A. Bilge Ozel
A. Bilge Ozel
Research Specialist Senior
Bestätigte E-Mail-Adresse bei
Zitiert von
Zitiert von
Genome Analyses of> 200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders
S Ligthart, A Vaez, U Võsa, MG Stathopoulou, PS de Vries, BP Prins, ...
The American Journal of Human Genetics 103 (5), 691-706, 2018
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155, 2013
Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia
MJ Kiel, T Velusamy, D Rolland, AA Sahasrabuddhe, F Chung, NG Bailey, ...
Blood 124 (9), 1460-1472, 2014
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126-1130, 2014
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era
Q Fang, AS George, ML Brinkmeier, AH Mortensen, P Gergics, ...
Endocrine Reviews 37 (6), 636-675, 2016
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects
E Seong, R Insolera, M Dulovic, EJ Kamsteeg, J Trinh, N Brüggemann, ...
Annals of neurology 83 (6), 1075-1088, 2018
Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels
M Sabater-Lleal, JE Huffman, PS de Vries, J Marten, MA Mastrangelo, ...
Circulation, 2019
Genome-wide association study and meta-analysis of intraocular pressure
AB Ozel, SE Moroi, DM Reed, M Nika, CM Schmidt, S Akbari, K Scott, ...
Human genetics 133 (1), 41-57, 2014
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association
KC Desch, AB Ozel, D Siemieniak, Y Kalish, JA Shavit, CD Thornburg, ...
Proceedings of the National Academy of Sciences 110 (2), 588-593, 2013
Genome-Wide Analysis of Central Corneal Thickness in Primary Open-Angle Glaucoma Cases in the NEIGHBOR and GLAUGEN ConsortiaThe Effects of CCT-Associated Variants on POAG Risk
M Ulmer, J Li, BL Yaspan, AB Ozel, JE Richards, SE Moroi, F Hawthorne, ...
Investigative ophthalmology & visual science 53 (8), 4468-4474, 2012
Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice
SJ Garnai, ML Brinkmeier, B Emery, TS Aleman, LC Pyle, B Veleva-Rotse, ...
PLoS genetics 15 (5), e1008130, 2019
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
FJA van Rooij, R Qayyum, AV Smith, Y Zhou, S Trompet, T Tanaka, ...
The American Journal of Human Genetics 100 (1), 51-63, 2017
Whole exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
K Desch, AB Ozel, M Halvorsen, PM Jacobi, KL Golden, MI Underwood, ...
Blood, 2020
Minimizing the Surface Effect on PCR in PDMS-Glass Chips by Dynamic Passivation
Y Xia, Z Hua, E Gular, O Srivannavit, AB Ozel
The 2005 Annual Meeting, 2005
COQ4 Mutation Leads to Childhood-Onset Ataxia Improved by CoQ10 Administration
AO Caglayan, H Gumus, E Sandford, TL Kubisiak, Q Ma, AB Ozel, H Per, ...
The Cerebellum 18 (3), 665-669, 2019
Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels
Q Ma, AB Ozel, S Ramdas, B McGee, R Khoriaty, D Siemieniak, HD Li, ...
Blood 124 (20), 3155-3164, 2014
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
G Hindy, DJ Tyrrell, A Vasbinder, C Wei, F Presswalla, H Wang, P Blakely, ...
The Journal of Clinical Investigation 132 (24), 2022
The endoplasmic reticulum cargo receptor SURF4 facilitates efficient erythropoietin secretion
Z Lin, R King, V Tang, G Myers, G Balbin-Cuesta, A Friedman, B McGee, ...
Molecular and Cellular Biology, 2020
Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 …
D Lessel, AB Ozel, SE Campbell, A Saadi, MF Arlt, KM McSweeney, ...
Human genetics 137 (11), 921-939, 2018
High-throughput splicing assays identify missense and silent splice-disruptive POU1F1 variants underlying pituitary hormone deficiency
P Gergics, C Smith, H Bando, AAL Jorge, D Rockstroh-Lippold, ...
medRxiv, 2021
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