S. Zeinali

S. Zeinali, Marzieh Mojbafan, Somayeh Takrim Nojehdeh, 2021, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Genetic Assessment of Mucopolysaccharidosis Type IV and the First Pathological Mutation of c.313A>G in the Iranian Population

S. Zeinali, M. Abiri, M. Hashemi, 2020 .

Investigating the influence of LCT rs3754689 polymorphism on inhibitor development in Iranian and Afghan patients with severe hemophilia A.

S. Zeinali, M. H. Samiee Aref, S. H. Mousavi, 2019, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

High-Resolution HLA-A Typing in Normal Iranian Population

S. Zeinali, Azadeh Hadadianpour, Mohammad Hasan Samiee Aref, 2018, Iranian biomedical journal.

Development and implementation of a novel panel consisting 20 markers for the detection of genetic causes of male infertility

S. Zeinali, M. Abiri, M. H. Samiee Aref, 2018, Andrologia.

Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group

S. Zeinali, M. Abiri, J. Tavakkoly-Bazzaz, 2016, Journal of Molecular Neuroscience.

A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping

S. Zeinali, Z. Sharifi, J. Tavakkoly-Bazzaz, 2016, Journal of neurogenetics.

Molecular Characterization of δ-Thalassemia in Iran

S. Zeinali, M. Karimipoor, A. Amirian, 2016, Hemoglobin.

A Large Cohort Study of Genotype and Phenotype Correlations of Beta- Thalassemia in Iranian Population

S. Zeinali, A. Azarkeivan, M. Fallah, 2015, International journal of hematology-oncology and stem cell research.

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia

S. Farashi, H. Najmabadi, S. Zeinali, 2015, Hemoglobin.

Analysis of Intron 1 Inversion at F8 Gene in Severe Hemophilia A Patients by Inverse Shifting-PCR Referred from Isfahan Seyedolshohada Hospital

S. Zeinali, L. Kokabee, M. Karimipoor, 2013 .

FREQUENCY OF ALPHA THALASSEMIA CARRIERS DETECTED IN TEHRAN PREMARRIAGE SCREENING USING MOLECULAR TECHNIQUES

S. Zeinali, M. Karimipoor, M. Fallah, 2013 .

Evaluation of intron 22 and intron 1 inversions of the factor 8 gene using an inverse shifting PCR method in severe haemophilia A patients

S. Zeinali, L. Kokabee, M. Karimipoor, 2013 .

Co-Inheritance of Beta & Delta-Globin Gene (HbYialousa) Mutations in an Iranian β-Thalassemia Carrier

S. Zeinali, M. Karimipoor, A. Valaei, 2012 .

Co-inheritance of α-and β-thalassemia : challenges in prenatal diagnosis of thalassemia

S. Zeinali, M. Karimipoor, A. Valaei, 2012 .

β-Thalassemia Mutations Found During 1 Year of Prenatal Diagnoses in Fars Province, Iran

S. Zeinali, A. Afrasiabi, A. Kord Valeshabad, 2011, Hemoglobin.

The Carrier Frequency of α-Globin Gene Triplication in an Iranian Population with Normal or Borderline Hematological Parameters

S. Zeinali, S. Moosavi, M. Karimipoor, 2011, Hemoglobin.

Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.

S. Zeinali, Leila Katouzian, M. Karimipoor, 2011, Archives of Iranian medicine.

First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.

S. Zeinali, M. Karimipoor, A. Amirian, 2011, Archives of Iranian medicine.

Molecular characterization of β-thalassemia intermedia: a report from Iran

A. Rajabi, S. Zeinali, M. Hamid, 2011, Molecular Biology Reports.

Identification of a Novel δ-Globin Gene Mutation in an Iranian Family

S. Zeinali, M. Karimipoor, A. Amirian, 2010, Hemoglobin.

Towards β-globin gene-targeting with integrase-defective lentiviral vectors

S. Zeinali, B. Yakhchali, R. A. Cohan, 2010, Biotechnology Letters.

A Novel Polymorphism Causes A Different Restriction Pattern by RsaI in the β-Globin Gene Cluster: Application in Prenatal Diagnosis

S. Zeinali, M. Karimipoor, A. Valaei, 2009, Hemoglobin.

The role of miRNA-377 as a tumor suppressor in lung cancer by negative regulation of genes belonging to ErbB signaling pathway

S. Zeinali, R. Mahdian, Saba Hashemi, 2021, Molecular Biology Reports.

Phenotypic heterogeneity in PIK3CA‐related overgrowth spectrum

J. Uitto, S. Zeinali, H. Vahidnezhad, 2016, The British journal of dermatology.

Gene-Targeted Next-Generation Sequencing Identifies a Novel CLDN1 Mutation in a Consanguineous Family With NISCH Syndrome

J. Uitto, S. Zeinali, H. Vahidnezhad, 2017, The American Journal of Gastroenterology.

A novel single step double positive double negative selection strategy for beta-globin gene replacement.

