How realistic is static traffic assignment? Analyzing automatic number-plate recognition data and image processing of real-time traffic maps for investigation
Mirzahossein, Hamid, Gholampour, Iman, Sedghi, Maryam, Zhu, Lei
Published in Transportation research interdisciplinary perspectives (01.03.2021)
Published in Transportation research interdisciplinary perspectives (01.03.2021)
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Journal Article
Clinical features of the myasthenic syndrome arising from mutations in GMPPB
Rodríguez Cruz, Pedro M, Belaya, Katsiaryna, Basiri, Keivan, Sedghi, Maryam, Farrugia, Maria Elena, Holton, Janice L, Liu, Wei Wei, Maxwell, Susan, Petty, Richard, Walls, Timothy J, Kennett, Robin, Pitt, Matthew, Sarkozy, Anna, Parton, Matt, Lochmüller, Hanns, Muntoni, Francesco, Palace, Jacqueline, Beeson, David
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2016)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2016)
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Journal Article
Association of SOD2 rs2758339, rs5746136 and rs2842980 polymorphisms with increased risk of breast cancer: a haplotype-based case–control study
Asadi, Sara, Abkar, Morteza, Zamanzadeh, Zahra, Taghipour Kamalabad, Setareh, Sedghi, Maryam, Yousefnia, Saghar
Published in Genes & genomics (01.09.2023)
Published in Genes & genomics (01.09.2023)
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Journal Article
Neurodevelopmental Outcome of Patients With Agenesis of Corpus Callosum
Nasiri, Jafar, Sedghi, Maryam, Hemat, Mohammad Hossein
Published in Caspian journal of neurological sciences (01.04.2021)
Published in Caspian journal of neurological sciences (01.04.2021)
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Journal Article
Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants
Mianesaz, Hamidreza, Ghalamkari, Safoura, Salehi, Mansoor, Behnam, Mahdiyeh, Hosseinzadeh, Majid, Basiri, Keivan, Ghasemi, Majid, Sedghi, Maryam, Ansari, Behnaz
Published in Molecular genetics & genomic medicine (01.02.2023)
Published in Molecular genetics & genomic medicine (01.02.2023)
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Journal Article
A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features
Sekiguchi, Futoshi, Nasiri, Jafar, Sedghi, Maryam, Salehi, Mansoor, Hosseinzadeh, Majid, Okamoto, Nobuhiko, Mizuguchi, Takeshi, Nakashima, Mitsuko, Miyatake, Satoko, Takata, Atsushi, Miyake, Noriko, Matsumoto, Naomichi
Published in Journal of human genetics (01.04.2018)
Published in Journal of human genetics (01.04.2018)
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Journal Article
Total graph of a $0$-distributive lattice
Ebrahimi Atani, Shahabaddin, Dolati Pishhesari, Saboura, Khoramdel, Mehdi, Sedghi, Maryam
Published in Categories and general algebraic structures with applications (01.07.2018)
Published in Categories and general algebraic structures with applications (01.07.2018)
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Journal Article
Early-onset Parkinson disease caused by a mutation in CHCHD2 and mitochondrial dysfunction
Lee, Richard G, Sedghi, Maryam, Salari, Mehri, Shearwood, Anne-Marie J, Stentenbach, Maike, Kariminejad, Ariana, Goullee, Hayley, Rackham, Oliver, Laing, Nigel G, Tajsharghi, Homa, Filipovska, Aleksandra
Published in Neurology. Genetics (01.10.2018)
Published in Neurology. Genetics (01.10.2018)
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Journal Article
Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries
Nouri, Narges, Fazel-Najafabadi, Esmat, Behnam, Mahdieh, Nouri, Nayereh, Aryani, Omid, Ghasemi, Majid, Nasiri, Jafar, Sedghi, Maryam
Published in Gene (10.02.2014)
Published in Gene (10.02.2014)
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Journal Article
Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study
Sedghi, Maryam, Moslemi, Ali‐Reza, Olive, Montse, Etemadifar, Masoud, Ansari, Behnaz, Nasiri, Jafar, Emrahi, Leila, Mianesaz, Hamid‐Reza, Laing, Nigel G., Tajsharghi, Homa
Published in Annals of clinical and translational neurology (01.11.2019)
Published in Annals of clinical and translational neurology (01.11.2019)
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Journal Article
Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families
Sedghi, Maryam, Esfandiari, Elham, Fazel-Najafabadi, Esmat, Salehi, Mansoor, Salavaty, Abbas, Fattahpour, Shirin, Dehghani, Leila, Nouri, Nayerossadat, Mokarian, Fariborz
Published in Journal of research in medical sciences (01.01.2016)
Published in Journal of research in medical sciences (01.01.2016)
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Journal Article
A case report of 22q11 deletion syndrome confirmed by array-CGH method
Sedghi, Maryam, Nouri, Narges, Abdali, Hossein, Memarzadeh, Mehrdad, Nouri, Nayereh
Published in Journal of research in medical sciences (01.03.2012)
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Published in Journal of research in medical sciences (01.03.2012)
Journal Article
Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset
Nouri, Nayereh, Fazel-Najafabadi, Esmat, Salehi, Mansoor, Hosseinzadeh, Majid, Behnam, Mahdieh, Ghazavi, Mohammad Reza, Sedghi, Maryam
Published in Advanced biomedical research (2014)
Published in Advanced biomedical research (2014)
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Journal Article
Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran
Sedghi, Maryam, Behnam, Mahdiyeh, Fazel, Esmat, Salehi, Mansoor, Ganji, Hamid, Meamar, Rokhsareh, Hosseinzadeh, Majid, Nouri, Nayereh
Published in Advanced biomedical research (2014)
Published in Advanced biomedical research (2014)
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Journal Article
An insight into genetics of non-syndromic cleft palate
Nouri, Nayereh, Karimi, Padideh, Mansoor, Salehi, Memarzadeh, Mehrdad, Ganji, Hamid, Sedghi, Maryam
Published in Advanced biomedical research (2013)
Published in Advanced biomedical research (2013)
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Journal Article
Association between Mismatch Repair Gene MSH3 codons 1036 and 222 Polymorphisms and Sporadic Prostate Cancer in the Iranian Population
Jafary, Fariba, Salehi, Mansoor, Sedghi, Maryam, Nouri, Nayereh, Jafary, Farzaneh, Sadeghi, Farzaneh, Motamedi, Shima, Talebi, Maede
Published in Asian Pacific journal of cancer prevention : APJCP (2012)
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Published in Asian Pacific journal of cancer prevention : APJCP (2012)
Journal Article