• Fjell, Anders Martin; Sørensen, Øystein; Wang, Yunpeng; Amlien, Inge; Baaré, William F. C. & Bartrés-Faz, David [Vis alle 24 forfattere av denne artikkelen] (2023). No phenotypic or genotypic evidence for a link between sleep duration and brain atrophy. Nature Human Behaviour. ISSN 2397-3374. 7, s. 2008–2022. doi: 10.1038/s41562-023-01707-5. Fulltekst i vitenarkiv
• Raud, Liisa; Sneve, Markus Handal; Vidal-Piñeiro, Didac; Sørensen, Øystein; Folvik, Line & Ness, Hedda Tvedten [Vis alle 10 forfattere av denne artikkelen] (2023). Hippocampal-cortical functional connectivity during memory encoding and retrieval. NeuroImage. ISSN 1053-8119. 279. doi: 10.1016/j.neuroimage.2023.120309.
• Carver, Rebecca Bruu; Fredheim, Nanna Alida Grit; Mowinckel, Athanasia Monika; Ebmeier, Klaus P.; Bodorkos Friedman, Barbara & Rosness, Tor Atle [Vis alle 20 forfattere av denne artikkelen] (2022). People's interest in brain health testing: Findings from an international, online cross-sectional survey. Frontiers in Public Health. ISSN 2296-2565. 10, s. 1–19. doi: 10.3389/fpubh.2022.998302. Fulltekst i vitenarkiv
• Binnewies, Julia; Nawijn, Laura; Brandmaier, Andreas M.; Baaré, William F.C.; Bartres-Faz, David & Drevon, Christian André [Vis alle 22 forfattere av denne artikkelen] (2022). Associations of depression and regional brain structure across the adult lifespan: Pooled analyses of six population-based and two clinical cohort studies in the European Lifebrain consortium. NeuroImage: Clinical. ISSN 2213-1582. 36. doi: 10.1016/j.nicl.2022.103180.
• Walhovd, Kristine B; Nyberg, Lars; Lindenberger, Ulman; Amlien, Inge; Sørensen, Øystein & Wang, Yunpeng [Vis alle 20 forfattere av denne artikkelen] (2022). Brain aging differs with cognitive ability regardless of education. Scientific Reports. ISSN 2045-2322. 12(1). doi: 10.1038/s41598-022-17727-6.
• Bråthen, Anne Cecilie Sjøli; Sørensen, Øystein; de Lange, Ann-Marie Glasø; Mowinckel, Athanasia Monika; Fjell, Anders Martin & Walhovd, Kristine B (2022). Cognitive and hippocampal changes weeks and years after memory training. Scientific Reports. ISSN 2045-2322. 12(1). doi: 10.1038/s41598-022-11636-4.
• Vidal-Piñeiro, Didac; Sørensen, Øystein; Blennow, Kaj; Capogna, Elettra; Halaas, Nathalie Bodd & Idland, Ane-Victoria [Vis alle 12 forfattere av denne artikkelen] (2022). Relationship between cerebrospinal fluid neurodegeneration biomarkers and temporal brain atrophy in cognitively healthy older adults. Neurobiology of Aging. ISSN 0197-4580. 116, s. 80–91. doi: 10.1016/j.neurobiolaging.2022.04.010. Fulltekst i vitenarkiv
• Solé-Padullés, Cristina; Macià, Dídac; Andersson, Micael; Stiernstedt, Mikael; Pudas, Sara & Düzel, Sandra [Vis alle 19 forfattere av denne artikkelen] (2022). No Association Between Loneliness, Episodic Memory and Hippocampal Volume Change in Young and Healthy Older Adults: A Longitudinal European Multicenter Study. Frontiers in Aging Neuroscience. ISSN 1663-4365. 14. doi: 10.3389/fnagi.2022.795764. Fulltekst i vitenarkiv
• Ljøsne, Isabelle Sylvie Budin; Mowinckel, Athanasia Monika; Bodorkos Friedman, Barbara; Ebmeier, Klaus P; Drevon, Christian A & Carver, Rebecca Bruu [Vis alle 22 forfattere av denne artikkelen] (2022). Public perceptions of brain health: an international, online cross-sectional survey. BMJ Open. ISSN 2044-6055. 12(4). doi: 10.1136/bmjopen-2021-057999. Fulltekst i vitenarkiv
• Vidal-Piñeiro, Didac; Wang, Yunpeng; Krogsrud, Stine Kleppe; Amlien, Inge; Baaré, William FC & Bartres-Faz, David [Vis alle 31 forfattere av denne artikkelen] (2021). Individual variations in ‘brain age’ relate to early-life factors more than to longitudinal brain change. eLIFE. ISSN 2050-084X. 10. doi: 10.7554/eLife.69995. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Grydeland, Håkon; Wang, Yunpeng; Amlien, Inge; Bartrés-Faz, David & Brandmaier, Andreas M. [Vis alle 24 forfattere av denne artikkelen] (2021). The genetic organization of longitudinal subcortical volumetric change is stable throughout the lifespan running title: Genetics of subcortical lifespan change. eLIFE. ISSN 2050-084X. 10, s. 1–22. doi: 10.7554/eLife.66466. Fulltekst i vitenarkiv Vis sammendrag

