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Kübra Adanur Sağlam

Observed names: A Saglam Kubra, Kubra Adanur Saglam, Kubra AdanurSaglam, Kubra Adanur Saglam, Kübra Adanur Saglam
ORCID: 0000-0003-0201-6877
Observed ORCID: 0000-0003-0201-6877
OpenAlex ID: A5102875488
A new case of Turnpenny‐Fry syndrome
2021 · Pelin Ercoskun, Cigdem Yuce Kahraman, et al. · American Journal of Medical Genetics Part A · 5
Genetic heterogeneity in pediatric short stature: insights from whole exome sequencing and snp- array analyses in a Turkish cohort
2025 · Kubra Adanur Saglam, Semiha Bekfilavioglu, et al. · European Journal of Pediatrics · 4
Secondary findings in genes related to cancer phenotypes in Turkish exome sequencing data from 2020 individuals
2024 · Oguzhan Demir, Kubra Adanur Saglam, et al. · American Journal of Medical Genetics Part A · 4
Biallelic Deletion of PEX26 Exon 4 in a Boy with Phenotypic Features of both Zellweger Syndrome and Infantile Refsum Disease
2024 · Burhanettin Yalçınkaya, Kübra Adanur Sağlam, et al. · Molecular Syndromology · 3
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A Strong Candidate Gene for Nonsyndromic Intellectual Disability Phenotype: SGSM3
2024 · Ayberk Turkyilmaz, Kubra Adanur Saglam, et al. · Clinical Genetics · 1
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Novel pathological genetic variant associated with DOCK8 deficiency: case report with successful hematopoietic stem cell transplantation
2026 · Hilal Karabag Citlak, Ayberk Turkyilmaz, et al. · Allergologia et Immunopathologia
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Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
2025 · T Apuhan, A Saglam Kubra, et al. · Balkan Journal of Medical Genetics
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Author response for "A Strong Candidate Gene for Nonsyndromic Intellectual Disability Phenotype: SGSM3"
2024 · Ayberk Turkyilmaz, Kubra Adanur Saglam, et al. · Publons reviews and discussion
An Unusual Case of Neonatal Hypotonia and Femur Fracture: Neuromuscular Variant of Glycogen Storage Disease Type IV
2023 · Handan Bezirganoglu, Kubra Adanur Saglam · Children
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Works count: 9
Citation count: 17
H-index: 3
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