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Hal Hoffman - Publications

Affiliations: 
University of California, San Diego, La Jolla, CA 
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28 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

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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