Author

Anastasia Shcherban

Institutions: University of Helsinki, Institute for Molecular Medicine Finland, HiLIFE – Elämäntieteiden Instituutti

Observed institutions: University of Helsinki, Pfizer (United States), Finnish Institute for Health and Welfare, Institute for Molecular Medicine Finland, University of Tampere, HiLIFE – Elämäntieteiden Instituutti

OpenAlex ID: A5107908554

Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries

2021 · Puya Gharahkhani, Eric Jorgenson, et al. · Nature Communications · 450

Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection

2021 · Seyedeh M. Zekavat, Shu-Hong Lin, et al. · Nature Medicine · 199

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

2019 · Rubina Tabassum, Joel T. Rämö, et al. · Nature Communications · 176

The role of polygenic risk and susceptibility genes in breast cancer over the course of life

2020 · Nina Mars, Elisabeth Widén, et al. · Nature Communications · 161

Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells

2020 · Erik L. Bao, Satish K. Nandakumar, et al. · Nature · 137

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

2021 · Pradeep Natarajan, Akhil Pampana, et al. · Nature Communications · 36

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

2020 · Sanni E. Ruotsalainen, Juulia J. Partanen, et al. · European Journal of Human Genetics · 24

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis

2022 · Sanni E. Ruotsalainen, Ida Surakka, et al. · Communications Biology · 19

Independent and cumulative coeliac disease-susceptibility loci are associated with distinct disease phenotypes

2021 · Juliana X. M. Cerqueira, Päivi Saavalainen, et al. · Journal of Human Genetics · 19

Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population

2021 · Perttu J. Liuska, Susanna Lemmelä, et al. · JAMA Ophthalmology · 9

Dissecting the contribution of single nucleotide polymorphisms in CCR9 and CCL25 genomic regions to the celiac disease phenotype

2021 · Laura Airaksinen, Juliana XM. Cerqueira, et al. · Journal of Translational Autoimmunity · 7

Works count: 11

Citation count: 1,237

H-index: 9

I10-index: 9