Gil Atzmon

2023

A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A: A rare human centenarian variant of SIRT6 enhances genome stability and interaction with Lamin A (The EMBO Journal, (2022), 41, 21, 10.15252/embj.2021110393)

Simon, M., Yang, J., Gigas, J., Earley, E. J., Hillpot, E., Zhang, L., Zagorulya, M., Tombline, G., Gilbert, M., Yuen, S. L., Pope, A., Van Meter, M., Emmrich, S., Firsanov, D., Athreya, A., Biashad, S. A., Han, J., Ryu, S., Tare, A., Zhu, Y., & 11 othersHudgins, A., Atzmon, G., Barzilai, N., Wolfe, A., Moody, K., Garcia, B. A., Robbins, P. D., Vijg, J., Seluanov, A., Suh, Y. & Gorbunova, V., 1 Feb 2023, In: EMBO Journal. 42, 3, e113326.

Research output: Contribution to journal › Comment/Debate

Open Access

2021

Author Correction: Transcript expression-aware annotation improves rare variant interpretation

Genome Aggregation Database Production Team & Genome Aggregation Database Consortium, 18 Feb 2021, In: Nature. 590, 7846, p. E54

Research output: Contribution to journal › Comment/Debate

Open Access

Author Correction: The effect of LRRK2 loss-of-function variants in humans

Genome Aggregation Database Production Team, Genome Aggregation Database Consortium & 23andMe Research Team, 1 Feb 2021, In: Nature Medicine. 27, 2, p. 355 1 p.

Research output: Contribution to journal › Comment/Debate

Open Access

Author Correction: Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Genome Aggregation Database Production Team & Genome Aggregation Database Consortium, 1 Dec 2021, In: Nature Communications. 12, 1, 827.

Research output: Contribution to journal › Comment/Debate

Open Access

Author Correction: Evaluating drug targets through human loss-of-function genetic variation

Genome Aggregation Database Production Team & Genome Aggregation Database Consortium, 18 Feb 2021, In: Nature. 590, 7846, p. E56

Research output: Contribution to journal › Comment/Debate

Open Access

Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans

Genome Aggregation Database Consortium, 18 Feb 2021, In: Nature. 590, 7846, p. E53

Research output: Contribution to journal › Comment/Debate

Open Access

Author Correction: A structural variation reference for medical and population genetics

Genome Aggregation Database Production Team & Genome Aggregation Database Consortium, 18 Feb 2021, In: Nature. 590, 7846, p. E55

Research output: Contribution to journal › Comment/Debate

Open Access

Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes

Deelen, J., Evans, D. S., Arking, D. E., Tesi, N., Nygaard, M., Liu, X., Wojczynski, M. K., Biggs, M. L., van der Spek, A., Atzmon, G., Ware, E. B., Sarnowski, C., Smith, A. V., Seppälä, I., Cordell, H. J., Dose, J., Amin, N., Arnold, A. M., Ayers, K. L., Barzilai, N., & 64 othersBecker, E. J., Beekman, M., Blanché, H., Christensen, K., Christiansen, L., Collerton, J. C., Cubaynes, S., Cummings, S. R., Davies, K., Debrabant, B., Deleuze, J. F., Duncan, R., Faul, J. D., Franceschi, C., Galan, P., Gudnason, V., Harris, T. B., Huisman, M., Hurme, M. A., Jagger, C., Jansen, I., Jylhä, M., Kähönen, M., Karasik, D., Kardia, S. L. R., Kingston, A., Kirkwood, T. B. L., Launer, L. J., Lehtimäki, T., Lieb, W., Lyytikäinen, L. P., Martin-Ruiz, C., Min, J., Nebel, A., Newman, A. B., Nie, C., Nohr, E. A., Orwoll, E. S., Perls, T. T., Province, M. A., Psaty, B. M., Raitakari, O. T., Reinders, M. J. T., Robine, J. M., Rotter, J. I., Sebastiani, P., Smith, J., Sørensen, T. I. A., Taylor, K. D., Uitterlinden, A. G., van der Flier, W., van der Lee, S. J., van Duijn, C. M., van Heemst, D., Vaupel, J. W., Weir, D., Ye, K., Zeng, Y., Zheng, W., Holstege, H., Kiel, D. P., Lunetta, K. L., Slagboom, P. E. & Murabito, J. M., Dec 2021, In: Nature Communications. 12, 1, p. 2463 2463.

