More than microglia: myeloid cells and biomarkers in neurodegeneration von Kodosaki, Eleftheria, Bell, Rosie, Sogorb-Esteve, Aitana, Wiltshire, Katharine, Zetterberg, Henrik, Heslegrave, Amanda

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Elevated Cerebrospinal Fluid Ubiquitin Carboxyl-Terminal Hydrolase Isozyme L1 in Asymptomatic C9orf72 Hexanucleotide Repeat Expansion Carriers von Dellar, Elizabeth R, Vendrell, Iolanda, Amein, Benazir, Lester, David G, Edmond, Evan C, Yoganathan, Katie, Dharmadasa, Thanuja, Sogorb-Esteve, Aitana, Fischer, Roman, Talbot, Kevin, Rohrer, Jonathan D, Turner, Martin R, Thompson, Alexander G

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Levels of ADAM10 are reduced in Alzheimer's disease CSF von Sogorb-Esteve, Aitana, García-Ayllón, María-Salud, Gobom, Johan, Alom, Jordi, Zetterberg, Henrik, Blennow, Kaj, Sáez-Valero, Javier

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Differential chemokine alteration in the variants of primary progressive aphasia-a role for neuroinflammation von Sogorb-Esteve, Aitana, Swift, Imogen J, Woollacott, Ione O C, Warren, Jason D, Zetterberg, Henrik, Rohrer, Jonathan D

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Decreased circulating ErbB4 ectodomain fragments as a read-out of impaired signaling function in amyotrophic lateral sclerosis von Lopez-Font, Inmaculada, Sogorb-Esteve, Aitana, Javier-Torrent, Míriam, Brinkmalm, Gunnar, Herrando-Grabulosa, Mireia, García-Lareu, Belen, Turon-Sans, Janina, Rojas-García, Ricardo, Lleó, Alberto, Saura, Carlos A., Zetterberg, Henrik, Blennow, Kaj, Bosch, Assumpció, Navarro, Xavier, Sáez-Valero, Javier

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Neurofilament light oligomers in neurodegenerative diseases: quantification by homogeneous immunoassay in cerebrospinal fluid von Meda, Francisco J., Knowles, Kathryn, Swift, Imogen J., Sogorb-Esteve, Aitana, Rohrer, Jonathan D., Dittrich, Anna, Skoog, Ingmar, Kern, Silke, Becker, Bruno, Blennow, Kaj, Andreasson, Ulf, Kvartsberg, Hlin, Zetterberg, Henrik

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Fluid biomarkers in frontotemporal dementia: past, present and future von Swift, IJ, Sogorb-Esteve, A, Heller, C, Synofzik, M, Otto, M, Graff, C, Galimberti, D, Todd, E, Heslegrave, AJ, van der Ende, EL, Van Swieten, JC, Zetterberg, H, Rohrer, JD

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Differential patterns of lysosomal dysfunction are seen in the clinicopathological forms of primary progressive aphasia von Swift, Imogen J., Sjödin, Simon, Gobom, Johan, Brinkmalm, Ann, Blennow, Kaj, Zetterberg, Henrik, Rohrer, Jonathan D., Sogorb-Esteve, Aitana

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Optimising remote sampling of NfL and GFAP using blood cards in the Genetic Frontotemporal Dementia Initiative (GENFI) cohort von Goldsmith, Sophie E, Swift, Imogen J, Oh, Lara, Laban, Rhiannon, Zetterberg, Henrik, Esteve, Aitana Sogorb, Rohrer, Jonathan D.

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A systematic review of progranulin concentrations in biofluids in over 7,000 people: Assessing the pathogenicity of GRN mutations and other influencing factors von Swift, Imogen J., Esteve, Aitana Sogorb, Heller, Carolin, Zetterberg, Henrik, Rohrer, Jonathan D.

