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Martino, Jeremiah
60
results:
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Online (59)
Print (1)
Mediatypes
Books (1)
Articles (Online) (18)
Bookchapter (Online) (1)
OpenAccess-fulltext (40)
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german (1)
english (49)
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1
Risk of meningomyelocele mediated by the common 22q11.2 del..:
Vong, Keng Ioi
;
Lee, Sangmoon
;
Au, Kit Sing
...
Science. 384 (2024) 6695 - p. 584-590 , 2024
Link:
https://doi.org/10.1126/..
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2
Strong protective effect of the APOL1 p.N264K variant again..:
Gupta, Yask
;
Friedman, David J.
;
McNulty, Michelle T.
...
Nature Communications. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
3
Mouse and human studies support DSTYK loss of function as a..:
Martino, Jeremiah
;
Liu, Qingxue
;
Vukojevic, Katarina
...
Genetics in Medicine. 25 (2023) 12 - p. 100983 , 2023
Link:
https://doi.org/10.1016/..
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4
Author Correction: The copy number variation landscape of c..:
Verbitsky, Miguel
;
Westland, Rik
;
Perez, Alejandra
...
Nature Genetics. 51 (2019) 4 - p. 764-764 , 2019
Link:
https://doi.org/10.1038/..
?
5
The copy number variation landscape of congenital anomalies..:
Verbitsky, Miguel
;
Westland, Rik
;
Perez, Alejandra
...
Nature Genetics. 51 (2018) 1 - p. 117-127 , 2018
Link:
https://doi.org/10.1038/..
?
6
Associative Pavlovian conditioning leads to an increase in ..:
Radley, Jason J.
;
Johnson, Luke R.
;
Janssen, William G. M.
...
European Journal of Neuroscience. 24 (2006) 3 - p. 876-884 , 2006
Link:
https://doi.org/10.1111/..
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7
De novo TRIM8 variants impair its protein localization to n..:
Weng, Patricia L
;
Majmundar, Amar J
;
Khan, Kamal
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895901/. , 2021
Link:
http://www.ncbi.nlm.nih...
?
8
The copy number variation landscape of congenital anomalies..:
Verbitsky, Miguel
;
Westland, Rik
;
Perez, Alejandra
...
info:eu-repo/semantics/altIdentifier/pmid/30578417. , 2019
Link:
http://hdl.handle.net/11..
?
9
The copy number variation landscape of congenital anomalies..:
Verbitsky, Miguel
;
Westland, Rik
;
Perez, Alejandra
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6668343/. , 2018
Link:
http://www.ncbi.nlm.nih...
?
10
Exome-wide Association Study Identifies GREB1L Mutations in..:
Sanna-Cherchi, Simone
;
Khan, Kamal
;
Westland, Rik
...
info:eu-repo/semantics/altIdentifier/pmid/29100090. , 2017
Link:
http://hdl.handle.net/11..
?
11
Exome-wide Association Study Identifies GREB1L Mutations in..:
Sanna-Cherchi, Simone
;
Khan, Kamal
;
Westland, Rik
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812917/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
12
Exome-wide Association Study Identifies GREB1L Mutations in..:
Sanna-Cherchi, Simone
;
Khan, Kamal
;
Westland, Rik
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673636/. , 2017
Link:
http://www.ncbi.nlm.nih...
?
13
Genetic Drivers of Kidney Defects in the DiGeorge Syndrome:
Lopez Rivera, Esther
;
Liu, Yangfan P
;
Verbitsky, Miguel
...
info:eu-repo/semantics/altIdentifier/pmid/28121514. , 2017
Link:
http://hdl.handle.net/11..
?
14
ROLES FOR NETRIN-4 AND LAMININS CONTAINING THE β2 OR γ3 SUB..:
Martino, Jeremiah
http://hdl.handle.net/20.500.12648/2020. , 2016
Link:
https://hdl.handle.net/2..
?
15
A susceptibility gene for kidney disease in an obese mouse ..:
Chua, Streamson
;
Li, Yifu
;
Liu, Shun Mei
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998677. , 2010
Link:
http://www.ncbi.nlm.nih...
1-15