Year |
Citation |
Score |
2023 |
Putnam CD, Broderick L, Hoffman HM. The discovery of NLRP3 and its function in cryopyrin-associated periodic syndromes and innate immunity. Immunological Reviews. PMID 38146057 DOI: 10.1111/imr.13292 |
0.616 |
|
2022 |
Broderick L, Hoffman HM. IL-1 and autoinflammatory disease: biology, pathogenesis and therapeutic targeting. Nature Reviews. Rheumatology. PMID 35729334 DOI: 10.1038/s41584-022-00797-1 |
0.309 |
|
2021 |
Stackowicz J, Gaudenzio N, Serhan N, Conde E, Godon O, Marichal T, Starkl P, Balbino B, Roers A, Bruhns P, Jönsson F, Moguelet P, Georgin-Lavialle S, Broderick L, Hoffman HM, et al. Neutrophil-specific gain-of-function mutations in Nlrp3 promote development of cryopyrin-associated periodic syndrome. The Journal of Experimental Medicine. 218. PMID 34477811 DOI: 10.1084/jem.20201466 |
0.322 |
|
2019 |
Broderick L, Yost S, Li D, McGeough MD, Booshehri LM, Guaderrama M, Brydges SD, Kucharova K, Patel NC, Harr M, Hakonarson H, Zackai E, Cowell IG, Austin CA, Hügle B, ... ... Hoffman HM, et al. Mutations in topoisomerase IIβ result in a B cell immunodeficiency. Nature Communications. 10: 3644. PMID 31409799 DOI: 10.1038/S41467-019-11570-6 |
0.571 |
|
2019 |
Hoss F, Mueller JL, Rojas Ringeling F, Rodriguez-Alcazar JF, Brinkschulte R, Seifert G, Stahl R, Broderick L, Putnam CD, Kolodner RD, Canzar S, Geyer M, Hoffman HM, Latz E. Alternative splicing regulates stochastic NLRP3 activity. Nature Communications. 10: 3238. PMID 31324763 DOI: 10.1038/S41467-019-11076-1 |
0.632 |
|
2019 |
Booshehri LM, Hoffman HM. CAPS and NLRP3. Journal of Clinical Immunology. 39: 277-286. PMID 31077002 DOI: 10.1007/s10875-019-00638-z |
0.308 |
|
2019 |
Gattorno M, Hofer M, Federici S, Vanoni F, Bovis F, Aksentijevich I, Anton J, Arostegui JI, Barron K, Ben-Cherit E, Brogan PA, Cantarini L, Ceccherini I, De Benedetti F, Dedeoglu F, ... ... Hoffman H, et al. Classification criteria for autoinflammatory recurrent fevers. Annals of the Rheumatic Diseases. PMID 31018962 DOI: 10.1136/Annrheumdis-2019-215048 |
0.31 |
|
2015 |
Broderick L, Carvalho D, Magit A, Jiang W, Leuin S, Bothwell M, Kearns D, Pransky S, Hoffman H. Immune dysregulation in Periodic Fever, Aphthous atomatitis, Pharyngitis, Adenitis (PFAPA) syndrome Pediatric Rheumatology. 13. DOI: 10.1186/1546-0096-13-S1-P196 |
0.352 |
|
2015 |
Broderick L, Carvalho D, Magit A, Jiang W, Leuin S, Bothwell M, Kearns D, Pransky S, Hoffman H. Long-term outcomes of tonsillectomy in children with periodic fever, aphthous stomatitis, pharyngitis, adenitis (PFAPA) syndrome Pediatric Rheumatology. 13. DOI: 10.1186/1546-0096-13-S1-O78 |
0.313 |
|
2015 |
McGeough M, Wree A, Pena C, Inzaugarat M, Feldstein A, Hoffman H. A significant role for tumor necrosis factor in Nlrp3 inflammasomeopathies. Pediatric Rheumatology. 13: 1-1. DOI: 10.1186/1546-0096-13-S1-O27 |
0.397 |
|
2013 |
Broderick L, Gandhi C, Mueller JL, Putnam CD, Shayan K, Giclas PC, Peterson KS, Aceves SS, Sheets RM, Peterson BM, Newbury RO, Hoffman HM, Bastian JF. Mutations of complement factor I and potential mechanisms of neuroinflammation in acute hemorrhagic leukoencephalitis. Journal of Clinical Immunology. 33: 162-71. PMID 22926405 DOI: 10.1007/S10875-012-9767-Z |
0.593 |
|
2013 |
Endres T, Hofer F, Goldbach-Mansky R, Hoffman H, Blank N, Krause K, Rietschel C, Horneff G, Lohse P, Kuemmerle-Deschner J. PReS-FINAL-2331: Low-penetrance NLRP3 variants Pediatric Rheumatology. 11: 321. DOI: 10.1186/1546-0096-11-S2-P321 |
0.433 |
|
2013 |
Broderick L, Carvalho D, Magit A, Jiang W, Leuin S, Bothwell M, Kearns D, Pransky S, Hoffman H. PW03-009 – Genetics of PFAPA syndrome Pediatric Rheumatology. 11: 1-1. DOI: 10.1186/1546-0096-11-S1-A235 |
0.387 |
|
2013 |
Broderick L, Brydges S, McGeough, Pena C, Mueller J, Hoffman H. OR11-004 - IL-1, IL-18 and cell death in NLRP3 driven disease Pediatric Rheumatology. 11: 1-1. DOI: 10.1186/1546-0096-11-S1-A193 |
0.382 |
|
2013 |
Endres T, Hofer F, Goldbach-Mansky R, Hoffman H, Blank N, Krause K, Rietschel C, Horneff G, Lohse P, Kuemmerle-Deschner J. PW02-040 - Low-penetrance NLRP3 variants Pediatric Rheumatology. 11: 1-2. DOI: 10.1186/1546-0096-11-S1-A181 |
