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001032380 1001_ $$0P:(DE-HGF)0$$aClaus, I.$$b0
001032380 245__ $$aContribution of rare and potentially functionally relevant sequence variants in Schizophrenia risk‐locus Xq28,distal
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001032380 7001_ $$0P:(DE-HGF)0$$aSivalingam, S.$$b1
001032380 7001_ $$0P:(DE-HGF)0$$aKoller, A. C.$$b2
001032380 7001_ $$0P:(DE-HGF)0$$aWeiß, A.$$b3
001032380 7001_ $$0P:(DE-HGF)0$$aMathey, C. M.$$b4
001032380 7001_ $$0P:(DE-HGF)0$$aSindermann, L.$$b5
001032380 7001_ $$0P:(DE-HGF)0$$aKlein, D.$$b6
001032380 7001_ $$0P:(DE-HGF)0$$aHenschel, L.$$b7
001032380 7001_ $$0P:(DE-HGF)0$$aLudwig, K. U.$$b8
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001032380 7001_ $$0P:(DE-HGF)0$$aKammerer-Ciernioch, J.$$b13
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001032380 7001_ $$0P:(DE-HGF)0$$aNenadić, I.$$b17
001032380 7001_ $$0P:(DE-HGF)0$$aBaune, B. T.$$b18
001032380 7001_ $$0P:(DE-HGF)0$$aHartmann, A. M.$$b19
001032380 7001_ $$0P:(DE-HGF)0$$aKonte, B.$$b20
001032380 7001_ $$0P:(DE-HGF)0$$aGiegling, I.$$b21
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001032380 7001_ $$0P:(DE-HGF)0$$aNöthen, M. M.$$b31$$eCorresponding author
001032380 7001_ $$0P:(DE-HGF)0$$aDegenhardt, F.$$b32
001032380 773__ $$0PERI:(DE-600)2143866-3$$a10.1002/ajmg.b.33011$$gp. e33011$$n3$$pe33011$$tAmerican journal of medical genetics / Part B$$v198$$x1552-4841$$y2025
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