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

per Bagherizadeh, Eiman, Shafaghati, Yousef, Hadipour, Fatemeh, Behjati, Farkhondeh
Publicat a Indian J Hum Genet (2014)

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...

per Taghizadeh, Sara, Najmabadi, Hossein, Kamali, Koorosh, Behjati, Farkhondeh
Publicat a J Environ Health Sci Eng (2014)

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

per Bagherizadeh, Eiman, Behjati, Farkhondeh, Saberi, Seyed Hoseinali, Shafeghati, Yousef
Publicat 2011

Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature

per TAFAZOLI, Alireza, BEHJATI, Farkhondeh, FARHUD, Dariush D., ABBASZADEGAN, Mohammad Reza
Publicat a Iran J Public Health (2019)

The Relationship between KIT Copy Number Variation, Protein Expression, and Angiogenesis in Sporadic Breast Cancer

per Rahimi, Maryam, Behjati, Farkhondeh, Hamid Reza, Khorram Khorshid, Karimlou, Masoud, Keyhani, Elahe
Publicat a Rep Biochem Mol Biol (2020)

Investigation of Aneusomy of Chromosome 21 in the Micronuclei of 13 Patients with Early Onset Alzheimer’s Disease Using Fluorescence in Situ Hybridization: A Pilot Study

per Biglari, Sajjad, Kamali, Koorosh, Banihashemi, Sousan, Faal Sezavari, Arash, Aghajanpour-Mir, Seyed Mohsen, Behjati, Farkhondeh
Publicat a Rep Biochem Mol Biol (2020)

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

per Aghajanpour-Mir, Seyed Mohsen, Zabihi, Ebrahim, Akhavan-Niaki, Haleh, Keyhani, Elahe, Bagherizadeh, Iman, Biglari, Sajjad, Behjati, Farkhondeh
Publicat a Int J Mol Cell Med (2016)

Application of Multiplex Ligation-Dependent Probe Amplification in Determining the Copy Number Alterations of HER Gene Family Members in Invasive Ductal Breast Carcinoma

per Soosanabadi, Mohsen, Mirfakhraie, Reza, Atanesyan, Lilit, Biglarian, Akbar, Aghakhani Moghadam, Fatemeh, Rahimi, Maryam, Behjati, Farkhondeh, Keyhani, Elaheh
Publicat a Rep Biochem Mol Biol (2019)

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

per Nozari, Ahoura, Aghaei-Moghadam, Ehsan, Zeinaloo, Aliakbar, Alavi, Afagh, Ghasemi Firouzabdi, Saghar, Minaee, Shohre, Eskandari Hesari, Marzieh, Behjati, Farkhondeh
Publicat a Cell J (2019)

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

per Garshasbi, Masoud, Hadavi, Valeh, Habibi, Haleh, Kahrizi, Kimia, Kariminejad, Roxana, Behjati, Farkhondeh, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas Walter
Publicat 2008

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

per Aristidou, Constantia, Koufaris, Costas, Theodosiou, Athina, Bak, Mads, Mehrjouy, Mana M., Behjati, Farkhondeh, Tanteles, George, Christophidou-Anastasiadou, Violetta, Tommerup, Niels, Sismani, Carolina
Publicat a PLoS One (2017)

Relationship Between PIK3CA Amplification and P110α and CD34 Tissue Expression as Angiogenesis Markers in Iranian Women with Sporadic Breast Cancer

per Hosseini, Shadi, Behjati, Farkhondeh, Rahimi, Maryam, Taheri, Nazanin, Khoram Khorshid, Hamidreza, Aghakhani Moghaddam, Fatemeh, Ghasemi, Saghar, Karimlou, Masoud, Sirati, Fereidoon, Keyhani, Elahe
Publicat a Iran J Pathol (2018)

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

per Najafi, Maryam, Kordi-Tamandani, Dor Mohammad, Behjati, Farkhondeh, Sadeghi-Bojd, Simin, Bakey, Zeineb, Karimiani, Ehsan Ghayoor, Schüle, Isabel, Azarfar, Anoush, Schmidts, Miriam
Publicat a Orphanet J Rare Dis (2019)

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

per Zorrieh Zahra, Atieh, Kadkhoda, Sepideh, Behjati, Farkhondeh, Aghakhani Moghaddam, Fatemeh, Badiei, Azadeh, Sirati, Fereidoon, Afshin Alavi, Hossein, Atri, Morteza, Omranipour, Ramesh, Keyhani, Elahe
Publicat a Int J Mol Cell Med (2016)

Investigation of CEBPA and CEBPA-AS Genes Expression in Acute Myeloid Leukemia

per Gholami, Milad, Bayat, Sahar, Manoochehrabadi, Saba, Pashaiefar, Hossein, Omrani, Mir Davood, Jalaeikhoo, Hasan, Yassaee, Vahid Reza, Ebrahimpour, Mohammad Reza, Behjati, Farkhondeh, Mirfakhraie, Reza
Publicat a Rep Biochem Mol Biol (2019)

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

per Behjati, Farkhondeh, Firouzabadi, Saghar Ghasemi, Kariminejad, Roxana, Vameghi, Roshanak, Sajedi, Firouzeh, Shafaghati, Yousef, Ghasemlou, Behruz Ebrahimizade, Shojaei, Azadeh, Jamali, Peyman, Bahman, Ideh, Najmabadi, Hossein
Publicat 2013

A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

per Najafi, Maryam, Tamandani, Dor Mohammad Kordi, Azarfar, Anoush, Bakey, Zeineb, Behjati, Farkhondeh, Antony, Dinu, Schüle, Isabel, Sadeghi-Bojd, Simin, Karimiani, Ehsan Ghayoor, Schmidts, Miriam
Publicat a Front Pediatr (2019)

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

per Farajzadeh Valilou, Saeed, Alavi, Afagh, Pashaei, Mahdiyeh, Ghasemi Firouzabadi, Saghar, Shafeghati, Yousef, Nozari, Ahoura, Hadipour, Fatemeh, Hadipour, Zahra, Maghsoodlou Estrabadi, Bijan, Gholamreza Noorazar, Seyed, Banihashemi, Susan, Karimian, Javad, Fattahi, Mahshid, Behjati, Farkhondeh
Publicat a Mol Syndromol (2020)

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

per Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Kahrizi, Kimia, Kariminejad, Roxana, Bagherizadeh, Iman, Ansari, Javad, Fallah, Masoumeh, Mojtahedi, Forough, Darvish, Hossein, Bahrami Monajemi, Gholamreza, Abedini, S. Sedigheh, Jamali, Payman, Mojahedi, Faezeh, Zadeh-Vakili, Azita, Najmabadi, Hossein
Publicat 2011

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

per Ghasemi Firouzabadi, Saghar, Vameghi, Roshanak, Kariminejad, Roxana, Darvish, Hossein, Banihashemi, Susan, Firouzkouhi Moghaddam, Mahboubeh, Jamali, Peyman, Farbod Mofidi Tehrani, Hassan, Dehghani, Hossein, Raeisoon, Mohammad Reza, Narooie-Nejad, Mehrnaz, Jamshidi, Javad, Tafakhori, Abbas, Sadabadi, Saeid, Behjati, Farkhondeh
Publicat a Int J Mol Cell Med (2016)