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Y. Nilipour · SciRah

Researcher profile · Semantic Scholar

Y. Nilipour

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Y. Nilipour — researcher profile on SciRah

h-index: 16
Works: 93
Citations: 1,043

Most-cited papers

Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.
J. Senderek, J. Müller, M. Dusl, T. Strom +35 more
2011American Journal of Human Genetics181 citations Open access
Semantic Scholar
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
V. Guergueltcheva, J. Müller, M. Dusl, J. Senderek +33 more
2012Journal of Neurology98 citations Open access
Semantic Scholar
An update on clinical, pathological, diagnostic, and therapeutic perspectives of childhood leukodystrophies
M. Ashrafi, Man Amanat, M. Garshasbi, Reyhaneh Kameli +4 more
2019Expert Review of Neurotherapeutics76 citations
Semantic Scholar
Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
C. Hedberg-Oldfors, A. Abramsson, D. Osborn, O. Danielsson +20 more
2019Human Molecular Genetics51 citations Open access
Semantic Scholar
Improved diagnostic yield of neuromuscular disorders applying clinical exome sequencing in patients arising from a consanguineous population
Zohreh Fattahi, Z. Kalhor, M. Fadaee, Raheleh Vazehan +10 more
2016Clinical Genetics50 citations
Semantic Scholar
Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies
Y. Nilipour, S. Nafissi, A. E. Tjust, G. Ravenscroft +12 more
2018European Journal of Neurology46 citations Open access
Semantic Scholar
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group
Fatma Al Jasmi, M. A. Al Jumah, Fatimah Alqarni, Nouriya A. Al-Sanna'a +12 more
2015BMC Neurology43 citations Open access
Semantic Scholar
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
J. Alonso-Pérez, L. González-Quereda, C. Bruno, C. Panicucci +24 more
2021Brain : a journal of neurology31 citations Open access
Semantic Scholar
Identification of COL6A2 mutations in progressive myoclonus epilepsy syndrome
S. Karkheiran, Catharine E. Krebs, Vladimir Makarov, Y. Nilipour +6 more
2013Human Genetics27 citations
Semantic Scholar
LGMD2E is the most common type of sarcoglycanopathies in the Iranian population
A. Alavi, Sara Esmaeili, Y. Nilipour, S. Nafissi +6 more
2017Journal of neurogenetics25 citations
Semantic Scholar
Genetics of GNE myopathy in the non-Jewish Persian population
A. Haghighi, S. Nafissi, A. Qurashi, Zheng Tan +5 more
2015European Journal of Human Genetics25 citations Open access
Semantic Scholar
Massive Ascites as the Only Sign of Ovarian Juvenile Granulosa Cell Tumor in an Adolescent: A Case Report and a Review of the Literature
A. Ashnagar, S. Alavi, Y. Nilipour, Roxana Azma +1 more
2013Case Reports in Oncological Medicine22 citations Open access
Semantic Scholar
Multiple acyl-coenzyme A dehydrogenase deficiency shows a possible founder effect and is the most frequent cause of lipid storage myopathy in Iran.
Y. Nilipour, F. Fatehi, Saleheh Sanatinia, Anna Bradshaw +4 more
2020Journal of Neurological Sciences21 citations Open access
Semantic Scholar
Osteoclast-Like Giant-Cell Tumor of the Parotid with Salivary Duct Carcinoma: Case Report and Cytologic, Histologic, and Immunohistochemical Findings
M. Kadivar, Y. Nilipour, A. Sadeghipour
2007Ear, nose, & throat journal21 citations Open access
Semantic Scholar
Adult-onset Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD)
F. Fatehi, A. Okhovat, Y. Nilipour, M. Mroczek +7 more
2020European Journal of Neurology17 citations Open access
Semantic Scholar
Increased number of regulatory T cells in esophageal tissue of patients with eosinophilic esophagitis in comparison to gastro esophageal reflux disease and control groups.
F. Mousavinasab, D. Babaie, Y. Nilipour, M. Mansouri +8 more
2019Allergologia et Immunopathologia17 citations Open access
Semantic Scholar
Recommendations for Infantile-Onset and Late-Onset Pompe Disease: An Iranian Consensus
F. Fatehi, M. Ashrafi, M. Babaee, B. Ansari +11 more
2021Frontiers in Neurology16 citations Open access
Semantic Scholar
Identification of a novel MICU1 nonsense variant causes myopathy with extrapyramidal signs in an Iranian consanguineous family
Fatemeh Bitarafan, Mehrnoosh Khodaeian, Elham Amjadi Sardehaei, F. Darvishi +3 more
