Maria Litvinova

Unique genetic profile of hereditary hemochromatosis in Russians: High frequency of C282Y mutation in population, but not in patients

Ekaterina Potekhina, L. М. Samokhodskaya, Anastasia Efimenko et al. · Blood Cells Molecules and Diseases · 2005 · 28 citations

C282y Mutation, Mendelian Disorder, Genetic Disorder +7

A novel ferroportin mutation in a Canadian family with autosomal dominant hemochromatosis

Tara Morris, Maria Litvinova, Diana Ralston et al. · Blood Cells Molecules and Diseases · 2005 · 20 citations

Mendelian Disorder, Genetic Disorder, Iron Metabolism +10

TLRs Gene Polymorphisms Associated with Pneumonia before and during COVID-19 Pandemic

Svetlana Salamaikina, V. I. Korchagin, Maria Litvinova · Diagnostics · 2022 · 13 citations · Full text

Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population

Maria Litvinova, K. Khafizov, V. I. Korchagin et al. · Frontiers in Genetics · 2021 · 10 citations · Full text