Research output: Contribution to journal › Comment/Debate

Open Access

2019

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population (PLOS Genetics, (2018), 14, 5, 10.1371/journal.pgen.1007329)

International IBD Genetics Consortium, NIDDK IBD Genetics Consortium & T2D-GENES Consortium, May 2019, In: PLoS Genetics. 15, 5, e1008190.

Research output: Contribution to journal › Comment/Debate

Open Access

2018

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Flannick, J., Fuchsberger, C., Mahajan, A., Teslovich, T. M., Agarwala, V., Gaulton, K. J., Caulkins, L., Koesterer, R., Ma, C., Moutsianas, L., McCarthy, D. J., Rivas, M. A., Perry, J. R. B., Sim, X., Blackwell, T. W., Robertson, N. R., Rayner, N. W., Cingolani, P., Locke, A. E., Tajes, J. F., & 281 othersHighland, H. M., Dupuis, J., Chines, P. S., Lindgren, C. M., Hartl, C., Jackson, A. U., Chen, H., Huyghe, J. R., van de Bunt, M., Pearson, R. D., Kumar, A., Müller-Nurasyid, M., Grarup, N., Stringham, H. M., Gamazon, E. R., Lee, J., Chen, Y., Scott, R. A., Below, J. E., Chen, P., Huang, J., Go, M. J., Stitzel, M. L., Pasko, D., Parker, S. C. J., Varga, T. V., Green, T., Beer, N. L., Day-Williams, A. G., Ferreira, T., Fingerlin, T., Horikoshi, M., Hu, C., Huh, I., Ikram, M. K., Kim, B. J., Kim, Y., Kim, Y. J., Kwon, M. S., Lee, J., Lee, S., Lin, K. H., Maxwell, T. J., Nagai, Y., Wang, X., Welch, R. P., Yoon, J., Zhang, W., Barzilai, N., Voight, B. F., Han, B. G., Jenkinson, C. P., Kuulasmaa, T., Kuusisto, J., Manning, A., Ng, M. C. Y., Palmer, N. D., Balkau, B., Stančáková, A., Abboud, H. E., Boeing, H., Giedraitis, V., Prabhakaran, D., Gottesman, O., Scott, J., Carey, J., Kwan, P., Grant, G., Smith, J. D., Neale, B. M., Purcell, S., Butterworth, A. S., Howson, J. M. M., Lee, H. M., Lu, Y., Kwak, S. H., Zhao, W., Danesh, J., Lam, V. K. L., Park, K. S., Saleheen, D., So, W. Y., Tam, C. H. T., Afzal, U., Aguilar, D., Arya, R., Aung, T., Chan, E., Navarro, C., Cheng, C. Y., Palli, D., Correa, A., Curran, J. E., Rybin, D., Farook, V. S., Fowler, S. P., Freedman, B. I., Griswold, M., Hale, D. E., Hicks, P. J., Khor, C. C., Kumar, S., Lehne, B., Thuillier, D., Lim, W. Y., Liu, J., Loh, M., Musani, S. K., Puppala, S., Scott, W. R., Yengo, L., Tan, S. T., Taylor, H. A., Thameem, F., Wilson, G., Wong, T. Y., Njølstad, P. R., Levy, J. C., Mangino, M., Bonnycastle, L. L., Schwarzmayr, T., Fadista, J., Surdulescu, G. L., Herder, C., Groves, C. J., Wieland, T., Bork-Jensen, J., Brandslund, I., Christensen, C., Koistinen, H. A., Doney, A. S. F., Kinnunen, L., Esko, T., Farmer, A. J., Hakaste, L., Hodgkiss, D., Kravic, J., Lyssenko, V., Hollensted, M., Jørgensen, M. E., Jørgensen, T., Ladenvall, C., Justesen, J. M., Käräjämäki, A., Kriebel, J., Rathmann, W., Lannfelt, L., Lauritzen, T., Narisu, N., Linneberg, A., Melander, O., Milani, L., Neville, M., Orho-Melander, M., Qi, L., Qi, Q., Roden, M., Rolandsson, O., Swift, A., Rosengren, A. H., Stirrups, K., Wood, A. R., Mihailov, E., Blancher, C., Carneiro, M. O., Maguire, J., Poplin, R., Shakir, K., Fennell, T., DePristo, M., de Angelis, M. H., Deloukas, P., Gjesing, A. P., Jun, G., Nilsson, P., Murphy, J., Onofrio, R., Thorand, B., Hansen, T., Meisinger, C., Hu, F. B., Isomaa, B., Karpe, F., Liang, L., Peters, A., Huth, C., O'Rahilly, S. P., Palmer, C. N. A., Pedersen, O., Rauramaa, R., Tuomilehto, J., Salomaa, V., Watanabe, R. M., Syvänen, A. C., Bergman, R. N., Bharadwaj, D., Bottinger, E. P., Cho, Y. S., Chandak, G. R., Chan, J. C. N., Chia, K. S., Daly, M. J., Ebrahim, S. B., Langenberg, C., Elliott, P., Jablonski, K. A., Lehman, D. M., Jia, W., Ma, R. C. W., Pollin, T. I., Sandhu, M., Tandon, N., Froguel, P., Barroso, I., Teo, Y. Y., Zeggini, E., Loos, R. J. F., Small, K. S., Ried, J. S., DeFronzo, R. A., Grallert, H., Glaser, B., Metspalu, A., Wareham, N. J., Walker, M., Banks, E., Gieger, C., Ingelsson, E., Im, H. K., Illig, T., Franks, P. W., Buck, G., Trakalo, J., Buck, D., Prokopenko, I., Mägi, R., Lind, L., Farjoun, Y., Owen, K. R., Gloyn, A. L., Strauch, K., Tuomi, T., Kooner, J. S., Lee, J. Y., Park, T., Donnelly, P., Morris, A. D., Hattersley, A. T., Bowden, D. W., Collins, F. S., Atzmon, G., Chambers, J. C., Spector, T. D., Laakso, M., Strom, T. M., Bell, G. I., Blangero, J., Duggirala, R., Tai, E. S., McVean, G., Hanis, C. L., Wilson, J. G., Seielstad, M., Frayling, T. M., Meigs, J. B., Cox, N. J., Sladek, R., Lander, E. S., Gabriel, S., Mohlke, K. L., Meitinger, T., Groop, L., Abecasis, G., Scott, L. J., Morris, A. P., Kang, H. M., Altshuler, D., Burtt, N. P., Florez, J. C., Boehnke, M. & McCarthy, M. I., 23 Jan 2018, In: Scientific data. 5, p. 180002 1 p.

