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20042019

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2019

Association of CamK2A genetic variants with transition time from occasional to regular heroin use in a sample of heroin-dependent individuals

Eirich, A., Biermann, T., Müller, C. P., Kornhuber, J., Benyamin, B., Hulse, G. K., Wildenauer, D. B. & Schwab, S. G., 1 Feb 2019, In : Psychiatric Genetics. 29, 1, p. 18-25 8 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Associations of genetically determined iron status across the phenome: A mendelian randomization study

Gill, D., Benyamin, B., Moore, L. S. P., Monori, G., Zhou, A., Koskeridis, F., Evangelou, E., Laffan, M., Walker, A. P., Tsilidis, K. K., Dehghan, A., Elliott, P., Hypponen, E. & Tzoulaki, I., 1 Jun 2019, In : PLoS Medicine. 16, 6, e1002833.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Comparative genetic architectures of schizophrenia in East Asian and European populations

Schizophrenia Working Group of the Psychiatric Genomics Consortium, Indonesia Schizophrenia Consortium & Genetic REsearch on schizophreniA neTwork-China and the Netherlands (GREAT-CN), 1 Dec 2019, In : Nature Genetics. 51, 12, p. 1670-1678 9 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)

Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expression

Tarr, I. S., McCann, E. P., Benyamin, B., Peters, T. J., Twine, N. A., Zhang, K. Y., Zhao, Q., Zhang, Z. H., Rowe, D. B., Nicholson, G. A., Bauer, D., Clark, S. J., Blair, I. P. & Williams, K. L., 1 Dec 2019, In : Scientific Reports. 9, 1, 8254.

Research output: Contribution to journalArticle

5 Citations (Scopus)
2017

Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis

Benyamin, B., He, J., Zhao, Q., Gratten, J., Garton, F., Leo, P. J., Liu, Z., Mangelsdorf, M., Al-Chalabi, A., Anderson, L., Butler, T. J., Chen, L., Chen, X. D., Cremin, K., Deng, H. W., Devine, M., Edson, J., Fifita, J. A., Furlong, S., Han, Y. Y. & 44 othersHarris, J., Henders, A. K., Jeffree, R. L., Jin, Z. B., Li, Z., Li, T., Li, M., Lin, Y., Liu, X., Marshall, M., McCann, E. P., Mowry, B. J., Ngo, S. T., Pamphlett, R., Ran, S., Reutens, D. C., Rowe, D. B., Sachdev, P., Shah, S., Song, S., Tan, L. J., Tang, L., Van Den Berg, L. H., Van Rheenen, W., Veldink, J. H., Wallace, R. H., Wheeler, L., Williams, K. L., Wu, J., Wu, X., Yang, J., Yue, W., Zhang, Z. H., Zhang, D., Noakes, P. G., Blair, I. P., Henderson, R. D., McCombe, P. A., Visscher, P. M., Xu, H., Bartlett, P. F., Brown, M. A., Wray, N. R. & Fan, D., 1 Dec 2017, In : Nature communications. 8, 1, 611.

Research output: Contribution to journalArticle

16 Citations (Scopus)

Identification of novel loci affecting circulating chromogranins and related peptides

Benyamin, B., Maihofer, A. X., Schork, A. J., Hamilton, B. A., Rao, F., Schmid-Schönbein, G. W., Zhang, K., Mahata, M., Stridsberg, M., Schork, N. J., Biswas, N., Hook, V. Y., Wei, Z., Montgomery, G. W., Martin, N. G., Nievergelt, C. M., Whitfield, J. B. & O'Connor, D. T., 1 Jan 2017, In : Human Molecular Genetics. 26, 1, p. 233-242 10 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)

Investigating the relationship between iron and depression

Mills, N. T., Maier, R., Whitfield, J. B., Wright, M. J., Colodro-Conde, L., Byrne, E. M., Scott, J. G., Byrne, G. J., Hansell, N. K., Vinkhuyzen, A. A. E., CouvyDuchesne, B., Montgomery, G. W., Henders, A. K., Martin, N. G., Wray, N. R. & Benyamin, B., 1 Nov 2017, In : Journal of Psychiatric Research. 94, p. 148-155 8 p.

Research output: Contribution to journalArticle

Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness

GEFOS Anytype of Fracture Consortium, 12 Jul 2017, In : Nature communications. 8, 16015.

