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Mahmut Selman Yıldırım

Observed names: Doç.Mahmut Selman Yildirim, M S Yildirim, M S Yıldırım, M Selman Yildirim, M. S. Yildirim, M. Selman Yildirim, M. Selman Yıldırım, M.S. Yildirim, M.Selman Yıldırım, Mahmut S Yildirim, Mahmut S. Yildirim, Mahmut Selman YILDIRIM, Mahmut Selman Yildirim, Mahmut Yildirim, Mahmut Selman Yildirim, YILDIRIM, M. Selman, Yıldırım, Mahmut Selman
Observed institutions: Dicle University, Sivas Cumhuriyet Üniversitesi, Selçuk University, Ankara University, Akdeniz University, Necmettin Erbakan University, Kırıkkale University
ORCID: 0000-0002-3986-5517
Observed ORCID: 0000-0002-3986-5517
OpenAlex ID: A5082553826
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
2015 · Ender Karaca, Tamar Harel, et al. · Neuron · 324
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Whole exome sequencing identifies three novel mutations in ANTXR1 in families with GAPO syndrome
2014 · Yavuz Bayram, Davut Pehlivan, et al. · American Journal of Medical Genetics Part A · 29
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Evaluation of segregation patterns of 21;21 Robertsonian translocation along with sex chromosomes and interchromosomal effects in sperm nuclei of carrier by FISH technique
2002 · Hasan Acar, M. Selman Yildirim, et al. · Molecular Reproduction and Development · 23
GAPO syndrome: Four new patients with congenital glaucoma and myelinated retinal nerve fiber layer
2013 · Banu Bozkurt, Mahmut Selman Yıldırım, et al. · American Journal of Medical Genetics Part A · 21
A girl with metopic synostosis and trisomy 13 mosaicism: Case report and review of the literature
2011 · Ebru Aypar, M. Selman Yildirim, et al. · American Journal of Medical Genetics Part A · 21
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
2022 · Munis Dundar, Umut Fahrioglu, et al. · Functional & Integrative Genomics · 20
Relation of glutathione S-transferase genotypes (GSTM1 and GSTT1) to laryngeal squamous cell carcinoma risk
2006 · Hasan Acar, Kayhan Ozturk, et al. · Cancer Genetics and Cytogenetics · 20
Ocular Findings in Children With 22q11.2 Deletion Syndrome
2016 · Bahar Gokturk, Pinar Topcu-Yilmaz, et al. · Journal of Pediatric Ophthalmology & Strabismus · 19
Evaluation of c-MYC Status in Primary Acquired Cholesteatoma by Using Fluorescence In Situ Hybridization Technique
2006 · Kayhan Ozturk, Mahmut Selman Yildirim, et al. · Otology & Neurotology · 16
K-ras oncogene mutation in pterygium
2016 · B T Ozturk, M S Yıldırım, et al. · Eye · 13
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Chromosome 8 Aneuploidy in Acquired Cholesteatoma
2003 · Mahmut Selman Yildirim, Kayhan Ozturk, et al. · Acta Oto-Laryngologica · 13
Association of Apolipoprotein E Polymorphism with Intravitreal Ranibizumab Treatment Outcomes in Age-Related Macular Degeneration
2015 · Berker Bakbak, Banu Turgut Ozturk, et al. · Current Eye Research · 12
Evaluation of chromosome 8 and 11 aneuploidies in washings and biopsy materials of bladder transitional cell carcinoma
2003 · Hasan Acar, Mehmet Kılınç, et al. · Cancer Genetics and Cytogenetics · 12
Novel findings, mini‐review and dysmorphological characterization of 16p13.11 microduplication syndrome
2022 · Ahmet Burak Arslan, Ayşe Gül Zamani, et al. · International Journal of Developmental Neuroscience · 11
Effect of mobile phone station on micronucleus frequency and chromosomal aberrations in human blood cells.
2010 · M S Yildirim, A Yildirim, et al. · PubMed · 10
Germline landscape of BRCAs by 7-site collaborations as a BRCA consortium in Turkey
2022 · Atil Bisgin, Sebnem Ozemri Sag, et al. · The Breast · 9
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Evaluation of immunological abnormalities in patients with rare syndromes
2023 · Yahya Gul, Hasan Kapakli, et al. · Central European Journal of Immunology · 8
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Hopelessness of mothers who have children with Down syndrome.
2010 · A Yildirim, M S Yildirim · PubMed · 8
LAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findings
2018 · Muserref Basdemirci, Ayse G. Zamani, et al. · Clinical Dysmorphology · 7
Micronuclei frequencies in lymphocytes and cervical cells of women with polycystic ovarian syndrome
2017 · Rengin Karataylı, Ayşe Gül Zamani, et al. · Journal of Turkish Society of Obstetric and Gynecology · 7
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Recurrent proximal 18p monosomy and 18q trisomy in a family due to a pericentric inversion
2014 · Ayse Gul Zamani, Aynur Acar, et al. · American Journal of Medical Genetics Part A · 7
Evaluation of death pathway genes FAS and FASL polymorphisms in chronic HBV infection
2013 · A. G. Zamani, I. O. Barlas, et al. · International Journal of Immunogenetics · 7
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Warburg micro syndrome in two children from a highly inbred Turkish family.
2012 · M S Yildirim, A G Zamani, et al. · PubMed · 7
Reliability and efficiency of interphase-fish with alpha-satellite probe for detection of aneuploidy.
2002 · H Acar, M S Yildirim, et al. · PubMed · 6
The XRCC1 and TP53 gene polymorphisms are associated with advanced-stage disease and early distant metastasis at diagnosis in non-small cell lung cancer
2023 · Mustafa Karaağaç, Çağlayan Geredeli, et al. · Journal of Cancer Research and Therapeutics · 5
Works count: 91
Citation count: 700
H-index: 12
I10-index: 15
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