EricHansonMD

PubMed

• 29 citations
  The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I...
  Kader Cetin Gedik, Lovro Lamot, Micol Romano, Erkan Demirkaya, David Piskin, Sofia Torreggiani, Laura A Adang, Thais Armangue, Kathe Barchus, Devon R Cordova, Yanick J...> ;Arthritis & Rheumatology. 2022 May 1
• 1 citations
  Distribution and Functional Consequences of Somatic MAP2K1 Variants in Affected Skin Associated with Bone Lesions in Melorheostosis.
  Smita Jha, Aleksandra Ivovic, Heeseog Kang, Françoise Meylan, Eric P. Hanson, Casey A. Rimland, Eileen Lange, James D. Katz, Alison A. McBride, Andrew C. Warner, Elija...> ;The Journal of Investigative Dermatology. 2021 Mar 1
• 20 citations
  Somatic SMAD3-activating mutations cause melorheostosis by up-regulating the TGF-β/SMAD pathway.
  Heeseog Kang, Smita Jha, Aleksandra Ivovic, Nadja Fratzl-Zelman, Zuoming Deng, Apratim Mitra, Wayne A. Cabral, Eric P. Hanson, Eileen Lange, Edward W. Cowen, James D. ...> ;The Journal of Experimental Medicine. 2020 May 4
• 113 citations
  Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases
  Adriana Almeida de Jesus, Yangfeng Hou, Stephen R. Brooks, Louise Malle, Angelique Biancotto, Yan Huang, Katherine R. Calvo, Bernadette Marrero, Susan Moir, Andrew J. ...> ;The Journal of Clinical Investigation. 2020 Apr 1
• 11 citations
  Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritis.
  Keith A. Sikora, Joshua R. Bennett, Laurens Vyncke, Zuoming Deng, Wanxia Li Tsai, Ewald Pauwels, Gerlinde Layh-Schmitt, April Brundidge, Fatemeh Navid, Kristien J. M. ...> ;The Journal of Allergy and Clinical Immunology. 2018 May 1
• 47 citations
  Somatic activating mutations in MAP2K1 cause melorheostosis
  Heeseog Kang, Smita Jha, Zuoming Deng, Nadja Fratzl-Zelman, Wayne A. Cabral, Aleksandra Ivovic, Françoise Meylan, Eric P. Hanson, Eileen Lange, James D. Katz, Paul Ros...> ;Nature Communications. 2018 Apr 11
• 48 citations
  Recruitment of A20 by the C-terminal domain of NEMO suppresses NF-κB activation and autoinflammatory disease
  Jevgenia Zilberman-Rudenko, Linda Monaco Shawver, Alex W. Wessel, Yongquan Luo, Martin Pelletier, Wanxia Li Tsai, Younglang Lee, Spiridon Vonortas, Laurence E. Cheng, ...> ;Proceedings of the National Academy of Sciences of the United States of America. 2016 Feb 9
• 372 citations
  Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
  Qing Zhou, Hongying Wang, Daniella M. Schwartz, Monique Stoffels, Yong Hwan Park, Yuan Zhang, Dan Yang, Erkan Demirkaya, Masaki Takeuchi, Wanxia Li Tsai, Jonathan J. L...> ;Nature Genetics. 2016 Jan 1
• 12 citations
  A method for the quantitative analysis of stimulation-induced nuclear translocation of the p65 subunit of NF-κB from patient-derived dermal fibroblasts.
  Alex W. Wessel, Eric P. Hanson> ;Methods in Molecular Biology. 2015 Jan 1
• 151 citations
  Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome
  Daniel Kotlarz, Natalia Ziętara, Gulbu Uzel, Thomas Weidemann, Christian Braun, Jana Diestelhorst, Peter Krawitz, Peter N. Robinson, Jochen Hecht, Jacek Puchałka, E. M...> ;The Journal of Experimental Medicine. 2013 Mar 11
• 20 citations
  Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations
  Michael D. Keller, Maureen M. Petersen, Peck Y. Ong, Joseph A. Church, Kimberly A. Risma, Jon Burham, Ashish Jain, E. Richard Stiehm, Eric P. Hanson, Gulbu Uzel, Matth...> ;Frontiers in Immunology. 2011 Nov 8
• 12 citations
  Congenital alterations of NEMO glutamic acid 223 result in hypohidrotic ectodermal dysplasia and immunodeficiency with normal serum IgG levels
  Gital Karamchandani-Patel, Eric P. Hanson, Rushani W. Saltzman, C. Eve Kimball, Ricardo U. Sorensen, Jordan S. Orange> ;Annals of Allergy, Asthma & Immunology. 2011 Jul 1
• 6 citations
  A Novel Missense Mutation in the Nuclear Factor-κB Essential Modulator (NEMO) Gene Resulting in Impaired Activation of the NF-κB Pathway and a Unique Clinical Phenotyp...
