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Genome-wide meta-analysis of heavy menstrual bleeding reveals 36 risk loci

Thibord F, Cunha J, Džigursk J, Tuftin B, Huffman JE, Pujol-Gualdo N, Cho K, Wilson PWF, Johnsen JM, Raffield LM, Chen MH, Laisk T, & Johnson AD
2025 Must-Read Heavy Menstrual Bleeding

Characterization of the clinical and laboratory phenotype of hemophilia carriers and trends of utilization of hemostatic therapies: Analysis of the American Thrombosis & Hemostasis Network (ATHN) dataset

Swaminathan N, Currie A, Hu J, Kulkarni R, Pipe S, Kouides P, Sharathkumar A
Bleeding Disorders Hemophilia

Diagnostic Accuracy of Imperforate Hymen at a Single Referral Center

Casey SR, Fang ME, Goytia K, Monestime G, & Dietrich JE
2025 Must-Read

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding

Friedman RK, Heath AS, Huffman JE, Baker JT, Hasbani NR, Gagliano Taliun SA, Chen MH, Howard TE, Lewis JP, Pankratz N, Patil S, Reiner AP, Thibord F, Yanek LR,Jie Yao J, et al.
Von Willebrand Disease

Sexual and Reproductive Health in Sickle Cell Disease: A Qualitative Analysis of Pediatric Hematologist Perspectives

Oberoi AR, Clarke AR, Jacob SA, Kazmerski TM, Fassel H, Askew M, Woolford T, Karol Walec K, Leroy-Melamed M
Sickle Cell Disease

Safety and Efficacy Of Fertility Preservation in Sickle Cell Disease and Transfusion Dependent Thalassemia Patients Undergoing Gene Editing Therapies

Hmaidan S, Van Heertum K, Bhatia S, Frangoul H
Fertility Sickle Cell Disease