Research output: Contribution to journalArticle

41 Citations (Scopus)

No Genetic Overlap between Circulating Iron Levels and Alzheimer's Disease

Lupton, M. K., Benyamin, B., Proitsi, P., Nyholt, D. R., Ferreira, M. A., Montgomery, G. W., Heath, A. C., Madden, P. A., Medland, S. E., Gordon, S. D., Lovestone, S., Tsolaki, M., Kloszewska, I., Soininen, H., Mecocci, P., Vellas, B., Powell, J. F., Bush, A. I., Wright, M. J., Martin, N. G. & 1 othersWhitfield, J. B., 1 Jan 2017, In : Journal of Alzheimer's Disease. 59, 1, p. 85-99 15 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Serum iron level and kidney function: A Mendelian randomization study

Del Greco, F. M., Foco, L., Pichler, I., Eller, P., Eller, K., Benyamin, B., Whitfield, J. B., Pramstaller, P. P., Thompson, J. R., Pattaro, C. & Minelli, C., 1 Feb 2017, In : Nephrology Dialysis Transplantation. 32, 2, p. 273-278 6 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)

Whole exome sequencing and DNA methylation analysis in a clinical amyotrophic lateral sclerosis cohort

Garton, F. C., Benyamin, B., Zhao, Q., Liu, Z., Gratten, J., Henders, A. K., Zhang, Z. H., Edson, J., Furlong, S., Morgan, S., Heggie, S., Thorpe, K., Pfluger, C., Mather, K. A., Sachdev, P. S., McRae, A. F., Robinson, M. R., Shah, S., Visscher, P. M., Mangelsdorf, M. & 3 othersHenderson, R. D., Wray, N. R. & McCombe, P. A., 1 Jan 2017, In : Molecular Genetics and Genomic Medicine. 5, 4, p. 418-428 11 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

Gratten, J., Zhao, Q., Benyamin, B., Garton, F., He, J., Leo, P. J., Mangelsdorf, M., Anderson, L., Zhang, Z. H., Chen, L., Chen, X. D., Cremin, K., Deng, H. W., Edson, J., Han, Y. Y., Harris, J., Henders, A. K., Jin, Z. B., Li, Z., Lin, Y. & 18 othersLiu, X., Marshall, M., Mowry, B. J., Ran, S., Reutens, D. C., Song, S., Tan, L. J., Tang, L., Wallace, R. H., Wheeler, L., Wu, J., Yang, J., Xu, H., Visscher, P. M., Bartlett, P. F., Brown, M. A., Wray, N. R. & Fan, D., 17 Nov 2017, In : Genome Medicine. 9, 1, 97.

Research output: Contribution to journalArticle

6 Citations (Scopus)
2016

EigenGWAS: Finding loci under selection through genome-wide association studies of eigenvectors in structured populations

Chen, G. B., Lee, H., Zhu, Z. X., Benyamin, B. & Robinson, M. R., 1 Jul 2016, In : Heredity. 117, 1, p. 51-61 11 p.

Research output: Contribution to journalArticle

23 Citations (Scopus)
2015

Adiposity as a cause of cardiovascular disease: A Mendelian randomization study

European Network for Genetic and Genomic Epidemiology (ENGAGE) consortium, 27 May 2015, In : International journal of epidemiology. 44, 2, p. 578-586 9 p.

Research output: Contribution to journalArticle

79 Citations (Scopus)

Age- And sex-specific causal effects of adiposity on cardiovascular risk factors

Fall, T., Hägg, S., Ploner, A., Mägi, R., Fischer, K., Draisma, H. H. M., Sarin, A. P., Benyamin, B., Ladenvall, C., Åkerlund, M., Kals, M., Esko, T., Nelson, C. P., Kaakinen, M., Huikari, V., Mangino, M., Meirhaeghe, A., Kristiansson, K., Nuotio, M. L., Kobl, M. & 68 othersGrallert, H., Dehghan, A., Kuningas, M., De Vries, P. S., De Bruijn, R. F. A. G., Willems, S. M., Heikkilä, K., Silventoinen, K., Pietiläinen, K. H., Legry, V., Giedraitis, V., Goumidi, L., Syvänen, A. C., Strauch, K., Koenig, W., Lichtner, P., Herder, C., Palotie, A., Menni, C., Uitterlinden, A. G., Kuulasmaa, K., Havulinna, A. S., Moreno, L. A., Gonzalez-Gross, M., Evans, A., Tregouet, D. A., Yarnell, J. W. G., Virtamo, J., Ferrières, J., Veronesi, G., Perola, M., Arveiler, D., Brambilla, P., Lind, L., Kaprio, J., Hofman, A., Stricker, B. H., Van Duijn, C. M., Ikram, M. A., Franco, O. H., Cottel, D., Dallongeville, J., Hall, A. S., Jula, A., Tobin, M. D., Penninx, B. W., Peters, A., Gieger, C., Samani, N. J., Montgomery, G. W., Whitfield, J. B., Martin, N. G., Groop, L., Spector, T. D., Magnusson, P. K., Amouyel, P., Boomsma, D. I., Nilsson, P. M., Järvelin, M. R., Lyssenko, V., Metspalu, A., Strachan, D. P., Salomaa, V., Ripatti, S., Pedersen, N. L., Prokopenko, I., Mccarthy, M. I. & Ingelsson, E., 1 May 2015, In : Diabetes. 64, 5, p. 1841-1852 12 p.

