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  • 1-6 of  6 results for ""Neurodevelopmental Disorders genetics""
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Academic Journal

Rare coding variants in ten genes confer substantial risk for schizophrenia

Subjects: Exome; Genetic Predisposition to Disease/genetics; Humans

  • Source: Singh , T , Poterba , T , Curtis , D , Akil , H , Al Eissa , M , Barchas , J D , Bass , N , Bigdeli , T B , Breen , G , Bromet , E J , Buckley , P F , Bunney , W E , Bybjerg-Grauholm , J , Byerley , W

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Academic Journal

ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9

Subjects: Adenosine Triphosphate/metabolism; Adolescent; Adult

  • Source: Smeland , M F , McClenaghan , C , Roessler , H I , Savelberg , S , Hansen , G Å M , Hjellnes , H , Arntzen , K A , Müller , K I , Dybesland , A R , Harter , T , Sala-Rabanal , M , Emfinger , C H ,

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Academic Journal

De novo variants in neurodevelopmental disorders with epilepsy

Subjects: Epilepsy/genetics; Exome/genetics; Female

  • Source: Heyne , H O , Singh , T , Stamberger , H , Abou Jamra , R , Caglayan , H , Craiu , D , De Jonghe , P , Guerrini , R , Helbig , K L , Koeleman , B P C , Kosmicki , J A , Linnankivi , T , May , P ,

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Rare coding variants in ten genes confer substantial risk for schizophrenia

Subjects: Multidisciplinary; Schizophrenia/genetics; MUTATIONS

  • Source: Singh, T, Poterba, T, Curtis, D, Akil, H, Al Eissa, M, Barchas, J D, Bass, N, Bigdeli, T B, Breen, G, Bromet, E J, Buckley, P F, Bunney, W E, Bybjerg-Grauholm, J, Byerley, W F, Chapman, S B, Chen, W

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De novo variants in neurodevelopmental disorders with epilepsy

Subjects: Exome/genetics; Male; 0301 basic medicine

  • Source: bioRxiv. Cold Spring Harbor Labs Journals (2017).Nature Genetics, Vol. 50, No 7 (2018) pp. 1048-1053Heyne, H O, Singh, T, Stamberger, H, Abou Jamra, R,

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  • 1-6 of  6 results for ""Neurodevelopmental Disorders genetics""