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Atieh Hajianpour

Observed names: A Hajianpour, A. Hajianpour, A.K. Hajianpour, Amirhossein Hajianpour, Atieh K. Hajianpour
Observed institutions: Guy's Hospital, Children's Hospital Los Angeles, Kaiser Permanente, Great Ormond Street Hospital, King Faisal Specialist Hospital & Research Centre, Hospital for Sick Children, Centre for Applied Genomics
ORCID: 0009-0004-3741-8694
Observed ORCID: 0009-0004-3741-8694
OpenAlex ID: A5035888786
A nonsense mutation and exon skipping in the Fanconi anaemia group C gene
1993 · Rachel A. Gibson, Atieh Hajianpour, et al. · Human Molecular Genetics · 83
Novel mutations and polymorphisms in the Fanconi anemia group C gene
1996 · Rachel A. Gibson, Neil V. Morgan, et al. · Human Mutation · 44
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Genotype-phenotype correlation in satellited 1p chromosome: Importance of fluorescence in situ hybridization (FISH) applications
1994 · R. Habibian, M.J. Hajianpour, et al. · The American Journal of Human Genetics · 16
A new autosomal recessive anomaly mimicking Fanconi's anaemia phenotype.
1993 · R D Milner, K A Khallouf, et al. · Archives of Disease in Childhood · 14
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Centromeric α-Satellite DNA Break in Reciprocal Translocations
2009 · J.-C. Wang, A. Hajianpour, et al. · Cytogenetic and Genome Research · 6
Multicenter Characterization and Validation of the Intron-8 Poly(T) Tract (IVS8-T) Status in 25 Coriell Cell Repository Cystic Fibrosis Reference Cell Lines for Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene Mutation Assays
2004 · Siby Sebastian, Silvia G Spitzer, et al. · Clinical Chemistry · 6
Leiomyoma of uterus in a patient with ring chromosome 12: Case presentation and literature review
1996 · M. J. Hajianpour, Atieh K. Hajianpour, et al. · American Journal of Medical Genetics · 6
Deletion size and background genetic variation shape congenital heart disease phenotypes in 3,016 individuals with 22q11.2 deletion syndrome
2026 · Jhih-Rong Lin, Daniella Miller, et al. · medRxiv · 1
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8. A partial deletion of the EP300 gene detected by microarray in an individual with mild autism
2021 · Casey J. Brewer, Abbas Padeganeh, et al. · Cancer Genetics · 1
Erratum
2009 · M. Teruel, J. Cabrero, et al. · Cytogenetic and Genome Research · 1
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Erratum
2009 · M. Teruel, J. Cabrero, et al. · Cytogenetic and Genome Research · 1
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Cerebrovascular accident leading to cortical blindness in a patient with bird-headed dwarfism
1999 · M.J. Hajianpour, A. Jamali, et al. · Genetics in Medicine · 1
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Beyond reference bias: Making pangenomes accessible with PangyPlot
2025 · Scott Mastromatteo, Shalvi Chirmade, et al. · bioRxiv (Cold Spring Harbor Laboratory)
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331 Is epigenetic age a marker of CF severity and drug response?
2025 · D. Roshandel, S. Chirmade, et al. · Journal of Cystic Fibrosis
P532: Incidental detection of chromothripsis in routine blood testing of a patient with breast cancer
2023 · Abbas Padeganeh, Mariam Ghochani, et al. · Genetics in Medicine Open
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Chromosome 8q22.3q23.3 interstitial duplication: a rare case report and review of the literature
2021 · Abbas Padeganeh, Atieh Hajianpour, et al. · Molecular Genetics and Metabolism
Cytogenomic microarray analysis as a first-tier clinical diagnostic test: Kaiser Permanente, Southern California Permanente Medical Group experience
2021 · Mariam Ghochani, Atieh Hajianpour, et al. · Molecular Genetics and Metabolism
41. Clinical significance of comprehensive genetic workup prior to use of assisted reproductive technology: A case study
2021 · Abbas Padeganeh, Mariam Ghochani, et al. · Cancer Genetics
Contents Vol. 125, 2009
2009 · M. Teruel, J. Cabrero, et al. · Cytogenetic and Genome Research
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Author Index Vol. 125, 2009
2009 · M. Teruel, J. Cabrero, et al. · Cytogenetic and Genome Research
Works count: 20
Citation count: 180
H-index: 6
I10-index: 4
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