Articles with public access mandates - Dan AndrewsLearn more
Not available anywhere: 5
Brief Report: Identification of a Pathogenic Variant in TREX1 in Early‐Onset Cerebral Systemic Lupus Erythematosus by Whole‐Exome Sequencing
JI Ellyard, R Jerjen, JL Martin, AYS Lee, MA Field, SH Jiang, J Cappello, ...
Arthritis & Rheumatology 66 (12), 3382-3386, 2014
Mandates: National Health and Medical Research Council, Australia
Understanding the immunological impact of the human mutation explosion
TD Andrews, G Sjollema, CC Goodnow
Trends in immunology 34 (3), 99-106, 2013
Mandates: US National Institutes of Health, National Health and Medical Research …
Systemic lupus erythematosus: A new autoimmune disorder in Kabuki syndrome
T Arsov, M Sestan, N Cekada, M Frkovic, D Andrews, Y He, N Shen, ...
European journal of medical genetics 62 (6), 103538, 2019
Mandates: National Health and Medical Research Council, Australia, National Natural …
Expanding the clinical spectrum of pathogenic variation in NR2F2: Asplenia
T Arsov, J Kelecic, SH Frkovic, M Sestan, N Kifer, D Andrews, M Adamski, ...
European journal of medical genetics 64 (12), 104347, 2021
Mandates: National Health and Medical Research Council, Australia, National Natural …
Increased burden of rare variants in genes of the endosomal Toll-like receptor pathway in patients with systemic lupus erythematosus
TN Lea-Henry, A Chuah, M Stanley, V Athanasopoulos, MR Starkey, ...
Lupus 30 (11), 1756-1763, 2021
Mandates: National Health and Medical Research Council, Australia
Available somewhere: 34
Global variation in copy number in the human genome
R Redon, S Ishikawa, KR Fitch, L Feuk, GH Perry, TD Andrews, H Fiegler, ...
nature 444 (7118), 444-454, 2006
Mandates: Genome Canada
Origins and functional impact of copy number variation in the human genome
DF Conrad, D Pinto, R Redon, L Feuk, O Gokcumen, Y Zhang, J Aerts, ...
Nature 464 (7289), 704-712, 2010
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls
Nature 464 (7289), 713-720, 2010
Mandates: Versus Arthritis, UK, British Heart Foundation
TLR7 gain-of-function genetic variation causes human lupus
GJ Brown, PF Cañete, H Wang, A Medhavy, J Bones, JA Roco, Y He, ...
Nature 605 (7909), 349-356, 2022
Mandates: US National Institutes of Health, National Health and Medical Research …
Comparison of predicted and actual consequences of missense mutations
LA Miosge, MA Field, Y Sontani, V Cho, S Johnson, A Palkova, ...
Proceedings of the National Academy of Sciences 112 (37), E5189-E5198, 2015
Mandates: US National Institutes of Health, National Health and Medical Research …
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization
JC Marioni, NP Thorne, A Valsesia, T Fitzgerald, R Redon, H Fiegler, ...
Genome biology 8, 1-14, 2007
Mandates: Cancer Research UK
Atypical B cells are part of an alternative lineage of B cells that participates in responses to vaccination and infection in humans
HJ Sutton, R Aye, AH Idris, R Vistein, E Nduati, O Kai, J Mwacharo, X Li, ...
Cell reports 34 (6), 2021
Mandates: US National Institutes of Health, National Health and Medical Research …
ATP11C is critical for the internalization of phosphatidylserine and differentiation of B lymphocytes
M Yabas, CE Teh, S Frankenreiter, D Lal, CM Roots, B Whittle, ...
Nature Immunology 12 (5), 441-449, 2011
Mandates: US National Institutes of Health, German Research Foundation
IRF2 transcriptionally induces GSDMD expression for pyroptosis
N Kayagaki, BL Lee, IB Stowe, OS Kornfeld, K O'Rourke, KM Mirrashidi, ...
Science signaling 12 (582), eaax4917, 2019
Mandates: US National Institutes of Health
Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models
TD Andrews, B Whittle, MA Field, B Balakishnan, Y Zhang, Y Shao, V Cho, ...
Open biology 2 (5), 120061, 2012
Mandates: US National Institutes of Health
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus
SH Jiang, V Athanasopoulos, JI Ellyard, A Chuah, J Cappello, A Cook, ...
Nature communications 10 (1), 2201, 2019
Mandates: National Health and Medical Research Council, Australia
B cell survival, surface BCR and BAFFR expression, CD74 metabolism, and CD8− dendritic cells require the intramembrane endopeptidase SPPL2A
H Bergmann, M Yabas, A Short, L Miosge, N Barthel, CE Teh, CM Roots, ...
Journal of Experimental Medicine 210 (1), 31-40, 2013
Mandates: US National Institutes of Health, Australian Research Council, National …
IgD attenuates the IgM-induced anergy response in transitional and mature B cells
Z Sabouri, S Perotti, E Spierings, P Humburg, M Yabas, H Bergmann, ...
Nature communications 7 (1), 13381, 2016
Mandates: US National Institutes of Health, National Health and Medical Research …
Gain-of-function IKBKB mutation causes human combined immune deficiency
C Cardinez, B Miraghazadeh, K Tanita, E Da Silva, A Hoshino, S Okada, ...
Journal of Experimental Medicine 215 (11), 2715-2724, 2018
Mandates: National Health and Medical Research Council, Australia
Interplay of dFOXO and Two ETS-Family Transcription Factors Determines Lifespan in Drosophila melanogaster
N Alic, ME Giannakou, I Papatheodorou, MP Hoddinott, TD Andrews, ...
PLoS genetics 10 (9), e1004619, 2014
Mandates: Wellcome Trust
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