1. A novel c.240_241insGG mutation in NDP gene in a family with Norrie disease. (18th September 2017) Authors: Andarva, Monavvar; Jamshidi, Javad; Ghaedi, Hamid; Daftarian, Narsis; Emamalizadeh, Babak; Alehabib, Elham; Taghavi, Shaghyegh; Pouriran, Ramin; Darvish, Hossein Journal: Clinical & experimental optometry Issue: Volume 101:Number 2(2018) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis. Issue 1 (2nd January 2023) Authors: Daneshmandpour, Yousef; Bahmanpour, Zahra; Kazeminasab, Somayeh; Aghaei Moghadam, Ehsan; Alehabib, Elham; Chapi, Marjan; Tafakhori, Abbas; Aghaei, Negar; Darvish, Hossein; Emamalizadeh, Babak Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 24:Issue 1/2(2023) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose?. (July 2021) Authors: Mortazavi, Sedigheh Sadat; Bahmanpour, Zahra; Daneshmandpour, Yousef; Roudbari, Faranak; Sheervalilou, Roghayeh; Kazeminasab, Somayeh; Emamalizadeh, Babak Journal: Computers in biology and medicine Issue: Volume 134(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Exhaled breath condensate efficacy to identify mutations in patients with lung cancer: A pilot study. (3rd April 2022) Authors: Kazeminasab, Somayeh; Ghanbari, Reza; Emamalizadeh, Babak; Jouyban-Gharamaleki, Vahid; Taghizadieh, Ali; Jouyban, Abolghasem; Khoubnasabjafari, Maryam Journal: Nucleosides, nucleotides & nucleic acids Issue: Volume 41:Number 4(2022) Page Start: 370 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Features, genetics and their correlation in Jalili syndrome: a systematic review. Issue 6 (31st January 2019) Authors: Daneshmandpour, Yousef; Darvish, Hossein; Pashazadeh, Fariba; Emamalizadeh, Babak Journal: Journal of medical genetics Issue: Volume 56:Issue 6(2019) Page Start: 358 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Incomplete penetrance of CRX gene for autosomal dominant form of cone-rod dystrophy. (4th May 2019) Authors: Chapi, Marjan; Sabbaghi, Hamideh; Suri, Fatemeh; Alehabib, Elham; Rahimi-Aliabadi, Simin; Jamali, Faezeh; Jamshidi, Javad; Emamalizadeh, Babak; Darvish, Hossein; Mirrahimi, Mehraban; Ahmadieh, Hamid; Daftarian, Narsis Journal: Ophthalmic genetics Issue: Volume 40:Number 3(2019) Page Start: 259 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population. (December 2020) Authors: Poursaei, Elham; Daneshmandpour, Yousef; Aghaei Moghadam, Ehsan; Abolghasemi, Mahsa; Jamshidi, Javad; Baradaran, Behzad; Asadi, Milad; Kazeminasab, Somayeh; Emamalizadeh, Babak Journal: Psychiatric genetics Issue: Volume 30:Number 6(2020:Dec.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. RAB7L1 promoter polymorphism and risk of Parkinson's disease; a case-control study. (4th May 2017) Authors: Khaligh, Ali; Goudarzian, Maryam; Moslem, Alireza; Mehrtash, Amirhosein; Jamshidi, Javad; Darvish, Hossein; Emamalizadeh, Babak Journal: Neurological research Issue: Volume 39:Number 5(2017) Page Start: 468 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population. (1st November 2016) Authors: Zarrabi Alhosseini, Mahjoubeh; Jamshidi, Javad; Zare Bidoki, Alireza; Ganji, Saeid; Eslami Amirabadi, Mohammad Reza; Emamalizadeh, Babak; Taghavi, Shaghayegh; Shokraeian, Parasto; Mohajerani, Fatemeh; Darvish, Hossein Journal: Neurological research Issue: Volume 38:Number 11(2016) Page Start: 959 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. The rs1572931 polymorphism of the RAB7L1 gene promoter is associated with reduced risk of Parkinson's disease. (November 2015) Authors: Goudarzian, Maryam; Khaligh, Ali; Fourozan, Reza; Jamal Mirmoosavi, Seyed; Darvish, Hossein; Safaralizadeh, Tannaz; Emamalizadeh, Babak Journal: Neurological research Issue: Volume 37:Number 11(2015) Page Start: 1029 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