2020Molecular and Cellular Pediatrics16 citations Open access
Semantic Scholar
Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report
Marzieh Mojbafan, S. Nojehdeh, F. Rahiminejad, Y. Nilipour +2 more
2020BMC Medical Genetics16 citations Open access
Semantic Scholar
A novel case report of spinal muscular atrophy with progressive myoclonic epilepsy from Iran
Reza Shervin Badv, Y. Nilipour, Shahram Rahimi-Dehgolan, A. Rashidi-Nezhad +1 more
2019International Medical Case Reports Journal14 citations Open access
Semantic Scholar
Tumefactive rebound of multiple sclerosis after the short-term cessation of fingolimod: A case report.
F. Ashtari, M. Sahraian, Marjan Oustad, Y. Nilipour
2019Multiple Sclerosis and Related Disorders13 citations
Semantic Scholar
Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families
M. Pashaei, Atefeh Davarzani, Reza Hajati, B. Zamani +5 more
2021Journal of neurogenetics12 citations Open access
Semantic Scholar
Effect of recurrent severe insulin-induced hypoglycemia on the cognitive function and brain oxidative status in the rats
Mahvash Nikpendar, M. Javanbakht, Hamidreza Moosavian, Sepideh Sajjadi +3 more
2024Diabetology & Metabolic Syndrome11 citations Open access
Semantic Scholar
Glioma Tumor Grading Using Radiomics on Conventional MRI: A Comparative Study of WHO 2021 and WHO 2016 Classification of Central Nervous Tumors
Farzan Moodi, Fereshteh Khodadadi Shoushtari, Delaram J. Ghadimi, Gelareh Valizadeh +6 more
2023Journal of Magnetic Resonance Imaging11 citations Open access
Semantic Scholar
Primary Signet-Ring Cell Carcinoma of the Urinary Bladder Successfully Managed with Radical Cystectomy in a Young Patient
F. Allameh, Morteza Fallah Karkan, Y. Nilipour, A. Rakhshan
2017Case Reports in Urology10 citations Open access
Semantic Scholar
Late‐onset pompe disease in Iran: A clinical and genetic report
Ferdos Nazari, F. Sinaei, Y. Nilipour, F. Fatehi +4 more
2017Muscle and Nerve10 citations
Semantic Scholar
Tumors of the Central Nervous System: An 18-Year Retrospective Review in a Tertiary Pediatric Referral Center
Hosein Aghayan Golkashani, H. Hatami, A. Farzan, Hassan Reza Mohammadi +3 more
2015Iranian journal of child neurology10 citations
Semantic Scholar
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patients.
A. Okhovat, Y. Nilipour, R. Boostani, F. Vahabizad +3 more
2020Neuromuscular Disorders9 citations
Semantic Scholar
Megaconial congenital muscular dystrophy due to CHKB gene variants, the first report of thirteen Iranian patients.
F. Zemorshidi, S. Nafissi, R. Boostani, E. G. Karimiani +5 more
2023Neuromuscular Disorders8 citations
Semantic Scholar
The Art of Muscle Biopsy in the New Genetic Era: A Narrative Review
Y. Nilipour
2019Iranian journal of child neurology8 citations
Semantic Scholar
Neutral lipid storage disease with myopathy: clinicopathological and genetic features of nine Iranian patients.
Hamed Shahriyari, M. Ramezani, Y. Nilipour, A. Okhovat +4 more
2023Neuromuscular Disorders7 citations
Semantic Scholar
BVVL/ FL: features caused by SLC52A3 mutations; WDFY4 and TNFSF13B may be novel causative genes.
Marzieh Khani, Hosein Shamshiri, Hanieh Taheri, J. Hardy +17 more
2020Neurobiology of Aging7 citations Open access
Semantic Scholar
Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation
G. Zamani, F. Karami, M. Mehdizadeh, A. Movafagh +2 more
2015Neurological Sciences7 citations
Semantic Scholar
Expression of neuronal markers, NFP and GFAP, in malignant astrocytoma.
F. Hashemi, Majid Naderian, M. Kadivar, Y. Nilipour +1 more
2014Asian Pacific Journal of Cancer Prevention7 citations Open access
Semantic Scholar
Retroperitoneal Malignant Peripheral Nerve Sheath Tumor Replacing an Absent Kidney in a Child
S. Alavi, M. Arzanian, Y. Nilipour
2013Case Reports in Oncological Medicine7 citations Open access
Semantic Scholar
Increased regulatory T cells in peripheral blood of children with eosinophilic esophagitis
Mahnaz Abdolahi, S. Rasouli, D. Babaie, N. Dara +10 more
2021Gastroenterology and hepatology from bed to bench6 citations
Semantic Scholar
Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group
Marzieh Mojbafan, S. Tonekaboni, M. Abiri, S. Kianfar +4 more
2016Journal of Molecular Neuroscience6 citations
