Items where authors include "Meitinger, T"

Article

Škorić-Milosavljević, D, Tadros, R, Bosada, FM et al. (77 more authors) (2022) Common genetic variants contribute to risk of transposition of the great arteries. Circulation Research, 130 (2). pp. 166-180. ISSN 0009-7330

Ruth, KS, Day, FR, Hussain, J et al. (265 more authors) (2021) Genetic insights into biological mechanisms governing human ovarian ageing. Nature, 596 (7872). pp. 393-397. ISSN 0028-0836

Lahrouchi, N, Tadros, R, Crotti, L et al. (103 more authors) (2020) Transethnic genome-wide association study provides insights in the genetic architecture and heritability of Long QT syndrome. Circulation, 142 (4). pp. 324-338. ISSN 0009-7322

Tedja, MS, Wojciechowski, R, Hysi, PG et al. (98 more authors) (2018) Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nature Genetics, 50 (6). pp. 834-848. ISSN 1061-4036

Nicolas, A, Kenna, KP, Renton, AE et al. (210 more authors) (2018) Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Neuron, 97 (6). 1268-1283.e6.

Webb, TR, Erdmann, J, Stirrups, KE et al. (131 more authors) (2017) Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease. Journal of the American College of Cardiology, 69 (7). pp. 823-836. ISSN 0735-1097

Kennedy, H, Haack, TB, Hartill, V et al. (32 more authors) (2016) Sudden Cardiac Death due to Deficiency of the Mitochondrial Inorganic Pyrophosphatase PPA2. American Journal of Human Genetics. ISSN 0002-9297

van Rheenen, W, Shatunov, A, Dekker, AM et al. (180 more authors) (2016) Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Nature Genetics. ISSN 1546-1718