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Showing results (481-490 of 551) with videos related to

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Cephalalgia : an International Journal of Headache|May 24, 2015
Improving the detection of chronic migraine: Development and validation of Identify Chronic Migraine (ID-CM)Richard B Lipton, Daniel Serrano, Dawn C Buse, et al.
American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
The Journal of Allergy and Clinical Immunology|April 4, 2016
DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitisChloé Sarnowski, Catherine Laprise, Giovanni Malerba, et al.
American Journal on Intellectual and Developmental Disabilities|March 4, 2017
Efficacy and Social Validity of Peer Network Interventions for High School Students With Severe DisabilitiesJennifer M Asmus, Erik W Carter, Colleen K Moss, et al.
Translational Psychiatry|October 17, 2022
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutationsRebecca S F Mok, Wenbo Zhang, Taimoor I Sheikh, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Nature Genetics|January 19, 2010
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1Francis J McMahon, Nirmala Akula, Thomas G Schulze, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|September 30, 2014
Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disordersClement C Zai, Mirko Manchia, Ida Elken Sønderby, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Pageof 56

Showing results (481-490 of 551) with videos related to

Sort By:
Pageof 56
Cephalalgia : an International Journal of Headache|May 24, 2015
Improving the detection of chronic migraine: Development and validation of Identify Chronic Migraine (ID-CM)Richard B Lipton, Daniel Serrano, Dawn C Buse, et al.
American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.
Human Molecular Genetics|June 13, 2018
Biallelic missense variants in ZBTB11 can cause intellectual disability in humansZohreh Fattahi, Taimoor I Sheikh, Luciana Musante, et al.
The Journal of Allergy and Clinical Immunology|April 4, 2016
DNA methylation within melatonin receptor 1A (MTNR1A) mediates paternally transmitted genetic variant effect on asthma plus rhinitisChloé Sarnowski, Catherine Laprise, Giovanni Malerba, et al.
American Journal on Intellectual and Developmental Disabilities|March 4, 2017
Efficacy and Social Validity of Peer Network Interventions for High School Students With Severe DisabilitiesJennifer M Asmus, Erik W Carter, Colleen K Moss, et al.
Translational Psychiatry|October 17, 2022
Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutationsRebecca S F Mok, Wenbo Zhang, Taimoor I Sheikh, et al.
Translational Psychiatry|January 8, 2021
Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disabilityTaimoor I Sheikh, Nasim Vasli, Stephen Pastore, et al.
Nature Genetics|January 19, 2010
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1Francis J McMahon, Nirmala Akula, Thomas G Schulze, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|September 30, 2014
Investigation of the genetic interaction between BDNF and DRD3 genes in suicidical behaviour in psychiatric disordersClement C Zai, Mirko Manchia, Ida Elken Sønderby, et al.
American Journal of Human Genetics|October 13, 2006
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxiaLars Feuk, Aino Kalervo, Marita Lipsanen-Nyman, et al.
Pageof 56