  Development and aging of the cerebral cortex show similar topographic organization and are governed by the same genes. It is unclear whether the same is true for subcortical regions, which follow fundamentally different ontogenetic and phylogenetic principles. We tested the hypothesis that genetically governed neurodevelopmental processes can be traced throughout life by assessing to which degree brain regions that develop together continue to change together through life. Analyzing over 6000 longitudinal MRIs of the brain, we used graph theory to identify five clusters of coordinated development, indexed as patterns of correlated volumetric change in brain structures. The clusters tended to follow placement along the cranial axis in embryonic brain development, suggesting continuity from prenatal stages, and correlated with cognition. Across independent longitudinal datasets, we demonstrated that developmental clusters were conserved through life. Twin-based genetic correlations revealed distinct sets of genes governing change in each cluster. Single-nucleotide polymorphisms-based analyses of 38,127 cross-sectional MRIs showed a similar pattern of genetic volume–volume correlations. In conclusion, coordination of subcortical change adheres to fundamental principles of lifespan continuity and genetic organization.

• Walhovd, Kristine Beate; Fjell, Anders Martin; Wang, Yunpeng; Amlien, Inge; Mowinckel, Athanasia Monika & Lindenberger, Ulman [Vis alle 29 forfattere av denne artikkelen] (2021). Education and income show heterogeneous relationships to lifespan brain and cognitive differences across European and US cohorts. Cerebral Cortex. ISSN 1047-3211. 32(4), s. 839–854. doi: 10.1093/cercor/bhab248. Fulltekst i vitenarkiv
• Krogsrud, Stine Kleppe; Mowinckel, Athanasia Monika; Sederevicius, Donatas; Vidal-Piñeiro, Didac; Amlien, Inge Kasbohm & Wang, Yunpeng [Vis alle 9 forfattere av denne artikkelen] (2021). Relationships between apparent cortical thickness and working memory across the lifespan - Effects of genetics and socioeconomic status. Developmental Cognitive Neuroscience. ISSN 1878-9293. 51, s. 1–11. doi: 10.1016/j.dcn.2021.100997.
• Roe, James Michael; Vidal-Piñeiro, Didac; Sørensen, Øystein; Brandmaier, Andreas M.; Düzel, Sandra & Gonzalez, Hector A. [Vis alle 18 forfattere av denne artikkelen] (2021). Asymmetric thinning of the cerebral cortex across the adult lifespan is accelerated in Alzheimer’s disease. Nature Communications. ISSN 2041-1723. 12:721, s. 1–11. doi: 10.1038/s41467-021-21057-y. Fulltekst i vitenarkiv
• Sørensen, Øystein; Brandmaier, Andreas M.; Macià, Dídac; Ebmeier, Klaus; Ghisletta, Paolo & Kievit, Rogier A. [Vis alle 10 forfattere av denne artikkelen] (2021). Meta-analysis of generalized additive models in neuroimaging studies. NeuroImage. ISSN 1053-8119. doi: 10.1016/j.neuroimage.2020.117416. Vis sammendrag

  Analyzing data from multiple neuroimaging studies has great potential in terms of increasing statistical power, enabling detection of effects of smaller magnitude than would be possible when analyzing each study separately and also allowing to systematically investigate between-study differences. Restrictions due to privacy or proprietary data as well as more practical concerns can make it hard to share neuroimaging datasets, such that analyzing all data in a common location might be impractical or impossible. Meta-analytic methods provide a way to overcome this issue, by combining aggregated quantities like model parameters or risk ratios. Most meta-analytic tools focus on parametric statistical models, and methods for meta-analyzing semi-parametric models like generalized additive models have not been well developed. Parametric models are often not appropriate in neuroimaging, where for instance age-brain relationships may take forms that are difficult to accurately describe using such models. In this paper we introduce meta-GAM, a method for meta-analysis of generalized additive models which does not require individual participant data, and hence is suitable for increasing statistical power while upholding privacy and other regulatory concerns. We extend previous works by enabling the analysis of multiple model terms as well as multivariate smooth functions. In addition, we show how meta-analytic p-values can be computed for smooth terms. The proposed methods are shown to perform well in simulation experiments, and are demonstrated in a real data analysis on hippocampal volume and self-reported sleep quality data from the Lifebrain consortium. We argue that application of meta-GAM is especially beneficial in lifespan neuroscience and imaging genetics. The methods are implemented in an accompanying R package metagam, which is also demonstrated.

