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Afife Büke
Observed names:
A., Büke,
Afife Büke¹,
Buke, Afife
Institution:
Ankara Etlik City Hospital
Observed institution:
Ankara Etlik City Hospital
ORCID:
0009-0006-0619-2340
Observed ORCID:
0009-0006-0619-2340
OpenAlex ID:
A5119217646
Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability
2025
·
Ariane Kröll-Hermi
, Corinne Stoetzel
, et al.
·
The American Journal of Human Genetics
·
1
PDF
A Founder Allele in SGCG Combining Missense Variant and Multi‐Exon Duplication in Turkish Patients With Sarcoglycanopathy
2025
·
Abdullah Sezer
, Afife Büke
, et al.
·
Clinical Genetics
·
1
PDF
Confirmation of the Hotspot Variant in MAP3K20 Responsible for Deafness, Ectodermal Dysplasia, Craniosynostosis, Ectrodactyly, and Skeletal Anomaly Spectrum
2025
·
Elifcan Taşdelen
, Müzeyyen Gönül
, et al.
·
Molecular Syndromology
·
1
Germline variant spectrum and pragmatic family history assessment in prostate cancer: a 250-patient Turkish cohort
2026
·
Zeynep Özdemir-Pehlivan¹
, Ezgi Çevik-Demir¹
, et al.
·
Research Square
PDF
Monoallelic NTHL1 p.(Gln90*) and cancer risk: evidence from a large Turkish cohort
2026
·
Esma Ertürkmen Aru
, Afife Büke
, et al.
·
Familial Cancer
Monoallelic germline RAD51C, RAD51D, and BRIP1 variants in hereditary cancer testing: Variant spectrum and clinical counselling implications
2026
·
Zeynep Özdemir-Pehlivan
, Afife Büke
, et al.
·
Mutation research. Fundamental and molecular mechanisms of mutagenesis
Clinical Consequences of Cancer-related RAS Signaling Pathway Beyond Malignancy
2025
·
Elifcan Taşdelen
, Afife Büke
, et al.
·
Acta haematologica oncologica Turcica.
PDF
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Works count:
9
Citation count:
3
H-index:
1
I10-index:
Year
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