Author

Haluk Akin

Professor of Medical Genetics, Ege University - Cited by 510 - Medical genetics - cancer genetics - genetic counseling

Biography

Dr. Haluk Akin is currently working as Head of department and Professor in Faculty of Medicine, Ege University, Turkey. He has done MBBS in Faculty of Medicine Firat University, Turkey. His research interests are Medicine, Health Sciences, Internal Medicine Sciences, Medical Genetics, Cytogenetics, Genetic Counseling, Clinical Genetics, Cancer Biology, Cancer Genetics.
Title
Cited by
Year
MEFV mutations in patients with familial Mediterranean fever from the Aegean region of Turkey
H Akin, H Onay, E Turker, O Cogulu, F OzkinayMolecular biology reports 37, 93-98, 2010201
82
2010
Primary male infertility in Izmir/Turkey: a cytogenetic and molecular study of 187 infertile Turkish patients
H Akin, H Onay, E Turker, F OzkinayJournal of assisted reproduction and genetics 28, 419-423, 2011201
31
2011
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, 2009200
27
2009
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, 2010201
18
2010
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 OzkinayGenetic testing and molecular biomarkers 16 (2), 0-3, 2012201
15
2012
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, 2012201
15
2012
Fragile X syndrome and cerebral perfusion abnormalities: single-photon emission computed tomographic study
N Kabakus, M Aydin, H Akin, TA Balci, A Kurt, E KekilliJournal of child neurology 21 (12), 1040-1046, 2006200
13
2006
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, 2020202
12
2020
Bilateral familial elastofibroma dorsi: is genetic abnormality essential?
Tİ Akçam, U Çağırıcı, A Çakan, H AkınThe Annals of Thoracic Surgery 8 (2), e31-e32, 2014201
9
2014
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), 42-4, 2020202
7
2020
Reactive oxygen species
C Boreera, O Akyol, M Yanik, H Elyas, M Namli, H Canatan, H Akin, ...Biol Psychiatry 32, 1123-31, 2015201
6
2015
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, 2022202
6
2022
Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven‐Year Period
Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 895 Cases over an Eleven‐Year PeriodO Cogulu, F Ozkinay, H Akin, H Onay, E Karaca, AA Durmaz, B Durmaz, ...Journal of Genetic Counseling 20 (3), 287-293, 2011201
6
2011
Whole-genome gene expression analysis in urine samples of patients with prostate cancer and benign prostate hyperplasia
TR Özdemir, A Şimşir, H Onay, İ Cüreklibatır, F Özkınay, H AkınUrologic Oncology: Seminars and Original Investigations 35 (10), 607. e15 …, 2017201
4
2017
20-year experience on prenatal diagnosis in a reference university medical geneticscenter in Turkey
MB DURMAZ, H Bolat, Z Cengisiz, F Akercan, TS Türk, E Pariltay, ...Turkish Journal of Medical Sciences 51 (), 1775-1780, 2021202
4
2021
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 SagolJournal of Assisted Reproduction and Genetics 7, 2019-2024, 2020202
3
2020
Elective Termination Decision in Sex Chromosomal Abnormalities-Current Situation in Decision Making Process
H AkinReprod Sys Sexual Disorders 1, e107, 2012201
3
2012
Investigation of possible associations of the BDNF, SNAP-25 and SYN III genes with the neurocognitive measures: BDNF and SNAP-25 genes might be involved in attention …
H Bolat, G Ünsel-Bolat, S Özgül, E Parıltay, A Tahıllıoğlu, LA Rohde, ...Nordic Journal of Psychiatry 76 (8), 610-615, 2022202
3
2022
The effects of IGF-1 and erythropoietin on apoptosis and telomerase activity in necrotizing enterocolitis model
M Akisu, B Durmaz, OA Koroglu, S Unlubay, M Yalaz, H Akin, U Ates, ...Pediatric Research 90 (3), 559-564, 010
2
2021
Investigation of genotype–phenotype correlation in patients with AZF microdeletion in a single‐reference centre
E Uzay, F Kızılay, B Altay, H Akın, MB DurmazAndrologia 53 (10), e14188, 010
2
2021

Referred From: https://scholar.google.com/citations?user=Hge8zacAAAAJ&hl=en

Cited by
Citations 510
h-index 12
i10-index 12
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