Ina R. Vogt - Concepedia

Author

Ina R. Vogt

University of Bonn ORCID

Also Known As

I Vogt, I. R. Vogt, I. Vogt, I.R Vogt, Ina R Vogt, Ina R. Vogt, Ina Vogt, Ina Rosemarie Vogt, Inte Vogt, Vogt, I.R.

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

University of Bonn German Center for Neurodegenerative Diseases Technical University of Munich Otto-von-Guericke University Magdeburg University of Rostock

About

Ina R. Vogt is an author at University of Bonn specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	620
2	Social Sciences	2	2	205
3	Cell Biology	2	2	209
4	Biology	1	1	153
5	Immunology	1	1	131

Ina R. Vogt

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Abnormal Pulmonary Artery Pressure Response in Asymptomatic Carriers of Primary Pulmonary Hypertension Gene Ekkehard Grünig, Bart Janssen, Derliz Mereles, Circulation	2000	255
Plasma extracellular vesicle tau and TDP-43 as diagnostic biomarkers in FTD and ALS Madhurima Chatterjee, Selcuk Özdemir, Christian Fritz, Nature Medicine	2024	160
Cloning, Genomic Organization, Alternative Transcripts and Mutational Analysis of the Gene Responsible for Autosomal Recessive Universal Congenital Alopecia Sven Cichon, M. Anker, Ina R. Vogt, Human Molecular Genetics BiologyDevelopmental BiologyMutational AnalysisMendelian DisorderGenetic Disorder	1998	153
Inflammatory Genes Are Upregulated in Expanded Ataxin-3-Expressing Cell Lines and Spinocerebellar Ataxia Type 3 Brains Bernd O. Evert, Ina R. Vogt, Claudia Kindermann, Journal of Neuroscience ImmunologyCell DeathSynaptic SignalingSocial SciencesNeuroinflammation	2001	131
Gene Expression Profiling in Ataxin-3 Expressing Cell Lines Reveals Distinct Effects of Normal and Mutant Ataxin-3 Bernd O. Evert, Ina R. Vogt, Ana Vieira‐Saecker, Journal of Neuropathology & Experimental Neurology GeneticsGene CharacterizationGene Expression ProfilingNeuroinflammationTranscriptional Regulation	2003	78
Investigation of the human serotonin 6 (5-HT6) receptor gene in bipolar affective disorder and schizophrenia Ina R. Vogt, Daphne Shimron‐Abarbanell, Helge Neidt, American Journal of Medical Genetics Bipolar Affective DisorderPsychotropic MedicationGeneticsPsychopharmacologyReceptor Gene	2000	74
A Gene for Universal Congenital Alopecia Maps to Chromosome 8p21-22 Markus M. Nöthen, Sven Cichon, Ina R. Vogt, The American Journal of Human Genetics Developmental BiologyGenetic DisorderGeneticsMolecular GeneticsGenetic Variation	1998	62
Transcriptional changes in multiple system atrophy and Parkinson's disease putamen Ina R. Vogt, Andrew J. Lees, Bernd O. Evert, Experimental Neurology Amyotrophic Lateral SclerosisGeneticsMultiple System AtrophyParkinson DiseaseDegenerative Disease	2006	53
Digital Gait Biomarkers Allow to Capture 1‐Year Longitudinal Change in Spinocerebellar Ataxia Type 3 Winfried Ilg, Björn Müller, Jennifer Faber, Movement Disorders	2022	52
Genetic linkage analysis with dyslexia: Evidence for linkage of spelling disability to chromosome 15 Markus M. Nöthen, Gerd Schulte‐Körne, T. Grimm, European Child & Adolescent Psychiatry Language DisorderGenetic DisorderGeneticsReading DisabilitiesMedicine	1999	51

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