Mark Consugar

4.0k citations

26 papers · 2.1k indexed · h-index 21

Molecular Biology top 5%
Genetics top 1%
Pediatrics, Perinatology and Child Health top 5%
Pathology and Forensic Medicine top 5%
Nephrology top 5%

Co-authors: Peter C. Harris Sandro Rossetti Vicente E. Torres Vickie Kubly Eric A. Pierce Lisa M. Guay‐Woodford Catherine M. Meyers Kyongtae T. Bae
Topics: Genetic and Kidney Cyst Diseases (12 papers)Renal and related cancers (10 papers)Genetic Syndromes and Imprinting (6 papers)
Cited by: Genetics Nephrology Molecular Biology
Journals: PLoS ONE Cancer Research Chemical Communications
Partner nations: United States United Kingdom Spain

In The Last Decade

Mark Consugar

26 papers receiving 2.0k citations

Peers

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

#	Work	Indexed citations
1	Whole exome sequencing identification of novel candidate genes in patients with proliferative diabetic retinopathy 2017 ·Vision Research ·Cindy Ung,(unknown),Li Shen,Samaneh Davoudi,(unknown),Daniel Navarro-Gomez,Ching J. Chen,Heather Hancock,Alan D. Penman,(unknown),Mark Consugar,(unknown),Vinay Shah,Joseph F. Arboleda‐Velásquez,Lucia Sobrin,Xiaowu Gai,Leo A. Kim	32
2	Serum molecular signature for proliferative diabetic retinopathy in Saudi patients with type 2 diabetes. 2016 ·PubMed ·Jianbo Pan,Sheng Liu,Michael H. Farkas,Mark Consugar,Donald J. Zack,Igor Kozak,J. Fernando Arévalo,Eric A. Pierce,Jiang Qian,(unknown)	10
3	A novelHSD17B10mutation impairing the activities of the mitochondrial RNase P complex causes X-linked intractable epilepsy and neurodevelopmental regression 2016 ·RNA Biology ·Marni J. Falk,Xiaowu Gai,Megumi Shigematsu,Elisa Vilardo,Ryuichi Takase,Elizabeth M. McCormick,Thomas Christian,Emily Place,Eric A. Pierce,Mark Consugar,Howard Gamper,Walter Rossmanith,Ya‐Ming Hou	41
4	Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations 2016 ·Genetics in Medicine ·Kinga M. Bujakowska,Rosario Fernández‐Godino,Emily Place,Mark Consugar,Daniel Navarro-Gomez,Joseph White,Emma Bedoukian,Xiaosong Zhu,Hongbo Xie,Xiaowu Gai,Bart P. Leroy,Eric A. Pierce	40
5	Efficient In Silico Identification of a Common Insertion in the MAK Gene which Causes Retinitis Pigmentosa 2015 ·PLoS ONE ·Kinga M. Bujakowska,Joseph White,Emily Place,Mark Consugar,Jason Comander	11
6	Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing 2014 ·Genetics in Medicine ·Mark Consugar,Daniel Navarro-Gomez,Emily Place,Kinga M. Bujakowska,Maria E Sousa,Zoë Fonseca-Kelly,Daniel G. Taub,(unknown),Dan Yi Wang,Elizabeth D. Au,Katherine B. Sims,David A. Sweetser,Anne B. Fulton,Qin Liu,Janey L. Wiggs,Xiaowu Gai,Eric A. Pierce	179
7	Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families 2013 ·Kidney International ·(unknown),Mark Consugar,(unknown),Jamie L. Sundsbak,Christina M. Heyer,Sandro Rossetti,Vickie Kubly,Katharina Hopp,Vicente E. Torres,Eliécer Coto,Maurizio Clementi,Nadja Bogdanova,Edgar Almeida,Daniel G. Bichet,Peter C. Harris	25
8	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 2013 ·BMC Genomics ·Michael H. Farkas,Gregory R. Grant,Joseph White,Maria E Sousa,Mark Consugar,Eric A. Pierce	120
9	A Novel Mutation of LAMB2 in a Multigenerational Mennonite Family Reveals a New Phenotypic Variant of Pierson Syndrome 2011 ·Ophthalmology ·Brian G. Mohney,José S. Pulido,Noralane M. Lindor,Marie C. Hogan,Mark Consugar,Justin P. Peters,V. Shane Pankratz,Samih H. Nasr,Stephen J. Smith,James M. Gloor,Vickie Kubly,(unknown),(unknown),Erik G. Puffenberger,Kevin A. Strauss,D. Holmes Morton,(unknown),Peter C. Harris	24
10	B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis 2011 ·Human Molecular Genetics ·Katharina Hopp,Christina M. Heyer,Cynthia J. Hommerding,(unknown),Jamie L. Sundsbak,(unknown),(unknown),Mark Consugar,Peter G. Czarnecki,Troy J. Gliem,Vicente E. Torres,Sandro Rossetti,Peter C. Harris	61
