1. Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults. (1st January 2020) Authors: Mehrdad, Mahsa; Doaei, Saeid; Gholamalizadeh, Maryam; Fardaei, Majid; Fararouei, Mohammad; Eftekhari, Mohammad Hassan Journal: Adipocyte Issue: Volume 9:Number 1(2020) Page Start: 51 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 gene. (19th August 2020) Authors: Khalili Alashti, Shayan; Fallahi, Jafar; Jokar, Arezoo; Fardaei, Majid 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) ↗
3. Development of biliary and renal stone and sludge after taking Ceftriaxone is associated with a defect in UDP‐Glucuronosyltransferase (ie Gilbert's syndrome). Issue 2 (21st March 2019) Authors: Heydari, Mohammad Reza; Fardaei, Majid; Kadivar, Mohammad Rahim; Rezaianzadeh, Abbas; Panjehshahin, Mohammad Reza; Bardeji, Zeinab Gholami; Heydari, Zahra Journal: GastroHep Issue: Volume 1:Issue 2(2019) Page Start: 55 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Featured Cover. Issue 6 (2nd May 2021) Authors: Rezaei, Maryam; Suresh, Beena; Bereke, Eric; Hadipour, Zahra; Aguinaga, Monic; Qian, Jianhua; Bagga, Rashmi; Fardaei, Majid; Hemida, Reda; Jagadeesh, Sujatha; Majewski, Jacek; Slim, Rima Journal: Clinical genetics Issue: Volume 99:Issue 6(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient. Issue 6 (4th May 2019) Authors: Taghdiri, Maryam; Kashef, Atie; Abbassi, Golemaryam; Moshtagh, Azadeh; Sadatian, Neda; Fardaei, Majid; Najafi, Kimia; Kariminejad, Roxana Journal: Clinical case reports Issue: Volume 7:Issue 6(2019) Page Start: 1149 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. High dietary inflammatory index (DII) scores increase odds of overweight in adults with rs9939609 polymorphism of FTO gene. (April 2021) Authors: Mehrdad, Mahsa; Vahid, Farhad; Shivappa, Nitin; Hébert, James R.; Fardaei, Majid; Hassan Eftekhari, Mohammad Journal: Clinical nutrition ESPEN Issue: Volume 42(2021) Page Start: 221 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome. Issue 1 (22nd November 2017) Authors: Taghdiri, Maryam; Kashef, Atie; Fardaei, Majid; Miryounesi, Mohammad Journal: Clinical case reports Issue: Volume 6:Issue 1(2018) Page Start: 32 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel mutation in the MED23 gene for intellectual disability: A case report and literature review. Issue 2 (9th January 2019) Authors: Hashemi‐Gorji, Feyzollah; Fardaei, Majid; Tabei, Seyed Mohammad Bagher; Miryounesi, Mohammad Journal: Clinical case reports Issue: Volume 7:Issue 2(2019) Page Start: 331 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Novel pathogenic variants in NLRP7, NLRP5, and PADI6 in patients with recurrent hydatidiform moles and reproductive failure. Issue 6 (23rd February 2021) Authors: Rezaei, Maryam; Suresh, Beena; Bereke, Eric; Hadipour, Zahra; Aguinaga, Monica; Qian, Jianhua; Bagga, Rashmi; Fardaei, Majid; Hemida, Reda; Jagadeesh, Sujatha; Majewski, Jacek; Slim, Rima Journal: Clinical genetics Issue: Volume 99:Issue 6(2021) Page Start: 823 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