Hassan Saei

发表

Description of biomechanical forces and physiological parameters of fruit cracking in pomegranate

E. Seifi, A. Dehghani, Hassan Saei, 2014 .

Whole-Exome Sequencing Uncovers Novel Causative Variants and Additional Findings in Three Patients Affected by Glycogen Storage Disease Type VI and Fanconi−Bickel Syndrome

M. Abiri, V. Yassaee, M. Modarressi, 2021, Frontiers in Genetics.

Exome sequencing identified a novel pathogenic RET variant with high variable expressivity and incomplete penetrance in an extended pedigree with Hirschsprung disease

M. Abiri, Hassan Saei, M. Eghbali, 2020 .

Identification of novel cis-mutations in the GJA8 gene in a 3-generation Iranian family with autosomal dominant congenital nuclear cataract

Mohammad Hossein Jabbarpoor Bonyadi, M. Bonyadi, Hassan Saei, 2022, Ophthalmic genetics.

The Effect of Alginate-Based Edible Coating Enriched with Citric Acid and Ascorbic Acid on Texture, Appearance and Eating Quality of Apple Fresh-Cut

S. Mortazavi, A. Mostaan, Hassan Saei, 2020, International Journal of Fruit Science.

Comprehensive transcriptome mining identified the gene expression signature and differentially regulated pathways of the late-onset preeclampsia.

M. Abiri, Hassan Saei, M. Eghbali, 2021, Pregnancy hypertension.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

Rapid methodologies for assessing Pseudomonas syringae pv. actinidiae colonization and effector-mediated hypersensitive response in kiwifruit.

A. Chatterjee, M. Templeton, C. Brendolise, 2021, Molecular plant-microbe interactions : MPMI.

A wave of deep intronic mutations in X-linked Alport Syndrome.

O. Gribouval, C. Antignac, C. Bole-Feysot, 2023, Kidney international.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

VNtyper enables accurate alignment-free genotyping of MUC1 coding VNTR using short-read sequencing data in autosomal dominant tubulointerstitial kidney disease

O. Gribouval, C. Antignac, P. Nitschké, 2023, iScience.

Hepatoprotective Effect of Ethanolic Extract of Lavandula officinalis L. in Alloxan-Induced Diabetic Rats

M. Azarmi, Hassan Saei, G. Dehghan, 2016 .