Janis Lem

5.1k total citations
50 papers, 4.1k citations indexed

About

Janis Lem is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Janis Lem has authored 50 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 30 papers in Cellular and Molecular Neuroscience and 8 papers in Ophthalmology. Recurrent topics in Janis Lem's work include Retinal Development and Disorders (41 papers), Photoreceptor and optogenetics research (26 papers) and Receptor Mechanisms and Signaling (13 papers). Janis Lem is often cited by papers focused on Retinal Development and Disorders (41 papers), Photoreceptor and optogenetics research (26 papers) and Receptor Mechanisms and Signaling (13 papers). Janis Lem collaborates with scholars based in United States, Switzerland and Italy. Janis Lem's co-authors include Clint L. Makino, Melvin I. Simon, Nataliia V. Krasnoperova, Edward N. Pugh, Peter D. Calvert, Béla Kosaras, Massimo Nicolò, Richard L. Sidman, Sergei Nikonov and Р. В. Холоденко and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Janis Lem

48 papers receiving 4.1k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Janis Lem 3.6k 2.1k 814 348 309 50 4.1k
Marie E. Burns 4.2k 1.2× 2.9k 1.4× 794 1.0× 819 2.4× 255 0.8× 91 5.6k
Clint L. Makino 2.9k 0.8× 2.1k 1.0× 459 0.6× 397 1.1× 211 0.7× 61 3.2k
Vladimir J. Kefalov 2.8k 0.8× 1.6k 0.8× 935 1.1× 288 0.8× 238 0.8× 116 3.3k
Maureen A. McCall 2.8k 0.8× 2.3k 1.1× 599 0.7× 236 0.7× 348 1.1× 99 3.7k
Wallace B. Thoreson 4.1k 1.1× 3.3k 1.5× 349 0.4× 743 2.1× 156 0.5× 141 5.0k
Ronald A. Bush 4.7k 1.3× 2.0k 1.0× 1.8k 2.2× 495 1.4× 249 0.8× 76 5.4k
Alexander M. Dizhoor 5.3k 1.5× 3.5k 1.6× 1.6k 2.0× 758 2.2× 132 0.4× 90 5.9k
Debora B. Farber 6.8k 1.9× 2.9k 1.4× 1.9k 2.3× 655 1.9× 311 1.0× 207 7.8k
Silke Haverkamp 4.9k 1.4× 4.2k 2.0× 542 0.7× 600 1.7× 283 0.9× 97 5.7k
Steven Nusinowitz 4.1k 1.1× 1.3k 0.6× 2.2k 2.7× 393 1.1× 220 0.7× 99 5.2k

Countries citing papers authored by Janis Lem

Since Specialization
Citations

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

Fields of papers citing papers by Janis Lem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janis Lem