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Inhibition of γ-Secretase Leads to an Increase in Presenilin-1 von Sogorb-Esteve, Aitana, García-Ayllón, María-Salud, Llansola, Marta, Felipo, Vicente, Blennow, Kaj, Sáez-Valero, Javier

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Development of a targeted proteomic assay for the quantitation of neurofilament light in cerebrospinal fluid: Correlation with Simoa‐based quantitation across neurodegenerative dis... von Leckey, Claire A., Coulton, John, Barthélemy, Nicolas R., He, Yingxin, Laban, Rhiannon, Heslegrave, Amanda, Giovannucci, Tatiana A., Byrne, Lauren M, Swift, Imogen J, Esteve, Aitana Sogorb, Rohrer, Jonathan D., Schott, Jonathan M, Wild, Edward J, Zetterberg, Henrik, Wray, Selina, Mills, Kevin, Bateman, Randall J., Paterson, Ross W.

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P2‐244: NEUROFILAMENT LIGHT IN ISOPOTENTIAL STEM CELL‐DERIVED NEURONS WITH FAMILIAL AD MUTATIONS AS A MARKER OF NEURODEGENERATION von Esteve, Aitana Sogorb, Leckey, Claire Alexandra, Arber, Charles, Toombs, Jamie, Wray, Selina, Heslegrave, Amanda J., De Strooper, Bart, Zetterberg, Henrik

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NEUROFILAMENT LIGHT IN ISOPOTENTIAL STEM CELL-DERIVED NEURONS WITH FAMILIAL AD MUTATIONS AS A MARKER OF NEURODEGENERATION von Esteve, Aitana Sogorb, Leckey, Claire Alexandra, Arber, Charles, Toombs, Jamie, Wray, Selina, Heslegrave, Amanda J., De Strooper, Bart, Zetterberg, Henrik

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A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia von van der Ende, Emma L, Bron, Esther E, Poos, Jackie M, Jiskoot, Lize C, Panman, Jessica L, Papma, Janne M, Meeter, Lieke H, Dopper, Elise GP, Wilke, Carlo, Synofzik, Matthis, Heller, Carolin, Swift, Imogen J, Sogorb-Esteve, Aitana, Bouzigues, Arabella, Borroni, Barbara, Sanchez-Valle, Raquel, Moreno, Fermin, Graff, Caroline, Laforce, Robert, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Finger, Elizabeth, Vandenberghe, Rik, Rowe, James B, de Mendonça, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Christopher R, Gerhard, Alexander, Levin, Johannes, Danek, Adrian, Otto, Markus, Pijnenburg, Yolande AL, Sorbi, Sandro, Zetterberg, Henrik, Niessen, Wiro J, Rohrer, Jonathan D, Klein, Stefan, van Swieten, John C, Venkatraghavan, Vikram, Seelaar, Harro, GENFI consortium

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Developing a mass spectrometric assay to measure granulin peptides in CSF for progranulin‐associated frontotemporal dementia von Swift, Imogen J, Weiner, Sophia, Sauer, Mathias, Nilsson, Johanna, van Swieten, John C., Jiskoot, Lize C., Seelaar, Harro, Moreno, Fermin, Sánchez‐Valle, Raquel, Laforce, Robert, Graff, Caroline, Masellis, Mario, Tartaglia, Carmela, Rowe, James B., Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, de Mendonça, Alexandre, Butler, Christopher, Gerhard, Alexander, Ducharme, Simon, Ber, Isabelle Le, Tiraboschi, Pietro, Santana, Isabel, Pasquier, Florence, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Brinkmalm, Ann, Zetterberg, Henrik, Rohrer, Jonathan D., Esteve, Aitana Sogorb, Gobom, Johan

