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Cisem Mail

Observed names: C., Mail, Mail, Çisem, Çisem MAİL, Çisem Mail
Institution: Trakya University
ORCID: 0000-0003-3559-5860
Observed ORCID: 0000-0003-3559-5860
OpenAlex ID: A5077358812
Concepts of Double Hit and Triple Hit Disease in Multiple Myeloma, Entity and Prognostic Significance
2020 · Mehmet Baysal, Ufuk Demirci, et al. · Scientific Reports · 64
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Clinical Implications of Chromosome 16 Copy Number Variation
2021 · Emine Ikbal Atli, Sinem Yalcintepe, et al. · Molecular Syndromology · 17
The Importance of Targeted Next-generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies
2020 · Emine Atli, Hakan Gurkan, et al. · Mediterranean Journal of Hematology and Infectious Diseases · 9
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De Novo Subtelomeric 6p25.3 Deletion with Duplication of 6q23.3-q27: Genotype–Phenotype Correlation
2019 · Emine Ikbal Atli, Hakan Gurkan, et al. · Journal of Pediatric Genetics · 9
Y chromosome polymorphism in Turkish patients with reproductive problems: a genetic centre experience
2023 · Emine İkbal Atlı, Çisem Mail, et al. · The European Research Journal · 6
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Investigation of the Relationship between Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2 and GABRA4 Genes
2021 · Sinem Yalcintepe, Isik Gorker, et al. · Nöro Psikiyatri Arşivi · 6
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The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method
2023 · Sinem Yalcintepe, Yasemin Karal, et al. · Global Medical Genetics · 4
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First Report of Jacobsen Syndrome with Dextrocardia Diagnosed with del(11)(q24q25)
2022 · Sinem Yalcintepe, Drenushe Zhuri, et al. · Molecular Syndromology · 4
The Phenotypic Spectrum of Desanto–Shinawi Syndrome: A Comparative Report of the First Reported Case in Turkey
2024 · Cisem Mail, Sinem Yalcintepe, et al. · Genetic Testing and Molecular Biomarkers · 2
Prenatal Sitogenetik Anormallikler ve Ultrasonografik olarak Saptanan Fetal Anomalilerin Korelasyonu
2022 · Emine İkbal ATLI, Engin ATLI, et al. · OSMANGAZİ JOURNAL OF MEDICINE · 2
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Clinical Features of Aberrations Chromosome 22q: A Pilot Study
2021 · Emine Ikbal Atli, Engin Atli, et al. · Global Medical Genetics · 2
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Comparison of Second Revision of the International Staging System (R2-ISS) and Mayo Additive Staging System (MASS) in Newly Diagnosed Multiple Myeloma Patients
2026 · Mehmet Baysal, Ufuk Demirci, et al. · Indian Journal of Hematology and Blood Transfusion · 1
Genotype-phenotype correlations of pathogenic copy number variations on X chromosome detected by comparative genomic hybridization
2022 · Sinem Yalcintepe, Engin Atli, et al. · Human Gene · 1
Investigation the etiology of syndromic autism with targeted gene analysis
2021 · Sinem Yalcintepe, Hakan Gurkan, et al. · Annals of Medical Research · 1
A Pilot Study of Identification Genetic Background of Craniosynostosis Cases
2020 · Emine Ikbal Atli, Sinem Yalcintepe, et al. · Journal of Craniofacial Surgery · 1
Supplemental Material for: Sifrim-Hitz-Weiss SyndromeCausedby a Novel De NovoNonsenseVariant in CHD4: A Case Report
2026 · figshare admin karger, Damla Eker, et al. · Figshare
Sifrim-Hitz-Weiss Syndrome Caused by a Novel De Novo Nonsense Variant in CHD4: A Case Report
2026 · Damla Eker, Cisem Mail, et al. · Molecular Syndromology
Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies
2022 · Emine Ikbal Atli, Engin Atli, et al. · Taiwanese Journal of Obstetrics and Gynecology
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Supplementary Material for: Clinical Implications of Chromosome 16 Copy Number Variation
2021 · E.I., Atli, S., Yalcintepe, et al. · Figshare
Can We Use Targeted Next-Generation Sequencing an Alternative Method to the Conventional Tests in Haematological Malignancies?
2020 · Emine Ikbal Atli, Hakan Gurkan, et al. · Research Square
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Works count: 21
Citation count: 129
H-index: 6
I10-index: 2
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