Segui
Mohammed Uddin
Mohammed Uddin
Associate Professor, MBRU, Dubai, UAE; Scientist, Cellular Intelligent Lab,GenomeArc Inc, Toronto
Email verificata su mbru.ac.ae
Titolo
Citata da
Citata da
Anno
Autoantibodies against type I IFNs in patients with life-threatening COVID-19
P Bastard, LB Rosen, Q Zhang, E Michailidis, HH Hoffmann, Y Zhang, ...
Science 370 (6515), eabd4585, 2020
14052020
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
Q Zhang, P Bastard, Z Liu, J Le Pen, M Moncada-Velez, J Chen, M Ogishi, ...
Science 370 (6515), eabd4570, 2020
12402020
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RKC Yuen, D Merico, M Bookman, JL Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
5472017
Whole-genome sequencing of quartet families with autism spectrum disorder
RKC Yuen, B Thiruvahindrapuram, D Merico, S Walker, K Tammimies, ...
Nature medicine 21 (2), 185-191, 2015
4932015
Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing
Y Jiang, RKC Yuen, X Jin, M Wang, N Chen, X Wu, J Ju, J Mei, Y Shi, ...
The American Journal of Human Genetics 93 (2), 249-263, 2013
4612013
Molecular diagnostic yield of chromosomal microarray analysis and whole-exome sequencing in children with autism spectrum disorder
K Tammimies, CR Marshall, S Walker, G Kaur, B Thiruvahindrapuram, ...
Jama 314 (9), 895-903, 2015
3262015
The COVID-19 host genetics initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic
COVID-19 Host Genetics Initiative
European Journal of Human Genetics 28 (6), 715, 2020
2442020
SARS-CoV-2/COVID-19: viral genomics, epidemiology, vaccines, and therapeutic interventions
M Uddin, F Mustafa, TA Rizvi, T Loney, H Al Suwaidi, AHH Al-Marzouqi, ...
Viruses 12 (5), 526, 2020
1952020
Genome-wide characteristics of de novo mutations in autism
RKC Yuen, D Merico, H Cao, G Pellecchia, B Alipanahi, ...
NPJ genomic medicine 1 (1), 1-10, 2016
1892016
Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
ET Lim, M Uddin, S De Rubeis, Y Chan, AS Kamumbu, X Zhang, ...
Nature neuroscience 20 (9), 1217-1224, 2017
1852017
Mapping the human genetic architecture of COVID-19.
COVID-19 Host Genetics Initiative
Springer Science and Business Media LLC, 2021
1662021
Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder
M Uddin, K Tammimies, G Pellecchia, B Alipanahi, P Hu, Z Wang, D Pinto, ...
Nature genetics 46 (7), 742-747, 2014
1522014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes
AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ...
Human molecular genetics 23 (10), 2752-2768, 2014
1392014
Sonic hedgehog (Shh) signaling promotes tumorigenicity and stemness via activation of epithelial‐to‐mesenchymal transition (EMT) in bladder cancer
SS Islam, RB Mokhtari, AS Noman, M Uddin, MZ Rahman, MA Azadi, ...
Molecular carcinogenesis 55 (5), 537-551, 2016
1232016
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
1082021
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
862021
Life-threatening COVID-19: defective interferons unleash excessive inflammation
Q Zhang, P Bastard, A Bolze, E Jouanguy, SY Zhang, CHG Effort, A Cobat, ...
Med 1 (1), 14-20, 2020
752020
Artificial intelligence for precision medicine in neurodevelopmental disorders
M Uddin, Y Wang, M Woodbury-Smith
NPJ Digital Medicine 2 (1), 1-10, 2019
742019
ARTS1 polymorphisms are associated with ankylosing spondylitis in Koreans
CB Choi, TH Kim, JB Jun, HS Lee, SC Shim, B Lee, A Pope, M Uddin, ...
Annals of the rheumatic diseases 69 (3), 582-584, 2010
742010
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy
M Zarrei, DL Fehlings, K Mawjee, L Switzer, B Thiruvahindrapuram, ...
Genetics in Medicine 20 (2), 172-180, 2018
702018
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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