Статии с изисквания за обществен достъп - Worrawat EngchuanНаучете повече
Налице някъде: 27
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
Genome-wide detection of tandem DNA repeats that are expanded in autism
B Trost, W Engchuan, CM Nguyen, B Thiruvahindrapuram, E Dolzhenko, ...
Nature 586 (7827), 80-86, 2020
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
Genomic architecture of autism from comprehensive whole-genome sequence annotation
B Trost, B Thiruvahindrapuram, AJS Chan, W Engchuan, ...
Cell 185 (23), 4409-4427. e18, 2022
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
A large data resource of genomic copy number variation across neurodevelopmental disorders
M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ...
NPJ genomic medicine 4 (1), 26, 2019
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
Genetic contributors to risk of schizophrenia in the presence of a 22q11. 2 deletion
I Cleynen, W Engchuan, MS Hestand, T Heung, AM Holleman, ...
Molecular psychiatry 26 (8), 4496-4510, 2021
Изисквания: Swiss National Science Foundation, US National Institutes of Health …
Machine learning methodologies versus cardiovascular risk scores, in predicting disease risk
AC Dimopoulos, M Nikolaidou, FF Caballero, W Engchuan, ...
BMC medical research methodology 18, 1-11, 2018
Изисквания: European Commission
Advanced analytical methodologies for measuring healthy ageing and its determinants, using factor analysis and machine learning techniques: the ATHLOS project
FF Caballero, G Soulis, W Engchuan, A Sánchez-Niubó, H Arndt, ...
Scientific reports 7 (1), 43955, 2017
Изисквания: US National Institutes of Health, European Commission
Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences
R Manshaei, D Merico, MS Reuter, W Engchuan, BA Mojarad, ...
Frontiers in genetics 11, 957, 2020
Изисквания: Canadian Institutes of Health Research
Neuron-specific protein network mapping of autism risk genes identifies shared biological mechanisms and disease-relevant pathologies
N Murtaza, AA Cheng, CO Brown, DP Meka, S Hong, JA Uy, J El-Hajjar, ...
Cell reports 41 (8), 2022
Изисквания: Canadian Institutes of Health Research, Natural Sciences and Engineering …
Genome-wide tandem repeat expansions contribute to schizophrenia risk
BA Mojarad, W Engchuan, B Trost, I Backstrom, Y Yin, ...
Molecular Psychiatry 27 (9), 3692-3698, 2022
Изисквания: Canadian Institutes of Health Research, Genome Canada, Natural Sciences and …
Sociodemographic indicators of health status using a machine learning approach and data from the English longitudinal study of aging (ELSA)
W Engchuan, AC Dimopoulos, S Tyrovolas, FF Caballero, ...
Medical science monitor: international medical journal of experimental and …, 2019
Изисквания: UK Economic and Social Research Council, UK Medical Research Council …
FAN1 exo-not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instability
AL Deshmukh, MC Caron, M Mohiuddin, S Lanni, GB Panigrahi, M Khan, ...
Cell Reports 37 (10), 2021
Изисквания: Canadian Institutes of Health Research, Natural Sciences and Engineering …
Performance of case-control rare copy number variation annotation in classification of autism
W Engchuan, K Dhindsa, AC Lionel, SW Scherer, JH Chan, D Merico
BMC medical genomics 8, 1-10, 2015
Изисквания: Canadian Institutes of Health Research, Genome Canada
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder
AJS Chan, W Engchuan, MS Reuter, Z Wang, B Thiruvahindrapuram, ...
Nature Communications 13 (1), 6463, 2022
Изисквания: Canadian Institutes of Health Research, Genome Canada, Autism Speaks Inc, USA
Copy number variation in fetal alcohol spectrum disorder
M Zarrei, GG Hicks, JN Reynolds, B Thiruvahindrapuram, W Engchuan, ...
Biochemistry and Cell Biology 96 (2), 161-166, 2018
Изисквания: Canadian Institutes of Health Research, Genome Canada
Gene copy number variation and pediatric mental health/neurodevelopment in a general population
M Zarrei, CL Burton, W Engchuan, EJ Higginbotham, J Wei, S Shaikh, ...
Human Molecular Genetics 32 (15), 2411-2421, 2023
Изисквания: Canadian Institutes of Health Research, Genome Canada, UK Medical Research …
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
J Wen, B Trost, W Engchuan, M Halvorsen, LM Pallotto, A Mitina, ...
Molecular Psychiatry 28 (1), 475-482, 2023
Изисквания: US National Institutes of Health, Canadian Institutes of Health Research …
Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy
DL Fehlings, M Zarrei, W Engchuan, N Sondheimer, ...
Nature genetics 56 (4), 585-594, 2024
Изисквания: Genome Canada
A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21. 22 microdeletion syndrome
M Zarrei, D Merico, B Kellam, W Engchuan, T Scriver, R Jokhan, ...
American Journal of Medical Genetics Part A 173 (5), 1287-1293, 2017
Изисквания: Canadian Institutes of Health Research, Genome Canada, Natural Sciences and …
Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathy
A Mitina, M Khan, R Lesurf, Y Yin, W Engchuan, O Hamdan, G Pellecchia, ...
EBioMedicine 101, 2024
Изисквания: Canadian Institutes of Health Research, Genome Canada, Heart and Stroke …
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