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Sibel Berker Karaüzüm

Observed names: S B Karauzum, S Berker Karaüzüm, S Karauzum, S. Berker Karauzum, SB Karauzum, Sibel BERKER KARAUZUM, Sibel BERKER KARAÜZÜM, Sibel Berker KARAÜZÜM, Sibel Berker Karauzum, Sibel Berker Karauzum, Sibel Karauzum, Sibel Karaüzüm, Sibel Karaüzum, Sibel Karaüzüm
Institution: Intergen (Turkey)
ORCID: 0000-0001-6415-3215
Observed ORCID: 0000-0001-6415-3215
OpenAlex ID: A5040019623
A familial interstitial 4q35 deletion with no discernible clinical effects
2015 · Sezin Yakut, Ozden Altiok Clarck, et al. · American Journal of Medical Genetics Part A · 44
Retinoic acid isomers protect hippocampal neurons from amyloid-β induced neurodegeneration
2005 · Mehmet Sahin, Sibel Berker Karaüzüm, et al. · Neurotoxicity Research · 42
Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12
2011 · Zafer Cetin, Ercan Mihci, et al. · American Journal of Medical Genetics Part A · 38
Differential PTEN Protein Expression Profiles in Superficial versus Invasive Bladder Cancers
2005 · Ismail Turker Koksal, Duygu Yasar, et al. · Urologia Internationalis · 29
Evaluation of PTEN and Mcl-1 expressions in NSCLC expressing wild-type or mutated EGFR
2009 · Zafer Cetin, Gulay Ozbilim, et al. · Medical Oncology · 25
Sensorimotor polyneuropathy in patients with SMA type‐1: Electroneuromyographic findings
2012 · Ozgur Duman, Hilmi Uysal, et al. · Muscle & Nerve · 21
Evaluation of ETV6/RUNX1 Fusion and Additional Abnormalities Involving ETV6 and/or RUNX1 Genes Using FISH Technique in Patients with Childhood Acute Lymphoblastic Leukemia
2015 · Cigdem Aydin, Zafer Cetin, et al. · Indian Journal of Hematology and Blood Transfusion · 17
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The value of donor lymphocyte infusions in thalassemia patients at imminent risk of graft rejection following stem cell transplantation
2011 · Gulsun Tezcan Karasu, M. Akif Yesilipek, et al. · Pediatric Blood & Cancer · 17
Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype
2010 · Gulseren Bagci, Atil Bisgin, et al. · Fertility and Sterility · 13
Partial trisomy 3q in a child with sacrococcygeal teratoma and Cornelia de Lange syndrome phenotype.
2011 · M Dundar, A Uzak, et al. · PubMed · 11
The Ratios of Estradiol and Progesterone to Testosterone Influence the Severity of Facioscapulohumeral Muscular Dystrophy
2020 · Ceren Hangül, Selen Bozkurt, et al. · Neurological Sciences and Neurophysiology · 10
Evaluation of exonic copy numbers of SMN1 and SMN2 genes in SMA
2022 · Yunus Arikan, Sibel Berker Karauzum, et al. · Gene · 8
Evaluation of eNOS gene polymorphisms in relation to BMD in postmenopausal women
2009 · Sibel Cubukcu Firat, Zafer Cetin, et al. · Maturitas · 8
Identification of a presymptomatic and early disease signature for amyotrophic lateral sclerosis (ALS): protocol of the premodiALS study
2025 · Laura Tzeplaeff, Ana Galhoz, et al. · Neurological Research and Practice · 7
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Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals
2021 · Ceren Hangül, Sibel Berker Karaüzüm, et al. · Current Neuropharmacology · 7
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Donor Cell-derived Acute Myeloblastic Leukemia After Allogeneic Peripheral Blood Hematopoietic Stem Cell Transplantation for Juvenile Myelomonocytic Leukemia
2006 · Zafer Cetin, Gulsun Tezcan, et al. · Journal of Pediatric Hematology/Oncology · 7
Estradiol differentially regulates DUX4, β-catenin and PAX3/PAX7 in primary myoblasts of facioscapulohumeral muscular dystrophy patients
2021 · Ceren Hangul, Esin Guvenir Celik, et al. · Turkish Journal of Biochemistry · 6
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Rare structural chromosomal abnormalities in prenatal diagnosis; clinical and cytogenetic findings on 10125 prenatal cases
2014 · Sezin Yakut, Zafer Cetin, et al. · Turkish Journal of Pathology · 6
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Gut Microbiota and Short-Chain Fatty Acid Profiles in Facioscapulohumeral Dystrophy: Associations with Epigenetic Alterations
2025 · Ceren Hangul, Ozlem Koyuncu Ozyurt, et al. · Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques · 5
Progesterone may be a regulator and B12 could be an indicator of the proximal D4Z4 repeat methylation status on 4q35ter
2024 · Ceren Hangul, Filiz Ozcan, et al. · Journal of Neurochemistry · 5
Coexistence of a Homozygous Chromosome 4q35.2 Deletion and Hidden IQSEC2 Pathogenic Variant in a Child with Intellectual Disability
2021 · Tuğba Karaman Mercan, Ozden Altiok Clark, et al. · Cytogenetic and Genome Research · 5
Conventional Cytogenetics and Interphase Fluorescence In Situ Hybridization Results in Multiple Myeloma: A Turkey Laboratory Analysis of 381 Cases
2019 · Cigdem Aydin, Turgay Ulas, et al. · Indian Journal of Hematology and Blood Transfusion · 5
Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia
2014 · Z. Cetin, O. Altiok-Clark, et al. · Andrologia · 5
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Previously Unreported Chromosomal Aberrations of t(3;3)(q29;q23), t(4;11)(q21;q23), and t(11;18)(q10;q10) in a Patient with Accelerated Phase Ph+ CML
2014 · Cigdem Aydin, Zafer Cetin, et al. · Case Reports in Genetics · 5
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M-FISH applications in clinical genetics.
2005 · Z Cetin, S Berker Karaüzüm, et al. · PubMed · 5
Works count: 65
Citation count: 383
H-index: 10
I10-index: 11
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