Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Identification of disease-causing variants in the EXOSC gene family underlying autosomal recessive intellectual disability in Iranian families.
Clin Genet. 2019 Jun;95(6):718-725. doi: 10.1111/cge.13549. Epub 2019 May 14.
Clin Genet. 2019.
PMID: 30950035
SZT2 mutation in a boy with intellectual disability, seizures and autistic features.
Kariminejad A, Yazdan H, Rahimian E, Kalhor Z, Fattahi Z, Zonooz MF, Najmabadi H, Ashrafi M.
Kariminejad A, et al. Among authors: kalhor z.
Eur J Med Genet. 2019 Sep;62(9):103556. doi: 10.1016/j.ejmg.2018.10.008. Epub 2018 Oct 22.
Eur J Med Genet. 2019.
PMID: 30359774
Item in Clipboard
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population.
Fattahi Z, Kalhor Z, Fadaee M, Vazehan R, Parsimehr E, Abolhassani A, Beheshtian M, Zamani G, Nafissi S, Nilipour Y, Akbari MR, Kahrizi K, Kariminejad A, Najmabadi H.
Fattahi Z, et al. Among authors: kalhor z.
Clin Genet. 2017 Mar;91(3):386-402. doi: 10.1111/cge.12810. Epub 2016 Jul 21.
Clin Genet. 2017.
PMID: 27234031
Item in Clipboard
De novo Mutation in CACNA1S Gene in a 20-Year-Old Man Diagnosed with Metabolic Myopathy.
Edizadeh M, Vazehan R, Javadi F, Dehdahsi S, Fadaee M, Faraji Zonooz M, Parsimehr E, Ahangari F, Abolhassani A, Kalhor Z, Fattahi Z, Beheshtian M, Kariminejad A, Akbari MR, Najmabadi H, Nafissi S.
Edizadeh M, et al. Among authors: kalhor z.
Arch Iran Med. 2017 Sep;20(9):617-620.
Arch Iran Med. 2017.
PMID: 29048924
Item in Clipboard
Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period.
Bazazzadegan N, Vazehan R, Fadaee M, Fattahi Z, Abolhassani A, Parsimehr E, Kalhor Z, Faraji Zonooz M, Ahangari F, Dehdahsi S, Samiee F, Jamali P, Habibi H, Nourizadeh Y, Mahdavi S, Beheshtian M, Kariminejad A, Smith RJ, Najmabadi H.
Bazazzadegan N, et al. Among authors: kalhor z.
Iran J Public Health. 2019 Oct;48(10):1910-1915.
Iran J Public Health. 2019.
PMID: 31850270
Free PMC article.
Item in Clipboard
Crosstalk between hypoxia-induced pyroptosis and immune escape in cancer: From mechanisms to therapy.
Meybodi SM, Ejlalidiz M, Manshadi MR, Raeisi M, Zarin M, Kalhor Z, Saberiyan M, Hamblin MR.
Meybodi SM, et al. Among authors: kalhor z.
Crit Rev Oncol Hematol. 2024 May;197:104340. doi: 10.1016/j.critrevonc.2024.104340. Epub 2024 Apr 1.
Crit Rev Oncol Hematol. 2024.
PMID: 38570176
Free article.
Review.
Item in Clipboard
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H.
Abolhassani A, et al. Among authors: kalhor z.
NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0.
NPJ Genom Med. 2024.
PMID: 38374194
Free PMC article.
Item in Clipboard
Cite
Cite