ABO Blood Group and the Risk of Thrombosis in Cancer Patients: A Mini-Review.
Elsherif S, Zidan A, Saville O, Othman M.

Role of the ABO Blood Groups as a Risk Factor for Retinal Vein Occlusion.
Posch-Pertl L, List W, Michelitsch M, Pinter-Hausberger S, Posch F, Innauer F, Renner W, Weger M.

Mother-newborn ABO group discrepancy caused by a rare BW.17 variant.
Marraccini C, Iotti B, Vanzanelli P, Bedeschi E, Farnetti E, Nicoli D, Berni P, Razzoli A, Maurizi E, Gavioli G, Mazzi A, Baricchi R, Merolle L, Schiroli D.

Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population.
Zhang Z, Li H, Weng H, Zhou G, Chen H, Yang G, Zhang P, Zhang X, Ji Y, Ying K, Liu B, Xu Q, Tang Y, Zhu G, Liu Z, Xia S, Yang X, Dong L, Zhu L, Zeng M, Yuan Y, Yang Y, Zhang N, Xu X, Pang W, Zhang M, Zhang Y, Zhen K, Wang D, Lei J, Wu S, Shu S, Zhang Y, Zhang S, Gao Q, Huang Q, Deng C, Fu X, Chen G, Duan W, Wan J, Xie W, Zhang P, Wang S, Yang P, Zuo X, Zhai Z, Wang C, China pUlmonary Thromboembolism REgistry Study (CURES) investigators., Free PMC Article

The rs8176740 T/A and rs512770 T/C Genetic Variants of the ABO Gene Increased the Risk of COVID-19, as well as the Plasma Concentration Platelets.
Vargas-Alarcón G, Ramírez-Bello J, Posadas-Sánchez R, Rojas-Velasco G, López-Reyes A, Martínez-Gómez L, Ortega-Peña S, Montúfar-Robles I, Barbosa-Cobos RE, Arellano-González M, Fragoso JM., Free PMC Article

Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis.
Ni X, Bai C, Nie C, Qi L, Liu Y, Yuan H, Zhu X, Sun L, Zhou Q, Li Y, Zhen H, Su H, Li R, Lan R, Pang G, Lv Y, Zhang W, Yang F, Yao Y, Chen C, Wang Z, Gao D, Zhang N, Zhang S, Zhang L, Wu Z, Hu C, Zeng Y, Yang Z., Free PMC Article

Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project.
Lopera-Maya EA, Kurilshikov A, van der Graaf A, Hu S, Andreu-Sánchez S, Chen L, Vila AV, Gacesa R, Sinha T, Collij V, Klaassen MAY, Bolte LA, Gois MFB, Neerincx PBT, Swertz MA, LifeLines Cohort Study, Harmsen HJM, Wijmenga C, Fu J, Weersma RK, Zhernakova A, Sanna S.

Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort.
Qin Y, Havulinna AS, Liu Y, Jousilahti P, Ritchie SC, Tokolyi A, Sanders JG, Valsta L, Brożyńska M, Zhu Q, Tripathi A, Vázquez-Baeza Y, Loomba R, Cheng S, Jain M, Niiranen T, Lahti L, Knight R, Salomaa V, Inouye M, Méric G., Free PMC Article

[Identification of B Antigen Weak Expression Caused by 5873CT Mutation in Blood Group Gene Based on Sequencing Technique].
Fang XM, Liu W, Yang B, Liu Y, Qu XJ.

[Different Subtypes Caused by c.721C>T Substitution in the Exon 7 of ABO Gene].
Xiao JY, Feng CC, Liu TX, Shi LL, Zhang RY, Huang CY, Chen Q.

A cell-specific regulatory region of the human ABO blood group gene regulates the neighborhood gene encoding odorant binding protein 2B.
Sano R, Takahashi Y, Fukuda H, Harada M, Hayakawa A, Okawa T, Kubo R, Takeshita H, Tsukada J, Kominato Y., Free PMC Article

A novel ABO allele with a 21-bp duplication identified in two unrelated European individuals with weak A expression.
Jakobsen MA, Hult AK, Hellberg Å, Crottet SL, Sprogøe U, Olsson ML.

The ABO histo-blood group, endothelial activation, and acute respiratory distress syndrome risk in critical illness.
Reilly JP, Meyer NJ, Shashaty MG, Anderson BJ, Ittner C, Dunn TG, Lim B, Forker C, Bonk MP, Kotloff E, Feng R, Cantu E, Mangalmurti NS, Calfee CS, Matthay MA, Mikacenic C, Walley KR, Russell J, Christiani DC, Wurfel MM, Lanken PN, Reilly MP, Christie JD., Free PMC Article

The ABO Locus is Associated with Increased Fibrin Network Formation in Patients with Stable Coronary Artery Disease.
Winther-Larsen A, Christiansen MK, Larsen SB, Nyegaard M, Neergaard-Petersen S, Ajjan RA, Würtz M, Grove EL, Jensen HK, Kristensen SD, Hvas AM.

Identification of a novel A allele with a c.731T>C mutation on the ABO*A1.02 allele.
Hong X, Ying Y, Ma K, Xu X, He J, Zhu F.

Identification of a novel A allele with a missense mutation (c.737A>G) in a Chinese individual with a weak A phenotype.
He B, Li B, Liu J, Liu X.

Mechanism evaluation for an amino acid substitution p.Y246C of B-glycosyltransferase enzyme with Bweak phenotype.
Ying Y, Hong X, Xu X, Zhang J, He J, Zhu F, Xie X.

The novel missense variant c.350G>T on the ABO*B.01 allele associated with a B(el) phenotype.
Kim TY, Yu H, Chung YN, Jang JH, Cho D.

A novel ABO*A allele with 21 base pair duplication in Polish individuals.
Guz K, Pelc-Kłopotowska M, Purchla-Szepioła S, Skulimowska J, Bednarz J, Lewicka M, Strażnikiewicz B, Orzińska A.

Two novel A alleles with c.322C>T or c.410C>T mutations on the ABO*A1.02 allele were identified in the Chinese individuals.
Hong X, Zhang J, Ying Y, He J, Zhu F.

Identification of a novel missense mutation (c.608A > G) in the ABO gene contributing to an A variant.
Wu X, Ji F, Huo N, Wu Y, Liu X, Zhang L, Liang W, Wang Z.

A novel B variant allele with c.586T>C (p.Cys196Arg) mutation identified at the ABO locus.
Chi X, Liu L, Feng Z, Zhang S.

Lung expression of genes putatively involved in SARS-CoV-2 infection is modulated in cis by germline variants.
Cotroneo CE, Mangano N, Dragani TA, Colombo F., Free PMC Article

A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.
Matzhold EM, Drexler C, Wagner A, Bernecker C, Pessentheiner A, Bogner-Strauß JG, Helmberg W, Wagner T., Free PMC Article

A novel A allele with c.287G > T mutation identified in a Chinese family.
Ma W, Zhang S, Jiao S, Feng Z.