Increased central microglial activation associated with peripheral cytokine levels in premanifest Huntington's disease gene carriers
Politis, Marios, Lahiri, Nayana, Niccolini, Flavia, Su, Paul, Wu, Kit, Giannetti, Paolo, Scahill, Rachael I, Turkheimer, Federico E, Tabrizi, Sarah J, Piccini, Paola
Published in Neurobiology of disease (01.11.2015)
Published in Neurobiology of disease (01.11.2015)
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Journal Article
Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study
Forde, Claire, Burkitt-Wright, Emma, Turnpenny, Peter D, Haan, Eric, Ealing, John, Mansour, Sahar, Holder, Muriel, Lahiri, Nayana, Dixit, Abhijit, Procter, Annie, Pacot, Laurence, Vidaud, Dominique, Capri, Yline, Gerard, Marion, Dollfus, Hélène, Schaefer, Elise, Quelin, Chloé, Sigaudy, Sabine, Busa, Tiffany, Vera, Gabriella, Damaj, Lena, Messiaen, Ludwine, Stevenson, David A, Davies, Peter, Palmer-Smith, Sheila, Callaway, Alison, Wolkenstein, Pierre, Pasmant, Eric, Upadhyaya, Meena
Published in European journal of human genetics : EJHG (01.03.2022)
Published in European journal of human genetics : EJHG (01.03.2022)
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Journal Article
A novel pathogenic pathway of immune activation detectable before clinical onset in Huntington's disease
Björkqvist, Maria, Wild, Edward J, Thiele, Jenny, Silvestroni, Aurelio, Andre, Ralph, Lahiri, Nayana, Raibon, Elsa, Lee, Richard V, Benn, Caroline L, Soulet, Denis, Magnusson, Anna, Woodman, Ben, Landles, Christian, Pouladi, Mahmoud A, Hayden, Michael R, Khalili-Shirazi, Azadeh, Lowdell, Mark W, Brundin, Patrik, Bates, Gillian P, Leavitt, Blair R, Möller, Thomas, Tabrizi, Sarah J
Published in The Journal of experimental medicine (04.08.2008)
Published in The Journal of experimental medicine (04.08.2008)
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Journal Article
Brain-derived neurotrophic factor in patients with Huntington's disease
Zuccato, Chiara, Marullo, Manuela, Vitali, Barbara, Tarditi, Alessia, Mariotti, Caterina, Valenza, Marta, Lahiri, Nayana, Wild, Edward J, Sassone, Jenny, Ciammola, Andrea, Bachoud-Lèvi, Anne Catherine, Tabrizi, Sarah J, Di Donato, Stefano, Cattaneo, Elena
Published in PloS one (12.08.2011)
Published in PloS one (12.08.2011)
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Journal Article
The phenotype of Sotos syndrome in adulthood: A review of 44 individuals
Foster, Alison, Zachariou, Anna, Loveday, Chey, Ashraf, Tazeen, Blair, Edward, Clayton‐Smith, Jill, Dorkins, Huw, Fryer, Alan, Gener, Blanca, Goudie, David, Henderson, Alex, Irving, Melita, Joss, Shelagh, Keeley, Vaughan, Lahiri, Nayana, Lynch, Sally Ann, Mansour, Sahar, McCann, Emma, Morton, Jenny, Motton, Nicole, Murray, Alexandra, Riches, Katie, Shears, Deborah, Stark, Zornitza, Thompson, Elizabeth, Vogt, Julie, Wright, Michael, Cole, Trevor, Tatton‐Brown, Katrina
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2019)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2019)
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Journal Article
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome
Pagnamenta, Alistair T., Kaisaki, Pamela J., Bennett, Fenella, Burkitt‐Wright, Emma, Martin, Hilary C., Ferla, Matteo P., Taylor, John M., Gompertz, Lianne, Lahiri, Nayana, Tatton‐Brown, Katrina, Newbury‐Ecob, Ruth, Henderson, Alex, Joss, Shelagh, Weber, Astrid, Carmichael, Jenny, Turnpenny, Peter D., McKee, Shane, Forzano, Francesca, Ashraf, Tazeen, Bradbury, Kimberley, Shears, Deborah, Kini, Usha, de Burca, Anna, Blair, Edward, Taylor, Jenny C., Stewart, Helen
Published in Clinical genetics (01.06.2019)
Published in Clinical genetics (01.06.2019)
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Journal Article
Duplication of 10q24 locus: broadening the clinical and radiological spectrum
Holder-Espinasse, Muriel, Jamsheer, Aleksander, Escande, Fabienne, Andrieux, Joris, Petit, Florence, Sowinska-Seidler, Anna, Socha, Magdalena, Jakubiuk-Tomaszuk, Anna, Gerard, Marion, Mathieu-Dramard, Michèle, Cormier-Daire, Valérie, Verloes, Alain, Toutain, Annick, Plessis, Ghislaine, Jonveaux, Philippe, Baumann, Clarisse, David, Albert, Farra, Chantal, Colin, Estelle, Jacquemont, Sébastien, Rossi, Annick, Mansour, Sahar, Ghali, Neeti, Moncla, Anne, Lahiri, Nayana, Hurst, Jane, Pollina, Elena, Patch, Christine, Ahn, Joo Wook, Valat, Anne-Sylvie, Mezel, Aurélie, Bourgeot, Philippe, Zhang, David, Manouvrier-Hanu, Sylvie
Published in European journal of human genetics : EJHG (01.04.2019)
Published in European journal of human genetics : EJHG (01.04.2019)
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Journal Article
Corrigendum to “Increased central microglial activation associated with peripheral cytokine levels in premanifest Huntington's disease gene carriers” [Neurobiol. Dis. 83 (2015) 115–121]
Politis, Marios, Lahiri, Nayana, Niccolini, Flavia, Su, Paul, Wu, Kit, Giannetti, Paolo, Scahill, Rachael I, Turkheimer, Federico E, Tabrizi, Sarah J, Piccini, Paola
Published in Neurobiology of disease (01.02.2017)
Published in Neurobiology of disease (01.02.2017)
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Journal Article
Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes
Perrino, Peter A., Talbot, Lidiya, Kirkland, Rose, Hill, Amanda, Rendall, Amanda R., Mountford, Hayley S., Taylor, Jenny, Buscarello, Alexzandrea N., Lahiri, Nayana, Saggar, Anand, Fitch, R. Holly, Newbury, Dianne F.
