Palmer, Colin

Professor, Associate Dean for Research

Calculated based on number of publications stored in Pure and citations from Scopus
1987 …2025

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  • 2022

    Common and rare variants in SLCO1B1 are associated with statin intolerance

    Bigossi, M., Maroteau, C., Dawed, A. Y., Taylor, A., Srinivasan, S., Melhem, A. L., Pearson, E. R., Pola, R., Palmer, C. N. A. & Siddiqui, M. K. (Lead / Corresponding author), 10 Aug 2022, medRxiv.

    Research output: Working paper/PreprintPreprint

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    38 Downloads (Pure)
  • 2021

    A meta-analysis of the genome-wide association studies on two genetically correlated phenotypes (self-reported headache and self-reported migraine) identifies four new risk loci for headaches (N=397,385)

    Meng, W. (Lead / Corresponding author), Reel, P. S., Nangia, C., Rajendrakumar, A. L., Hebert, H. L., Adams, M. J., Zheng, H., Lu, Z. H., Team, 2. R., Ray, D., Colvin, L. A., Palmer, C. N., McIntosh, A. & Smith, B. H., 22 Sept 2021, Cold Spring Harbor Laboratory: medRxiv, 25 p.

    Research output: Working paper/PreprintPreprint

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  • A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

    Smith, B. H., Palmer, C., Zhu, X. (Lead / Corresponding author) & Brown, C. D. (Lead / Corresponding author), 8 Dec 2021, Cold Spring Harbor Laboratory: BioRxiv.

    Research output: Working paper/PreprintPreprint

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    375 Downloads (Pure)
  • Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

    Kanoni, S., Graham, S. E., Wang, Y., Surakka, I., Ramdas, S., Zhu, X., Clarke, S. L., Bhatti, K. F., Vedantam, S., Winkler, T. W., Locke, A. E., Marouli, E., Zajac, G. J. M., Wu, K.-H. H., Ntalla, I., Hui, Q., Klarin, D., Hilliard, A. T., Wang, Z. & Palmer, C. & 3 others, Smith, B. H., Willer, C. J. (Lead / Corresponding author) & Peloso, G. M. (Lead / Corresponding author), 16 Dec 2021, Cold Spring Harbor Laboratory: medRxiv.

    Research output: Working paper/PreprintPreprint

    Open Access
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    210 Downloads (Pure)
  • 2019

    Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure

    B.A.F. Investigators, Regeneron Genetics Center, EchoGen Consortium, Shah, S., Henry, A., Roselli, C., Lin, H., Sveinbjörnsson, G., Fatemifar, G., Hedman, Å. K., Wilk, J. B., Morley, M. P., Chaffin, M. D., Helgadottir, A., Verweij, N., Dehghan, A., Almgren, P., Andersson, C., Aragam, K. G. & Ärnlöv, J. & 129 others, Backman, J. D., Biggs, M. L., Bloom, H. L., Brandimarto, J., Brown, M. R., Buckbinder, L., Carey, D. J., Chasman, D. I., Chen, X., Chen, X., Chung, J., Chutkow, W., Cook, J. P., Delgado, G. E., Denaxas, S., Doney, A. S., Dörr, M., Dudley, S. C., Dunn, M. E., Engström, G., Esko, T., Felix, S. B., Finan, C., Ford, I., Ghanbari, M., Ghasemi, S., Giedraitis, V., Giulianini, F., Gottdiener, J. S., Gross, S., Guðbjartsson, D. F., Gutmann, R., Haggerty, C. M., van der Harst, P., Hyde, C. L., Ingelsson, E., Jukema, J. W., Kavousi, M., Khaw, K.-T., Kleber, M. E., Køber, L., Koekemoer, A., Langenberg, C., Lind, L., Lindgren, C. M., London, B., Lotta, L. A., Lovering, R. C., Luan, J., Magnusson, P. K. E., Mahajan, A., Margulies, K. B., März, W., Melander, O., Mordi, I., Morgan, T., Morris, A., Morris, A. P., Morrison, A. C., Nagle, M. W., Nelson, C. P., Niessner, A., Niiranen, T., O'Donoghue, M. L., Owens, A. T., Palmer, C., Parry, H., Perola, M., Portilla-Fernandez, E., Psaty, B. M., Rice, K. M., Ridker, P. M., Romaine, S. P. R., Rotter, J. I., Salo, P., Salomaa, V., van Setten, J., Shalaby, A. A., Smelser, D. T., Smith, N. L., Stender, S., Stott, D. J., Svensson, P., Tammesoo, M.-L., Taylor, K. D., Teder-Laving, M., Teumer, A., Thorgeirsson, G., Thorsteinsdottir, U., Torp-Pedersen, C., Trompet, S., Tyl, B., Uitterlinden, A. G., Veluchamy, A., Völker, U., Voors, A. A., Wang, X., Wareham, N. J., Waterworth, D. M., Weeke, P. E., Weiss, R., Wiggins, K. L., Xing, H., Yerges-Armstrong, L. M., Yu, B., Zannad, F., Zhao, J. H., Hemingway, H., Samani, N. J., McMurray, J. J. V., Yang, J., Visscher, P. M., Newton-Cheh, C., Mälarstig, A., Holm, H., Lubitz, S. A., Sattar, N., Holmes, M. V., Cappola, T. P., Asselbergs, F. W., Hingorani, A. D., Kuchenbaecker, K., Ellinor, P. T., Lang, C., Stefansson, K., Smith, J. G., Vasan, R. S., Swerdlow, D. I. & Lumbers, R. T. (Lead / Corresponding author), 10 Jun 2019, BioRxiv, 46 p.

    Research output: Working paper/PreprintPreprint

  • 2018

    Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease

    Veluchamy, A., Ballerini, L., Vitart, V., Schraut, K. E., Kirin, M., Campbell, H., Joshi, P. K., Relan, D., Harris, S., Vaidya, S. S. .., Dhillon, B., Zhou, K., Pearson, E., Hayward, C., Polašek, O., Deary, I. J., MacGillivray, T. J., Wilson, J. F., Trucco, M. & Palmer, C. (Lead / Corresponding author) & 1 others, Doney, A. (Lead / Corresponding author), 20 Jun 2018, BioRxiv.

    Research output: Working paper/PreprintPreprint

    Open Access
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    27 Downloads (Pure)