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Aidin Foroutan
Aidin Foroutan
Department of AFNS, University of Alberta
Verified email at ualberta.ca
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Cited by
Cited by
Year
Chemical composition of commercial cow’s milk
A Foroutan, AC Guo, R Vazquez-Fresno, M Lipfert, L Zhang, J Zheng, ...
Journal of agricultural and food chemistry 67 (17), 4897-4914, 2019
2092019
The bovine metabolome
A Foroutan, C Fitzsimmons, R Mandal, H Piri-Moghadam, J Zheng, ...
Metabolites 10 (6), 233, 2020
1112020
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
MA Levy, H McConkey, J Kerkhof, M Barat-Houari, S Bargiacchi, ...
Human Genetics and Genomics Advances 3 (1), 2022
1032022
Detection of Candidatus Phytoplasma aurantifolia with a quantum dots fret-based biosensor
F Rad, A Mohsenifar, M Tabatabaei, MR Safarnejad, F Shahryari, ...
Journal of Plant Pathology, 525-534, 2012
962012
Functional correlation of genome‐wide DNA methylation profiles in genetic neurodevelopmental disorders
MA Levy, R Relator, H McConkey, E Pranckeviciene, J Kerkhof, ...
Human mutation 43 (11), 1609-1628, 2022
322022
Serum metabolite biomarkers for predicting residual feed intake (RFI) of young angus bulls
A Foroutan, C Fitzsimmons, R Mandal, MV Berjanskii, DS Wishart
Metabolites 10 (12), 491, 2020
262020
Childhood-onset dystonia-causing KMT2B variants result in a distinctive genomic hypermethylation profile
A Ciolfi, A Foroutan, A Capuano, L Pedace, L Travaglini, S Pizzi, ...
Clinical epigenetics 13 (1), 157, 2021
242021
Evaluation of anti-phytoplasma properties of surfactin and tetracycline towards lime witches' broom disease using real-time PCR
N Askari, GS Jouzani, M Mousivand, AH Nazari, S Abbasalizadeh, ...
Journal of Microbiology and Biotechnology 21 (1), 81-88, 2011
212011
SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile
R Al-Jawahiri, A Foroutan, J Kerkhof, H McConkey, M Levy, ...
Genetics in medicine 24 (6), 1261-1273, 2022
202022
Could gene therapy cure HIV?
M Sheykhhasan, A Foroutan, H Manoochehri, SG Khoei, N Poondla, ...
Life Sciences 277, 119451, 2021
162021
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene
MR Pérez Baca, EZ Jacobs, L Vantomme, P Leblanc, E Bogaert, ...
medRxiv, 2023.05. 22.23289895, 2023
82023
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome
A Foroutan, S Haghshenas, P Bhai, MA Levy, J Kerkhof, H McConkey, ...
International journal of molecular sciences 23 (3), 1815, 2022
82022
Clinical findings and a DNA methylation signature in kindreds with alterations in ZNF711
J Wang, A Foroutan, E Richardson, SA Skinner, J Reilly, J Kerkhof, ...
European Journal of Human Genetics 30 (4), 420-427, 2022
72022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders. HGG Adv. 3, 100075
MA Levy, H McConkey, J Kerkhof, M Barat-Houari, S Bargiacchi, ...
52021
Serum metabolite biomarkers for predicting residual feed intake (RFI) of young angus bulls. Metabolites 10, 491
A Foroutan, C Fitzsimmons, R Mandal, MV Berjanskii, DS Wishart
52020
Impact of prenatal maternal nutrition and parental residual feed intake (RFI) on mRNA abundance of metabolic drivers of growth and development in young Angus bulls
A Foroutan, J Devos, DS Wishart, C Li, M Colazo, J Kastelic, J Thundathil, ...
Livestock Science 243, 104365, 2021
42021
Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy
S Haghshenas, A Foroutan, P Bhai, MA Levy, R Relator, J Kerkhof, ...
European Journal of Human Genetics 31 (8), 879-886, 2023
32023
Exploring biological impacts of prenatal nutrition and selection for residual feed intake on beef cattle using Omics technologies: A review
A Foroutan, DS Wishart, C Fitzsimmons
Frontiers in Genetics 12, 720268, 2021
32021
Food Constituent and Food Metabolite Databases
A Foroutan, DS Wishart
Elsevier, 2021
32021
Single-cell chromatin accessibility data combined with GWAS improves detection of relevant cell types in 59 complex phenotypes
AC Das, A Foroutan, B Qian, N Hosseini Naghavi, K Shabani, ...
International Journal of Molecular Sciences 23 (19), 11456, 2022
22022
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