1. Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation. Issue 1 (December 2018) Authors: Ahlberg, Gustav; Refsgaard, Lena; Lundegaard, Pia; Andreasen, Laura; Ranthe, Mattis; Linscheid, Nora; Nielsen, Jonas; Melbye, Mads; Haunsø, Stig; Sajadieh, Ahmad; Camp, Lu; Olesen, Søren-Peter; Rasmussen, Simon; Lundby, Alicia; Ellinor, Patrick; Holst, Anders; Svendsen, Jesper; Olesen, Morten Journal: Nature communications Issue: Volume 9:Issue 1(2018) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm. (January 2019) Authors: Gould, Russell; Aziz, Hamza; Woods, Courtney; Seman-Senderos, Manuel; Sparks, Elizabeth; Preuss, Christoph; Wünnemann, Florian; Bedja, Djahida; Moats, Cassandra; McClymont, Sarah; Rose, Rebecca; Sobreira, Nara; Ling, Hua; MacCarrick, Gretchen; Kumar, Ajay; Luyckx, Ilse; Cannaerts, Elyssa; Verstra... Journal: Nature genetics Issue: Volume 51:Number 1(2019) Page Start: 42 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Leveraging Human Genetics to Estimate Clinical Risk Reductions Achievable by Inhibiting Factor XI. Issue 11 (November 2019) Authors: Georgi, Benjamin; Mielke, Johanna; Chaffin, Mark; Khera, Amit V.; Gelis, Lian; Mundl, Hardi; van Giezen, J.J.J.; Ellinor, Patrick; Kathiresan, Sekar; Ziegelbauer, Karl; Freitag, Daniel F. Journal: Stroke Issue: Volume 50:Issue 11(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genetic Susceptibility for Atrial Fibrillation in Patients Undergoing Atrial Fibrillation Ablation. (March 2020) Authors: Shoemaker, M. Benjamin; Husser, Daniela; Roselli, Carolina; Al Jazairi, Meelad; Chrispin, Jonathan; Kühne, Michael; Neumann, Benjamin; Knight, Stacey; Sun, Han; Mohanty, Sanghamitra; Shaffer, Christian; Thériault, Sébastien; Rinke, Lauren Lee; Siland, Joylene E.; Crawford, Diane M.; Ueberham, Lau... Journal: Circulation Issue: Volume 13:Number 3(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels. Issue 13 (25th September 2018) Authors: Montasser, May E.; O'Hare, Elizabeth A.; Wang, Xiaochun; Howard, Alicia D.; McFarland, Rebecca; Perry, James A.; Ryan, Kathleen A.; Rice, Kenneth; Jaquish, Cashell E.; Shuldiner, Alan R.; Miller, Michael; Mitchell, Braxton D.; Zaghloul, Norann A.; Chang, Yen-Pei C.; Abe, Namiko; Abecasis, Goncalo... Journal: Circulation Issue: Volume 138:Issue 13(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. Issue 1 (December 2016) Authors: Hanley, Alan; Walsh, Katie; Joyce, Caroline; McLellan, Michael; Clauss, Sebastian; Hagen, Amaya; Shea, Marisa; Tucker, Nathan; Lin, Honghuang; Fahy, Gerard; Ellinor, Patrick Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