Sequencing of human genomes with nanopore technology by Bowden, Rory, Davies, Robert W., Heger, Andreas, Pagnamenta, Alistair T., de Cesare, Mariateresa, Oikkonen, Laura E., Parkes, Duncan, Freeman, Colin, Dhalla, Fatima, Patel, Smita Y., Popitsch, Niko, Ip, Camilla L. C., Roberts, Hannah E., Salatino, Silvia, Lockstone, Helen, Lunter, Gerton, Taylor, Jenny C., Buck, David, Simpson, Michael A., Donnelly, Peter

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Inborn errors of thymic stromal cell development and function by Kreins, Alexandra Y., Maio, Stefano, Dhalla, Fatima

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Biologically indeterminate yet ordered promiscuous gene expression in single medullary thymic epithelial cells by Dhalla, Fatima, Baran‐Gale, Jeanette, Maio, Stefano, Chappell, Lia, Holländer, Georg A, Ponting, Chris P

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Ageing compromises mouse thymus function and remodels epithelial cell differentiation by Baran-Gale, Jeanette, Morgan, Michael D, Maio, Stefano, Dhalla, Fatima, Calvo-Asensio, Irene, Deadman, Mary E, Handel, Adam E, Maynard, Ashley, Chen, Steven, Green, Foad, Sit, Rene V, Neff, Norma F, Darmanis, Spyros, Tan, Weilun, May, Andy P, Marioni, John C, Ponting, Chris P, Holländer, Georg A

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Challenges in the Role of Gammaglobulin Replacement Therapy and Vaccination Strategies for Hematological Malignancy by Sánchez-Ramón, Silvia, Dhalla, Fatima, Chapel, Helen

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Histology of Interstitial Lung Disease in Common Variable Immune Deficiency by Dhalla, Fatima, Lochlainn, Dylan J Mac, Chapel, Helen, Patel, Smita Y

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Combined multidimensional single-cell protein and RNA profiling dissects the cellular and functional heterogeneity of thymic epithelial cells by Klein, Fabian, Veiga-Villauriz, Clara, Börsch, Anastasiya, Maio, Stefano, Palmer, Sam, Dhalla, Fatima, Handel, Adam E., Zuklys, Saulius, Calvo-Asensio, Irene, Musette, Lucas, Deadman, Mary E., White, Andrea J., Lucas, Beth, Anderson, Graham, Holländer, Georg A.

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Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations by Giardino, Giuliana, Sharapova, Svetlana O., Ciznar, Peter, Dhalla, Fatima, Maragliano, Luca, Radha Rama Devi, Akella, Islamoglu, Candan, Ikinciogullari, Aydan, Haskologlu, Sule, Dogu, Figen, Hanna-Wakim, Rima, Dbaibo, Ghassan, Chou, Janet, Cirillo, Emilia, Borzacchiello, Carla, Kreins, Alexandra Y., Worth, Austen, Rota, Ioanna A., Marques, José G., Sayitoglu, Muge, Firtina, Sinem, Mahdi, Moaffaq, Geha, Raif, Neven, Bénédicte, Sousa, Ana E., Benfenati, Fabio, Hollander, Georg A., Davies, E. Graham, Pignata, Claudio

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COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience by Shields, Adrian M., Burns, Siobhan O., Savic, Sinisa, Richter, Alex G., Anantharachagan, Ariharan, Arumugakani, Gururaj, Baker, Kenneth, Bahal, Sameer, Bermingham, William, Bhole, Malini, Boules, Evon, Bright, Philip, Burns, Siobhan, Cleave, Betsy, Dempster, John, Devlin, Lisa, Dhalla, Fatima, Drewe, Elizabeth, Duncan, Christopher, Dziadzio, Magdalena, Elkhalifa, Shuayb, Gennery, Andrew, Goddard, Sarah, Grigoriadou, Sofia, Hayman, Grant, Herwadkar, Archana, Huissoon, Aarnoud, Jain, Rashmi, Jolles, Stephen, Johnston, Sarah, Leeman, Lucy, Mahabir, Shanti, MacLochlainn, Dylan, McDermott, Elizabeth, Misbah, Siraj, Morsi, Hadeil, Murng, Sai, Noorani, Sadia, O’Brien, Rachael, Patel, Smita, Price, Arthur, Richter, Alex, Savic, Sinisa, Seneviratne, Suranjith, Shields, Adrian, Shrimpton, Anna, Stroud, Catherine, Vaitla, Prashantha, Verma, Nisha

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FOXN1 deficient nude severe combined immunodeficiency by Rota, Ioanna A, Dhalla, Fatima

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SARS-CoV-2 Vaccine Responses in Individuals with Antibody Deficiency: Findings from the COV-AD Study by Shields, Adrian M., Faustini, Sian E., Hill, Harriet J., Al-Taei, Saly, Tanner, Chloe, Ashford, Fiona, Workman, Sarita, Moreira, Fernando, Verma, Nisha, Wagg, Hollie, Heritage, Gail, Campton, Naomi, Stamataki, Zania, Klenerman, Paul, Thaventhiran, James E. D., Goddard, Sarah, Johnston, Sarah, Huissoon, Aarnoud, Bethune, Claire, Elcombe, Suzanne, Lowe, David M., Patel, Smita Y., Savic, Sinisa, Burns, Siobhan O., Richter, Alex G.

