Jessika E. Sussmann

发表

Common genetic variants influence human subcortical brain structures

Thomas E. Nichols, Robert W. Williams, Benjamin S. Aribisala, 2015, Nature.

Identification of common variants associated with human hippocampal and intracranial volumes

Marisa O. Hollinshead, Lorna M. Lopez, Thomas W. Mühleisen, 2012, Nature Genetics.

White Matter Tractography in Bipolar Disorder and Schizophrenia

Mark E. Bastin, Eve C. Johnstone, Susana Muñoz Maniega, 2008, Biological Psychiatry.

Low birthweight and preterm birth in young people with special educational needs: a magnetic resonance imaging analysis

Eve C Johnstone, Stephen M Lawrie, S. Lawrie, 2008, BMC medicine.

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2016, Nature Neuroscience.

Do Candidate Genes Affect the Brain’s White Matter Microstructure? Large-Scale Evaluation of 6,165 Diffusion MRI Scans

Peter Kochunov, Thomas E. Nichols, Neda Jahanshad, 2017, bioRxiv.

Polygenic Risk and White Matter Integrity in Individuals at High Risk of Mood Disorder

S. Lawrie, H. Whalley, D. Glahn, 2013, Biological Psychiatry.

An investigation of a genomewide supported psychosis variant in ZNF804A and white matter integrity in the human brain☆

Mark E. Bastin, Norbert Dahmen, Georg Winterer, 2012, Magnetic resonance imaging.

White matter abnormalities in bipolar disorder and schizophrenia detected using diffusion tensor magnetic resonance imaging.

James McKirdy, Mark E Bastin, Eve C Johnstone, 2009, Bipolar disorders.

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Michael W. Weiner, Anders M. Dale, Robert C. Green, 2017, bioRxiv.

Novel genetic loci associated with hippocampal volume

Benjamin S Aribisala, Wiro J Niessen, Peter Kochunov, 2017, Nature Communications.

Genetic architecture of subcortical brain structures in 38,851 individuals

Benjamin S Aribisala, Tien Yin Wong, Wiro J Niessen, 2019, Nature Genetics.

Obstetric complications and mild to moderate intellectual disability

S. Lawrie, E. Johnstone, A. McIntosh, 2009, British Journal of Psychiatry.

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals

Heather C Whalley, Eve C Johnstone, Stephen M Lawrie, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Review of functional magnetic resonance imaging studies comparing bipolar disorder and schizophrenia

Heather C Whalley, Stephen M Lawrie, Emma Sprooten, 2012, Bipolar disorders.

Multi-site study of additive genetic effects on fractional anisotropy of cerebral white matter: Comparing meta and megaanalytical approaches for data pooling

Arthur W. Toga, Thomas E. Nichols, Joanna M. Wardlaw, 2014, NeuroImage.

Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group

Paul M. Thompson, Arthur W. Toga, Thomas E. Nichols, 2013, NeuroImage.

Corrigendum to “Multi-site genetic analysis of diffusion images and voxelwise heritability analysis: A pilot project of the ENIGMA–DTI working group” [NeuroImage 81 (2013) 455–469]

Paul M. Thompson, Arthur W. Toga, Thomas E. Nichols, 2014, NeuroImage.

Effect of Variation in Diacylglycerol Kinase Eta (DGKH) Gene on Brain Function in a Cohort at Familial Risk of Bipolar Disorder

S. Lawrie, H. Whalley, E. Johnstone, 2012, Neuropsychopharmacology.

Identification of common variants associated with human hippocampal and intracranial volumes

Marisa O. Hollinshead, Lorna M. Lopez, Thomas W. Mühleisen, 2012, Nature Genetics.

Novel genetic loci associated with hippocampal volume

Thomas E. Nichols, Benjamin S. Aribisala, Amelia A. Assareh, 2017, Nature Communications.

Prospective longitudinal voxel-based morphometry study of major depressive disorder in young individuals at high familial risk

S. Lawrie, H. Whalley, T. Nickson, 2016, Psychological Medicine.

Low birthweight and preterm birth in young people with special educational needs: a magnetic resonance imaging analysis

S. Lawrie, E. Johnstone, A. McIntosh, 2008 .

White Matter Integrity in Individuals at High Genetic Risk of Bipolar Disorder

Mark E. Bastin, Eve C. Johnstone, Seonaid Anderson, 2011, Biological Psychiatry.

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

Andrew D. Johnson, Dan J Stein, Benjamin S. Aribisala, 2017 .

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Benjamin S. Aribisala, Nicola J. Armstrong, Amelia A. Assareh, 2016, Nature Neuroscience.

Deactivation in anterior cingulate cortex during facial processing in young individuals with high familial risk and early development of depression: fMRI findings from the Scottish Bipolar Family Study.

H. Whalley, Jessika E. Sussmann, L. Romaniuk, 2016, Journal of child psychology and psychiatry, and allied disciplines.

Prospective longitudinal voxel-based morphometry study of major depressive disorder in young individuals at high familial risk

H. Whalley, T. Nickson, A. McIntosh, 2016, Psychological Medicine.