Suma P. Shankar

3.6k total citations
71 papers, 1.5k citations indexed

About

Suma P. Shankar is a scholar working on Molecular Biology, Physiology and Organic Chemistry. According to data from OpenAlex, Suma P. Shankar has authored 71 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 35 papers in Physiology and 17 papers in Organic Chemistry. Recurrent topics in Suma P. Shankar's work include Lysosomal Storage Disorders Research (33 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Trypanosoma species research and implications (12 papers). Suma P. Shankar is often cited by papers focused on Lysosomal Storage Disorders Research (33 papers), Carbohydrate Chemistry and Synthesis (17 papers) and Trypanosoma species research and implications (12 papers). Suma P. Shankar collaborates with scholars based in United States, United Kingdom and Canada. Suma P. Shankar's co-authors include Stephen P. Daiger, Lori S. Sullivan, Sara J. Bowne, Dianna K. Hughbanks-Wheaton, David G. Birch, Edwin M. Stone, Robert R. German, Katherine A. Rauen, John R. Heckenlively and Kathy Nicholls and has published in prestigious journals such as Blood, PLoS ONE and PEDIATRICS.

In The Last Decade

Suma P. Shankar

70 papers receiving 1.4k citations

Peers

Countries citing papers authored by Suma P. Shankar

Since Specialization

Citations

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

Fields of papers citing papers by Suma P. Shankar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Suma P. Shankar. 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 Suma P. Shankar. The network helps show where Suma P. Shankar may publish in the future.

