Maryam Tahmasebi Birgani (M Tahmasebi Birgani, Maryam Tahmasebi-Birgani)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 7

Top Topics

Breast Cancer Risk

Polycystic Ovary Syndrome

Genome Wide Identification

Top Venues

International journal of reproductive biomedicine

Annals of human genetics

The journal of gene medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi Birgani, Javad Mohammadi-Asl
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study. International journal of reproductive biomedicine 22 (2) (2024)
Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi Birgani, Javad Mohammadi-Asl
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study. International journal of reproductive biomedicine 22 (2) (2024)
Neda Farajnezhad, Pegah Ghandil, Maryam Tahmasebi Birgani, Javad Mohammadi-Asl
Folate gene polymorphisms CBS 844ins68 and RFC1 A80G and risk of Down syndrome offspring in young Iranian women: A cross-sectional study. International journal of reproductive biomedicine 22 (2) (2024)
Mahzad Nasirshalal, Maryam Tahmasebi Birgani, Mohammadreza Dadfar, Roshan Nikbakht, Alihossein Saberi, Pegah Ghandil
Identification of the PRM1 gene mutations in oligoasthenoteratozoospermic men. Andrologia 52 (11) (2020)
Hossein Ansari, Javad Mohammadi-Asl, Mohammadreza Hajjari, Maryam Tahmasebi Birgani, Abolghasem Kollaee, Farzad Jassemi-Zergani, Amin Vakili-Hajiagha
Exome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia. The journal of gene medicine 21 (8) (2019)
Mahsa Ghaffari, Maryam Tahmasebi Birgani, Roxana Kariminejad, Alihossein Saberi
Genotype-phenotype correlation and the size of microdeletion or microduplication of 7q11.23 region in patients with Williams-Beuren syndrome. Annals of human genetics 82 (6) (2018)
J Mohammadi-Asl, Mohammadreza Hajjari, Maryam Tahmasebi Birgani, K Riahi, H Nasiri, A Kollaee
Exome sequencing revealed a novel deletion in the ERCC8 gene in an Iranian family with Cockayne syndrome. Annals of human genetics 82 (5) (2018)