Luan M. Streb

3.2k total citations
23 papers, 2.1k citations indexed

About

Luan M. Streb is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Luan M. Streb has authored 23 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Ophthalmology and 4 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Luan M. Streb's work include Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (8 papers) and Retinoids in leukemia and cellular processes (3 papers). Luan M. Streb is often cited by papers focused on Retinal Development and Disorders (10 papers), Retinal Diseases and Treatments (8 papers) and Retinoids in leukemia and cellular processes (3 papers). Luan M. Streb collaborates with scholars based in United States, Canada and Israel. Luan M. Streb's co-authors include Edwin M. Stone, Val C. Sheffield, Brian E. Nichols, Robert F. Mullins, Arlene V. Drack, Terry A. Braun, Wallace L.M. Alward, A. Tim Johnson, Budd A. Tucker and Alan Kimura and has published in prestigious journals such as Nature Genetics, IEEE Transactions on Industrial Electronics and Ophthalmology.

In The Last Decade

Luan M. Streb

21 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Luan M. Streb United States	14	1.5k	1.0k	472	429	245	23	2.1k
Bernhard Jurklies Germany	21	1.8k 1.1×	1.6k 1.6×	243 0.5×	608 1.4×	253 1.0×	49	2.6k
Isabelle Perrault France	30	2.7k 1.7×	1.5k 1.5×	628 1.3×	329 0.8×	452 1.8×	71	3.0k
Christian P. Hamel France	26	2.0k 1.3×	933 0.9×	273 0.6×	269 0.6×	366 1.5×	71	2.4k
Panagiotis I. Sergouniotis United Kingdom	30	1.8k 1.2×	1.1k 1.1×	579 1.2×	325 0.8×	279 1.1×	83	2.3k
Arne Nystuen United States	19	1.4k 0.9×	1.2k 1.1×	215 0.5×	324 0.8×	275 1.1×	28	2.3k
Pete Humphries Ireland	26	1.3k 0.8×	553 0.5×	249 0.5×	241 0.6×	428 1.7×	55	1.7k
Mary J. van Schooneveld Netherlands	27	1.9k 1.2×	1.3k 1.3×	347 0.7×	453 1.1×	282 1.2×	69	2.4k
Nicole Weisschuh Germany	27	1.3k 0.9×	964 0.9×	377 0.8×	270 0.6×	124 0.5×	73	1.8k
John Neidhardt Germany	29	2.1k 1.4×	677 0.7×	572 1.2×	163 0.4×	592 2.4×	63	2.4k
Alice E. Davidson United Kingdom	26	1.3k 0.8×	987 1.0×	288 0.6×	741 1.7×	187 0.8×	54	2.0k

Countries citing papers authored by Luan M. Streb

Since Specialization

Citations

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

Fields of papers citing papers by Luan M. Streb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Luan M. Streb. 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 Luan M. Streb. The network helps show where Luan M. Streb may publish in the future.

Co-authorship network of co-authors of Luan M. Streb

This figure shows the co-authorship network connecting the top 25 collaborators of Luan M. Streb. A scholar is included among the top collaborators of Luan M. Streb 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 Luan M. Streb. Luan M. Streb 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

Stone, Edwin M., Jeaneen L. Andorf, S. Scott Whitmore, et al.. (2017). Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease. Ophthalmology. 124(9). 1314–1331. 299 indexed citations

Tucker, Budd A., Cathryn M. Cranston, Luan M. Streb, et al.. (2015). Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trial. Translational research. 166(6). 740–749.e1. 24 indexed citations

Small, Kent W., Adam P. DeLuca, S. Scott Whitmore, et al.. (2015). North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13. Ophthalmology. 123(1). 9–18. 71 indexed citations

Tucker, Budd A., Robert F. Mullins, Luan M. Streb, et al.. (2013). Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa. eLife. 2. e00824–e00824. 157 indexed citations

Mullins, Robert F., et al.. (2011). Elevated membrane attack complex in human choroid with high risk complement factor H genotypes. Experimental Eye Research. 93(4). 565–567. 104 indexed citations

Tucker, Budd A., Edwin M. Stone, Luan M. Streb, et al.. (2011). Use Of A Synthetic Xeno-Free Culture Substrate For iPSC Induction And Retinal Differentiation. 52(14). 2223–2223.

Fishman, Gerald A., et al.. (2007). DE NOVO MUTATION IN A CHOROIDEREMIA CARRIER. Retinal Cases & Brief Reports. 1(3). 182–184. 3 indexed citations

Allen, Richard C., et al.. (2005). Phenotypic heterogeneity associated with a novel mutation (Gly112Glu) in the Norrie disease protein. Eye. 20(2). 234–241. 19 indexed citations

Fingert, John H., et al.. (2003). Linkage of a Large Pattern Dystrophy Pedigree to Chromosome 6p21. Investigative Ophthalmology & Visual Science. 44(13). 1497–1497. 1 indexed citations

10.

Mykytyn, Kirk, Darryl Nishimura, Charles Searby, et al.. (2002). Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome. Nature Genetics. 31(4). 435–438. 258 indexed citations

11.

Chung, Mina, Kean T. Oh, Luan M. Streb, Alan Kimura, & Edwin M. Stone. (2001). VISUAL OUTCOME FOLLOWING SUBRETINAL HEMORRHAGE IN BEST DISEASE. Retina. 21(6). 575–580. 32 indexed citations

12.

Haider, Neena B., Samuel G. Jacobson, Artur V. Cideciyan, et al.. (2000). Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate. Nature Genetics. 24(2). 127–131. 374 indexed citations

13.

Héon, Elise, Francis L. Munier, Scott R. Sneed, et al.. (1998). Linkage of Autosomal Dominant Radial Drusen (Malattia Leventinese) to Chromosome p 16–21. Retina. 18(2). 191–191. 3 indexed citations

14.

Héon, Elise, Bhavna P. Sheth, Jeffrey W. Kalenak, et al.. (1995). Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). Human Molecular Genetics. 4(8). 1435–1439. 50 indexed citations

15.

Héon, Elise, Bhavna P. Sheth, Jeffrey W. Kalenak, et al.. (1995). 3127 Linkage of autosomal dominant iris hypoplasia to the rieger syndrome locus (4q25). Vision Research. 35. S122–S122. 4 indexed citations

16.

Stone, Edwin M., William D. Mathers, George O. D. Rosenwasser, et al.. (1994). Three autosomal dominant corneal dystrophies map to chromosome 5q. Nature Genetics. 6(1). 47–51. 115 indexed citations

17.

Sheffield, Val C., Edwin M. Stone, Wallace L.M. Alward, et al.. (1993). Genetic linkage of familial open angle glaucoma to chromosome 1q21–q31. Nature Genetics. 4(1). 47–50. 340 indexed citations

18.

Stone, Edwin M., Brian E. Nichols, Luan M. Streb, Alan Kimura, & Val C. Sheffield. (1992). Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nature Genetics. 1(4). 246–250. 169 indexed citations

19.

Stone, Edwin M., Alan Kimura, James C. Folk, et al.. (1992). Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13. Human Molecular Genetics. 1(9). 685–689. 54 indexed citations

20.

Streb, Luan M., et al.. (1992). Board-level boundary scan: regaining observability with an additional IC. IEEE Transactions on Computer-Aided Design of Integrated Circuits and Systems. 11(1). 68–75. 1 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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