Denna sida på svenska
Loading profile information...

Publications

A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relationship to chronic lymphocytic leukemia
Chen X, Gustafsson S, Whitington T, Borné Y, Lorentzen E, Sun J, et al
Human molecular genetics 2018;27(10):1809-1818

A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
Lifelines Cohort Study, Charge Neurology Working Group, Cogent-kidney Consortium, Giant Consortium, Sung Yj, Winkler Tw, et al
American journal of human genetics 2018;102(3):375-400

Genetic and Environmental Contributions to the Covariation Between Cardiometabolic Traits
Chen X, Kuja-halkola R, Chang Z, Karlsson R, Hägg S, Svensson P, et al
Journal of the American Heart Association 2018;7(9):-

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries
Interact Consortium, Feitosa Mf, Kraja At, Chasman Di, Sung Yj, Winkler Tw, et al
PloS one 2018;13(6):e0198166-

Polygenic link between blood lipids and amyotrophic lateral sclerosis
Chen X, Yazdani S, Piehl F, Magnusson Pke, Fang F
Neurobiology of aging 2018;67():202.e1-202.e6

Cystatin C Predicts Incident Cardiovascular Disease in Twins
Arpegård J, Magnusson Pk, Chen X, Ridefelt P, Pedersen Nl, De Faire U, et al
Journal of the American Heart Association 2016;5(6):-

One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins
Magnusson Pk, Lee D, Chen X, Szatkiewicz J, Pramana S, Teo S, et al
Twin research and human genetics : the official journal of the International Society for Twin Studies 2016;19(2):97-103

Dominant Genetic Variation and Missing Heritability for Human Complex Traits: Insights from Twin versus Genome-wide Common SNP Models
Chen X, Kuja-halkola R, Rahman I, Arpegård J, Viktorin A, Karlsson R, et al
American journal of human genetics 2015;97(5):708-14

Heterogeneity of chronic obstructive pulmonary disease: from phenotype to genotype
Chen X, Xu X, Xiao F
Frontiers of medicine 2013;7(4):425-32

[The mechanisms of palindrome-stimulated mutation and related human diseases]
Chen X, Xiao F, Guo J
Yi chuan = Hereditas 2013;35(5):571-7

Map

Presentations