Sandra Hing

1.5k citations

24 papers · 916 indexed · h-index 16

Impact in

Pathology and Forensic Medicine top 10%
- Tumors and Oncological Cases
Genetics top 10%
- Genetic and rare skin diseases.

Papers in ⓘ

Molecular Biology 10
- Renal and related cancers 3
Pulmonary and Respiratory Medicine 7
- Sarcoma Diagnosis and Treatment 5

Co-authors: Kathy Pritchard‐Jones (6 shared papers)Yong‐Jie Lu (2 shared papers)Janet Shipley (2 shared papers)Paul O’Donnell (3 shared papers)David Delaney (3 shared papers)Adrienne M. Flanagan (3 shared papers)Paul E. Grundy (2 shared papers)Richard D. Williams (3 shared papers)
Journals: Blood (3 papers)Annals of Human Genetics (2 papers)Modern Pathology (2 papers)Genes Chromosomes and Cancer (2 papers)British Journal of Haematology (1 paper)
Partner nations: United Kingdom United States Switzerland

In The Last Decade

Sandra Hing

23 papers receiving 899 citations

Peers

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-authors

The 25 scholars most cited alongside Sandra Hing, 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 Sandra Hing Line = papers co-authored together Sandra Hing links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Multiple Congenital Melanocytic Nevi and Neurocutaneous Melanosis Are Caused by Postzygotic Mutations in Codon 61 of NRAS Journal of Investigative Dermatology ·Veronica A. Kinsler, Anna Thomas, Miho Ishida, Neil Bulstrode, Sam Loughlin, Sandra Hing, Jane Chalker, Kathryn J. McKenzie, Sayeda Abu‐Amero, Olga Slater, Estelle Chanudet, Rodger Palmer, Deborah Morrogh, Philip Stanier, Eugene Healy, Neil J. Sebire, Gudrun E. Moore	2013	196
2	Gain of 1q Is Associated with Adverse Outcome in Favorable Histology Wilms’ Tumors American Journal Of Pathology ·Sandra Hing, Yong‐Jie Lu, Brenda Summersgill, Linda King‐Underwood, James C. Nicholson, Paul E. Grundy, Richard G. Grundy, Manfred Gessler, Janet Shipley, Kathy Pritchard‐Jones	2001	102
3	Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization Oncogene ·Jonathan C. Strefford, Helen Worley, Kerry E. Barber, Sarah Wright, Adam Stewart, Hazel M. Robinson, G Bettney, Frederik W. van Delft, Mark Atherton, T. Davies, Mike Griffiths, Sandra Hing, F. M. Ross, P. Talley, Vaskar Saha, Anthony V. Moorman, Christine J. Harrison	2007	78
4	GNAS1 mutations occur more commonly than previously thought in intramuscular myxoma Modern Pathology ·David Delaney, Tim C. Diss, Nadège Presneau, Sandra Hing, Fitim Berisha, Bernadine Idowu, Paul O’Donnell, John Skinner, Roberto Tirabosco, Adrienne M. Flanagan	2009	72
5	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 ·I. Karen Temple, J A Hurst, Sandra Hing, L. J. Butler, M Baraitser	1990	54
6	Sensitivity of MDM2 amplification and unexpected multiple faint alphoid 12 (alpha 12 satellite sequences) signals in atypical lipomatous tumor Modern Pathology ·Takeshi Kashima, Dina Halai, Hongtao Ye, Sandra Hing, David Delaney, Robin Pollock, Paul O’Donnell, Roberto Tirabosco, Adrienne M. Flanagan	2012	52
7	MULTIPLE SCLEROSIS IN NORTH-EAST SCOTLAND AN ASSOCIATION WITH HLA-DOW1 Brain ·D. A. Francis, J. R. Batchelor, W. I. McDonald, Sandra Hing, I. Anthony Dodi, A.H.L. Fielder, Jaclyn Hern, A. W. Downie	1987	51
8	Chromosome 1q expression profiling and relapse in Wilms' tumour The Lancet ·Yong‐Jie Lu, Sandra Hing, Richard D. Williams, Ross Pinkerton, Janet Shipley, Kathy Pritchard‐Jones	2002	46
9	Molecular profiling reveals frequent gain of MYCN and anaplasia‐specific loss of 4q and 14q in wilms tumor Genes Chromosomes and Cancer ·Richard D. Williams, Reem Al‐Saadi, Rachael Natrajan, Alan Mackay, Tasnim Chagtai, Suzanne E. Little, Sandra Hing, Kerry Fenwick, Alan Ashworth, Paul E. Grundy, James R. Anderson, Jeffrey S. Dome, Elizabeth J. Perlman, Chris Jones, Kathy Pritchard‐Jones	2011	38
10	Prognostic classification of relapsing favorable histology Wilms tumor using cDNA microarray expression profiling and support vector machines Genes Chromosomes and Cancer ·Richard D. Williams, Sandra Hing, Braden T. Greer, Craig C. Whiteford, Jun S. Wei, Rachael Natrajan, Anna Kelsey, Simon Rogers, Colin Campbell, Kathy Pritchard‐Jones, Javed Khan	2004	36
11	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 ·Joshua Kapp, Tim C. Diss, James Spicer, Michael Gandy, Iris Schrijver, Lawrence J. Jennings, Marilyn M. Li, Gregory J. Tsongalis, David González de Castro, Julia A. Bridge, Andrew J. Wallace, Joshua L. Deignan, Sandra Hing, Rachel Butler, Eldo T. Verghese, Gary J. Latham, Rifat Hamoudi	2014	36
12	Expression profile of wild‐type ETV6 in childhood acute leukaemia British Journal of Haematology ·Naina Patel, Lindsey K. Goff, Taane G. Clark, Anthony M. Ford, Nicola Foot, Debra M. Lillington, Sandra Hing, Kathy Pritchard‐Jones, Louise Jones, Vaskar Saha	2003	22
13	SEROLOGIC AND DNA FOLLOW-UP DATA FROM HBsAg-POSITIVE PATIENTS TREATED WITH ORTHOTOPIC LIVER TRANSPLANTATION Transplantation ·Richard B. Freeman, Herminio Sanchez, W. DAVID LEWIS, Bradford Sherburne, Sunny Dzik, Urmila Khettry, Sandra Hing, Jerome B. Zeldis, Roger L. Jenkins	1991	22
14	Familial tumoral calcinosis and hyperostosis–hyperphosphataemia syndrome are different manifestations of the same disease: novel missense mutations in GALNT3 Skeletal Radiology ·Leo Joseph, Sandra Hing, Nadège Presneau, Paul O’Donnell, Tim Diss, Bernadine Idowu, Selvanayagam Joseph, Adrienne M. Flanagan, David Delaney	2009	22
15	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 ·E. Solomon, Rodger W. Palmer, Sandra Hing, S.K. Alex Law	1988	22
16	HLA genetic determinants in familial MS Tissue Antigens ·D A Francis, J. R. Batchelor, W. I. McDonald, I. Anthony Dodi, Sandra Hing, Jaclyn Hern, A. W. Downie	1987	15
17	Primary Pericardial Synovial Sarcoma Confirmed by Molecular Genetic Studies Journal of Pediatric Hematology/Oncology ·Sandra Hing, Lynley Marshall, Reem Al‐Saadi, Darren Hargrave	2007	12
18	HLA Haplotypes with C4B5; evidence for further allelic heterogeneity Immunogenetics ·Sandra Hing, Carolyn M. Giles, A.H.L. Fielder, J. R. Batchelor	1986	11
19	Assignment of complement components C4 binding protein (C4BP) and factor H (FH) to human chromosome 1q, using cDNA probes Annals of Human Genetics ·Sandra Hing, Anthony J. Day, S. J. LINTON, Jean Ripoche, Robert B. Sim, K.B.M. Reid, E. Solomon	1988	10
20	Clinical features of molecular pathology of solid tumours in childhood The Lancet Oncology ·Boo Messahel, Ruth Nash, Iona Jeffrey, Kathy Pritchard‐Jones, Sandra Hing	2005	7

