Heidi Stöhr

3.7k total citations · 1 hit paper
60 papers, 2.4k citations indexed

About

Heidi Stöhr is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Heidi Stöhr has authored 60 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 30 papers in Ophthalmology and 14 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Heidi Stöhr's work include Retinal Development and Disorders (36 papers), Retinal Diseases and Treatments (28 papers) and Cellular transport and secretion (12 papers). Heidi Stöhr is often cited by papers focused on Retinal Development and Disorders (36 papers), Retinal Diseases and Treatments (28 papers) and Cellular transport and secretion (12 papers). Heidi Stöhr collaborates with scholars based in Germany, United States and United Kingdom. Heidi Stöhr's co-authors include Bernhard H. F. Weber, Ute Felbor, Gudrun Vogt, Ronald C. Pruett, Karen L. White, Andreas Marquardt, Heidi L. Schulz, E Apfelstedt-Sylla, Vladimir M. Milenkovic and Olaf Strauß and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Heidi Stöhr

59 papers receiving 2.4k citations

Hit Papers

align trajectories

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.

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy

1994 495 citations Bernhard H. F. Weber, Gudrun Vogt et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Heidi Stöhr Germany	24	1.7k	1.0k	425	379	280	60	2.4k
Marijana Samardzija Switzerland	29	2.2k 1.3×	1.3k 1.3×	340 0.8×	639 1.7×	221 0.8×	71	3.1k
Yusuke Takahashi United States	26	1.9k 1.1×	785 0.8×	239 0.6×	270 0.7×	176 0.6×	47	2.5k
Gennadiy Moiseyev United States	27	2.2k 1.3×	1.1k 1.1×	261 0.6×	493 1.3×	294 1.1×	55	2.5k
Eeva Nikoskelainen Finland	28	3.7k 2.2×	697 0.7×	117 0.3×	401 1.1×	97 0.3×	70	4.4k
Panagiotis I. Sergouniotis United Kingdom	30	1.8k 1.1×	1.1k 1.1×	325 0.8×	279 0.7×	273 1.0×	83	2.3k
Galina Dvoriantchikova United States	26	1.1k 0.7×	492 0.5×	116 0.3×	260 0.7×	77 0.3×	52	1.9k
M. Rosario Hernandez United States	42	2.5k 1.5×	3.4k 3.2×	1.1k 2.5×	532 1.4×	563 2.0×	87	5.0k
Neena B. Haider United States	23	1.4k 0.8×	584 0.6×	190 0.4×	383 1.0×	199 0.7×	46	2.0k
Stephanie A. Hagstrom United States	24	1.3k 0.8×	1.6k 1.6×	1.1k 2.5×	325 0.9×	313 1.1×	73	2.8k

Countries citing papers authored by Heidi Stöhr

Since Specialization

Citations

This map shows the geographic impact of Heidi Stöhr'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 Heidi Stöhr with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heidi Stöhr more than expected).

Fields of papers citing papers by Heidi Stöhr

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Heidi Stöhr. 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 Heidi Stöhr. The network helps show where Heidi Stöhr may publish in the future.

Co-authorship network of co-authors of Heidi Stöhr

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi Stöhr. A scholar is included among the top collaborators of Heidi Stöhr 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 Heidi Stöhr. Heidi Stöhr is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Stöhr, Heidi & Bernhard H. F. Weber. (2025). Genetics and diagnostics of inherited retinal diseases in the era of whole genome sequencing. Medizinische Genetik. 37(1). 3–10. 1 indexed citations

Cardon, Iseline, Caroline Nothdurfter, Mark Berneburg, et al.. (2024). Mitochondrial and Cellular Function in Fibroblasts, Induced Neurons, and Astrocytes Derived from Case Study Patients: Insights into Major Depression as a Mitochondria-Associated Disease. International Journal of Molecular Sciences. 25(2). 963–963. 8 indexed citations

Kiel, Christina, Heidi Stöhr, Georg Spital, et al.. (2024). 18-Years of single-centre DNA testing in over 7000 index cases with inherited retinal dystrophies and optic neuropathies. Scientific Reports. 14(1). 25529–25529. 2 indexed citations

Framme, Carsten, et al.. (2022). Investigation of Structural Alterations in Inherited Retinal Diseases: A Quantitative SD-OCT-Analysis of Retinal Layer Thicknesses in Light of Underlying Genetic Mutations. International Journal of Molecular Sciences. 23(24). 16007–16007. 10 indexed citations

