Transcriptional and epigenetic mechanisms of promiscuous gene expression by thymic epithelial cells by Dhalla, F

FOXN1 deficient nude severe combined immunodeficiency by Rota, I, Dhalla, F

Challenges in the role of gammaglobulin replacement therapy and vaccination strategies for hematological malignancy by Sánchez-Ramón, S, Dhalla, F, Chapel, H

Review of gastric cancer risk factors in patients with common variable immunodeficiency disorders, resulting in a proposal for a surveillance programme by Dhalla, F, da Silva, S, Lucas, M, Travis, S, Chapel, H

Review of gastric cancer risk factors in patients with common variable immunodeficiency disorders, resulting in a proposal for a surveillance programme. by Dhalla, F, da Silva, S, Lucas, M, Travis, S, Chapel, H

Secondary immunodeficiency in lymphoproliferative malignancies. by Friman, V, Winqvist, O, Blimark, C, Langerbeins, P, Chapel, H, Dhalla, F

Biologically indeterminate yet ordered promiscuous gene expression in single medullary thymic epithelial cells by Dhalla, F, Baran-Gale, J, Maio, S, Chappell, L, Holländer, G, Ponting, C

Antibody deficiency secondary to chronic lymphocytic leukemia: Should patients be treated with prophylactic replacement immunoglobulin? by Dhalla, F, Lucas, M, Schuh, A, Bhole, M, Jain, R, Patel, S, Misbah, S, Chapel, H

Antibody deficiency secondary to chronic lymphocytic leukemia: Should patients be treated with prophylactic replacement immunoglobulin? by Dhalla, F, Lucas, M, Schuh, A, Bhole, M, Jain, R, Patel, S, Misbah, S, Chapel, H

X-MEN: The new mutants by Dhalla, F, Murray, S, Miller, J, Sadler, R, Soilleux, E, Bhole, M, Uzel, G, Ferry, B, Patel, S, Chapel, H

Developmental dynamics of the neural crest-mesenchymal axis in creating the thymic microenvironment by Handel, A, Cheuk, S, Dhalla, F, Maio, S, Hübscher, T, Rota, I, Deadman, M, Ekwall, O, Lutolf, M, Weinberg, K, Hollander, G

Identification of a Novel Mutation in MAGT1 and Progressive Multifocal Leucoencephalopathy in a 58-Year-Old Man with XMEN Disease. by Dhalla, F, Murray, S, Sadler, R, Chaigne-Delalande, B, Sadaoka, T, Soilleux, E, Uzel, G, Miller, J, Collins, G, Hatton, C, Bhole, M, Ferry, B, Chapel, H, Cohen, J, Patel, S

Ageing compromises mouse thymus function and remodels epithelial cell differentiation by Baran-Gale, J, Morgan, MD, Maio, S, Dhalla, F, Calvo-Asensio, I, Deadman, ME, Handel, AE, Maynard, A, Chen, S, Green, F, Sit, RV, Neff, NF, Darmanis, S, Tan, W, May, AP, Marioni, JC, Ponting, CP, Hollander, G

Sequencing of human genomes with nanopore technology by Bowden, R, Davies, R, Heger, A, Pagnamenta, A, De Cesare, M, Oikkonen, L, Parkes, D, Freeman, C, Dhalla, F, Patel, S, Popitsch, N, Ip, C, Roberts, H, Salatino, S, Lockstone, H, Lunter, G, Taylor, J, Buck, D, Simpson, M, Donnelly, P

Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations by Giardino, G, Sharapova, SO, Ciznar, P, Dhalla, F, Maragliano, L, Radha Rama Devi, A, Islamoglu, C, Ikinciogullari, A, Haskologlu, S, Dogu, F, Hanna-Wakim, R, Dbaibo, G, Chou, J, Cirillo, E, Borzacchiello, C, Kreins, AY, Worth, A, Rota, IA, Marques, JG, Sayitoglu, M, Firtina, S, Mahdi, M, Geha, R, Neven, B, Sousa, AE, Benfenati, F, Hollander, GA, Davies, EG, Pignata, C

