Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

A. Bişgin · SciRah

Researcher profile · Semantic Scholar

A. Bişgin

Share profile

A. Bişgin — researcher profile on SciRah

h-index: 20
Works: 167
Citations: 1,351

Most-cited papers

Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
L. Schottlaender, R. Abeti, Z. Jaunmuktane, C. Macmillan +83 more
2020American Journal of Human Genetics79 citations Open access
Semantic Scholar
An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer
Alakesh Das, S. Adhikari, D. Deka, N. Baildya +5 more
2023Medicina52 citations Open access
Semantic Scholar
Interaction of CD200 Overexpression on Tumor Cells with CD200R1 Overexpression on Stromal Cells: An Escape from the Host Immune Response in Rectal Cancer Patients
A. Bişgin, W. Meng, G. Adell, Xiao-Feng Sun
2019Journal of Oncology21 citations Open access
Semantic Scholar
An Updated Review on Recent Advances in the Usage of Novel Therapeutic Peptides for Breast Cancer Treatment
Alakesh Das, S. Adhikari, D. Deka, A. Bişgin +5 more
2023International Journal of Peptide Research and Therapeutics20 citations
Semantic Scholar
Monogenic lupus due to DNASE1L3 deficiency in a pediatric patient with urticarial rash, hypocomplementemia, pulmonary hemorrhage, and immune-complex glomerulonephritis.
Rabia Miray Kışla Ekinci, S. Balcı, D. Ozcan, B. Atmış +1 more
2021European Journal of Medical Genetics20 citations
Semantic Scholar
Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey
Rabia Miray Kışla Ekinci, S. Balcı, H. Dogan, S. Ceylaner +4 more
2021Molecular Syndromology20 citations Open access
Semantic Scholar
Congenital myasthenic syndrome in Turkey: clinical and genetic features in the long-term follow-up of patients
Gulen Gul Mert, N. Özcan, Ö. Hergüner, Ş. Altunbaşak +3 more
2019Acta Neurologica Belgica20 citations
Semantic Scholar
The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID)
A. Bişgin, Ozge Sonmezler, I. Boga, M. Yılmaz
2021Scientific Reports19 citations Open access
Semantic Scholar
Primary melanoma of the urinary tract; Clinicopathologic and molecular review of a case series.
A. Açıkalın, E. Bağır, Savalan Karim, A. Bişgin +2 more
2020Pathology, Research and Practice19 citations
Semantic Scholar
Functional Foods: A Promising Strategy for Restoring Gut Microbiota Diversity Impacted by SARS-CoV-2 Variants
A. Banerjee, I. Somasundaram, Diptimay Das, Samatha Jain Manoj +8 more
2023Nutrients18 citations Open access
Semantic Scholar
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
M. Dundar, U. Fahrioğlu, S. Yıldız, Burcu Bakir-Gungor +178 more
2022Functional & Integrative Genomics18 citations Open access
Semantic Scholar
Altered expression of apoptosis-related, circulating cell-free miRNAs in children with familial Mediterranean fever: a cross-sectional study
Emin Murat Karpuzoglu, Rabia Miray Kışla Ekinci, S. Balcı, A. Bişgin +1 more
2020Rheumatology International17 citations
Semantic Scholar
Current Update on Severe Acute Respiratory Syndrome Coronavirus 2 Vaccine Development with a Special Emphasis on Gene Therapy Viral Vector Design and Construction for Vaccination
A. Bişgin, A. Şanlioğlu, Y. E. Ekşi, Thomas S. Griffith +1 more
2021Human Gene Therapy16 citations
Semantic Scholar
Morquio A syndrome and effect of enzyme replacement therapy in different age groups of Turkish patients: a case series
S. Kılavuz, S. Başaran, D. Kor, F. Bulut +5 more
2021Orphanet Journal of Rare Diseases16 citations Open access
Semantic Scholar
Nanobubble Ozone Stored in Hyaluronic Acid Decorated Liposomes: Antibacterial, Anti-SARS-CoV-2 Effect and Biocompatibility Tests
A. Ü. Sabancı, Perihan Erkan Alkan, Cem Mujde, H. Polat +4 more
2022International Journal of Nanomedicine15 citations Open access
Semantic Scholar
Evaluation of phenotypic and genotypic features of children with distal kidney tubular acidosis
B. Atmış, D. Cevizli, E. Melek, A. Bişgin +3 more
2020Pediatric nephrology (Berlin, West)15 citations
Semantic Scholar
The contribution of diet preference to the disease course in children with familial Mediterranean fever: a cross-sectional study
R. M. K. Ekinci, S. Balcı, A. Bişgin, F. Çetin +1 more
2020Rheumatology13 citations Open access
Semantic Scholar