Co-authorship network of co-authors of Suma P. Shankar

This figure shows the co-authorship network connecting the top 25 collaborators of Suma P. Shankar. A scholar is included among the top collaborators of Suma P. Shankar 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 Suma P. Shankar. Suma P. Shankar 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	Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosome 2022 ·BMJ Case Reports ·(unknown), (unknown), Flora Tassone, Suma P. Shankar, Randi J. Hagerman	1
2	Retinal dystrophies: A look beyond the eyes 2022 ·American Journal of Ophthalmology Case Reports ·(unknown), (unknown), Glenn Yiu, (unknown), Ala Moshiri, Suma P. Shankar	2
3	Clinical outcomes after 4.5 years of eliglustat therapy for Gaucher disease type 1: Phase 3 ENGAGE trial final results 2021 ·American Journal of Hematology ·Pramod K. Mistry, Elena Lukina, Hadhami Ben Turkia, Suma P. Shankar, Hagit Baris Feldman, Marwan Ghosn, Atul Mehta, Seymour Packman, Heather Lau, Мilan Petakov, Sarit Assouline, Manisha Balwani, Sumita Danda, Evgueniy Hadjiev, Andres Ortega, Meredith C. Foster, Sebastiaan J.M. Gaemers, Michel Peterschmitt	31
4	Genetic testing for inherited colorectal cancer and polyposis, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG) 2021 ·Genetics in Medicine ·Rong Mao, Patti Krautscheid, Rondell P. Graham, Arupa Ganguly, Suma P. Shankar, (unknown), Madhuri Hegde	36
5	Retinal degeneration in mice and humans with neuronal ceroid lipofuscinosis type 8 2021 ·Annals of Translational Medicine ·(unknown), Brian C. Leonard, (unknown), Christopher J. Murphy, Sara M. Thomasy, Denise M. Imai, Kristin Grimsrud, K. C. Kent Lloyd, Jiong Yan, Rossana Sanchez Russo, Suma P. Shankar, Ala Moshiri	3
6	Costello syndrome: Clinical phenotype, genotype, and management guidelines 2019 ·American Journal of Medical Genetics Part A ·Karen W. Gripp, (unknown), Marni E. Axelrad, Kathryn C. Chatfield, Aaron Chidekel, William B. Dobyns, Daniel Doyle, Bronwyn Kerr, Angela E. Lin, David D. Schwartz, Barbara Sibbles, Dawn H. Siegel, Suma P. Shankar, David A. Stevenson, Mihir M. Thacker, K. Nicole Weaver, Sue M. White, Katherine A. Rauen	72
7	Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial 2019 ·Molecular Genetics and Metabolism ·Uma Ramaswami, Daniel G. Bichet, L. Clarke, Gabriela Dostálová, (unknown), Andreas Fellgiebel, Cassiano Mateus Forcelini, Kristina An Haack, Robert J. Hopkin, Michael Mauer, Behzad Najafian, C. Ronald Scott, Suma P. Shankar, Beth L. Thurberg, Camilla Tøndel, Anna Tylki‐Szymańska, Bernard Bénichou, Frits A. Wijburg	24
8	Phenotypic characteristics of the p.Asn215Ser (p.N215S) GLA mutation in male and female patients with Fabry disease: A multicenter Fabry Registry study 2018 ·Molecular Genetics & Genomic Medicine ·Dominique P. Germain, Eva Brand, Alessandro P. Burlina, Franco Cecchi, Scott C. Garman, Judy Kempf, Dawn A. Laney, Aleš Linhart, László Maródi, Kathy Nicholls, Alberto Ortíz, Federico Pieruzzi, Suma P. Shankar, Stephen Waldek, Christoph Wanner, Ana Jovanović	81
9	Migalastat improves diarrhea in patients with Fabry disease: clinical-biomarker correlations from the phase 3 FACETS trial 2018 ·Orphanet Journal of Rare Diseases ·Raphael Schiffmann, Daniel G. Bichet, Ana Jovanović, Derralynn Hughes, Roberto Giugliani, Ulla Feldt‐Rasmussen, Suma P. Shankar, Laura Barisoni, Robert B. Colvin, J. Charles Jennette, Fred Holdbrook, Andrew E. Mulberg, Jeffrey P. Castelli, Nina Skuban, Jay Barth, Kathy Nicholls	25
10	An open-label clinical trial of agalsidase alfa enzyme replacement therapy in children with Fabry disease who are naïve to enzyme replacement therapy 2016 ·Drug Design Development and Therapy ·Özlem Göker-Alpan, Nicola Longo, Timothy J. McDonald, Suma P. Shankar, Raphael Schiffmann, Peter Chang, Yinghua Shen, Arian Pano	18
11	Effect and Tolerability of Agalsidase Alfa in Patients with Fabry Disease Who Were Treatment Naïve or Formerly Treated with Agalsidase Beta or Agalsidase Alfa 2015 ·JIMD Reports ·Özlem Göker-Alpan, Khan Nedd, Suma P. Shankar, Yeong‐Hau H. Lien, Neal J. Weinreb, Anna Wijatyk, (unknown), Rick Martin	17
12	Contribution of Family History in Co-occurring Down Syndrome and Ehlers-Danlos Syndrome 2013 ·PubMed ·(unknown), (unknown), Suma P. Shankar, (unknown), (unknown), Jeannie Visootsak	3
13	Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the proband 2010 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·Phoebe Lin, Suma P. Shankar, John S. Duncan, Anne Slavotinek, Edwin M. Stone, Tina Rutar	11
14	Genetic Screening for OPA1 and OPA3 Mutations in Patients with Suspected Inherited Optic Neuropathies 2010 ·Ophthalmology ·Patrick Yu‐Wai‐Man, Suma P. Shankar, Valérie Biousse, Neil R. Miller, Lora Jh Bean, Bradford Coffee, Madhuri Hegde, Nancy J. Newman	41
15	Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy 2008 ·Ophthalmic Genetics ·Suma P. Shankar, John H. Fingert, Valério Carelli, Maria Lucia Valentino, Terri M. King, Stephen P. Daiger, Solange Rios Salomão, Adriana Berezovsky, Rubens Belfort, (unknown), Val C. Sheffield, Alfredo A. Sadun, Edwin M. Stone	88
16	Genetic Factors Modifying Clinical Expression of Autosomal Dominant RP 2007 ·Advances in experimental medicine and biology ·Stephen P. Daiger, Suma P. Shankar, Alice B. Schindler, Lori S. Sullivan, Sara J. Bowne, Terri M. King, (unknown), Edwin M. Stone, John R. Heckenlively	9
17	Linkage Mapping in Families With Autosomal Dominant Retinitis Pigmentosa (adRP) 2005 ·Investigative Ophthalmology & Visual Science ·L.S. Sullivan, Sara J. Bowne, Suma P. Shankar, Susan H. Blanton, John R. Heckenlively, David G. Birch, Dianna H. Wheaton, Mary Z. Pelias, (unknown)	1
18	Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON) 2005 ·Investigative Ophthalmology & Visual Science ·Suma P. Shankar, Valério Carelli, Terri M. King, Christine Taylor, (unknown), (unknown), Stephen P. Daiger, Solange Rios Salomão, (unknown), Edwin M. Stone	3
19	Autosomal dominant retinitis pigmentosa: exclusion of known and mapped genes in three families. 2004 ·Investigative Ophthalmology & Visual Science ·L.S. Sullivan, Sara J. Bowne, Suma P. Shankar, David G. Birch, Dianna K. Hughbanks-Wheaton, J. R. Heckenlively, Susan H. Blanton, Stephen P. Daiger	1
20	Segregation Analysis of a Large Lhon Pedigree Is Consistent With the Existence of a Nuclear Modifying Gene 2003 ·Investigative Ophthalmology & Visual Science ·Valério Carelli, (unknown), Maria Lucia Valentino, Suma P. Shankar, Solange Rios Salomão, (unknown), Alfredo A. Sadun, Edwin M. Stone	2

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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