Ivan Prokudin

401 citations

6 papers · 191 indexed · h-index 5

Co-authors: Maree Flaherty Robyn V. Jamieson John Grigg James E. Smith Bruce Bennetts Alan Ma Clare L. Fraser Frank Martin
Topics: Connexins and lens biology (3 papers)Ocular Disorders and Treatments (3 papers)Intraocular Surgery and Lenses (3 papers)
Cited by: Ophthalmology Genetics Molecular Biology
Journals: PROTEOMICS Human Mutation European Journal of Human Genetics
Partner nations: Australia China United States

In The Last Decade

Ivan Prokudin

6 papers receiving 190 citations

Peers

Countries citing papers authored by Ivan Prokudin

Since Specialization

Citations

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

Fields of papers citing papers by Ivan Prokudin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivan Prokudin

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

All Works

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6 of 6 papers shown

#	Work	Indexed citations
1	New mutations in GJA8 expand the phenotype to include total sclerocornea 2017 ·Clinical Genetics ·(unknown),John Grigg,Ivan Prokudin,Maree Flaherty,Bruce Bennetts,Robyn V. Jamieson	13
2	Sporadic and Familial Congenital Cataracts: Mutational Spectrum and New Diagnoses Using Next‐Generation Sequencing 2015 ·Human Mutation ·Alan Ma,John Grigg,Gladys Ho,Ivan Prokudin,Elizabeth Farnsworth,Katherine Holman,(unknown),Frank A. Billson,Frank Martin,Clare L. Fraser,David Mowat,James E. Smith,John Christodoulou,Maree Flaherty,Bruce Bennetts,Robyn V. Jamieson	103
3	Advantage of Whole Exome Sequencing over Allele-Specific and Targeted Segment Sequencing in Detection of NovelTULP1Mutation in Leber Congenital Amaurosis 2014 ·Ophthalmic Genetics ·Yiran Guo,Ivan Prokudin,Cong Yu,Jinlong Liang,Yi Xie,Maree Flaherty,Lifeng Tian,Stephanie Crofts,Fengxiang Wang,James W. Snyder,Craig Donaldson,Nada Abdelmagid,Lyam Vazquez,Brendan J. Keating,Håkon Håkonarson,Jun Wang,Robyn V. Jamieson	12
4	Value of whole exome sequencing for syndromic retinal dystrophy diagnosis in young patients 2014 ·Clinical and Experimental Ophthalmology ·Ivan Prokudin,Dong Li,(unknown),Yiran Guo,Linda Goodwin,Meredith Wilson,(unknown),Lifeng Tian,Yulan Chen,Jinlong Liang,Brendan J. Keating,Xun Xu,Robyn V. Jamieson,Håkon Håkonarson	7
5	Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1 2013 ·European Journal of Human Genetics ·Ivan Prokudin,Cas Simons,John Grigg,(unknown),Vikrant Kumar,(unknown),James E. Smith,Maree Flaherty,Sonia Dávila,Robyn V. Jamieson	52
6	Comprehensive proteomic and transcriptomic characterization of hepatic expression signatures affected in p14 liver conditional knockout mice 2010 ·PROTEOMICS ·Ivan Prokudin,Taras Stasyk,Johannes Rainer,Guenther K. Bonn,Reinhard Kofler,Lukas A. Huber	4

About Ivan Prokudin

Ivan Prokudin is a scholar working on Ophthalmology, Genetics and Molecular Biology, having authored 6 papers that have together received 191 indexed citations. Recurring topics across this work include Connexins and lens biology (3 papers), Ocular Disorders and Treatments (3 papers) and Intraocular Surgery and Lenses (3 papers). The work is most often cited by research in Ophthalmology (88 citations), Genetics (103 citations) and Molecular Biology (145 citations). Ivan Prokudin has collaborated with scholars based in Australia, China and United States. Frequent co-authors include Maree Flaherty, Robyn V. Jamieson, John Grigg, James E. Smith, Bruce Bennetts, Alan Ma, Clare L. Fraser, Frank Martin, Elizabeth Farnsworth and Katherine Holman. Their work appears in journals such as PROTEOMICS, Human Mutation and European Journal of Human Genetics.

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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