Nayereh Nouri - Concepedia

Author

Nayereh Nouri

Isfahan University of Medical Sciences

Also Known As

Günter E. Schubert, Majid Hosseinzadeh, N Nouri, N. Nouri, Nayereh Nouri, Nima Nouri, Nouri, Nayereh, Rokhsareh Meamar

Publications

299

Citations

H-Index

Concepts

All Affiliations

Isfahan University of Medical Sciences Alzahra University University of Bologna IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola University of Ferrara

About

Nayereh Nouri is an author at Isfahan University of Medical Sciences specializing in genetics, medicine, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	55
2	Public Health	3	3	37
3	Pathology	2	2	22
4	Biostatistics	1	1	15
5	Cancer Genetics	1	1	10

Nayereh Nouri

Publications

193

Citations

H-Index

Page 1

	Year	Citations
Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11. Bronya J.B. Keats, Nayereh Nouri, Mary Z. Pelias, PubMed	1994	49
Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents Wolfram Demaerel, Majid Hosseinzadeh, Nayereh Nouri, Cytogenetic and Genome Research	2016	35
Non-syndromic cleft lip with or without cleft palate in Asian populations: Association analysis on three gene polymorphisms of the folate pathway Marcella Martinelli, Ambra Girardi, Francesca Curà, Archives of Oral Biology Association AnalysisGenetic DisorderGeneticsGenetic EpidemiologyHuman Polymorphism	2015	18
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 Maryam Sedghi, Nayereh Nouri, Esmat Fazel-Najafabadi, Advanced Biomedical Research	2014	18
Family-based association analysis between nonsyndromic cleft lip with or without cleft palate and IRF6 polymorphism in an Iranian population Nayereh Nouri, Mehrdad Memarzadeh, Francesco Carinci, Clinical Oral Investigations Genotype-phenotype AssociationMedicineGeneticsGenetic EpidemiologyHuman Polymorphism	2014	15
Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran Nayereh Nouri, Maryam Sedghi, Mahdiyeh Behnam, Advanced Biomedical Research	2014	13
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East Flavia Palombo, Claudio Graziano, Nadia Al-Wardy, Human Genetics Genetic TestingMendelian DisorderGenetic DisorderMedicineGenetics	2020	12
Biallelic loss of LDB3 leads to a lethal pediatric dilated cardiomyopathy Tamara T. Koopmann, Yalda Jamshidi, Mohammad Naghibi-Sistani, European Journal of Human Genetics	2022	12
Consanguineous marriages in the genetic counseling centers of Isfahan and the ethical issues of clinical consultations. Narges Nouri, Nayereh Nouri, Samane Tirgar, PubMed	2017	11
Association between Mismatch Repair Gene MSH3 codons 1036 and 222 Polymorphisms and Sporadic Prostate Cancer in the Iranian Population Fariba Jafary, Mansoor Salehi, Maryam Sedghi, Asian Pacific Journal of Cancer Prevention UrologyIranian PopulationSomatic VariantMedicineGenetics	2012	10

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