Research output: Contribution to journalArticle

33 Citations (Scopus)

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

He, J., Tang, L., Benyamin, B., Shah, S., Hemani, G., Liu, R., Ye, S., Liu, X., Ma, Y., Zhang, H., Cremin, K., Leo, P., Wray, N. R., Visscher, P. M., Xu, H., Brown, M. A., Bartlett, P. F., Mangelsdorf, M. & Fan, D., 1 Sep 2015, In : Neurobiology of Aging. 36, 9, p. 2660.e1-2660.e8

Research output: Contribution to journalArticle

32 Citations (Scopus)

Iron and hepcidin as risk factors in atherosclerosis: What do the genes say?

Galesloot, T. E., Janss, L. L., Burgess, S., Kiemeney, L. A. L. M., den Heijer, M., de Graaf, J., Holewijn, S., Benyamin, B., Whitfield, J. B., Swinkels, D. W. & Vermeulen, S. H., 11 Jul 2015, In : BMC Genetics. 16, 1, 79.

Research output: Contribution to journalArticle

16 Citations (Scopus)

Meta-analysis of the heritability of human traits based on fifty years of twin studies

Polderman, T. J. C., Benyamin, B., De Leeuw, C. A., Sullivan, P. F., Van Bochoven, A., Visscher, P. M. & Posthuma, D., 1 Jan 2015, In : Nature Genetics. 47, 7, p. 702-709 8 p.

Research output: Contribution to journalArticle

611 Citations (Scopus)

Sharing a Placenta is Associated With a Greater Similarity in DNA Methylation in Monochorionic Versus Dichorionic Twin Pars in Blood at Age 14

Bui, M., Benyamin, B., Shah, S., Henders, A. K., Martin, N. G., Montgomery, G. W. & McRae, A. F., 1 Dec 2015, In : Twin Research and Human Genetics. 18, 6, p. 680-685 6 p.

Research output: Contribution to journalArticle

5 Citations (Scopus)
2014

Childhood intelligence is heritable, highly polygenic and associated with FNBP1L

Benyamin, B., Pourcain, B., Davis, O. S., Davies, G., Hansell, N. K., Brion, M. J., Kirkpatrick, R. M., Cents, R. A. M., Franić, S., Miller, M. B., Haworth, C. M. A., Meaburn, E., Price, T. S., Evans, D. M., Timpson, N., Kemp, J., Ring, S., McArdle, W., Medland, S. E., Yang, J. & 23 othersHarris, S. E., Liewald, D. C., Scheet, P., Xiao, X., Hudziak, J. J., De Geus, E. J. C., Jaddoe, V. W. V., Starr, J. M., Verhulst, F. C., Pennell, C., Tiemeier, H., Iacono, W. G., Palmer, L. J., Montgomery, G. W., Martin, N. G., Boomsma, D. I., Posthuma, D., McGue, M., Wright, M. J., Davey Smith, G., Deary, I. J., Plomin, R. & Visscher, P. M., 1 Feb 2014, In : Molecular Psychiatry. 19, 2, p. 253-258 6 p.

Research output: Contribution to journalArticle

128 Citations (Scopus)

Common genetic variants associated with cognitive performance identified using the proxy-phenotype method