FOXN1 forms higher-order nuclear condensates displaced by mutations causing immunodeficiency by Rota, I, Handel, A, Maio, S, Klein, F, Dhalla, F, Deadman, M, Cheuk, S, Newman, J, Michaels, Y, Zuklys, S, Prevot, N, Hublitz, P, Charles, P, Gkazi, A, Adamopoulou, E, Quasim, W, Davies, EG, Hanson, C, Pagnamenta, A, Camps, C, Dreau, H, White, A, James, K, Fischer, R, Gileadi, O, Taylor, J, Fulga, T, Lagerholm, BC, Anderson, G, Sezgin, E, Hollander, G

Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK by Shields, AM, Anantharachagan, A, Arumugakani, G, Baker, K, Bahal, S, Baxendale, H, Bermingham, W, Bhole, M, Boules, E, Bright, P, Chopra, C, Cliffe, L, Cleave, B, Dempster, J, Devlin, L, Dhalla, F, Diwakar, L, Drewe, E, Duncan, C, Dziadzio, M, Elcombe, S, Elkhalifa, S, Gennery, A, Ghanta, H, Goddard, S, Grigoriadou, S, Hackett, S, Hayman, G, Herriot, R, Herwadkar, A, Huissoon, A, Jain, R, Jolles, S, Johnston, S, Khan, S, Laffan, J, Lane, P, Leeman, L, Lowe, DM, Mahabir, S, Lochlainn, DJM, McDermott, E, Misbah, S, Moghaddas, F, Morsi, H, Murng, S, Noorani, S, O'Brien, R, Patel, S, Price, A

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases by Pagnamenta, AT, Camps, C, Giacopuzzi, E, Taylor, JM, Hashim, M, Calpena, E, Kaisaki, PJ, Hashimoto, A, Yu, J, Sanders, E, Schwessinger, R, Hughes, JR, Lunter, G, Dreau, H, Ferla, M, Lange, L, Kesim, Y, Ragoussis, V, Vavoulis, DV, Allroggen, H, Ansorge, O, Babbs, C, Banka, S, Baños-Piñero, B, Beeson, D, Ben-Ami, T, Bennett, DL, Bento, C, Blair, E, Brasch-Andersen, C, Bull, KR, Cario, H, Cilliers, D, Conti, V, Davies, EG, Dhalla, F, Dacal, BD, Dong, Y, Dunford, JE, Guerrini, R, Harris, AL, Hartley, J, Hollander, G, Javaid, K, Kane, M, Kelly, D, Kelly, D, Knight, SJL, Kreins, AY, Kvikstad, EM, Lines, KE, Lord, SR, Lu, X, Marsden, B, Ormondroyd, E, Stevenson, M, Twigg, SRF, Uhlig, HH, Watkins, H, Schuh, AH, Wilkie, AOM, Taylor, JC

Long term outcomes of 176 patients with X-linked hyper IgM syndrome treated with or without hematopoietic cell transplantation by de la Morena, M, Leonard, D, Torgerson, T, Cabral-Marques, O, Slatter, M, Aghamohammadi, A, Chandra, S, Murguia-Favela, L, Bonilla, F, Kanariou, M, Damrongwatanasuk, R, Kuo, C, Dvorak, C, Meyts, I, Chen, K, Kobrynski, L, Kapoor, N, Richter, D, DiGiovanni, D, Dhalla, F, Farmaki, E, Speckmann, C, Espanol, T, Shcherbina, A, Hanson, C, Litzman, J, Routes, J, Wong, M, Fuleihan, R, Seneviratne, S, Small, T, Janda, A, Bezrodnik, L, Seger, R, Raccio, A, Edgar, J, Chou, J, Abbott, J, van Montfrans, J, Gonzalez-Granado, L, Bunin, N, Kutukculer, N, Gray, P, Seminario, G, Pasic, S, Aquino, V, Wysocki, C, Abolhassani, H, Grunebaum, E, Dorsey, M, Costa Carvalho, B, Condino-Neto, A, Cunningham-Rundles, C, Knutsen, A, Sleasman, J, Chapel, H, Ochs, H, Filipovich, A, Cowan, M, Gennery, A, Cant, A, Notarangelo, L, Roifman, C