S. Zeinali, B. Rabbani, H. Khanahmad, 2006, Biochemical and biophysical research communications.

Beta thalassemia gene therapy using lentiviral vectors

S. Zeinali, M. Karimipoor, M. Abbasalipour, 2020 .

Transient Expression Assay of Aγ-588 (A/G) Mutations in the K562 Cell Line

S. Zeinali, M. Hamid, M. Karimipoor, 2011 .

Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

S. Zeinali, M. Hamid, M. Karimipoor, 2011, Iranian biomedical journal.

Missense mutations in the human beta fibrinogen gene cause congenital afibrinogenemia by impairing fibrinogen secretion.

P. Mannucci, E. Santagostino, P. Mannucci, 2000, Blood.

Identification of factor IX mutations in Iranian haemophilia B patients by SSCP and sequencing.

N. Nafissi, S. Zeinali, E. Tuddenham, 2007, Thrombosis research.

Carrier testing and prenatal diagnosis of haemophilia B by SSCP in an Iranian family

S. Zeinali, M. Karimipoor, R. Safaee, 2003, Haemophilia : the official journal of the World Federation of Hemophilia.

Allele frequencies of two polymorphisms associated with the factor IX gene in Iranian population.

S. Zeinali, P. Ghandil, A. Ghadiri, 2004, Thrombosis research.

The locus for combined factor V-factor VIII deficiency (F5F8D) maps to 18q21, between D18S849 and D18S1103.

S. Zeinali, J. Blouin, E. Tuddenham, 1997, American journal of human genetics.

Iranian national program for the prevention of thalassemia and prenatal diagnosis : mandatory premarital screening and legal medical abortion

S. Zeinali, A. Samavat, M. Fallah, 2009, Prenatal diagnosis.

Lessons for preparedness and reasons for concern from the early COVID-19 epidemic in Iran

Mohammad Hossein Khosravi, L. Ferretti, A. Katzourakis, 2021, Epidemics.

Therapeutic targeting of angiogenesis molecular pathways in angiogenesis-dependent diseases.

Asghar Fallah, Ali Sadeghinia, S. Zeinali, 2019, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinity

J. Uitto, S. Zeinali, M. Abiri, 2016, Journal of Pediatric Endocrinology & Metabolism (JPEM).

Genomics‐based treatment in a patient with two overlapping heritable skin disorders: Epidermolysis bullosa and acrodermatitis enteropathica

J. Uitto, J. McGrath, A. Kariminejad, 2020, Human mutation.

Targeted deletion of BCL11A gene by CRISPR-Cas9 system for fetal hemoglobin reactivation: A promising approach for gene therapy of beta thalassemia disease.

J. Concordet, S. Zeinali, K. Azadmanesh, 2019, European journal of pharmacology.

Autosomal recessive congenital ichthyosis: Genomic landscape and phenotypic spectrum in a cohort of 125 consanguineous families

P. Fortina, J. Uitto, K. K. Hesari, 2019, Human mutation.

Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity.

P. Fortina, J. Uitto, S. Zeinali, 2017, The Journal of investigative dermatology.

Keratitis‐ichthyosis‐deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation

J. Uitto, Z. Naraghi, S. Zeinali, 2020, Dermatologic therapy.

Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

S. Zeinali, A. Surguchov, Y. Nilipour, 2019, Molecular genetics & genomic medicine.

The Molecular Analysis of β-Thalassemia Mutations in Lorestan Province, Iran

S. Zeinali, Y. Mortazavi, A. Kiani, 2007, Hemoglobin.

Molecular Analysis of γ-Globin Promoters, HS-111 and 3′HS1, in β-thalassemia Intermedia Patients Associated with High Levels of Hb F

S. Zeinali, M. Hamid, M. Karimipoor, 2009, Hemoglobin.

A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran

S. Zeinali, M. Ghaffari Novin, Z. Sharifi, 2021, BMC Pregnancy and Childbirth.

Development of a quantitative real-time PCR assay for detection of unknown alpha-globin gene deletions.

