Ali Oghabian

Helsinki, Finland

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications

Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-Sequencing.

Poly(A)+ selection limits detection of long and alternatively spliced transcripts compared with rRNA depletion in RNA-Sequencing.

Journal: BMC genomics
Published: January 07, 2026

Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2-related osteoporosis.

Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2-related osteoporosis.

Journal: JBMR plus
Published: May 26, 2025

A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.

A homozygous single-nucleotide variant in TNNT1 causes abnormal troponin T isoform expression in a patient with severe nemaline myopathy: A case report.

Journal: Journal of neuromuscular diseases
Published: May 21, 2025

Correction: OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development.

Correction: OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development.

Journal: Skeletal muscle
Published: April 08, 2025

Inferring disease course from differential exon usage in the wide titinopathy spectrum.

Inferring disease course from differential exon usage in the wide titinopathy spectrum.

Journal: Annals of clinical and translational neurology
Published: July 23, 2024

OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development.

OBSCN undergoes extensive alternative splicing during human cardiac and skeletal muscle development.

Journal: Skeletal muscle
Published: July 23, 2024

Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions.

Revealing myopathy spectrum: integrating transcriptional and clinical features of human skeletal muscles with varying health conditions.

Journal: Communications biology
Published: August 22, 2023

Baseline gene expression in subcutaneous adipose tissue predicts diet-induced weight loss in individuals with obesity.

Baseline gene expression in subcutaneous adipose tissue predicts diet-induced weight loss in individuals with obesity.

Journal: PeerJ
Published: November 01, 2022

Molecular pathways behind acquired obesity: Adipose tissue and skeletal muscle multiomics in monozygotic twin pairs discordant for BMI.

Molecular pathways behind acquired obesity: Adipose tissue and skeletal muscle multiomics in monozygotic twin pairs discordant for BMI.

Journal: Cell reports. Medicine
Published: October 09, 2020

Chromosomal instability by mutations in the novel minor spliceosome component CENATAC.

Chromosomal instability by mutations in the novel minor spliceosome component CENATAC.

Journal: The EMBO journal
Published: August 14, 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.

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.

Journal: International journal of molecular sciences
Published: April 10, 2018

IntEREst: intron-exon retention estimator.

IntEREst: intron-exon retention estimator.

Journal: BMC bioinformatics
Published: September 22, 2017
Showing 1-12 of 15

Last Updated: 09/26/2026