Published Papers (listed alphabetically by first author, most recent year first)

2009

  • Kathiresan, S., Willer, C.J., Peloso, G.M., Demissie, S., Musunuru, K., Schadt, E.E., Kaplan, L., Bennett, D., Li, Y., Tanaka, T., Voight, B.F., Bonnycastle, L.L., Jackson, A.U., Crawford, G., Surti, A., Guiducci, C., Burtt, N.P., Parish, S., Clarke, R., Zelenika, D., Kubalanza, K.A., Morken, M.A., Scott, L.J., Stringham, H.M., Galan, P., Swift, A.J., Kuusisto, J., Bergman, R.N., Sundvall, Laakso, M., Ferrucci, L., Scheet, P., Sanna, S., Uda, M., Yang, Q., Lunetta, K.L., Dupuis, J., de Bakker, P.I.W., O'Donnell, C.J., Chambers, J.C., Kooner, J.S., Hercberg, S., Meneton, P., Lakatta, E.G., Scuteri, A., Schlessinger, D., Tuomilehto, J., Collins, F.S., Groop, L., Altshuler, D., Collins, R., Lathrop, G.M., Melander, O., Salomaa, V., Peltonen, L., Orho-Melander, M., Ordovas, J.M., Boehnke, M., Abecasis, G.R., Mohlke, K.L., and Cupples, L.A. (2009) Common Variants at 30 Loci Contribute to Polygenic Dyslipidemia. Nature Genetics 41(1):56-65.

  • Lindgren, C.M., Heid, I.M., Randall, J.C., Lamina, C., Steinthorsdottir, V., Qi, L., Speliotes, E.K., Thorleifsson, G., Willer, C.J., Herrera, B.M., Jackson, A.U., Lim, N., Scheet, Pl, Soranzo, N., Amin, N., Aulchenko, Y.S., Chambers, Y.S., Chambers, J.D., Drong, A., Luan, Jl, Lyon, H.N., Rivadeneira, F., Sanna, S., Timpson, N.J., Zillikens, M.C., Zhao, J.H., Almgren, P., Bandinelli, S., Bennett, A.J., Bergman, R.N., Bonnycastle, L.L., Bumpstead, S.J., Chanock, S.J., Cherkas, L., Chines, P., Coin, L., Cooper, C., Crawford, G., Doering, A., Dominiczak, A., Doney, A.S., Ebrahim, S., Elliott, P., Erdos, M.R., Estrada, K., Ferrucci, L., Fischer G, Forouhi NG, Gieger C, Grallert H, Groves CJ, Grundy S, Guiducci C, Hadley D, Hamsten A, Havulinna AS, Hofman A, Holle R, Holloway JW, Illig T, Isomaa B, Jacobs LC, Jameson K, Jousilahti P, Karpe F, Kuusisto J, Laitinen J, Lathrop GM, Lawlor DA, Mangino M, McArdle WL, Meitinger T, Morken MA, Morris AP, Munroe P, Narisu N, Nordström A, Nordström P, Oostra BA, Palmer CN, Payne F, Peden JF, Prokopenko I, Renström F, Ruokonen A, Salomaa V, Sandhu MS, Scott LJ, Scuteri A, Silander K, Song K, Yuan X, Stringham HM, Swift AJ, Tuomi T, Uda M, Vollenweider P, Waeber G, Wallace C, Walters GB, Weedon MN; Wellcome Trust Case Control Consortium, Witteman JC, Zhang C, Zhang W, Caulfield MJ, Collins FS, Davey Smith G, Day IN, Franks PW, Hattersley AT, Hu FB, Jarvelin MR, Kong A, Kooner JS, Laakso M, Lakatta E, Mooser V, Morris AD, Peltonen L, Samani NJ, Spector TD, Strachan DP, Tanaka T, Tuomilehto J, Uitterlinden AG, van Duijn CM, Wareham NJ, Hugh Watkins; Procardis Consortia, Waterworth DM, Boehnke M, Deloukas P, Groop L, Hunter DJ, Thorsteinsdottir U, Schlessinger D, Wichmann HE, Frayling TM, Abecasis GR, Hirschhorn JN, Loos RJ, Stefansson K, Mohlke KL, Barroso I, McCarthy MI, and the Giant Consortium (2009) Genome wide association scan meta-analysis identifies novel loci influencing adiposity and fat distribution. Public Library of Science Genetics 5:e1000508. PMCID: PMC2695778.