About Sandra Hing

Sandra Hing is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine, Genetics, Pathology and Forensic Medicine and Radiology, Nuclear Medicine and Imaging, having authored 24 papers that have together received 916 indexed citations. Recurring topics across this work include Sarcoma Diagnosis and Treatment (5 papers), Monoclonal and Polyclonal Antibodies Research (4 papers), Tumors and Oncological Cases (4 papers), Renal and related cancers (3 papers), Acute Lymphoblastic Leukemia research (3 papers), Cancer Genomics and Diagnostics (3 papers), Soft tissue tumor case studies (2 papers) and Hemoglobinopathies and Related Disorders (2 papers). The work is most often cited by research in Pathology and Forensic Medicine (160 citations), Genetics (211 citations), Rheumatology (113 citations), Pulmonary and Respiratory Medicine (242 citations) and Hematology (76 citations). Sandra Hing has collaborated with scholars based in United Kingdom, United States and Switzerland. Frequent co-authors include Kathy Pritchard‐Jones, Yong‐Jie Lu, Janet Shipley, Paul O’Donnell, David Delaney, Adrienne M. Flanagan, Paul E. Grundy, Richard D. Williams, Roberto Tirabosco and Philip Stanier. Their work appears in journals such as Blood, Annals of Human Genetics, Modern Pathology, Genes Chromosomes and Cancer and British Journal of Haematology.

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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