Srirangan Sampath

523 total citations
12 papers, 246 citations indexed

About

Srirangan Sampath is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Srirangan Sampath has authored 12 papers receiving a total of 246 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Srirangan Sampath's work include Retinal Development and Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Srirangan Sampath is often cited by papers focused on Retinal Development and Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Srirangan Sampath collaborates with scholars based in United States, Australia and Germany. Srirangan Sampath's co-authors include Shirly G. Panicker, Aramati B. M. Reddy, Anil K. Mandal, Yves Lacassie, Dorairajan Balasubramanian, Subhabrata Chakrabarti, Seyed E. Hasnain, Sherri J. Bale, Katherine A. Rauen and William E. Tidyman and has published in prestigious journals such as PLoS ONE, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Srirangan Sampath

12 papers receiving 241 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Srirangan Sampath United States 8 165 102 36 35 27 12 246
Aušra Matulevičienė Lithuania 10 222 1.3× 216 2.1× 61 1.7× 17 0.5× 17 0.6× 24 348
Bellinda van den Helm Netherlands 11 320 1.9× 201 2.0× 40 1.1× 31 0.9× 36 1.3× 17 465
Jesús Javier Martínez García United States 6 216 1.3× 105 1.0× 24 0.7× 33 0.9× 14 0.5× 10 313
Isabella Rau Germany 6 138 0.8× 97 1.0× 66 1.8× 27 0.8× 43 1.6× 9 236
Ali Muhammad Waryah Pakistan 12 191 1.2× 77 0.8× 53 1.5× 38 1.1× 150 5.6× 39 412
Muriel Holder France 9 283 1.7× 185 1.8× 19 0.5× 26 0.7× 92 3.4× 14 408
Sanne Broekman Netherlands 10 199 1.2× 33 0.3× 50 1.4× 62 1.8× 38 1.4× 19 244
Raffaella Stallone Italy 9 110 0.7× 147 1.4× 37 1.0× 5 0.1× 12 0.4× 16 312
Michaela Thoenes Germany 7 132 0.8× 88 0.9× 12 0.3× 28 0.8× 24 0.9× 9 226
Ascensión Gimenez-Pardo Spain 4 198 1.2× 50 0.5× 40 1.1× 17 0.5× 102 3.8× 4 266

Countries citing papers authored by Srirangan Sampath

Since Specialization
Citations

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

Fields of papers citing papers by Srirangan Sampath

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Srirangan Sampath

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

All Works

12 of 12 papers shown
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Wortmann, Saskia B., Roberto Colombo, Alessandro Pontoglio, et al.. (2017). Mild orotic aciduria in UMPS heterozygotes: a metabolic finding without clinical consequences. Journal of Inherited Metabolic Disease. 40(3). 423–431. 9 indexed citations
4.
Shaw, Chad A., Amber N. Pursley, Patricia Hixson, et al.. (2014). Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases. European Journal of Human Genetics. 22(8). 969–978. 35 indexed citations
5.
Loupe, Jacob M., Srirangan Sampath, & Yves Lacassie. (2014). Familial co-segregation of Coffin–Lowry syndrome inherited from the mother and autosomal dominant Waardenburg type IV syndrome due to deletion of EDNRB inherited from the father. European Journal of Medical Genetics. 57(10). 562–566. 3 indexed citations
6.
Sampath, Srirangan, Simone Gupta, Ashley O’Connor, et al.. (2013). Defining the Contribution of CNTNAP2 to Autism Susceptibility. PLoS ONE. 8(10). e77906–e77906. 31 indexed citations
7.
Sampath, Srirangan, et al.. (2013). Correction: Defining the Contribution of CNTNAP2 to Autism Susceptibility. PLoS ONE. 8(12). 2 indexed citations
8.
Sampath, Srirangan, Bronya J.B. Keats, & Yves Lacassie. (2011). HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31. American Journal of Medical Genetics Part A. 155(5). 976–985. 2 indexed citations
9.
Phillips, Jennifer B., Bernardo Blanco‐Sánchez, Jennifer J Lentz, et al.. (2011). Harmonin (Ush1c) is required in zebrafish Müller glial cells for photoreceptor synaptic development and function. Disease Models & Mechanisms. 4(6). 786–800. 48 indexed citations
10.
Rauen, Katherine A., William E. Tidyman, Anne L. Estep, et al.. (2010). Molecular and functional analysis of a novel MEK2 mutation in cardio‐facio‐cutaneous syndrome: Transmission through four generations. American Journal of Medical Genetics Part A. 152A(4). 807–814. 37 indexed citations
11.
Chakrabarti, Subhabrata, Anil K. Mandal, Aramati B. M. Reddy, et al.. (2003). Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.. PubMed. 9. 43–8. 42 indexed citations
12.
Panicker, Shirly G., Srirangan Sampath, Anil K. Mandal, et al.. (2002). Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.. PubMed. 43(12). 3613–6. 27 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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