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B Talcott

Showing results (51-60 of 68) with videos related to

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Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
BMC Medicine|March 22, 2021
Effects of maternal folic acid supplementation during the second and third trimesters of pregnancy on neurocognitive development in the child: an 11-year follow-up from a randomised controlled trialAoife Caffrey, Helene McNulty, Mark Rollins, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.
Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Developmental Medicine and Child Neurology|October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Nature Genetics|February 24, 2023
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|April 17, 2021
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measuresAngela Martinelli, Mabel L Rice, Joel B Talcott, et al.
Translational Psychiatry|July 26, 2017
The DCDC2 deletion is not a risk factor for dyslexiaT S Scerri, E Macpherson, A Martinelli, et al.
BMC Medicine|March 22, 2021
Effects of maternal folic acid supplementation during the second and third trimesters of pregnancy on neurocognitive development in the child: an 11-year follow-up from a randomised controlled trialAoife Caffrey, Helene McNulty, Mark Rollins, et al.
Plos One|December 5, 2012
The dyslexia candidate locus on 2p12 is associated with general cognitive ability and white matter structureThomas S Scerri, Fahimeh Darki, Dianne F Newbury, et al.
Plos Genetics|September 27, 2013
Common variants in left/right asymmetry genes and pathways are associated with relative hand skillWilliam M Brandler, Andrew P Morris, David M Evans, et al.
Nature Genetics|December 18, 2001
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexiaSimon E Fisher, Clyde Francks, Angela J Marlow, et al.
Developmental Medicine and Child Neurology|October 15, 2013
Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexiaNuala H Simpson, Laura Addis, William M Brandler, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Nature Genetics|October 20, 2022
Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Nature Genetics|February 24, 2023
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexiaCatherine Doust, Pierre Fontanillas, Else Eising, et al.
Pageof 7