Autoinflammatory keratinization diseases: An emerging concept encompassing various inflammatory keratinization disorders of the skin von Akiyama, Masashi, Takeichi, Takuya, McGrath, John A., Sugiura, Kazumitsu

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Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation von Zhong, Franklin L., Mamaï, Ons, Sborgi, Lorenzo, Boussofara, Lobna, Hopkins, Richard, Robinson, Kim, Szeverényi, Ildikó, Takeichi, Takuya, Balaji, Reshmaa, Lau, Aristotle, Tye, Hazel, Roy, Keya, Bonnard, Carine, Ahl, Patricia J., Jones, Leigh Ann, Baker, Paul J., Lacina, Lukas, Otsuka, Atsushi, Fournie, Pierre R., Malecaze, François, Lane, E. Birgitte, Akiyama, Masashi, Kabashima, Kenji, Connolly, John E., Masters, Seth L., Soler, Vincent J., Omar, Salma Samir, McGrath, John A., Nedelcu, Roxana, Gribaa, Moez, Denguezli, Mohamed, Saad, Ali, Hiller, Sebastian, Reversade, Bruno

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Novel and emerging therapies in the treatment of recessive dystrophic epidermolysis bullosa von Rashidghamat, Ellie, McGrath, John A.

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Metabolic perturbations in fibrosis disease von Ung, Chuin Ying, Onoufriadis, Alexandros, Parsons, Maddy, McGrath, John A., Shaw, Tanya J.

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The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB von Fine, Jo-David, MD, MPH, FRCP, Eady, Robin A.J., DSc, FRCP, FMedSci, Bauer, Eugene A., MD, Bauer, Johann W., MD, Bruckner-Tuderman, Leena, MD, PhD, Heagerty, Adrian, MD, FRCP, Hintner, Helmut, MD, Hovnanian, Alain, MD, PhD, Jonkman, Marcel F., MD, PhD, Leigh, Irene, MD, FRCP, FMedSci, McGrath, John A., MD, FRCP, Mellerio, Jemima E., MD, FRCP, Murrell, Dedee F., MD, Shimizu, Hiroshi, MD, PhD, Uitto, Jouni, MD, PhD, Vahlquist, Anders, MD, PhD, Woodley, David, MD, Zambruno, Giovanna, MD

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Recently Identified Forms of Epidermolysis Bullosa von McGrath, John A

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Prediction of Real-World Functional Disability in Chronic Mental Disorders: A Comparison of Schizophrenia and Bipolar Disorder von Bowie, Christopher R., Depp, Colin, McGrath, John A., Wolyniec, Paula, Mausbach, Brent T., Thornquist, Mary H., Luke, James, Patterson, Thomas L., Harvey, Philip D., Pulver, Ann E.

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Current topics in Epidermolysis bullosa: Pathophysiology and therapeutic challenges von Natsuga, Ken, Shinkuma, Satoru, Hsu, Chao-Kai, Fujita, Yasuyuki, Ishiko, Akira, Tamai, Katsuto, McGrath, John A.

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Amlexanox Enhances Premature Termination Codon Read-Through in COL7A1 and Expression of Full Length Type VII Collagen: Potential Therapy for Recessive Dystrophic Epidermolysis Bull... von Atanasova, Velina S., Jiang, Qiujie, Prisco, Marco, Gruber, Christina, Piñón Hofbauer, Josefina, Chen, Mei, Has, Cristina, Bruckner-Tuderman, Leena, McGrath, John A., Uitto, Jouni, South, Andrew P.

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WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation von Xu, Mingang, Horrell, Jeremy, Snitow, Melinda, Cui, Jiawei, Gochnauer, Heather, Syrett, Camille M., Kallish, Staci, Seykora, John T., Liu, Fei, Gaillard, Dany, Katz, Jonathan P., Kaestner, Klaus H., Levin, Brooke, Mansfield, Corinne, Douglas, Jennifer E., Cowart, Beverly J., Tordoff, Michael, Liu, Fang, Zhu, Xuming, Barlow, Linda A., Rubin, Adam I., McGrath, John A., Morrisey, Edward E., Chu, Emily Y., Millar, Sarah E.

