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David V. Hansen et al.
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Naomi R. Wray et al.
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Nathan G Skene et al.
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Antonio F. Pardinas et al.
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Laura E. Clarke et al.
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Verneri Anttila et al.
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Michael J. Gandal et al.
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Daifeng Wang et al.
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Jeremy F. McRae et al.
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Huwenbo Shi et al.
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Hyejung Won et al.
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Neelroop N. Parikshak et al.
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C. L. Muller et al.
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Blue B. Lake et al.
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Till F. M. Andlauer et al.
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Jason Ernst et al.
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Colm O'Dushlaine et al.
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Jerzy Wegiel et al.
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Rank-rank hypergeometric overlap: identification of statistically significant overlap between gene-expression signatures
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AM Clement et al.
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