Rietveld, C. A., Esko, T., Davies, G., Pers, T. H., Turley, P., Benyamin, B., Chabris, C. F., Emilsson, V., Johnson, A. D., Lee, J. J., De Leeuw, C., Marioni, R. E., Medland, S. E., Miller, M. B., Rostapshova, O., Van Der Lee, S. J., Vinkhuyzen, A. A. E., Amin, N., Conley, D., Derringer, J. & 39 othersVan Duijn, C. M., Fehrmann, R., Franke, L., Glaeser, E. L., Hansell, N. K., Hayward, C., Iacono, W. G., Ibrahim-Verbaas, C., Jaddoe, V., Karjalainen, J., Laibson, D., Lichtenstein, P., Liewald, D. C., Magnusson, P. K. E., Martin, N. G., McGue, M., McMahon, G., Pedersen, N. L., Pinker, S., Porteous, D. J., Posthuma, D., Rivadeneira, F., Smithk, B. H., Starr, J. M., Tiemeier, H., Timpsonm, N. J., Trzaskowskin, M., Uitterlinden, A. G., Verhulst, F. C., Ward, M. E., Wright, M. J., Smith, G. D., Deary, I. J., Johannesson, M., Plomin, R., Visscher, P. M., Benjamin, D. J., Cesarini, D. & Koellinger, P. D., 23 Sep 2014, In : Proceedings of the National Academy of Sciences of the United States of America. 111, 38, p. 13790-13794 5 p.

Research output: Contribution to journalArticle

126 Citations (Scopus)

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

Hoggart, C. J., Venturini, G., Mangino, M., Gomez, F., Ascari, G., Zhao, J. H., Teumer, A., Winkler, T. W., Tšernikova, N., Luan, J., Mihailov, E., Ehret, G. B., Zhang, W., Lamparter, D., Esko, T., Macé, A., Rüeger, S., Bochud, P. Y., Barcella, M., Dauvilliers, Y. & 33 othersBenyamin, B., Evans, D. M., Hayward, C., Lopez, M. F., Franke, L., Russo, A., Heid, I. M., Salvi, E., Vendantam, S., Arking, D. E., Boerwinkle, E., Chambers, J. C., Fiorito, G., Grallert, H., Guarrera, S., Homuth, G., Huffman, J. E., Porteous, D., Moradpour, D., Iranzo, A., Hebebrand, J., Kemp, J. P., Lammers, G. J., Aubert, V., Heim, M. H., Martin, N. G., Montgomery, G. W., Peraita-Adrados, R., Santamaria, J., Hyppönen, E., The GIANT Consortium, Generation Scotland Consortium & The LifeLines Cohort study, 1 Jan 2014, In : PLoS genetics. 10, 7, p. 1-12 12 p., e1004508.

Research output: Contribution to journalArticle

32 Citations (Scopus)

Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis

Benyamin, B., Esko, T., Ried, J. S., Radhakrishnan, A., Vermeulen, S. H., Traglia, M., Gögele, M., Anderson, D., Broer, L., Podmore, C., Luan, JA., Kutalik, Z., Sanna, S., Van Der Meer, P., Tanaka, T., Wang, F., Westra, H. J., Franke, L., Mihailov, E., Milani, L. & 49 othersHäldin, J., Winkelmann, J., Meitinger, T., Thiery, J., Peters, A., Waldenberger, M., Rendon, A., Jolley, J., Sambrook, J., Kiemeney, L. A., Sweep, F. C., Sala, C. F., Schwienbacher, C., Pichler, I., Hui, J., Demirkan, A., Isaacs, A., Amin, N., Steri, M., Waeber, G., Verweij, N., Powell, J. E., Nyholt, D. R., Heath, A. C., Madden, P. A. F., Visscher, P. M., Wright, M. J., Montgomery, G. W., Martin, N. G., Hernandez, D., Bandinelli, S., Van Der Harst, P., Uda, M., Vollenweider, P., Scott, R. A., Langenberg, C., Wareham, N. J., Van Duijn, C., Beilby, J., Pramstaller, P. P., Hicks, A. A., Ouwehand, W. H., Oexle, K., Gieger, C., Metspalu, A., Camaschella, C., Toniolo, D., Swinkels, D. W. & Whitfield, J. B., 1 Jan 2014, In : Nature communications. 5, 5926.

Research output: Contribution to journalArticle

63 Citations (Scopus)
2013

Association of rs1344706 in the ZNF804A gene with schizophrenia in a case/control sample from Indonesia

Schwab, S. G., Kusumawardhani, A. A. A. A., Dai, N., Qin, W. W., Wildenauer, M. D. B., Agiananda, F., Amir, N., Antoni, R., Arsianti, T., Asmarahadi, A., Diatri, H., Djatmiko, P., Irmansyah, I., Khalimah, S., Kusumadewi, I., Kusumaningrum, P., Lukman, P. R., Mustar, L., Nasrun, M. W., Naswati, S. & 9 othersPrasetiyawan, P., Semen, G. M., Siste, K., Tobing, H., Widiasih, N., Wiguna, T., Wulandari, W. D., Benyamin, B. & Wildenauer, D. B., 1 Jun 2013, In : Schizophrenia Research. 147, 1, p. 46-52 7 p.

