Publications by authors named "Ingrid Goebel"

22Publications

Dynamic mA methylation facilitates mRNA triaging to stress granules.

Life Sci Alliance 2018 Aug 3;1(4):e201800113. Epub 2018 Jul 3.

Institute for Biochemistry and Molecular Biology, Department of Chemistry, University of Hamburg, Hamburg, Germany.

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http://www.life-science-alliance.org/lookup/doi/10.26508/lsa
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http://dx.doi.org/10.26508/lsa.201800113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238392PMC
August 2018

AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance.

Audiol Neurootol 2017 10;22(1):30-40. Epub 2017 Jun 10.

Department of Otorhinolaryngology, Head and Neck Surgery, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1159/000474929DOI Listing
September 2018

De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients.

Neurobiol Aging 2015 Nov 15;36(11):3117.e1-3117.e6. Epub 2015 Aug 15.

Institute of Human Genetics, University of Ulm, Ulm, Germany; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.08.005DOI Listing
November 2015

Interactive effects of citalopram and serotonin transporter genotype on neural correlates of response inhibition and attentional orienting.

Neuroimage 2015 Aug 6;116:59-67. Epub 2015 May 6.

Otto-von-Guericke University, Institute of Psychology II, Magdeburg, Germany; Max Planck Institute for Neurological Research, Cologne, Germany; Radboud University, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, Netherlands; Center for Behavioral Brain Sciences, Magdeburg, Germany.

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http://dx.doi.org/10.1016/j.neuroimage.2015.04.064DOI Listing
August 2015

A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate.

Am J Med Genet A 2015 Mar;167A(3):670-3

Section of Phoniatrics and Pedaudiology, Department of Otolaryngology - Head and Neck Surgery, University of Ulm, Ulm, Germany.

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http://dx.doi.org/10.1002/ajmg.a.36891DOI Listing
March 2015

A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.

Eur J Med Genet 2012 Dec 30;55(12):727-31. Epub 2012 Aug 30.

Department of Biotechnology and Informatics, BUITEMS, Quetta, Pakistan.

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http://dx.doi.org/10.1016/j.ejmg.2012.08.010DOI Listing
December 2012

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.

Nat Genet 2010 Oct 29;42(10):869-73. Epub 2010 Aug 29.

Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Cambridge, UK.

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https://openaccess.leidenuniv.nl/bitstream/handle/1887/16353
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ftp://ftp.sanger.ac.uk/pub/resources/theses/sc14/chapter3.pd
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http://www.nature.com/doifinder/10.1038/ng.652
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http://dx.doi.org/10.1038/ng.652DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2948563PMC
October 2010

New genetic evidence for involvement of the dopamine system in migraine with aura.

Hum Genet 2009 Apr 17;125(3):265-79. Epub 2009 Jan 17.

Institute of Human Genetics, University of Cologne, Germany.

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http://dx.doi.org/10.1007/s00439-009-0623-zDOI Listing
April 2009

Replication study of the insulin receptor gene in migraine with aura.

Genomics 2008 Jun 2;91(6):503-7. Epub 2008 May 2.

Institute of Human Genetics, University of Cologne, 50931 Cologne, Germany.

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http://dx.doi.org/10.1016/j.ygeno.2008.03.006DOI Listing
June 2008

Haplotype-based systematic association studies of ATP1A2 in migraine with aura.

Am J Med Genet B Neuropsychiatr Genet 2006 Apr;141B(3):257-60

Institute of Human Genetics, University of Cologne, Cologne, Germany.

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http://dx.doi.org/10.1002/ajmg.b.30283DOI Listing
April 2006