| Cancer/testis antigens: expression, regulation, tumor invasion, and use in immunotherapy of cancers A Salmaninejad, MR Zamani, M Pourvahedi, Z Golchehre, ... Immunological investigations 45 (7), 619-640, 2016 | 175 | 2016 |
| Clinical and genetic aspects of oral lichen planus MA Haqiqi, N Pourmoshir, AH Bereshneh Int J Biomed Adv Res 7 (6), 251, 2016 | 11 | 2016 |
| The first comprehensive cohort of the Duchenne muscular dystrophy in Iranian population: mutation spectrum of 314 patients and identifying two novel nonsense mutations G Zamani, A Hosseini Bereshneh, R Azizi Malamiri, S Bagheri, K Moradi, ... Journal of Molecular Neuroscience 70, 1565-1573, 2020 | 10 | 2020 |
| Genetic counseling and genetic tests ethical challenges AH Bereshneh, AS Nejad, SM Akrami Journal of Clinical Research & Bioethics 6 (5), 1, 2015 | 10 | 2015 |
| Horizons of personalized medicine in breast cancer treatment A Hosseini Bereshneh, D Soltani, N Veisi, M Khademi, MH Modarressi Tehran University of Medical Sciences Journal 74 (9), 607-613, 2016 | 9 | 2016 |
| Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy G Zamani, S Hosseinpour, MR Ashrafi, M Mohammadi, RS Badv, ... BMC neurology 22 (1), 162, 2022 | 7 | 2022 |
| Expanding the clinical and neuroimaging features of NKX6-2-related hereditary spastic ataxia type 8 AH Bereshneh, S Hosseipour, MS Rasoulinezhad, N Pak, M Garshasbi, ... European Journal of Medical Genetics 63 (5), 103868, 2020 | 7 | 2020 |
| Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report A Hosseini Bereshneh, M Garshasbi Journal of Medical Case Reports 12, 1-9, 2018 | 7 | 2018 |
| Crystallographic modeling of the PNPT1: c. 1453A> G variant as a cause of mitochondrial dysfunction and autosomal recessive deafness; expanding the neuroimaging and clinical … AH Bereshneh, Z Rezaei, E Jafarinia, F Rajabi, MR Ashrafi, AR Tavasoli, ... Mitochondrion 59, 1-7, 2021 | 5 | 2021 |
| Pharmacogenetics and personalized medicine in pancreatic cancer AH Bereshneh, F Morshedi, M Hematyar, A Kaki, M Garshasbi Acta Medica Iranica, 194-199, 2017 | 5 | 2017 |
| Ethical issues in prenatal diagnosis and therapeutic abortion in Iran AH Bereshneh, A Salmaninejad, SM Akrami Arvand Journal of Health and Medical Sciences 1 (2), 2016 | 5 | 2016 |
| Case report of RANBP2 mutation and familial acute necrotizing encephalopathy M Paktinat, K Hessami, S Inaloo, H Nemati, P Katibeh, M Nejabat, ... International Journal of Pediatrics 2021, 2021 | 4 | 2021 |
| Methylation assessment of two DKK2 and DKK4 genes in oral squamous cell carcinoma patients S Kheirandish, N Eshghyar, F Yazdani, PA Shakib, A Hosseini-Bereshneh, ... Iranian Journal of Public Health 49 (10), 1947, 2020 | 4 | 2020 |
| The molecular signature of breast cancer metastasis to bone T Bahrami, S Mokmeli, H Hossieni, R Pourpaknia, Z Makani, ... Anti-Cancer Drugs 27 (9), 824-831, 2016 | 4 | 2016 |
| Medical genetics, criteria of miscarriage and ethical challenges of genetic tests A Bereshneh, A Sadr-Nabavi Genetics in the 3rd Millennium 12, 3478-3487, 2014 | 4 | 2014 |
| Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report F Rajabi, AH Bereshneh, M Ramezanzadeh, M Garshasbi BMC pediatrics 22 (1), 63, 2022 | 2 | 2022 |
| Leukoencephalopathy in Al‐Raqad syndrome: Expanding the clinical and neuroimaging features caused by a biallelic novel missense variant in DCPS M Masoudi, AH Bereshneh, M Rasoulinezhad, MR Ashrafi, M Garshasbi, ... American journal of medical genetics Part A 182 (10), 2391-2398, 2020 | 2 | 2020 |
| Frequent Novel Variations Within MSH2 and MLH1 Genes in a Subset of Iranian Families With Hereditary Non-Polyposis Colorectal Cancer Shadi S Javan, A Andalib, AH Bereshneh, MH Emami, R Salehi, F Karami Acta Medica Iranica, 2019 | 2 | 2019 |
| High genetic heterogeneity of leukodystrophies in Iranian children: the first report of Iranian Leukodystrophy Registry M Ashrafi, R Kameli, S Hosseinpour, E Razmara, Z Zamani, Z Rezaei, ... neurogenetics 24 (4), 279-289, 2023 | 1 | 2023 |
| A comprehensive study of mutation and phenotypic heterogeneity of childhood mitochondrial leukodystrophies S Hosseinpour, E Razmara, M Heidari, Z Rezaei, MR Ashrafi, AZ Dehnavi, ... Brain and Development 46 (4), 167-179, 2024 | | 2024 |
Arash SalmaninejadPhD in Medical GeneticsVerified email at mums.ac.ir
