受强制性开放获取政策约束的文章 - Burcu Yaldiz了解详情
无法在其他位置公开访问的文章：1 篇
Effect of sterilization methods on the mechanical stability and extracellular matrix constituents of decellularized brain tissues
B Yaldiz, P Saglam-Metiner, SB Cam, P Korkusuz, O Yesil-Celiktas
The Journal of Supercritical Fluids 175, 105299, 2021
强制性开放获取政策： Scientific and Technological Research Council of Turkey
可在其他位置公开访问的文章：11 篇
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data
L Matalonga, C Hernández-Ferrer, D Piscia, R Schüle, M Synofzik, A Töpf, ...
European Journal of Human Genetics 29 (9), 1337-1347, 2021
强制性开放获取政策： Department of Science & Technology, India, UK Medical Research Council …
Spatio-temporal dynamics enhance cellular diversity, neuronal function and further maturation of human cerebral organoids
P Saglam-Metiner, U Devamoglu, Y Filiz, S Akbari, G Beceren, B Goker, ...
Communications Biology 6 (1), 173, 2023
强制性开放获取政策： Scientific and Technological Research Council of Turkey
Advances in microfluidic synthesis and coupling with synchrotron SAXS for continuous production and real-time structural characterization of nano-self-assemblies
E Ilhan-Ayisigi, B Yaldiz, G Bor, A Yaghmur, O Yesil-Celiktas
Colloids and Surfaces B: Biointerfaces 201, 111633, 2021
强制性开放获取政策： Danish Council for Independent Research
Decellularised extracellular matrix-based biomaterials for repair and regeneration of central nervous system
B Yaldiz, P Saglam-Metiner, O Yesil-Celiktas
Expert Reviews in Molecular Medicine 23, e25, 2021
强制性开放获取政策： Scientific and Technological Research Council of Turkey
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing
AS Denommé-Pichon, L Matalonga, E de Boer, A Jackson, E Benetti, ...
Genetics in Medicine 25 (4), 100018, 2023
强制性开放获取政策： UK Medical Research Council, European Commission, Government of Spain
Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples
R Wijngaard, G Demidov, L O’Gorman, J Corominas-Galbany, B Yaldiz, ...
European Journal of Human Genetics 32 (2), 200-208, 2024
强制性开放获取政策： National Institute for Health Research, UK, European Commission
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
B Yaldiz, E Kucuk, J Hampstead, T Hofste, R Pfundt, ...
Human genomics 17 (1), 39, 2023
强制性开放获取政策： UK Medical Research Council, Wellcome Trust, European Commission
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing
AEJ Janssen, RM Koeck, R Essers, P Cao, W van Dijk, M Drüsedau, ...
Nature Communications 15 (1), 7164, 2024
强制性开放获取政策： European Commission
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14
A Jackson, SJ Lin, EA Jones, KE Chandler, D Orr, C Moss, Z Haider, ...
Human Genetics and Genomics Advances 4 (2), 2023
强制性开放获取政策： Cancer Research UK, UK Medical Research Council, National Institute for …
Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant
E de Boer, B Yaldiz, AS Denommé-Pichon, L Matalonga, S Laurie, ...
European Journal of Medical Genetics 65 (1), 104402, 2022
强制性开放获取政策： UK Medical Research Council, European Commission, Netherlands Organisation …
Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses
G Demidov, B Yaldiz, J Garcia-Pelaez, E de Boer, N Schuermans, ...
NPJ genomic medicine 9 (1), 49, 2024
强制性开放获取政策： European Commission
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