Hum Mol Genet

A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis

Munz M, Willenborg C, Richter GM, Jockel-Schneider Y, Graetz C, Staufenbiel I, Wellmann J, Berger K, Krone B, Hoffmann P, van der Velde N, Uitterlinden AG, de Groot LCPGM, Sawalha AH, Direskeneli H, Saruhan-Direskeneli G, Guzeldemir-Akcakanat E, Keceli G, Laudes M, Noack B, Teumer A, Holtfreter B, Kocher T, Eickholz P, Meyle J, Doerfer C, Bruckmann C, Lieb W, Franke A, Schreiber S, Nohutcu RM, Erdmann J, Loos BG, Jepsen S, Dommisch H, Schaefer AS.

Hum Mol Genet. 2017 Jul 1;26(13):2577-2588. doi: 10.1093/hmg/ddx151.

https://www.ncbi.nlm.nih.gov/pubmed/28449029

A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis Read More »

Genome-wide association study of biologically-informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease

Offenbacher S, Divaris K, Barros SP, Moss KL, Marchesan JT, Morelli T, Zhang S, Kim S, Sun L, Beck JD, Laudes M, Munz M, Schaefer AS, North KE.

Hum Mol Genet. 2016, Mar 8. pii: ddw069. [Epub ahead of print] PubMed PMID: 26962152.

http://www.ncbi.nlm.nih.gov/pubmed/?term=26962152

Genome-wide association study of biologically-informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease Read More »

Genome-wide meta-analysis of common variant differences between men and women

Boraska, V., Jeroncic, A., Colonna, V., Southam, L., Nyholt, D. R., Rayner, N. W., Perry, J. R., Toniolo, D., Albrecht, E., Ang, W., Bandinelli, S., Barbalic, M., Barroso, I., Beckmann, J. S., Biffar, R., Boomsma, D., Campbell, H., Corre, T., Erdmann, J., Esko, T., Fischer, K., Franceschini, N., Frayling, T. M., Girotto, G., Gonzalez, J. R., Harris, T. B., Heath, A. C., Heid, I. M., Hoffmann, W., Hofman, A., Horikoshi, M., Zhao, J. H., Jackson, A. U., Hottenga, J. J., Jula, A., Kahonen, M., Khaw, K. T., Kiemeney, L. A., Klopp, N., Kutalik, Z., Lagou, V., Launer, L. J., Lehtimaki, T., Lemire, M., Lokki, M. L., Loley, C., Luan, J., Mangino, M., Mateo Leach, I., Medland, S. E., Mihailov, E., Montgomery, G. W., Navis, G., Newnham, J., Nieminen, M. S., Palotie, A., Panoutsopoulou, K., Peters, A., Pirastu, N., Polasek, O., Rehnstrom, K., Ripatti, S., Ritchie, G. R., Rivadeneira, F., Robino, A., Samani, N. J., Shin, S. Y., Sinisalo, J., Smit, J. H., Soranzo, N., Stolk, L., Swinkels, D. W., Tanaka, T., Teumer, A., Tonjes, A., Traglia, M., Tuomilehto, J., Valsesia, A., van Gilst, W. H., van Meurs, J. B., Smith, A. V., Viikari, J., Vink, J. M., Waeber, G., Warrington, N. M., Widen, E., Willemsen, G., Wright, A. F., Zanke, B. W., Zgaga, L., Wellcome Trust Case Control, Consortium, Boehnke, M., d’Adamo, A. P., de Geus, E., Demerath, E. W., den Heijer, M., Eriksson, J. G., Ferrucci, L., Gieger, C., Gudnason, V., et al.

Hum Mol Genet. 2012 Nov 1;21(21):4805-15. doi: 10.1093/hmg/dds304. Epub 2012 Jul 27.

http://www.ncbi.nlm.nih.gov/pubmed/22843499

Genome-wide meta-analysis of common variant differences between men and women Read More »

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene

Davison, L. J., Wallace, C., Cooper, J. D., Cope, N. F., Wilson, N. K., Smyth, D. J., Howson, J. M., Saleh, N., Al-Jeffery, A., Angus, K. L., Stevens, H. E., Nutland, S., Duley, S., Coulson, R. M., Walker, N. M., Burren, O. S., Rice, C. M., Cambien, F., Zeller, T., Munzel, T., Lackner, K., Blakenberg, S., Cardiogenics, Consortium, Fraser, P., Gottgens, B., Todd, J. A., Attwood, T., Belz, S., Braund, P., Cambien, F., Cooper, J., Crisp-Hihn, A., Diemert, P., Deloukas, P., Foad, N., Erdmann, J., Goodall, A. H., Gracey, J., Gray, E., Williams, R. G., Heimerl, S., Hengstenberg, C., Jolley, J., Krishnan, U., Lloyd-Jones, H., Lugauer, I., Lundmark, P., Maouche, S., Moore, J. S., Muir, D., Murray, E., Nelson, C. P., Neudert, J., Niblett, D., O’Leary, K., Ouwehand, W. H., Pollard, H., Rankin, A., Rice, C. M., Sager, H., Samani, N. J., Sambrook, J., Schmitz, G., Scholz, M., Schroeder, L., Schunkert, H., Syvannen, A. C., Tennstedt, S., Wallace, C.

Hum Mol Genet. 2012 Jan 15;21(2):322-33. doi: 10.1093/hmg/ddr468. Epub 2011 Oct 11.

http://www.ncbi.nlm.nih.gov/pubmed/21989056

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene Read More »

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease

Baessler, A., Fischer, M., Mayer, B., Koehler, M., Wiedmann, S., Stark, K., Doering, A., Erdmann, J., Riegger, G., Schunkert, H., Kwitek, A. E., Hengstenberg, C.

Hum Mol Genet. 2007 Apr 15;16(8):887-99. Epub 2007 Feb 26.

http://www.ncbi.nlm.nih.gov/pubmed/17324965

Epistatic interaction between haplotypes of the ghrelin ligand and receptor genes influence susceptibility to myocardial infarction and coronary artery disease Read More »

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