WA
Wei Ang

Highly Cited

11
Works
1,306
Citations
9
H-Index
Search Authors
Author Statistics
  • OpenAlex ID A5111910059
  • i10-Index 8
  • 2-Yr Mean Citedness 0.00
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Wei Ang

Also known as: Ang, W., W Ang, Wei Ang

11

Total Works

1,306

Citations

9

H-Index

8

i10-Index

Citation & Works Trend by Year
5 years active
Top Research Topics
Genetic Associations and Epidemiology (9) Asthma and respiratory diseases (2) Pregnancy and preeclampsia studies (2) Birth, Development, and Health (2) Ocular Disorders and Treatments (2)
Recent Publications
11 shown
Year Publication Title Citations Action
2017 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks Nature Genetics 550
2016 Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index Molecular Psychiatry 74
2014 A novel common variant in DCST2 is associated with length in early life and height in adulthood Human Molecular Genetics 120
2014 Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22 Pregnancy Hypertension 16
2014 Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype Journal of Allergy and Clinical Immunology 216
2014 Further Evidence for the Involvement of Two Functional Polymorphisms in Folate Metabolising Genes, SHMT1 (1420) T and MTRR (66) A, with an Increased Risk of Early Spontaneous Preterm Birth from the PGP Consortium GWAS:T-076 UWA Profiles and Research Repository (UWA) 0
2013 Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia Nature Genetics 9
2013 OP004. A SNP associated with susceptibility to preeclampsia near the inhibin, beta B gene, is also associated with cardiovascular disease risk traits Pregnancy Hypertension 0
2013 Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity Human Molecular Genetics 209
2012 Genome-wide meta-analysis of common variant differences between men and women Human Molecular Genetics 41
2012 X-Linked Megalocornea Caused by Mutations in CHRDL1 Identifies an Essential Role for Ventroptin in Anterior Segment Development The American Journal of Human Genetics 72

Data source: OpenAlex API