Linn Gieser

4.2k total citations
29 papers, 1.5k citations indexed

About

Linn Gieser is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Linn Gieser has authored 29 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 8 papers in Ophthalmology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Linn Gieser's work include Retinal Development and Disorders (21 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (6 papers). Linn Gieser is often cited by papers focused on Retinal Development and Disorders (21 papers), Retinal Diseases and Treatments (8 papers) and Photoreceptor and optogenetics research (6 papers). Linn Gieser collaborates with scholars based in United States, United Kingdom and Spain. Linn Gieser's co-authors include Anand Swaroop, Matthew J. Brooks, Koray Dogan Kaya, Ashley Walton, Norimoto Gotoh, Rinki Ratnapriya, Margaret R. Starostik, Tyler J. DiStefano, Nicole Y. Morgan and Christopher J. Panebianco and has published in prestigious journals such as Nature Genetics, Scientific Reports and Developmental Cell.

In The Last Decade

Linn Gieser

29 papers receiving 1.4k citations

Peers

Linn Gieser

OPHTH

CMN

GENET

Matthew J. Brooks United States

Sacha Reichman France

Alexander B. Quiambao United States

Claudio Punzo United States

Arpad Palfi Ireland

Christian P. Hamel France

Xitiz Chamling United States

Ani V. Das United States

Adrian M. Timmers United States

Vijender Chaitankar United States

Matthew J. Brooks United States

Linn Gieser

1.0k ×0.8

251 ×0.6

OPHTH

325 ×1.1

CMN

98 ×0.5

GENET

115 ×0.7

Citations per year, relative to Linn Gieser Linn Gieser (= 1×) peers Matthew J. Brooks

Countries citing papers authored by Linn Gieser

Since Specialization

Citations

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

Fields of papers citing papers by Linn Gieser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linn Gieser

This figure shows the co-authorship network connecting the top 25 collaborators of Linn Gieser. A scholar is included among the top collaborators of Linn Gieser 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 Linn Gieser. Linn Gieser 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

Batz, Zachary, Ryan A. Kelley, Linn Gieser, et al.. (2022). Nicotinamide Promotes Formation of Retinal Organoids From Human Pluripotent Stem Cells via Enhanced Neural Cell Fate Commitment. Frontiers in Cellular Neuroscience. 16. 878351–878351. 9 indexed citations

Kruczek, Kamil, James L. Gentry, Linn Gieser, et al.. (2021). Gene Therapy of Dominant CRX-Leber Congenital Amaurosis using Patient Stem Cell-Derived Retinal Organoids. Stem Cell Reports. 16(2). 252–263. 65 indexed citations

Gumerson, Jessica, Jacob Nellissery, Angel Aponte, et al.. (2020). Loss of endocytosis-associated RabGEF1 causes aberrant morphogenesis and altered autophagy in photoreceptors leading to retinal degeneration. PLoS Genetics. 16(12). e1009259–e1009259. 10 indexed citations

Corso‐Díaz, Ximena, James L. Gentry, Ryan J. Rebernick, et al.. (2020). Genome-wide Profiling Identifies DNA Methylation Signatures of Aging in Rod Photoreceptors Associated with Alterations in Energy Metabolism. Cell Reports. 31(3). 107525–107525. 29 indexed citations

Lukovic, Dunja, Ana Artero‐Castro, Koray Dogan Kaya, et al.. (2020). Retinal Organoids derived from hiPSCs of an AIPL1-LCA Patient Maintain Cytoarchitecture despite Reduced levels of Mutant AIPL1. Scientific Reports. 10(1). 5426–5426. 44 indexed citations

Ratnapriya, Rinki, Olukayode Sosina, Margaret R. Starostik, et al.. (2019). Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration. Nature Genetics. 51(4). 606–610. 175 indexed citations

Li, Yan, Amanda Ray, Todd Duncan, et al.. (2019). Aberrant RNA splicing is the major pathogenic effect in a knock‐in mouse model of the dominantly inherited c.1430A>G humanRPE65mutation. Human Mutation. 40(4). 426–443. 19 indexed citations