S. Zeinali, R. Mahdian, M. Fallah, 2010, Blood cells, molecules & diseases.

Detection of unknown deletions in β‐globin gene cluster using relative quantitative PCR methods

S. Zeinali, M. Karimipoor, R. Mahdian, 2009, European journal of haematology.

Reporting Two Novel Mutations in Two Iranian Families with Cystic Fibrosis, Molecular and Bioinformatic Analysis

M. Kabiri, S. Zeinali, Amin Hosseini Nami, 2022, Iranian biomedical journal.

Archive of SID Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene

S. Zeinali, H. Khanahmad, E. Kamali, 2010 .

Whole-transcriptome sequencing–based concomitant detection of viral and human genetic determinants of cutaneous lesions

J. Casanova, P. Fortina, J. Uitto, 2022, JCI insight.

Recalcitrant Cutaneous Warts in a Family with Inherited ICOS Deficiency.

J. Casanova, J. Uitto, S. Zeinali, 2022, The Journal of investigative dermatology.

Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations

S. Zeinali, N. Mahdieh, B. Rabbani, 2010, Journal of Human Genetics.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

Multipotent mesenchymal stromal cells: optimization and comparison of five cationic polymer-based gene delivery methods.

M. Soleimani, Y. Gheisari, S. Zeinali, 2008, Cytotherapy.

The role of miRNA-377 as a tumor suppressor in lung cancer by negative regulation of genes belonging to ErbB signaling pathway

S. Zeinali, R. Mahdian, Saba Hashemi, 2021, Molecular Biology Reports.

TCF4 silencing sensitizes the colon cancer cell line to oxaliplatin as a common chemotherapeutic drug

S. Zeinali, L. Teimoori-Toolabi, Fatemeh Gheidari, 2014, Anti-cancer drugs.

Frequency and Correlation of Common Genes Copy Number Alterations in Childhood Acute Lymphoblastic Leukemia with Prognosis

R. Sheervalilou, S. Zeinali, J. Toporski, 2020, Asian Pacific journal of cancer prevention : APJCP.

Whole-Transcriptome Analysis by RNA Sequencing for Genetic Diagnosis of Mendelian Skin Disorders in the Context of Consanguinity.

P. Fortina, J. Uitto, F. Abdollahimajd, 2021, Clinical chemistry.

Next generation sequencing identifies double homozygous mutations in two distinct genes (EXPH5 and COL17A1) in a patient with concomitant simplex and junctional epidermolysis bullosa

J. Uitto, J. McGrath, A. Kariminejad, 2018, Human mutation.

KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.

J. Uitto, S. Zeinali, H. Vahidnezhad, 2016, The Journal of investigative dermatology.

Mutation update: The spectra of PLEC sequence variants and related plectinopathies

J. Uitto, S. Zeinali, H. Vahidnezhad, 2022, Human mutation.

Kindler epidermolysis bullosa-like skin phenotype and downregulated basement membrane zone gene expression in poikiloderma with neutropenia and a homozygous USB1 mutation.

J. Uitto, J. McGrath, A. Kariminejad, 2021, Matrix biology : journal of the International Society for Matrix Biology.

Comprehensive Mutation Analysis and Report of 12 Novel Mutations in a Cohort of Patients with Spinal Muscular Atrophy in Iran

M. Taheri, S. Zeinali, M. Abiri, 2021, Journal of Molecular Neuroscience.

Molecular genetic diagnosis of Glanzmann syndrome in Iranian population; reporting novel and recurrent mutations

S. Zeinali, M. Abiri, Z. Salehi, 2019, Orphanet Journal of Rare Diseases.

Targeted Integration into Pseudo attP Sites of CHO Cells Using CRISPR/Cas9.

S. Zeinali, F. Davami, E. Bayat, 2021, Journal of biotechnology.

Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder

J. Schuurs-Hoeijmakers, S. Antonarakis, R. Płoski, 2021, Genetics in Medicine.

Selective Suicide Gene Therapy of Colon Cancer Exploiting the Urokinase Plasminogen Activator Receptor Promoter

S. Zeinali, K. Azadmanesh, L. Teimoori-Toolabi, 2010, BioDrugs.

Selective suicide gene therapy of colon cancer cell lines exploiting fibroblast growth factor 18 promoter.

S. Zeinali, K. Azadmanesh, L. Teimoori-Toolabi, 2010, Cancer biotherapy & radiopharmaceuticals.

Potential circulating miRNA signature for early detection of NSCLC.

