Mobile phone and cordless phone use and the risk for glioma – Analysis of pooled case- control studies in Sweden, 1997–2003 and 2007–2009 Lennart Hardell,

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Mobile phone and cordless phone use and the risk for glioma – Analysis of pooled case- control studies in Sweden, 1997–2003 and 2007–2009 Lennart Hardell, Michael Carlberg Pathophysiology Volume 22, Issue 1, Pages 1-13 (March 2015) DOI: 10.1016/j.pathophys.2014.10.001 Copyright © 2014 Elsevier B.V. Terms and Conditions

Fig. 1 Restricted cubic spline plot of the relationship between cumulative use of wireless phones and glioma. The solid line indicates the OR estimate and the broken lines represent the 95% CI. Adjustment was made for age at diagnosis, gender, SEI-code, and year for diagnosis. Population based controls were used. Pathophysiology 2015 22, 1-13DOI: (10.1016/j.pathophys.2014.10.001) Copyright © 2014 Elsevier B.V. Terms and Conditions

Fig. 2 Restricted cubic spline plot of the relationship between latency of wireless phones and glioma. The solid line indicates the OR estimate and the broken lines represent the 95% CI. Adjustment was made for age at diagnosis, gender, SEI-code, and year for diagnosis. Population based controls were used. Pathophysiology 2015 22, 1-13DOI: (10.1016/j.pathophys.2014.10.001) Copyright © 2014 Elsevier B.V. Terms and Conditions

Fig. 3 Restricted cubic spline plot of the relationship between latency of ipsilateral mobile phone use and glioma. The solid line indicates the OR estimate and the broken lines represent the 95% CI. Adjustment was made for age at diagnosis, gender, SEI-code, and year for diagnosis. Population based controls were used. Pathophysiology 2015 22, 1-13DOI: (10.1016/j.pathophys.2014.10.001) Copyright © 2014 Elsevier B.V. Terms and Conditions

Fig. 4 Restricted cubic spline plot of the relationship between latency of contralateral mobile phone use and glioma. The solid line indicates the OR estimate and the broken lines represent the 95% CI. Adjustment was made for age at diagnosis, gender, SEI-code, and year for diagnosis. Population based controls were used. Pathophysiology 2015 22, 1-13DOI: (10.1016/j.pathophys.2014.10.001) Copyright © 2014 Elsevier B.V. Terms and Conditions