Errata

• Jelenčić, Vedrana; Šestan, Marko; Kavazović, Inga et al. (2024). Correction to: NK cell receptor NKG2D sets activation threshold for the NCR1 receptor early in NK cell development (Nature Immunology, (2018), 19, 10, (1083-1092), 10.1038/s41590-018-0209-9). (ekstern lenke)
• Theorell, Jakob; Bileviciute-Ljungar, Indre; Tesi, Bianca et al. (2019). Corrigendum: Unperturbed cytotoxic lymphocyte phenotype and function in myalgic encephalomyelitis/chronic fatigue syndrome patients. (ekstern lenke)

Vitenskapelig artikkel

• Bastard, Paul; Gervais, Adrian; Taniguchi, Maki et al. (2024). Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children. (ekstern lenke)
• Dick, Jenna K.; Sangala, Jules A.; Krishna, Venkatramana D. et al. (2024). NK Cell and Monocyte Dysfunction in Multisystem Inflammatory Syndrome in Children. (ekstern lenke)
• Chiang, Samuel C. C.; Covill, Laura E.; Tesi, Bianca et al. (2024). Efficacy of T-cell assays for the diagnosis of primary defects in cytotoxic lymphocyte exocytosis. (ekstern lenke)
• Covill, L.E.; Sendel, A.; Campbell, T.M. et al. (2024). Evaluation of Genetic or Cellular Impairments in Type I IFN Immunity in a Cohort of Young Adults with Critical COVID-19. (ekstern lenke)
• Kögl, Tamara; Chang, Hsin-Fang; Staniek, Julian et al. (2024). Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect. (ekstern lenke)
• Rebuffet, Lucas; Melsen, Janine E; Escaliere, Bertrand et al. (2024). High-dimensional single-cell analysis of human natural killer cell heterogeneity. (ekstern lenke)
• Bastard, Paul; Vazquez, Sara E.; Liu, Jamin et al. (2023). Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs. (ekstern lenke)
• Carlsten, Mattias; Bryceson, Yenan (2023). Rough operators: sphingomyelinase inhibitors spike NK cells to kill cancer. (ekstern lenke)
• Gahr, Stine; Casoni, Giovanna Perinetti; Falk-Paulsen, Maren et al. (2023). Viral host range factors antagonize pathogenic SAMD9 and SAMD9L variants. (ekstern lenke)
• Zitti, Beatrice; Hoffer, Elena; Zheng, Wenning et al. (2023). Human skin-resident CD8⁺ T cells require RUNX2 and RUNX3 for induction of cytotoxicity and expression of the integrin CD49a. (ekstern lenke)
• Schmied, Laurent; Luu, Thuy T.; Søndergaard, Jonas N. et al. (2023). SHP-1 localization to the activating immune synapse promotes NK cell tolerance in MHC class I deficiency. (ekstern lenke)
• Helm, Eric Y.; Zelenka, Tomas; Cismasiu, Valeriu B. et al. (2023). Bcl11b sustains multipotency and restricts effector programs of intestinal-resident memory CD8⁺ T cells. (ekstern lenke)
• Campbell, Tessa Mollie; Liu, Zhiyong; Zhang, Qian et al. (2022). Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency. (ekstern lenke)
• Zondag, Timo C. E.; Torralba-Raga, Lamberto; Van Laar, Jan A. M. et al. (2022). Novel RAB27A Variant Associated with Late-Onset Hemophagocytic Lymphohistiocytosis Alters Effector Protein Binding. (ekstern lenke)
• Groß, Miriam; Speckmann, Carsten; May, Annette et al. (2022). Rubella vaccine–induced granulomas are a novel phenotype with incomplete penetrance of genetic defects in cytotoxicity. (ekstern lenke)
• Asano, Takaki; Boisson, Bertrand; Onodi, Fanny et al. (2021). X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. (ekstern lenke)
• Paucar, Martin; Tesi, Bianca; Eshtad, Saeed et al. (2021). Adult-Onset Ataxia with Neuropathy and White Matter Abnormalities Due to a Novel SAMD9L Variant. (ekstern lenke)
• Kalinichenko, Artem; Perinetti Casoni, Giovanna; Dupré, Loïc et al. (2021). RhoG deficiency abrogates cytotoxicity of human lymphocytes and causes hemophagocytic lymphohistiocytosis. (ekstern lenke)
• Holmes, Timothy Dunstan; Pandey, Ram Vinay; Helm, Eric Y. et al. (2021). The transcription factor Bcl11b promotes both canonical and adaptive NK cell differentiation. (ekstern lenke)
• Hetemäki, Iivo; Kaustio, Meri; Kinnunen, Matias et al. (2021). Loss-of-function mutation in IKZF2 leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cells. (ekstern lenke)
