Suma P. Shankar

3.6k citations

71 papers · 1.5k indexed · h-index 21

Physiology top 5%
- Lysosomal Storage Disorders Research 33
Ophthalmology top 5%
Cell Biology top 5%
- Cellular transport and secretion 6
Molecular Biology top 10%
- Retinal Development and Disorders 7
- Glycosylation and Glycoproteins Research 6
Rheumatology top 10%
- Glycogen Storage Diseases and Myoclonus 9
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 17
Epidemiology
- Trypanosoma species research and implications 12
Genetics
- Genetic Syndromes and Imprinting 4

Co-authors: 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
Cited by: Physiology Ophthalmology Cell Biology
Partner nations: United States United Kingdom Canada

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

The 25 scholars most cited alongside Suma P. Shankar, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Suma P. Shankar Line = papers co-authored together Suma P. Shankar links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Fragile X syndrome in a girl with variant Turner syndrome and an isodicentric X chromosome Nattaporn Tassanakijpanich,Rachel Wright,Flora Tassone,Suma P. Shankar,Randi J. Hagerman	2022	1
2	Retinal dystrophies: A look beyond the eyes Vincent Tang,Alena Egense,Glenn Yiu,Elijah Meyers,Ala Moshiri,Suma P. Shankar	2022	2
3	Clinical outcomes after 4.5 years of eliglustat therapy for Gaucher disease type 1: Phase 3 ENGAGE trial final results 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	2021	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) Rong Mao,Patti Krautscheid,Rondell P. Graham,Arupa Ganguly,Suma P. Shankar,Matthew Ferber,Madhuri Hegde	2021	36
5	Retinal degeneration in mice and humans with neuronal ceroid lipofuscinosis type 8 Elyse M. Salpeter,Brian C. Leonard,Antonio Jacobo Lopez,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	2021	3
6	Costello syndrome: Clinical phenotype, genotype, and management guidelines Karen W. Gripp,Lindsey A. Morse,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	2019	72
7	Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial Uma Ramaswami,Daniel G. Bichet,L. Clarke,Gabriela Dostálová,Alejandro Fainboim,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	2019	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 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	2018	81
9	Migalastat improves diarrhea in patients with Fabry disease: clinical-biomarker correlations from the phase 3 FACETS trial 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	2018	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 Özlem Göker-Alpan,Nicola Longo,Timothy J. McDonald,Suma P. Shankar,Raphael Schiffmann,Peter Chang,Yinghua Shen,Arian Pano	2016	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 Özlem Göker-Alpan,Khan Nedd,Suma P. Shankar,Yeong‐Hau H. Lien,Neal J. Weinreb,Anna Wijatyk,Peter Chang,Rick Martin	2015	17
12	Contribution of Family History in Co-occurring Down Syndrome and Ehlers-Danlos Syndrome Allison Buterbaugh,Henry J. Mroczkowski,Suma P. Shankar,(unknown),(unknown),Jeannie Visootsak	2013	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 Phoebe Lin,Suma P. Shankar,John S. Duncan,Anne Slavotinek,Edwin M. Stone,Tina Rutar	2010	11
14	Genetic Screening for OPA1 and OPA3 Mutations in Patients with Suspected Inherited Optic Neuropathies Patrick Yu‐Wai‐Man,Suma P. Shankar,Valérie Biousse,Neil R. Miller,Lora Jh Bean,Bradford Coffee,Madhuri Hegde,Nancy J. Newman	2010	41
15	Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy Suma P. Shankar,John H. Fingert,Valério Carelli,Maria Lucia Valentino,Terri M. King,Stephen P. Daiger,Solange Rios Salomão,Adriana Berezovsky,Rubens Belfort,Tobias Braun,Val C. Sheffield,Alfredo A. Sadun,Edwin M. Stone	2008	88
16	Genetic Factors Modifying Clinical Expression of Autosomal Dominant RP Stephen P. Daiger,Suma P. Shankar,Alice B. Schindler,Lori S. Sullivan,Sara J. Bowne,Terri M. King,E. Warick Daw,Edwin M. Stone,John R. Heckenlively	2007	9
17	Linkage Mapping in Families With Autosomal Dominant Retinitis Pigmentosa (adRP) L.S. Sullivan,Sara J. Bowne,Suma P. Shankar,Susan H. Blanton,John R. Heckenlively,David G. Birch,Dianna H. Wheaton,Mary Z. Pelias,S.P. Daiger	2005	1
18	Linkage Analysis of the X Chromosome in a Brazilian Family With Leber Hereditary Optic Neuropathy (LHON) Suma P. Shankar,Valério Carelli,Terri M. King,Christine Taylor,Hakeem Abdulkawy,Tobias Braun,Stephen P. Daiger,Solange Rios Salomão,A.A. Sadun,Edwin M. Stone	2005	3
19	Autosomal dominant retinitis pigmentosa: exclusion of known and mapped genes in three families. 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	2004	1
20	Segregation Analysis of a Large Lhon Pedigree Is Consistent With the Existence of a Nuclear Modifying Gene Valério Carelli,K. Wang,Maria Lucia Valentino,Suma P. Shankar,Solange Rios Salomão,Richard Belford,Alfredo A. Sadun,Edwin M. Stone	2003	2

About Suma P. Shankar

Suma P. Shankar is a scholar working on Physiology, Rheumatology and Organic Chemistry, having authored 71 papers that have together received 1.5k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (33 papers), Carbohydrate Chemistry and Synthesis (17 papers), Trypanosoma species research and implications (12 papers), Glycogen Storage Diseases and Myoclonus (9 papers), Retinal Development and Disorders (7 papers), Glycosylation and Glycoproteins Research (6 papers), Cellular transport and secretion (6 papers) and Genetic Syndromes and Imprinting (4 papers). The work is most often cited by research in Physiology (628 citations), Ophthalmology (175 citations) and Cell Biology (282 citations). Suma P. Shankar has collaborated with scholars based in United States, United Kingdom and Canada. Frequent 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.

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