Research output: Contribution to journalArticle

21 Citations (Scopus)

Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

Pichler, I., Del Greco, M. F., Gögele, M., Lill, C. M., Bertram, L., Do, C. B., Eriksson, N., Foroud, T., Myers, R. H., Nalls, M., Keller, M. F., Benyamin, B., Whitfield, J. B., Pramstaller, P. P., Hicks, A. A., Thompson, J. R. & Minelli, C., 1 Jun 2013, In : PLoS Medicine. 10, 6, e1001462.

Research output: Contribution to journalArticle

67 Citations (Scopus)

The genetic aetiology of cannabis use initiation: A meta-analysis of genome-wide association studies and a SNP-based heritability estimation

Verweij, K. J. H., Vinkhuyzen, A. A. E., Benyamin, B., Lynskey, M. T., Quaye, L., Agrawal, A., Gordon, S. D., Montgomery, G. W., Madden, P. A. F., Heath, A. C., Spector, T. D., Martin, N. G. & Medland, S. E., 1 Sep 2013, In : Addiction Biology. 18, 5, p. 846-850 5 p.

Research output: Contribution to journalArticle

32 Citations (Scopus)

The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis

Fall, T., Hägg, S., Mägi, R., Ploner, A., Fischer, K., Horikoshi, M., Sarin, A. P., Thorleifsson, G., Ladenvall, C., Kals, M., Kuningas, M., Draisma, H. H. M., Ried, J. S., van Zuydam, N. R., Huikari, V., Mangino, M., Sonestedt, E., Benyamin, B., Nelson, C. P., Rivera, N. V. & 105 othersKristiansson, K., Shen, H. Y., Havulinna, A. S., Dehghan, A., Donnelly, L. A., Kaakinen, M., Nuotio, M. L., Robertson, N., de Bruijn, R. F. A. G., Ikram, M. A., Amin, N., Balmforth, A. J., Braund, P. S., Doney, A. S. F., Döring, A., Elliott, P., Esko, T., Franco, O. H., Gretarsdottir, S., Hartikainen, A. L., Heikkilä, K., Herzig, K. H., Holm, H., Hottenga, J. J., Hyppönen, E., Illig, T., Isaacs, A., Isomaa, B., Karssen, L. C., Kettunen, J., Koenig, W., Kuulasmaa, K., Laatikainen, T., Laitinen, J., Lindgren, C., Lyssenko, V., Läärä, E., Rayner, N. W., Männistö, S., Pouta, A., Rathmann, W., Rivadeneira, F., Ruokonen, A., Savolainen, M. J., Sijbrands, E. J. G., Small, K. S., Smit, J. H., Steinthorsdottir, V., Syvänen, A. C., Taanila, A., Tobin, M. D., Uitterlinden, A. G., Willems, S. M., Willemsen, G., Witteman, J., Perola, M., Evans, A., Ferrières, J., Virtamo, J., Kee, F., Tregouet, D. A., Arveiler, D., Amouyel, P., Ferrario, M. M., Brambilla, P., Hall, A. S., Heath, A. C., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Whitfield, J. B., Jula, A., Knekt, P., Oostra, B., van Duijn, C. M., Penninx, B. W. J. H., Davey Smith, G., Kaprio, J., Samani, N. J., Gieger, C., Peters, A., Wichmann, H. E., Boomsma, D. I., de Geus, E. J. C., Tuomi, T. M., Power, C., Hammond, C. J., Spector, T. D., Lind, L., Orho-Melander, M., Palmer, C. N. A., Morris, A. D., Groop, L., Järvelin, M. R., Salomaa, V., Vartiainen, E., Hofman, A., Ripatti, S., Metspalu, A., Thorsteinsdottir, U., Stefansson, K., Pedersen, N. L., McCarthy, M. I., Ingelsson, E. & Prokopenko, I., 1 Jan 2013, In : PLoS Medicine. 10, 6, e1001474.

Research output: Contribution to journalArticle

126 Citations (Scopus)
2012

Genetic Variation within a metabolic motif in the chromogranin a promoter: Pleiotropic influence on cardiometabolic risk traits in twins

Rao, F., Chiron, S., Wei, Z., Fung, M. M., Chen, Y., Wen, G., Khandrika, S., Ziegler, M. G., Benyamin, B., Montgomery, G., Whitfield, J. B., Martin, N. G., Waalen, J., Hamilton, B. A., Mahata, S. K. & O'Connor, D. T., 1 Jan 2012, In : American Journal of Hypertension. 25, 1, p. 29-40 12 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations

Middelberg, R. P., Benyamin, B., de Moor, M. H. M., Warrington, N. M., Gordon, S., Henders, A. K., Medland, S. E., Nyholt, D. R., de Geus, E. J. C., Hottenga, J. J., Willemsen, G., Beilin, L. J., Mori, T. A., Wright, M. J., Heath, A. C., Madden, P. A. F., Boomsma, D. I., Pennell, C. E., Montgomery, G. W., Martin, N. G. & 1 othersWhitfield, J. B., 1 Jan 2012, In : Human Molecular Genetics. 21, 2, p. 446-455 10 p., ddr478.