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Secondary immunodeficiency in lymphoproliferative malignancies by Friman, Vanda, Winqvist, Ola, Blimark, Cecilie, Langerbeins, Petra, Chapel, Helen, Dhalla, Fatima

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European Society for Immunodeficiencies guidelines for the management of patients with congenital athymia by Kreins, Alexandra Y., Dhalla, Fatima, Flinn, Aisling M., Howley, Evey, Ekwall, Olov, Villa, Anna, Staal, Frank J.T., Anderson, Graham, Gennery, Andrew R., Holländer, Georg A., Davies, E. Graham, Burns, Siobhan O., Carrabba, Maria, Gardulf, Ann, Haerynck, Filomeen, Hauck, Fabian, Jandus, Peter, Meyts, Isabelle, Klocperk, Adam, Neven, Bénédicte, Pac, Malgorzata, Pergent, Martine, Sediva, Anna, Soler-Palacín, Pere, Velcheva, Margarita, Warnatz, Klaus

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Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation by de la Morena, M. Teresa, MD, Leonard, David, PhD, Torgerson, Troy R., MD, PhD, Cabral-Marques, Otavio, PhD, Slatter, Mary, MD, Aghamohammadi, Asghar, MD, Chandra, Sharat, MD, Murguia-Favela, Luis, MD, Bonilla, Francisco A., MD, PhD, Kanariou, Maria, MD, Damrongwatanasuk, Rongras, MD, Kuo, Caroline Y., MD, Dvorak, Christopher C., MD, Meyts, Isabelle, MD, Chen, Karin, MD, Kobrynski, Lisa, MD, MPH, Kapoor, Neena, MD, Richter, Darko, MD, DiGiovanni, Daniela, MD, Dhalla, Fatima, MD, Farmaki, Evangelia, MD, Speckmann, Carsten, MD, Español, Teresa, MD, Shcherbina, Anna, MD, Hanson, Imelda Celine, MD, Litzman, Jiri, MD, Routes, John M., MD, Wong, Melanie, MD, PhD, Fuleihan, Ramsay, MD, Seneviratne, Suranjith L., MD, Small, Trudy N., MD, Janda, Ales, MD, Bezrodnik, Liliana, MD, Seger, Reinhard, MD, Raccio, Andrea Gomez, MD, Edgar, J. David M., MD, Chou, Janet, MD, Abbott, Jordan K., MD, van Montfrans, Joris, MD, González-Granado, Luis Ignacio, MD, Bunin, Nancy, MD, Kutukculer, Necil, MD, Gray, Paul, MD, Seminario, Gisela, MD, Pasic, Srdjan, MD, Aquino, Victor, MD, Wysocki, Christian, MD, PhD, Abolhassani, Hassan, MD, Dorsey, Morna, MD, Cunningham-Rundles, Charlotte, MD, PhD, Knutsen, Alan P., MD, Sleasman, John, MD, Costa Carvalho, Beatriz Tavares, MD, Condino-Neto, Antonio, MD, Grunebaum, Eyal, MD, Chapel, Helen, MD, Ochs, Hans D., MD, PhD, Filipovich, Alexandra, MD, Cowan, Mort, MD, Gennery, Andrew, MD, Cant, Andrew, MD, Notarangelo, Luigi D., MD, Roifman, Chaim M., MD

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Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK by Shields, Adrian M, Anantharachagan, Ariharan, Arumugakani, Gururaj, Baker, Kenneth, Bahal, Sameer, Baxendale, Helen, Bermingham, William, Bhole, Malini, Boules, Evon, Bright, Philip, Chopra, Charu, Cliffe, Lucy, Cleave, Betsy, Dempster, John, Devlin, Lisa, Dhalla, Fatima, Diwakar, Lavanya, Drewe, Elizabeth, Duncan, Christopher, Dziadzio, Magdalena, Elcombe, Suzanne, Elkhalifa, Shuayb, Gennery, Andrew, Ghanta, Harichandrana, Goddard, Sarah, Grigoriadou, Sofia, Hackett, Scott, Hayman, Grant, Herriot, Richard, Herwadkar, Archana, Huissoon, Aarnoud, Jain, Rashmi, Jolles, Stephen, Johnston, Sarah, Khan, Sujoy, Laffan, James, Lane, Peter, Leeman, Lucy, Lowe, David M, Mahabir, Shanti, Lochlainn, Dylan James Mac, McDermott, Elizabeth, Misbah, Siraj, Moghaddas, Fiona, Morsi, Hadeil, Murng, Sai, Noorani, Sadia, O'Brien, Rachael, Patel, Smita, Price, Arthur, Rahman, Tasneem, Seneviratne, Suranjith, Shrimpton, Anna, Stroud, Catherine, Thomas, Moira, Townsend, Katie, Vaitla, Prashantha, Verma, Nisha, Williams, Anthony, Burns, Siobhan O, Savic, Sinisa, Richter, Alex G

