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  1. No Access

    Article

    Refining the accuracy of validated target identification through coding variant fine-map** in type 2 diabetes

    We aggregated coding variant data for 81,412 type 2 diabetes cases and 370,832 controls of diverse ancestry, identifying 40 coding variant association signals (P < 2.2 × 10−7); of these, 16 map outside known risk...

    Anubha Mahajan, Jennifer Wessel, Sara M. Willems, Wei Zhao in Nature Genetics (2018)

  2. Article

    Open Access

    Efficient clearance of Aβ protofibrils in AβPP-transgenic mice treated with a brain-penetrating bifunctional antibody

    Amyloid-β (Aβ) immunotherapy is one of the most promising disease-modifying strategies for Alzheimer’s disease (AD). Despite recent progress targeting aggregated forms of Aβ, low antibody brain penetrance rema...

    Stina Syvänen, Greta Hultqvist, Tobias Gustavsson in Alzheimer's Research & Therapy (2018)

  3. Article

    Open Access

    Alzheimer’s disease pathology propagation by exosomes containing toxic amyloid-beta oligomers

    The gradual deterioration of cognitive functions in Alzheimer’s disease is paralleled by a hierarchical progression of amyloid-beta and tau brain pathology. Recent findings indicate that toxic oligomers of amy...

    Maitrayee Sardar Sinha, Anna Ansell-Schultz, Livia Civitelli in Acta Neuropathologica (2018)

  4. No Access

    Article

    Fine-map** type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

    We expanded GWAS discovery for type 2 diabetes (T2D) by combining data from 898,130 European-descent individuals (9% cases), after imputation to high-density reference panels. With these data, we (i) extend th...

    Anubha Mahajan, Daniel Taliun, Matthias Thurner, Neil R. Robertson in Nature Genetics (2018)

  5. Article

    Open Access

    Secretion and Uptake of α-Synuclein Via Extracellular Vesicles in Cultured Cells

    In Parkinson’s disease and other Lewy body disorders, the propagation of pathology has been accredited to the spreading of extracellular α-synuclein (α-syn). Although the pathogenic mechanisms are not fully un...

    Gabriel Gustafsson, Camilla Lööv, Emma Persson in Cellular and Molecular Neurobiology (2018)

  6. No Access

    Article

    Mosaic loss of chromosome Y in leukocytes matters

    Lars A. Forsberg, Jonatan Halvardson, Edyta Rychlicka-Buniowska in Nature Genetics (2019)

  7. Article

    Open Access

    Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

    Rare coding variants in TREM2, PLCG2, and ABI3 were recently associated with the susceptibility to Alzheimer’s disease (AD) in Caucasians. Frequencies and AD-associated effects of variants differ across ethniciti...

    Maria Carolina Dalmasso, Luis Ignacio Brusco, Natividad Olivar in Translational Psychiatry (2019)

  8. No Access

    Article

    Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    Risk for late-onset Alzheimer’s disease (LOAD), the most prevalent dementia, is partially driven by genetics. To identify LOAD risk loci, we performed a large genome-wide association meta-analysis of clinicall...

    Brian W. Kunkle, Benjamin Grenier-Boley, Rebecca Sims, Joshua C. Bis in Nature Genetics (2019)

  9. Article

    Open Access

    Binding of α-synuclein oligomers to Cx32 facilitates protein uptake and transfer in neurons and oligodendrocytes

    The intercellular transfer of alpha-synuclein (α-syn) has been implicated in the progression of Parkinson’s disease (PD) and multiple system atrophy (MSA). The cellular mechanisms underlying this process are n...

    Juan F. Reyes, Christopher Sackmann, Alana Hoffmann in Acta Neuropathologica (2019)

  10. Article

    Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    Brian W. Kunkle, Benjamin Grenier-Boley, Rebecca Sims, Joshua C. Bis in Nature Genetics (2019)

  11. Article

    Open Access

    High levels of AAV vector integration into CRISPR-induced DNA breaks

    Adeno-associated virus (AAV) vectors have shown promising results in preclinical models, but the genomic consequences of transduction with AAV vectors encoding CRISPR-Cas nucleases is still being examined. In ...