Research output: Contribution to journalArticle

22 Citations (Scopus)

Seventy-five genetic loci influencing the human red blood cell

Van Der Harst, P., Zhang, W., Mateo Leach, I., Rendon, A., Verweij, N., Sehmi, J., Paul, D. S., Elling, U., Allayee, H., Li, X., Radhakrishnan, A., Tan, S. T., Voss, K., Weichenberger, C. X., Albers, C. A., Al-Hussani, A., Asselbergs, F. W., Ciullo, M., Danjou, F., Dina, C. & 175 othersEsko, T., Evans, D. M., Franke, L., Gögele, M., Hartiala, J., Hersch, M., Holm, H., Hottenga, J. J., Kanoni, S., Kleber, M. E., Lagou, V., Langenberg, C., Lopez, L. M., Lyytikäinen, L. P., Melander, O., Murgia, F., Nolte, I. M., O'Reilly, P. F., Padmanabhan, S., Parsa, A., Pirastu, N., Porcu, E., Portas, L., Prokopenko, I., Ried, J. S., Shin, S. Y., Tang, C. S., Teumer, A., Traglia, M., Ulivi, S., Westra, H. J., Yang, J., Hua Zhao, J., Anni, F., Abdellaoui, A., Attwood, A., Balkau, B., Bandinelli, S., Bastardot, F., Benyamin, B., Boehm, B. O., Cookson, W. O., Das, D., De Bakker, P. I. W., De Boer, R. A., De Geus, E. J. C., De Moor, M. H., Dimitriou, M., Domingues, F. S., Döring, A., Engström, G., Eyjolfsson, G. I., Ferrucci, L., Fischer, K., Galanello, R., Garner, S. F., Genser, B., Gibson, Q. D., Girotto, G., Gudbjartsson, D. F., Harris, S. E., Hartikainen, A. L., Hastie, C. E., Hedblad, B., Illig, T., Jolley, J., Kähönen, M., Kema, I. P., Kemp, J. P., Liang, L., Lloyd-Jones, H., Loos, R. J. F., Meacham, S., Medland, S. E., Meisinger, C., Memari, Y., Mihailov, E., Miller, K., Moffatt, M. F., Nauck, M., Novatchkova, M., Nutile, T., Olafsson, I., Onundarson, P. T., Parracciani, D., Penninx, B. W., Perseu, L., Piga, A., Pistis, G., Pouta, A., Puc, U., Raitakari, O., Ring, S. M., Robino, A., Ruggiero, D., Ruokonen, A., Saint-Pierre, A., Sala, C., Salumets, A., Sambrook, J., Schepers, H., Schmidt, C. O., Silljé, H. H. W., Sladek, R., Smit, J. H., Starr, J. M., Stephens, J., Sulem, P., Tanaka, T., Thorsteinsdottir, U., Tragante, V., Van Gilst, W. H., Joost Van Pelt, L., Van Veldhuisen, D. J., Völker, U., Whitfield, J. B., Willemsen, G., Winkelmann, B. R., Wirnsberger, G., Algra, A., Cucca, F., D'Adamo, A. P., Danesh, J., Deary, I. J., Dominiczak, A. F., Elliott, P., Fortina, P., Froguel, P., Gasparini, P., Greinacher, A., Hazen, S. L., Jarvelin, M. R., Khaw, K. T., Lehtimäki, T., Maerz, W., Martin, N. G., Metspalu, A., Mitchell, B. D., Montgomery, G. W., Moore, C., Navis, G., Pirastu, M., Pramstaller, P. P., Ramirez-Solis, R., Schadt, E., Scott, J., Shuldiner, A. R., Smith, G. D., Gustav Smith, J., Snieder, H., Sorice, R., Spector, T. D., Stefansson, K., Stumvoll, M., Wilson Tang, W. H., Toniolo, D., Tönjes, A., Visscher, P. M., Vollenweider, P., Wareham, N. J., Wolffenbuttel, B. H. R., Boomsma, D. I., Beckmann, J. S., Dedoussis, G. V., Deloukas, P., Ferreira, M. A., Sanna, S., Uda, M., Hicks, A. A., Penninger, J. M., Gieger, C., Kooner, J. S., Ouwehand, W. H., Soranzo, N. & Chambers, J. C., 20 Dec 2012, In : Nature. 492, 7429, p. 369-375 7 p.

