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Hans Brightbill Email & Phone Number

Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen at Amgen
Location: San Francisco, California, United States 13 work roles 3 schools
3 work emails found @gene.com 1 phone found area 510 LinkedIn matched
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Role
Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen
Location
San Francisco, California, United States

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Hans Brightbill is listed as Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen at Amgen, based in San Francisco, California, United States. AeroLeads shows a work email signal at gene.com, phone signal with area code 510, and a matched LinkedIn profile for Hans Brightbill.

Hans Brightbill previously worked as Scientific Director, In Vivo Pharmacology - Inflammation at Amgen and Review Editor at Frontiers In Immunology. Hans Brightbill holds Ph.D., Microbiology And Immunology from Ucla.

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About Hans Brightbill

Hans Brightbill is a Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen at Amgen. He possess expertise in immunology, cell, molecular biology, cell biology, cell culture and 14 more skills.

Listed skills include Immunology, Cell, Molecular Biology, Cell Biology, and 15 others.

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Amgen
Amgen
Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen
Website
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13 roles · 35 years

Hans Brightbill work experience

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Scientific Director, In Vivo Pharmacology - Inflammation

Current

Thousand Oaks, Ca, Us

Jun 2024 - Present

Review Editor

Current
Frontiers In Immunology
Nov 2022 - Present

Voting Member, Institutional Animal Care And Use Committee (Iacuc)

South San Francisco, California, Us

Jan 2023 - Jun 2024

Principal Scientific Manager (Group Leader), Translational Immunology

South San Francisco, California, Us

Publications:Sun. T., Huang, Z., Liang, W.C., Yin, J., Lin, W.Y., Wu, J., Vernes, J.M., Lutman, J., Caplazi, P., Jeet, S., Wong, T., Wong, M., DePianto, D.J., Morshead, K.B., Sun, K.H., Modrusan, Z., Vander Heiden, J.A., Abbas, A.R., Zhang, H., Xu, M., N'Diaye, E.N., Roose-Girma, M., Wolters, P.J., Yadav, R., Sukumaran, S., Ghilardi, N., Corpuz, R., Emson, C., Meng, Y.G., Ramalingam, T.R., Lupardus, P., Brightbill, H.D., Seshasayee, D., Wu, Y., Arron, J.R. (2021) TGFβ2 and TGFβ3 isoforms drive fibrotic disease pathogenesis. Sci. Transl. Med. 13(605):eabe0407. doi: 10.1126/scitranslmed.abe0407.Gu, M., Zhou, X. , Sohn, J.H., Zhu, L-L. , Jie, Z., Yang, J-Y. , Zheng, X., Xie, X., Yang, J., Shi, Y., Brightbill, H., Kim, J.B., Wang, J., Cheng, X., S-C. Sun. (2021) NF-kB inducing kinase maintains T cell metabolic fitness in antitumor immunity. Nat Immunol. 22:530. doi: 10.1038/s41590-021-00892-7.Presentations:Anti-Fibrotic Drug Development Conference (AFDD) 2020. “A Comparison of CDA-HFD & High Cholesterol Diet Induced NASH Models Using Automated Quantitative Image Analysis and Deuterated Hydroxyproline Mass Spectrometry”. November 2020. Virtual Conference.IPF Summit 2020. Panel discussion: Preclinical Fibrosis Models. August 2020.