  • Lyssenko, V., Nagorny, C.L.F., Erdos, M.R., Wierup, N., Jonsson, A., Spegel, P., Bugliani, M., Saxena, R., Fex, M., Pulizzi, N., Isomaa, B., Tuomi, T., Nilsson, P., Kuusisto, J., Tuomilehto, J., Boehnke, M., Altshuler, D., Sundler, F., Eriksson, J.G., Jackson, A.U., Laakso, M., Marchetti, P., Watanabe, R.M., Mulder, H., and Groop, L. (2009) Common Variant in MTNR1B Associated with Increased Risk of Type 2 Diabetes and Impaired Early Insulin Secretion. Nature Genetics 41(1):82-88.

  • Prokopenko, I., Langenberg, C., Florez, J.C., Saxena, R., Soranzo, N., Thorleifsson, G., Loos, R.J.F., Manning, A.K., Jackson, A.U., Aulchenko, Y., Potter, S.C., Erdos, M.R., Sanna, S., Hottenga, J-J., Wheeler, E., Kaakinen, M., Lyssenko, V., Chen, W-M., Kourosh, K., Beckmann, J.S., Bergman, R.N., Bochud, M., Bonnycastle, L.L., Buchanan, T.A., Cao, A., Cervino, A., Coin, L., Collins, F.S., Crisponi, L., de Geus, E.J.C., Dehghan, A., Deloukas, P., Doney, A.S.F., Elliott, P., Freimer, N., Gateva, V., Herder, C., Hofman, A., Hughes, T.E., Hunt, S., Illig, T., Inouye, M., Isomaa, B., Johnson, T., Kong, A., Krestyaninova, M., Kuusisto, J., Laakso, M., Lim, N., Lindblad, U., Lindgren, C.M., McCann, O.T., Mohlke, K.L., Morris, A.D., Naitza, S., Orru, M., Palmer, C.N.A., Pouta, A., Randall, J., Rathmann, W., Saramies, J., Scheet, P., Scott, L.J., Scuteri, A., Sharp, S., Sijbrands, E., Smit, J.H., Song, K., Steinthorsdottir, V., Stringham, H.M., Tuomi, T., Tuomilehto, J., Uitterlinden, A.G., Voight, B.F., Waterworth, D., Wichmann, H-E., Willemsen, G., Witteman, J.C.M., Yuan, X., Zhao, J.H., Zeggini, E., Schlessinger, D., Sandhu, M., Boomsma, D.I., Uda, M., Spector, T.D., Penninx, B.W.J.H., Altshuler, D., Vollenweider, P., Jarvelin, M.R., Lakatta, E., Waeber, G., Fox, C.S., Peltonen8, L., Groop, L.C., Mooser, V., Cupples, L.A., Thorsteinsdottir, U., Boehnke, M., Barroso, I., Van Duijn, C., Dupuis, J., Watanabe, R.M., Stefansson, K., McCarthy, M.I., Wareham, N.J., Meigs, J.B., and Abecasis, G.R. (2009) Variants in MTNR1B Influence Fasting Glucose Levels. Nature Genetics 41(1):77-81.