• Woan, Karrune V.; Kim, Hansol; Bjordahl, Ryan et al. (2021). Harnessing features of adaptive NK cells to generate iPSC-derived NK cells for enhanced immunotherapy. (ekstern lenke)
• Parga-Vidal, Loreto; Behr, Felix M.; Kragten, Natasja A.M. et al. (2021). Hobit identifies tissue-resident memory t cell precursors that are regulated by eomes. (ekstern lenke)
• Galgano, Donatella; Soheili, Tayebeh; Voss, Matthias et al. (2020). Alternative UNC13D Promoter Encodes a Functional Munc13-4 Isoform Predominantly Expressed in Lymphocytes and Platelets. (ekstern lenke)
• Kavazović, Inga; Han, Hongya; Balzaretti, Giulia et al. (2020). Eomes broadens the scope of CD8 T-cell memory by inhibiting apoptosis in cells of low affinity. (ekstern lenke)
• Torralba-Raga, Lamberto; Tesi, Bianca; Chiang, Samuel C.C. et al. (2020). Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease. (ekstern lenke)
• Solberg, Silje Michelsen; Aarebrot, Anders K.; Sarkar, Irene et al. (2020). Mass cytometry analysis of blood immune cells from psoriasis patients on biological therapy. (ekstern lenke)
• Keskitalo, Salla; Haapaniemi, Emma M.; Glumoff, Virpi et al. (2019). Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease. (ekstern lenke)
• Theorell, Axel; Bryceson, Yenan; Theorell, Jakob (2019). Determination of essential phenotypic elements of clusters in high-dimensional entities—DEPECHE. (ekstern lenke)
• Jun, Eunsung; Song, Ah Young; Choi, Ji-Wan et al. (2019). Progressive impairment of NK cell cytotoxic degranulation is associated with TGF-β1 deregulation and disease progression in pancreatic cancer. (ekstern lenke)
• Lam, Michael T.; Coppola, Simona; Krumbach, Oliver H.F. et al. (2019). A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function. (ekstern lenke)
• Wu, Chuanfeng; Espinoza, Diego A; Koelle, Samson J et al. (2018). Clonal expansion and compartmentalized maintenance of rhesus macaque NK cell subsets. (ekstern lenke)
• Aarebrot, Anders Krogh; Solberg, Silje Michelsen; Davies, Richard Allan et al. (2018). Phosphorylation of intracellular signaling molecules in peripheral blood cells from psoriasis patients on originator or biosimilar infliximab. (ekstern lenke)
• Hagberg, Niklas; Joelsson, Martin; Leonard, Dag et al. (2018). The STAT4 SLE risk allele rs7574865[T] is associated with increased IL-12-induced IFN-γ production in t cells from patients with SLE. (ekstern lenke)
• Chiang, Samuel C.C.; Vergamini, Sue M; Husami, Ammar et al. (2018). Screening for Wiskott-Aldrich syndrome by flow cytometry. (ekstern lenke)
• Solberg, Silje Michelsen; Sandvik, Lene Frøyen; Eidsheim, Marianne et al. (2018). Serum cytokine measurements and biological therapy of psoriasis - Prospects for personalized treatment?. (ekstern lenke)
• Tesi, Bianca; Rascon, Jelena; Chiang, Samuel C.C. et al. (2018). A RAB27A 5' untranslated region structural variant associated with late-onset hemophagocytic lymphohistiocytosis and normal pigmentation. (ekstern lenke)
• Cichocki, Frank; Wu, Cheng-Ying; Zhang, Bin et al. (2018). ARID5B regulates metabolic programming in human adaptive NK cells. (ekstern lenke)
• Jelencic, Vedrana; Sestan, Marko; Kavazovic, Inga et al. (2018). NK cell receptor NKG2D sets activation threshold for the NCR1 receptor early in NK cell development. (ekstern lenke)
• Ilander, Mette; Olsson-Strömberg, Ulla; Schlums, Heinrich et al. (2017). Increased proportion of mature NK cells is associated with successful imatinib discontinuation in chronic myeloid leukemia. (ekstern lenke)
• Theorell, Jakob; Bileviciute-Ljungar, Indre; Tesi, Bianca et al. (2017). Unperturbed cytotoxic lymphocyte phenotype and function in myalgic encephalomyelitis/chronic fatigue syndrome patients. (ekstern lenke)
• Voss, Matthias; Bryceson, Yenan (2017). Natural killer cell biology illuminated by primary immunodeficiency syndromes in humans. (ekstern lenke)