Jul 2020 - Jun 2024

Interim Fibrosis Disease Area Strategy Lead

South San Francisco, California, Us

Jul 2021 - Jan 2023

Senior Scientific Manager (Lab Head), Translational Immunology

South San Francisco, California, Us

Awards:2019 Research Biology Recognition AwardPublications:Corzo C., U., et al. The kinase IRAK4 promotes endosomal TLR and immune complex signaling in B cells and plasmacytoid dendritic cells. Science Signaling 13:eaaz1053. Doi:10.1126/scisignal.aaz1053 (2020).Rajapaksa, N.S., et al. Discovery of Potent Benzolactam IRAK4 Inhibitors with Robust in Vivo Activity. ACS Med Chem Lett. 11:327-333. doi: 10.1021/acsmedchemlett.9b00380 (2019).Sun T, et al. (2019) TAZ is required for lung alveolar epithelial cell differentiation after injury. JCI Insight. pii:128674. doi: 10.1172/jci.insight.128674.Bryan MC, Drobnick J, Gobbi A, Kolesnikov A, Chen Y, Rajapaksa N, Ndubaku C, Feng J, Chang W, Francis R, Yu C, Choo EF, DeMent K, Ran Y, An L, Emson C, Huang Z, Sujatha-Bhaskar S, Brightbill H, DiPasquale A, Maher J, Wai J, McKenzie BS, Lupardus PJ, Zarrin AA, Kiefer JR. (2019) Development of Potent and Selective Pyrazolopyrimidine IRAK4 Inhibitors. J Med Chem. doi:10.1021/acs.jmedchem.9b00439.Jie Z, et al. (2018) NIK signaling axis regulates dendritic cell function in intestinal immunity and homeostasis. Nat Immunol. 19:1224-1235. doi: 10.1038/s41590-018-0206-z. Epub 2018 Sep 24.Blaquiere N, et al. (2018) A scaffold-hopping approach to discover potent, selective and efficacious inhibitors of NF-κB inducing kinase. J. Med. Chem. doin:10.1021/acs.jmedchem.8b00678.Presentations:H.D. Brightbill. “Looking at the kinetics of transcriptional and extracellular matrix responses to Bleomycin induced lung fibrosis”. IPF Summit 2019, San Diego, CA.

Jan 2018 - Jul 2020

Senior Principal Scientific Researcher(Scientist 4)-Manager, Immunology Discovery Smi Assay Core Lab

South San Francisco, California, Us

Biology Lead for NIK small molecule program.Publications:Brightbill HD, et al. (2017) NF-kB inducing kinase is a therapeutic target for systemic lupus erythematosus. Nature Communications 9:179.Castanedo GM, et al. (2017) Structure-Based Design of Tricyclic NF-κB Inducing Kinase (NIK) Inhibitors That Have High Selectivity over Phosphoinositide-3-kinase (PI3K). J Med Chem. 60:627-640.Li Y, Wang H, et al. (2016) Cell intrinsic role of NF-κB-inducing kinase in regulating T cell mediated immune and autoimmune responses. Scientific Reports 6:22115.Katakam AK, Brightbill H, et al. (2015) Dendritic cells require NIK for CD40-dependent cross-priming of CD8+ T cells. Proc Natl Acad Sci U S A 112:14664-9. Presentations:American Association of Immunologists Conference 2017. Talk and poster, “Selective inhibition of NF-kappaB inducing kinase reduces disease and inflammation in IFNa-accelerated lupus nephritis prone mice.”Keystone Conference 2017, Immune regulation in Autoimmunity and Cancer. Poster, “Selective inhibition of NF-kappaB inducing kinase reduces disease and inflammation in IFNa-accelerated lupus nephritis prone mice.”Cytokine 2016 Conference. Poster, “Selective inhibition of NF-kappaB inducing kinase reduces disease and inflammation in IFNa-accelerated lupus nephritis prone mice.”LEADERSHIP:Summer Intern Mentor, 2017