  • Willer, C.J., Speliotes, E.K., Loos, R.J.F., Li, S., Lindgren, C.M., Heid, I.M., Berndt, S.I., Elliott, A.L., Jackson, A.U., Lamina, C., Lettre, G., Lim, N., Lyon, H.N., McCarroll, S.A., Papadakis, K., Qi, Ll, Randall, J.C., Roccasecca, R.M., Sanna, S., Scheet, P., Weedon, M.N., Wheeler, E., Zhao, J.H., Jacobs, L.C., Prokopenko, I., Soranzo, N., Tanaka, T., Timpson, N.J., Almgren, P., Bennett, A., Bergman, R.N., Bingham, S.A., Bonnycastle, L.L., Brown, M., Burtt, N., Chines, P., Coin, L., Collins, F.S., Connell, J.M., Cooper, C., Smith, G.D., Dennison, E.M., Deodhar, P., Elliott, P., Erdos, M.R., Estrada, K., Evans, D.M., Gianniny, O.L., Gieger, C., Gillson, C.J., Guiducci, C., Hackett, R., Hadley, D., Hall, A.S., Havulinna, A.S., Hebebrand, J., Hofman, A., Isomaa, B., Jacobs, K.B., Johnson, T., Jousilahti, P., Jovanovic, Z., Khaw, K-T., Kraft, P., Kuokkanen, M., Kuusisto, J., Laitinen, J., Lakatta, E.G., Luan, J., Luben, R.N., Mangino, M., McArdle, W.L., Meitinger, T., Mulas, A., Munroe, P.B., Narisu, N., Ness, A.R., Northstone, K., O'Rahilly, S., Purmann, C., Rees, M.G., Ridderstrale, M., Ring, S.M., Rivadeneira, F., Ruokonen, A., Sandhu, M.S., Saramies, J., Scott, L.J., Scuteri, A., Silander, K., Sims, M.A., Song, K., Stephens, J., Stevens, S., Stringham, H.M., Tung, Y.C.L., Valle, T.T., Van Duijn, C.M., Vimaleswaran, K.S., Vollenweider, P., Waeber, G., Wallace, C., Watanabe, R.M., Waterworth, D.M., Watkins, N., The Wellcome Trust Case Control Consortium, Witteman, J.C.M., Zeggini, E., Zhai, G., Zillikens, M.C., Altshuler, D., Caulfield, M.D., Chanock, S.J., Farooqi, I.S., Ferrucci, L., Guralnik, J.M., Hattersley, A.T., Hu, F.B., Jarvelin, M.R., Laakso, M., Mooser, V., Ong, K.K., Ouwehand, W.H., Salomaa, V., Samani, N.J., Spector, T.D., Tuomi, T., Tuomilehto, J., Uda, M., Uitterlinden, A.G., Wareham, N.J., Deloukas, P., Frayling, T.M., Groop, L.C., Hayes, R.B., Hunter, D.J., Mohlke, K.L., Peltonen, L., Schlessinger, D., Strachan, D.P., Wichmann, H-E., McCarthy, M.I., Boehnke, M., Barroso, I., Abecasis, G.R., and Hirschhorn, J.N. for the GIANT Consortium (2009) Six New Loci Associated with Body Mass Index Highlight a Neuronal Influence on Body Weight Regulation. Nature Genetics 41(1):25-34.

2008

  • Chen, W-M, Erdos, M.R., Jackson, A.U., Saxena, R., Sanna, S., Silver, K.D., Timpson, N.J., Hansen, T., Orrů, M., Piras, M.G., Bonnycastle, L.L., Willer, C.J., Lyssenko, V., Shen, H., Kuusisto, J., Ebrahim, S., Sestu, N., Duren, W.L., Spada, M.C., Stringham, H.M., Scott, L.J., Olla, N., Swift, A.J., Najjar, S., Mitchell, B.D., Lawlor, D.A., Smith, G.D., Ben-Shlomo, Y., Andersen, G., Borch-Johnsen, K., Jřrgensen, T., Saramies, J., Valle, T.T., Buchanan, T.A., Shuldiner, A.R., Lakatta, E., Bergman, R.N., Uda, M., Tuomilehto, J., Pedersen, O., Cao, A., Groop, L., Mohlke, K.L., Laakso, M., Schlessinger, D., Collins, F.S., Altshuler, D., Abecasis, G.R., Boehnke, M., Scuteri, A., Watanabe, R.M. (2008) Variations in the G6PC2/ABCB11 Genomic Region are Associated with Fasting Glucose Levels. Journal of Clinical Investigation 118:2620-2628. Published online 2 June 2008, doi:10.1172/JCI34566.

  • Franks, P.W., Rolandsson, O., Debenham, S.L., Fawcett, K.A., Payne, F., Dina, C., Froguel, P., Mohlke, K.L., Willer, C., Olsson, T., Wareham, N.J., Hallmans, G., Barroso, I., and Sandhu, M.S. (2008) Replication of the Association Between Variants in WFS1 and Risk of Type 2 Diabetes in European Populations Diabetologia51(3):458-463.

  • Lettre, G., Jackson, A.U., Gieger, C., Schumacher, F.R., Berndt, S.I., Sanna, S., Eyheramendy, S., Voight, B.F., Butler, J.L, Guiducci, C., Illig, T., Hackett, R., Heid, I.M., Jacobs, K.B., Lyssenko, V., Uda, M., The Diabetes Genetics Initiative, FUSION, KORA, The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial, The Nurses' Health Study, SardiNIA, Boehnke, M., Chanock, S.J., Groop, L.C., Hu, F.B., Isomaa, B., Kraft, P., Peltonen, L., Salomaa, V., Schlessinger, D., Hunter, D.J., Hayes, R.B., Abecasis, G.R., Wichmann, H-Erich, Mohlke, K.L., and Hirschhorn, J.N. (2008) Identification of Ten Loci Associated with Height Highlights New Biological Pathways in Human Growth, Nature Genetics, 40:584-591. Published Online 6 April 2008, doi:10.1038/ng.125.
    Supplementary Text and Figures