    Killian S. Hanlon, Benjamin P. Kleinstiver, Sara P. Garcia in Nature Communications (2019)

  12. No Access

    Article

    Genetic predisposition to mosaic Y chromosome loss in blood

    Mosaic loss of chromosome Y (LOY) in circulating white blood cells is the most common form of clonal mosaicism15, yet our knowledge of the causes and consequences of this is limited. Here, using a computational ...

    Deborah J. Thompson, Giulio Genovese, Jonatan Halvardson, Jacob C. Ulirsch in Nature (2019)

  13. No Access

    Article

    α-Synuclein strains target distinct brain regions and cell types

    The clinical and pathological differences between synucleinopathies such as Parkinson’s disease and multiple system atrophy have been postulated to stem from unique strains of α-synuclein aggregates, akin to w...

    Angus Lau, Raphaella W. L. So, Heather H. C. Lau, Jason C. Sang in Nature Neuroscience (2020)

  14. Article

    Open Access

    Altered levels of CSF proteins in patients with FTD, presymptomatic mutation carriers and non-carriers

    The clinical presentations of frontotemporal dementia (FTD) are diverse and overlap with other neurological disorders. There are, as of today, no biomarkers in clinical practice for diagnosing the disorders. H...

    Julia Remnestål, Linn Öijerstedt, Abbe Ullgren in Translational Neurodegeneration (2020)

  15. Article

    Open Access

    Dual-task tests discriminate between dementia, mild cognitive impairment, subjective cognitive impairment, and healthy controls – a cross-sectional cohort study

    Discrimination between early-stage dementia and other cognitive impairment diagnoses is central to enable appropriate interventions. Previous studies indicate that dual-task testing may be useful in such diffe...

    Hanna B. Åhman, Ylva Cedervall, Lena Kilander, Vilmantas Giedraitis in BMC Geriatrics (2020)

  16. Article

    Open Access

    Self-reported difficulty initiating sleep and early morning awakenings are associated with nocturnal diastolic non-dip** in older white Swedish men

    Chronically blunted nocturnal blood pressure (BP) dip** has been shown to increase the future risk of cardiovascular diseases. In the present cross-sectional study, we investigated whether self-reported inso...

    **ao Tan, Lars Lind, Martin Ingelsson, Johan Sundström in Scientific Reports (2020)

  17. Article

    Open Access

    Extracellular vesicles from amyloid-β exposed cell cultures induce severe dysfunction in cortical neurons

    Alzheimer’s disease (AD) is characterized by a substantial loss of neurons and synapses throughout the brain. The exact mechanism behind the neurodegeneration is still unclear, but recent data suggests that sp...

    Chiara Beretta, Elisabeth Nikitidou, Linn Streubel-Gallasch in Scientific Reports (2020)

  18. Article

    Open Access

    Accumulation of alpha-synuclein within the liver, potential role in the clearance of brain pathology associated with Parkinson’s disease

    Alpha-synuclein (α-syn) aggregation is the hallmark pathological lesion in brains of patients with Parkinson’s disease (PD) and related neurological disorders characterized as synucleinopathies. Accumulating e...

    Juan F. Reyes, Sara Ekmark-Léwen, Marina Perdiki in Acta Neuropathologica Communications (2021)

  19. Article

    Open Access

    Immune cells lacking Y chromosome show dysregulation of autosomal gene expression

    Epidemiological investigations show that mosaic loss of chromosome Y (LOY) in leukocytes is associated with earlier mortality and morbidity from many diseases in men. LOY is the most common acquired mutation a...

    Jan P. Dumanski, Jonatan Halvardson, Hanna Davies in Cellular and Molecular Life Sciences (2021)

  20. Article

    Open Access

    Crosstalk between astrocytes and microglia results in increased degradation of α-synuclein and amyloid-β aggregates

    Alzheimer’s disease (AD) and Parkinson’s disease (PD) are characterized by brain accumulation of aggregated amyloid-beta (Aβ) and alpha-synuclein (αSYN), respectively. In order to develop effective therapies, ...

    **ar Rostami, Tobias Mothes, Mahshad Kolahdouzan in Journal of Neuroinflammation (2021)

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