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David A Collier

Showing results (141-150 of 176) with videos related to

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Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 17, 2015
123I-iododexetimide preferentially binds to the muscarinic receptor subtype M1 in vivoGeor Bakker, Wilhelmina A Vingerhoets, Jan-Peter van Wieringen, et al.
Human Mutation|May 27, 2015
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental RetardationLaura Addis, Joo Wook Ahn, Richard Dobson, et al.
Genome Biology|August 31, 2016
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylationEilis Hannon, Emma Dempster, Joana Viana, et al.
Human Molecular Genetics|April 30, 2004
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populationsMarta Ribasés, Mònica Gratacòs, Fernando Fernández-Aranda, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populationsMarta Ribasés, Mònica Gratacòs, Fernando Fernández-Aranda, et al.
American Journal of Human Genetics|January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorderAndrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|January 24, 2017
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on GeneticsIna Giegling, Ladislav Hosak, Rainald Mössner, et al.
Translational Psychiatry|April 13, 2021
HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestryBettina Konte, James T R Walters, Dan Rujescu, et al.
Journal of Medical Genetics|April 14, 2016
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditionsMaria Tropeano, Deirdre Howley, Matthew J Gazzellone, et al.
Psychiatric Genetics|March 16, 2006
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosaElena Cellini, Benedetta Nacmias, Maria Brecelj-Anderluh, et al.
Pageof 18

Showing results (141-150 of 176) with videos related to

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Pageof 18
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine|January 17, 2015
123I-iododexetimide preferentially binds to the muscarinic receptor subtype M1 in vivoGeor Bakker, Wilhelmina A Vingerhoets, Jan-Peter van Wieringen, et al.
Human Mutation|May 27, 2015
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental RetardationLaura Addis, Joo Wook Ahn, Richard Dobson, et al.
Genome Biology|August 31, 2016
An integrated genetic-epigenetic analysis of schizophrenia: evidence for co-localization of genetic associations and differential DNA methylationEilis Hannon, Emma Dempster, Joana Viana, et al.
Human Molecular Genetics|April 30, 2004
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populationsMarta Ribasés, Mònica Gratacòs, Fernando Fernández-Aranda, et al.
European Journal of Human Genetics : EJHG|January 20, 2005
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populationsMarta Ribasés, Mònica Gratacòs, Fernando Fernández-Aranda, et al.
American Journal of Human Genetics|January 3, 2012
Rare deletions at the neurexin 3 locus in autism spectrum disorderAndrea K Vaags, Anath C Lionel, Daisuke Sato, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|January 24, 2017
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on GeneticsIna Giegling, Ladislav Hosak, Rainald Mössner, et al.
Translational Psychiatry|April 13, 2021
HLA-DQB1 6672G>C (rs113332494) is associated with clozapine-induced neutropenia and agranulocytosis in individuals of European ancestryBettina Konte, James T R Walters, Dan Rujescu, et al.
Journal of Medical Genetics|April 14, 2016
Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditionsMaria Tropeano, Deirdre Howley, Matthew J Gazzellone, et al.
Psychiatric Genetics|March 16, 2006
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosaElena Cellini, Benedetta Nacmias, Maria Brecelj-Anderluh, et al.
Pageof 18