  • Loos, R.J.F., Lindgren, C.M., Li, S., Wheeler, E., Zhao, J.H., Prokopenko, I., Inouye, M., Freathy, R.M., Attwood, A.P., Beckmann, J.S., Berndt, S.I., The Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial, Bergmann, S., Bennett, A.M., Bingham, S.A., Bochud, M., Brown, M., Cauchi, S., Connell, J.M., Cooper, C., Smith, G.D., Day, I., Dina, C., De, S., Dermitzakis, E.T., Doney, A.S., Elliott, K.S., Elliott, P., Evans, D.M., Farooqi, S., Froguel, P., Ghori, J., Groves, J., Gwilliam, R., Hadley, D., Hall, A.S., Hattersley, A.T., Hebebrand, J. Heid, I.M., KORA, Herrera, B., Hinney, A., Hunt, S.E., Jarvelin, M-R., Johnson, T., Jolley, J.D.M., Karpe, F., Keniry, A., Khaw, K-T., Luben, R.N., Mangino, M., Marchini, J., McArdle, W., McGinnis, R., Meyre, D., Munroe, P.B., Morris, A.D., Ness, A.R., Neville, M.J., Nica, A.C., Ong, K.K., O'Rahilly, S., Owen, K.R., Palmer, C.N.A., Papadakis, K., Potter, S., Pouta, A., Qi, L., Nurses' Health Study, Randall, J.C., Rayner, N.W., Ring, S.M., Sandhu, M.S., Scherag, A., Sims, M.A., Song, K., Soranzo, N., Speliotes, E.K., Diabetes Genetics Initiative, Syddall, H.E., Teichmann, S.A., Timpson, N.J., Tobias, J.H., Uda, M., The SardiNIA Study, Ganz Vogel, C.I., Wallace, C., Waterworth, D.M., Weedon, M.N., The Wellcome Trust Case Control Consortium, Willer, C.J., FUSION, Wraight, V.L., Yuan, X., Zeggini, E., Hirschhorn, J.N., Strachan, D.P., Ouwehand, W.H., Caulfield, M.J., Samani, N.J., Frayling, T.M., Vollenweider, P., Waeber, G., Mooser, V., Deloukas, P., McCarthy, M., Wareham, N.J., and Barroso, I. (2008) Common Variants Near MC4R are Associated with Fat Mass, Weight, and Risk of Obesity, Nature Genetics 40:768-775. Published Online 4 May 2008, doi:10.1038/ng.140.
    Supplementary Text and Figures

  • Sanna, S., Jackson, A.U., Nagaraja, R., Willer, C.J., Chen, W-M., Bonnycastle, L.L., Shen, H., Timpson, N., Lettre, G., Usala, G., Chines, P.S., Stringham, H.M., Scott, L.J., Dei, M., Lai, S., Albai, G., Crisponi, L., Naitza, S., Doheny, K.F., Pugh, E.W., Shlomo, Y.B., Ebrahim, S., Lawlor, D.A., Bergman, R.N., Watanabe, R.M., Uda, M., Tuomilehto, J., Coresh, J., Hirschhorn, J.N., Shuldiner, A.R., Schlessinger, D., Collins, F.S., Smith, G.D., Boerwinkle, E., Cao, A., Boehnke, M., Abecasis, G.R., Mohlke, K.L. (2008) Common Variants in the GDF5-UQCC Region are Associated with Variation in Human Height. Nature Genetics 40:198-203. Published online 13 January 2008, doi:10.1038/ng.74. Supplemental Material

  • Willer, C.J., Sanna, S., Jackson, A.U., Scuteri, A., Bonnycastle, L.L., Clarke, R., Heath, S.C., Timpson, N.J., Najjar, S.S., Stringham, H.M., Strait, J., Duren, W.L., Maschio, A., Busonero, F., Mulas, A., Albai, G., Swift, A.J., Morken, M.A., Narisu, N., Bennett, D., Parish, S., Shen, H., Galan, P., Meneton, P., Hercberg, S., Zelenika, D., Chen, W-M., Li, Y., Scott, L.J., Sheet, P.A., Sundvall, J., Watanabe, R.M., Nagaraja, R., Ebrahim, S., Lawlor, D.A., Ben-Shlomo, Y., Davey-Smith, G., Shuldiner, A.R., Collins, R., Bergman, R.N., Uda, M., Tuomilehto, J., Cao, A., Collins, F.S., Lakatta, E., Lathrop, G.M., Boehnke, M., Schlessinger, D., Mohlke, K.L., Abecasis, G.R. (2008) Newly Identified Loci that Influence Lipid Concentrations and Risk of Coronary Artery Disease. Nature Genetics 40:161-169. Published online 13 January 2008, doi:10.1038/ng.76. Supplemental Material

