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Showing results (571-580 of 576) with videos related to

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Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Nature Communications|February 24, 2025
Insights from a methylome-wide association study of antidepressant exposureE Davyson, X Shen, F Huider, et al.
Translational Psychiatry|February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Nature Communications|April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertensionStefan Gräf, Matthias Haimel, Marta Bleda, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Dissecting heterogeneity in cortical thickness abnormalities in major depressive disorder: a large-scale ENIGMA MDD normative modelling studyJ M M Bayer, L S van Velzen, E Pozzi, et al.
Pageof 58

Showing results (571-580 of 576) with videos related to

Sort By:
Pageof 58
You have reached the last page of results.This site can display upto 576 results.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Nature Communications|February 24, 2025
Insights from a methylome-wide association study of antidepressant exposureE Davyson, X Shen, F Huider, et al.
Translational Psychiatry|February 12, 2019
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Molecular Psychiatry|October 15, 2020
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexiaAlessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Nature Communications|April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertensionStefan Gräf, Matthias Haimel, Marta Bleda, et al.
Biorxiv : the Preprint Server for Biology|April 1, 2025
Dissecting heterogeneity in cortical thickness abnormalities in major depressive disorder: a large-scale ENIGMA MDD normative modelling studyJ M M Bayer, L S van Velzen, E Pozzi, et al.
Pageof 58