• Ljøsne, Isabelle Sylvie Budin; Bodorkos Friedman, Barbara; Suri, Sana; Solé-Padullés, Cristina; Düzel, Sandra & Drevon, Christian André [Vis alle 24 forfattere av denne artikkelen] (2020). The Global Brain Health Survey: Development of a Multi-Language Survey of Public Views on Brain Health. Frontiers in Public Health. ISSN 2296-2565. doi: 10.3389/fpubh.2020.00387.
• Walhovd, Kristine B; Bråthen, Anne Cecilie Sjøli; Panizzon, Matthew S.; Mowinckel, Athanasia Monika; Sørensen, Øystein & de Lange, Ann-Marie Glasø [Vis alle 11 forfattere av denne artikkelen] (2020). Within-session verbal learning slope is predictive of lifespan delayed recall, hippocampal volume, and memory training benefit, and is heritable. Scientific Reports. ISSN 2045-2322. 10, s. 1–13. doi: 10.1038/s41598-020-78225-1. Fulltekst i vitenarkiv Vis sammendrag

  Memory performance results from plasticity, the ability to change with experience. We show that benefit from practice over a few trials, learning slope, is predictive of long-term recall and hippocampal volume across a broad age range and a long period of time, relates to memory training benefit, and is heritable. First, in a healthy lifespan sample (n = 1825, age 4–93 years), comprising 3483 occasions of combined magnetic resonance imaging (MRI) scans and memory tests over a period of up to 11 years, learning slope across 5 trials was uniquely related to performance on a delayed free recall test, as well as hippocampal volume, independent from first trial memory or total memory performance across the five learning trials. Second, learning slope was predictive of benefit from memory training across ten weeks in an experimental subsample of adults (n = 155). Finally, in an independent sample of male twins (n = 1240, age 51–50 years), learning slope showed significant heritability. Within-session learning slope may be a useful marker beyond performance per se, being heritable and having unique predictive value for long-term memory function, hippocampal volume and training benefit across the human lifespan.

• Danielsen, Vilde Marie; Vidal-Piñeiro, Didac; Mowinckel, Athanasia Monika; Sederevicius, Donatas; Fjell, Anders Martin & Walhovd, Kristine B [Vis alle 7 forfattere av denne artikkelen] (2020). Lifespan trajectories of relative corpus callosum thickness: Regional differences and cognitive relevance. Cortex. ISSN 0010-9452. 130, s. 127–141. doi: 10.1016/j.cortex.2020.05.020. Vis sammendrag

  The cerebral hemispheres are specialized for different cognitive functions and receive divergent information from the sensory organs, so that the interaction between the hemispheres is a crucial aspect of perception and cognition. At the same time, the major fiber tract responsible for this interaction, the corpus callosum, shows a structural development across the lifespan which is over-proportional. That is, compared to changes in overall forebrain volume, the corpus callosum shows an accentuated growth during childhood, adolescence, and early adulthood, as well as pronounced decline in older age. However, this over-proportionality of growth and decline along with potential consequences for cognition, have been largely overlooked in empirical research. In the present study we systematically address the proportionality of callosal development in a large mixed cross-sectional and longitudinal sample (1867 datasets from 1014 unique participants), covering the human lifespan (age range 4–93 years), and examine the cognitive consequences of the observed changes. Relative corpus callosum thickness was measured at 60 segments along the midsagittal surface, and lifespan trajectories were clustered to identify callosal subsections of comparable lifespan development. While confirming the expected inverted u-shaped lifespan trajectories, we also found substantial regional variation. Compared with anterior clusters, the most posterior sections exhibited an accentuated growth during development which extends well into the third decade of life, and a protracted decline in older age which is delayed by about 10 years (starting mid to late 50s). We further showed that the observed longitudinal changes in relative thickness of the mid splenium significantly mediates age-related changes in tests assessing verbal knowledge and non-verbal visual-spatial abilities across the lifespan. In summary, we demonstrate that analyzing the proportionality of callosal growth and decline offers valuable insight into lifespan development of structural connectivity between the hemispheres, and suggests consequences for the cognitive development of perception and cognition.

