Journal of Human Genetics
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Cao, T., O’Reilly, M. E., Selvaggi, C., Cynn, E., Lumish, H., Xue, C., Jha, A., Reilly, M. P., & Foulkes, A. S. (2022). Cis-regulated expression of non-conserved lincRNAs associates with cardiometabolic related traits. Journal of Human Genetics, 67(5), 307–310. https://doi.org/10.1038/s10038-022-01012-5
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Columbia Affiliation
Adadey, S. M., Schrauwen, I., Aboagye, E. T., Bharadwaj, T., Esoh, K. K., Basit, S., Acharya, A., Nouel-Saied, L. M., Liaqat, K., Wonkam-Tingang, E., Mowla, S., Awandare, G. A., Ahmad, W., Leal, S. M., & Wonkam, A. (2021). Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment. Journal of human genetics, 66(12), 1169–1175. https://doi.org/10.1038/s10038-021-00954-6
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Columbia Affiliation
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Acharya, A., Raza, S. I., Anwar, M. Z., Bharadwaj, T., Liaqat, K., Khokhar, M. A. S., Everard, J. L., Nasir, A., Nickerson, D. A., Bamshad, M. J., Ansar, M., Schrauwen, I., Ahmad, W., & Leal, S. M. (2021). Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13. Journal of Human Genetics, 66(10), 1009–1018. https://doi.org/10.1038/s10038-021-00922-0
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Columbia Affiliation
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