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Dominant dystrophic epidermolysis bullosa is associated with glycolytically active GATA3+ T helper 2 cells which may contribute to pruritus in lesional skin von Aala, Wilson Jr F, Hou, Ping-Chen, Hong, Yi-Kai, Lin, Yu-Chen, Lee, Yu-Rong, Tu, Wei-Ting, Papanikolaou, Marieta, Benzian-Olsson, Natashia, Onoufriadis, Alexandros, I Chen Harn, Hans, Hwang, Daw-Yang, Cheng, Siao Muk, Lu, Kurt, Chen, Peng-Chieh, McGrath, John A, Hsu, Chao-Kai

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Publications in the BJD: the impact of being read (and cited) von McGrath, John A

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Tofacitinib ameliorates skin inflammation in a patient with severe autosomal recessive congenital ichthyosis von Lin, Yu-Chen, Hong, Yi-Kai, Aala, Wilson Jr F, Hitomi, Kiyotaka, Akiyama, Masashi, McGrath, John A, Hsu, Chao-Kai

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Expression of interferon-regulated genes in juvenile dermatomyositis versus Mendelian autoinflammatory interferonopathies von Kim, Hanna, Gunter-Rahman, Fatima, McGrath, John A., Lee, Esther, de Jesus, Adriana A., Targoff, Ira N., Huang, Yan, O'Hanlon, Terrance P., Tsai, Wanxia L., Gadina, Massimo, Miller, Frederick W., Goldbach-Mansky, Raphaela, Rider, Lisa G.

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WNT10A variant and severe scoliosis? von Kantaputra, Piranit, Olsen, Bjorn, McGrath, John A.

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Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome von Petrof, Gabriela, Nanda, Arti, Howden, Jake, Takeichi, Takuya, McMillan, James R., Aristodemou, Sophia, Ozoemena, Linda, Liu, Lu, South, Andrew P., Pourreyron, Celine, Dafou, Dimitra, Proudfoot, Laura E., Al-Ajmi, Hejab, Akiyama, Masashi, McLean, W.H. Irwin, Simpson, Michael A., Parsons, Maddy, McGrath, John A.

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BJD: striving to be the Best Journal in Dermatology in a changing world von McGrath, John A

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Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa von Wagner, John E, Ishida-Yamamoto, Akemi, McGrath, John A, Hordinsky, Maria, Keene, Douglas R, Woodley, David T, Chen, Mei, Riddle, Megan J, Osborn, Mark J, Lund, Troy, Dolan, Michelle, Blazar, Bruce R, Tolar, Jakub

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ABE8e adenine base editor precisely and efficiently corrects a recurrent COL7A1 nonsense mutation von Sheriff, Adam, Guri, Ina, Zebrowska, Paulina, Llopis-Hernandez, Virginia, Brooks, Imogen R., Tekkela, Stavroula, Subramaniam, Kavita, Gebrezgabher, Ruta, Naso, Gaetano, Petrova, Anastasia, Balon, Katarzyna, Onoufriadis, Alexandros, Kujawa, Dorota, Kotulska, Martyna, Newby, Gregory, Łaczmański, Łukasz, Liu, David R., McGrath, John A., Jacków, Joanna

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Pain in recessive dystrophic epidermolysis bullosa (RDEB): findings of the Prospective Epidermolysis Bullosa Longitudinal Evaluation Study (PEBLES) von Jeffs, Eunice, Pillay, Elizabeth I, Ledwaba-Chapman, Lesedi, Bisquera, Alessandra, Robertson, Susan J, McGrath, John A, Wang, Yanzhong, Martinez, Anna E, Mellerio, Jemima E

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