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Ali Oghabian
Ali Oghabian
未知所在单位机构
在 helsinki.fi 的电子邮件经过验证
标题
引用次数
引用次数
年份
Biclustering methods: biological relevance and application in gene expression analysis
A Oghabian, S Kilpinen, S Hautaniemi, E Czeizler
PloS one 9 (3), e90801, 2014
1412014
Defective minor spliceosome mRNA processing results in isolated familial growth hormone deficiency
J Argente, R Flores, A Gutiérrez‐Arumí, B Verma, GÁ Martos‐Moreno, ...
EMBO molecular medicine 6 (3), 299-306, 2014
1172014
Molecular pathways behind acquired obesity: Adipose tissue and skeletal muscle multiomics in monozygotic twin pairs discordant for BMI
BW van der Kolk, S Saari, A Lovric, M Arif, M Alvarez, A Ko, Z Miao, ...
Cell Reports Medicine 2 (4), 2021
532021
Multiple Isoforms of ANRIL in Melanoma Cells: Structural Complexity Suggests Variations in Processing
D Sarkar, A Oghabian, PK Bodiyabadu, WR Joseph, EY Leung, GJ Finlay, ...
International journal of molecular sciences 18 (7), 1378, 2017
472017
Global analysis of the nuclear processing of transcripts with unspliced U12-type introns by the exosome
EH Niemelä, A Oghabian, RHJ Staals, D Greco, GJM Pruijn, MJ Frilander
Nucleic acids research 42 (11), 7358-7369, 2014
442014
Chromosomal instability by mutations in the novel minor spliceosome component CENATAC
B de Wolf, A Oghabian, MV Akinyi, S Hanks, EC Tromer, JJE van Hooff, ...
The EMBO journal 40 (14), e106536, 2021
332021
IntEREst: intron-exon retention estimator
A Oghabian, D Greco, MJ Frilander
BMC bioinformatics 19, 1-10, 2018
292018
Inferring disease course from differential exon usage in the wide titinopathy spectrum
MF Di Feo, A Oghabian, E Nippala, M Gautel, H Jungbluth, F Forzano, ...
Annals of clinical and translational neurology 11 (10), 2745-2755, 2024
22024
Chromosomal instability by mutations in a novel specificity factor of the minor spliceosome
B de Wolf, A Oghabian, MV Akinyi, S Hanks, EC Tromer, J van Hooff, ...
bioRxiv, 2020.08. 06.239418, 2020
22020
FlowAnd: Comprehensive Computational Framework for Flow Cytometry Data Analysis
AMK Lahesmaa-Korpinen, S Jalkanen, P Chen, EA Valo, ...
Journal of Proteomics and Bioinformatics 4 (11), 245-249, 2011
22011
Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions
H Zhong, V Sian, M Johari, S Katayama, A Oghabian, PH Jonson, ...
Communications Biology 7 (1), 438, 2024
12024
Baseline gene expression in subcutaneous adipose tissue predicts diet-induced weight loss in individuals with obesity
A Oghabian, BW van der Kolk, P Marttinen, A Valsesia, D Langin, ...
PeerJ 11, e15100, 2023
12023
Bioinformatics analysis of intron retention events associated with the minor spliceosome
A Oghabian
Helsingin yliopisto, 2018
12018
474P Identifying biological pathomechanisms of TTN-affected Myopathies using RNA-sequencing data
SN Gayathri, P Jonson, A Oghabian, V Lillback, V Sian, A Roos, ...
Neuromuscular Disorders 43, 104441.311, 2024
2024
682P Differential splicing of OBSCN throughout human cardiac and skeletal muscle development
A Oghabian, P Jonson, M Johari, D Andres, F Munell, J Soriano, M Duran, ...
Neuromuscular Disorders 43, 104441.383, 2024
2024
OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development
A Oghabian, PH Jonson, M Johari, DG Andres, F Munell, JC Soriano, ...
2024
Splicing analysis of RNAseq data using IntEREst R/Bioconductor package (V1. 24.0)
A Oghabian, M Frilander, M Savarese
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 658-658, 2024
2024
P184 Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions
H Zhong, M Johari, S Katayama, A Oghabian, V Sian, P Jonson, ...
Neuromuscular Disorders 33, S111, 2023
2023
Corrigendum to: Expanding the phenotype of biallelic RNPC3 variants associated with growth hormone deficiency (American Journal of Medical Genetics Part A,(2020), 182, 8,(1952 …
J Argente, R Flores, A Gutiérrez-Arumí, B Verma, G Martos-Moreno, ...
EMBO Molecular Medicine 12 (9), e13133, 2020
2020
Correction: Sarkar, D., et al. Multiple Isoforms of ANRIL in Melanoma Cells: Structural Complexity Suggests Variations in Processing. Int. J. Mol. Sci. 2017, 18, 1378
D Sarkar, A Oghabian, PK Bodiyabadu, WR Joseph, EY Leung, GJ Finlay, ...
International Journal of Molecular Sciences 19 (5), 1343, 2018
2018
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