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Clyde Francks

Showing results (11-20 of 115) with videos related to

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Scientific Reports|April 14, 2019
The molecular genetics of hand preference revisitedCarolien G F de Kovel, Clyde Francks
The Lancet. Neurology|July 10, 2003
The genetic basis of dyslexiaClyde Francks, I Laurence MacPhie, Anthony P Monaco
Neuropsychologia|November 20, 2015
Whole exome sequencing for handedness in a large and highly consanguineous familyTulya Kavaklioglu, Muhammad Ajmal, Abdul Hameed, et al.
Science Advances|February 17, 2023
Genetic architecture of the white matter connectome of the human brainZhiqiang Sha, Dick Schijven, Simon E Fisher, et al.
Brain and Language|August 1, 2016
Neuroimaging genetic analyses of novel candidate genes associated with reading and languageAlessandro Gialluisi, Tulio Guadalupe, Clyde Francks, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Persistence and transmission of recessive deafness and sign language: new insights from village sign languagesAlessandro Gialluisi, Dan Dediu, Clyde Francks, et al.
Nature Communications|April 2, 2024
Exome-wide analysis implicates rare protein-altering variants in human handednessDick Schijven, Sourena Soheili-Nezhad, Simon E Fisher, et al.
Scientific Data|September 5, 2018
Transcriptomic analysis of left-right differences in human embryonic forebrain and midbrainCarolien G F de Kovel, Steven N Lisgo, Clyde Francks
Scientific Reports|January 26, 2019
A large-scale population study of early life factors influencing left-handednessCarolien G F de Kovel, Amaia Carrión-Castillo, Clyde Francks
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 12, 2014
Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophreniaNicolas Brucato, Lynn E DeLisi, Simon E Fisher, et al.
Pageof 12

Showing results (11-20 of 115) with videos related to

Sort By:
Pageof 12
Scientific Reports|April 14, 2019
The molecular genetics of hand preference revisitedCarolien G F de Kovel, Clyde Francks
The Lancet. Neurology|July 10, 2003
The genetic basis of dyslexiaClyde Francks, I Laurence MacPhie, Anthony P Monaco
Neuropsychologia|November 20, 2015
Whole exome sequencing for handedness in a large and highly consanguineous familyTulya Kavaklioglu, Muhammad Ajmal, Abdul Hameed, et al.
Science Advances|February 17, 2023
Genetic architecture of the white matter connectome of the human brainZhiqiang Sha, Dick Schijven, Simon E Fisher, et al.
Brain and Language|August 1, 2016
Neuroimaging genetic analyses of novel candidate genes associated with reading and languageAlessandro Gialluisi, Tulio Guadalupe, Clyde Francks, et al.
European Journal of Human Genetics : EJHG|January 17, 2013
Persistence and transmission of recessive deafness and sign language: new insights from village sign languagesAlessandro Gialluisi, Dan Dediu, Clyde Francks, et al.
Nature Communications|April 2, 2024
Exome-wide analysis implicates rare protein-altering variants in human handednessDick Schijven, Sourena Soheili-Nezhad, Simon E Fisher, et al.
Scientific Data|September 5, 2018
Transcriptomic analysis of left-right differences in human embryonic forebrain and midbrainCarolien G F de Kovel, Steven N Lisgo, Clyde Francks
Scientific Reports|January 26, 2019
A large-scale population study of early life factors influencing left-handednessCarolien G F de Kovel, Amaia Carrión-Castillo, Clyde Francks
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 12, 2014
Hypomethylation of the paternally inherited LRRTM1 promoter linked to schizophreniaNicolas Brucato, Lynn E DeLisi, Simon E Fisher, et al.
Pageof 12