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Gökberk Alagöz
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Discovery of 42 genome-wide significant loci associated with dyslexia
C Doust, P Fontanillas, E Eising, SD Gordon, Z Wang, G Alagöz, B Molz, ...
Nature genetics 54 (11), 1621-1629, 2022
962022
Genome-wide analyses of individual differences in quantitatively assessed reading-and language-related skills in up to 34,000 people
E Eising, N Mirza-Schreiber, EL De Zeeuw, CA Wang, DT Truong, ...
Proceedings of the National Academy of Sciences 119 (35), e2202764119, 2022
832022
Stationary patterns in a two-protein reaction-diffusion system
P Glock, B Ramm, T Heermann, S Kretschmer, J Schweizer, J Mücksch, ...
ACS synthetic biology 8 (1), 148-157, 2018
512018
Using neuroimaging genomics to investigate the evolution of human brain structure
G Alagöz, B Molz, E Eising, D Schijven, C Francks, JL Stein, SE Fisher
Proceedings of the National Academy of Sciences 119 (40), e2200638119, 2022
82022
NANOGP1, a tandem duplicate of NANOG, exhibits partial functional conservation in human naïve pluripotent stem cells
K Maskalenka, G Alagöz, F Krueger, J Wright, M Rostovskaya, A Nakhuda, ...
Development 150 (2), dev201155, 2023
32023
SETBP1 variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental …
MMK Wong, RA Kampen, RO Braden, G Alagöz, MS Hildebrand, ...
medRxiv, 2022.03. 04.22271462, 2022
32022
Neuroimaging genomics as a window into the evolution of human sulcal organization
O Goltermann, G Alagöz, B Molz, SE Fisher
Cerebral Cortex 34 (3), bhae078, 2024
12024
The shared genetic architecture and evolution of human language and musical rhythm
G Alagöz, E Eising, Y Mekki, G Bignardi, P Fontanillas, MG Nivard, ...
bioRxiv, 2023
12023
No phenotypic consequences of archaic hominin alleles in present-day humans
B Molz, M Lana Alberro, E Eising, D Schijven, G Alagöz, C Francks, ...
bioRxiv, 2024.07. 05.602242, 2024
2024
Imaging genomics reveals genetic architecture of the globular human braincase
B Molz, E Eising, G Alagoz, D Schijven, C Francks, P Gunz, SE Fisher
bioRxiv, 2024.03. 20.585712, 2024
2024
Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia
C Doust, P Fontanillas, E Eising, SD Gordon, Z Wang, G Alagöz, B Molz, ...
nature genetics 55 (3), 520-520, 2023
2023
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