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A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia von van der Ende, Emma L, Bron, Esther E, Poos, Jackie M, Jiskoot, Lize C, Panman, Jessica L, Papma, Janne M, Meeter, Lieke H, Dopper, Elise G.P, Wilke, Carlo, Synofzik, Matthis, Heller, Carolin, Swift, Imogen J, Sogorb-Esteve, Aitana, Bouzigues, Arabella, Borroni, Barbara, Sanchez-Valle, Raquel, Moreno, Fermin, Graff, Caroline, Laforce, Robert, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Finger, Elizabeth, Vandenberghe, Rik, Rowe, James B, de Mendonca, Alexandre, Tagliavini, Fabrizio, Santana, Isabel, Ducharme, Simon, Butler, Christopher R, Gerhard, Alexander, Levin, Johannes, Danek, Adrian, Otto, Markus, Pijnenburg, Yolande A.L, Sorbi, Sandro, Zetterberg, Henrik, Niessen, Wiro J, Rohrer, Jonathan D, Klein, Stefan, van Swieten, John C, Venkatraghavan, Vikram, Seelaar, Harro

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Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis von Wilson, Katherine M, Katona, Eszter, Glaria, Idoia, Carcole, Mireia, Swift, Imogen J, Sogorb-Esteve, Aitana, Heller, Carolin, Bouzigues, Arabella, Heslegrave, Amanda J, Keshavan, Ashvini, Knowles, Kathryn, Patil, Saurabh, Mohapatra, Susovan, Liu, Yuanjing, Goyal, Jaya, Sanchez-Valle, Raquel, Laforce, Robert, Synofzik, Matthis, Rowe, James B, Finger, Elizabeth, Vandenberghe, Rik, Butler, Christopher R, Gerhard, Alexander, Van Swieten, John C, Seelaar, Harro, Borroni, Barbara, Galimberti, Daniela, de Mendonca, Alexandre, Masellis, Mario, Tartaglia, M. Carmela, Otto, Markus, Graff, Caroline, Ducharme, Simon, Schott, Jonathan M, Malaspina, Andrea, Zetterberg, Henrik, Boyanapalli, Ramakrishna, Rohrer, Jonathan D, Isaacs, Adrian M

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Development of a sensitive trial-ready poly(GP) CSF biomarker assay for C9orf72 -associated frontotemporal dementia and amyotrophic lateral sclerosis von Wilson, Katherine M, Katona, Eszter, Glaria, Idoia, Carcolé, Mireia, Swift, Imogen J, Sogorb-Esteve, Aitana, Heller, Carolin, Bouzigues, Arabella, Heslegrave, Amanda J, Keshavan, Ashvini, Knowles, Kathryn, Patil, Saurabh, Mohapatra, Susovan, Liu, Yuanjing, Goyal, Jaya, Sanchez-Valle, Raquel, Laforce, Robert Jr, Synofzik, Matthis, Rowe, James B, Finger, Elizabeth, Vandenberghe, Rik, Butler, Christopher R, Gerhard, Alexander, Van Swieten, John C, Seelaar, Harro, Borroni, Barbara, Galimberti, Daniela, de Mendonça, Alexandre, Masellis, Mario, Tartaglia, M Carmela, Otto, Markus, Graff, Caroline, Ducharme, Simon, Schott, Jonathan M, Malaspina, Andrea, Zetterberg, Henrik, Boyanapalli, Ramakrishna, Rohrer, Jonathan D, Isaacs, Adrian M, Genetic FTD Initiative (GENFI)

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Targeted proteomic search reveals new actors in the synaptic and lysosomal dysfunction in genetic FTD, a GENFI study von Weiner, Sophia, Malichova, Frederika, Simrén, Joel, Sauer, Mathias, Swift, Imogen J, Heller, Carolin, Knowles, Kathryn, van Swieten, John C., Jiskoot, Lize C., Seelaar, Harro, Moreno, Fermin, Sanchez‐Valle, Raquel, Laforce, Robert, Graff, Caroline, Masellis, Mario, Tartaglia, Carmela, Rowe, James B., Borroni, Barbara, Finger, Elizabeth, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, de Mendonça, Alexandre, Butler, Christopher, Gerhard, Alexander, Ducharme, Simon, Ber, Isabelle Le, Tiraboschi, Pietro, Santana, Isabel, Pasquier, Florence, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Blennow, Kaj, Zetterberg, Henrik, Rohrer, Jonathan D., Gobom, Johan, Esteve, Aitana Sogorb

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