SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population-Reference-Cited by-同舟云学术

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population

Published:2017-08-23 Issue:11 Volume:25 Page:1253-1260
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Ameur Adam,Dahlberg Johan,Olason Pall,Vezzi Francesco,Karlsson Robert^ORCID,Martin Marcel,Viklund Johan,Kähäri Andreas Kusalananda,Lundin Pär,Che Huiwen,Thutkawkorapin Jessada,Eisfeldt Jesper,Lampa Samuel,Dahlberg Mats,Hagberg Jonas^ORCID,Jareborg Niclas^ORCID,Liljedahl Ulrika,Jonasson Inger,Johansson Åsa,Feuk Lars^ORCID,Lundeberg Joakim,Syvänen Ann-Christine,Lundin Sverker,Nilsson Daniel,Nystedt Björn,Magnusson Patrik KE,Gyllensten Ulf

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2017130.pdf

Reference38 articles.

1. 1000 Genomes Project Consortium 1000 Genomes Project Consortium, Abecasis GR 1000 Genomes Project Consortium, Auton A et al: An integrated map of genetic variation from 1,092 human genomes. Nature 2012; 491: 56–65.

2. Besenbacher S, Liu S, Izarzugaza JM et al: Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios. Nat Commun 2015; 6: 5969.

3. Boomsma DI, Wijmenga C, Slagboom EP et al: The Genome of the Netherlands: design, and project goals. Eur J Hum Genet 2014; 22: 221–227.

4. Gudbjartsson DF, Helgason H, Gudjonsson SA et al: Large-scale whole-genome sequencing of the Icelandic population. Nat Genet 2015; 47: 435–444.

5. UK10K Consortium UK10K Consortium, Walter K UK10K Consortium, Min JL et al: The UK10K project identifies rare variants in health and disease. Nature 2015; 526: 82–90.

Cited by 149 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Spinocerebellar ataxia type 4 is caused by a GGC expansion in the ZFHX3 gene and is associated with prominent dysautonomia and motor neuron signs;Journal of Internal Medicine;2024-07-07

2. Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population;JID Innovations;2024-07

3. Predicting human and viral protein variants affecting COVID-19 susceptibility and repurposing therapeutics;Scientific Reports;2024-06-20

4. Egypt Genome: Towards an African new genomic era;Journal of Advanced Research;2024-06

5. Genetic determinants of renal scarring in children with febrile UTI;Pediatric Nephrology;2024-05-20