1. Genetic analysis for a shared biological basis between migraine and coronary artery disease. (June 2015) Authors: Winsvold, Bendik S.; Nelson, Christopher P.; Malik, Rainer; Gormley, Padhraig; Anttila, Verneri; Vander Heiden, Jason; Elliott, Katherine S.; Jacobsen, Line M.; Palta, Priit; Amin, Najaf; de Vries, Boukje; Hämäläinen, Eija; Freilinger, Tobias; Ikram, M. Arfan; Kessler, Thorsten; Koiranen, Markku;... Journal: Neurology Issue: Volume 1:Number 1(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies. Issue 9 (29th July 2017) Authors: Pérez-Palma, Eduardo; Helbig, Ingo; Klein, Karl Martin; Anttila, Verneri; Horn, Heiko; Reinthaler, Eva Maria; Gormley, Padhraig; Ganna, Andrea; Byrnes, Andrea; Pernhorst, Katharina; Toliat, Mohammad R; Saarentaus, Elmo; Howrigan, Daniel P; Hoffman, Per; Miquel, Juan Francisco; De Ferrari, Giancar... Journal: Journal of medical genetics Issue: Volume 54:Issue 9(2017) Page Start: 598 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Migraine genetics: from genome-wide association studies to translational insights. Issue 1 (December 2016) Authors: Gormley, Padhraig; Winsvold, Bendik; Nyholt, Dale; Kallela, Mikko; Chasman, Daniel; Palotie, Aarno Journal: Genome medicine Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. (1st February 2022) Authors: Daghals, Iyas; Sargurupremraj, Muralidharan; Danning, Rebecca; Gormley, Padhraig; Malik, Rainer; Amouyel, Philippe; Metso, Tiina; Pezzini, Alessandro; Kurth, Tobias; Debette, Stéphanie; Chasman, Daniel Journal: Neurology Issue: Volume 8:Number 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. (1st February 2022) Authors: Daghals, Iyas; Sargurupremraj, Muralidharan; Danning, Rebecca; Gormley, Padhraig; Malik, Rainer; Amouyel, Philippe; Metso, Tiina; Pezzini, Alessandro; Kurth, Tobias; Debette, Stéphanie; Chasman, Daniel Journal: Neurology Issue: Volume 8:Number 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. (February 2022) Authors: Daghals, Iyas; Sargurupremraj, Muralidharan; Danning, Rebecca; Gormley, Padhraig; Malik, Rainer; Amouyel, Philippe; Metso, Tiina; Pezzini, Alessandro; Kurth, Tobias; Debette, Stéphanie; Chasman, Daniel Journal: Neurology Issue: Volume 8:Number 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions. (30th November 2021) Authors: Guo, Yanjun; Daghlas, Iyas; Gormley, Padhraig; Giulianini, Franco; Ridker, Paul M.; Mora, Samia; Kurth, Tobias; Rist, Pamela M.; Chasman, Daniel I. Journal: Neurology Issue: Volume 97:Number 22(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Phenotypic and Genotypic Associations Between Migraine and Lipoprotein Subfractions. (30th November 2021) Authors: Guo, Yanjun; Daghlas, Iyas; Gormley, Padhraig; Giulianini, Franco; Ridker, Paul M.; Mora, Samia; Kurth, Tobias; Rist, Pamela M.; Chasman, Daniel I. Journal: Neurology Issue: Volume 97:Number 22(2021) Page Start: e2223 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Phenotypic Consequences of a Genetic Predisposition to Enhanced Nitric Oxide Signaling. Issue 3 (16th January 2018) Authors: Emdin, Connor A.; Khera, Amit V.; Klarin, Derek; Natarajan, Pradeep; Zekavat, Seyedeh M.; Nomura, Akihiro; Haas, Mary; Aragam, Krishna; Ardissino, Diego; Wilson, James G.; Schunkert, Heribert; McPherson, Ruth; Watkins, Hugh; Elosua, Roberto; Bown, Matthew J.; Samani, Nilesh J.; Baber, Usman; Erdm... Journal: Circulation Issue: Volume 137:Issue 3(2018) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Pitfalls in genetic testing: the story of missed SCN1A mutations. Issue 4 (14th April 2016) Authors: Djémié, Tania; Weckhuysen, Sarah; von Spiczak, Sarah; Carvill, Gemma L.; Jaehn, Johanna; Anttonen, Anna‐Kaisa; Brilstra, Eva; Caglayan, Hande S.; de Kovel, Carolien G.; Depienne, Christel; Gaily, Eija; Gennaro, Elena; Giraldez, Beatriz G.; Gormley, Padhraig; Guerrero‐López, Rosa; Guerrini, Renzo;... Journal: Molecular genetics & genomic medicine Issue: Volume 4:Issue 4(2016) Page Start: 457 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