Comorbid and inflammatory characteristics of genetic subtypes of clonal hematopoiesis EK Cook, T Izukawa, S Young, G Rosen, M Jamali, L Zhang, D Johnson, ... Blood advances 3 (16), 2482-2486, 2019 | 109 | 2019 |
Association of clonal hematopoiesis of indeterminate potential with worse kidney function and anemia in two cohorts of patients with advanced chronic kidney disease C Vlasschaert, AJM McNaughton, M Chong, EK Cook, W Hopman, ... Journal of the American Society of Nephrology 33 (5), 985-995, 2022 | 55 | 2022 |
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability A Heidari, C Tongsook, R Najafipour, L Musante, N Vasli, M Garshasbi, ... Human molecular genetics 24 (20), 5697-5710, 2015 | 40 | 2015 |
Interplay between maternal Slc6a4 mutation and prenatal stress: a possible mechanism for autistic behavior development CP Sjaarda, P Hecht, AJM McNaughton, A Zhou, ML Hudson, MJ Will, ... Scientific Reports 7 (1), 8735, 2017 | 34 | 2017 |
Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort DB Callaghan, S Rogic, PPC Tan, K Calli, Y Qiao, R Baldwin, M Jacobson, ... Clinical genetics 96 (3), 199-206, 2019 | 21 | 2019 |
Schizophrenia risk conferred by rare protein-truncating variants is conserved across diverse human populations D Liu, D Meyer, B Fennessy, C Feng, E Cheng, JS Johnson, YJ Park, ... Nature genetics 55 (3), 369-376, 2023 | 18 | 2023 |
Exome sequencing identifies de novo splicing variant in XRCC6 in sporadic case of autism CP Sjaarda, S Wood, AJM McNaughton, S Taylor, ML Hudson, X Liu, ... Journal of Human Genetics 65 (3), 287-296, 2020 | 9 | 2020 |
Homozygosity for the 10-repeat dopamine transporter (DAT1) allele is associated with reduced EEG response in males with ASD CP Sjaarda, M Sabbagh, S Wood, J Ward-King, AJM McNaughton, ... Research in Autism Spectrum Disorders 60, 25-35, 2019 | 4 | 2019 |
Noninvasive prenatal detection of trisomy 21 by targeted semiconductor sequencing: a technical feasibility study Y Xi, A Arbabi, AJM McNaughton, A Hamilton, D Hull, H Perras, T Chiu, ... Fetal diagnosis and therapy 42 (4), 302-310, 2017 | 2 | 2017 |
Impact of temperature on the expression of Kennedy Pathway genes in developing soybean seeds AJM McNaughton, BJ Shelp, I Rajcan Canadian journal of plant science 95 (1), 87-101, 2015 | 2 | 2015 |
Evaluation of genes encoding the enzymes of the Kennedy pathway in soybeans with altered fatty acid profiles AJM McNaughton University of Guelph, 2012 | 2 | 2012 |
Neutrophil-mediated innate immune resistance to bacterial pneumonia is dependent on Tet2 function C Quin, EN DeJong, EK Cook, YZ Luo, C Vlasschaert, S Sadh, ... The Journal of Clinical Investigation, 2024 | | 2024 |
The Impact of Clonal Hematopoiesis on Clinical Outcomes and Clonal Dynamics in Older Lymphoma Patients Receiving Chemotherapy R Buckstein, O Lopes, AJM McNaughton, MC Cheung, L Mozessohn, ... Blood 142, 442, 2023 | | 2023 |
Chronic TNF in the Aging Microenvironment Exacerbates TET2-loss-of-Function Myeloid Expansion C Quin, E DeJong, AJM McNaughton, MM Buttigieg, S Basrai, S Abelson, ... Blood 142, 938, 2023 | | 2023 |
Topic: AS07-Singular Entities/Subtypes/AS07a-ARCH, CCUS, ICUS: THE IMPACT OF CHIP ON CHEMOTHERAPY-RELATED OUTCOMES AND CLONAL DYNAMICS IN OLDER LYMPHOMA PATIENTS R Buckstein, M Cheung, L Mozessohn, L Chodirker, K Imrie, N Berinstein, ... Leukemia Research 128, 107239, 2023 | | 2023 |
A Lower Frequency of Spliceosome Mutations Distinguishes Clonal Cytopenias of Undetermined Significance From Low-Risk Myelodysplastic Syndromes, Despite Inherent Similarities … CK Ferrone, AJM McNaughton, I Rashedi, B Ring, R Buckstein, H Tsui, ... Modern Pathology 36 (3), 100068, 2023 | | 2023 |
Germline and Somatic Mutations in DNA Methyltransferase 3A (DNMT3A) Predispose to Pulmonary Arterial Hypertension (PAH) in Humans and Mice: Implications for Associated PAH R Al-Qazazi, IM Emon, F Potus, AY Martin, PDA Lima, C Vlasschaert, ... medRxiv, 2023.12. 30.23300391, 2023 | | 2023 |
CCUS and Low-Risk MDS Are Inherently Similar, Sharing Clonal and Clinical Features CK Ferrone, AJM McNaughton, I Rashedi, R Buckstein, H Tsui, MJ Rauh Blood 140 (Supplement 1), 6915-6916, 2022 | | 2022 |
U2AF1S34/Q157 Variants Detected in cis Arise Sequentially in an MDS Patient With Serial Sequencing Spanning 18 Years CK Ferrone, AJM McNaughton, F Vincelli, P Zuzarte, D Lee, HE Feilotter, ... HemaSphere 6 (10), e779, 2022 | | 2022 |
Clinical Utility of Hematopathologist-Triaged NGS Testing When Investigating Patients with Suspected MDS CK Ferrone, AJM McNaughton, I Rashedi, H Tsui, MJ Rauh Blood 138, 4675, 2021 | | 2021 |