Suchergebnisse - "Burren, Oliver S."

PubPharm (74)

31

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

enthalten in: Genome biology | 2017

von Burren, O. | Rubio García, A. | Javierre, B. | +20

32

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

enthalten in: Genome biology | 2017

von Burren, O. | Rubio García, A. | Javierre, B. | +20

33

Chromosome contacts in activated T cells identify autoimmune disease candidate genes

enthalten in: Genome biology | 2017

von Burren, O. | Rubio García, A. | Javierre, B. | +20

34

Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

enthalten in: Cell | 2016

von Javierre, B. | Burren, O. | Wilder, S. | +37

35

Lineage-Specific Genome Architecture Links Enhancers and Non-coding Disease Variants to Target Gene Promoters

enthalten in: Cell | 2016

von Javierre, B. | Burren, O. | Wilder, S. | +25

36

Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping

enthalten in: PLoS genetics | 2015

von Wallace, C. | Cutler, A. | Pontikos, N. | +15

37

Integration of disease association and eQTL data using a Bayesian colocalisation approach highlights six candidate causal genes in immune-mediated diseases

enthalten in: Human molecular genetics | 2015

von Guo, H. | Fortune, M. | Burren, O. | +3

38

Widespread seasonal gene expression reveals annual differences in human immunity and physiology

enthalten in: Nature communications | 2015

von Dopico, X. | Evangelou, M. | Ferreira, R. | +12

39

Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes

enthalten in: Human molecular genetics | 2015

von Cooper, N. | Shtir, C. | Smyth, D. | +12

40

Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes

enthalten in: Human molecular genetics | 2015

von Cooper, N. | Shtir, C. | Smyth, D. | +12