Seyed Hassan Tonekaboni

Author

Shahid Beheshti University of Medical Sciences ORCID

Also Known As

H. Tonekaboni, Hassan Tonekaboni, Rawda Sunbul, S. H. Tonekaboni, S. Hassan Tonekaboni, S. Tonekaboni, S.H. Tonekaboni, Sayed Hassan Tonekaboni, Seyed H. Tonekaboni, Seyed Hasan Tonekaboni

144

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Shahid Beheshti University of Medical Sciences University of Social Welfare and Rehabilitation Sciences Children's Medical Center Tehran University of Medical Sciences Isfahan Fertility and Infertility Center

About

Seyed Hassan Tonekaboni is an author at Shahid Beheshti University of Medical Sciences specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	16	616
2	Education	1	1	34
3	Health Sciences	1	1	28
4	Nursing	1	1	11
5	Public Health	1	1	79

Seyed Hassan Tonekaboni

Publications

Citations

H-Index

Page 1

	Year	Citations
Genetics of intellectual disability in consanguineous families Hao Hu, Kimia Kahrizi, Luciana Musante, Molecular Psychiatry Intellectual ImpairmentComplex Trait GeneticsGenetic DisorderGeneticsDisability	2018	206
Effect of inbreeding on intellectual disability revisited by trio sequencing Kimia Kahrizi, Hao Hu, Masoumeh Hosseini, Clinical Genetics Genetic TestingGeneticsGenetic EpidemiologyLinkage AnalysisDisease Gene Identification	2018	79
Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity Giovanni Stévanin, Giorgia Montagna, Hamid Azzedine, Neurogenetics MedicineGeneticsThin Corpus CallosumSpg11 LocusRehabilitation	2006	45
Ryanodine receptor type 3 (<i><scp>RYR</scp>3</i>) as a novel gene associated with a myopathy with nemaline bodies Yalda Nilipour, Shahriar Nafissi, Anton Tjust, European Journal of Neurology	2018	45
GM2-Gangliosidosis (Sandhoff and Tay Sachs disease): Diagnosis and Neuroimaging Findings (An Iranian Pediatric Case Series). Parvaneh Karimzadeh, Narjes Jafari, Habibeh Nejad Biglari, PubMed	2014	40
Efficacy of the Atkins diet as therapy for intractable epilepsy in children. Seyed Hassan Tonekaboni, Parvin Mostaghimi, Parvin Mirmiran, PubMed	2010	38
<i>PANK2</i> and <i>C19orf12</i> mutations are common causes of neurodegeneration with brain iron accumulation Mitra Ansari Dezfouli, Afagh Alavi, Mohammad Rohani, Movement Disorders	2012	36
Novel mutations in the ciliopathy-associated gene CPLANE1 (C5orf42) cause OFD syndrome type VI rather than Joubert syndrome Carine Bonnard, Mohammad Shboul, Seyed Hassan Tonekaboni, European Journal of Medical Genetics Ciliopathy-associated Gene Cplane1Joubert SyndromeGenetic DisorderGeneticsNovel Mutations	2018	36
Knowledge, attitudes, and practices among mothers of children with epilepsy: A study in a teaching hospital Ali‐Asghar Kolahi, Mohsen Abbasi‐Kangevari, Pouya Bakhshaei, Epilepsy & Behavior Family MedicinePediatricsTeaching HospitalMaternal HealthEducation	2017	34
Autosomal recessive mutations in <i><scp>THOC6</scp></i> cause intellectual disability: syndrome delineation requiring forward and reverse phenotyping J. Amos, Linda Huang, Julien Thévenon, Clinical Genetics	2016	33

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