Christie‐Ann McCarl

Author

Christie‐Ann McCarl

NYU Langone Health

Also Known As

Christie-Ann McCarl, Christie-Ann Mccarl, Christie‐Ann McCarl

Publications

914

Citations

H-Index

Concepts

All Affiliations

NYU Langone Health Biogen (United States)University of Freiburg Harvard University New York University

About

Christie‐Ann McCarl is an author at NYU Langone Health specializing in immunology, medicine, and signal transduction.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	464
2	Immunology	3	3	464
3	Cell Biology	2	2	148
4	Cellular Physiology	1	1	28
5	Molecular Medicine	1	1	316

Christie‐Ann McCarl

Publications

896

Citations

H-Index

Page 1

	Year	Citations
ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia Christie‐Ann McCarl, Capucine Pïcard, Sara Khalil, Journal of Allergy and Clinical Immunology MedicinePathogenesisImmunologyOrai1 DeficiencyPathology	2009	316
ORAI1-mediated calcium influx is required for human cytotoxic lymphocyte degranulation and target cell lysis Andrea Maul‐Pavicic, Samuel C. C. Chiang, Anne Rensing‐Ehl, Proceedings of the National Academy of Sciences	2011	213
R93W mutation in Orai1 causes impaired calcium influx in platelets Wolfgang Bergmeier, Masatsugu Oh‐hora, Christie‐Ann McCarl, Blood	2008	120
T‐cell‐specific deletion of STIM1 and STIM2 protects mice from EAE by impairing the effector functions of Th1 and Th17 cells Jian Ma, Christie‐Ann McCarl, Sara Khalil, European Journal of Immunology T-regulatory CellImmune RegulationImmunologyImmunologic MechanismCd4 T Cell Responses	2010	120
MOG autoantibodies trigger a tightly-controlled FcR and BTK-driven microglia proliferative response Kathryn Pellerin, Stephen Rubino, Jeremy C. Burns, Brain	2021	59
Effect of in vivo Hydroxychloroquine and ex vivo Anti-BDCA2 mAb Treatment on pDC IFNα Production From Patients Affected With Cutaneous Lupus Erythematosus Agnès Gardet, Alex Pellerin, Christie‐Ann McCarl, Frontiers in Immunology	2019	40
Interference with <scp>C</scp>a<sup>2+</sup> release activated <scp>C</scp>a<sup>2+</sup> (<scp>CRAC</scp>) channel function delays <scp>T</scp>‐cell arrest in vivo Janelle Waite, Santosha A. Vardhana, Patrick J. Shaw, European Journal of Immunology Channel FunctionT-regulatory CellImmunologyImmunologic MechanismAntigen Processing	2013	28

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