Melanie M. Sohocki

1.4k total citations
18 papers, 1.1k citations indexed

About

Melanie M. Sohocki is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Melanie M. Sohocki has authored 18 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 11 papers in Ophthalmology and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Melanie M. Sohocki's work include Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (10 papers) and Glaucoma and retinal disorders (5 papers). Melanie M. Sohocki is often cited by papers focused on Retinal Development and Disorders (13 papers), Retinal Diseases and Treatments (10 papers) and Glaucoma and retinal disorders (5 papers). Melanie M. Sohocki collaborates with scholars based in United States, United Kingdom and Canada. Melanie M. Sohocki's co-authors include Stephen P. Daiger, David G. Birch, Lori S. Sullivan, John R. Heckenlively, Helen A. Mintz-Hittner, Sara J. Bowne, Carol L. Freund, Roderick R. McInnes, Annette Payne and Wilbur R. Harrison and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and The American Journal of Human Genetics.

In The Last Decade

Melanie M. Sohocki

16 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Melanie M. Sohocki United States 14 1.0k 501 267 177 160 18 1.1k
Dominique Ducroq France 17 1.2k 1.1× 756 1.5× 182 0.7× 246 1.4× 161 1.0× 20 1.3k
Christian Hamel France 9 851 0.8× 461 0.9× 283 1.1× 123 0.7× 108 0.7× 14 972
Mai M. Abd El-Aziz Egypt 12 751 0.7× 355 0.7× 198 0.7× 171 1.0× 144 0.9× 18 950
Sassan M. Azarian United States 10 1.1k 1.1× 575 1.1× 237 0.9× 102 0.6× 206 1.3× 16 1.3k
Nancy Ransom United States 12 942 0.9× 451 0.9× 241 0.9× 253 1.4× 289 1.8× 15 1.3k
Shirley He United States 11 995 1.0× 548 1.1× 173 0.6× 376 2.1× 154 1.0× 14 1.3k
Britta Baumann Germany 16 936 0.9× 429 0.9× 146 0.5× 123 0.7× 156 1.0× 23 1.0k
Nele Schwarz United Kingdom 12 840 0.8× 174 0.3× 250 0.9× 211 1.2× 176 1.1× 14 931
Lina Zelinger Israel 15 653 0.6× 246 0.5× 135 0.5× 183 1.0× 109 0.7× 19 733
Mònica Aguilà United Kingdom 13 911 0.9× 238 0.5× 367 1.4× 89 0.5× 205 1.3× 20 1.0k

Countries citing papers authored by Melanie M. Sohocki

Since Specialization
Citations

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

Fields of papers citing papers by Melanie M. Sohocki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Melanie M. Sohocki

This figure shows the co-authorship network connecting the top 25 collaborators of Melanie M. Sohocki. A scholar is included among the top collaborators of Melanie M. Sohocki 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 Melanie M. Sohocki. Melanie M. Sohocki 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.
Sohocki, Melanie M., Stacy L. Donovan, J. Zhang, et al.. (2005). Characterization of Retinal Development in Aipl1 Deficient Mice. 46(13). 3182–3182.
2.
Sohocki, Melanie M., et al.. (2004). Pinealocyte expression of retinopathy genes: a role in circadian rhythm abnormalities?. Investigative Ophthalmology & Visual Science. 45(13). 5284–5284. 1 indexed citations
3.
Wilkie, Susan E., Evelyne Deery, R. Newbold, et al.. (2004). Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1690(2). 141–149. 6 indexed citations
4.
Kanaya, Kōichi, Melanie M. Sohocki, & Tetsu Kamitani. (2004). Abolished interaction of NUB1 with mutant AIPL1 involved in Leber congenital amaurosis. Biochemical and Biophysical Research Communications. 317(3). 768–773. 14 indexed citations
5.
Dyer, Michael A., Stacy L. Donovan, Jiakun Zhang, et al.. (2004). Retinal degeneration in Aipl1-deficient mice: a new genetic model of Leber congenital amaurosis. Molecular Brain Research. 132(2). 208–220. 36 indexed citations
6.
Akey, Dayna T., Xuemei Zhu, Michael A. Dyer, et al.. (2003). Functional Studies of AIPL1. Advances in experimental medicine and biology. 533. 287–295.
7.
Lith-Verhoeven, Janneke J.C. van, et al.. (2002). Clinical characterization, linkage analysis, and PRPC8 mutation analysis of a family with autosomal dominant retinitis pigmentosa type 13 (RP13). Ophthalmic Genetics. 23(1). 1–12. 25 indexed citations
8.
Damji, Karim F., Melanie M. Sohocki, Sanjoy K. Gupta, et al.. (2001). Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. Canadian Journal of Ophthalmology. 36(5). 252–259. 30 indexed citations
9.
Sohocki, Melanie M., et al.. (2001). Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans. Mammalian Genome. 12(7). 566–568. 14 indexed citations
10.
Tzekov, Radouil, Yuhui Liu, Melanie M. Sohocki, et al.. (2001). Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene.. PubMed. 42(6). 1319–27. 31 indexed citations
11.
Sohocki, Melanie M., Isabelle Perrault, Bart P. Leroy, et al.. (2000). Prevalence of AIPL1 Mutations in Inherited Retinal Degenerative Disease. Molecular Genetics and Metabolism. 70(2). 142–150. 129 indexed citations
12.
Sohocki, Melanie M., Stephen P. Daiger, Sara J. Bowne, et al.. (2000). Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Human Mutation. 17(1). 42–51. 265 indexed citations
13.
Sohocki, Melanie M., Sara J. Bowne, Lori S. Sullivan, et al.. (2000). Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. Nature Genetics. 24(1). 79–83. 229 indexed citations
14.
Tzekov, Radouil, Melanie M. Sohocki, Stephen P. Daiger, & David G. Birch. (2000). Visual phenotype in patients with Arg41Gln and Ala196+1bp mutations in the CRX gene. Ophthalmic Genetics. 21(2). 89–99. 21 indexed citations
15.
Sohocki, Melanie M., et al.. (1999). Localization of Retina/Pineal-Expressed Sequences: Identification of Novel Candidate Genes for Inherited Retinal Disorders. Genomics. 58(1). 29–33. 23 indexed citations
16.
Sohocki, Melanie M., et al.. (1999). Identifying and mapping novel retinal-expressed ESTs from humans.. PubMed. 5. 5–5. 19 indexed citations
17.
Sohocki, Melanie M., Lori S. Sullivan, Helen A. Mintz-Hittner, et al.. (1998). A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene. The American Journal of Human Genetics. 63(5). 1307–1315. 220 indexed citations
18.
Sohocki, Melanie M., Lori S. Sullivan, Wilbur R. Harrison, et al.. (1997). Human Glutamate Pyruvate Transaminase (GPT): Localization to 8q24.3, cDNA and Genomic Sequences, and Polymorphic Sites. Genomics. 40(2). 247–252. 44 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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