11	Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease 2009 ·Kidney International ·Sandro Rossetti,Vickie Kubly,Mark Consugar,Katharina Hopp,Sushmita Roy,Sharon W. Horsley,Dominique Chauveau,Lesley Rees,T M Barratt,William G. van’t Hoff,(unknown),Vicente E. Torres,Peter C. Harris	229
12	Comprehensive Molecular Diagnostics in Autosomal Dominant Polycystic Kidney Disease 2007 ·Journal of the American Society of Nephrology ·Sandro Rossetti,Mark Consugar,Arlene B. Chapman,Vicente E. Torres,Lisa M. Guay‐Woodford,Jared J. Grantham,William M. Bennett,Catherine M. Meyers,Denise L. Walker,Kyongtae T. Bae,Qin Zhang,Paul A. Thompson,J. Philip Miller,Peter C. Harris	311
13	Molecular diagnostics of Meckel–Gruber syndrome highlights phenotypic differences between MKS1 and MKS3 2007 ·Human Genetics ·Mark Consugar,Vickie Kubly,Donna J. Lager,Cynthia J. Hommerding,(unknown),Egbert Bakker,Vincent H. Gattone,Vicente E. Torres,Martijn H. Breuning,Peter C. Harris	53
14	Loss of Polycystin-1 in Human Cyst-Lining Epithelia Leads to Ciliary Dysfunction 2006 ·Journal of the American Society of Nephrology ·Surya M. Nauli,Sandro Rossetti,Robert J. Kolb,Francis J. Alenghat,Mark Consugar,Peter C. Harris,Donald E. Ingber,Mahmoud Loghman‐Adham,Jing Zhou	151
15	Clinical and Molecular Characterization Defines a Broadened Spectrum of Autosomal Recessive Polycystic Kidney Disease (ARPKD) 2006 ·Medicine ·Magdalena Adeva,Mounif El‐Youssef,Sandro Rossetti,Patrick S. Kamath,Vickie Kubly,Mark Consugar,(unknown),Bernard F. King,Vicente E. Torres,Peter C. Harris	152
16	Cyst Number but Not the Rate of Cystic Growth Is Associated with the Mutated Gene in Autosomal Dominant Polycystic Kidney Disease 2006 ·Journal of the American Society of Nephrology ·Peter C. Harris,Kyongtae T. Bae,Sandro Rossetti,Vicente E. Torres,Jared J. Grantham,Arlene B. Chapman,Lisa M. Guay‐Woodford,Bernard F. King,Louis H. Wetzel,Deborah A. Baumgarten,Philip J. Kenney,Mark Consugar,Saulo Klahr,William M. Bennett,Catherine M. Meyers,Qin Zhang,Paul A. Thompson,Fang Zhu,J. Philip Miller	196
17	Haplotype analysis improves molecular diagnostics of autosomal recessive polycystic kidney disease 2005 ·American Journal of Kidney Diseases ·Mark Consugar,Sarah Anderson,Sandro Rossetti,V. Shane Pankratz,Christopher J. Ward,Roser Torrá,Eliécer Coto,(unknown),Sibel Kantarci,Boris Utsch,Friedhelm Hildebrandt,William E. Sweeney,Ellis D. Avner,Vicente E. Torres,Julie M. Cunningham,Peter C. Harris	24
18	Self-hydroxylation of perbenzoic acids at a nonheme iron(ii) center 2005 ·Chemical Communications ·(unknown),Mi Sook Seo,Mi Hee Lim,Mark Consugar,Mi Joo Park,Jan‐Uwe Rohde,Jaehong Han,Kwan Mook Kim,Jinheung Kim,Lawrence Que,Wonwoo Nam	59
19	A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigrees 2003 ·Kidney International ·Sandro Rossetti,Roser Torrá,Eliécer Coto,Mark Consugar,Vickie Kubly,S Málaga,Mercedes Navarro,Mounif El‐Youssef,Vicente E. Torres,Peter C. Harris	82
20	The ENOS polymorphism is not associated with severity of renal disease in polycystic kidney disease 1 2002 ·American Journal of Kidney Diseases ·Denise L. Walker,Mark Consugar,Jeff Slezak,Sandro Rossetti,Vicente E. Torres,Christopher G. Winearls,Peter C. Harris	29

About Mark Consugar

Mark Consugar is a scholar working on Genetics, Ophthalmology and Nephrology, having authored 26 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetic and Kidney Cyst Diseases (12 papers), Renal and related cancers (10 papers) and Genetic Syndromes and Imprinting (6 papers). The work is most often cited by research in Genetics (1.4k citations), Nephrology (177 citations) and Molecular Biology (1.5k citations). Mark Consugar has collaborated with scholars based in United States, United Kingdom and Spain. Frequent 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. Their work appears in journals such as PLoS ONE, Cancer Research and Chemical Communications.

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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