• Gorbach, Tetiana; Pudas, Sara; Bartrés-Faz, David; Brandmaier, Andreas M.; Düzel, Sandra & Henson, Rik [Vis alle 17 forfattere av denne artikkelen] (2020). Longitudinal association between hippocampus atrophy and episodic‐memory decline in non‐demented APOE ε4 carriers. Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. ISSN 2352-8729. 12(1). doi: 10.1002/dad2.12110. Fulltekst i vitenarkiv Vis sammendrag

  Introduction The apolipoprotein E (APOE) ε4 allele is the main genetic risk factor for Alzheimer's disease (AD), accelerated cognitive aging, and hippocampal atrophy, but its influence on the association between hippocampus atrophy and episodic‐memory decline in non‐demented individuals remains unclear. Methods We analyzed longitudinal (two to six observations) magnetic resonance imaging (MRI)–derived hippocampal volumes and episodic memory from 748 individuals (55 to 90 years at baseline, 50% female) from the European Lifebrain consortium. Results The change‐change association for hippocampal volume and memory was significant only in ε4 carriers (N = 173, r = 0.21, P = .007; non‐carriers: N = 467, r = 0.073, P = .117). The linear relationship was significantly steeper for the carriers [t(629) = 2.4, P = .013]. A similar trend toward a stronger change‐change relation for carriers was seen in a subsample with more than two assessments. Discussion These findings provide evidence for a difference in hippocampus‐memory association between ε4 carriers and non‐carriers, thus highlighting how genetic factors modulate the translation of the AD‐related pathophysiological cascade into cognitive deficits.

• Fjell, Anders Martin; Sørensen, Øystein; Amlien, Inge Kasbohm; Bartrés-Faz, David; Brandmaier, Andreas M. & Buchmann, Nikolaus [Vis alle 32 forfattere av denne artikkelen] (2020). Poor Self-Reported Sleep is Related to Regional Cortical Thinning in Aging but not Memory Decline-Results From the Lifebrain Consortium. Cerebral Cortex. ISSN 1047-3211. s. 1–17. doi: 10.1093/cercor/bhaa332. Fulltekst i vitenarkiv Vis sammendrag

  We examined whether sleep quality and quantity are associated with cortical and memory changes in cognitively healthy participants across the adult lifespan. Associations between self-reported sleep parameters (Pittsburgh Sleep Quality Index, PSQI) and longitudinal cortical change were tested using five samples from the Lifebrain consortium (n = 2205, 4363 MRIs, 18–92 years). In additional analyses, we tested coherence with cell-specific gene expression maps from the Allen Human Brain Atlas, and relations to changes in memory performance. “PSQI # 1 Subjective sleep quality” and “PSQI #5 Sleep disturbances” were related to thinning of the right lateral temporal cortex, with lower quality and more disturbances being associated with faster thinning. The association with “PSQI #5 Sleep disturbances” emerged after 60 years, especially in regions with high expression of genes related to oligodendrocytes and S1 pyramidal neurons. None of the sleep scales were related to a longitudinal change in episodic memory function, suggesting that sleep-related cortical changes were independent of cognitive decline. The relationship to cortical brain change suggests that self-reported sleep parameters are relevant in lifespan studies, but small effect sizes indicate that self-reported sleep is not a good biomarker of general cortical degeneration in healthy older adults.

