Beziat, V., S. J. Tavernier, Y. H. Chen, C. S. Ma, M. Materna, A. Laurence, J. Staal, D. Aschenbrenner, L. Roels, L. Worley, K. Claes, L. Gartner, L. A. Kohn, M. De Bruyne, K. Schmitz-Abe, L. M. Charbonnier, S. Keles, J. Nammour, N. Vladikine, M. R. L. Maglorius Renkilaraj, Y. Seeleuthner, M. Migaud, J. Rosain, M. Jeljeli, B. Boisson, E. Van Braeckel, J. A. Rosenfeld, H. Dai, L. C. Burrage, D. R. Murdock, B. N. Lambrecht, V. Avettand-Fenoel, T. P. Vogel, N. Undiagnosed Diseases, C. R. Esther, S. Haskologlu, F. Dogu, P. Ciznar, D. Boutboul, M. Ouachee-Chardin, J. Amourette, M. N. Lebras, C. Gauvain, C. Tcherakian, A. Ikinciogullari, R. Beyaert, L. Abel, J. D. Milner, B. Grimbacher, L. J. Couderc, M. J. Butte, A. F. Freeman, E. Catherinot, C. Fieschi, T. A. Chatila, S. G. Tangye, H. H. Uhlig, F. Haerynck, J. L. Casanova, and A. Puel. 2020. Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome. J Exp Med 217. pii: e20191804. doi: 10.1084/jem.20191804.

Erny, D., and M. Prinz. 2020. How microbiota shape microglial phenotypes and epigenetics. Glia. doi: 10.1002/glia.23822. [Epub ahead of print]

Klocperk, A., S. Unger, D. Friedmann, M.  Seidl, K. Zoldan, J. Pfeiffer, O. Hausmann, V. Benes, G. Andrieux, T. Boettler, A. Sediva, B. Bengsch, and K. Warnatz. 2020. Exhausted phenotype of follicular CD8 T cells in CVID. J Allergy Clin Immunol. pii: S0091-6749(20)30333-X. doi: 10.1016/j.jaci.2020.02.025. [Epub ahead of print]

Troilo, A., C. Wehr, I. Janowska, N. Venhoff, J. Thiel, J. Rawluk, N. Frede, J. Staniek, R. Lorenzetti, M. T. Schleyer, G. W. Herget, L. Konstantinidis, M. Erlacher, M. Proietti, N. Camacho-Ordonez, R. E. Voll, B. Grimbacher, K. Warnatz, U. Salzer, and M. Rizzi. 2020. Nonpermissive bone marrow environment impairs early B-cell development in common variable immunodeficiency. Blood 135: 1452-1457.

Marschner, D., M. Falk, N. R. Javorniczky, K. Hanke-Muller, J. Rawluk, Schmitt-Graeff, F. Simonetta, E. Haring, S. Dicks, M. Ku, S. Duquesne, K. Aumann, D. Rafei-Shamsabadi, F. Meiss, P. Marschner, M. Boerries, R. S. Negrin, J. Duyster, R. Zeiser, and N. Kohler. 2020. MicroRNA-146a regulates immune-related adverse events caused by immune checkpoint inhibitors. JCI insight 5. pii: 132334. doi: 10.1172/jci.insight.132334.

Zenke S, Palm MM, Braun J, Gavrilov A, Meiser P, Böttcher JP, Beyersdorf N, Ehl S, Gerard A, Lämmermann T, Schumacher TN, Beltman JB, Rohr JC. 2020. Quorum Regulation via Nested Antagonistic Feedback Circuits Mediated by the Receptors CD28 and CTLA-4 Confers Robustness to T Cell Population Dynamics. Immunity. 52(2):313-327.e7.

Thian, M., B. Hoeger, A. Kamnev, F. Poyer, S. Kostel Bal, M. Caldera, R. Jimenez-Heredia, J. Huemer, W. F. Pickl, M. Gross, S. Ehl, C. L. Lucas, J. Menche, C. Hutter, A. Attarbaschi, L. Dupre, and K. Boztug. 2020. Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation. Haematologica. pii: haematol.2019.231399. doi: 10.3324/haematol.2019.231399. [Epub ahead of print]

Ammann, S., S. Fuchs, L. Martin-Martin, C. N. Castro, B. Spielberger, C. Klemann, R. Elling, M. Heeg, C. Speckmann, I. Hainmann, P. Kaiser-Labusch, G. Horneff, J. Thalhammer, R. G. Bredius, U. Z. Stadt, K. Lehmberg, I. Fuchs, C. von Spee-Mayer, P. Henneke, and S. Ehl. 2020. Functional flow cytometry of monocytes for routine diagnosis of innate primary immunodeficiencies. J Allergy Clin Immunol 145: 434-437 e434.

Binder, B., and R. Thimme. 2020. CD4+ T cell responses in human viral infection: lessons from hepatitis C. J Clin Invest. pii: 133222. doi: 10.1172/JCI133222. [Epub ahead of print]

Cekic, S., J. M. Hartberger, S. Frey-Jakobs, H. Huriyet, M. B. Hortoglu, J. C. Neubauer, Y. Karali, C. D. Abakay, O. Saraydaroglu, T. Cavas, B. Grimbacher, and S. S. Kilic. 2020. Cancer Tendency in a Patient with ZNF341 Deficiency. J Clin Immunol. doi: 10.1007/s10875-020-00756-z. [Epub ahead of print]

Masuda, T., R. Sankowski, O. Staszewski, and M. Prinz. 2020. Microglia Heterogeneity in the Single-Cell Era. Cell Rep 30: 1271-1281.

Castro CN, Rosenzwajg M, Carapito R, Shahrooei M, Konantz M, Khan A, Miao Z, Groß M, Tranchant T, Radosavljevic M, Paul N, Stemmelen T, Pitoiset F, Hirschler A, Nespola B, Molitor A, Rolli V, Pichot A, Faletti LE, Rinaldi B, Friant S, Mednikov M, Karauzum H, Aman MJ, Carapito C, Lengerke C, Ziaee V, Eyaid W, Ehl S, Alroqi F, Parvaneh N, Bahram S. 2020. NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation. J Exp Med. 217(12):e20192275. doi: 10.1084/jem.20192275.