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ArticlesPeer ReviewedFull Text
Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing
Author / Creator:Aristidou, Constantia ; Koufaris, Costas ; Theodosiou, Athina ; Bak, Mads ; Mehrjouy, Mana M. ; Behjati, Farkhondeh ; Tanteles, George ; Christophidou-Anastasiadou, Violetta ; Tommerup, Niels ; Sismani, Carolina
Publisher:United States: Public Library of Science
Journal title:PloS one, 2017-01, Vol.12 (1), p.e0169935-e0169935
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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
Author / Creator:Najafi, Maryam ; Kordi-Tamandani, Dor Mohammad ; Behjati, Farkhondeh ; Sadeghi-Bojd, Simin ; Bakey, Zeineb ; Karimiani, Ehsan Ghayoor ; Schüle, Isabel ; Azarfar, Anoush ; Schmidts, Miriam
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2019-02, Vol.14 (1), p.41-41, Article 41
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BOD1 Is Required for Cognitive Function in Humans and Drosophila
Author / Creator:Esmaeeli-Nieh, Sahar ; Fenckova, Michaela ; Porter, Iain M. ; Motazacker, M. Mahdi ; Nijhof, Bonnie ; Castells-Nobau, Anna ; Asztalos, Zoltan ; Weißmann, Robert ; Behjati, Farkhondeh ; Tzschach, Andreas ; Felbor, Ute ; Scherthan, Harry ; Sayfati, Seyed Morteza ; Ropers, H. Hilger ; Kahrizi, Kimia ; Najmabadi, Hossein ; Swedlow, Jason R. ; Schenck, Annette ; Kuss, Andreas W.
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2016-05, Vol.12 (5), p.e1006022-e1006022
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Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans
Author / Creator:Pak, ChangHui ; Garshasbi, Masoud ; Kahrizi, Kimia ; Gross, Christina ; Apponi, Luciano H ; Noto, John J ; Kelly, Seth M ; Leung, Sara W ; Tzschach, Andreas ; Behjati, Farkhondeh ; Abedini, Seyedeh Sedigheh ; Mohseni, Marzieh ; Jensen, Lars R ; Hu, Hao ; Huang, Brenda ; Stahley, Sara N ; Liu, Guanglu ; Williams, Kathryn R ; Burdick, Sharon ; Feng, Yue ; Sanyal, Subhabrata ; Bassell, Gary J ; Ropers, Hans-Hilger ; Najmabadi, Hossein ; Corbett, Anita H ; Moberg, Kenneth H ; Kuss, Andreas W
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2011-07, Vol.108 (30), p.12390-12395
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The Genotoxic and Cytotoxic Effects of Bisphenol-A (BPA) in MCF-7 Cell Line and Amniocytes
Author / Creator:Aghajanpour-Mir, Seyed Mohsen ; Zabihi, Ebrahim ; Akhavan-Niaki, Haleh ; Keyhani, Elahe ; Bagherizadeh, Iman ; Biglari, Sajjad ; Behjati, Farkhondeh
Publisher:Iran: Babol University of Medical Sciences
Journal title:International journal of molecular and cellular medicine, 2016, Vol.5 (1), p.19-29
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Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature
Author / Creator:TAFAZOLI, Lireza ; BEHJATI, Farkhondeh ; D. FARHUD, Dariush ; ABBASZADEGAN, Mohammad Reza
Publisher:Iran: Tehran University of Medical Sciences
Journal title:Iranian journal of public health, 2019-03, Vol.48 (3), p.371-378
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Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies
Author / Creator:Mohammadzadeh, Akbar ; Akbaroghli, Susan ; Aghaei-Moghadam, Ehsan ; Mahdieh, Nejat ; Badv, Reza Shervin ; Jamali, Payman ; Kariminejad, Roxana ; Chavoshzadeh, Zahra ; Ghasemi Firouzabadi, Saghar ; Mansour Ghanaie, Roxana ; Nozari, Ahoura ; Banihashemi, Sussan ; Hadipour, Fatemeh ; Hadipour, Zahra ; Kariminejad, Ariana ; Najmabadi, Hossein ; Shafeghati, Yousef ; Behjati, Farkhondeh
Publisher:Iran: Royan Institute of Iran
Journal title:Cell journal (Yakhteh), 2019-10, Vol.21 (3), p.337-349
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Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications
Author / Creator: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
Publisher:Iran: Babol University of Medical Sciences
