Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants.
Clin Genet. 2017 Jan;91(1):63-72. doi: 10.1111/cge.12847. Epub 2016 Sep 26.
Clin Genet. 2017.
PMID: 27538377
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts.
Paludan-Müller C, Ghouse J, Vad OB, Herfelt CB, Lundegaard P, Ahlberg G, Schmitt N, Svendsen JH, Haunsø S, Bundgaard H, Hansen T, Kanters JK, Olesen MS.
Paludan-Müller C, et al. Among authors: herfelt cb.
Eur J Hum Genet. 2019 Sep;27(9):1427-1435. doi: 10.1038/s41431-019-0416-3. Epub 2019 May 1.
Eur J Hum Genet. 2019.
PMID: 31043699
Free PMC article.
Item in Clipboard
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.
Gregers E, Ahlberg G, Christensen T, Jabbari J, Larsen KO, Herfelt CB, Henningsen KM, Andreasen L, Thiis JJ, Lund J, Holme S, Haunsø S, Bentzen BH, Schmitt N, Svendsen JH, Olesen MS.
Gregers E, et al. Among authors: herfelt cb.
Heart Rhythm. 2017 Oct;14(10):1531-1538. doi: 10.1016/j.hrthm.2017.05.027. Epub 2017 May 24.
Heart Rhythm. 2017.
PMID: 28549997
Item in Clipboard
Cite
Cite