Search Results

Reporting three rare pathogenic variants at the CFTR gene in two unrelated Iranian Azeri children with cystic fibrosis.

• Authors : Hosseini-Asl, S. Erfan¹ (AUTHOR); Khalafi, Jafar² (AUTHOR); Seyedhashemi, Effat³ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 10/7/2024, Vol. 25 Issue 1, p1-5. 5p.

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A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems.

• Authors : Mir, Atefeh¹ (AUTHOR); Song, Yongjun² (AUTHOR); Lee, Hane² (AUTHOR)

• Source: Molecular Genetics & Genomic Medicine. Jan2024, Vol. 12 Issue 1, p1-7. 7p.

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Trait profiling and genotype selection in oilseed rape using genotype by trait and genotype by yield*trait approaches.

• Authors : Bakhshi, Behnam¹ (AUTHOR); Amiri Oghan, Hassan² (AUTHOR) ; Rameeh, Valiollah³ (AUTHOR)

Subjects: *RAPESEED; *CULTIVARS; *GENOTYPESIRAN

• Source: Food Science & Nutrition. Jun2023, Vol. 11 Issue 6, p3083-3095. 13p.

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In silico analysis and the pathogenicity classification of PTS gene variants among Iranian population.

• Authors : Khamooshian, Sahand¹ (AUTHOR); Kazeminia, Mohsen¹ (AUTHOR); Moradi, Keivan² (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 9/15/2022, Vol. 23 Issue 1, p1-10. 10p.

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A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case.

• Authors : Ghasemnejad, Tohid^1,2,3 (AUTHOR); Shekari Khaniani, Mahmoud² (AUTHOR); Nouri Nojadeh, Jafar² (AUTHOR)

• Source: BMC Medical Genomics. 2/1/2022, Vol. 15 Issue 1, p1-10. 10p.

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Identification of a Novel Homozygous Mutation in BBS10 Gene in an Iranian Family with Bardet-Biedl Syndrome.

• Authors : Dehani, Mohammad¹; Zare-Abdollahi, Davood² ; Bushehri, Ata¹

• Source: Avicenna Journal of Medical Biotechnology. Oct-Dec2021, Vol. 13 Issue 4, p230-233. 4p.

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A novel pathogenic variant in the LRTOMT gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.

• Authors : Sarmadi, Akram^1,2 (AUTHOR); Nasrniya, Samane¹ (AUTHOR); Soleimani Farsani, Maryam³ (AUTHOR)

• Source: BMC Medical Genetics. 6/9/2020, Vol. 21 Issue 1, p1-9. 9p.

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Gene Panel Testing in Hereditary Breast Cancer.

• Authors : Rostami, Parvin¹; Zendehdel, Kazem^2,3,4; Shirkoohi MD, Reza^3,4

• Source: Archives of Iranian Medicine (AIM). Mar2020, Vol. 23 Issue 3, p155-162. 8p.

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Changes in maize transcriptome in response to maize Iranian mosaic virus infection.

• Authors : Izadpanah, Keramatollah¹; Ghorbani, Abozar^1,2; Dietzgen, Ralf G.²

Subjects: *CORN; *MOSAIC viruses; *RNAIRAN

• Source: PLoS ONE. 4/10/2018, Vol. 13 Issue 4, p1-17. 17p.

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Genetics and genomic medicine in Iran.

• Authors : Behnam, Babak¹ ; Zakeri, Maryam²

• Source: Molecular Genetics & Genomic Medicine. Feb2019, Vol. 7 Issue 2, pN.PAG-N.PAG. 1p.

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