I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Yasuno, Katsuhito
93
results:
Search for persons
X
Format
Online (93)
Mediatypes
Articles (Online) (33)
OpenAccess-fulltext (60)
Sorted by: Relevance
Sorted by: Year
?
1
EPCO-47. HETEROZYGOUS CDKN2A LOSS IS ASSOCIATED WITH HIGHER..:
Tabor, Joanna
;
Chavez, Miguel Millares
;
O'Brien, Joseph
...
Neuro-Oncology. 25 (2023) Supplement_5 - p. v134-v135 , 2023
Link:
https://doi.org/10.1093/..
?
2
METAP1 mutation is a novel candidate for autosomal recessiv..:
Caglayan, Ahmet Okay
;
Aktar, Fesih
;
Bilguvar, Kaya
...
Journal of Human Genetics. 66 (2020) 2 - p. 215-218 , 2020
Link:
https://doi.org/10.1038/..
?
3
Correction: Author Correction: Integrated genomic analyses ..:
Harmancı, Akdes Serin
;
Youngblood, Mark W.
;
Clark, Victoria E.
...
Nature Communications. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
4
Loss of Protocadherin‐12Leads to Diencephalic‐Mesencephalic..:
Guemez‐Gamboa, Alicia
;
Çağlayan, Ahmet Okay
;
Stanley, Valentina
...
Annals of Neurology. 84 (2018) 5 - p. 638-647 , 2018
Link:
https://doi.org/10.1002/..
?
5
Genotype–phenotype investigation of 35 patients from 11 unr..:
Yilmaz, Saliha
;
Uludağ Alkaya, Dilek
;
Kasapçopur, Özgür
...
Molecular Genetics & Genomic Medicine. 6 (2018) 2 - p. 230-248 , 2018
Link:
https://doi.org/10.1002/..
?
6
Exome analysis of the evolutionary path of hepatocellular a..:
Vilarinho, Sílvia
;
Erson-Omay, E. Zeynep
;
Mitchell-Richards, Kisha
...
Journal of Hepatology. 67 (2017) 1 - p. 186-191 , 2017
Link:
https://doi.org/10.1016/..
?
7
Longitudinal analysis of treatment-induced genomic alterati..:
Erson-Omay, E. Zeynep
;
Henegariu, Octavian
;
Omay, S. Bülent
...
Genome Medicine. 9 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
8
Integrated genomic analyses of de novo pathways underlying ..:
Harmancı, Akdes Serin
;
Youngblood, Mark W.
;
Clark, Victoria E.
...
Nature Communications. 8 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
9
Constitutive mismatch repair defect syndrome: New insights ..:
Caglayan, Ahmet Okay
;
Omay, Zeynep E. Erson
;
Koksal, Yavuz
...
Journal of Biotechnology. 231 (2016) - p. S12 , 2016
Link:
https://doi.org/10.1016/..
?
10
A patient with a novel homozygous missense mutation in FTO ..:
Çağlayan, Ahmet O
;
Tüysüz, Beyhan
;
Coşkun, Süleyman
...
Journal of Human Genetics. 61 (2016) 5 - p. 395-403 , 2016
Link:
https://doi.org/10.1038/..
?
11
Recurrent somatic mutations in POLR2A define a distinct sub..:
Clark, Victoria E
;
Harmancı, Akdes Serin
;
Bai, Hanwen
...
Nature Genetics. 48 (2016) 10 - p. 1253-1259 , 2016
Link:
https://doi.org/10.1038/..
?
12
GENO-15IDENTIFICATION AND GENOMIC ANALYSIS OF HYPER-MUTATED..:
Erson-Omay, E. Zeynep
;
Schultz, Nikolaus
;
Omay, S. Bulent
...
Neuro-Oncology. 17 (2015) suppl 5 - p. v94.3-v94 , 2015
Link:
https://doi.org/10.1093/..
?
13
Whole‐exome sequencing defines the mutational landscape of ..:
Juhlin, C. Christofer
;
Stenman, Adam
;
Haglund, Felix
...
Genes, Chromosomes and Cancer. 54 (2015) 9 - p. 542-554 , 2015
Link:
https://doi.org/10.1002/..
?
14
NGLY1 mutation causes neuromotor impairment, intellectual d..:
Caglayan, Ahmet Okay
;
Comu, Sinan
;
Baranoski, Jacob F.
...
European Journal of Medical Genetics. 58 (2015) 1 - p. 39-43 , 2015
Link:
https://doi.org/10.1016/..
?
15
SomaticPOLEmutations cause an ultramutated giant cell high-..:
Erson-Omay, E. Zeynep
;
Çağlayan, Ahmet Okay
;
Schultz, Nikolaus
...
Neuro-Oncology. 17 (2015) 10 - p. 1356-1364 , 2015
Link:
https://doi.org/10.1093/..
1-15