Hull LE, Flannery K, Kaimal A, Sepucha K, Rehm HL, Haas JS. Multilevel barriers and facilitators to widespread use of preconception carrier screening in the United States. Genetics in medicine : official journal of the American College of Medical Genetics. 2023:100946. doi:10.1016/j.gim.2023.100946
Publications
Okonechnikov K, Joshi P, Sepp M, et al. Mapping pediatric brain tumors to their origins in the developing cerebellum. Neuro-oncology. 2023. doi:10.1093/neuonc/noad124
McNamara RP, Maron JS, Boucau J, et al. Anamnestic humoral correlates of immunity across SARS-CoV-2 variants of concern. mBio. 2023:e0090223. doi:10.1128/mbio.00902-23
Cai Y, Franceschini N, Surapaneni A, et al. Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait. Clinical journal of the American Society of Nephrology : CJASN. 2023. doi:10.2215/CJN.0000000000000257
Berryer MH, Tegtmeyer M, Binan L, et al. Robust induction of functional astrocytes using NGN2 expression in human pluripotent stem cells. iScience. 2023;26(7):106995. doi:10.1016/j.isci.2023.106995
He W, Ou T, Skamangas N, et al. Heavy-chain CDR3-engineered B cells facilitate in vivo evaluation of HIV-1 vaccine candidates. Immunity. 2023. doi:10.1016/j.immuni.2023.07.003
van de Vegte YJ, Eppinga RN, van der Ende Y, et al. Genetic insights into resting heart rate and its role in cardiovascular disease. Nature communications. 2023;14(1):4646. doi:10.1038/s41467-023-39521-2
Wang H, Fu T, Du Y, et al. Scientific discovery in the age of artificial intelligence. Nature. 2023;620(7972):47-60. doi:10.1038/s41586-023-06221-2
Thomas S, Guenther G, Rowe JH, et al. Severe congenital neutropenia due to jagunal homolog 1 () mutation: a case report and literature review. Frontiers in pediatrics. 2023;11:1223191. doi:10.3389/fped.2023.1223191
Hilal N, Chen Z, Chen MH, Choudhury S. RASopathies and cardiac manifestations. Frontiers in cardiovascular medicine. 2023;10:1176828. doi:10.3389/fcvm.2023.1176828