S. Irani, S. Zeinali, Elham Tafsiri, 2017, Cancer genetics.

Detection of Numerical Aneuploidy of Chromosomes X, Y, 13, 18 and 21 in 100 Blood and Fetals Samples by QF-PCR Method

A. Kariminejad, S. Zeinali, M. Hashemi, 2012 .

Transduction of an optimized recombinant lentivirus expressing E-cadherin shRNA resulted in stable downregulation of CDH1 gene and obvious cell morphological change in the human colorectal cancer cell line HT29

A. Fallah, S. Zeinali, Behrooz Johari, 2016 .

Comprehensive Analysis via Exome Sequencing Uncovers Genetic Etiology in Autosomal Recessive Non-Syndromic Deafness in a Large Multiethnic Cohort

M. Tekin, S. Blanton, Shengru Guo, 2015, Genetics in Medicine.

A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effect.

S. Zeinali, M. Tabatabaiefar, N. Mahdieh, 2013, International journal of pediatric otorhinolaryngology.

MiR-377 reverses cancerous phenotypes of pancreatic cells via suppressing DNMT1 and demethylating tumor suppressor genes.

S. Zeinali, H. Mahmoodzadeh, K. Azadmanesh, 2017, Epigenomics.

G allele at −924 A > G position of FoxP3 gene promoter as a risk factor for tuberculosis

S. Abediankenari, S. Zeinali, M. Goudarzi, 2017, BMC Infectious Diseases.

The human CIB1–EVER1–EVER2 complex governs keratinocyte-intrinsic immunity to β-papillomaviruses

J. Casanova, E. Fuchs, J. Franco, 2018, The Journal of experimental medicine.

Expression analysis data of BCL11A and γ-globin genes in KU812 and KG-1 cell lines after CRISPR/Cas9-mediated BCL11A enhancer deletion

J. Concordet, S. Zeinali, T. Buch, 2019, Data in brief.

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

A. Noor, J. Vincent, M. Rafiq, 2017, Molecular Psychiatry.

Identification and characterization of a novel nanobody against human placental growth factor to modulate angiogenesis.

S. Muyldermans, H. Rahimi, S. Zeinali, 2016, Molecular immunology.

In Vitro Evaluation of Vegf-Pseudomonas Exotoxin: A Conjugated on Tumor Cells

S. Zeinali, M. Behdani, M. Karimipoor, 2017, Advanced biomedical research.

Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing

S. Zeinali, J. Tavakkoly-Bazzaz, M. Fallah, 2015, Acta oto-laryngologica.

Molecular Analysis of KCNQ1, KCNH2 and SCN5A Genes in Iranian Patients with Long QT Syndrome

S. Zeinali, S. Saber, A. Fazelifar, 2018 .

Aberrant promoter hypermethylation of miR-335 and miR-145 is involved in breast cancer PD-L1 overexpression

S. Zeinali, Masoumeh Azizi, N. Nafissi, 2023, Scientific Reports.

Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous Marriages.

P. Fortina, J. Uitto, A. Ertel, 2017, The Journal of investigative dermatology.

Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

S. Zeinali, Z. Sharifi, S. Bagheri, 2020, Orphanet journal of rare diseases.

Identification of a Novel KCNQ1 Frameshift Mutation and Review of the Literature among Iranian Long QT Families

S. Zeinali, S. Saber, A. Fazelifar, 2019, Iranian biomedical journal.

Molecular genetic study of Calpainopathy in Iran.

S. Zeinali, A. Khajeh, H. Bagherian, 2018, Gene.

In silico analysis of novel mutations in maple syrup urine disease patients from Iran

M. Alaei, S. Zeinali, M. Abiri, 2016, Metabolic Brain Disease.

Molecular Investigation of Iranian Patients Suspected to Hereditary Spherocytosis

S. Zeinali, A. Majd, Z. Shahab-Movahed, 2021, Journal of Blood Disorders.

Screening of OTOF mutations in Iran: a novel mutation and review.

M. Tekin, S. Zeinali, N. Mahdieh, 2012, International journal of pediatric otorhinolaryngology.

Severely damaged kidneys possess multipotent renoprotective stem cells.

M. Soleimani, M. Vasei, Y. Gheisari, 2010, Cytotherapy.

8q24.3 and 11q25 chromosomal loci association with low HDL‐C in metabolic syndrome

F. Azizi, Ahmed Rebai, M. Hedayati, 2011, European journal of clinical investigation.

A gene-based anti-angiogenesis therapy as a novel strategy for cancer treatment.

S. Zeinali, A. Fallah, H. Heidari, 2019, Life sciences.

MicroRNA-148b and microRNA-152 reactivate tumor suppressor genes through suppression of DNA methyltransferase-1 gene in pancreatic cancer cell lines

S. Zeinali, K. Azadmanesh, L. Teimoori-Toolabi, 2014, Cancer biology & therapy.

Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency.

