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Najafi, Maryam [Author]; Kordi-Tamandani, Dor Mohammad [Author]; Azarfar, Anoush [Author]; Bakey, Zeineb [Author]; Behjati, Farkhondeh [Author]; Antony, Dinu [Author]; Schüle, Isabel [Author]; Sadeghi-Bojd, Simin [Author]; Karimiani, Ehsan Ghayoor [Author]; Schmidts, Miriam [Author]

A 57 kB genomic deletion causing CTNS loss of function contributes to the CTNS mutational spectrum in the Middle East

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Lausanne: Frontiers Media, 2019

Published in: Frontiers in pediatrics ; 7 (2019), 89
Najafi, Maryam [Author]; Kordi-Tamandani, Dor Mohammad [Author]; Behjati, Farkhondeh [Author]; Sadeghi-Bojd, Simin [Author]; Bakey, Zeineb [Author]; Karimiani, Ehsan Ghayoor [Author]; Schüle, Isabel [Author]; Azarfar, Anoush [Author]; Schmidts, Miriam [Author]

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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... to E-book via Resolving system (Volltext ; freely accessible)

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London: BioMed Central, 2019

Published in: Orphanet journal of rare dise ; 14, 1 (2019), 41$z1750-1172
Taghizadeh, Sara; Behjati, Farkhondeh

COVID-19; History, Taxonomy, and Diagnostic Molecular and Immunological Techniques

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Knowledge E DMCC, 2022

Published in: International Journal of Medical Laboratory (2022)
Rahimi, Maryam; Keyhani, Elahe; Behjati, Farkhondeh

The Relation between Exon Variations of KIT Gene and Clinical Pathological Factors of Breast Cancer

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Farname, Inc., 2020

Published in: Journal of Obstetrics, Gynecology and Cancer Research, 5 (2020) 4, Seite 137-148
TAFAZOLI, Lireza; BEHJATI, Farkhondeh; D. FARHUD, Dariush; ABBASZADEGAN, Mohammad Reza

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

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Knowledge E, 2019

Published in: Iranian Journal of Public Health (2019)
Rahimi, Maryam; Behjati, Farkhondeh; Moghaddam, Fatemeh; Keyhani, Elahe

Investigation KIT Gene Expression in Sporadic Breast Cancer Tissues

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Farname, Inc., 2017

Published in: Multidisciplinary Cancer Investigation, 1 (2017) Supplementary 1, Seite 0-0
Taghizadeh, Sara; Najmabadi, Hossein; Kamali, Koorosh; Behjati, Farkhondeh

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

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Springer Science and Business Media LLC, 2014

Published in: Journal of Environmental Health Science and Engineering, 12 (2014) 1
Behjati, Farkhondeh; Bagherizadeh, Eiman; Shafaghati, Yousef; Hadipour, Fatemeh

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

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CLOCKSS Archive, 2014

Published in: Indian Journal of Human Genetics, 20 (2014) 2, Seite 203
Fatemeh Hadipour; Yousef Shafeghati; Eiman Bagherizadeh; Farkhondeh Behjati; Zahra Hadipour

Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family

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2013

Published in: Acta Medica Iranica, 51 (2013) 12
Behjati, Farkhondeh; Shafeghati, Yousef; Bagherizadeh, Eiman; Saberi, SeyedHoseinali

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

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CLOCKSS Archive, 2011

Published in: Indian Journal of Human Genetics, 17 (2011) 2, Seite 111
Khaksari, Soheila; Aghaei Moghadam, Ehsan; Nozari, Ahoura; Boroughani, Zahra; Ghasemi Firouzabadi, Saghar; Behjati, Farkhondeh

CNV Analysis Using Multiplex Ligation-Dependent Probe Amplification in Iranian Families with Non-Syndromic Congenital Heart Defects: Early Diagnosis of Non-Syndromic Patients

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Knowledge E DMCC, 2022

Published in: International Journal of Medical Laboratory (2022)
Rahimi, Maryam; Behjati, Farkhondeh; Khorram Khorshid, Hamid Reza; Karimlou, Masoud; Keyhani, Elahe

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

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CMV Verlag, 2020

Published in: Reports of Biochemistry and Molecular Biology, 9 (2020) 1, Seite 40-49
Muhammadnejad, Ahad; Keyhani, Elahe; Mortazavi, Pejman; Behjati, Farkhondeh; Haghdoost, Iraj Sohrabi

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

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Asian Pacific Organization for Cancer Prevention, 2012

Published in: Asian Pacific Journal of Cancer Prevention, 13 (2012) 12, Seite 6415-6421
Behjati, Farkhondeh; Shafeghati, Yousef; Kahrizi, Kimia; Firouzabadi, Saghar Ghasemi; Najmabadi, Hossein; Dixon, Neil; Davies, Angela F.

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

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Wiley, 2008

Published in: American Journal of Medical Genetics Part A, 146A (2008) 24, Seite 3223-3226
Behjati, Farkhondeh; Atri, Morteza; Najmabadi, Hossein; Nouri, Keramat; Zamani, Mahdi; Mehdipour, Parvin

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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Springer Science and Business Media LLC, 2005

Published in: Pathology & Oncology Research, 11 (2005) 3, Seite 157-163
Agha Gholizadeh, Mehdi; Behjati, Farkhondeh; Ghasemi Firouzabadi, Saghar; Heidari, Erfan; Razmara, Ehsan; Almadani, Navid; Sharifi Zarchi, Ali; Garshasbi, Masoud

Novel splicing variant and gonadal mosaicism in DYRK1A gene identified by whole-genome sequencing in multiplex autism spectrum disorder families

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Springer Science and Business Media LLC, 2024

Published in: Neurogenetics (2024)
Soosanabadi, Mohsen; Ghahfarokhi, Arezoo Mosharraf; Pourghazi, Farzad; Ehtesham, Naeim; Mirfakhraie, Reza; Atanesyan, Lilit; Keyhani, Elahe; Behjati, Farkhondeh

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

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Springer Science and Business Media LLC, 2022

Published in: Molecular Biology Reports, 49 (2022) 9, Seite 8547-8553
Ahoura Nozari; Ehsan Aghaei-Moghadam; Aliakbar Zeinaloo; Afagh Alavi; Saghar Ghasemi Firouzabad; Shohre Minaee; Marzeieh Eskandari Hesari; Farkhondeh Behjati

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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2018

Published in: Cell Journal, 21 (2018) 1, Seite 70-77
Keyhani, Elahe; Muhammadnejad, Ahad; Behjati, Farkhondeh; Sirati, Fereidoon; Khodadadi, Faranak; Karimlou, Masoud; Moghaddam, Fatemeh A.; Pazhoomand, Reza

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

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Asian Pacific Organization for Cancer Prevention, 2013

Published in: Asian Pacific Journal of Cancer Prevention, 14 (2013) 12, Seite 7651-7656
Aristidou, Constantia; Theodosiou, Athina; Alexandrou, Angelos; Papaevripidou, Ioannis; Evangelidou, Paola; Kosmaidou-Aravidou, Zoe; Behjati, Farkhondeh; Christophidou-Anastasiadou, Violetta; Tanteles, George A.; Sismani, Carolina

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

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MDPI AG, 2022

Published in: Genes, 14 (2022) 1, Seite 82

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