• Davies, Richard Allan; Hammenfors, Daniel; Bergum, Brith et al. (2017). Patients with primary Sjögren's syndrome have alterations in absolute quantities of specific peripheral leucocyte populations. (ekstern lenke)
• Marcais, Antoine; Marotel, Marie; Degouve, Sophie et al. (2017). High mTOR activity is a hallmark of reactive natural killer cells and amplifies early signaling through activating receptors. (ekstern lenke)
• Chiang, Samuel C.C.; Wood, Stephanie M.; Tesi, Bianca et al. (2017). Differences in granule morphology yet equally impaired exocytosis among cytotoxic T cells and NK cells from Chediak-Higashi syndrome patients. (ekstern lenke)
• Tesi, Bianca; Davidsson, Josef; Voss, Matthias et al. (2017). Gain-of-function SAMD9L mutations cause a syndrome of cytopenia, immunodeficiency, MDS, and neurological symptoms. (ekstern lenke)
• Corat, Marcus A F; Schlums, Heinrich; Wu, Chuanfeng et al. (2017). Acquired somatic mutations in PNH reveal long-term maintenance of adaptive NK cells independent of HSPCs. (ekstern lenke)
• Cheuk, Stanley; Schlums, Heinrich; Gallais Serezal, Irene et al. (2017). CD49a Expression Defines Tissue-Resident CD8+ T Cells Poised for Cytotoxic Function in Human Skin. (ekstern lenke)
• Schlums, Heinrich; Jung, Moonjung; Han, Hongya et al. (2017). Adaptive NK cells can persist in patients with GATA2 mutation depleted of stem and progenitor cells. (ekstern lenke)
• Sand, Kristoffer; Theorell, Jakob; Bruserud, Øystein et al. (2016). Reduced potency of cytotoxic T lymphocytes from patients with high-risk myelodysplastic syndromes. (ekstern lenke)
• Cichocki, Frank; Verneris, Michael R.; Cooley, Sarah et al. (2016). The past, present, and future of NK cells in hematopoietic cell transplantation and adoptive transfer. (ekstern lenke)
• Cichocki, Frank; Cooley, Sarah; Davis, Zachary et al. (2016). CD56dim CD57+ NKG2C+ NK cell expansion is associated with reduced leukemia relapse after reduced intensity HCT. (ekstern lenke)
• Cichocki, Frank; Schlums, Heinrich; Theorell, Jakob et al. (2016). Diversification and functional specialization of human NK cell subsets. (ekstern lenke)
• Tesi, Bianca; Lagerstedt-Robinson, Kristina; Chiang, Samuel C.C. et al. (2015). Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis. (ekstern lenke)
• Meeths, Marie; Horne, Annacarin; Sabel, Magnus et al. (2015). Incidence and clinical presentation of primary hemophagocytic lymphohistiocytosis in Sweden. (ekstern lenke)
• Schlums, Heinrich; Cichocki, Frank; Tesi, Bianca et al. (2015). Cytomegalovirus infection drives adaptive epigenetic diversification of NK cells with altered signaling and effector function. (ekstern lenke)
• Hagberg, Niklas; Theorell, Jakob; Hjorton, Karin et al. (2015). Functional anti-CD94/NKG2A and anti-CD94/NKG2C autoantibodies in patients with systemic lupus erythematosus. (ekstern lenke)
• Theorell, Jakob; Gustavsson, Anna-Lena; Tesi, Bianca et al. (2014). Immunomodulatory activity of commonly used drugs on Fc-receptor-mediated human natural killer cell activation. (ekstern lenke)
• Cichocki, Frank; Schlums, Heinrich; Li, Hongchuan et al. (2014). Transcriptional regulation of Munc13-4 expression in cytotoxic lymphocytes is disrupted by an intronic mutation associated with a primary immunodeficiency. (ekstern lenke)
• Chiang, Samuel C.C.; Theorell, Jakob; Entesarian, Miriam et al. (2013). Comparison of primary human cytotoxic T-cell and natural killer cell responses reveal similar molecular requirements for lytic granule exocytosis but differences in cytokine production. (ekstern lenke)
• Machaczka, Maciej; Klimkowska, Monika; Chiang, Samuel C.C. et al. (2013). Development of classical Hodgkin's lymphoma in an adult with biallelic STXBP2 mutations. (ekstern lenke)
• Cohnen, André; Chiang, Samuel C.C.; Stojanovic, Ana et al. (2013). Surface CD107a/LAMP-1 protects natural killer cells from degranulation-associated damage. (ekstern lenke)

