D.J. Sidjanin

1.1k total citations
35 papers, 724 citations indexed

About

D.J. Sidjanin is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, D.J. Sidjanin has authored 35 papers receiving a total of 724 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 9 papers in Genetics and 8 papers in Cell Biology. Recurrent topics in D.J. Sidjanin's work include Connexins and lens biology (13 papers), Retinal Development and Disorders (5 papers) and Ubiquitin and proteasome pathways (3 papers). D.J. Sidjanin is often cited by papers focused on Connexins and lens biology (13 papers), Retinal Development and Disorders (5 papers) and Ubiquitin and proteasome pathways (3 papers). D.J. Sidjanin collaborates with scholars based in United States, Australia and Germany. D.J. Sidjanin's co-authors include Dwight Stambolian, Bo Chang, Joseph A. Toonen, William T. Jackson, Richard R. Dubielzig, Seymour Zigman, John R. Reddan, Martin Rosenberg, Gregory M. Acland and Derk J. Bergsma and has published in prestigious journals such as Nature Genetics, PLoS ONE and Journal of Virology.

In The Last Decade

D.J. Sidjanin

35 papers receiving 702 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
D.J. Sidjanin United States 14 514 197 119 105 67 35 724
Alka Chaubey United States 15 371 0.7× 218 1.1× 44 0.4× 69 0.7× 46 0.7× 49 782
James R. Lupski United States 7 653 1.3× 330 1.7× 265 2.2× 81 0.8× 35 0.5× 11 875
Sílvia Albert United States 16 614 1.2× 99 0.5× 143 1.2× 80 0.8× 47 0.7× 58 889
Chunqiao Liu China 17 554 1.1× 279 1.4× 70 0.6× 112 1.1× 32 0.5× 41 820
Nallathambi Jeyabalan India 18 355 0.7× 172 0.9× 238 2.0× 82 0.8× 137 2.0× 31 841
Jayeeta Roychoudhury United States 11 494 1.0× 64 0.3× 313 2.6× 69 0.7× 88 1.3× 12 907
Yasushi Isashiki Japan 17 474 0.9× 89 0.5× 271 2.3× 33 0.3× 68 1.0× 48 933
Jacob Nellissery United States 14 518 1.0× 83 0.4× 170 1.4× 52 0.5× 144 2.1× 25 657
Kerry B. Gunning United States 6 420 0.8× 213 1.1× 27 0.2× 54 0.5× 49 0.7× 7 652
Kei Adachi Japan 16 586 1.1× 312 1.6× 116 1.0× 27 0.3× 52 0.8× 36 942

Countries citing papers authored by D.J. Sidjanin

Since Specialization
Citations

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

Fields of papers citing papers by D.J. Sidjanin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D.J. Sidjanin. 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 D.J. Sidjanin. The network helps show where D.J. Sidjanin may publish in the future.

