Association between Ala–9Val polymorphism of Mn-SOD gene and schizophrenia O Akyol, M Yanik, H Elyas, M Namli, H Canatan, H Akin, H Yuce, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 29 (1), 123-131, 2005 | 125 | 2005 |
MEFV mutations in patients with familial Mediterranean fever from the Aegean region of Turkey H Akin, H Onay, E Turker, O Cogulu, F Ozkinay Molecular biology reports 37, 93-98, 2010 | 86 | 2010 |
Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients H Akin, H Onay, E Turker, F Ozkinay Journal of assisted reproduction and genetics 28, 419-423, 2011 | 34 | 2011 |
The activities of purine catabolizing enzymes in plasma and bronchial washing fluid in patients with lung cancer and pneumonia Ö Akyol, I Gökbulut, N Köksal, H Akin, H Özyurt, Z Yildirim Clinical biochemistry 34 (3), 251-254, 2001 | 30 | 2001 |
A severe α thalassemia case compound heterozygous for Hb Adana in α1 gene and 20.5 kb double gene deletion AA Durmaz, H Akin, AY Ekmekci, H Onay, B Durmaz, O Cogulu, ... Journal of Pediatric Hematology/Oncology 31 (8), 592-594, 2009 | 26 | 2009 |
Adenosine deaminase and xanthine oxidase activities in bladder washing fluid from patients with bladder cancer: a preliminary study M Güleç, H Akın, H üseyin Yüce, E Ergin, H Elyas, O Yalçın, Ö Akyol Clinical biochemistry 36 (3), 193-196, 2003 | 25 | 2003 |
Interferon-γ gene and interferon-γ receptor-1 gene polymorphisms in children with tuberculosis from Turkey H Onay, A Ekmekci, B Durmaz, E Sayin, H Cosar, N Bayram, D Can, ... Scandinavian journal of infectious diseases 42 (1), 39-42, 2010 | 19 | 2010 |
Molecular analysis and clinical findings of Griscelli syndrome patients A Durmaz, F Ozkinay, H Onay, M Tombuloglu, A Atay, O Gursel, E Peker, ... Journal of Pediatric Hematology/Oncology 34 (7), 541-544, 2012 | 17 | 2012 |
DRD4 genotyping may differentiate symptoms of attention-deficit/hyperactivity disorder and sluggish cognitive tempo H Bolat, ES Ercan, G Ünsel-Bolat, A Tahillioğlu, KU Yazici, A Bacanli, ... Brazilian Journal of Psychiatry 42, 630-637, 2020 | 15 | 2020 |
The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey E Ataman, O Cogulu, A Durmaz, E Karaca, B Durmaz, H Akin, F Ozkinay Genetic testing and molecular biomarkers 16 (2), 150-153, 2012 | 15 | 2012 |
The Ala-9Val polymorphism in the mitochondrial targeting sequence (MTS) of the manganese superoxide dismutase gene is not associated with juvenile-onset asthma A Gurel, N Tomac, HR Yilmaz, I Tekedereli, O Akyol, F Armutcu, H Yuce, ... Clinical biochemistry 37 (12), 1117-1120, 2004 | 14 | 2004 |
Fragile X syndrome and cerebral perfusion abnormalities: single-photon emission computed tomographic study N Kabakus, M Aydin, H Akin, TA Balci, A Kurt, E Kekilli Journal of child neurology 21 (12), 1040-1046, 2006 | 13 | 2006 |
Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure Y Karaca, E Pariltay, L Mardan, E Karaca, A Durmaz, B Durmaz, A Aykut, ... Reproductive biology 20 (1), 42-47, 2020 | 10 | 2020 |
Multiple pterygium syndrome F Ferda Özkinay, C Özkinay, H Akin, S Azarsiz, C Gündüz The Indian Journal of Pediatrics 64, 113-116, 1997 | 10 | 1997 |
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 9 | 2022 |
Bilateral familial elastofibroma dorsi: is genetic abnormality essential? Tİ Akçam, U Çağırıcı, A Çakan, H Akın The Annals of Thoracic Surgery 98 (2), e31-e32, 2014 | 9 | 2014 |
Reactive oxygen species C Boreera, O Akyol, M Yanik, H Elyas, M Namli, H Canatan, H Akin, ... Biol Psychiatry 32, 1123-31, 2015 | 8 | 2015 |
Comparison of indications and results of prenatal invasive diagnostic tests before and after the implementation of the use of cell-free fetal DNA: a tertiary referral center … F Okmen, H Ekici, I Hortu, M Imamoglu, D Arican, H Akın, S Sagol Journal of Assisted Reproduction and Genetics 37, 2019-2024, 2020 | 7 | 2020 |
SUBTELOMERIC REARRANGEMENTS IN PATIENTS WITH IDIOPATHIC INTELLECTUAL DISABILITY/MULTIPLE CONGENITAL ANOMALIES AND RECURRENT MISCARRIAGES: SEVEN YEARS'EXPERIENCE B Durmaz, E Karaca, A Durmaz, T Atik, H Akin, O Cogulu, F Ozkinay Genetic counseling 24 (2), 167, 2013 | 6 | 2013 |
Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven‐Year Period O Cogulu, F Ozkinay, H Akin, H Onay, E Karaca, AA Durmaz, B Durmaz, ... Journal of Genetic Counseling 20 (3), 287-293, 2011 | 6 | 2011 |