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Original Research

A simple method for assessing the strength of evidence for association at the level of the whole gene

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Pages 115-120 | Published online: 17 Nov 2008

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David Curtis. (2013) Approaches to the detection of recessive effects using next generation sequencing data from outbred populations. Advances and Applications in Bioinformatics and Chemistry 6, pages 29-35.
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David Curtis. (2012) A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway. Advances and Applications in Bioinformatics and Chemistry 5, pages 1-9.
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Noomi Gregersen, Hans A Dahl, Henriette N Buttenschøn, Mette Nyegaard, Anne Hedemand, Thomas D Als, August G Wang, Sofus Joensen, David PD Woldbye, Pernille Koefoed, Ann S Kristensen, Torben A Kruse, Anders D Børglum & Ole Mors. (2011) A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene. European Journal of Human Genetics 20:1, pages 84-90.
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H. N. Buttenschøn, A. S. Kristensen, H. N. Buch, J. H. Andersen, J. P. Bonde, M. Grynderup, A. M. Hansen, H. Kolstad, A. Kaergaard, L. Kaerlev, S. Mikkelsen, J. F. Thomsen, P. Koefoed, A. Erhardt, D. P. D. Woldbye, A. D. Børglum & O. Mors. (2011) The norepinephrine transporter gene is a candidate gene for panic disorder. Journal of Neural Transmission 118:6, pages 969-976.
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