Qiang Pan-Hammarström
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Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans
U Salzer, HM Chapel, ADB Webster, Q Pan-Hammarström, ...
Nature genetics 37 (8), 820-828, 2005
Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity
G Lopez-Herrera, G Tampella, Q Pan-Hammarström, P Herholz, ...
The American Journal of Human Genetics 90 (6), 986-1001, 2012
B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans
K Warnatz, U Salzer, M Rizzi, B Fischer, S Gutenberger, J Böhm, ...
Proceedings of the National Academy of Sciences 106 (33), 13945-13950, 2009
Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency
Q Pan-Hammarström, U Salzer, L Du, J Björkander, ...
Nature genetics 39 (4), 429-430, 2007
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
U Salzer, C Bacchelli, S Buckridge, Q Pan-Hammarström, S Jennings, ...
Blood 113 (9), 1967-1976, 2009
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases
JD Rioux, P Goyette, TJ Vyse, L Hammarström, MMA Fernando, T Green, ...
Proceedings of the National Academy of Sciences 106 (44), 18680-18685, 2009
In situ delivery of passive immunity by lactobacilli producing single-chain antibodies
C Krüger, Y Hu, Q Pan, H Marcotte, A Hultberg, D Delwar, PJ van Dalen, ...
Nature biotechnology 20 (7), 702-706, 2002
Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR
S Borte, U von Döbeln, A Fasth, N Wang, M Janzi, J Winiarski, U Sack, ...
Blood, The Journal of the American Society of Hematology 119 (11), 2552-2555, 2012
B cell super-enhancers and regulatory clusters recruit AID tumorigenic activity
J Qian, Q Wang, M Dose, N Pruett, KR Kieffer-Kwon, W Resch, G Liang, ...
Cell 159 (7), 1524-1537, 2014
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency
RC Ferreira, Q Pan-Hammarström, RR Graham, V Gateva, G Fontán, ...
Nature genetics 42 (9), 777, 2010
Role for Msh5 in the regulation of Ig class switch recombination
H Sekine, RC Ferreira, Q Pan-Hammarström, RR Graham, B Ziemba, ...
Proceedings of the National Academy of Sciences 104 (17), 7193-7198, 2007
Selective IgA deficiency in early life: association to infections and allergic diseases during childhood
M Janzi, I Kull, R Sjöberg, J Wan, E Melén, N Bayat, E Östblom, ...
Clinical immunology 133 (1), 78-85, 2009
Lactobacilli expressing variable domain of llama heavy-chain antibody fragments (lactobodies) confer protection against rotavirus-induced diarrhea
N Pant, A Hultberg, Y Zhao, L Svensson, Q Pan-Hammarström, ...
The Journal of infectious diseases 194 (11), 1580-1588, 2006
Risk for myasthenia gravis maps to a 151Pro→Ala change in TNIP1 and to human leukocyte antigen‐B*08
PK Gregersen, R Kosoy, AT Lee, J Lamb, J Sussman, D McKee, ...
Annals of neurology 72 (6), 927-935, 2012
Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells
Q Pan-Hammarström, AM Jones, A Lähdesmäki, W Zhou, RA Gatti, ...
The Journal of experimental medicine 201 (2), 189-194, 2005
Artiodactyl IgD: the missing link
Y Zhao, I Kacskovics, Q Pan, DA Liberles, J Geli, SK Davis, H Rabbani, ...
The Journal of Immunology 169 (8), 4408-4416, 2002
Molecular basis of IgG subclass deficiency.
Q Pan, L Hammarström
Immunological reviews 178, 99-110, 2000
Genetic landscapes of relapsed and refractory diffuse large B-cell lymphomas
RD Morin, S Assouline, M Alcaide, A Mohajeri, RL Johnston, L Chong, ...
Clinical cancer research 22 (9), 2290-2300, 2016
AID from bony fish catalyzes class switch recombination
VM Barreto, Q Pan-Hammarstrom, Y Zhao, L Hammarstrom, Z Misulovin, ...
The Journal of experimental medicine 202 (6), 733-738, 2005
Pan-cancer analysis of whole genomes
I The, TPCA of Whole, Genomes Consortium
Nature 578 (7793), 82, 2020
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