Semantic Scholar
Nemaline myopathy: reclassification of previously reported variants according to ACMG guidelines, and report of novel genetic variants
A. Haghighi, Z. Alvandi, Y. Nilipour, Amirreza Haghighi +3 more
2023European Journal of Human Genetics5 citations Open access
Semantic Scholar
Distinct Clinical and Genetic Findings in Iranian Patients With Glycogen Storage Disease Type 3
Ferdos Nazari, F. Sinaei, Y. Nilipour, F. Petit +5 more
2018Journal of Clinical Neuromuscular Disease5 citations
Semantic Scholar
A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping
Marzieh Mojbafan, Y. Nilipour, S. Tonekaboni, S. Bagheri +5 more
2016Journal of neurogenetics5 citations
Semantic Scholar
A 33-year-old male farmer with progressive gingival swelling and bleeding
Taghi Azizi, A. Sadeghipour, Aliasghar Roohi, Y. Nilipour
2005Annals of Saudi Medicine5 citations Open access
Semantic Scholar
A novel heterozygous missense MYH7 mutation potentially causes an autosomal dominant form of myosin storage myopathy with dilated cardiomyopathy
Niloofar Naderi, N. Mohsen-Pour, Y. Nilipour, Maryam Pourirahim +2 more
2023BMC Cardiovascular Disorders4 citations Open access
Semantic Scholar
Neurological Complications of COVID-19: A Rare Case of Bilateral Blindness
Behnam Safarpour Lima, Negar Mohammadi Khorasani, S. H. Aghamiri, Fatemeh Omidi +1 more
2021Journal of Emergency Medicine4 citations Open access
Semantic Scholar
Estrogen Receptor Expression in Glial Tumors of Iranian Patients: A Single Center Experience
M. Shafiee, Ahmad R. Mafi, Y. Nilipour, A. Sourati +2 more
2020Iranian Journal of Pathology4 citations Open access
Semantic Scholar
Juvenile Clinically Amyopathic Dermatomyositis: A Case Report and Review of Literature
V. Javadi Parvaneh, M. Yasaei, K. Rahmani, Y. Nilipour
2019Iranian journal of child neurology4 citations
Semantic Scholar
A novel mutation in alpha sarcoglycan gene in an Iranian family with limb girdle muscular dystrophy 2D
Marzieh Mojbafan, Y. Nilipour, S. Tonekaboni, J. Tavakkoly-Bazzaz +1 more
2016Neurological Research4 citations
Semantic Scholar
Soft palatine mass with diagnosis of mature teratoma
M. Rouzrokh, F. Azizi, Y. Nilipour
2015International journal of surgery case reports4 citations Open access
Semantic Scholar
A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy
M. Behnam, Jin-Hong Shin, Dae-Seong Kim, Keivan Basiri +2 more
2014Journal of Research in Medical Sciences4 citations
Semantic Scholar
Survey on Childhood Solid Malignant Tumors in Cases Admitted to Mofid Pediatric Hospital From 1996-2010: a Single-Center Study
F. Jadali, Hosein Aghayan Golkashani, G. Habibi, M. Rouzrokh +6 more
2012Iranian Journal of Cancer Prevention4 citations
Semantic Scholar
A case of diffuse leptomeningeal glioneuronal tumor in a 10‐year‐old boy: First report from Iran
P. Karimzadeh, Y. Nilipour, M. Khalili, A. Nikkhah +2 more
2021Clinical Case Reports3 citations Open access
Semantic Scholar

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S. Nafissi×19
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S. Nafissi — researcher profile on SciRah
S. Tonekaboni×8
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S. Tonekaboni — researcher profile on SciRah
F. Fatehi×6
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F. Fatehi — researcher profile on SciRah
H. Najmabadi×5
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H. Najmabadi — researcher profile on SciRah

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A. Kariminejad — researcher profile on SciRah

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V. Straub — researcher profile on SciRah

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A. Alavi — researcher profile on SciRah

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A. Okhovat — researcher profile on SciRah

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R. Boostani — researcher profile on SciRah

Marzieh Mojbafan×4

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Marzieh Mojbafan — researcher profile on SciRah

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S. Zeinali — researcher profile on SciRah

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N. Muelas — researcher profile on SciRah