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Goebel, Ingrid
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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