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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
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
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). Correction: Wolfram-like syndrome with bicuspid aortic valve due to a homozygous missense variant in CDK13. Journal of Human Genetics, 66(10), 1019–1019. https://doi.org/10.1038/s10038-021-00949-3
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Alkelai, A., Shohat, S., Greenbaum, L., Schechter, T., Draiman, B., Chitrit-Raveh, E., Rienstein, S., Dagaonkar, N., Hughes, D., Aggarwal, V. S., Heinzen, E. L., Shifman, S., Goldstein, D. B., & Kohn, Y. (2020). Expansion of the GRIA2 phenotypic representation: a novel de novo loss of function mutation in a case with childhood onset schizophrenia. Journal of Human Genetics, 66(3), 339–343. https://doi.org/10.1038/s10038-020-00846-1
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Columbia Affiliation
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