S. Banihashemi

Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots

H. Ropers, D. Wieczorek, A. Tzschach, 2011, Human Genetics.

Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems

F. Hadipour, Z. Hadipour, F. Behjati, 2020, Molecular Syndromology.

Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome

H. Najmabadi, H. Ghaedi, H. Darvish, 2016, Molecular Neurobiology.

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications

H. Darvish, M. Raeisoon, F. Behjati, 2016, International journal of molecular and cellular medicine.

Development of Enzyme Linked Immunosorbent Assay for humoral immuneresponse and infection monitoring of anthrax

H. Nouri, K. Tadayon, M. Taghdiri, 2020 .

A Comparison of Transdiagnostic Components in Generalized Anxiety Disorder, Unipolar Mood Disorder and Nonclinical Population

L. Fata, I. Abasi, M. Sadeghi, 2013 .

Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population.

H. Ropers, K. Kahrizi, H. Najmabadi, 2009, European journal of medical genetics.

A novel splicing variant in FLNC gene responsible for a highly penetrant familial dilated cardiomyopathy in an extended Iranian family.

H. Najmabadi, F. Behjati, R. Mollazadeh, 2018, Gene.

Comparison of Chromosome Instabilities (Chromo- some Breakage and Aneusomy) Between Patients with Early- Onset Alzheimer Disease , Parkinson Disease and Normal Controls using Micronucleus Assay

M. Rohani, K. Kamali, F. Behjati, 2014 .