/j.ajhg.2016.02.016. Epub 2016 Mar 3.
Am J Hum Genet. 2016.
PMID: 28863274
Free PMC article.
No abstract available.
Rare variants in NR2F2 cause congenital heart defects in humans.
Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium; Wilson DI, Mital S, Hurles ME.
Al Turki S, et al. Among authors: arndt ak.
Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007.
Am J Hum Genet. 2014.
PMID: 24702954
Free PMC article.
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Reponse to De Leeuw and Houge.
Arndt AK, Macrae CA, Klaassen S.
Arndt AK, et al.
Am J Hum Genet. 2014 Jan 2;94(1):154-5. doi: 10.1016/j.ajhg.2013.11.011.
Am J Hum Genet. 2014.
PMID: 24387996
Free PMC article.
No abstract available.
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Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S.
Arndt AK, et al.
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13.
Am J Hum Genet. 2013.
PMID: 23768516
Free PMC article.
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Genetic testing in cardiovascular diseases.
Arndt AK, MacRae CA.
Arndt AK, et al.
Curr Opin Cardiol. 2014 May;29(3):235-40. doi: 10.1097/HCO.0000000000000055.
Curr Opin Cardiol. 2014.
PMID: 24717670
Free PMC article.
Review.
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RAGE-mediated interstitial fibrosis in neonatal obstructive nephropathy is independent of NF-κB activation.
Gasparitsch M, Arndt AK, Pawlitschek F, Oberle S, Keller U, Kasper M, Bierhaus A, Schaefer F, Weber LT, Lange-Sperandio B.
Gasparitsch M, et al. Among authors: arndt ak.
Kidney Int. 2013 Nov;84(5):911-9. doi: 10.1038/ki.2013.171. Epub 2013 May 15.
Kidney Int. 2013.
PMID: 23677242
Free article.
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Staged surgical palliation in identical twins with concordance for hypoplastic left heart syndrome (HLHS).
Arndt AK, Petko C, Scheewe J, Kramer HH.
Arndt AK, et al.
Klin Padiatr. 2012 Jul;224(4):268-9. doi: 10.1055/s-0032-1312589. Epub 2012 Jun 1.
Klin Padiatr. 2012.
PMID: 22661338
No abstract available.
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