Hoshino, Akina, Rinki Ratnapriya, Matthew J. Brooks, et al.. (2017). Molecular Anatomy of the Developing Human Retina. Developmental Cell. 43(6). 763–779.e4. 169 indexed citations

DiStefano, Tyler J., Christopher J. Panebianco, Koray Dogan Kaya, et al.. (2017). Accelerated and Improved Differentiation of Retinal Organoids from Pluripotent Stem Cells in Rotating-Wall Vessel Bioreactors. Stem Cell Reports. 10(1). 300–313. 150 indexed citations

10.

Hamon, Annaïg, Christel Masson, Juliette Bitard, et al.. (2017). Retinal Degeneration Triggers the Activation of YAP/TEAD in Reactive Müller Cells. Investigative Ophthalmology & Visual Science. 58(4). 1941–1941. 38 indexed citations

11.

Chen, Yuanyuan, Matthew J. Brooks, Linn Gieser, Anand Swaroop, & Krzysztof Palczewski. (2016). Transcriptome profiling of NIH3T3 cell lines expressing opsin and the P23H opsin mutant identifies candidate drugs for the treatment of retinitis pigmentosa. Pharmacological Research. 115. 1–13. 8 indexed citations

12.

Kim, Jung-Woong, Hyun‐Jin Yang, Matthew J. Brooks, et al.. (2016). NRL-Regulated Transcriptome Dynamics of Developing Rod Photoreceptors. Cell Reports. 17(9). 2460–2473. 91 indexed citations

13.

Ma, Wenxin, Radu Cojocaru, Norimoto Gotoh, et al.. (2013). Gene expression changes in aging retinal microglia: relationship to microglial support functions and regulation of activation. Neurobiology of Aging. 34(10). 2310–2321. 81 indexed citations

14.

Kim, Douglas S., Bernward Klocke, Kory R. Johnson, et al.. (2012). Transcriptional Regulation of Rod Photoreceptor Homeostasis Revealed by In Vivo NRL Targetome Analysis. PLoS Genetics. 8(4). e1002649–e1002649. 92 indexed citations

15.

Dorris, David, Allen Nguyen, Linn Gieser, et al.. (2003). Oligodeoxyribonucleotide probe accessibility on a three-dimensional DNA microarray surface and the effect of hybridization time on the accuracy of expression ratios. BMC Biotechnology. 3(1). 6–6. 46 indexed citations

16.

Mears, Alan J., Suja Hiriyanna, R. Vervoort, et al.. (2000). Remapping of the RP15 Locus for X-Linked Cone-Rod Degeneration to Xp11.4-p21.1, and Identification of a De Novo Insertion in the RPGR Exon ORF15. The American Journal of Human Genetics. 67(4). 1000–1003. 55 indexed citations

17.

Gieser, Linn, Ricardo Fujita, Harald H.H. Göring, et al.. (1998). A Novel Locus (RP24) for X-linked Retinitis Pigmentosa Maps to Xq26-27. The American Journal of Human Genetics. 63(5). 1439–1447. 59 indexed citations

18.

Fujita, Ricardo, Monika Buraczyńska, Linn Gieser, et al.. (1997). Analysis of the RPGRGene in 11 Pedigrees with the Retinitis Pigmentosa Type 3 Genotype: Paucity of Mutations in the Coding Region but Splice Defects in Two Families. The American Journal of Human Genetics. 61(3). 571–580. 53 indexed citations

19.

Agarwal, Neeraj, Anand Swaroop, Jui‐Der Liou, et al.. (1995). Expression and chromosomal localization of cDNA clones from an enriched human retinal pigment epithelial (RPE) cell line library: identification of two RPE-specific genes. Cytogenetic and Genome Research. 69(1-2). 71–74. 12 indexed citations

20.

Gieser, Linn & Anand Swaroop. (1992). Expressed sequence tags and chromosomal localization of cDNA clones from a subtracted retinal pigment epithelium library. Genomics. 13(3). 873–876. 51 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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