Lista de obras - Farkhondeh Behjati - Dominio Público Uruguay

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

artículo científico publicado en 2010

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

artículo científico publicado en 2008

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

artículo científico publicado el 1 de noviembre de 2012

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

artículo científico publicado en 2018

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

artículo científico publicado en 2017

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

artículo científico publicado en 2013

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

artículo científico publicado en 2010

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

artículo científico publicado en 2016

Chromosomal Abnormalities in Dupuytren’s Contracture and Carpal Tunnel Syndrome

artículo científico publicado en 1992

Chromosomal studies in infertile men

article

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

artículo científico publicado en 2011

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

artículo científico publicado en 1997

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

artículo científico publicado en 2016

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

artículo científico publicado en 2012

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

artículo científico publicado en 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 1993

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

artículo científico publicado en 2013

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

artículo científico publicado en 2009

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

artículo científico publicado en 2015

Genetic and environmental factors affecting immunoglobulin levels in Iran

artículo científico publicado en 1987

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

artículo científico publicado en 2013

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

artículo científico publicado en 2006

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

artículo científico publicado en 1985

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

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

artículo científico publicado en 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

artículo científico publicado en 2008

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

artículo científico publicado el 1 de febrero de 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 2008

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

artículo científico publicado en 2016

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

artículo científico publicado en 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

artículo científico publicado en 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.

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 2017

Lista de obras de Farkhondeh Behjati

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

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

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

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

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

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

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

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

Chromosomal Abnormalities in Dupuytren’s Contracture and Carpal Tunnel Syndrome

Chromosomal studies in infertile men

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

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

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

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

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

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

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

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

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

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

Genetic and environmental factors affecting immunoglobulin levels in Iran

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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.

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

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

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

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

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

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

The Iranian human mutation database

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

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