Tugce Balci
Overview
Explore the profile of Tugce Balci including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
16
Citations
155
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Richer J, Velchev J, Goobie S, Boswell-Patterson C, van de Laar I, Verhagen J, et al.
J Med Genet
. 2025 Jan;
62(3):199-205.
PMID: 39746778
Background: Individuals harbouring pathogenic variants are at risk for aneurysms/dissections throughout the arterial tree. Based on prior reports of sex differences in thoracic aortic aneurysm/dissection, we investigated the sexual dimorphism...
2.
Layo-Carris D, Lubin E, Sangree A, Clark K, Durham E, Gonzalez E, et al.
Eur J Hum Genet
. 2024 Jul;
32(8):1032.
PMID: 39060653
No abstract available.
3.
Layo-Carris D, Lubin E, Sangree A, Clark K, Durham E, Gonzalez E, et al.
Eur J Hum Genet
. 2024 Apr;
32(8):928-937.
PMID: 38678163
Bryant-Li-Bhoj syndrome (BLBS), which became OMIM-classified in 2022 (OMIM: 619720, 619721), is caused by germline variants in the two genes that encode histone H3.3 (H3-3A/H3F3A and H3-3B/H3F3B) [1-4]. This syndrome...
4.
Sabbagh Q, Haghshenas S, Piard J, Trouve C, Amiel J, Attie-Bitach T, et al.
Genet Med
. 2023 Oct;
26(1):101007.
PMID: 37860968
Purpose: BCL11B-related disorder (BCL11B-RD) arises from rare genetic variants within the BCL11B gene, resulting in a distinctive clinical spectrum encompassing syndromic neurodevelopmental disorder, with or without intellectual disability, associated with...
5.
Stefanski A, Perez-Palma E, Brunger T, Montanucci L, Gati C, Klockner C, et al.
Brain
. 2023 Aug;
146(12):5198-5208.
PMID: 37647852
Genetic variants in the SLC6A1 gene can cause a broad phenotypic disease spectrum by altering the protein function. Thus, systematically curated clinically relevant genotype-phenotype associations are needed to understand the...
6.
Algouneh A, Caudle M, Balci T, Andrade A, Penava D, Saleh M
Clin Case Rep
. 2022 Aug;
10(8):e6202.
PMID: 35957765
Pathogenic variants in the and genes are associated with increased risk for breast and ovarian cancers. Concurrent mutations in both genes in the same individual are rare but pose specific...
7.
Levy M, McConkey H, Kerkhof J, Barat-Houari M, Bargiacchi S, Biamino E, et al.
HGG Adv
. 2022 Jan;
3(1):100075.
PMID: 35047860
Overlapping clinical phenotypes and an expanding breadth and complexity of genomic associations are a growing challenge in the diagnosis and clinical management of Mendelian disorders. The functional consequences and clinical...
8.
Haghshenas S, Levy M, Kerkhof J, Aref-Eshghi E, McConkey H, Balci T, et al.
Int J Mol Sci
. 2021 Jan;
22(3).
PMID: 33498634
A growing number of genetic neurodevelopmental disorders are known to be associated with unique genomic DNA methylation patterns, called episignatures, which are detectable in peripheral blood. The intellectual developmental disorder,...
9.
Aref-Eshghi E, Kerkhof J, Carere D, Volodarsky M, Bhai P, Colaiacovo S, et al.
J Hum Genet
. 2020 Oct;
66(5):451-464.
PMID: 33093641
The adaptation of a broad genomic sequencing approach in the clinical setting has been accompanied by considerations regarding the clinical utility, technical performance, and diagnostic yield compared to targeted genetic...
10.
Ozmen Yelken B, Balci T, Yilmaz Susluer S, Kayabasi C, Biray Avci C, Kirmizibayrak P, et al.
Gene
. 2017 Jul;
627:408-411.
PMID: 28669925
Breast cancer is one of the most common malignancies in women and metastasis is the cause of morbidity and mortality in patients. In the development of metastasis, the matrix metalloproteinase...