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Saeed Reza Ghaffari
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Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies
T Eisenberger, C Neuhaus, AO Khan, C Decker, MN Preising, ...
PloS one 8 (11), e78496, 2013
2392013
Prevalence of human papillomavirus genotypes in women with normal and abnormal cervical cytology in Iran
SR Ghaffari, T Sabokbar, H Mollahajian, J Dastan, F Ramezanzadeh, ...
Asian Pacific Journal of Cancer Prevention 7 (4), 529-532, 2006
1092006
Ataxia-telangiectasia in Iran: clinical and laboratory features of 104 patients
M Moin, A Aghamohammadi, A Kouhi, S Tavassoli, N Rezaei, SR Ghaffari, ...
Pediatric neurology 37 (1), 21-28, 2007
1042007
First‐trimester screening for chromosomal abnormalities by integrated application of nuchal translucency, nasal bone, tricuspid regurgitation and ductus venosus flow combined …
SR Ghaffari, AR Tahmasebpour, A Jamal, S Hantoushzadeh, L Eslamian, ...
Ultrasound in obstetrics & gynecology 39 (5), 528-534, 2012
892012
A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.
SR Ghaffari, E Boyd, JL Tolmie, YJ Crow, AH Trainer, JM Connor
Journal of medical genetics 35 (3), 225-233, 1998
811998
Human papillomavirus in saliva of patients with oral squamous cell carcinoma
M SahebJamee, M Boorghani, SR Ghaffari, F AtarbashiMoghadam, ...
Medicina Oral Patología Oral y Cirugia Bucal 14 (10), E525-E528, 2009
722009
Chromosomal radiosensitivity in patients with common variable immunodeficiency
A Aghamohammadi, M Moin, A Kouhi, MA Mohagheghi, A Shirazi, ...
Immunobiology 213 (5), 447-454, 2008
702008
Automatic locating the centromere on human chromosome pictures
M Moradi, SK Setarehdan, SR Ghaffari
16th IEEE Symposium Computer-Based Medical Systems, 2003. Proceedings., 56-61, 2003
502003
Experiences of infertile women seeking assisted pregnancy in Iran: a qualitative study
F Ranjbar, Z Behboodi-Moghadam, L Borimnejad, SR Ghaffari, ...
Journal of reproduction & infertility 16 (4), 221, 2015
472015
Increased nuchal translucency and pregnancy outcome
A Tahmasebpour, NB Rafiee, S Ghaffari, A Jamal
Iranian Journal of Public Health 41 (11), 92, 2012
372012
Automatic landmark detection on chromosomes' images for feature extraction purposes
M Moradi, SK Setarehdan, SR Ghaffari
3rd International Symposium on Image and Signal Processing and Analysis …, 2003
292003
Paradox of modern pregnancy: A phenomenological study of women’s lived experiences from assisted pregnancy
F Ranjbar, MM Akhondi, L Borimnejad, SR Ghaffari, ...
Journal of Pregnancy 2015, 2015
272015
A novel truncating mutation in the E-cadherin gene in the first Iranian family with hereditary diffuse gastric cancer
SR Ghaffari, M Rafati, T Sabokbar, J Dastan
European Journal of Surgical Oncology (EJSO) 36 (6), 559-562, 2010
272010
Normal ranges for fetal femur and humerus diaphysis length during the second trimester in an Iranian population
AR Tahmasebpour, R Pirjani, A Rahimi-Foroushani, SR Ghaffari, ...
Journal of Ultrasound in Medicine 31 (7), 991-995, 2012
212012
Her2 amplification status in Iranian breast cancer patients: comparison of immunohistochemistry (IHC) and fluorescence in situ hybridisation (FISH)
SR Ghaffari, T Sabokbar, J Dastan, M Rafati, S Moossavi
Asian Pac J Cancer Prev 12 (4), 1031-4, 2011
202011
Combining mammaglobin and carcinoembryonic mRNA markers for early detection of micrometastases from breast cancers-a molecular study of 59 patients
SR Ghaffari, T Sabokbar, S Tahmasebi, J Dastan, S Shorakae, A Moradi, ...
Asian Pacific Journal of Cancer Prevention 7 (3), 396-398, 2006
192006
Mosaic supernumerary ring chromosome 19 identified by comparative genomic hybridisation.
SR Ghaffari, E Boyd, JM Connor, AM Jones, JL Tolmie
Journal of medical genetics 35 (10), 836-840, 1998
191998
Determination of human papillomavirus type 16 genotype and construction of cloning vector pTZ57R encoding HPV16 E7 gene
Z Meshkat, H Soleimanjahi, M Mahmoudi, H Mirshahabi, ZM Hassan, ...
Saudi medical journal 28 (10), 1511, 2007
182007
" Familial" versus" Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes
M Rafati, E Seyyedaboutorabi, MR Ghadirzadeh, Y Heshmati, H Adibi, ...
Molecular cytogenetics 5, 1-5, 2012
162012
Rhodopsin gene mutation analysis in Iranian patients with autosomal dominant retinitis pigmentosa
D Roshandel, M Rafati, S Khorami, N Novin Baheran, S Jalali, ...
International Ophthalmology 39, 2523-2531, 2019
142019
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