Optimizing A Lipocomplex-Based Gene Transfer Method into HeLa Cell Line

by Alimohammad Asgharian, Mehdi Banan, Hossein Najmabadi
Published 2013-01-01

A Novel Homozygous ATP8A2 Variant in a Patient With Phenotypic Features of Dysequilibrium Syndrome

by Amene Saghazadeh, Seyed Hassan Tonekaboni, Hossein Najmabadi, Nima Rezaei
Published 2019-01-01

Investigation of the Relationship Between a Genetic Polymorphism in ACTN3 and Elite Sport Performance Among Iranian Soccer Players

by Asal Honarpour, Marzieh Mohseni, Siamak Ghavidel Hajiagha, Shiva Irani, Hossein Najmabadi
Published 2017-06-01

Genetic Causes of Putative Autosomal Recessive Intellectual Disability Cases in Hamedan Province

by Milad Bastami, Elaheh Papari, Seyedeh Sedigheh Abedini, Kimia Kahrizi, Hossein Najmabadi
Published 2012-04-01

Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss

by Reihaneh Alikhani, Fatemeh Ostaresh, Mojgan Babanejad, Nilofar Bazazzadegan, Hossein Najmabadi, Kimia Kahrizi
Published 2015-09-01

Molecular Study Of Pkd1 & Pkd2 Genes By Linkage Analysis And Determining The Genotype/Phenotype Correlations In Several Iranian Families With Autosomal Dominant Polycystic Kidney D...

by Behrooz Broumand, Hossein Najmabadi, ASghar Hagibeigi, Ramin Radpour, Mahdi M. Haghighi, Mina Ohadi
Published 2005-05-01

Serotonin Transporter Polymorphism (5-HTTLPR) and Citalopram Effectiveness in Iranian Patients with Major Depressive Disorder.

by Shima Sahraian, Mohammad Babashams, Pouria Reza-Soltani, Hossein Najmabadi, Kimia Kahrizi, Sahel Hemmati Gorgani
Published 2013-06-01

Serotonin Transporter Polymorphism (5-HTTLPR) and Citalopram Effectiveness in Iranian Patients with Major Depressive Disorder

by Shima Sahraian, Mohammad Babashams, Pouria Reza-Soltani, Hossein Najmabadi, Kimia Kahrizi, Sahel Hemmati Gorgani
Published 2013-06-01

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

by Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi
Published 2021-03-01

Genotype–Phenotype Correlations in Iranian Myotonic Dystrophy Type I Patients

by Kimia Kahrizi, Neda Moradin, Mojtaba Azimian, Bahareh Shojasaffar, Kaveh Alavi, Shahriar Nafisi, Mandana Hasanzad, Seyed Mohammad Ebrahim Moosavi, Azadeh Shirazian, Hossein Najmabadi
Published 2010-04-01

Association of Polymorphisms at LDLR Locus with Coronary Artery Disease Independently from Lipid Profile

by Seyed Hamid Jamaldini, Mojgan Babanejad, Reza Mozaffari, Nooshin Nikzat, Khadijeh Jalalvand, Azadeh Badiei, Hamidreza Sanati, Farshad Shakerian, Mahdi Afshari, Kimia Kahrizi, Hossein Najmabadi
Published 2014-05-01

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.

by Behzad Davarniya, Hao Hu, Kimia Kahrizi, Luciana Musante, Zohreh Fattahi, Masoumeh Hosseini, Fariba Maqsoud, Reza Farajollahi, Thomas F Wienker, H Hilger Ropers, Hossein Najmabadi
Published 2015-01-01

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

by Kimia Najafi, Soheila Gholami, Azadeh Moshtagh, Masood Bazrgar, Neda Sadatian, Golemaryam Abbasi, Parvin Rostami, Soheila Khalili, Mojgan Babanejad, Bahareh Nourmohammadi, Negin Faramarzi Garous, Hossein Najmabadi, Roxana Kariminejad
Published 2019-08-01

Genetic Causes of Mental Retardation in Golestan Province

by Hossein Darvish, Saghar Ghasemi-Firouzabadi, Gholam Reza Bahrami-Monajemi, Ideh Bahman, Marziyeh Mohseni, Mohammad Javad Soltani-Banavandi, Sousan Banihashemi , Sanaz Arjangi, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi
Published 2010-10-01

Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability

by Sepideh Mehvari, Farzaneh Larti, Hao Hu, Zohreh Fattahi, Maryam Beheshtian, Seyedeh Sedigheh Abedini, Sanaz Arzhangi, Hans‐Hilger Ropers, Vera M. Kalscheuer, Daniel Auld, Kimia Kahrizi, Yasser Riazalhosseini, Hossein Najmabadi
Published 2020-10-01

Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period

by Niloofar BAZAZZADEGAN, Raheleh VAZEHAN, Mahsa FADAEE, Zohreh FATTAHI, Ayda ABOLHASSANI, Elham PARSIMEHR, Zahra KALHOR, Mehrshid FARAJI ZONOOZ, Fatemeh AHANGARI, Shima DEHDAHSI, Farshide SAMIEE, Payman JAMALI, Haleh HABIBI, Younes NOURIZADEH, Shokouh MAHDAVI, Maryam BEHESHTIAN, Ariana KARIMINEJAD, Richard JH SMITH, Hossein NAJMABADI
Published 2019-10-01

Investigation of Chromosomal Abnormalities and Microdeletion/Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

by Akbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, Nejat Mahdieh, Reza Shervin Badv, Payman Jamali, Roxana Kariminejad, Zahra Chavoshzadeh, Saghar Ghasemi Firouzabadi, Roxana Mansour Ghanaie, Ahoura Nozari, Sussan Banihashemi, Fatemeh Hadipour, Zahra Hadipour, Ariana Kariminejad, Hossein Najmabadi, Yousef Shafeghati, Farkhondeh Behjati
Published 2019-06-01

Grxcr2 is required for stereocilia morphogenesis in the cochlea.

by Matthew R Avenarius, Jae-Yun Jung, Charles Askew, Sherri M Jones, Kristina L Hunker, Hela Azaiez, Atteeq U Rehman, Margit Schraders, Hossein Najmabadi, Hannie Kremer, Richard J H Smith, Gwenaëlle S G Géléoc, David F Dolan, Yehoash Raphael, David C Kohrman
Published 2018-01-01

Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia

by Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï
Published 2013-01-01

Correction: A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia.

by Asma Ben Ammar, Payam Soltanzadeh, Stéphanie Bauché, Pascale Richard, Evelyne Goillot, Ruth Herbst, Karen Gaudon, Caroline Huzé, Laurent Schaeffer, Yuji Yamanashi, Osamu Higuchi, Antoine Taly, Jeanine Koenig, Jean-Paul Leroy, Fayçal Hentati, Hossein Najmabadi, Kimia Kahrizi, Manouchehr Ilkhani, Michel Fardeau, Bruno Eymard, Daniel Hantaï
Published 2013-01-01