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Annals of Clinical and Translational Neurology
|
December 16, 2025
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
Darren Cameron, Nicholas E Clifton, Daniel Cabezas de la Fuente, et al.
Scientific Reports
|
June 21, 2022
Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation
Ye Hyun Hwang, Bruce Eliot Hayward, Marwa Zafarullah, et al.
Journal of Alzheimer'S Disease : JAD
|
September 6, 2021
Cognitive Decline in Alzheimer's Disease Is Not Associated with APOE
Ioanna Katzourou, Ganna Leonenko, Dobril Ivanov, et al.
American Journal of Human Genetics
|
February 18, 2005
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
Natalie Cope, Denise Harold, Gary Hill, et al.
Molecular Psychiatry
|
March 14, 2023
Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia
Alexandros Rammos, George Kirov, Leon Hubbard, et al.
Biological Psychiatry
|
April 13, 2011
An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction
Valentina Moskvina, Nick Craddock, Bertram Müller-Myhsok, et al.
Human Molecular Genetics
|
February 3, 2009
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
George Kirov, Detelina Grozeva, Nadine Norton, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
November 3, 2011
Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants
Kate Langley, Joanna Martin, Sharifah Shameem Agha, et al.
Genetic Epidemiology
|
March 14, 2018
POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data
Emily Baker, Karl Michael Schmidt, Rebecca Sims, et al.
Neuroepidemiology
|
February 20, 2024
Modelling Disease Progression of Multiple Sclerosis in a South Wales Cohort
Emeka C Uzochukwu, Katharine E Harding, James Hrastelj, et al.
Page
of 18
Search research articles
Search
Showing results (21-30 of 173) with videos related to
Sort By:
Page
of 18
Annals of Clinical and Translational Neurology
|
December 16, 2025
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia
Darren Cameron, Nicholas E Clifton, Daniel Cabezas de la Fuente, et al.
Scientific Reports
|
June 21, 2022
Both cis and trans-acting genetic factors drive somatic instability in female carriers of the FMR1 premutation
Ye Hyun Hwang, Bruce Eliot Hayward, Marwa Zafarullah, et al.
Journal of Alzheimer'S Disease : JAD
|
September 6, 2021
Cognitive Decline in Alzheimer's Disease Is Not Associated with APOE
Ioanna Katzourou, Ganna Leonenko, Dobril Ivanov, et al.
American Journal of Human Genetics
|
February 18, 2005
Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia
Natalie Cope, Denise Harold, Gary Hill, et al.
Molecular Psychiatry
|
March 14, 2023
Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia
Alexandros Rammos, George Kirov, Leon Hubbard, et al.
Biological Psychiatry
|
April 13, 2011
An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction
Valentina Moskvina, Nick Craddock, Bertram Müller-Myhsok, et al.
Human Molecular Genetics
|
February 3, 2009
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
George Kirov, Detelina Grozeva, Nadine Norton, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
November 3, 2011
Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants
Kate Langley, Joanna Martin, Sharifah Shameem Agha, et al.
Genetic Epidemiology
|
March 14, 2018
POLARIS: Polygenic LD-adjusted risk score approach for set-based analysis of GWAS data
Emily Baker, Karl Michael Schmidt, Rebecca Sims, et al.
Neuroepidemiology
|
February 20, 2024
Modelling Disease Progression of Multiple Sclerosis in a South Wales Cohort
Emeka C Uzochukwu, Katharine E Harding, James Hrastelj, et al.
Page
of 18