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Goebel, Ingrid
75
results:
Search for persons
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Online (75)
Mediatypes
E-Books (2)
Articles (Online) (29)
Bookchapter (Online) (1)
OpenAccess-fulltext (43)
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1
smORFer: a modular algorithm to detect small ORFs in prokar..:
Bartholomäus, Alexander
;
Kolte, Baban
;
Mustafayeva, Ayten
...
Nucleic Acids Research. 49 (2021) 15 - p. e89-e89 , 2021
Link:
https://doi.org/10.1093/..
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2
Author Correction: Octa-repeat domain of the mammalian prio..:
Czech, Andreas
;
Konarev, Petr V.
;
Goebel, Ingrid
...
Scientific Reports. 10 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1038/..
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3
Octa-repeat domain of the mammalian prion protein mRNA form..:
Czech, Andreas
;
Konarev, Petr V.
;
Goebel, Ingrid
...
Scientific Reports. 9 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1038/..
?
4
Dynamic m6A methylation facilitates mRNA triaging to stress..:
Anders, Maximilian
;
Chelysheva, Irina
;
Goebel, Ingrid
...
Life Science Alliance. 1 (2018) 4 - p. e201800113 , 2018
Link:
https://doi.org/10.26508..
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5
A post GWAS association study of SNPs associated with cleft..:
Reiter, Rudolf
;
Brosch, Sibylle
;
Goebel, Ingrid
...
American Journal of Medical Genetics Part A. 167 (2015) 3 - p. 670-673 , 2015
Link:
https://doi.org/10.1002/..
?
6
De novo FUS mutations are the most frequent genetic cause i..:
Hübers, Annemarie
;
Just, Walter
;
Rosenbohm, Angela
...
Neurobiology of Aging. 36 (2015) 11 - p. 3117.e1-3117.e6 , 2015
Link:
https://doi.org/10.1016/..
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7
Interactive effects of citalopram and serotonin transporter..:
Fischer, Adrian G.
;
Endrass, Tanja
;
Goebel, Ingrid
...
NeuroImage. 116 (2015) - p. 59-67 , 2015
Link:
https://doi.org/10.1016/..
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8
A homozygous splice site mutation in TRAPPC9 causes intelle..:
Kakar, Naseebullah
;
Goebel, Ingrid
;
Daud, Shakeela
...
European Journal of Medical Genetics. 55 (2012) 12 - p. 727-731 , 2012
Link:
https://doi.org/10.1016/..
?
9
Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessi..:
Borck, Guntram
;
Rehman, Atteeq Ur
;
Lee, Kwanghyuk
...
The American Journal of Human Genetics. 88 (2011) 2 - p. 127-137 , 2011
Link:
https://doi.org/10.1016/..
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10
New genetic evidence for involvement of the dopamine system..:
Todt, Unda
;
Netzer, Christian
;
Toliat, Mohammad
...
Human Genetics. 125 (2009) 3 - p. 265-279 , 2009
Link:
https://doi.org/10.1007/..
?
11
A novel HSF4gene mutation (p.R405X) causing autosomal reces..:
Sajjad, Naheed
;
Goebel, Ingrid
;
Kakar, Naseebullah
...
BMC Medical Genetics. 9 (2008) 1 - p. , 2008
Link:
https://doi.org/10.1186/..
?
12
Replication study of the insulin receptor gene in migraine ..:
Netzer, Christian
;
Freudenberg, Jan
;
Heinze, Axel
...
Genomics. 91 (2008) 6 - p. 503-507 , 2008
Link:
https://doi.org/10.1016/..
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13
Genetic association studies of the chromosome 15 GABA-A rec..:
Netzer, Christian
;
Freudenberg, Jan
;
Toliat, Mohammad R.
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 147B (2007) 1 - p. 37-41 , 2007
Link:
https://doi.org/10.1002/..
?
14
Haplotype‐based systematic association studies of ATP1A2 in..:
Netzer, Christian
;
Todt, Unda
;
Heinze, Axel
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 141B (2006) 3 - p. 257-260 , 2006
Link:
https://doi.org/10.1002/..
?
15
Hereditary parkinsonism with dementia is caused by mutation..:
Ramirez, Alfredo
;
Heimbach, André
;
Gründemann, Jan
...
Nature Genetics. 38 (2006) 10 - p. 1184-1191 , 2006
Link:
https://doi.org/10.1038/..
1-15