Serum creatinine and fat-free mass (lean body mass). by Swaminathan, R, Major, P, Snieder, H, Spector, T

Explaining the associations of education and occupation with childlessness: the role of desires and expectations to remain childless by Verweij, RM, Stulp, G, Snieder, H, Mills, MC

Sexual dimorphism in the genetic influence on human childlessness by Verweij, R, Mills, M, Tropf, F, Veenstra, R, Nyman, A, Snieder, H

Genetic contribution to renal function and electrolyte balance: a twin study. by Hunter, D, Lange, M, Snieder, H, MacGregor, A, Swaminathan, R, Thakker, R, Spector, T

Genetic contribution to bone metabolism, calcium excretion, and vitamin D and parathyroid hormone regulation. by Hunter, D, De Lange, M, Snieder, H, MacGregor, A, Swaminathan, R, Thakker, R, Spector, T

A randomized controlled trial of vitamin D supplementation on preventing postmenopausal bone loss and modifying bone metabolism using identical twin pairs. by Hunter, D, Major, P, Arden, N, Swaminathan, R, Andrew, T, MacGregor, A, Keen, R, Snieder, H, Spector, T

SNP-based heritability estimates of common and specific variance in self- and informant-reported neuroticism scales. by Realo, A, van der Most, P, Allik, J, Esko, T, Jeronimus, B, Kööts-Ausmees, L, Mõttus, R, Tropf, F, Snieder, H, Ormel, J

Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour by Mills, MC, Tropf, FC, Brazel, DM, van Zuydam, N, Vaez, A, Pers, TH, Snieder, H, Perry, JRB, Ong, KK, den Hoed, M, Barban, N, Day, FR

Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus by Mathieson, I, Day, FR, Barban, N, Tropf, FC, Brazel, D, Vaez, A, van Zuydam, N, Bitarello, BD, Snieder, H, den Hoed, M, Ong, K, Mills, MC, Perry, JRB

Association of complement C3 gene variants with renal transplant outcome of deceased cardiac dead donor kidneys by Damman, J, Leuvenink, H, Ploeg, R, Daha, MR, Born, J, De Borst, M, Bakker, S, Navis, G, Seelen, M, Van Goor, H, Hillebrands, J, Dijk, M, Hepkema, BG, Snieder, H

Association of complement C3 gene variants with renal transplant outcome of deceased cardiac dead donor kidneys. by Damman, J, Daha, MR, Leuvenink, H, van Goor, H, Hillebrands, J, Dijk, M, Hepkema, BG, Snieder, H, Born, J, de Borst, M, Bakker, S, Navis, G, Ploeg, R, Seelen, M

Leveraging functional genomic annotations and genome coverage to improve polygenic prediction of complex traits within and between ancestries by Zheng, Z, Liu, S, Sidorenko, J, Wang, Y, Lin, T, Yengo, L, Turley, P, Ani, A, Wang, R, Nolte, IM, Snieder, H, Yang, J, Wray, NR, Goddard, ME, Visscher, PM, Zeng, J

Using polygenic scores in social science research: Unraveling childlessness by Verweij, RM, Mills, MC, Stulp, G, Nolte, IM, Barban, N, Tropf, FC, Carrell, DT, Aston, KI, Zondervan, KT, Rahmioglu, N, Dalgaard, M, Skaarup, C, Hayes, MG, Dunaif, A, Guo, G, Snieder, H

Lectin complement pathway gene profile of the donor and recipient does not influence graft outcome after kidney transplantation by Damman, J, Kok, J, Leuvenink, H, Ploeg, R, Reznichenko, A, Van den Born, J, De Borst, M, Bakker, S, Navis, G, Seelen, M, Snieder, H, Van Goor, H, Hillebrands, J, Dijk, V, Hepkema, BG

Lectin complement pathway gene profile of the donor and recipient does not influence graft outcome after kidney transplantation. by Damman, J, Kok, J, Snieder, H, Leuvenink, H, van Goor, H, Hillebrands, J, Dijk, v, Hepkema, BG, Reznichenko, A, van den Born, J, de Borst, M, Bakker, S, Navis, G, Ploeg, R, Seelen, M

Hidden heritability due to heterogeneity across seven populations. by Tropf, FC, Lee, SH, Verweij, RM, Stulp, G, van der Most, PJ, de Vlaming, R, Bakshi, A, Briley, DA, Rahal, C, Hellpap, R, Nyman, A, Esko, T, Metspalu, A, Medland, SE, Martin, NG, Barban, N, Snieder, H, Robinson, MR, Mills, MC

Hidden heritability due to heterogeneity across seven populations by Tropf, FC, Lee, SH, Verweij, RM, Stulp, G, van der Moost, PJ, de Vlaming, R, Bakshi, A, Briley, DA, Rahal, C, Hellpap, R, Nyman, A, Esko, T, Metspalu, A, Medland, SE, Martin, NG, Barban, N, Snieder, H, Robinson, MR, Mills, MC

Evidence for genetic overlap between schizophrenia and age at first birth in women by Tropf, F, Mills, M, Barban, N, Mehta, D, Gratten, J, Bakshi, A, Zhu, Z, Bacanu, S, Hermani, G, Magnusson, P, Esko, T, Metspalu, A, Snieder, H, Mowry, B, Kendler, K, Yang, J, Visscher, P, McGrath, J, Wray, N, Lee, S, Schizophrenia Working Group of the Psychiatric Genomics Consortium, LifeLines Cohort Study, TwinsUK

Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. by Nolte, I, Wallace, C, Newhouse, S, Waggott, D, Fu, J, Soranzo, N, Gwilliam, R, Deloukas, P, Savelieva, I, Zheng, D, Dalageorgou, C, Farrall, M, Samani, N, Connell, J, Brown, M, Dominiczak, A, Lathrop, M, Zeggini, E, Wain, L, Newton-Cheh, C, Eijgelsheim, M, Rice, K, de Bakker, P, Pfeufer, A, Sanna, S, Arking, D, Asselbergs, F, Spector, T, Carter, N, Jeffery, S, Tobin, M, Caulfield, M, Snieder, H, Paterson, A, Munroe, P, Jamshidi, Y

Investigating the causal relationship of c-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium mendelian randomization study by Prins, B, Abbasi, A, Wong, A, Vaez, A, Nolte, I, Franceschini, N, Stuart, P, Guterriez Achury, J, Mistry, V, Bradfield, J, Valdes, A, Bras, J, Shatunov, A, Lu, C, Han, B, Raychaudhuri, S, Bevan, S, Mayes, M, Tsoi, L, Evangelou, E, Nair, R, Grant, S, Polychronakos, C, Radstake, T, van Heel, D, Dunstan, M, Wood, N, Al-Chalabi, A, Dehghan, A, Hakonarson, H, Markus, H, Elder, J, Knight, J, Arking, D, Spector, T, Koeleman, B, van Duijn, C, Martin, J, Morris, A, Weersma, R, Wijmenga, C, Munroe, P, Perry, J, Pouget, J, Jamshidi, Y, Snieder, H, Alizadeh, B