Ingrid Goebel

3.1k total citations · 1 hit paper
18 papers, 1.4k citations indexed

About

Ingrid Goebel is a scholar working on Molecular Biology, Psychiatry and Mental health and Endocrine and Autonomic Systems. According to data from OpenAlex, Ingrid Goebel has authored 18 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Psychiatry and Mental health and 4 papers in Endocrine and Autonomic Systems. Recurrent topics in Ingrid Goebel's work include Migraine and Headache Studies (6 papers), Neuroscience of respiration and sleep (4 papers) and Restraint-Related Deaths (3 papers). Ingrid Goebel is often cited by papers focused on Migraine and Headache Studies (6 papers), Neuroscience of respiration and sleep (4 papers) and Restraint-Related Deaths (3 papers). Ingrid Goebel collaborates with scholars based in Germany, United States and United Kingdom. Ingrid Goebel's co-authors include Christian Kubisch, Alfredo Ramı́rez, C. Geoffrey Woods, L. Pablo Cid, André Heimbach, Birgit Liss, Meliha Karsak, A. S. Najim Al-Din, Ammar F. Mubaidin and Axel M. Hillmer and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and NeuroImage.

In The Last Decade

Ingrid Goebel

18 papers receiving 1.4k citations

Hit Papers

Hereditary parkinsonism with dementia is caused by mutati... 2006 2026 2012 2019 2006 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
    2006 881 citations Alfredo Ramı́rez, André Heimbach et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ingrid Goebel Germany 13 675 619 315 310 307 18 1.4k
Sarah Mizielinska United Kingdom 17 1.3k 1.9× 971 1.6× 398 1.3× 454 1.5× 227 0.7× 28 2.1k
Elize D. Haasdijk Netherlands 22 994 1.5× 910 1.5× 421 1.3× 405 1.3× 340 1.1× 28 2.1k
Luigia Atorino Italy 7 348 0.5× 598 1.0× 277 0.9× 320 1.0× 238 0.8× 8 1.4k
Rubén Fernández‐Santiago Spain 23 849 1.3× 643 1.0× 243 0.8× 372 1.2× 202 0.7× 46 1.5k
Ikuko Mizuta Japan 26 891 1.3× 736 1.2× 334 1.1× 762 2.5× 478 1.6× 98 2.0k
Yasuhiro Kawamoto Japan 20 522 0.8× 469 0.8× 203 0.6× 486 1.6× 263 0.9× 46 1.3k
Una‐Marie Sheerin United Kingdom 13 1.3k 1.9× 495 0.8× 296 0.9× 567 1.8× 370 1.2× 19 1.7k
Nicol Birsa United Kingdom 15 265 0.4× 786 1.3× 143 0.5× 153 0.5× 57 0.2× 17 1.1k
Xian Lin China 19 1.4k 2.1× 764 1.2× 540 1.7× 842 2.7× 520 1.7× 44 2.3k
Patricia Kramer United States 15 853 1.3× 848 1.4× 137 0.4× 927 3.0× 270 0.9× 21 1.9k

Countries citing papers authored by Ingrid Goebel

Since Specialization
Citations

This map shows the geographic impact of Ingrid Goebel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ingrid Goebel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingrid Goebel more than expected).

Fields of papers citing papers by Ingrid Goebel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ingrid Goebel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ingrid Goebel. The network helps show where Ingrid Goebel may publish in the future.

