ติดตาม
Worrawat Engchuan
Worrawat Engchuan
The Centre for Applied Genomics, The Hospital for Sick Children
ยืนยันอีเมลแล้วที่ sickkids.ca
ชื่อ
อ้างโดย
อ้างโดย
ปี
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
8392017
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
2012020
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
1602022
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
1562019
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
1292021
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
1082018
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
972017
Identification of novel microRNAs in Hevea brasiliensisand computational prediction of their targets
V Gébelin, X Argout, W Engchuan, B Pitollat, C Duan, P Montoro, ...
BMC Plant Biology 12, 1-18, 2012
632012
Pathway activity transformation for multi-class classification of lung cancer datasets
W Engchuan, JH Chan
Neurocomputing 165, 81-89, 2015
462015
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
372020
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
332022
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
322022
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
322019
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
232021
GSNFS: Gene subnetwork biomarker identification of lung cancer expression data
N Doungpan, W Engchuan, JH Chan, A Meechai
BMC medical genomics 9, 241-250, 2016
212016
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
212015
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
202022
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
202018
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
162023
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
152023
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บทความ 1–20