Hufendiek, Karsten, Herbert Jägle, Heidi Stöhr, et al.. (2020). Clinical Heterogeneity in Autosomal Recessive Bestrophinopathy with Biallelic Mutations in the BEST1 Gene. International Journal of Molecular Sciences. 21(24). 9353–9353. 8 indexed citations

Nasser, Fadi, Melanie Kempf, Anne Kurtenbach, et al.. (2020). Correlating Adaptive Optics Images to Clinical Findings in Juvenile Macular Dystrophy with Hypotrichosis in Siblings with Homozygous <b><i>CDH3</i></b> Pathogenic Variation. Ophthalmic Research. 63(2). 141–151. 1 indexed citations

Khan, Mubeen, Stéphanie S. Cornelis, Muhammad Imran Khan, et al.. (2019). Cost‐effective molecular inversion probe‐based ABCA4 sequencing reveals deep‐intronic variants in Stargardt disease. Human Mutation. 40(10). 1749–1759. 37 indexed citations

Schulz, Heidi L., Felix Graßmann, Ulrich Kellner, et al.. (2017). Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort—Impact of Selected Deep Intronic Variants and Common SNPs. Investigative Ophthalmology & Visual Science. 58(1). 394–394. 103 indexed citations

Kaufman, Stuart J., et al.. (2016). Long-Term Macular Changes in the First Proband of Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) Due to a Newly Identified Mutation inBEST1. Ophthalmic Genetics. 37(1). 102–108. 14 indexed citations

10.

Kellner, Ulrich, et al.. (2015). Inherited Retinal or Optic Nerve Disorders – Five Steps to Diagnosis (Originaltitel: Erbliche Netzhaut- und Sehbahnerkrankungen – 5 Schritte zur Diagnose). University of Regensburg Publication Server (University of Regensburg). 1 indexed citations

11.

Fung, Adrian T., Heidi Stöhr, Bernhard H. F. Weber, Frank G. Holz, & Lawrence A. Yannuzzi. (2012). ATYPICAL SORSBY FUNDUS DYSTROPHY WITH A NOVEL TYR159CYS TIMP-3 MUTATION. Retinal Cases & Brief Reports. 7(1). 71–74. 8 indexed citations

12.

Langmann, Thomas, Silvio Alessandro Di Gioia, Isabella Rau, et al.. (2010). Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa. The American Journal of Human Genetics. 87(3). 376–381. 64 indexed citations

13.

Janßen, Andreas, et al.. (2008). Molecular dissection of TIMP3 mutation S156C associated with Sorsby fundus dystrophy. Matrix Biology. 27(5). 381–392. 20 indexed citations

14.

Stöhr, Heidi, et al.. (2007). Three novel ABCC5 splice variants in human retina and their role as regulators of ABCC5 gene expression. BMC Molecular Biology. 8(1). 42–42. 21 indexed citations

15.

Stöhr, Heidi, et al.. (2005). VMD2 und seine Rolle bei Morbus Best und anderen Retinopathien -- VMD2 and its role in Best's disease and other retinopathies. University of Regensburg Publication Server (University of Regensburg). 1 indexed citations

16.

Stöhr, Heidi, et al.. (2002). Cloning and characterization of WDR17, a novel WD repeat-containing gene on chromosome 4q34. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1579(1). 18–25. 11 indexed citations

17.

Stöhr, Heidi, et al.. (2000). EST mining of the UniGene dataset to identify retina-specific genes. Cytogenetic and Genome Research. 91(1-4). 267–277. 21 indexed citations

18.

Marquardt, Andreas, Heidi Stöhr, Karen L. White, & Bernhard H. F. Weber. (2000). cDNA Cloning, Genomic Structure, and Chromosomal Localization of Three Members of the Human Fatty Acid Desaturase Family. Genomics. 66(2). 175–183. 244 indexed citations

19.

Stöhr, Heidi, Andreas Marquardt, Paul R. Cooper, et al.. (1998). A Gene Map of the Best’s Vitelliform Macular Dystrophy Region in Chromosome 11q12–q13.1. Genome Research. 8(1). 48–56. 20 indexed citations

20.

Weber, Bernhard H. F., Gudrun Vogt, Ronald C. Pruett, Heidi Stöhr, & Ute Felbor. (1994). Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy. Nature Genetics. 8(4). 352–356. 495 indexed citations breakdown →

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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