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Füsun Düzcan

Observed names: DÜZCAN, FÜSUN, Düzcan, F, Düzcan, Füsun, F. Duzcan, Fusun Duzcan, Füsun DÜZCAN, füsun düzcan
ORCID: 0000-0002-3973-1404
Observed ORCID: 0000-0002-3973-1404
OpenAlex ID: A5052185192
The role of RELN in lissencephaly and neuropsychiatric disease
2006 · Bernard S. Chang, Fusun Duzcan, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 79
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No Strong Association Between HER-2/neu Protein Overexpression and Gene Amplification in High-grade Invasive Urothelial Carcinomas
2008 · Vildan Caner, Nilay Sen Turk, et al. · Pathology & Oncology Research · 64
Cytogenetic studies in patients with reproductive failure
2003 · Füsun Düzcan, Münevver Atmaca, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 51
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Expanding the phenotypic spectrum of ECEL1‐related congenital contracture syndromes
2013 · S. Shaaban, F. Duzcan, et al. · Clinical Genetics · 27
Detection of Y Chromosomal Material in Patients with a 45,X Karyotype by PCR Method
2007 · C. Nur Semerci, N. Lale Satiroglu-Tufan, et al. · The Tohoku Journal of Experimental Medicine · 21
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Familial influence on parkinsonism in a rural area of Turkey (Kızılcaboluk–Denizli): A community‐based case‐control study
2003 · Fusun Duzcan, Mehmet Zencir, et al. · Movement Disorders · 18
Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family
2002 · Serap Özden, Füsun Düzcan, et al. · Ophthalmic Genetics · 17
Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer
2011 · Emre Tepeli, Vildan Caner, et al. · Molecular Biology Reports · 10
A Newborn with Congenital Mixed Phenotype Acute Leukemia After In Vitro Fertilization
2013 · Hacer Ergin, Özmert M.A. Özdemir, et al. · Pediatrics & Neonatology · 9
Expression and Amplification of Topoisomerase-2α in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2/neu Amplification
2011 · Fusun Duzcan, Suleyman Ender Duzcan, et al. · Pathology & Oncology Research · 5
A case with proximal femoral focal deficiency (PFFD) and fibular A/hypoplasia (FA/H) associated with urogenital anomalies.
2006 · Hacer Ergin, C Nur Semerci, et al. · PubMed · 5
Sex chromosome aneuploidy rates in the somatic cells of infertile men.
2006 · Fusun Duzcan, Zafer Aybek, et al. · PubMed · 5
Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation
2024 · Samim Özen, Damla Gökşen, et al. · Journal of Clinical Research in Pediatric Endocrinology · 4
Sister Chromatid Exchange Frequency in Lymphocytes Cultured from Cotton Gin Workers
2004 · Münevver Atmaca, Hüseyin Bağcı, et al. · DergiPark (Istanbul University) · 4
Dicentric Recombinant Chromosome 18 due to Maternal Paracentric Inversion Analyzed by Array CGH
2023 · Özlem Anlaş, Akgün Ölmez, et al. · Molecular Syndromology · 3
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Determination of apoptosis, proliferation status and O6-methylguanine DNA methyltransferase methylation profiles in different immunophenotypic profiles of diffuse large B-cell lymphoma
2010 · Nilay Sen Turk, Nazan Ozsan, et al. · Turkish Journal of Hematology · 3
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Non-Mosaic Tetrasomy 9p in An Infant With Multiple Congenital Anomalies
2007 · Füsun Düzcan, Hacer Ergin, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 2
A new syndrome with cardiac malformation, cleft lip‐palate, microcephaly and digital anomalies?
1995 · E. Ferda Perçin, Füsun Düzcan, et al. · Clinical Genetics · 2
Pseudohypoparathyroidism Type IA (PHP-Ia): Maternally Inherited GNAS Gene Mutation
2009 · S. Semiz, F. Duzcan, et al. · Journal of Pediatric Endocrinology and Metabolism · 1
[Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].
2003 · Füsun Düzcan, Bernd Wollnik, et al. · PubMed · 1
Laurence-Moon-Biedl Syndrome with Vaginal Atresia
2002 · Inci Gökalan Kara, Füsun Düzcan, et al. · Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery · 1
46, XY,t(1;2;12;6;16)(q42;q23;q22;q13;q13) REPORT OF A CASE WITH SEX DIFFERENTIATION DISORDER (DSD) WITH COMPLEX CHROMOSOMAL REARRANGEMENT
2025 · Diclehan Oral, Gülbahar Güzel Erdal, et al. · Middle East Journal of Science
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Bir Rekombinant Kromozom 4 Olgusunun Klinik Özelliklerinin Ayrıntılı Tanımlanması
2020 · Özlem Anlaş, Gökhan Ozan Çetin, et al. · Pamukkale Medical Journal
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A case of recombinant chromosome 4: further delineation of the clinical features. Bir Rekombinant Kromozom 4 Olgusunun Klinik Özelliklerinin Ayrıntılı Tanımlanması 201913(1):229-234
2019 · DÜZCAN, FÜSUN, BAĞCI, GÜLSEREN, et al. · AYBU AVESIS
Co-existence of Goldenhar and Klinefelter Syndromes in a Patient Born Following ICSI
2018 · Selcan Zeybek, Bilge Sarikepe, et al. · Journal of Clinical Practice and Research
Works count: 52
Citation count: 336
H-index: 9
I10-index: 8
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