Immunodeficiency associated with a novel functionally defective variant of SLC19A1 benefits from folinic acid treatment
Veysel Gök, Ş. Erdem, Yesim Haliloğlu, A. Bişgin +12 more
2022Genes and Immunity12 citations Open access
Semantic Scholar
BMAP-27 Peptide Reduces Proliferation and Increases Apoptosis in Primary and Metastatic Colon Cancer Cell Lines
Alakesh Das, D. Deka, N. Baildya, A. Banerjee +4 more
2023International Journal of Peptide Research and Therapeutics10 citations Open access
Semantic Scholar
Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population
Nilgün Duman, G. Tuncel, A. Bişgin, S. Bozdoğan +23 more
2022Journal of Medical Virology10 citations Open access
Semantic Scholar
Gender Identity and Assignment Recommendations in Disorders of Sex Development Patients: 20 Years’ Experience and Challenges
Fatih Gürbüz, M. Alkan, G. Çelik, A. Bişgin +6 more
2020Journal of Clinical Research in Pediatric Endocrinology10 citations Open access
Semantic Scholar
Renal features of Bardet Biedl syndrome: A single center experience.
B. Atmış, Aysun Karabay-Bayazıt, E. Melek, A. Bişgin +1 more
2019Turkish Journal of Pediatrics10 citations Open access
Semantic Scholar
A concise review on miRNAs as regulators of colon cancer stem cells and associated signalling pathways
A. Banerjee, D. Deka, Makalakshmi Muralikumar, Alexander Sun Zhang +5 more
2023Clinical and Translational Oncology8 citations
Semantic Scholar
Ethylmalonic Encephalopathy: a literature review and two new cases of mild phenotype
Isobel Platt, A. Bişgin, S. Kılavuz
2023Neurological Sciences8 citations Open access
Semantic Scholar
Current Status of Genetic Diagnosis Laboratories and Frequency of Genetic Variants Associated with Cystic Fibrosis through a Newborn-Screening Program in Turkey
S. Bozdoğan, Cem Mujde, I. Boga, Ozge Sonmezler +5 more
2021Genes8 citations Open access
Semantic Scholar
First pediatric case with primary familial brain calcification due to a novel variant on the MYORG gene and review of the literature.
Leman Tekin Orgun, Seyda Besen, Özlem Sangün, A. Bişgin +2 more
2021Brain & development (Tokyo. 1979)8 citations
Semantic Scholar
A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction.
F. Ekıncı, R. Yıldızdaş, O. Horoz, O. Herguner +1 more
2020European Journal of Medical Genetics8 citations
Semantic Scholar
A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia
R. M. K. Ekinci, S. Balcı, A. Bişgin, I. Şaşmaz +3 more
2019Pediatric Hematology & Oncology8 citations
Semantic Scholar
Congenital erythropoietic porphyria with erythrodontia: A case report.
Volkan Ciftci, S. Kılavuz, F. Bulut, H. Mungan +2 more
2019International Journal of Paediatric Dentistry8 citations
Semantic Scholar
Clinical and genetic profiles of patients with X-linked agammaglobulinemia from southeast Turkey: Novel mutations in BTK gene.
Dilek Doğruel, M. Serbes, Ayşe Şenay Şaşihüseyinoğlu, M. Yilmaz +2 more
2019Allergologia et Immunopathologia8 citations Open access
Semantic Scholar
Bi-allelic pathogenic variants in TRMT1 disrupt tRNA modification and induce a neurodevelopmental disorder
S. Efthymiou, C. Leo, C. Deng, Sheng-Jia Lin +96 more
2025American Journal of Human Genetics7 citations Open access
Semantic Scholar
Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia
A. Kiraz, O. Sezer, A. Alemdar, Sezin Canbek +46 more
2023Journal of Medical Virology7 citations Open access
Semantic Scholar
Real-world patient data on immunity and COVID-19 status of patients with MPS, Gaucher, and Pompe diseases from Turkey
S. Kılavuz, D. Kor, F. Bulut, M. Serbes +5 more
2022Archives de pédiatrie7 citations Open access
Semantic Scholar
Determination of the etiology of pediatric urinary stone disease by multigene panel and metabolic screening evaluation.
Elnur Ziyadov, A. Bişgin, M. Değer, Nebil Akdoğan +3 more
2021Journal of Pediatric Urology7 citations
Semantic Scholar
Deficiency of adenosine deaminase 2: a case series revealing clinical manifestations, genotypes and treatment outcomes from Turkey.
Rabia Miray Kışla Ekinci, S. Balcı, Michael S. Hershfield, A. Bişgin +3 more
2019Rheumatology7 citations
Semantic Scholar
Differentiating children with familial Mediterranean fever from other recurrent fever syndromes: The utility of new Eurofever/PRINTO classification criteria
