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Yassaee, Vahid Reza
31  Ergebnisse:
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1

Association of HOTAIR rs2366152 and rs1899663 polymorphisms..:

Eivazi, Nasim ; Mirfakhraie, Reza ; Nazemalhosseini Mojarad, Ehsan...
Journal of Clinical Laboratory Analysis.  37 (2023)  9-10 - p. , 2023
Link: https://doi.org/10.1002/..
 
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2

Identification of a novel de novo mutation in the CTNNB1 ge..:

Dashti, Sepide ; Salehpour, Shadab ; Ghasemi, Mohammad-Reza...
Neurological Sciences.  43 (2022)  4 - p. 2859-2863 , 2022
Link: https://doi.org/10.1007/..
 
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3

Gnathodiaphyseal dysplasia with a novel genetic variant in ..:

Yassaee, Vahid Reza ; Khojasteh, Arash ; Hashemi‐Gorji, Farzad...
Molecular Genetics & Genomic Medicine.  10 (2022)  9 - p. , 2022
Link: https://doi.org/10.1002/..
 
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4

Overexpression of GABRP Gene in Triple Negative Breast Canc..:

Azizi-Tabesh, Ghasem ; Kamaliyan, Zeeba ; Darbeheshti, Farzaneh...
International Journal of Cancer Management.  14 (2021)  11 - p. , 2021
Link: https://doi.org/10.5812/..
 
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5

Delineating the expanding phenotype of HERC2‐related disord..:

Vincent, Krista M. ; Eaton, Alison ; Yassaee, Vahid Reza...
Clinical Genetics.  100 (2021)  5 - p. 637-640 , 2021
Link: https://doi.org/10.1111/..
 
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6

Whole-Exome Sequencing Uncovers Novel Causative Variants an..:

Eghbali, Maryam ; Fatemi, Kiyana Sadat ; Salehpour, Shadab...
Frontiers in Genetics.  11 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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7

Autophagy ATG16L1 rs2241880 impacts the colorectal cancer r..:

Jamali, Leila ; Sadeghi, Hossein ; Ghasemi, Mohammad‐Reza...
Journal of Clinical Laboratory Analysis.  36 (2021)  1 - p. , 2021
Link: https://doi.org/10.1002/..
 
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8

Association between single nucleotide polymorphisms rs12722..:

Ahmadi, Habib ; Yassaee, Vahid Reza ; Mirfakhraie, Reza.
Current Journal of Neurology.  , 2020
Link: https://doi.org/10.18502..
 
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9

Could CYP24A1 promoter methylation status affect the gene e..:

Sadeghi, Hossein ; Nazemalhosseini-Mojarad, Ehsan ; Yassaee, Vahid Reza...
Meta Gene.  24 (2020)  - p. 100656 , 2020
Link: https://doi.org/10.1016/..
 
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10

A novelSRD5A2mutation in an Iranian family with sex develop..:

Hashemi‐Gorji, Feyzollah ; Salehpour, Shadab ; Miryounesi, Mohammad..
Andrologia.  53 (2020)  1 - p. , 2020
Link: https://doi.org/10.1111/..
 
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11

Next generation sequencing elucidated a clinically undiagno..:

Ravesh, Zeinab ; Yassaee, Vahid Reza ; Tonekaboni, Seyed Hasan...
Gene Reports.  16 (2019)  - p. 100457 , 2019
Link: https://doi.org/10.1016/..
 
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12

Whole exome sequencing unraveled the mystery of neurodevelo..:

Ravesh, Zeinab ; Ghafouri-Fard, Soudeh ; Rostami, Masoumeh...
Gene Reports.  13 (2018)  - p. 141-145 , 2018
Link: https://doi.org/10.1016/..
 
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13

miR‐30a promoter variation contributes to the increased ris..:

Sadeghi, Hossein ; Nazemalhosseini‐Mojarad, Ehsan ; Yaghoob‐Taleghani, Mohammad...
Journal of Cellular Biochemistry.  120 (2018)  5 - p. 7734-7740 , 2018
Link: https://doi.org/10.1002/..
 
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14

Neurodegeneration with brain iron accumulation 2A: Report o..:

Miryounesi, Mohammad ; Salehpour, Shadab ; Tonekaboni, Seyed Hassan...
Meta Gene.  15 (2018)  - p. 87-89 , 2018
Link: https://doi.org/10.1016/..
 
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15

A new mutation in steroidogenic acute regulatory protein (S..:

Ghafouri-Fard, Soudeh ; Yassaee, Vahid Reza ; Alipour, Nasrin..
Meta Gene.  16 (2018)  - p. 196-198 , 2018
Link: https://doi.org/10.1016/..
 
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