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List of works by Farkhondeh Behjati

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly.

scientific article published on 26 October 2010

A defect in the TUSC3 gene is associated with autosomal recessive mental retardation

scientific article published on May 2008

A novel mutation in MCPH1 gene in an Iranian family with primary microcephaly

scientific article published on November 1, 2012

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

scientific article published on 15 March 2018

Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing

scientific article

Angiogenesis Markers in Breast Cancer - Potentially Useful Tools for Priority Setting of Anti-Angiogenic Agents

Angiogenesis markers in breast cancer--potentially useful tools for priority setting of anti-angiogenic agents

scientific article published in January 2013

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

scientific article published on 10 November 2010

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

scientific article

Chromosomal Abnormalities in Dupuytren’s Contracture and Carpal Tunnel Syndrome

scientific article published on 01 June 1992

Chromosomal studies in infertile men

article

Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages.

scientific article published on April 2011

Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation

scientific article published in January 1997

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

scientific article published on 28 October 2016

Cytogenetic abnormalities in 222 infertile men with azoospermia and oligospermia in Iran: Report and review

scientific article

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

scientific article

Detection of HER2 Status in Breast Cancer: Comparison of Current Methods with MLPA and Real-time RT-PCR

Detection of increased level of chromosome breakage in peripheral blood of Iranian women with sporadic breast cancer using neural networks

Evaluation of chromosomal aberrations caused by air pollutants in some taxi drivers from two polluted districts of urban Tehran and its comparison with drivers from rural areas of Lahijan: a pilot study

scientific article

FACC gene mutations and early prenatal diagnosis of Fanconi's anaemia

scientific article

Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family

scientific article published on January 2013

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

scientific article published on 8 April 2009

Frequency of PTEN alterations, TMPRSS2-ERG fusion and their association in prostate cancer.

scientific article

Genetic and environmental factors affecting immunoglobulin levels in Iran

scientific article published on 01 January 1987

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization.

scientific article published on October 2013

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.

scientific article published on 21 November 2006

Human leukocyte antigens and circulating immunoglobulin levels in Indian patients with pulmonary tuberculosis

scientific article published on 01 March 1985

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation

scientific article published on 05 October 2013

Improvement of hepatogenic differentiation of iPS cells on an aligned polyethersulfone compared to random nanofibers.

scientific article published on 11 July 2017

In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer.

scientific article published on 12 August 2016

Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation

scientific article published on 01 December 2008

Investigation of genetic causes of intellectual disability in kerman province, South East of iran ⬇️

scientific article published on February 1, 2012

Investigation of primary microcephaly in Bushehr province of Iran: novel STIL and ASPM mutations.

scientific article published on 18 September 2012

M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism.

scientific article published on 12 July 2008

Mutation Screening of BRCA Genes in 10 Iranian Males with Breast Cancer

scientific article published on 09 May 2016

Mutation analysis of androgen receptor gene: multiple uses for a single test.

scientific article published on 18 September 2014

Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans

scientific journal article

Mutational screening of ARX gene in Iranian families with X-linked intellectual disability

scientific article published in June 2012

Overexpression of HER-2/neu in Malignant Mammary Tumors: Translation of Clinicopathological Features from Dog to Human

Overexpression of her-2/neu in malignant mammary tumors; translation of clinicopathological features from dog to human.

scientific article

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.

scientific article published on 30 November 2012

Phenotypical characterization of 13q deletion syndrome: Report of two cases

scientific article

Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18

scientific article published on May 2011

Prognostic value of chromosome 1 and 8 copy number in invasive ductal breast carcinoma among Iranian women: an interphase FISH analysis

scientific article published on 29 September 2005

SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly

scientific article published on 26 November 2005

The Genotoxic and Cytotoxic Effects of Bisphenol-A (BPA) in MCF-7 Cell Line and Amniocytes

scientific article published on January 2016

The Iranian human mutation database

scientific article published on 01 July 2007

Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester

scientific article

miRNA-Related Polymorphisms in miR-423 (rs6505162) and PEX6 (rs1129186) and Risk of Esophageal Squamous Cell Carcinoma in an Iranian Cohort

scientific article published on 21 April 2017

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