• Vidal-Piñeiro, Didac; Sneve, Markus Handal; Amlien, Inge Kasbohm; Grydeland, Håkon; Mowinckel, Athanasia Monika & Roe, James Michael [Vis alle 10 forfattere av denne artikkelen] (2020). The Functional Foundations of Episodic Memory Remain Stable Throughout the Lifespan. Cerebral Cortex. ISSN 1047-3211. doi: 10.1093/cercor/bhaa348. Fulltekst i vitenarkiv
• Vidal-Piñeiro, Didac; Parker, Nadine; Shin, Jean; French, Leon; Grydeland, Håkon & Jackowski, Andrea [Vis alle 14 forfattere av denne artikkelen] (2020). Cellular correlates of cortical thinning throughout the lifespan. Scientific Reports. ISSN 2045-2322. 10(1), s. 1–14. doi: 10.1038/s41598-020-78471-3. Fulltekst i vitenarkiv
• Mowinckel, Athanasia Monika & Vidal-Piñeiro, Didac (2020). Visualization of Brain Statistics With R Packages ggseg and ggseg3d. Advances in Methods and Practices in Psychological Science (AMPPS). ISSN 2515-2459. 3(4), s. 466–483. doi: 10.1177/2515245920928009.
• Walhovd, Kristine B; Fjell, Anders Martin; Sørensen, Øystein; Mowinckel, Athanasia Monika; Reinbold, Céline Sonja & Idland, Ane-Victoria [Vis alle 12 forfattere av denne artikkelen] (2020). Genetic risk for Alzheimer disease predicts hippocampal volume through the human lifespan. Neurology: Genetics. ISSN 2376-7839. 6(5). doi: 10.1212/NXG.0000000000000506. Fulltekst i vitenarkiv
• Ljøsne, Isabelle Sylvie Budin; Friedman, Barbara Bodorkos; Suri, Sana; Solé-Padullés, Cristina; Düzel, Sandra & Drevon, Christian A [Vis alle 24 forfattere av denne artikkelen] (2020). The global brain health survey: Development of a multi-language survey of public views on brain health. Frontiers in Public Health. ISSN 2296-2565. 8:387, s. 1–13. doi: 10.3389/fpubh.2020.00387. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Sørensen, Øystein; Amlien, Inge Kasbohm; Bartrés-Faz, David; Bros, Didac Macia & Buchmann, Nikolaus [Vis alle 28 forfattere av denne artikkelen] (2019). Self-reported sleep relates to hippocampal atrophy across the adult lifespan – results from the Lifebrain consortium. Sleep. ISSN 0161-8105. doi: 10.1093/sleep/zsz280. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Sneve, Markus Handal; Sederevicius, Donatas; Sørensen, Øystein; Krogsrud, Stine Kleppe & Mowinckel, Athanasia Monika [Vis alle 7 forfattere av denne artikkelen] (2019). Volumetric and microstructural regional changes of the hippocampus underlying development of recall performance after extended retention intervals. Developmental Cognitive Neuroscience. ISSN 1878-9293. 40:100723, s. 1–12. doi: 10.1016/j.dcn.2019.100723. Fulltekst i vitenarkiv
• Fjell, Anders Martin; Chen, Chi-Hua Chen; Sederevicius, Donatas; Sneve, Markus Handal; Grydeland, Håkon & Krogsrud, Stine Kleppe [Vis alle 17 forfattere av denne artikkelen] (2019). Continuity and discontinuity in human cortical development and change from embryonic stages to old age. Cerebral Cortex. ISSN 1047-3211. 29(9), s. 3879–3890. doi: 10.1093/cercor/bhy266. Fulltekst i vitenarkiv
• Vidal-Piñeiro, Didac; Sneve, Markus Handal; Nyberg, Lars; Mowinckel, Athanasia Monika; Sederevicius, Donatas & Walhovd, Kristine B [Vis alle 7 forfattere av denne artikkelen] (2019). Maintained Frontal Activity Underlies High Memory Function Over 8 Years in Aging. Cerebral Cortex. ISSN 1047-3211. 29(7), s. 3111–3123. doi: 10.1093/cercor/bhy177. Fulltekst i vitenarkiv
• Mowinckel, Athanasia Monika; Alnæs, Dag; Pedersen, Mads Lund; Ziegler, Sigurd; Fredriksen, Mats & Kaufmann, Tobias [Vis alle 10 forfattere av denne artikkelen] (2017). Increased default-mode variability is related to reduced task-performance and is evident in adults with ADHD. NeuroImage: Clinical. ISSN 2213-1582. 16, s. 369–382. doi: 10.1016/j.nicl.2017.03.008. Fulltekst i vitenarkiv
• Ziegler, Sigurd; Pedersen, Mads Lund; Mowinckel, Athanasia Monika & Biele, Guido (2016). Modelling ADHD: A review of ADHD theories through their predictions for computational models of decision-making and reinforcement learning. Neuroscience and Biobehavioral Reviews. ISSN 0149-7634. 71, s. 633–656. doi: 10.1016/j.neubiorev.2016.09.002.
• Mowinckel, Athanasia Monika; Pedersen, Mads Lund; Eilertsen, Espen Moen & Biele, Guido (2015). A Meta-Analysis of Decision-Making and Attention in Adults With ADHD. Journal of Attention Disorders. ISSN 1087-0547. 19(5), s. 355–367. doi: 10.1177/1087054714558872. Vis sammendrag