Journal title:International journal of molecular and cellular medicine, 2016, Vol.5 (4), p.236-245
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Mutation Screening of BRCA Genes in 10 Iranian Males with Breast Cancer
Author / Creator:Zorrieh Zahra, Atieh ; Kadkhoda, Sepideh ; Behjati, Farkhondeh ; Aghakhani Moghaddam, Fatemeh ; Badiei, Azadeh ; Sirati, Fereidoon ; Afshin Alavi, Hossein ; Atri, Morteza ; Omranipour, Ramesh ; Keyhani, Elahe
Publisher:Iran: Babol University of Medical Sciences
Journal title:International journal of molecular and cellular medicine, 2016-01, Vol.5 (2), p.114-122
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ArticlesPeer ReviewedFull Text
Prognostic value of chromosome 1 and 8 copy number in invasive ductal breast carcinoma among iranian women: An interphase FISH analysis
Author / Creator:Behjati, Farkhondeh ; Atri, Morteza ; Najmabadi, Hossein ; Nouri, Keramat ; Zamani, Mahdi ; Mehdipour, Parvin
Publisher:Switzerland: Springer Nature B.V
Journal title:Pathology oncology research, 2005-01, Vol.11 (3), p.157-163
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Deep sequencing reveals 50 novel genes for recessive cognitive disorders
Author / Creator:Najmabadi, Hossein ; Hu, Hao ; Garshasbi, Masoud ; Zemojtel, Tomasz ; Abedini, Seyedeh Sedigheh ; Chen, Wei ; Hosseini, Masoumeh ; Behjati, Farkhondeh ; Haas, Stefan ; Jamali, Payman ; Zecha, Agnes ; Mohseni, Marzieh ; Püttmann, Lucia ; Vahid, Leyla Nouri ; Jensen, Corinna ; Moheb, Lia Abbasi ; Bienek, Melanie ; Larti, Farzaneh ; Mueller, Ines ; Weissmann, Robert ; Darvish, Hossein ; Wrogemann, Klaus ; Hadavi, Valeh ; Lipkowitz, Bettina ; Esmaeeli-Nieh, Sahar ; Wieczorek, Dagmar ; Kariminejad, Roxana ; Firouzabadi, Saghar Ghasemi ; Cohen, Monika ; Fattahi, Zohreh ; Rost, Imma ; Mojahedi, Faezeh ; Hertzberg, Christoph ; Dehghan, Atefeh ; Rajab, Anna ; Banavandi, Mohammad Javad Soltani ; Hoffer, Julia ; Falah, Masoumeh ; Musante, Luciana ; Kalscheuer, Vera ; Ullmann, Reinhard ; Kuss, Andreas Walter ; Tzschach, Andreas ; Kahrizi, Kimia ; Ropers, H. Hilger
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2011-10, Vol.478 (7367), p.57-63
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Genetic Investigation of Inherited Variants in a Multiplex Autism Spectrum Disorder (ASD) Family Using Whole-Genome Sequencing (WGS)
Author / Creator:Gholizadeh, Mehdi Agha ; Behjati, Farkhondeh ; Garshasbi, Masoud Garshasbi
Publisher:Tehran: Tehran University of Medical Sciences
Journal title:Iranian journal of public health, 2025, Vol.54 (5), p.1087
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Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease
Author / Creator:Soosanabadi, Mohsen ; Ghahfarokhi, Arezoo Mosharraf ; Pourghazi, Farzad ; Ehtesham, Naeim ; Mirfakhraie, Reza ; Atanesyan, Lilit ; Keyhani, Elahe ; Behjati, Farkhondeh
Publisher:Dordrecht: Springer Netherlands
Journal title:Molecular biology reports, 2022-09, Vol.49 (9), p.8547-8553
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Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing
Author / Creator:Aristidou, Constantia ; Theodosiou, Athina ; Alexandrou, Angelos ; Papaevripidou, Ioannis ; Evangelidou, Paola ; Kosmaidou-Aravidou, Zoe ; Behjati, Farkhondeh ; Christophidou-Anastasiadou, Violetta ; Tanteles, George A. ; Sismani, Carolina
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2022-12, Vol.14 (1), p.82
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In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer
Author / Creator:Nariman-Saleh-Fam, Ziba ; Bastami, Milad ; Somi, Mohammad Hossein ; Samadi, Naser ; Abbaszadegan, Mohammad Reza ; Behjati, Farkhondeh ; Ghaedi, Hamid ; Tavakkoly-Bazzaz, Javad ; Masotti, Andrea
Publisher:New York: Springer US
Journal title:Cell biochemistry and biophysics, 2016-12, Vol.74 (4), p.483-497
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Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome
