1. A biallelic variant in POLR2C is associated with congenital hearing loss and male infertility: Case report. (10th January 2023) Authors: Bitarafan, Fatemeh; Razmara, Ehsan; Jafarinia, Ehsan; Almadani, Navid; Garshasbi, Masoud Journal: European journal of clinical investigation Issue: Volume 53:Number 4(2023) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A homozygote variant in the tRNA splicing endonuclease subunit 54 causes pontocerebellar hypoplasia in a consanguineous Iranian family. Issue 10 (22nd July 2020) Authors: Sepahvand, Afrooz; Razmara, Ehsan; Bitarafan, Fatemeh; Galehdari, Mohammad; Tavasoli, Ali Reza; Almadani, Navid; Garshasbi, Masoud Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 10(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel variant of ST3GAL3 causes non‐syndromic autosomal recessive intellectual disability in Iranian patients. (3rd August 2020) Authors: Farajollahi, Zahra; Razmara, Ehsan; Heidari, Erfan; Jafarinia, Ehsan; Garshasbi, Masoud Journal: Journal of gene medicine Issue: Volume 22:Number 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Association between TBXT rs2305089 polymorphism and chordoma in Iranian patients identified by a developed T‐ARMS‐PCR assay. Issue 1 (27th November 2021) Authors: Jalessi, Maryam; Gholami, Mohammad Saeed; Razmara, Ehsan; Hassanzadeh, Sajad; Sadeghipour, Alireza; Jahanbakhshi, Amin; Tabibkhooei, Alireza; Bahrami, Eshagh; Falah, Masoumeh Journal: Journal of clinical laboratory analysis Issue: Volume 36:Issue 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Functions of the SNAI family in chondrocyte‐to‐osteocyte development. Issue 1 (17th August 2021) Authors: Razmara, Ehsan; Bitaraf, Amirreza; Karimi, Behnaz; Babashah, Sadegh Other Names: Zaidi Mone guestEditor. Journal: Annals of the New York Academy of Sciences Issue: Volume 1503:Issue 1(2021) Page Start: 5 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Graves' disease: introducing new genetic and epigenetic contributors. (February 2021) Authors: Razmara, Ehsan; Salehi, Mehrnaz; Aslani, Saeed; Bitaraf, Amirreza; Yousefi, Hassan; Colón, Jonathan Rosario; Mahmoudi, Mahdi Journal: Journal of molecular endocrinology Issue: Volume 66:Number 2(2021) Page Start: R33 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Homozygous in‐frame variant of SCL6A3 causes dopamine transporter deficiency syndrome in a consanguineous family. (20th February 2020) Authors: Heidari, Erfan; Razmara, Ehsan; Hosseinpour, Sareh; Tavasoli, Ali Reza; Garshasbi, Masoud Journal: Annals of human genetics Issue: Volume 84:Number 4(2020:Jul.) Page Start: 315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. How Transmembrane Inner Ear (TMIE) plays role in the auditory system: A mystery to us. Issue 13 (13th May 2021) Authors: Farhadi, Mohammad; Razmara, Ehsan; Balali, Maryam; Hajabbas Farshchi, Yeganeh; Falah, Masoumeh Journal: Journal of cellular and molecular medicine Issue: Volume 25:Issue 13(2021) Page Start: 5869 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of a six‐microRNA signature as a potential diagnostic biomarker in breast cancer tissues. Issue 11 (15th September 2021) Authors: Mahmoudian, Mojdeh; Razmara, Ehsan; Mahmud Hussen, Bashdar; Simiyari, Mandana; Lotfizadeh, Nazanin; Motaghed, Hoda; Khazraei Monfared, Arefeh; Montazeri, Maryam; Babashah, Sadegh Journal: Journal of clinical laboratory analysis Issue: Volume 35:Issue 11(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Issue 12 (18th November 2020) Authors: Zardadi, Safoura; Razmara, Ehsan; Asgaritarghi, Golareh; Jafarinia, Ehsan; Bitarafan, Fatemeh; Rayat, Sima; Almadani, Navid; Morovvati, Saeid; Garshasbi, Masoud Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 12(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