J. Uitto, J. McGrath, A. Kariminejad, 2019, Matrix biology : journal of the International Society for Matrix Biology.

The Evaluation of miR-21 Level in Lung Tissue and Plasma of Nsclc Patients

S. Irani, S. Zeinali, Elham Tafsiri, 2017 .

Expression Levels of Key Components of the Hedgehog Pathway and an Investigation of the Correlation of this Pathway with Expression Levels of Claudin-1 in Invasive Breast Carcinoma

S. Zeinali, M. Salehi, S. Babashah, 2022 .

The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family

S. Zeinali, M. Hamid, M. Karimipoor, 2009, Annals of Hematology.

Detection of a new KCNQ1 frameshift mutation associated with Jervell and Lange‐Nielsen syndrome in 2 Iranian families

S. Zeinali, S. Saber, A. Fazelifar, 2018, Journal of arrhythmia.

Efficacy and antitumor activity of a mutant type of interleukin 2

S. Zeinali, S. Ajdary, M. Behdani, 2022, Scientific Reports.

Human IL-2Rɑ subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approach

M. Shokrgozar, S. Zeinali, S. Ajdary, 2022, PloS one.

Genetic testing of Mucopolysaccharidoses disease using multiplex PCR- based panels of STR markers: in silico analysis of novel mutations

S. Zeinali, M. Abiri, M. Hashemi, 2019, Metabolic Brain Disease.

Multigene Next-Generation Sequencing Panel Identifies Pathogenic Variants in Patients with Unknown Subtype of Epidermolysis Bullosa: Subclassification with Prognostic Implications.

P. Fortina, J. Uitto, S. Zeinali, 2017, The Journal of investigative dermatology.

Arrhythmogenic right ventricular cardiomyopathy in patients with biallelic JUP-associated skin fragility

J. Uitto, J. McGrath, Z. Sani, 2020, Scientific Reports.

Genome‐wide single nucleotide polymorphism‐based autozygosity mapping facilitates identification of mutations in consanguineous families with epidermolysis bullosa

H. Hakonarson, Cecilia Kim, J. Bradfield, 2019, Experimental dermatology.

Molecular genetics of a cohort of 635 cases of phenylketonuria in a consanguineous population

M. Alaei, S. Zeinali, M. Abiri, 2018, Journal of Inherited Metabolic Disease.

Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort

S. Zeinali, M. Abiri, M. Hashemi, 2018, Metabolic Brain Disease.

GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss

S. Zeinali, L. Rejali, Sarah Azadmehr, 2015, European Archives of Oto-Rhino-Laryngology.

Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.

S. Zeinali, N. Mahdieh, B. Rabbani, 2011, Genetic testing and molecular biomarkers.

Archive of SID Molecular Analysis of Iranian Patients with Duchenne/Becker Muscular Dystrophies

F. Pourfarzad, H. Najmabadi, S. Zeinali, 2003 .

Expression of VGRNb-PE immunotoxin in transplastomic lettuce (Lactuca sativa L.)

S. Zeinali, M. Behdani, A. Moieni, 2018, Plant Molecular Biology.

Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 beta-thalassemia.

S. Zeinali, M. Naderi, R. Mahdian, 2009, Blood cells, molecules & diseases.

In silico design, construction and cloning of Trastuzumab humanized monoclonal antibody: A possible biosimilar for Herceptin

M. Shokrgozar, S. Zeinali, B. Yakhchali, 2012, Advanced biomedical research.

8q24.3and11q25chromosomallociassociation with low HDL-C in metabolic syndrome

F. Azizi, Ahmed Rebai, M. Hedayati, 2011 .

Allele frequency distribution for D11S1304, D11S1998, and D11S934 and metabolic syndrome in TLGS

F. Azizi, M. Hedayati, M. Zarkesh, 2010 .

Allele Frequency Distribution Data for D8S1132, D8S1779, D8S514, and D8S1743 in Four Ethnic Groups in Relation to Metabolic Syndrome: Tehran Lipid and Glucose Study

F. Azizi, M. Hedayati, M. Zarkesh, 2009, Biochemical Genetics.

Validation and comparison of two quantitative real-time PCR assays for direct detection of DMD/BMD carriers.

S. Zeinali, M. Karimipoor, R. Mahdian, 2009, Clinical biochemistry.

Novel mutations in the BRCA1 and BRCA2 genes in Iranian women with early-onset breast cancer

D. Hornby, A. Dalton, S. Zeinali, 2002, Breast Cancer Research.

Transfection of Human Hematopoietic Stem Cells by a Gene Targeting Construct Containing the β-Globin Gene

S. Zeinali, H. Khanahmad, E. Kamali, 2010 .

Molecular cloning and expression of human trophoblast antigen FDO161G and its identification as 3 beta-hydroxy-5-ene steroid dehydrogenase.