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

All Works

20 of 20 papers shown
1.
Cowan, Cameron S., Muhammad M. Abd‐El‐Barr, Meike E. van der Heijden, et al.. (2016). Connexin 36 and rod bipolar cell independent rod pathways drive retinal ganglion cells and optokinetic reflexes. Vision Research. 119. 99–109. 26 indexed citations
2.
Richey, Lauren, et al.. (2012). CCN5 Expression in mammals. III. Early embryonic mouse development. Journal of Cell Communication and Signaling. 6(4). 217–223. 10 indexed citations
3.
Makino, Clint L., Xiaohong Wen, Norman Michaud, et al.. (2012). Rhodopsin Expression Level Affects Rod Outer Segment Morphology and Photoresponse Kinetics. PLoS ONE. 7(5). e37832–e37832. 42 indexed citations
4.
Pang, Ji‐Jie, Fan Gao, Janis Lem, et al.. (2009). Direct rod input to cone BCs and direct cone input to rod BCs challenge the traditional view of mammalian BC circuitry. Proceedings of the National Academy of Sciences. 107(1). 395–400. 67 indexed citations
5.
Lem, Janis, et al.. (2009). Chapter 1 Rhodopsin‐Mediated Retinitis Pigmentosa. Progress in molecular biology and translational science. 88. 1–31. 37 indexed citations
6.
Abd‐El‐Barr, Muhammad M., Mark E. Pennesi, Shannon Saszik, et al.. (2009). Genetic Dissection of Rod and Cone Pathways in the Dark-Adapted Mouse Retina. Journal of Neurophysiology. 102(3). 1945–1955. 77 indexed citations
7.
Wen, Xiaohong, Lixin Shen, Richard S. Brush, et al.. (2009). Overexpression of Rhodopsin Alters the Structure and Photoresponse of Rod Photoreceptors. Biophysical Journal. 96(3). 939–950. 70 indexed citations
8.
Rajala, Ammaji, Robert E. Anderson, Jian‐xing Ma, et al.. (2007). G-protein-coupled Receptor Rhodopsin Regulates the Phosphorylation of Retinal Insulin Receptor. Journal of Biological Chemistry. 282(13). 9865–9873. 36 indexed citations
9.
Rosenzweig, Derek H., K. Saidas Nair, Junhua Wei, et al.. (2007). Subunit Dissociation and Diffusion Determine the Subcellular Localization of Rod and Cone Transducins. Journal of Neuroscience. 27(20). 5484–5494. 55 indexed citations
10.
Bemelmans, Alexis‐Pierre, Corinne Kostic, Muriel Jaquet, et al.. (2006). Lentiviral Vectors Containing a Retinal Pigment Epithelium Specific Promoter for Leber Congenital Amaurosis Gene Therapy. Advances in experimental medicine and biology. 572. 247–253. 8 indexed citations
11.
Bemelmans, Alexis‐Pierre, Corinne Kostic, Sylvain V. Crippa, et al.. (2006). Lentiviral Gene Transfer of Rpe65 Rescues Survival and Function of Cones in a Mouse Model of Leber Congenital Amaurosis. PLoS Medicine. 3(10). e347–e347. 100 indexed citations
12.
Ko, Tony H., Vivek J. Srinivasan, Mariana T. Carvalho, et al.. (2005). Three Dimensional Retinal Imaging of Small Animals With High–speed, Ultrahigh Resolution Optical Coherence Tomography. Investigative Ophthalmology & Visual Science. 46(13). 1051–1051.
13.
He, Wei, Keiko Yasumatsu, Ayako Yamada, et al.. (2004). UmamiTaste Responses Are Mediated by α-Transducin and α-Gustducin. Journal of Neuroscience. 24(35). 7674–7680. 126 indexed citations
14.
Naash, Muna I., Dibyendu Chakraborty, Steven J. Fliesler, et al.. (2004). Retinal abnormalities associated with the G90D mutation in opsin. The Journal of Comparative Neurology. 478(2). 149–163. 30 indexed citations
15.
Woodruff, Michael L., et al.. (2003). Spontaneous activity of opsin apoprotein is a cause of Leber congenital amaurosis. Nature Genetics. 35(2). 158–164. 159 indexed citations
16.
Lyubarsky, Arkady, et al.. (2002). Functionally rodless mice: transgenic models for the investigation of cone function in retinal disease and therapy. Vision Research. 42(4). 401–415. 52 indexed citations
17.
Hao, Wenshan, Andreas Wenzel, Martin S. Obin, et al.. (2002). Evidence for two apoptotic pathways in light-induced retinal degeneration. Nature Genetics. 32(2). 254–260. 212 indexed citations
18.
Calvert, Peter D., V. I. Govardovskii, Nataliia V. Krasnoperova, et al.. (2001). Membrane protein diffusion sets the speed of rod phototransduction. Nature. 411(6833). 90–94. 153 indexed citations
19.
Méndez, Ana, Marie E. Burns, Janis Lem, et al.. (2000). Rapid and Reproducible Deactivation of Rhodopsin Requires Multiple Phosphorylation Sites. Neuron. 28(1). 153–164. 221 indexed citations
20.
Lem, Janis, Meredithe Applebury, Jeffrey Falk, John G. Flannery, & Melvin I. Simon. (1991). Tissue-specific and developmental regulation of rod opsin chimeric genes in transgenic mice. Neuron. 6(2). 201–210. 150 indexed citations

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