Author / Creator:Firouzabadi, Saghar Ghasemi ; Kariminejad, Roxana ; Vameghi, Roshanak ; Darvish, Hossein ; Ghaedi, Hamid ; Banihashemi, Susan ; Firouzkouhi Moghaddam, Mahboubeh ; Jamali, Peyman ; Mofidi Tehrani, Hassan Farbod ; Dehghani, Hossein ; Narooie-Nejad, Mehrnaz ; Jamshidi, Javad ; Tafakhori, Abbas ; Sadabadi, Saeid ; Najmabadi, Hossein ; Behjati, Farkhondeh
Publisher:New York: Springer US
Journal title:Molecular neurobiology, 2017-11, Vol.54 (9), p.7019-7027
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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 stu...
Author / Creator:Taghizadeh, Sara ; Najmabadi, Hossein ; Kamali, Koorosh ; Behjati, Farkhondeh
Publisher:London: BioMed Central
Journal title:Journal of environmental health science and engineering, 2014-12, Vol.12 (1), p.144, Article 144
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A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family A Pathogenic Homozygous Mutation In The Pl...
Author / Creator:Ahoura Nozari ; Ehsan Aghaei-Moghadam ; Aliakbar Zeinaloo ; Afagh Alavi ; Saghar Ghasemi Firouzabad ; Shohre Minaee ; Marzeieh Eskandari Hesari ; Farkhondeh Behjati
Publisher:Royan Institute (ACECR), Tehran
Journal title:Cell journal (Yakhteh), 2018-12, Vol.21 (1), p.70-77
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A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family
Author / Creator:Nozari, Ahoura ; Aghaei-Moghadam, Ehsan ; Zeinaloo, Aliakbar ; Alavi, Afagh ; Ghasemi Firouzabdi, Saghar ; Minaee, Shohre ; Eskandari Hesari, Marzieh ; Behjati, Farkhondeh
Publisher:Iran: Royan Institute of Iran
Journal title:Cell journal (Yakhteh), 2019-04, Vol.21 (1), p.70-77
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Phenotypical characterization of 13q deletion syndrome: Report of two cases
Author / Creator:Behjati, Farkhondeh ; Bagherizadeh, Eiman ; Shafaghati, Yousef ; Hadipour, Fatemeh
Publisher:India: Medknow Publications and Media Pvt. Ltd
Journal title:Indian journal of human genetics, 2014-04, Vol.20 (2), p.203-205
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Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing

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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

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BOD1 Is Required for Cognitive Function in Humans and Drosophila

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

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

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

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

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

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

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

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders

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Genetic Investigation of Inherited Variants in a Multiplex Autism Spectrum Disorder (ASD) Family Using Whole-Genome Sequencing (WGS)

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Expression of ERBB gene family in females with breast cancer and its correlation with clinicopathological characteristics of the disease

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Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing

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

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

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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 stu...

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A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family A Pathogenic Homozygous Mutation In The Pl...

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

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

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