M. McBride, R. Sutcliffe, S. Zeinali, 1991, Journal of reproduction and fertility.

Three common CARD15 mutations are not responsible for the pathogenesis of Crohn's disease in Iranians.

R. Malekzadeh, S. Zeinali, S. Rashtak, 2010, Hepato-Gastroenterology.

Characterization of Niemann-Pick diseases genes mutation spectrum in Iran and identification of a novel mutation in SMPD1 gene

S. Zeinali, M. Karimipoor, Elham Davoudi-Dehaghani, 2019, Medical journal of the Islamic Republic of Iran.

Improved Microsatellite Instability detection in colorectal cancer patients by a combination of fourteen markers especially DNMT3a, DCD, and MT1X.

S. Zeinali, H. Mahmoodzadeh, M. Fazeli, 2021, Cancer biomarkers : section A of Disease markers.

A. Fallah, S. Zeinali, Mansoureh Soleimani, 2019, Cell journal.

BRCA1 and BRCA2 germline mutations in 85 Iranian breast cancer patients

G. Javadi, S. Zeinali, F. Keshavarzi, 2012, Familial Cancer.

Sequence Variants of BRCA1 and BRCA2 Genes in Four Iranian Families with Breast and Ovarian Cancer

S. Zeinali, F. Keshavarzi, A. E. Noughani, 2011, Iranian journal of public health.

BRCA 1 and BRCA 2 germline mutations in 85 Iranian breast cancer patients

G. Javadi, S. Zeinali, F. Keshavarzi, 2022 .

Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of miR-200b, miR-145, and let7b in A Functional Imbalanced Epigenetic Disease

S. Zeinali, P. Mashayekhi, M. Noruzinia, 2019, Cell journal.

Thrombophilic Mutations in Iran

P. Mannucci, S. Zeinali, A. Eckardstein, 2000, Thrombosis and Haemostasis.

Microsatellite Marker Analysis for Laboratory Mice Profiling

S. Zeinali, M. H. Samiee Aref, Reza Ahangari Cohan, 2019, Advanced biomedical research.

Molecular Characterisation and Three-Dimensional Structural Analysis of Mutations in 21 Unrelated Families with Inherited Factor VII Deficiency

S. Perkins, P. Mannucci, S. Zeinali, 2000, Thrombosis and Haemostasis.

Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2017, Nature Genetics.

Homozygosity mapping and CDH23 mutation analysis in Iranian deaf families

S. Zeinali, N. Mahdieh, Atefeh Shirkavand, 2016 .

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

S. Merat, S. Zeinali, M. Khatami, 2021, Journal of clinical laboratory analysis.

Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia.

S. Leal, M. Zeviani, P. Striano, 2021, American journal of human genetics.

The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families.

J. Uitto, S. Zeinali, Qiaoli Li, 2015, The Journal of investigative dermatology.

Epidermodysplasia Verruciformis: Genetic Heterogeneity and EVER1 and EVER2 Mutations Revealed by Genome-Wide Analysis.

J. Casanova, J. Uitto, S. Zeinali, 2019, The Journal of investigative dermatology.

CROSS-RESISTANCE TO VINCRISTIN AND ETOPOSIDE IN A SUB LINE OF THE HUMAN BREAST CANCER T47D CELLS SELECTED FOR ADRIAMYCIN-RESISTANCE

E. Azizi, S. Ostad, S. Zeinali, 2004 .

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

J. Uitto, V. Ziaee, M. Yousefi, 2021, JAMA dermatology.

Hypotrichosis with juvenile macular dystrophy: Combination of whole‐genome sequencing and genome‐wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole‐exome sequencing—A lesson from next‐generation sequencing

J. Uitto, S. Zeinali, H. Vahidnezhad, 2019, Molecular genetics & genomic medicine.

Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis

S. Zeinali, A. Majd, Elham siasi torbati, 2021, Iranian biomedical journal.

ANTISERUM PRODUCTION IN IMMUNIZED CAMEL BY THE VENOM OF HEMISCORPIUS LEPTURUS SCORPION: EVALUATION OF NEUTRALIZING TEST IN VIVO

S. Zeinali, M. Behdani, D. Shahbazzadeh, 2010 .

Recombinant expression and purification of human placental growth factor 1 and specific camel heavy chain polyclonal antibody preparation.

S. Zeinali, M. Behdani, H. Khanahmad, 2014, Saudi journal of biological sciences.

High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene.

