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Alexandra Y. Kreins, M.D.
Alexandra Y. Kreins, M.D.
Graduate Fellow, The Rockefeller University
Verified email at mail.rockefeller.edu
Title
Cited by
Cited by
Year
Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis
L Liu, S Okada, XF Kong, AY Kreins, S Cypowyj, A Abhyankar, J Toubiana, ...
The Journal of Experimental Medicine 208 (8), 1635, 2011
8782011
Mycobacterial disease and impaired IFN-γ immunity in humans with inherited ISG15 deficiency
D Bogunovic, M Byun, LA Durfee, A Abhyankar, O Sanal, D Mansouri, ...
Science 337 (6102), 1684-1688, 2012
5392012
Functional STAT3 deficiency compromises the generation of human T follicular helper cells
CS Ma, DT Avery, A Chan, M Batten, J Bustamante, S Boisson-Dupuis, ...
Blood, The Journal of the American Society of Hematology 119 (17), 3997-4008, 2012
3422012
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
AY Kreins, MJ Ciancanelli, S Okada, XF Kong, N Ramírez-Alejo, SS Kilic, ...
Journal of Experimental Medicine 212 (10), 1641-1662, 2015
3362015
Induction of nuclear factor-κB and its downstream genes by TNF-α and IL-1β has a pro-apoptotic role in pancreatic beta cells
F Ortis, P Pirot, N Naamane, AY Kreins, J Rasschaert, F Moore, E Theatre, ...
Diabetologia 51, 1213-1225, 2008
2162008
A patient with tyrosine kinase 2 deficiency without hyper-IgE syndrome
SS Kilic, M Hacimustafaoglu, S Boisson-Dupuis, AY Kreins, AV Grant, ...
The Journal of pediatrics 160 (6), 1055-1057, 2012
1132012
A novel form of human STAT1 deficiency impairing early but not late responses to interferons
XF Kong, M Ciancanelli, S Al-Hajjar, L Alsina, T Zumwalt, J Bustamante, ...
Blood 116 (26), 5895, 2010
1042010
Haploinsufficiency at the human IFNGR2 locus contributes to mycobacterial disease
XF Kong, G Vogt, Y Itan, A Macura-Biegun, A Szaflarska, D Kowalczyk, ...
Human molecular genetics 22 (4), 769-781, 2013
732013
Partial IFN-γR2 deficiency is due to protein misfolding and can be rescued by inhibitors of glycosylation
M Moncada-Vélez, R Martinez-Barricarte, D Bogunovic, XF Kong, ...
Blood, The Journal of the American Society of Hematology 122 (14), 2390-2401, 2013
392013
Current and future therapeutic approaches for thymic stromal cell defects
AY Kreins, P Bonfanti, EG Davies
Frontiers in immunology 12, 655354, 2021
312021
Inborn errors of thymic stromal cell development and function
AY Kreins, S Maio, F Dhalla
Seminars in Immunopathology 43 (1), 85-100, 2021
212021
Hematopoietic stem cell transplantation positively affects the natural history of cancer in Nijmegen breakage syndrome
B Wolska-Kusnierz, A Pastorczak, W Fendler, A Wakulinska, ...
Clinical Cancer Research 27 (2), 575-584, 2021
212021
Prospective newborn screening for SCID in Germany: a first analysis by the Pediatric Immunology Working Group (API)
C Speckmann, U Nennstiel, M Hönig, MH Albert, S Ghosh, C Schuetz, ...
Journal of clinical immunology 43 (5), 965-978, 2023
172023
Expanding the nude SCID/CID phenotype associated with FOXN1 homozygous, compound heterozygous, or heterozygous mutations
G Giardino, SO Sharapova, P Ciznar, F Dhalla, L Maragliano, ...
Journal of Clinical Immunology 41, 756-768, 2021
152021
Correction of both immunodeficiency and hypoparathyroidism by thymus transplantation in complete DiGeorge syndrome
AY Kreins, F Junghanns, W Mifsud, K Somana, N Sebire, D Rampling, ...
American Journal of Transplantation 20 (5), 1447-1450, 2020
132020
Long-term immune recovery after hematopoietic stem cell transplantation for ADA deficiency: a single-center experience
AY Kreins, HF Velasco, KN Cheong, K Rao, P Veys, A Worth, HB Gaspar, ...
Journal of clinical immunology, 1-14, 2022
112022
Replacing defective thymus function
AY Kreins, EG Davies
Current Opinion in Allergy and Clinical Immunology 20 (6), 541-548, 2020
112020
Congenital athymia: Unmet needs and practical guidance
E Howley, EG Davies, AY Kreins
Therapeutics and Clinical Risk Management, 239-254, 2023
42023
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases
AT Pagnamenta, C Camps, E Giacopuzzi, JM Taylor, M Hashim, ...
Genome medicine 15 (1), 94, 2023
42023
First use of thymus transplantation in PAX1 deficiency
AY Kreins, A Worth, S Ghosh, RW Mohammed, EG Davies
Journal of Clinical Immunology 43 (6), 1127-1130, 2023
42023
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Articles 1–20