Mark Consugar

4.0k total citations
26 papers, 2.1k citations indexed

About

Mark Consugar is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Mark Consugar has authored 26 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, 14 papers in Genetics and 4 papers in Ophthalmology. Recurrent topics in Mark Consugar's work include Genetic and Kidney Cyst Diseases (12 papers), Renal and related cancers (10 papers) and Genetic Syndromes and Imprinting (6 papers). Mark Consugar is often cited by papers focused on Genetic and Kidney Cyst Diseases (12 papers), Renal and related cancers (10 papers) and Genetic Syndromes and Imprinting (6 papers). Mark Consugar collaborates with scholars based in United States, United Kingdom and Spain. Mark Consugar's co-authors include Peter C. Harris, Sandro Rossetti, Vicente E. Torres, Vickie Kubly, Eric A. Pierce, Lisa M. Guay‐Woodford, Catherine M. Meyers, Kyongtae T. Bae, Qin Zhang and William M. Bennett and has published in prestigious journals such as PLoS ONE, Cancer Research and Chemical Communications.

In The Last Decade

Mark Consugar

26 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
Mark Consugar United States	21	1.5k	1.4k	249	238	177	26	2.1k
Hennie T. Brüggenwirth Netherlands	25	1.3k 0.9×	786 0.6×	183 0.7×	91 0.4×	6 0.0×	73	2.1k
Sunil K. Parapuram Canada	17	937 0.6×	385 0.3×	38 0.2×	159 0.7×	14 0.1×	24	1.5k
Ghada M. H. Abdel‐Salam Egypt	20	895 0.6×	437 0.3×	177 0.7×	34 0.1×	29 0.2×	89	1.4k
Irfan Saadi United States	18	623 0.4×	347 0.2×	75 0.3×	95 0.4×	9 0.1×	36	1.1k
Dimitra Micha Netherlands	22	521 0.3×	633 0.5×	49 0.2×	29 0.1×	91 0.5×	73	1.5k
Satyajit Karnik United States	12	844 0.6×	556 0.4×	73 0.3×	42 0.2×	22 0.1×	15	2.0k
Nicoletta Resta Italy	27	887 0.6×	408 0.3×	67 0.3×	540 2.3×	15 0.1×	115	2.0k
Monika Goś Poland	19	769 0.5×	331 0.2×	68 0.3×	66 0.3×	8 0.0×	49	1.2k
Hagit Baris Israel	17	385 0.3×	203 0.1×	83 0.3×	158 0.7×	8 0.0×	49	965
Andrew Beenken United States	9	1.6k 1.1×	238 0.2×	13 0.1×	69 0.3×	48 0.3×	11	2.0k

Countries citing papers authored by Mark Consugar

Since Specialization

Citations

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

Fields of papers citing papers by Mark Consugar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Consugar

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Consugar. A scholar is included among the top collaborators of Mark Consugar 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 Mark Consugar. Mark Consugar 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

Ung, Cindy, Li Shen, Samaneh Davoudi, et al.. (2017). Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy. Vision Research. 139. 168–176. 32 indexed citations

Pan, Jianbo, Sheng Liu, Michael H. Farkas, et al.. (2016). Serum molecular signature for proliferative diabetic retinopathy in Saudi patients with type 2 diabetes.. PubMed. 22. 636–45. 10 indexed citations

Falk, Marni J., Xiaowu Gai, Megumi Shigematsu, et al.. (2016). A novelHSD17B10mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression. RNA Biology. 13(5). 477–485. 41 indexed citations

Bujakowska, Kinga M., Rosario Fernández‐Godino, Emily Place, et al.. (2016). Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations. Genetics in Medicine. 19(6). 643–651. 40 indexed citations

Bujakowska, Kinga M., Joseph White, Emily Place, Mark Consugar, & Jason Comander. (2015). Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa. PLoS ONE. 10(11). e0142614–e0142614. 11 indexed citations

Consugar, Mark, Daniel Navarro-Gomez, Emily Place, et al.. (2014). Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. Genetics in Medicine. 17(4). 253–261. 179 indexed citations

Consugar, Mark, Jamie L. Sundsbak, Christina M. Heyer, et al.. (2013). Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families. Kidney International. 85(2). 383–392. 25 indexed citations

Farkas, Michael H., Gregory R. Grant, Joseph White, et al.. (2013). Transcriptome analyses of the human retina identify unprecedented transcript diversity and 3.5 Mb of novel transcribed sequence via significant alternative splicing and novel genes. BMC Genomics. 14(1). 486–486. 120 indexed citations

Mohney, Brian G., José S. Pulido, Noralane M. Lindor, et al.. (2011). A Novel Mutation of LAMB2 in a Multigenerational Mennonite Family Reveals a New Phenotypic Variant of Pierson Syndrome. Ophthalmology. 118(6). 1137–1144. 24 indexed citations

10.

Hopp, Katharina, Christina M. Heyer, Cynthia J. Hommerding, et al.. (2011). B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis. Human Molecular Genetics. 20(13). 2524–2534. 61 indexed citations

11.

Rossetti, Sandro, Vickie Kubly, Mark Consugar, et al.. (2009). Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease. Kidney International. 75(8). 848–855. 229 indexed citations

12.

Rossetti, Sandro, Mark Consugar, Arlene B. Chapman, et al.. (2007). Comprehensive Molecular Diagnostics in Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 18(7). 2143–2160. 311 indexed citations

13.

Consugar, Mark, Vickie Kubly, Donna J. Lager, et al.. (2007). Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3. Human Genetics. 121(5). 591–599. 53 indexed citations

14.

Nauli, Surya M., Sandro Rossetti, Robert J. Kolb, et al.. (2006). Loss of Polycystin-1 in Human Cyst-Lining Epithelia Leads to Ciliary Dysfunction. Journal of the American Society of Nephrology. 17(4). 1015–1025. 151 indexed citations

15.

Adeva, Magdalena, Mounif El‐Youssef, Sandro Rossetti, et al.. (2006). Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD). Medicine. 85(1). 1–21. 152 indexed citations

16.

Harris, Peter C., Kyongtae T. Bae, Sandro Rossetti, et al.. (2006). Cyst Number but Not the Rate of Cystic Growth Is Associated with the Mutated Gene in Autosomal Dominant Polycystic Kidney Disease. Journal of the American Society of Nephrology. 17(11). 3013–3019. 196 indexed citations

17.

Consugar, Mark, Sarah Anderson, Sandro Rossetti, et al.. (2005). Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease. American Journal of Kidney Diseases. 45(1). 77–87. 24 indexed citations

18.

Seo, Mi Sook, Mi Hee Lim, Mark Consugar, et al.. (2005). Self-hydroxylation of perbenzoic acids at a nonheme iron(ii) center. Chemical Communications. 5644–5644. 59 indexed citations

19.

Rossetti, Sandro, Roser Torrá, Eliécer Coto, et al.. (2003). A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees. Kidney International. 64(2). 391–403. 82 indexed citations

20.

Walker, Denise L., Mark Consugar, Jeff Slezak, et al.. (2002). The ENOS polymorphism is not associated with severity of renal disease in polycystic kidney disease 1. American Journal of Kidney Diseases. 41(1). 90–94. 29 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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