Co-authorship network of co-authors of D.J. Sidjanin

This figure shows the co-authorship network connecting the top 25 collaborators of D.J. Sidjanin. A scholar is included among the top collaborators of D.J. Sidjanin 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 D.J. Sidjanin. D.J. Sidjanin 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.
Toonen, Joseph A., et al.. (2016). A Disintegrin and Metalloproteinase10 (ADAM10) Regulates NOTCH Signaling during Early Retinal Development. PLoS ONE. 11(5). e0156184–e0156184. 15 indexed citations
2.
Ebert, Allison D., et al.. (2014). Targeted disruption of Tbc1d20with zinc-finger nucleases causes cataracts and testicular abnormalities in mice. BMC Genetics. 15(1). 135–135. 19 indexed citations
3.
Sidjanin, D.J., et al.. (2014). Alkylglycerone phosphate synthase (AGPS) deficient mice: Models for rhizomelic chondrodysplasia punctata type 3 (RCDP3) malformation syndrome. Molecular Genetics and Metabolism Reports. 1. 299–311. 21 indexed citations
4.
Toonen, Joseph A. & D.J. Sidjanin. (2013). The role of ADAM10 in retinal development. Investigative Ophthalmology & Visual Science. 54(15). 5151–5151. 1 indexed citations
5.
Sidjanin, D.J., et al.. (2013). Functional Analysis ofHSF4Mutations Found in Patients With Autosomal Recessive Congenital Cataracts. Investigative Ophthalmology & Visual Science. 54(10). 6646–6646. 13 indexed citations
6.
Toonen, Joseph A., Lina Liang, & D.J. Sidjanin. (2012). Waved with open eyelids 2 (woe2) is a novel spontaneous mouse mutation in the protein phosphatase 1, regulatory (inhibitor) subunit 13 like (Ppp1r13l)gene. BMC Genetics. 13(1). 76–76. 15 indexed citations
7.
Chang, Bo, et al.. (2011). A spontaneous mutation in Srebf2 leads to cataracts and persistent skin wounds in the lens opacity 13 (lop13) mouse. Mammalian Genome. 22(11-12). 661–673. 10 indexed citations
8.
Chang, Bo, et al.. (2011). Blind sterile 2 (bs2), a hypomorphic mutation in Agps, results in cataracts and male sterility in mice. Molecular Genetics and Metabolism. 103(1). 51–59. 35 indexed citations
9.
Kim, Judy E., et al.. (2009). Genetic and clinical evaluation of juvenile retinoschisis. Journal of American Association for Pediatric Ophthalmology and Strabismus. 13(2). 215–217. 4 indexed citations
10.
Iannaccone, Alessandro, et al.. (2007). Identification of two novel mutations in families with X-linked ocular albinism.. PubMed. 13. 1856–61. 3 indexed citations
11.
Goldstein, Orly, Barbara Zangerl, Sue Pearce‐Kelling, et al.. (2006). Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod–cone degeneration interval and identifies ancestral disease-transmitting chromosome. Genomics. 88(5). 541–550. 57 indexed citations
12.
Talamas, Elijah J., et al.. (2005). Mapping of the Mouse Lens Opacity Locus 11 (lop11). Investigative Ophthalmology & Visual Science. 46(13). 823–823. 1 indexed citations
13.
Sidjanin, D.J., John L. McElwee, Barbara Miller, & Gustavo D. Aguirre. (2005). Cloning of canine galactokinase (GALK1) and evaluation as a candidate gene for hereditary cataracts in Labrador retrievers. Animal Genetics. 36(3). 265–266. 3 indexed citations
14.
Goldstein, Orly, et al.. (2004). A Linkage Disequilibrium Map of the Progressive Rod Cone Degeneration Interval. Investigative Ophthalmology & Visual Science. 45(13). 4756–4756. 1 indexed citations
15.
16.
Sidjanin, D.J.. (2002). Canine CNGB3 mutations establish cone degeneration as orthologous to the human achromatopsia locus ACHM3. Human Molecular Genetics. 11(16). 1823–1833. 146 indexed citations
17.
Grimes, P, Jack Favor, Brigitte Koeberlein, et al.. (1997). Genetic mapping of a mouse ocular malformation locus, tcm, to chromosome 4. Mammalian Genome. 8(3). 178–181. 17 indexed citations
18.
Sidjanin, D.J., David J. Grdina, & Gayle E. Woloschak. (1996). UV‐Induced Changes in Cell Cycle and Gene Expression within Rabbit Lens Epithelial Cells. Photochemistry and Photobiology. 63(1). 79–85. 11 indexed citations
19.
Stambolian, Dwight, Yunjun Ai, D.J. Sidjanin, et al.. (1995). Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts. Nature Genetics. 10(3). 307–312. 72 indexed citations
20.
Sidjanin, D.J., Seymour Zigman, & John R. Reddan. (1993). DNA damage and repair in rabbit lens epithelial cells following UVA radiation. Current Eye Research. 12(9). 773–781. 33 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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