Research output: Contribution to journal › Comment/Debate

Open Access

2017

Correction: The complex genetics of gait speed: Genome-wide metaanalysis approach [Aging, (Albany NY), 9, 1, (2017), (209-246)]doi 10.18632/aging.101151

Ben-Avraham, D., Karasik, D., Verghese, J., Lunetta, K. L., Smith, J. A., Eicher, J. D., Vered, R., Deelen, J., Arnold, A. M., Buchman, A. S., Tanaka, T., Faul, J. D., Nethander, M., Fornage, M., Adams, H. H., Matteini, A. M., Callisaya, M. L., Smith, A. V., Yu, L., De Jager, P. L., & 50 othersEvans, D. A., Gudnason, V., Hofman, A., Pattie, A., Corley, J., Launer, L. J., Knopman, D. S., Parimi, N., Turner, S. T., Bandinelli, S., Beekman, M., Gutman, D., Sharvit, L., Mooijaart, S. P., Liewald, D. C., Houwing-Duistermaat, J. J., Ohlsson, C., Moed, M., Verlinden, V. J., Mellström, D., van der Geest, J. N., Karlsson, M., Hernandez, D., McWhirter, R., Liu, Y., Thomson, R., Tranah, G. J., Uitterlinden, A. G., Weir, D. R., Zhao, W., Starr, J. M., Johnson, A. D., Arfan Ikram, M., Bennett, D. A., Cummings, S. R., Deary, I. J., Harris, T. B., Kardia, S. L. R., Mosley, T. H., Srikanth, V. K., Windham, B. G., Newman, A. B., Walston, J. D., Davies, G., Evans, D. S., Slagboom, E. P., Ferrucci, L., Kiel, D. P., Murabito, J. M. & Atzmon, G., 1 Jul 2017, In: Aging. 9, 7, p. 1844-1846 3 p.

Research output: Contribution to journal › Comment/Debate

Open Access

Gil Atzmon

Research output

Search results