Published in Communications biology (20.04.2020)
Published in Communications biology (20.04.2020)
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Journal Article
Abnormal peripheral chemokine profile in Huntington's disease
Wild, Edward, Magnusson, Anna, Lahiri, Nayana, Krus, Ulrika, Orth, Michael, Tabrizi, Sarah J, Björkqvist, Maria
Published in PLoS currents (13.04.2011)
Published in PLoS currents (13.04.2011)
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Journal Article
Genetic risk for Huntington Disease and reproductive decision‐making: A systematic review
Fahy, Neil, Rice, Charlotte, Lahiri, Nayana, Desai, Roopal, Stott, Joshua
Published in Clinical genetics (01.08.2023)
Published in Clinical genetics (01.08.2023)
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Journal Article
H13 Co-production of a proposed new Huntington’s disease service model for patients in surrey heartlands health and care partnership
Lahiri, Nayana, Walters, Ben, Kane, Wendy, Sands, Ruth, Coebergh, Jan, Carpenter, Peter, Williams, Jane
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
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Journal Article
The prognostic value of a normal Tc-99m sestamibi SPECT study in suspected coronary artery disease
Soman, Prem, Parsons, Ann, Lahiri, Nayana, Lahiri, Avijit
Published in Journal of nuclear cardiology (01.05.1999)
Published in Journal of nuclear cardiology (01.05.1999)
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Journal Article
Stability of white matter changes related to Huntington's disease in the presence of imaging noise: a DTI study
Müller, Hans-Peter, Glauche, Volkmar, Novak, Marianne J U, Nguyen-Thanh, Thao, Unrath, Alexander, Lahiri, Nayana, Read, Joy, Say, Miranda Julia, Tabrizi, Sarah J, Kassubek, Jan, Kloppel, Stefan
Published in PLoS currents (07.06.2011)
Published in PLoS currents (07.06.2011)
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Journal Article
Developing a consensus protocol for genetic testing in frontotemporal dementia
Greaves, Caroline V, Lahiri, Nayana, Rohrer, Jonathan D
Published in Alzheimer's & dementia (01.12.2021)
Published in Alzheimer's & dementia (01.12.2021)
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Journal Article
HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulation
TRÄGER, Ulrike, ANDRE, Ralph, MOSER, Roger, HUMMERICH, Holger, ANTONIOU, Michael, BATES, Gillian P, LUTHI-CARTER, Ruth, LOWDELL, Mark W, BJÖRKQVIST, Maria, OSTROFF, Gary R, ARONIN, Neil, TABRIZI, Sarah J, LAHIRI, Nayana, MAGNUSSON-LIND, Anna, WEISS, Andreas, GRUENINGER, Stephan, MCKINNON, Chris, SIRINATHSINGHJI, Eva, KAHLON, Shira, PFISTER, Edith L
Published in Brain (London, England : 1878) (01.03.2014)
Published in Brain (London, England : 1878) (01.03.2014)
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Journal Article
C12 HTT repeat instability in family trios in the 100,000 genomes project
Hensman Moss, Davina, Dalmia, Anupriya, Galassi Deforie, Valentina, Ibanez, Kristina, Tabrizi, Sarah J, Lahiri, Nayana, Houlden, Henry, Holmans, Peter, Jones, Lesley, Tucci, Arianna
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
Published in Journal of neurology, neurosurgery and psychiatry (12.09.2022)
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Journal Article
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disability
Jadhav, Bharati, Garg, Paras, van Vugt, Joke J. F. A., Ibanez, Kristina, Gagliardi, Delia, Lee, William, Shadrina, Mariya, Mokveld, Tom, Dolzhenko, Egor, Martin-Trujillo, Alejandro, Gies, Scott J., Altman, Gabrielle, Rocca, Clarissa, Barbosa, Mafalda, Jain, Miten, Lahiri, Nayana, Lachlan, Katherine, Houlden, Henry, Paten, Benedict, Veldink, Jan, Tucci, Arianna, Sharp, Andrew J.
Published in Nature genetics (23.09.2024)
Published in Nature genetics (23.09.2024)
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