Follow
Ashish marwaha
Ashish marwaha
University of Calgary
Verified email at ahs.ca
Title
Cited by
Cited by
Year
Cutting edge: increased Il-17–secreting T cells in children with new-onset type 1 diabetes
AK Marwaha, SQ Crome, C Panagiotopoulos, KB Berg, H Qin, Q Ouyang, ...
The Journal of Immunology 185 (7), 3814-3818, 2010
2812010
TH17 cells in autoimmunity and immunodeficiency: protective or pathogenic?
AK Marwaha, NJ Leung, AN McMurchy, MK Levings
Frontiers in immunology 3, 129, 2012
1752012
Combined immunodeficiency associated with homozygous MALT1 mutations
ML McKinnon, J Rozmus, SY Fung, AF Hirschfeld, KL Del Bel, L Thomas, ...
Journal of allergy and clinical immunology 133 (5), 1458-1462. e7, 2014
1272014
Profiling of circulating microRNAs in children with recent onset of type 1 diabetes
S Erener, A Marwaha, R Tan, C Panagiotopoulos, TJ Kieffer
JCI insight 2 (4), 2017
1142017
Targeting the IL-17/IFN-γ axis as a potential new clinical therapy for type 1 diabetes
AK Marwaha, S Tan, JP Dutz
Clinical immunology 154 (1), 84-89, 2014
512014
Treg gene signatures predict and measure type 1 diabetes trajectory
AM Pesenacker, V Chen, J Gillies, C Speake, AK Marwaha, A Sun, ...
JCI insight 4 (6), 2019
332019
Pre-diagnostic genotyping identifies T1D subjects with impaired Treg IL-2 signaling and an elevated proportion of FOXP3+ IL-17+ cells
AK Marwaha, C Panagiotopoulos, CM Biggs, S Staiger, KL Del Bel, ...
Genes & Immunity 18 (1), 15-21, 2017
242017
The point‐of‐care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning
A Marwaha, D Chitayat, MS Meyn, R Mendoza‐Londono, L Chad
American Journal of Medical Genetics Part A 185 (4), 1151-1158, 2021
212021
Two cases of carbonic anhydrase VA deficiency—An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcome
A Marwaha, J Ibrahim, T Rice, N Hamwi, CA Rupar, D Cresswell, ...
JIMD reports 57 (1), 9-14, 2021
122021
Congenital hypothyroidism, cardiac defects, and pancreatic agenesis in an infant with GATA6 mutation
N Raghuram, A Marwaha, MLC Greer, E Gauda, D Chitayat
American Journal of Medical Genetics Part A 182 (6), 1496-1499, 2020
112020
A chromosomal duplication encompassing interleukin-33 causes a novel hyper IgE phenotype characterized by eosinophilic esophagitis and generalized autoimmunity
AK Marwaha, R Laxer, M Liang, AM Muise, T Eiwegger, E Pope, ...
Gastroenterology 163 (2), 510-513. e3, 2022
92022
A phase 1b open-label dose-finding study of ustekinumab in young adults with type 1 diabetes
AK Marwaha, S Chow, AM Pesenacker, L Cook, A Sun, SA Long, ...
Immunotherapy advances 2 (1), ltab022, 2022
92022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome
RY Oh, AR Deshwar, A Marwaha, N Sabha, M Tropak, H Hou, KE Yuki, ...
Genetics in Medicine 24 (11), 2399-2407, 2022
62022
Progressive decline of T and B cell numbers and function in a patient with CDC42 deficiency
P Kashani, A Marwaha, S Feanny, VHD Kim, AR Atkinson, M Leon-Ponte, ...
Immunologic Research 69, 53-58, 2021
62021
Genotype–phenotype data from a case series of patients with mosaic neurofibromatosis type 1
A Marwaha, J Malach, A Shugar, S Hedges, M Weinstein, PC Parkin, ...
British Journal of Dermatology 179 (5), 1216-1217, 2018
62018
CCL3 and CCL4 secretion by T regulatory cells attracts CD4+ and CD8+ T cells (P1077)
A Wang, S Patterson, A Marwaha, R Tan, M Levings
The Journal of Immunology 190 (1_Supplement), 121.10-121.10, 2013
62013
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
C Gehin, MA Lone, W Lee, L Capolupo, S Ho, AM Adeyemi, EH Gerkes, ...
The Journal of clinical investigation 133 (10), 2023
52023
The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13‐related disorder
A Marwaha, G Costain, C Cytrynbaum, R Mendoza‐Londono, L Chad, ...
American Journal of Medical Genetics Part A 188 (5), 1368-1375, 2022
42022
Phase II multicentre, double-blind, randomised trial of ustekinumab in adolescents with new-onset type 1 diabetes (USTEK1D): trial protocol
JW Gregory, K Carter, WY Cheung, G Holland, J Bowen-Morris, S Luzio, ...
BMJ open 11 (10), e049595, 2021
32021
Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancy
BR Earl, M Szybowska, A Marwaha, V Belostotsky, I Lara‐Corrales, ...
The Journal of Dermatology 47 (8), 898-902, 2020
32020
The system can't perform the operation now. Try again later.
Articles 1–20