Rabia Miray Kışla Ekinci, S. Balcı, A. Erol, Dilek Karagöz +2 more
2021Archives of Rheumatology6 citations Open access
Semantic Scholar
From infancy to adulthood: challenges in congenital nephrogenic diabetes insipidus
B. Atmış, A. Bayazıt, E. Melek, A. Bişgin +1 more
2020Journal of Pediatric Endocrinology & Metabolism (JPEM)6 citations
Semantic Scholar
Phenotypic variability in two patients with tumor necrosis factor receptor associated periodic fever syndrome emphasizes a rare manifestation: Immunoglobulin a nephropathy.
S. Balcı, Rabia Miray Kışla Ekinci, E. Melek, B. Atmış +2 more
2020European Journal of Medical Genetics6 citations
Semantic Scholar
Integration of Liquid Biopsies into Clinical Laboratory Applications via NGS in Cancer Diagnostics.
Ozge Sonmezler, I. Boga, A. Bişgin
2020Clinical Laboratory6 citations
Semantic Scholar
Results of Liquid Biopsy Studies by Next Generation Sequencing in Patients with Advanced Stage Non-small Cell Lung Cancer: Single Center Experience from Turkey
M. Buyuksimsek, M. Togun, K. Oguz, A. Bişgin +7 more
2019Balkan Journal of Medical Genetics6 citations Open access
Semantic Scholar
Hemophagocytic lymphohistiocytosis in children with Griscelli syndrome type 2: genetics, laboratory findings and treatment.
E. Çay, Ahmet Sezer, Veysel Karakulak, M. Serbes +7 more
2023American Journal of Clinical and Experimental Immunology5 citations
Semantic Scholar
Real-world applications of tumor mutation burden (TMB) analysis using ctDNA and FFPE samples in various cancer types of Turkish population
I. Boga, A. Bişgin
2022International journal of experimental research and review5 citations Open access
Semantic Scholar
Experience with the targeted next-generation sequencing in the diagnosis of hereditary hypophosphatemic rickets
Ihsan Turan, Sevcan Erdem, L. D. Kotan, Semine Özdemir Dilek +6 more
2021Journal of Pediatric Endocrinology & Metabolism (JPEM)5 citations
Semantic Scholar
More than tubular dysfunction: cystinosis and kidney outcomes
B. Atmış, A. Bayazıt, D. Cevizli, D. Kor +9 more
2021JN. Journal of Nephrology (Milano. 1992)5 citations
Semantic Scholar
Spectrum of FAR1 (Fatty Acyl‐CoA Reductase 1) Variants and Related Neurological Conditions
A. Westenberger, A. Ruiz-Herrera, S. Bozdoğan, A. Bişgin +10 more
2023Movement Disorders4 citations Open access
Semantic Scholar
A Multicenter Study of Genotype Variation/Demographic Patterns in 2475 Individuals Including 1444 Cases With Breast Cancer in Turkey.
I. Boga, S. Ozemri Sag, Nilgün Duman, Sevda Yesim Ozdemir +33 more
2023European Journal of Breast Health4 citations Open access
Semantic Scholar
Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey
A. Bişgin, S. Sag, M. Doğan, M. Yıldırım +21 more
2022Breast4 citations Open access
Semantic Scholar
Experience of Autoimmune and autoinflammatory diseases in a Turkish pediatric cohort with primary immunodeficiencies.
Dilek Özcan, M. Serbes, R. M. K. Ekinci, Sibel Balcı Çetinkaya +3 more
2021Allergologia et Immunopathologia4 citations Open access
Semantic Scholar
Serum lubricin levels in patients with juvenile idiopathic arthritis
R. M. K. Ekinci, S. Balcı, F. Çoban, A. Bişgin
2021Rheumatology4 citations Open access
Semantic Scholar
Autoimmune Manifestations in Heterozygote Type I Complement 2 Deficiency: A Child Eventually Diagnosed With Systemic Lupus Erythematosus
R. M. K. Ekinci, S. Balcı, A. Bişgin, B. Atmış +2 more
2019Archives of Rheumatology4 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

I. Boga×10
Invite
I. Boga — researcher profile on SciRah
S. Balcı×10
Invite
S. Balcı — researcher profile on SciRah
B. Atmış×7
Invite
B. Atmış — researcher profile on SciRah
M. Yılmaz×7
Invite
M. Yılmaz — researcher profile on SciRah

×7

Invite

S. Bozdoğan — researcher profile on SciRah

Rabia Miray Kışla Ekinci×6

Invite

Rabia Miray Kışla Ekinci — researcher profile on SciRah

Invite

A. Banerjee — researcher profile on SciRah

Invite

S. Pathak — researcher profile on SciRah

Ozge Sonmezler×5

Invite

Ozge Sonmezler — researcher profile on SciRah

Invite

M. Dundar — researcher profile on SciRah

Invite

S. Temel — researcher profile on SciRah

Invite

A. Alemdar — researcher profile on SciRah