Fedik Rahimov

FinnGen: Unique genetic insights from combining isolated population and national health register data

Mitja Kurki, Juha Karjalainen, Priit Palta et al. · 2022 · 412 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +21

Systematic single-variant and gene-based association testing of thousands of phenotypes in 394,841 UK Biobank exomes

Konrad J. Karczewski, Matthew Solomonson, Katherine R. Chao et al. · Cell Genomics · 2022 · 275 citations · Full text

Genome-wide Association Study, Genetic Analysis, Functional Genomics +13

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

Haifa H. Jabara, Steven E. Boyden, Janet Chou et al. · Nature Genetics · 2015 · 266 citations · Full text

Primary Immunodeficiency, Autoimmune Disease, Human Retrovirus +10

Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate

Alexandre R. Vieira, Joseph R. Avila, Sandra Daack‐Hirsch et al. · PLoS Genetics · 2005 · 259 citations · Full text

Nonsyndromic Cleft Lip, Genetics, Genetic Epidemiology +22

Variation in the HLA-G Promoter Region Influences Miscarriage Rates

Carole Ober, Carrie Aldrich, Inna Chervoneva et al. · The American Journal of Human Genetics · 2003 · 249 citations · Full text

Fertility, Genetics, Reproductive Health +4