Detalhe da pesquisa
1.
High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population.
Am J Hum Genet
; 108(10): 1981-2005, 2021 10 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34582790
2.
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance.
Am J Hum Genet
; 105(1): 132-150, 2019 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31230720
3.
Mitochondrial DNA copy number may be associated with attention deficit/hyperactivity disorder severity in treatment: a one-year follow-up study.
Int J Psychiatry Clin Pract
; 25(1): 37-42, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33555215
4.
SMN1 gene copy number analysis for spinal muscular atrophy (SMA) in a Turkish cohort by CODE-SEQ technology, an integrated solution for detection of SMN1 and SMN2 copy numbers and the "2+0" genotype.
Neurol Sci
; 41(9): 2575-2584, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32249332
5.
Spectrum of germline cancer susceptibility gene mutations in Turkish colorectal cancer patients: a single center study
Turk J Med Sci
; 50(4): 1015-1021, 2020 06 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32283892
6.
Mitochondrial DNA Copy Number is Associated with Attention Deficit Hyperactivity Disorder.
Psychiatr Danub
; 32(2): 168-175, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32796781
7.
The Frequency of Monocyte Chemoattractant Protein-1 Gene Polymorphism in Obstructive Sleep Apnea Syndrome.
Lung
; 197(5): 585-592, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31388753
8.
Mitochondrial DNA deletions in patients with chronic suppurative otitis media.
Eur Arch Otorhinolaryngol
; 273(9): 2473-9, 2016 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26620342
9.
Higher TP53 somatic mutation prevalence from liquid biopsy analysis in ever smoker non-small-cell lung cancer patients.
Mutat Res
; 828: 111847, 2023 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38071953
10.
Uncommon variants detected via hereditary cancer panel and suggestions for genetic counseling.
Mutat Res
; 827: 111831, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37453313
11.
Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy.
Anatol J Cardiol
; 26(6): 460-465, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35703482
12.
Liquid biopsy: Novel perspectives on the importance and spectrum of PIK3CA, PTEN and RET mutations in solid tumors.
Mol Clin Oncol
; 16(1): 1, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34824841
13.
A rare cause of dyspnea in emergency medicine: Keutel syndrome.
Am J Emerg Med
; 34(5): 935.e3-5, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26462901
14.
Function of telomere in aging and age related diseases.
Environ Toxicol Pharmacol
; 85: 103641, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33774188
15.
Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature.
Acta Neurol Belg
; 121(6): 1457-1462, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170608
16.
High Expression of Stem Cell-Related Genes in Polyps with Villous Features and High-Grade Dysplasia Support Malignant Phenotype and Colorectal Carcinogenesis.
Asian Pac J Cancer Prev
; 22(8): 2429-2435, 2021 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34452555
17.
Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders.
Mol Cytogenet
; 11: 54, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30258496
18.
Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, ß-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
Neuromolecular Med
; 18(2): 170-6, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26951304
19.
Association Between Human Hair Loss and the Expression Levels of Nucleolin, Nucleophosmin, and UBTF Genes.
Genet Test Mol Biomarkers
; 20(4): 197-202, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26866305