  Gene A. Devora, Lijun Sun, Zhijian J. Chen, Nicolai S. C. van Oers, Eric P. Hanson, Jordan S. Orange, M. Teresa de la Morena> ;Journal of Clinical Immunology. 2010 Jul 23
• ACTN3 genotype does not influence muscle power.
  Hanson, E. D.,Ludlow, A. T.,Sheaff, A. K.,Park, J.,Roth, S. M.> ;Int J Sports Med. 2010 Sep 11
• 5 citations
  Cutting Edge: Association with IκB Kinase β Regulates the Subcellular Localization of Homer3
  Gayatri Yatherajam, Pinaki P. Banerjee, Kelly A. McCorkell, Laura A. Solt, Eric P. Hanson, Lisa A. Madge, Shin Kang, Paul F. Worley, Jordan S. Orange, Michael J. May> ;Journal of Immunology. 2010 Sep 1
• 165 citations
  Hypomorphic nuclear factor-κB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity
  Eric P. Hanson, Linda Monaco-Shawver, Laura A. Solt, Lisa A. Madge, Pinaki P. Banerjee, Michael J. May, Jordan S. Orange> ;The Journal of Allergy and Clinical Immunology. 2008 Dec 1
• 36 citations
  IKBKG (nuclear factor-κB essential modulator) mutation can be associated with opportunistic infection without impairing Toll-like receptor function
  Bryn H. Salt, Julie E. Niemela, Rahul Pandey, Eric P. Hanson, Raquel P. Deering, Ralph Quinones, Ashish Jain, Jordan S. Orange, Erwin W. Gelfand> ;The Journal of Allergy and Clinical Immunology. 2008 Apr 1
• 90 citations
  Autosomal SCID caused by a point mutation in the N-terminus of Jak3: mapping of the Jak3-receptor interaction domain.
  Nicholas A. Cacalano, Thi-Sau Migone, Fernando Bazan, Eric P. Hanson, Min Chen, Fabio Candotti, John J. O'Shea, James A. Johnston> ;The EMBO Journal. 1999 Mar 15
• 94 citations
  Distinct tyrosine phosphorylation sites in JAK3 kinase domain positively and negatively regulate its enzymatic activity
  Yong-Jie Zhou, Eric P. Hanson, Yi-Qing Chen, Kelly S. Magnuson, Min Chen, Patrick G. Swann, Ronald L. Wange, Paul S. Changelian, John J. O'Shea> ;Proceedings of the National Academy of Sciences of the United States of America. 1997 Dec 9
• 121 citations
  The amino terminus of JAK3 is necessary and sufficient for binding to the common γ chain and confers the ability to transmit interleukin 2-mediated signals
  Min Chen, Alan C. Cheng, Yi-Qing Chen, Anka Hymel, Eric P. Hanson, Lida H. Kimmel, Yasuhiro Minami, Tadatsugu Taniguchi, Paul S. Changelian, John J. O'Shea> ;Proceedings of the National Academy of Sciences of the United States of America. 1997 Jun 24
• 117 citations
  Interleukins 2, 4, 7, and 15 Stimulate Tyrosine Phosphorylation of Insulin Receptor Substrates 1 and 2 in T Cells POTENTIAL ROLE OF JAK KINASES
  James A. Johnston, Ling-Mei Wang, Eric P. Hanson, Xiao Jian Sun, Morris F. White, Scott A. Oakes, Jacalyn H. Pierce, John J. O'Shea> ;The Journal of Biological Chemistry. 1995 Dec 1
• 9 citations
  Recurrent salmonella infection with a single strain in the acquired immunodeficiency syndrome. Confirmation by plasmid fingerprinting.
  Kenneth H. Mayer, Eric P. Hanson> ;Diagnostic Microbiology and Infectious Disease. 1986 Jan 1
• Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome.
  Rider, N. L.,Boisson, B.,Jyonouchi, S.,Hanson, E. P.,Rosenzweig, S. D.,Cassanova, J. L.,Orange, J. S.> ;Front Pediatr. 2015 Feb 18
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