Bassett, Anne
358  Ergebnisse:
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Genetic contributors to risk of schizophrenia in the presen..:

Cleynen, Isabelle ; Engchuan, Worrawat ; Hestand, Matthew...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41380-020-0654-3.  , 2020
 
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Genetic contributors to risk of schizophrenia in the presen..:

Cleynen, Isabelle ; Engchuan, Worrawat ; Hestand, Matthew...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41380-020-0654-3.  , 2020
 
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7

Using common genetic variation to examine phenotypic expres..:

Davies, Robert ; Fiksinski, Ania ; Breetvelt, Elemi...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41591-020-1103-1.  , 2020
 
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Nested Inversion Polymorphisms Predispose Chromosome 22q11...:

Demaerel, Wolfram ; Hestand, Matthew S ; Vergaelen, Elfi...
Demaerel , W , Hestand , M S , Vergaelen , E , Swillen , A , López-Sánchez , M , Pérez-Jurado , L A , Mcdonald-Mcginn , D , Zackai , E , Emanuel , B , Morrow , B E , Breckpot , J , Devriendt , K , Vermeesch , J , Antshel , K , Arango , C , Armando , M , Bassett , A , Bearden , C , Boot , E , Bravo-sanchez , M , Breetvelt , E , Busa , T , Butcher , N , Campbell , L , Carmel , M , Chow , E , Crowley , T B , Cubells , J , Cutler , D , Demaerel , W , Digilio , M C , Duijff , S , Eliez , S , Emanuel , B , Epstein , M , Evers , R , Fernandez Garcia-moya , L , Fiksinski , A , Fraguas , D , Fremont , W , Fritsch , R , Garcia-Minaur , S , Golden , A , Gothelf , D , Guo , T , Gur , R , Murphy , D , Murphy , K & Murphy , C & Van Amelsvoort , T 2017 , ' Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements ' , American Journal of Human Genetics , vol. 101 , no. 4 , pp. 616-622 . https://doi.org/10.1016/j.ajhg.2017.09.002.  , 2017
 
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Nested Inversion Polymorphisms Predispose Chromosome 22q11...:

Demaerel, Wolfram ; Hestand, Matthew S ; Vergaelen, Elfi...
Demaerel , W , Hestand , M S , Vergaelen , E , Swillen , A , López-Sánchez , M , Pérez-Jurado , L A , Mcdonald-Mcginn , D , Zackai , E , Emanuel , B , Morrow , B E , Breckpot , J , Devriendt , K , Vermeesch , J , Antshel , K , Arango , C , Armando , M , Bassett , A , Bearden , C , Boot , E , Bravo-sanchez , M , Breetvelt , E , Busa , T , Butcher , N , Campbell , L , Carmel , M , Chow , E , Crowley , T B , Cubells , J , Cutler , D , Demaerel , W , Digilio , M C , Duijff , S , Eliez , S , Emanuel , B , Epstein , M , Evers , R , Fernandez Garcia-moya , L , Fiksinski , A , Fraguas , D , Fremont , W , Fritsch , R , Garcia-Minaur , S , Golden , A , Gothelf , D , Guo , T , Gur , R , Murphy , D , Murphy , K & Murphy , C & Van Amelsvoort , T 2017 , ' Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements ' , American Journal of Human Genetics , vol. 101 , no. 4 , pp. 616-622 . https://doi.org/10.1016/j.ajhg.2017.09.002.  , 2017
 
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Parental Origin of Interstitial Duplications at 15q11.2-q13..:

Isles, Anthony R ; Ingason, Andrés ; Lowther, Chelsea...
Isles , A R , Ingason , A , Lowther , C , Walters , J , Gawlick , M , Stöber , G , Rees , E , Martin , J , Little , R B , Potter , H , Georgieva , L , Pizzo , L , Ozaki , N , Aleksic , B , Kushima , I , Ikeda , M , Iwata , N , Levinson , D F , Gejman , P V , Shi , J , Sanders , A R , Duan , J , Willis , J , Sisodiya , S , Costain , G , Werge , T M , Degenhardt , F , Giegling , I , Rujescu , D , Hreidarsson , S J , Saemundsen , E , Ahn , J W , Ogilvie , C , Girirajan , S D , Stefansson , H , Stefansson , K , O'Donovan , M C , Owen , M J , Bassett , A & Kirov , G 2016 , ' Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders ' ..  , 2016
 
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Enhanced Maternal Origin of the 22q11.2 Deletion in Velocar..:

Delio, Maria ; Guo, Tingwei ; McDonald-McGinn, Donna M...
Delio , M , Guo , T , McDonald-McGinn , D M , Zackai , E , Herman , S , Kaminetzky , M , Higgins , A M , Coleman , K , Chow , C , Jarlbrzkowski , M , Bearden , C E , Bailey , A , Vangkilde , A , Olsen , L , Olesen , C , Skovby , F , Werge , T M , Templin , L , Busa , T , Philip , N , Swillen , A , Vermeesch , J R , Devriendt , K , Schneider , M , Dahoun , S , Eliez , S , Schoch , K , Hooper , S R , Shashi , V , Samanich , J , Marion , R , van Amelsvoort , T , Boot , E , Klaassen , P , Duijff , S N , Vorstman , J , Yuen , T , Silversides , C , Chow , E , Bassett , A , Frisch , A , Weizman , A , Gothelf , D , Niarchou , M , van den Bree , M , Owen , M J , Heine Suner , D , Rosell Andreo , J , Armando , M , Vicari , S , Digilio , M C , Auton , A , Kates , W R , Wang , T , Shprintzen , R J , Emanuel , B S & Morrow , B E 2013 , ' Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes ' , American Journal of Human Genetics , vol. 92 , no.....  , 2013
 
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