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Abedini, Seyedeh Sedigheh
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1

A critical review of the impact of candidate copy number va..:

Abedini, Seyedeh Sedigheh ; Akhavantabasi, Shiva ; Liang, Yuheng...
Mutation Research - Reviews in Mutation Research.  794 (2024)  - p. 108509 , 2024
Link: https://doi.org/10.1016/..
 
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2

DNA Technologies in Precision Medicine and Pharmacogenetics:

, In: Precision Medicine in Clinical Practice,
Abedini, Seyedeh Sedigheh ; Bazazzadegan, Niloofar ; Hasanzad, Mandana - p. 129-149 , 2022
Link: https://doi.org/10.1007/..
 
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3

Detection of a rare AXIN2 variant in an Iranian family with..:

Safari, Shiva ; Ebadifar, Asghar ; Najmabadi, Hossien...
Journal of Dental Research, Dental Clinics, Dental Prospects.  16 (2022)  2 - p. 107-111 , 2022
Link: https://doi.org/10.34172..
 
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4

Subcellular relocalization and nuclear redistribution of th..:

Jonkhout, Nicky ; Cruciani, Sonia ; Santos Vieira, Helaine Graziele...
RNA Biology.  18 (2021)  11 - p. 1905-1919 , 2021
Link: https://doi.org/10.1080/..
 
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5

Novel phenotype and genotype spectrum of NARS2 and literatu..:

Vafaee-Shahi, Mohammad ; Farhadi, Mohammad ; Razmara, Ehsan...
Irish Journal of Medical Science (1971 -).  191 (2021)  4 - p. 1877-1890 , 2021
Link: https://doi.org/10.1007/..
 
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6

Comprehensive genotype‐phenotype correlation in AP‐4 defici..:

Beheshtian, Maryam ; Akhtarkhavari, Tara ; Mehvari, Sepideh...
Clinical Genetics.  99 (2020)  1 - p. 187-192 , 2020
Link: https://doi.org/10.1111/..
 
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7

Whole genome sequencing identifies a duplicated region enco..:

Mehvari, Sepideh ; Larti, Farzaneh ; Hu, Hao...
Molecular Genetics & Genomic Medicine.  8 (2020)  10 - p. , 2020
Link: https://doi.org/10.1002/..
 
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8

Identification of disease‐causing variants in the EXOSC gen..:

Beheshtian, Maryam ; Fattahi, Zohreh ; Fadaee, Mahsa...
Clinical Genetics.  95 (2019)  6 - p. 718-725 , 2019
Link: https://doi.org/10.1111/..
 
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9

GPR126: A novel candidate gene implicated in autosomal rece..:

Hosseini, Masoumeh ; Fattahi, Zohreh ; Abedini, Seyedeh Sedigheh...
American Journal of Medical Genetics Part A.  179 (2018)  1 - p. 13-19 , 2018
Link: https://doi.org/10.1002/..
 
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10

Genetics of intellectual disability in consanguineous famil..:

Hu, Hao ; Kahrizi, Kimia ; Musante, Luciana...
Molecular Psychiatry.  24 (2018)  7 - p. 1027-1039 , 2018
Link: https://doi.org/10.1038/..
 
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11

Association Study of the TREM2 Gene and Identification of a..:

Mehrjoo, Zohreh ; Najmabadi, Amin ; Abedini, Seyedeh Sedigheh...
Medical Principles and Practice.  24 (2015)  4 - p. 351-354 , 2015
Link: https://doi.org/10.1159/..
 
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12

The influence of the BCL11A polymorphism on the phenotype o..:

Neishabury, Maryam ; Zamani, Fahimeh ; Keyhani, Elahe...
Blood Cells, Molecules, and Diseases.  51 (2013)  2 - p. 80-84 , 2013
Link: https://doi.org/10.1016/..
 
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13

The modifying effect of Xmn1-HBG2 on thalassemic phenotype ..:

Neishabury, Maryam ; Zamani, Shahbaz ; Azarkeivan, Azita...
Blood Cells, Molecules, and Diseases.  48 (2012)  1 - p. 1-5 , 2012
Link: https://doi.org/10.1016/..
 
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14

Analyzing 5′HS3 and 5′HS4 LCR core regions and NF-E2 in Ira..:

Neishabury, Maryam ; Azarkeivan, Azita ; Oberkanins, Christian...
Blood Cells, Molecules, and Diseases.  46 (2011)  3 - p. 201-205 , 2011
Link: https://doi.org/10.1016/..
 
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15

Mutation of the conserved polyadenosine RNA binding protein..:

Pak, ChangHui ; Garshasbi, Masoud ; Kahrizi, Kimia...
Proceedings of the National Academy of Sciences.  108 (2011)  30 - p. 12390-12395 , 2011
Link: https://doi.org/10.1073/..
 
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