Research output: Contribution to journalArticle

198 Citations (Scopus)

Unraveling the Genetic Etiology of Adult Antisocial Behavior: A Genome-Wide Association Study

Tielbeek, J. J., Medland, S. E., Benyamin, B., Byrne, E. M., Heath, A. C., Madden, P. A. F., Martin, N. G., Wray, N. R. & Verweij, K. J. H., 15 Oct 2012, In : PloS one. 7, 10, e45086.

Research output: Contribution to journalArticle

47 Citations (Scopus)
2011

Cognitive function in adolescence: Testing for interactions between breast-feeding and FADS2 polymorphisms

Martin, N. W., Benyamin, B., Hansell, N. K., Montgomery, G. W., Martin, N. G., Wright, M. J. & Bates, T. C., 1 Jan 2011, In : Journal of the American Academy of Child and Adolescent Psychiatry. 50, 1, p. 55-62.e4

Research output: Contribution to journalArticle

25 Citations (Scopus)

Genome-wide association study identifies two loci strongly affecting transferrin glycosylation

Kutalik, Z., Benyamin, B., Bergmann, S., Mooser, V., Waeber, G., Montgomery, G. W., Martin, N. G., Madden, P. A. F., Heath, A. C., Beckmann, J. S., Vollenweider, P., Marques-Vidal, P. & Whitfield, J. B., 1 Sep 2011, In : Human Molecular Genetics. 20, 18, p. 3710-3717 8 p., ddr272.

Research output: Contribution to journalArticle

21 Citations (Scopus)

GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors

Benyamin, B., Middelberg, R. P., Lind, P. A., Valle, A. M., Gordon, S., Nyholt, D. R., Medland, S. E., Henders, A. K., Heath, A. C., Madden, P. A. F., Visscher, P. M., O'Connor, D. T., Montgomery, G. W., Martin, N. G. & Whitfield, J. B., 1 Nov 2011, In : Human Molecular Genetics. 20, 22, p. 4504-4514 11 p., ddr375.

Research output: Contribution to journalArticle

37 Citations (Scopus)
2010

A genome-wide association study of Cloninger's temperament scales: Implications for the evolutionary genetics of personality

Verweij, K. J. H., Zietsch, B. P., Medland, S. E., Gordon, S. D., Benyamin, B., Nyholt, D. R., McEvoy, B. P., Sullivan, P. F., Heath, A. C., Madden, P. A. F., Henders, A. K., Montgomery, G. W., Martin, N. G. & Wray, N. R., 1 Oct 2010, In : Biological Psychology. 85, 2, p. 306-317 12 p.

Research output: Contribution to journalArticle

73 Citations (Scopus)

Common SNPs explain a large proportion of the heritability for human height

Yang, J., Benyamin, B., McEvoy, B. P., Gordon, S., Henders, A. K., Nyholt, D. R., Madden, P. A., Heath, A. C., Martin, N. G., Montgomery, G. W., Goddard, M. E. & Visscher, P. M., 1 Jul 2010, In : Nature Genetics. 42, 7, p. 565-569 5 p.

Research output: Contribution to journalArticle

2192 Citations (Scopus)
2009

Common variants in TMPRSS6 are associated with iron status and erythrocyte volume

Benyamin, B., Ferreira, M. A. R., Willemsen, G., Gordon, S., Middelberg, R. P. S., McEvoy, B. P., Hottenga, J. J., Henders, A. K., Campbell, M. J., Wallace, L., Frazer, I. H., Heath, A. C., De Geus, E. J. C., Nyholt, D. R., Visscher, P. M., Penninx, B. W., Boomsma, D. I., Martin, N. G., Montgomery, G. W. & Whitfield, J. B., 1 Nov 2009, In : Nature Genetics. 41, 11, p. 1173-1175 3 p.

