» Authors » David E Linden

David E Linden

Explore the profile of David E Linden including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 16
Citations 217
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Goebel R, Luhrs M, Ciarlo A, Esposito F, Linden D
Philos Trans R Soc Lond B Biol Sci . 2024 Oct; 379(1915):20230084. PMID: 39428873
During fMRI neurofeedback participants learn to self-regulate activity in relevant brain areas and networks based on ongoing feedback extracted from measured responses in those regions. This closed-loop approach has been...
2.
Bressler R, Raible S, Luhrs M, Tier R, Goebel R, Linden D
Neuropsychologia . 2023 Oct; 190:108699. PMID: 37816480
Police officers of the Special Forces are confronted with highly demanding situations in terms of stress, high tension and threats to their lives. Their tasks are specifically high-risk operations, such...
3.
Boen R, Kaufmann T, van der Meer D, Frei O, Agartz I, Ames D, et al.
Biol Psychiatry . 2023 Sep; 95(2):147-160. PMID: 37661008
Background: Carriers of the 1q21.1 distal and 15q11.2 BP1-BP2 copy number variants exhibit regional and global brain differences compared with noncarriers. However, interpreting regional differences is challenging if a global...
4.
Lancaster T, Dimitriadis S, Perry G, Zammit S, ODonovan M, Linden D
Schizophr Bull . 2021 Oct; 48(2):524-532. PMID: 34662406
Schizophrenia (SCZ) is associated with structural brain changes, with considerable variation in the extent to which these cortical regions are influenced. We present a novel metric that summarises individual structural...
5.
Dimitriadis S, Lancaster T, Perry G, Tansey K, Jones D, Singh K, et al.
Biol Psychiatry Cogn Neurosci Neuroimaging . 2021 Feb; 6(12):1176-1184. PMID: 33524599
Background: Altered functional brain connectivity has been proposed as an intermediate phenotype between genetic risk loci and clinical expression of schizophrenia. Genetic high-risk groups of healthy subjects are particularly suited...
6.
Ching C, Gutman B, Sun D, Villalon Reina J, Ragothaman A, Isaev D, et al.
Am J Psychiatry . 2020 Feb; 177(7):589-600. PMID: 32046535
Objective: 22q11.2 deletion syndrome (22q11DS) is among the strongest known genetic risk factors for schizophrenia. Previous studies have reported variable alterations in subcortical brain structures in 22q11DS. To better characterize...
7.
Dimitriadis S, Brindley L, Evans L, Linden D, Singh K
Front Neuroinform . 2018 Dec; 12:59. PMID: 30510507
Both amplitude and latency of single-trial EEG/MEG recordings provide valuable information regarding functionality of the human brain. In this article, we provided a data-driven graph and network-based framework for mining...
8.
Sykes L, Haddon J, Lancaster T, Sykes A, Azzouni K, Ihssen N, et al.
Schizophr Bull . 2018 Oct; 45(5):1024-1032. PMID: 30304534
Genetic variation in CACNA1C, which encodes the alpha-1 subunit of Cav1.2 L-type voltage-gated calcium channels (VGCCs), has been strongly linked to risk for psychiatric disorders including schizophrenia and bipolar disorder....
9.
Dimitriadis S, Routley B, Linden D, Singh K
Front Neurosci . 2018 Aug; 12:506. PMID: 30127710
The resting activity of the brain can be described by so-called intrinsic connectivity networks (ICNs), which consist of spatially and temporally distributed, but functionally connected, nodes. The coordinated activity of...
10.
Lancaster T, Dimitriadis S, Tansey K, Perry G, Ihssen N, Jones D, et al.
Schizophr Bull . 2018 Apr; 45(2):405-414. PMID: 29608775
Risk profile scores (RPS) derived from genome-wide association studies (GWAS) explain a considerable amount of susceptibility for schizophrenia (SCZ). However, little is known about how common genetic risk factors for...