  Abstract Objective: Deficient reward processing has gained attention as an important aspect of ADHD, but little is known about reward-based decision-making (DM) in adults with ADHD. This article summarizes research on DM in adult ADHD and contextualizes DM deficits by comparing them to attention deficits. Method: Meta-analytic methods were used to calculate average effect sizes for different DM domains and continuous performance task (CPT) measures. Results: None of the 59 included studies (DM: 12 studies; CPT: 43; both: 4) had indications of publication bias. DM and CPT measures showed robust, small to medium effects. Large effect sizes were found for a drift diffusion model analysis of the CPT. Conclusion: The results support the existence of DM deficits in adults with ADHD, which are of similar magnitude as attention deficits. These findings warrant further examination of DM in adults with ADHD to improve the understanding of underlying neurocognitive mechanisms

• Mowinckel, Athanasia Monika; Espeseth, Thomas & Westlye, Lars Tjelta (2012). Network-specific effects of age and in-scanner subject motion: A resting-state fMRI study of 238 healthy adults. NeuroImage. ISSN 1053-8119. 63(3), s. 1364–1373. doi: 10.1016/j.neuroimage.2012.08.004. Vis sammendrag

  Cognitive aging is accompanied by a range of structural and functional differences in the brain, even in the absence of neurodegenerative disease. Functional magnetic resonance imaging (fMRI) studies have reported increased bilateral activation during task performance in elderly participants compared to their younger counterparts, particularly in frontal regions. Alterations have also been observed in the functional architecture of the resting brain, suggesting that aging is associated with changes in the organization of the networks of the brain. However, previous studies have largely focused on the default mode network, and little is known about the effects of age on other resting state-networks (RSNs). The aim of the present study was to investigate age-differences in resting state functional connectivity (RSFC) using fMRI data obtained during rest from 238 healthy participants aged 21–80 years. Using independent component analysis (ICA) and dual-regression, the results revealed age-related increases in RSFC across a range of RSNs, including task-positive networks in frontal and parietal regions. In contrast, age-related reductions in the default mode network and occipital visual networks were observed. Furthermore, whereas the effects of age on the various RSNs were found independent of age-related decreases in gray matter volume, sex and subject motion, we report strong positive and widespread effects of estimated subject motion on the RSFC across RSNs. The results provide support for the notion of network-specific effects in aging, manifested as increased tonic activation of task-positive networks, supporting higher-order cognitive functions and cognitive control, along with reduced task-negative default mode network and sensory visual networks during rest. The present results also corroborate recent evidence of strong influence of subject motion on estimated functional connectivity measures and strongly suggest that studies using RSFC measures as imaging phenotypes should adjust for individual differences in in-scanner subject motion.

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• Mowinckel, Athanasia Monika; Bodorkos Friedman, Barbara; Walhovd, Kristine B & Fjell, Anders Martin (2022). Global Brain Health Survey raw data .
• Roe, James Michael; Vidal-Piñeiro, Didac; Sørensen, Øystein; Brandmaier, Andreas M.; Düzel, Sandra & Gonzalez, Hector A. [Vis alle 78 forfattere av denne artikkelen] (2022). Author Correction: Asymmetric thinning of the cerebral cortex across the adult lifespan is accelerated in Alzheimer’s disease (Nature Communications, (2021), 12, 1, (721), 10.1038/s41467-021-21057-y). Nature Communications. ISSN 2041-1723. 13(1). doi: 10.1038/s41467-022-28514-2.
• Mowinckel, Athanasia Monika (2021). R and the tidyverse.
• Mowinckel, Athanasia Monika (2021). Make something random - learn something useful.
• Mowinckel, Athanasia Monika (2021). Zhoosh up your ggplots .
• Mowinckel, Athanasia Monika (2021). Advanced R use - package development in R .
• Mowinckel, Athanasia Monika (2021). A different type of database - talk about LCBC data base .
• Mowinckel, Athanasia Monika (2021). Talk on nettskjema R package.
• Mowinckel, Athanasia Monika (2021). Talk on the LCBC ggseg R-package.
• Mowinckel, Athanasia Monika (2020). Talk on gg-seg R package .
• Mowinckel, Athanasia Monika (2020). Talk on the LCBC ggseg R-package.
• Mowinckel, Athanasia Monika (2016). Re: Kronisk utmattelsessyndrom og erfaring med Lightning Process. Tidsskrift for Den norske legeforening. ISSN 0029-2001. 136(7).

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