Sep 2015 - Jan 2018

Principal Scientific Researcher (Scientist 3), Immunology

South San Francisco, California, Us

R&D. Basic research and therapeutics for the treatment of allergy, asthma, and autoimmune disease.THERAPEUTIC PROJECTS:Quilizumab, anti-M1'​-IgE. Late stage, Early Development, IND Filing. 2007, 2009.Small Molecule therapeutic. Late stage transition, 2014.PRESENTATIONS:Keystone Symposium: The NF-κB System in Health and Disease, Keystone, CO, 2014. Poster: Conditional deletion of NF-κB Inducing Kinase (NIK) in adult mice disrupts mature B cell homeostasis and survival.AAI. Honolulu, 2013. Poster presentation entitled "Development of a Conditional NIK knockout Mouse".FOCIS Meeting. San Francisco, 2009. Oral presentation entitled “Therapeutic anti-human membrane IgE antibodies reduce serum IgE and deplete IgE producing cells in vivo” in session entitled “IgE”.Keystone Symposium: Allergy and Asthma. Keystone, C.O. Poster Presentation. January, 2009LEADERSHIP:Summer Intern Mentor, 2011 and 2014Research Trouble Shooters Committee, 2008-2014Department Representative, Radiation Safety Committee, 2015

Jan 2006 - Aug 2015

Associate Specialist

Berkeley, Ca, Us

Research on the role of c-Abl in early B cell development and survival. 2004-2005: National Institutes of Health Fellowship, #CA09179-29.

Jul 2005 - Jan 2006

Post-Doctoral Fellow

Berkeley, Ca, Us

AWARDS:2001-2004. Leukemia and Lymphoma Society Fellowship #5325-02.

May 2000 - Jun 2005

Undergraduate Researcher

Irvine, Ca, Us

PUBLICATIONS:Burger, R.A., et al. (1994) Host-tumor interaction in ovarian cancer. Spontaneous release of Tumor Necrosis Factor and Interluekin-1 inhibitors by purified cell populations form human ovarian carcinoma in vitro. Gynecol. Oncol. 55:294 – 303.Abe, Y., M. et al. (1993) The role of lymphotoxin in the IL-2-driven differentiation of human lymphokine-activated T-killer (T-LAK) cell in vitro. Lymphokine Cytokine Res. 12:279-283.

1992 - 1994 ~2 yrs
Team & coworkers

Colleagues at Amgen

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3 education records

Hans Brightbill education

Ph.D., Microbiology And Immunology

Ucla

B.S. Biological Sciences, B.M. Cello Performance, Biological Sciences, Music

Uc Irvine

Education record

Dana Hills High School
FAQ

Frequently asked questions about Hans Brightbill

Quick answers generated from the profile data available on this page.

What company does Hans Brightbill work for?

Hans Brightbill works for Amgen.

What is Hans Brightbill's role at Amgen?

Hans Brightbill is listed as Scientific Director, In Vivo Pharmacology - Inflammation Research, Amgen at Amgen.

What is Hans Brightbill's email address?

AeroLeads has found 3 work email signals at @gene.com for Hans Brightbill at Amgen.

What is Hans Brightbill's phone number?

AeroLeads has found 1 phone signal(s) with area code 510 for Hans Brightbill at Amgen.

Where is Hans Brightbill based?

Hans Brightbill is based in San Francisco, California, United States while working with Amgen.

What companies has Hans Brightbill worked for?

Hans Brightbill has worked for Amgen, Frontiers In Immunology, Genentech, Uc Berkeley, and Ucla, Department Of Microbiology And Immunology, School Of Medicine.

Who are Hans Brightbill's colleagues at Amgen?

Hans Brightbill's colleagues at Amgen include James Schmidt, Salvador Ruperez, Alli Moeller, Erin Coghlan (Formerly Hau), and Vanessa Alejandra Ibañez Garzon.

How can I contact Hans Brightbill?

You can use AeroLeads to view verified contact signals for Hans Brightbill at Amgen, including work email, phone, and LinkedIn data when available.

What schools did Hans Brightbill attend?

Hans Brightbill holds Ph.D., Microbiology And Immunology from Ucla.

What skills is Hans Brightbill known for?

Hans Brightbill is listed with skills including Immunology, Cell, Molecular Biology, Cell Biology, Cell Culture, Elisa, Science, and Tissue Culture.

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