Vitenskapelig oversiktsartikkel/review

• Sekine, Takuya; Galgano, Donatella; Casoni, Giovanna Perinetti et al. (2024). CD8⁺ T Cell Biology in Cytokine Storm Syndromes. (ekstern lenke)
• Lindahl, Hannes; Bryceson, Yenan (2022). Neuroinflammation Associated With Inborn Errors of Immunity. (ekstern lenke)
• Zhang, Qian; Bastard, Paul; Karbuz, Adem et al. (2022). Human genetic and immunological determinants of critical COVID-19 pneumonia. (ekstern lenke)
• Smith, Carl Inge Edvard; Zain, Rula; Österborg, Anders et al. (2022). Do reduced numbers of plasmacytoid dendritic cells contribute to the aggressive clinical course of COVID-19 in chronic lymphocytic leukaemia?. (ekstern lenke)
• Meeths, Marie; Bryceson, Yenan (2021). Genetics and pathophysiology of haemophagocytic lymphohistiocytosis. (ekstern lenke)
• Tesi, Bianca; Bryceson, Yenan (2018). HLH: Genomics illuminates pathophysiological diversity. (ekstern lenke)
• Zitti, Beatrice; Bryceson, Yenan (2018). Natural killer cells in inflammation and autoimmunity. (ekstern lenke)
• Malmberg, Karl-Johan; Carlsten, Mattias; Björklund, Andreas et al. (2017). Natural killer cell-mediated immunosurveillance of human cancer. (ekstern lenke)
• Tesi, Bianca; Schlums, Heinrich; Cichocki, Frank et al. (2016). Epigenetic Regulation of Adaptive NK Cell Diversification. (ekstern lenke)
• Holmes, Timothy; Bryceson, Yenan (2016). Natural killer cell memory in context. (ekstern lenke)
• Cichocki, Frank; Sitnicka, Ewa; Bryceson, Yenan (2014). NK cell development and function - Plasticity and redundancy unleashed. (ekstern lenke)
• Meeths, Marie; Chiang, Samuel C.C.; Löfstedt, Alexandra et al. (2014). Pathophysiology and spectrum of diseases caused by defects in lymphocyte cytotoxicity. (ekstern lenke)

Brev til redaktøren

• Brodin, Petter; Casari, Giorgio; Townsend, Liam et al. (2022). Studying severe long COVID to understand post-infectious disorders beyond COVID-19. (ekstern lenke)
• Lemarquis, Andri; Campbell, Tessa; Aranda-Guillén, Maribel et al. (2021). Severe COVID-19 in an APS1 patient with interferon autoantibodies treated with plasmapheresis. (ekstern lenke)
• Järviaho, Tekla; Zachariadis, Vasilios; Tesi, Bianca et al. (2019). Microdeletion of 7p12.1p13, including IKZF1, causes intellectual impairment, overgrowth, and susceptibility to leukaemia. (ekstern lenke)
• Tesi, Bianca; Sieni, Elena; Neves, Conceicao et al. (2015). Hemophagocytic lymphohistiocytosis in 2 patients with underlying IFN-γ receptor deficiency. (ekstern lenke)
• Borte, Stephan; Meeths, Marie; Liebscher, Inés et al. (2014). Combined newborn screening for familial hemophagocytic lymphohistiocytosis and severe T- and B-cell immunodeficiencies. (ekstern lenke)

Leder

• Manna, Paul T.; Chiang, Samuel C.C.; Bryceson, Yenan et al. (2021). Editorial: Membrane Trafficking in Immunology - How Membrane Transport and Exocytosis Defects Underlie Immunodeficiencies. (ekstern lenke)
• Sitnicka, Ewa; Bryceson, Yenan; Freud, Aharon G. et al. (2020). Editorial: Molecular and Cellular Pathways in NK Cell Development. (ekstern lenke)

Doktorgradsavhandling

• Solberg, Silje Michelsen; Appel, Silke; Bryceson, Yenan et al. (2019). Systemic inflammation in psoriasis: Circulating immune cells and cytokines. (ekstern lenke)

Leserinnlegg

• Entesarian, Miriam; Chiang, Samuel CC; Sclums, Heinrich et al. (2013). Novel deep intronic and missense UNC13D mutations in familial haemophagocytic lymphohistiocytosis type 3. (ekstern lenke)

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