0.43 |
|
2012 |
Sivagnanam M, Mueller JL, McGeough MD, Pena C, Hoffman HM. Mo1982 Epcam Deficient Mice Demonstrate Intestinal Permeability Defects Gastroenterology. 142. DOI: 10.1016/S0016-5085(12)62762-0 |
0.633 |
|
2011 |
Piram M, Frenkel J, Gattorno M, Ozen S, Lachmann HJ, Goldbach-Mansky R, Hentgen V, Neven B, Stojanovic KS, Simon A, Kuemmerle-Deschner J, Hoffman H, Stojanov S, Duquesne A, Pillet P, et al. A preliminary score for the assessment of disease activity in hereditary recurrent fevers: results from the AIDAI (Auto-Inflammatory Diseases Activity Index) Consensus Conference. Annals of the Rheumatic Diseases. 70: 309-14. PMID 21081528 DOI: 10.1136/Ard.2010.132613 |
0.339 |
|
2011 |
Sivagnanam M, Mueller JL, Mcgeough MD, Pena C, Hoffman HM. Epcam Deficient Mice Show Significant Morbidity and Pathology Resembling Congenital Tufting Enteropathy Gastroenterology. 140. DOI: 10.1016/S0016-5085(11)62674-7 |
0.64 |
|
2010 |
Broderick L, Page N, Hong P, Carvalho D, Magit A, Jiang W, Simon L, Bothwell M, Kearns D, Pransky S, Hoffman H. Cellular Immunity in Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis (PFAPA) Syndrome Clinical Immunology. 135. DOI: 10.1016/J.Clim.2010.03.190 |
0.309 |
|
2009 |
Brydges SD, Mueller JL, McGeough MD, Pena CA, Misaghi A, Gandhi C, Putnam CD, Boyle DL, Firestein GS, Horner AA, Soroosh P, Watford WT, O'Shea JJ, Kastner DL, Hoffman HM. Inflammasome-mediated disease animal models reveal roles for innate but not adaptive immunity. Immunity. 30: 875-87. PMID 19501000 DOI: 10.1016/J.Immuni.2009.05.005 |
0.622 |
|
2009 |
Brydges S, Mueller J, McGeough M, Pena C, Misaghi A, Gandhi C, Boyle D, Firestein G, Horner A, Soroosh P, Putnam C, Watford W, O'Shea J, Kastner D, Hoffman H. OR.26. Animal Models of Inflammasomapathy Solely Implicate the Innate Immune System in Pathogenesis, with an Important but not Universal Role for IL-1β Clinical Immunology. 131: S13-S14. DOI: 10.1016/J.Clim.2009.03.033 |
0.58 |
|
2008 |
Anderson JP, Mueller JL, Misaghi A, Anderson S, Sivagnanam M, Kolodner RD, Hoffman HM. Initial description of the human NLRP3 promoter Genes and Immunity. 9: 721-726. PMID 18719602 DOI: 10.1038/Gene.2008.66 |
0.699 |
|
2008 |
Sivagnanam M, Mueller JL, Lee H, Chen Z, Nelson SF, Turner D, Zlotkin SH, Pencharz PB, Ngan BY, Libiger O, Schork NJ, Lavine JE, Taylor S, Newbury RO, Kolodner RD, ... Hoffman HM, et al. Identification of EpCAM as the gene for congenital tufting enteropathy. Gastroenterology. 135: 429-37. PMID 18572020 DOI: 10.1053/J.Gastro.2008.05.036 |
0.689 |
|
2007 |
Aksentijevich I, Putnam CD, Remmers EF, Mueller JL, Le J, Kolodner RD, Moak Z, Chuang M, Austin F, Goldbach-Mansky R, Hoffman HM, Kastner DL. The clinical continuum of cryopyrinopathies: Novel CIAS1 mutations in North American patients and a new cryopyrin model Arthritis and Rheumatism. 56: 1273-1285. PMID 17393462 DOI: 10.1002/Art.22491 |
0.651 |
|
2003 |
Hoffman HM, Gregory SG, Mueller JL, Tresierras M, Broide DH, Wanderer AA, Kolodner RD. Fine structure mapping of CIAS1: Identification of an ancestral haplotype and a common FCAS mutation, L353P Human Genetics. 112: 209-216. PMID 12522564 DOI: 10.1007/S00439-002-0860-X |
0.504 |
|
2002 |
Aksentijevich I, Nowak M, Mallah M, Chae JJ, Watford WT, Hofmann SR, Stein L, Russo R, Goldsmith D, Dent P, Rosenberg HF, Austin F, Remmers EF, Balow JE, Rosenzweig S, ... ... Hoffman H, et al. De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases. Arthritis and Rheumatism. 46: 3340-8. PMID 12483741 DOI: 10.1002/Art.10688 |
0.445 |
|
2001 |
Hoffman HM, Mueller JL, Broide DH, Wanderer AA, Kolodner RD. Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome. Nature Genetics. 29: 301-5. PMID 11687797 DOI: 10.1038/Ng756 |
0.524 |
|
2000 |
Hoffman HM, Wright FA, Broide DH, Wanderer AA, Kolodner RD. Identification of a locus on chromosome 1q44 for familial cold urticaria. American Journal of Human Genetics. 66: 1693-8. PMID 10741953 DOI: 10.1086/302874 |
0.454 |
|
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