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The American Journal of Psychiatry
|
February 13, 2020
Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness
Christopher R K Ching, Boris A Gutman, Daqiang Sun, et al.
Research Square
|
January 8, 2026
Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis
Mansoureh Shahsavani, Josephine Wincent, Ricarda Reiter, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study
Rune Boen, Kathleen P O'Hora, Hoki Fung, et al.
Brain : a Journal of Neurology
|
November 15, 2025
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency
Kajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben, et al.
Human Brain Mapping
|
February 22, 2021
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
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of 27
Search research articles
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Showing results (261-270 of 266) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 266 results.
The American Journal of Psychiatry
|
February 13, 2020
Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness
Christopher R K Ching, Boris A Gutman, Daqiang Sun, et al.
Research Square
|
January 8, 2026
Characterization of CTNND2-related neurodevelopmental disease, phenotype-genotype spectrum and WNT dynamics in early neurogenesis
Mansoureh Shahsavani, Josephine Wincent, Ricarda Reiter, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 4, 2026
The Hidden Architecture of Brain Structural Variability in 22q11.2 Deletion Syndrome: A Multi-site Study
Rune Boen, Kathleen P O'Hora, Hoki Fung, et al.
Brain : a Journal of Neurology
|
November 15, 2025
The genotypic and phenotypic landscape of PDHA1-related pyruvate dehydrogenase complex deficiency
Kajus Merkevicius, Dmitrii Smirnov, Lea D Schlieben, et al.
Human Brain Mapping
|
February 22, 2021
Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs
Ida E Sønderby, Christopher R K Ching, Sophia I Thomopoulos, et al.
Molecular Psychiatry
|
February 5, 2020
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Isabelle Cleynen, Worrawat Engchuan, Matthew S Hestand, et al.
Page
of 27