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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 schizophrenia
C Francks, S Maegawa, J Laurén, et al.
Nature Communications
|
February 24, 2025
Insights from a methylome-wide association study of antidepressant exposure
E 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 dyslexia
Alessandro 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 dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Nature Communications
|
April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Stefan 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 study
J M M Bayer, L S van Velzen, E Pozzi, et al.
Page
of 58
Search research articles
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Showing results (571-580 of 576) with videos related to
Sort By:
Page
of 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 schizophrenia
C Francks, S Maegawa, J Laurén, et al.
Nature Communications
|
February 24, 2025
Insights from a methylome-wide association study of antidepressant exposure
E 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 dyslexia
Alessandro 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 dyslexia
Alessandro Gialluisi, Till F M Andlauer, Nazanin Mirza-Schreiber, et al.
Nature Communications
|
April 14, 2018
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Stefan 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 study
J M M Bayer, L S van Velzen, E Pozzi, et al.
Page
of 58