S. Zeinali, N. Mahdieh, Atefeh Shirkavand, 2010, International journal of pediatric otorhinolaryngology.

A novel autosomal recessive GJB2‐associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma

P. Fortina, J. Uitto, A. Kariminejad, 2018, Human mutation.

Genetic attributes of Iranian cystic fibrosis patients: the diagnostic efficiency of CFTR mutations in over a decade

M. Kabiri, S. Zeinali, A. Karimi, 2023, Frontiers in Genetics.

Expression Enhancement in Trastuzumab Therapeutic Monoclonal Antibody Production using Genomic Amplification with Methotrexate

M. Shokrgozar, S. Zeinali, B. Yakhchali, 2013, Avicenna journal of medical biotechnology.

Allele Frequency of CYP2C9 Gene Polymorphisms in Iran

S. Zeinali, F. Peyvandi, M. Karimi, 2002, Thrombosis and Haemostasis.

Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutations

S. Zeinali, M. Abiri, Razieh Karamzadeh, 2019, Metabolic Brain Disease.

The 3rd National Festival & International Congress on Stem Cell & Regenerative Medicine

A. Seifalian, H. Ahmadieh, H. Poustchi, 2018, BioImpacts : BI.

Isolation of stem cells from adult rat kidneys.

M. Soleimani, Y. Gheisari, S. Zeinali, 2009, Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al.

Sequence heterogeneity of the merozoite surface protein-1 gene (MSP-1) of Plasmodium vivax wild isolates in southeastern Iran.

S. Zeinali, S. Zakeri, Navid Dinparast Djadid, 2003, Acta tropica.

Linkage Study Revealed Complex Haplotypes in a Multifamily due to Different Mutations in CAPN3 Gene in an Iranian Ethnic Group

S. Zeinali, M. Abiri, J. Tavakkoly-Bazzaz, 2016, Journal of Molecular Neuroscience.

Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report

S. Zeinali, Y. Nilipour, S. Tonekaboni, 2020, BMC Medical Genetics.

Very-Early-Onset Inflammatory Bowel Disease in a Patient With Junctional Epidermolysis Bullosa With a Homozygous Mutation in the α6 Integrin Gene (ITGA6).

J. Uitto, S. Zeinali, H. Vahidnezhad, 2021, Inflammatory bowel diseases.

Inhibitory Effect of miRNA-145 on PD-L1 Expression in Breast Cancer Cell Line

S. Zeinali, Masoumeh Azizi, N. Nafisi, 2022, Iranian Journal of Breast Diseases.

Cohort profile update: Tehran cardiometabolic genetic study

A. Ghasemi, D. Khalili, P. Mirmiran, 2023, European Journal of Epidemiology.

Globin Chain Synthesis is a Useful Complementary Tool in the Differential Diagnosis of Thalassemias

H. Najmabadi, S. Zeinali, M. Akbari, 2007, Hemoglobin.

Molecular Dynamics Simulation of the Consequences of a PYCR1 Mutation (p.Ala189Val) in Patients with Complex Connective Tissue Disorder and Severe Intellectual Disability.

J. Uitto, M. Vasei, S. Zeinali, 2017, The Journal of investigative dermatology.

Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene.

J. Uitto, V. Ziaee, S. Zeinali, 2017, Acta dermato-venereologica.

Ichthyosis follicularis syndromes in patients with mutations in GJB2

J. Uitto, S. Zeinali, F. Rajabi, 2022, Clinical and experimental dermatology.

Genetic counselling of Mucopolysaccharidosis type III: case report and literature review

S. Zeinali, M. Fallah, Jamileh Malbin, 2019, International Journal of Genetic Medicine and Gene Therapy.

Development of Transgenic Mice Expressing Calcitonin as a Beta-lactoglobulin Fusion Protein in Mammary Gland

S. Zeinali, M. Magliano, M. Karimi, 2005, Transgenic Research.

Development of Transgenic Mice Harboring Ovine Beta Lactoglobulin-Calcitonin Transgene

S. Zeinali, M. Karimi, M. Rassoulzadegan, 2004 .

Inherited Interleukin 2-Inducible T-Cell (ITK) Kinase Deficiency in Siblings With Epidermodysplasia Verruciformis and Hodgkin Lymphoma.

J. Casanova, P. Fortina, J. Uitto, 2019, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Allele frequencies of three factor VIII gene polymorphisms in Iranian populations and their application in hemophilia A carrier detection

S. B. Azimifar, S. Zeinali, S. Y. Seyedna, 2006, American journal of hematology.

The value of St14 (DXS52) VNTR analysis for genetic diagnosis of hemophilia A in Iranian population.

