Sandhya Parkash

1.1k total citations
6 papers, 75 citations indexed

About

Sandhya Parkash is a scholar working on Genetics, Surgery and Neurology. According to data from OpenAlex, Sandhya Parkash has authored 6 papers receiving a total of 75 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Genetics, 2 papers in Surgery and 2 papers in Neurology. Recurrent topics in Sandhya Parkash's work include Connective tissue disorders research (2 papers), Intestinal Malrotation and Obstruction Disorders (2 papers) and Cerebrovascular and genetic disorders (2 papers). Sandhya Parkash is often cited by papers focused on Connective tissue disorders research (2 papers), Intestinal Malrotation and Obstruction Disorders (2 papers) and Cerebrovascular and genetic disorders (2 papers). Sandhya Parkash collaborates with scholars based in Canada and United States. Sandhya Parkash's co-authors include Andrea L. Rideout, Heidi Thiese, Dianna M. Milewicz, Sarah Dyack, Beth S. Torchia, Lisa G. Shaffer, Patricia G. Wheeler, Shimul Chowdhury, Kathleen A. Leppig and Jay W. Ellison and has published in prestigious journals such as Neurology, American Journal of Medical Genetics Part A and European Journal of Medical Genetics.

In The Last Decade

Sandhya Parkash

6 papers receiving 64 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandhya Parkash Canada	4	35	27	23	19	17	6	75
Regan Klatt Canada	6	32 0.9×	19 0.7×	47 2.0×	17 0.9×	53 3.1×	10	155
Yonit A. Addissie United States	6	66 1.9×	13 0.5×	77 3.3×	6 0.3×	12 0.7×	11	144
Paul IW de Bakker Netherlands	3	29 0.8×	11 0.4×	27 1.2×	9 0.5×	10 0.6×	3	79
Alice Masurel France	4	40 1.1×	21 0.8×	29 1.3×	32 1.7×	8 0.5×	5	99
Manali Chitre United Kingdom	6	10 0.3×	33 1.2×	19 0.8×	46 2.4×	18 1.1×	11	116
Cécile Zordan France	5	27 0.8×	16 0.6×	37 1.6×	45 2.4×	30 1.8×	7	98
S. Hande Çağlayan Türkiye	9	41 1.2×	11 0.4×	89 3.9×	4 0.2×	23 1.4×	15	159
Nigel Osborne United Kingdom	2	15 0.4×	7 0.3×	22 1.0×	16 0.8×	14 0.8×	4	68
Olivier Patat France	4	50 1.4×	7 0.3×	60 2.6×	4 0.2×	22 1.3×	4	107
C. Cancès France	6	12 0.3×	8 0.3×	20 0.9×	36 1.9×	9 0.5×	14	82

Countries citing papers authored by Sandhya Parkash

Since Specialization

Citations

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

Fields of papers citing papers by Sandhya Parkash

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandhya Parkash

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

All Works

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6 of 6 papers shown

1.

Pinard, Amélie, Alana C. Cecchi, Andrea L. Rideout, et al.. (2021). Association of De Novo RNF213 Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy. Neurology. 96(13). e1783–e1791. 23 indexed citations

2.

Rideout, Andrea L., Sara MacKay, Jill Beis, et al.. (2019). A family with Classical Ehlers-Danlos Syndrome (cEDS), mild bone fragility and without vascular complications, caused by the p.Arg312Cys mutation in COL1A1. European Journal of Medical Genetics. 63(2). 103730–103730. 9 indexed citations

3.

Kwartler, Callie, Ellen S. Regalado, Rana O. Afifi, et al.. (2019). Grange syndrome due to homozygous YY1AP1 missense rare variants. American Journal of Medical Genetics Part A. 179(12). 2500–2505. 7 indexed citations

4.

Rashid, Mohsin, et al.. (2018). Chylomicron Retention Disease: An Infant Presenting with Vomiting and Failure to Thrive without Diarrhea. 2(2). 1 indexed citations

5.

Parkash, Sandhya, et al.. (2018). A177 CHYLOMICRON RETENTION DISEASE: A CASE OF INFANT PRESENTING WITH VOMITING AND FAILURE TO THRIVE WITHOUT DIARRHEA. Journal of the Canadian Association of Gastroenterology. 1(suppl_2). 261–261. 2 indexed citations

6.

Chowdhury, Shimul, Anne M. Bandholz, Sandhya Parkash, et al.. (2013). Phenotypic and molecular characterization of 19q12q13.1 deletions: A report of five patients. American Journal of Medical Genetics Part A. 164(1). 62–69. 33 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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