Research output: Contribution to journalArticle

154 Citations (Scopus)

Multicenter dizygotic twin cohort study confirms two linkage susceptibility loci for body mass index at 3q29 and 7q36 and identifies three further potential novel loci

Kettunen, J., Perola, M., Martin, N. G., Cornes, B. K., Wilson, S. G., Montgomery, G. W., Benyamin, B., Harris, J. R., Boomsma, D., Willemsen, G., Hottenga, J. J., Slagboom, P. E., Christensen, K., Kyvik, K. O., Sørensen, T. I. A., Pedersen, N. L., Magnusson, P. K. E., Andrew, T., Spector, T. D., Widen, E. & 4 othersSilventoinen, K., Kaprio, J., Palotie, A. & Peltonen, L., 2 Sep 2009, In : International Journal of Obesity. 33, 11, p. 1235-1242 8 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)

Variants in TF and HFE Explain ∼40% of Genetic Variation in Serum-Transferrin Levels

Benyamin, B., McRae, A. F., Zhu, G., Gordon, S., Henders, A. K., Palotie, A., Peltonen, L., Martin, N. G., Montgomery, G. W., Whitfield, J. B. & Visscher, P. M., 9 Jan 2009, In : American Journal of Human Genetics. 84, 1, p. 60-65 6 p.

Research output: Contribution to journalArticle

116 Citations (Scopus)
2008

Common genetic components of obesity traits and serum leptin

Hasselbalch, A. L., Benyamin, B., Visscher, P. M., Heitmann, B. L., Kyvik, K. O. & Sørensen, T. I. A., 1 Dec 2008, In : Obesity. 16, 12, p. 2723-2729 7 p.

Research output: Contribution to journalArticle

17 Citations (Scopus)

Within-family outliers: Segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs

Benyamin, B., Perola, M., Cornes, B. K., Madden, P. A. F., Palotie, A., Nyholt, D. R., Montgomery, G. W., Peltonen, L., Martin, N. G. & Visscher, P. M., 1 Apr 2008, In : European Journal of Human Genetics. 16, 4, p. 516-524 9 p.

Research output: Contribution to journalArticle

11 Citations (Scopus)
2007

Are there common genetic and environmental factors behind the endophenotypes associated with the metabolic syndrome?

Benyamin, B., Sørensen, T. I. A., Schousboe, K., Fenger, M., Visscher, P. M. & Kyvik, K. O., 1 Sep 2007, In : Diabetologia. 50, 9, p. 1880-1888 9 p.

Research output: Contribution to journalArticle

81 Citations (Scopus)

Bodyweight QTL on mouse chromosomes 4 and 11 by selective genotyping: Regression v. maximum likelihood

Benyamin, B., Martin, I. C. A., Cheung, C. C., Buckley, M. F., Thomson, P. C., Visscher, P. M. & Moran, C., 28 May 2007, In : Australian Journal of Experimental Agriculture. 47, 6, p. 677-682 6 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Combined genome scans for body stature in 6,602 European twins: Evidence for common caucasian loci

Perola, M., Sammalisto, S., Hiekkalinna, T., Martin, N. G., Visscher, P. M., Montgomery, G. W., Benyamin, B., Harris, J. R., Boomsma, D., Willemsen, G., Hottenga, J. J., Christensen, K., Kyvik, K. O., Sørensen, T. I. A., Pedersen, N. L., Magnusson, P. K. E., Spector, T. D., Widen, E., Silventoinen, K., Kaprio, J. & 2 othersPalotie, A. & Peltonen, L., 1 Jun 2007, In : PLoS genetics. 3, 6, p. 1019-1028 10 p.

Research output: Contribution to journalArticle

135 Citations (Scopus)

Genome partitioning of genetic variation for height from 11,214 sibling pairs

Visscher, P. M., Macgregor, S., Benyamin, B., Zhu, G., Gordon, S., Medland, S., Hill, W. G., Hottenga, J. J., Willemsen, G., Boomsma, D. I., Liu, Y. Z., Deng, H. W., Montgomery, G. W. & Martin, N. G., 1 Jan 2007, In : American Journal of Human Genetics. 81, 5, p. 1104-1110 7 p.

Research output: Contribution to journalArticle

90 Citations (Scopus)
2006
7 Citations (Scopus)
2005

Large, consistent estimates of the heritability of cognitive ability in two entire populations of 11-year-old twins from Scottish Mental Surveys of 1932 and 1947

Benyamin, B., Wilson, V., Whalley, L. J., Visscher, P. M. & Deary, I. J., 1 Sep 2005, In : Behavior genetics. 35, 5, p. 525-534 10 p.

Research output: Contribution to journalArticle

26 Citations (Scopus)
2004

The use of linear mixed models to estimate variance components from data on twin pairs by maximum likelihood

Visscher, P. M., Benyamin, B. & White, I., 1 Dec 2004, In : Twin Research. 7, 6, p. 670-674 5 p.

Research output: Contribution to journalArticle

31 Citations (Scopus)