Atil Yuksel
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Explore the profile of Atil Yuksel including associated specialties, affiliations and a list of published articles.
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Articles
49
Citations
131
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Recent Articles
1.
Senturk L, Gulec C, Sarac Sivrikoz T, Kayserili H, Kalelioglu I, Avci S, et al.
Fetal Diagn Ther
. 2024 Feb;
51(3):285-299.
PMID: 38346409
Introduction: Counseling osteogenesis imperfecta (OI) pregnancies is challenging due to the wide range of onsets and clinical severities, from perinatal lethality to milder forms detected later in life. Methods: Thirty-eight...
2.
Turgut G, Altunoglu U, Gulec C, Sarac Sivrikoz T, Kalayci T, Toksoy G, et al.
Clin Genet
. 2024 Jan;
105(6):596-610.
PMID: 38278647
Multiple congenital contractures (MCC) due to fetal akinesia manifest across a broad spectrum of diseases, ranging from mild distal arthrogryposis to lethal fetal akinesia deformation sequence. We hereby present a...
3.
Uygur L, Sarac Sivrikoz T, Kalelioglu I, Has R, Kunt Isguder C, Oktar T, et al.
J Perinat Med
. 2023 May;
51(7):932-939.
PMID: 37144940
Objectives: This study aims to assess the diagnostic accuracy of targeted ultrasound examination in prenatal diagnosis of hypospadias and to evaluate the predictive values of defined ultrasonographic findings of hypospadias....
4.
Uzunhan T, Erturk B, Aydin K, Ayaz A, Altunoglu U, Yarar M, et al.
Clin Neurol Neurosurg
. 2022 Dec;
224:107560.
PMID: 36580738
Objective: Joubert syndrome is a neurodevelopmental disorder with a distinctive hindbrain malformation called molar tooth sign, causing motor and cognitive impairments. More than 40 genes have been associated with Joubert...
5.
Basaran S, Has R, Kalelioglu I, Sarac Sivrikoz T, Karaman B, Kirgiz M, et al.
Genes (Basel)
. 2022 Dec;
13(12).
PMID: 36553656
The scope of cell-free DNA (cfDNA) testing was expanded to the genome, which allowed screening for rare chromosome anomalies (RCAs). Since the efficiency of the test for RCAs remains below...
6.
Kalayci T, Altunoglu U, Corbacioglu Esmer A, Avci S, Sarac Sivrikoz T, Karaman B, et al.
Am J Med Genet A
. 2022 Nov;
191(2):498-509.
PMID: 36398383
We report on 314 fetal cases from 297 unrelated families with skeletal dysplasia evaluated in the postmortem period from 2000 to 2017 at a single clinical genetics center in İstanbul,...
7.
Can S, Has R, Turkyilmaz G, Aktoz F, Yuksel A
J Clin Ultrasound
. 2022 Jun;
50(7):958-963.
PMID: 35665512
Purpose: Multiple pregnancy is associated with high perinatal mortality and morbidity. Abnormal cord insertions more common in twin pregnancies compared to singleton pregnancies and velamentous cord insertion is related with...
8.
Sarac Sivrikoz T, Demir O, Kalelioglu I, Has R, Karakas Paskal E, Kundakci Ozdemir P, et al.
Eur J Obstet Gynecol Reprod Biol
. 2022 Jan;
270:195-200.
PMID: 35093827
Objective: The aim of the study was to compare the effect of early or late fetal reduction (FR) procedures on perinatal outcomes in multiple pregnancies reduced to twins or singletons....
9.
Sarac Sivrikoz T, Basaran S, Has R, Karaman B, Kalelioglu I, Kirgiz M, et al.
Arch Gynecol Obstet
. 2021 Jun;
305(2):323-342.
PMID: 34145474
Purpose: We aimed to present the fetal ultrasound, cytogenetic/molecular testing and postmortem or postnatal clinical findings of cases with 22q11.2DS diagnosed prenatally. Materials And Methods: A retrospective medical record review...
10.
Turkyilmaz G, Cetin B, Erturk E, Sivrikoz T, Kalelioglu I, Has R, et al.
J Obstet Gynaecol
. 2021 Jan;
41(7):1071-1075.
PMID: 33459097
We reviewed the records of 144 patients. The mean gestational age at first US diagnosis was 27.5 ± 4.3 weeks. An anomaly of the contralateral kidney was detected in 25%...