Sandra Hing

1.5k total citations
24 papers, 916 citations indexed

About

Sandra Hing is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Sandra Hing has authored 24 papers receiving a total of 916 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Pulmonary and Respiratory Medicine and 5 papers in Genetics. Recurrent topics in Sandra Hing's work include Sarcoma Diagnosis and Treatment (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers) and Tumors and Oncological Cases (4 papers). Sandra Hing is often cited by papers focused on Sarcoma Diagnosis and Treatment (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers) and Tumors and Oncological Cases (4 papers). Sandra Hing collaborates with scholars based in United Kingdom, United States and Switzerland. Sandra Hing's co-authors include Kathy Pritchard‐Jones, Janet Shipley, Yong‐Jie Lu, David Delaney, Paul O’Donnell, Adrienne M. Flanagan, Paul E. Grundy, Richard D. Williams, Roberto Tirabosco and Gudrun E. Moore and has published in prestigious journals such as The Lancet, Blood and Brain.

In The Last Decade

Sandra Hing

23 papers receiving 899 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Hing United Kingdom 16 408 242 211 181 160 24 916
Christian Herens Belgium 16 275 0.7× 101 0.4× 295 1.4× 101 0.6× 106 0.7× 35 877
Takafumi Nishizaki Japan 18 477 1.2× 112 0.5× 266 1.3× 188 1.0× 192 1.2× 62 1.3k
Jennifer Willert United States 13 485 1.2× 178 0.7× 129 0.6× 223 1.2× 70 0.4× 37 926
Massimo Brisigotti Italy 20 488 1.2× 326 1.3× 91 0.4× 232 1.3× 107 0.7× 55 1.4k
Carol Berger United States 22 831 2.0× 308 1.3× 530 2.5× 296 1.6× 304 1.9× 43 1.6k
Pierre Heimann Belgium 16 543 1.3× 224 0.9× 117 0.6× 335 1.9× 180 1.1× 49 1.2k
Marion C. Baker United Kingdom 17 469 1.1× 236 1.0× 310 1.5× 206 1.1× 160 1.0× 27 1.2k
Regina Kunzmann Germany 20 496 1.2× 137 0.6× 185 0.9× 257 1.4× 104 0.7× 33 1.5k
Annet Simons Netherlands 17 239 0.6× 145 0.6× 181 0.9× 144 0.8× 154 1.0× 29 800
Roberta La Starza Italy 24 796 2.0× 165 0.7× 183 0.9× 170 0.9× 211 1.3× 91 1.8k

Countries citing papers authored by Sandra Hing

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Hing

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Hing

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

All Works

20 of 20 papers shown
1.
Kapp, Joshua, Tim C. Diss, James Spicer, et al.. (2014). Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial. Journal of Clinical Pathology. 68(2). 111–118. 36 indexed citations
2.
Kinsler, Veronica A., Anna Thomas, Miho Ishida, et al.. (2013). Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS. Journal of Investigative Dermatology. 133(9). 2229–2236. 196 indexed citations
3.
Kashima, Takeshi, Dina Halai, Hongtao Ye, et al.. (2012). Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor. Modern Pathology. 25(10). 1384–1396. 52 indexed citations
4.
Williams, Richard D., Reem Al‐Saadi, Rachael Natrajan, et al.. (2011). Molecular profiling reveals frequent gain of MYCN and anaplasia‐specific loss of 4q and 14q in wilms tumor. Genes Chromosomes and Cancer. 50(12). 982–995. 38 indexed citations
5.
Delaney, David, Tim C. Diss, Nadège Presneau, et al.. (2009). GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma. Modern Pathology. 22(5). 718–724. 72 indexed citations
6.
Hing, Sandra, Nadège Presneau, Paul O’Donnell, et al.. (2009). Familial tumoral calcinosis and hyperostosis–hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3. Skeletal Radiology. 39(1). 63–68. 22 indexed citations
7.
Hing, Sandra, et al.. (2007). Primary Pericardial Synovial Sarcoma Confirmed by Molecular Genetic Studies. Journal of Pediatric Hematology/Oncology. 29(7). 492–495. 12 indexed citations
8.
Strefford, Jonathan C., Helen Worley, Kerry E. Barber, et al.. (2007). Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization. Oncogene. 26(29). 4306–4318. 78 indexed citations
9.
Messahel, Boo, et al.. (2005). Clinical features of molecular pathology of solid tumours in childhood. The Lancet Oncology. 6(6). 421–430. 7 indexed citations
10.
Williams, Richard D., Sandra Hing, Braden T. Greer, et al.. (2004). Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines. Genes Chromosomes and Cancer. 41(1). 65–79. 36 indexed citations
11.
Patel, Naina, Lindsey K. Goff, Taane G. Clark, et al.. (2003). Expression profile of wild‐type ETV6 in childhood acute leukaemia. British Journal of Haematology. 122(1). 94–98. 22 indexed citations
12.
Lu, Yong‐Jie, Sandra Hing, Richard D. Williams, et al.. (2002). Chromosome 1q expression profiling and relapse in Wilms' tumour. The Lancet. 360(9330). 385–386. 46 indexed citations
13.
Hing, Sandra, Yong‐Jie Lu, Brenda Summersgill, et al.. (2001). Gain of 1q Is Associated with Adverse Outcome in Favorable Histology Wilms’ Tumors. American Journal Of Pathology. 158(2). 393–398. 102 indexed citations
14.
Freeman, Richard B., Sunny Dzik, Urmila Khettry, et al.. (1991). SEROLOGIC AND DNA FOLLOW-UP DATA FROM HBsAg-POSITIVE PATIENTS TREATED WITH ORTHOTOPIC LIVER TRANSPLANTATION. Transplantation. 51(4). 793–796. 22 indexed citations
15.
Temple, I. Karen, J A Hurst, Sandra Hing, L. J. Butler, & M Baraitser. (1990). De novo deletion of Xp22.2-pter in a female with linear skin lesions of the face and neck, microphthalmia, and anterior chamber eye anomalies.. Journal of Medical Genetics. 27(1). 56–58. 54 indexed citations
16.
Moore, Gudrun E., Philip Hedge, S.H. Rider, et al.. (1989). Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17. Genomics. 4(2). 152–161. 6 indexed citations
17.
Hing, Sandra, Anthony J. Day, Jean Ripoche, et al.. (1988). Assignment of complement components C4 binding protein (C4BP) and factor H (FH) to human chromosome 1q, using cDNA probes. Annals of Human Genetics. 52(2). 117–122. 10 indexed citations
18.
Solomon, E., Rodger W. Palmer, Sandra Hing, & S.K. Alex Law. (1988). Regional localization of CD18, the β‐subunit of the cell surface adhesion molecule LFA‐1, on human chromosome 21 by in situ hybridization. Annals of Human Genetics. 52(2). 123–128. 22 indexed citations
19.
Francis, D. A., J. R. Batchelor, W. I. McDonald, et al.. (1987). MULTIPLE SCLEROSIS IN NORTH-EAST SCOTLAND AN ASSOCIATION WITH HLA-DOW1. Brain. 110(1). 181–196. 51 indexed citations
20.
Hing, Sandra, Carolyn M. Giles, A.H.L. Fielder, & J. R. Batchelor. (1986). HLA Haplotypes with C4B5; evidence for further allelic heterogeneity. Immunogenetics. 23(3). 151–155. 11 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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