Heidi L. Schulz

1.0k total citations
18 papers, 589 citations indexed

About

Heidi L. Schulz is a scholar working on Molecular Biology, Cell Biology and Ophthalmology. According to data from OpenAlex, Heidi L. Schulz has authored 18 papers receiving a total of 589 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 4 papers in Cell Biology and 3 papers in Ophthalmology. Recurrent topics in Heidi L. Schulz's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (3 papers) and interferon and immune responses (2 papers). Heidi L. Schulz is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (3 papers) and interferon and immune responses (2 papers). Heidi L. Schulz collaborates with scholars based in Germany, Netherlands and United Kingdom. Heidi L. Schulz's co-authors include Bernhard H. F. Weber, Heidi Stöhr, Jan Wijnholds, Vladimir M. Milenkovic, P. Benz, Julia Heisig, Wendy M. Aartsen, Olaf Strauß, Ulrich Kellner and Felix Graßmann and has published in prestigious journals such as Journal of Neuroscience, International Journal of Molecular Sciences and Investigative Ophthalmology & Visual Science.

In The Last Decade

Heidi L. Schulz

17 papers receiving 574 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heidi L. Schulz Germany 12 451 161 119 75 63 18 589
F de Pablo Spain 16 474 1.1× 101 0.6× 45 0.4× 53 0.7× 32 0.5× 24 769
Wendy M. Aartsen Netherlands 13 574 1.3× 167 1.0× 149 1.3× 68 0.9× 62 1.0× 16 815
Li‐Ting Chien United States 9 663 1.5× 314 2.0× 112 0.9× 50 0.7× 90 1.4× 9 806
Ahmad Usman Zafar Pakistan 11 347 0.8× 60 0.4× 80 0.7× 19 0.3× 113 1.8× 30 471
Colin A. Bretz United States 14 196 0.4× 150 0.9× 133 1.1× 45 0.6× 14 0.2× 19 479
Piotr Stawiński Poland 15 514 1.1× 77 0.5× 40 0.3× 37 0.5× 42 0.7× 58 782
Ismail Zaitoun United States 17 447 1.0× 75 0.5× 124 1.0× 32 0.4× 12 0.2× 31 904
Nora Overlack Germany 10 638 1.4× 92 0.6× 49 0.4× 24 0.3× 244 3.9× 13 726
Katharine K. Miller United States 12 348 0.8× 41 0.3× 30 0.3× 23 0.3× 130 2.1× 23 563

Countries citing papers authored by Heidi L. Schulz

Since Specialization
Citations

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

Fields of papers citing papers by Heidi L. Schulz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heidi L. Schulz

This figure shows the co-authorship network connecting the top 25 collaborators of Heidi L. Schulz. A scholar is included among the top collaborators of Heidi L. Schulz 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 L. Schulz. Heidi L. Schulz 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.
Moitinho‐Silva, Lucas, Hila Emmert, Hansjörg Baurecht, et al.. (2021). Host traits, lifestyle and environment are associated with human skin bacteria. British Journal of Dermatology. 185(3). 573–584. 15 indexed citations
2.
Brandl, Caroline, Heidi L. Schulz, Gabriele E. Lang, et al.. (2020). Mutation-Dependent Pathomechanisms Determine the Phenotype in the Bestrophinopathies. International Journal of Molecular Sciences. 21(5). 1597–1597. 20 indexed citations
3.
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
4.
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
5.
Brandl, Caroline, Heidi L. Schulz, Peter Charbel Issa, et al.. (2017). Mutations in the Genes for Interphotoreceptor Matrix Proteoglycans, IMPG1 and IMPG2, in Patients with Vitelliform Macular Lesions. Genes. 8(7). 170–170. 24 indexed citations
6.
Ried, Janina S., Hansjörg Baurecht, Ferdinand Stückler, et al.. (2013). Integrative genetic and metabolite profiling analysis suggests altered phosphatidylcholine metabolism in asthma. Allergy. 68(5). 629–636. 71 indexed citations
7.
Grzmil, Paweł, J Konietzko, Alicia Aguilar, et al.. (2009). Targeted Disruption of the Mouse <i>Npal3</i> Gene Leads to Deficits in Behavior, Increased IgE Levels, and Impaired Lung Function. Cytogenetic and Genome Research. 125(3). 186–200. 7 indexed citations
8.
Stöhr, Heidi, Julia Heisig, P. Benz, et al.. (2009). TMEM16B, A Novel Protein with Calcium-Dependent Chloride Channel Activity, Associates with a Presynaptic Protein Complex in Photoreceptor Terminals. Journal of Neuroscience. 29(21). 6809–6818. 183 indexed citations
9.
Schulz, Heidi L., et al.. (2004). Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization. Cytogenetic and Genome Research. 106(1). 74–81. 10 indexed citations
10.
Schulz, Heidi L., et al.. (2004). The Retinome – Defining a reference transcriptome of the adult mammalian retina/retinal pigment epithelium. BMC Genomics. 5(1). 50–50. 23 indexed citations
11.
Schulz, Heidi L.. (2003). Towards a comprehensive description of the human retinal transcriptome: identification and characterization of differentially expressed genes. Online Publication Service of Würzburg University (Würzburg University). 1 indexed citations
13.
Schulz, Heidi L., Heidi Stöhr, & Bernhard H. F. Weber. (2002). Characterization of three novel isoforms of the metabotrobic glutamate receptor 7 (GRM7). Neuroscience Letters. 326(1). 37–40. 25 indexed citations
14.
Mah, Nancy, et al.. (2001). Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 1522(3). 167–174. 20 indexed citations
15.
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
16.
Grosser, D., et al.. (1991). Histologische Untersuchungen über das Schutzholz einheimischer Laubbäume. European Journal of Wood and Wood Products. 49(2). 65–73. 13 indexed citations
17.
Grosser, D. & Heidi L. Schulz. (1985). Trabeculae (intrazelluläre Stabbildungen) als anatomische Anomalie im Stammholz erkrankter Nadelbäume. European Journal of Wood and Wood Products. 43(1). 32–32. 1 indexed citations
18.
Schulz, Heidi L., et al.. (1985). Ein ungewöhnlicher Spritzkern an Buche (Fagus sylvatica L.) und seine Auswirkung auf die Druckfestigkeit. European Journal of Wood and Wood Products. 43(8). 350–350. 6 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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