Items where authors include "van den Berg, LH"

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Number of items: 8.

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

van Rheenen, W, van der Spek, RAA, Bakker, MK et al. (279 more authors) (2021) Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Nature Genetics, 53 (12). pp. 1636-1648. ISSN 1061-4036

Johnson, JO, Chia, R, Miller, DE et al. (295 more authors) (2021) Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis. JAMA Neurology, 78 (10). pp. 1236-1248. ISSN 2168-6149

Nabais, MF, Laws, SM, Lin, T et al. (67 more authors) (2021) Meta-analysis of genome-wide DNA methylation identifies shared associations across neurodegenerative disorders. Genome Biology, 22. 90. ISSN 1474-760X

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

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.

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

Yasuno, K, Bilguvar, K, Bijlenga, P et al. (66 more authors) (2010) Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nature Genetics, 42 (5). pp. 420-425. ISSN 1061-4036

This list was generated on Mon Mar 25 04:03:41 2024 GMT.