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Ercan-Sencicek, A. Gulhan
72
results:
Search for persons
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Online (72)
Mediatypes
Articles (Online) (26)
Bookchapter (Online) (2)
OpenAccess-fulltext (44)
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1
Pleiotropic role of TRAF7 in skull-base meningiomas and con..:
Mishra-Gorur, Ketu
;
Barak, Tanyeri
;
Kaulen, Leon D.
...
Proceedings of the National Academy of Sciences. 120 (2023) 16 - p. , 2023
Link:
https://doi.org/10.1073/..
?
2
Induced pluripotent stem cells for modeling Noonan, Noonan ..:
, In:
Current Progress in iPSC Disease Modeling
,
Ercan-Sencicek, A. Gulhan
;
Chennappan, Saravanakkumar
;
Aromalaran, Kelly
. - p. 65-110 , 2022
Link:
https://doi.org/10.1016/..
?
3
Contributors:
, In:
Current Progress in iPSC Disease Modeling
,
Al Sayed, Zeina R.
;
Aromalaran, Kelly
;
Azad, Priti
... - p. xiii-xvi , 2022
Link:
https://doi.org/10.1016/..
?
4
Engineering spatial-organized cardiac organoids for develop..:
Hoang, Plansky
;
Kowalczewski, Andrew
;
Sun, Shiyang
...
Stem Cell Reports. 16 (2021) 5 - p. 1228-1244 , 2021
Link:
https://doi.org/10.1016/..
?
5
PPIL4 is essential for brain angiogenesis and implicated in..:
Barak, Tanyeri
;
Ristori, Emma
;
Ercan-Sencicek, A. Gulhan
...
Nature Medicine. 27 (2021) 12 - p. 2165-2175 , 2021
Link:
https://doi.org/10.1038/..
?
6
Both proliferation and lipogenesis of brown adipocytes cont..:
Negron, Steven G.
;
Ercan-Sencicek, A. Gulhan
;
Freed, Jessica
..
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
?
7
Neurogenetic analysis of childhood disintegrative disorder:
Gupta, Abha R.
;
Westphal, Alexander
;
Yang, Daniel Y. J.
...
Molecular Autism. 8 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
8
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/..
?
9
Insights into Autism Spectrum Disorder Genomic Architecture..:
Sanders, Stephan J.
;
He, Xin
;
Willsey, A. Jeremy
...
Neuron. 87 (2015) 6 - p. 1215-1233 , 2015
Link:
https://doi.org/10.1016/..
?
10
Integrated genomic characterization of IDH1-mutant glioma m..:
Bai, Hanwen
;
Harmancı, Akdes Serin
;
Erson-Omay, E Zeynep
...
Nature Genetics. 48 (2015) 1 - p. 59-66 , 2015
Link:
https://doi.org/10.1038/..
?
11
De Novo Insertions and Deletions of Predominantly Paternal ..:
Dong, Shan
;
Walker, Michael F.
;
Carriero, Nicholas J.
...
Cell Reports. 9 (2014) 1 - p. 16-23 , 2014
Link:
https://doi.org/10.1016/..
?
12
Histidine Decarboxylase Deficiency Causes Tourette Syndrome..:
Castellan Baldan, Lissandra
;
Williams, Kyle A.
;
Gallezot, Jean-Dominique
...
Neuron. 81 (2014) 1 - p. 77-90 , 2014
Link:
https://doi.org/10.1016/..
?
13
Histidine Decarboxylase Deficiency Causes Tourette Syndrome..:
Castellan Baldan, Lissandra
;
Williams, Kyle A.
;
Gallezot, Jean-Dominique
...
Neuron. 82 (2014) 5 - p. 1186-1187 , 2014
Link:
https://doi.org/10.1016/..
?
14
Coexpression Networks Implicate Human Midfetal Deep Cortica..:
Willsey, A. Jeremy
;
Sanders, Stephan J.
;
Li, Mingfeng
...
Cell. 155 (2013) 5 - p. 997-1007 , 2013
Link:
https://doi.org/10.1016/..
?
15
A balanced t(10;15) translocation in a male patient with de..:
Ercan-Sencicek, A. Gulhan
;
Davis Wright, Nicole R.
;
Sanders, Stephan J.
...
European Journal of Medical Genetics. 55 (2012) 2 - p. 128-131 , 2012
Link:
https://doi.org/10.1016/..
1-15