  • Zeggini, E., Scott, L.J., Saxena, R., and Voight, B.F., for the Diabetes Genetics Replication and Meta-analysis (DIAGRAM) Consortium (2008) Meta-analysis of Genome-wide Association Data and Large-scale Replication Identifies Additional Susceptibility Loci for Type 2 Diabetes, Nature Genetics 40:638-645. Published Online 30 March 2008, doi:10.1038/ng.120.
    Supplementary Text and Figures
    Supplementary Table 5

2007

2006

  • Bonnycastle, L.L., Willer, C.J., Conneely, K.N., Jackson, A.U., Burrill, C.P., Watanabe, R.M., Chines, P.S., Narisu, N., Scott, L.J., Enloe, S.T., Swift, A.J., Duren, W.L., Stringham, H.M., Erdos, M.R., Riebow, N.L., Buchanan, T.A., Valle, T.T., Tuomilehto, J., Bergman, R.N., Mohlke, K.L., Boehnke, M., Collins, F.S. (2006) Common Variants in Maturity-Onset Diabetes of the Young Genes Contribute to Risk of Type 2 Diabetes in Finns. Diabetes 55:2534-2540.

  • Huth, C., Heid, I.M., Vollmert, C., Gieger, C., Grallert, H., Wolford, J.K., Langer, B., Thorand, B., Klopp, N., Hamid, Y.H., Pedersen, O., Hansen, T., Lyssenko, V., Groop, L., Meisinger, C., Doring, A., Lowel, H., Lieb, W., Hengstenberg, C., Rathmann, W., Martin, S., Stephens, J.W., Ireland, H., Mather, H., Miller, G.J., Stringham, H.M., Boehnke, M., Tuomilehto, J., Boeing, H., Mohlig, M., Spranger, J., Pfeiffer, A., Wernstedt, I., Niklason, A., Lopez-Bermejo, A., Fernandez-Real, J.M., Hanson, R.L., Gallart, L., Vendrell, J., Tsiavou, A., Hatziagelaki, E., Humphries, S.E., Wichmann, H.E., Herder, C., Illig T. (2006) IL6 Gene Promoter Polymorphisms and Type 2 Diabetes Joint Analysis of Individual Participants' Data From 21 Studies. Diabetes 55:2915-2921 (Also online appendix).

  • Scott, L.J., Bonnycastle, L.L., Willer, C.J., Sprau, A.G., Jackson, A.U., Narisu, N., Duren, W.L., Chines, P.S., Stringham, H.M., Erdos, M.R., Valle, T.T., Tuomilehto, J., Bergman, R.N., Mohlke, K.L., Collins, F.S., Boehnke, M. (2006) Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample. Diabetes 55:2649-2653.

  • Tsuchiya, T., Schwarz, P., del Bosque-Plata, L., Hayes, M.G., Dina, C., Froguel, P., Towers, G.W., Fischer, S., Temelkova-Kurktschiev, T., Rietzsch, H., Graessler, J., Vcelák, J., Palyzová, D., Selisko, T., Bendlová, B., Schulze, J., Julius, U., Hanefeld, M., Weedon, M.N., Evans, J.C., Frayling, T.M., Hattersley, A.T., Orho-Melander, M., Groop, L., Malecki, M.T., Hansen, T., Pedersen, O., Fingerlin, T.E., Boehnke, M., Hanis, C.L., Cox, N.J., and Bell, G.I. (2006) Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analyses. Molecular Genetics and Metabolism 89:174-184.

  • Willer, C.J., Scott, L.J., Bonnycastle, L.L, Jackson, A.U., Chines, P., Pruim, R., Bark, C.W., Tsai, Y., Pugh, E.W., Doheny, K.F., Kinnunen, L., Mohlke, K.L., Valle, T.T., Bergman, R.N., Tuomilehto, J., Collins, F.S., and Boehnke, M. (2006) Tag SNP Selection for Finnish Individuals Based on the CEPH Utah HapMap Database. Genetic Epidemiology 30:180-190.