S. Zeinali, S. Babak Azimifar, S. Yoosef Seyedna, 2006, Thrombosis research.

The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series

J. Uitto, V. Ziaee, S. Zeinali, 2018, BMC Medical Genetics.

Digital

J. Uitto, V. Ziaee, S. Zeinali, 2015, Sales Excellence.

Transient expression of anti-VEFGR2 nanobody in Nicotiana tabacum and N. benthamiana

S. Zeinali, M. Behdani, M. Shams-bakhsh, 2018, 3 Biotech.

Molecular Characterization of QDPR Gene in Iranian Families with BH4 Deficiency: Reporting Novel and Recurrent Mutations.

M. Alaei, S. Zeinali, M. Abiri, 2015, JIMD reports.

DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21–12.1

M. Lathrop, C. Petit, D. Weil, 2003, European Journal of Human Genetics.

Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach

H. Rahimi, S. Zeinali, S. Talebi, 2023, Hereditas.

Identification and characterization of the largest deletion in the PCCA gene causing severe acute early-onset form of propionic acidemia

H. Rahimi, S. Zeinali, S. Talebi, 2023, Molecular Genetics and Genomics.

NPM1 Mutation Detection in Acute Myeloid Leukemia: A Method Comparison Study.

M. Yaghmaie, K. Alimoghaddam, A. Ghavamzadeh, 2016, Genetic testing and molecular biomarkers.

MOLECULAR CHARACTERIZATION OF THE FACTOR IX GENE IN 28 IRANIAN HEMOPHILIA B PATIENTS

S. Zeinali, E. Tuddenham, M. Karimipour, 2009 .

Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia

S. Zeinali, S. Ghadami, Samira DabbaghBagheri, 2016, Indian Journal of Hematology and Blood Transfusion.

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients

P. Mannucci, S. Zeinali, F. Peyvandi, 1998, British journal of haematology.

STUDYING THE ACTIVITY OF FIBROBLAST GROWTH FACTOR 18 AND UROKINASE PLASMINOGEN ACTIVATOR RECEPTOR PROMOTERS IN TWO COLON CANCER CELL LINES

S. Zeinali, K. Azadmanesh, M. Karimipoor, 2009 .

Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate

S. Zeinali, K. Azadmanesh, M. Karimipoor, 2019, BioMed research international.

Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

S. Zeinali, M. Karimipoor, Z. Sharifi, 2019, Turkish journal of medical sciences.

Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.

S. Zeinali, N. Mahdieh, Atefeh Shirkavand, 2010, Clinical laboratory.

The first successful application of preimplantation genetic diagnosis for hearing loss in Iran.

S. Zeinali, F. Ramezanzadeh, S. Amanpour, 2018, Cellular and molecular biology.

Severely damaged kidneys possess multipotent renoprotective stem cells.

M. Soleimani, M. Vasei, Y. Gheisari, 2010, Cytotherapy.

In silico Analysis of Two Novel Variants in the Pyruvate Carboxylase (PC) Gene Associated with the Severe Form of PC Deficiency

S. Zeinali, Elham Davoudi-Dehaghani, N. Khalesi, 2023, Iranian biomedical journal.

High level of intrafamilial phenotypic variability of non-syndromic hearing loss in a Lur family due to delE120 mutation in GJB2 gene.

S. Zeinali, N. Mahdieh, Atefeh Shirkavand, 2010, International journal of pediatric otorhinolaryngology.

A CIB1 Splice-Site Founder Mutation in Families with Typical Epidermodysplasia Verruciformis.

J. Casanova, J. Uitto, M. Yousefi, 2019, The Journal of investigative dermatology.

Human Mutation

S. Zeinali, H. Vahidnezhad, P. Lovell, 2020 .

MiR-377 reverses cancerous phenotypes of pancreatic cells via suppressing DNMT1 and demethylating tumor suppressor genes.

S. Zeinali, H. Mahmoodzadeh, K. Azadmanesh, 2017, Epigenomics.

TuMV as an efficient transient vector for expressing heterologous proteins in Nicotiana tabacum and N. benthamiana

S. Zeinali, M. Mirzaee, M. Modarresi, 2019 .

a including phenotype with abnormal anchoring and

A. Kariminejad, S. Zeinali, H. Vahidnezhad, 2018 .

MicroRNA-561-3p indirectly regulates the PD-L1 expression by targeting ZEB1, HIF1A, and MYC genes in breast cancer

S. Zeinali, Masoumeh Azizi, N. Nafissi, 2024, Scientific reports.