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Resolving the polygenic aetiology of a late onset combined immune deficiency caused by NFKB1 haploinsufficiency and modified by PIK3R1 and TNFRSF13B variants by Hargreaves, Chantal E., Dhalla, Fatima, Patel, Arzoo M., de Oteyza, Andrés Caballero Garcia, Bateman, Elizabeth, Miller, Joanne, Anzilotti, Consuelo, Ayers, Lisa, Grimbacher, Bodo, Patel, Smita Y.

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Antibody Deficiency Secondary to Chronic Lymphocytic Leukemia: Should Patients be Treated with Prophylactic Replacement Immunoglobulin? by Dhalla, Fatima, Lucas, Mary, Schuh, Anna, Bhole, Malini, Jain, Rashmi, Patel, Smita Y., Misbah, Siraj, Chapel, Helen

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Increased Seroprevalence and Improved Antibody Responses Following Third Primary SARS-CoV-2 Immunisation: An Update From the COV-AD Study by Shields, Adrian M, Faustini, Sian E, Hill, Harriet J, Al-Taei, Saly, Tanner, Chloe, Ashford, Fiona, Workman, Sarita, Moreira, Fernando, Verma, Nisha, Wagg, Hollie, Heritage, Gail, Campton, Naomi, Stamataki, Zania, Drayson, Mark T, Klenerman, Paul, Thaventhiran, James E D, Elkhalifa, Shuayb, Goddard, Sarah, Johnston, Sarah, Huissoon, Aarnoud, Bethune, Claire, Elcombe, Suzanne, Lowe, David M, Patel, Smita Y, Savic, Sinisa, Richter, Alex G, Burns, Siobhan O

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Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases by Pagnamenta, Alistair T, Camps, Carme, Giacopuzzi, Edoardo, Taylor, John M, Hashim, Mona, Calpena, Eduardo, Kaisaki, Pamela J, Hashimoto, Akiko, Yu, Jing, Sanders, Edward, Schwessinger, Ron, Hughes, Jim R, Lunter, Gerton, Dreau, Helene, Ferla, Matteo, Lange, Lukas, Kesim, Yesim, Ragoussis, Vassilis, Vavoulis, Dimitrios V, Allroggen, Holger, Ansorge, Olaf, Babbs, Christian, Banka, Siddharth, Baños-Piñero, Benito, Beeson, David, Ben-Ami, Tal, Bennett, David L, Bento, Celeste, Blair, Edward, Brasch-Andersen, Charlotte, Bull, Katherine R, Cario, Holger, Cilliers, Deirdre, Conti, Valerio, Davies, E Graham, Dhalla, Fatima, Dacal, Beatriz Diez, Dong, Yin, Dunford, James E, Guerrini, Renzo, Harris, Adrian L, Hartley, Jane, Hollander, Georg, Javaid, Kassim, Kane, Maureen, Kelly, Deirdre, Kelly, Dominic, Knight, Samantha J L, Kreins, Alexandra Y, Kvikstad, Erika M, Langman, Craig B, Lester, Tracy, Lines, Kate E, Lord, Simon R, Lu, Xin, Mansour, Sahar, Manzur, Adnan, Maroofian, Reza, Marsden, Brian, Mason, Joanne, McGowan, Simon J, Mei, Davide, Mlcochova, Hana, Murakami, Yoshiko, Németh, Andrea H, Okoli, Steven, Ormondroyd, Elizabeth, Ousager, Lilian Bomme, Palace, Jacqueline, Patel, Smita Y, Pentony, Melissa M, Pugh, Chris, Rad, Aboulfazl, Ramesh, Archana, Riva, Simone G, Roberts, Irene, Roy, Noémi, Salminen, Outi, Schilling, Kyleen D, Scott, Caroline, Sen, Arjune, Smith, Conrad, Stevenson, Mark, Thakker, Rajesh V, Twigg, Stephen R F, Uhlig, Holm H, van Wijk, Richard, Vona, Barbara, Wall, Steven, Wang, Jing, Watkins, Hugh, Zak, Jaroslav, Schuh, Anna H, Kini, Usha, Wilkie, Andrew O M, Popitsch, Niko, Taylor, Jenny C

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Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease by Dhalla, Fatima, Murray, Sarah, Sadler, Ross, Chaigne-Delalande, Benjamin, Sadaoka, Tomohiko, Soilleux, Elizabeth, Uzel, Gulbu, Miller, Joanne, Collins, Graham Peter, Hatton, Christian Simon Ross, Bhole, Malini, Ferry, Berne, Chapel, Helen M., Cohen, Jeffrey I., Patel, Smita Y.

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