2005

2004

2002

2001

2000

  • Ghosh, S., Watanabe, R.M., Valle, T., Hauser, E.R., Magnuson, V.L., Langefeld, C.D., Ally, D.S., Mohlke, K.L., Silander, K., Kohtamaki, K., Chines, P., Balow, J., Birznieks, G., Chang, J., Eldridge, W., Erdos, M.R., Karanjawala, Z.E., Knapp, J.I., Kudelko, K., Martin, C., Morales-Mena, A., Musick, A., Musick, T., Pfahl, C., Porter, R., Rayman, J.B., Rha, D., Segal, L., Shapiro, S., Sharaf, R., Shurtleff, B., So, A., Tannenbaum, J., Te, C., Tovar, J., Unni, A., Welch, C., Whiten, R., Witt, A., Blaschak-Harvan, J., Douglas, J.A., Duren, W.L., Epstein, M.P., Fingerlin, T.E., Kaleta, H.S., Lange, E.M., Li, C., McEachin, R.C., Stringham, H.M., Trager, E., White, P.P., Eriksson, J., Toivanen, L., Vidgren, G., Nylund, S.J., Tuomilehto-Wolf, E., Ross, E.H., Demirchyan, E., Hagopian, W.A., Buchanan, T.A., Tuomilehto, J., Bergman, R.N., Collins, F.S., and Boehnke, M. (2000) The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. I. An Autosomal Genome Scan for Genes that Predispose to Type 2 Diabetes. American Journal of Human Genetics 67:1174-1185.

  • Karanjawala, Z.E., Kaariainen, H., Ghosh, S., Tannenbaum, J., Martin, C., Ally, D., Tuomilehto, J., Valle, T., and Collins, F.S. (2000) Complete Maternal Isodisomy of Chromosome 8 in an Individual with an Early-Onset Ileal Carcinoid Tumor. American Journal of Medical Genetics 93:207-210.

  • Watanabe, R.M., Ghosh, S., Langefeld, C.D., Valle, T., Hauser, E.R., Magnuson, V.L., Mohlke, K.L., Silander, K., Ally, D.S., Chines, P., Blaschak-Harvan, J., Douglas, J.A., Duren, W.L., Epstein, M.P., Fingerlin, T.E., Kaleta, H.S., Lange, E.M., Li, C., McEachin, R.C., Stringham, H.M., Trager, E., White, P.P., Balow, J., Birznieks, G., Chang, J., Eldridge, W., Erdos, M.R., Karanjawala, Z.E., Knapp, J.I., Kudelko, K., Martin, C., Morales-Mena, A., Musick, A., Musick, T., Pfahl, C., Porter, R., Rayman, J.B., Rha, D., Segal, L., Shapiro, S., Sharaf, R., Shurtleff, B., So, A., Tannenbaum, J., Te, C., Tovar, J., Unni, A., Welch, C., Whiten, R., Witt, A., Kohtamaki, K., Ehnholm, C., Eriksson, J., Toivanen, L., Vidgren, G., Nylund, S.J., Tuomilehto-Wolf, E., Ross, E.H., Demirchyan, E., Hagopian, W.A., Buchanan, T.A., Tuomilehto, J., Bergman, R.N., Collins, F.S., and Boehnke, M. (2000) The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) Study. II. An Autosomal Genome Scan for Diabetes-Related Quantitative-Trait Loci. American Journal of Human Genetics 67:1186-1200.

1999

1998

1997

1996


FUSION-Related Papers (Published)

2009

  • Xiao, R. and Boehnke, M. (2009) Quantifying and correcting for the winner's curse in genetic association studies. Genetic Epidemiology 33:453-462. PMCID: PMC2706290.

  • Guan W, Liang L, Boehnke M, and Abecasis GR (2009) Genotype-based matching to correct for population stratification in large-scale case-control genetic association studies. Genetic Epidemiology 33:508-517. PMCID: PMC2732762.

  • Salanti G, Southam L, Altshuler D, Ardlie K, Barroso I, Boehnke M, Cornelis MC, Frayling TM, Grallert H, Grarup N, Groop L, Hansen T, Hattersley AT, Hu FB, Hveem K, Illig T, Kuusisto J, Laakso M, Langenberg C, Lyssenko V, McCarthy MI, Morris A, Morris AD, Palmer CN, Payne F, Platou CG, Scott LJ, Voight BF, Wareham NJ, Zeggini E, and Ioannidis JP (2009) Underlying genetic models of inheritance in established type 2 diabetes associations. American Journal of Epidemiology 170:537-545. PMCID: PMC2732984.

2007

2006

2005

2004

2003

1997
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