Co-authorship network of co-authors of Ingrid Goebel

This figure shows the co-authorship network connecting the top 25 collaborators of Ingrid Goebel. A scholar is included among the top collaborators of Ingrid Goebel based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ingrid Goebel. Ingrid Goebel is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Barroso, Madalena, Ingrid Goebel, Karl Kuchler, et al.. (2024). Use of the Novel Site-Directed Enzyme Enhancement Therapy (SEE-Tx) Drug Discovery Platform to Identify Pharmacological Chaperones for Glutaric Acidemia Type 1. Journal of Medicinal Chemistry. 67(19). 17087–17100. 1 indexed citations
2.
Bartholomäus, Alexander, Ingrid Goebel, Stephan Fuchs, et al.. (2021). smORFer: a modular algorithm to detect small ORFs in prokaryotes. Nucleic Acids Research. 49(15). e89–e89. 21 indexed citations
3.
Czech, Andreas, Petr V. Konarev, Ingrid Goebel, et al.. (2019). Octa-repeat domain of the mammalian prion protein mRNA forms stable A-helical hairpin structure rather than G-quadruplexes. Scientific Reports. 9(1). 4 indexed citations
4.
Chelysheva, Irina, Ingrid Goebel, Jun Zhou, et al.. (2018). Dynamic m 6 A methylation facilitates mRNA triaging to stress granules. Life Science Alliance. 1(4). e201800113–e201800113. 135 indexed citations
5.
Lang‐Roth, Ruth, Cornelia Kornblum, Gudrun Nürnberg, et al.. (2017). AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance. Audiology and Neurotology. 22(1). 30–40. 8 indexed citations
6.
Kakar, Naseebullah, Ingrid Goebel, Tahir Yaqub, et al.. (2016). Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(3-4). 260–265. 10 indexed citations
7.
Fischer, Adrian G., Tanja Endraß, Ingrid Goebel, et al.. (2015). Interactive effects of citalopram and serotonin transporter genotype on neural correlates of response inhibition and attentional orienting. NeuroImage. 116. 59–67. 5 indexed citations
8.
Hübers, Annemarie, Walter Just, Angela Rosenbohm, et al.. (2015). De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients. Neurobiology of Aging. 36(11). 3117.e1–3117.e6. 56 indexed citations
9.
Kakar, Naseebullah, Ingrid Goebel, Gudrun Nürnberg, et al.. (2012). A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly. European Journal of Medical Genetics. 55(12). 727–731. 34 indexed citations
10.
Todt, Unda, Christian Netzer, Mohammad R. Toliat, et al.. (2009). New genetic evidence for involvement of the dopamine system in migraine with aura. Human Genetics. 125(3). 265–279. 53 indexed citations
11.
Netzer, Christian, Jan Freudenberg, Axel Heinze, et al.. (2008). Replication study of the insulin receptor gene in migraine with aura. Genomics. 91(6). 503–507. 17 indexed citations
12.
Goebel, Ingrid, et al.. (2008). A novel HSF4gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan. BMC Medical Genetics. 9(1). 99–99. 34 indexed citations
13.
Netzer, Christian, Jan Freudenberg, Mohammad R. Toliat, et al.. (2007). Genetic association studies of the chromosome 15 GABA‐A receptor cluster in migraine with aura. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(1). 37–41. 17 indexed citations
14.
Ramı́rez, Alfredo, André Heimbach, Jan Gründemann, et al.. (2006). Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nature Genetics. 38(10). 1184–1191. 881 indexed citations breakdown →
15.
Netzer, Christian, Unda Todt, Axel Heinze, et al.. (2006). Haplotype‐based systematic association studies of ATP1A2 in migraine with aura. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(3). 257–260. 15 indexed citations
16.
Todt, Unda, Jan Freudenberg, Ingrid Goebel, et al.. (2006). Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura. Neurology. 67(9). 1707–1709. 21 indexed citations
17.
Todt, Unda, Martin Dichgans, Karin Jurkat‐Rott, et al.. (2005). Rare missense variants inATP1A2 in families with clustering of common forms of migraine. Human Mutation. 26(4). 315–321. 61 indexed citations
18.
Ramı́rez, Alfredo, Ingrid Goebel, Susanne Beyer, et al.. (2004). Identification of a novel mutation in the coding region of the grey-lethal geneOSTM1in human malignant infantile osteopetrosis. Human Mutation. 23(5). 471–476. 48 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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