Ingrid Slade

740 total citations
10 papers, 431 citations indexed

About

Ingrid Slade is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Ingrid Slade has authored 10 papers receiving a total of 431 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Ingrid Slade's work include BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers) and Cancer Genomics and Diagnostics (3 papers). Ingrid Slade is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Genomics and Rare Diseases (4 papers) and Cancer Genomics and Diagnostics (3 papers). Ingrid Slade collaborates with scholars based in United Kingdom, Canada and United States. Ingrid Slade's co-authors include Nazneen Rahman, Helen Hanson, Angela George, Ann Strydom, Zoe Kemp, Michael Dunn, Susana Banerjee, Sheila Seal, Sabrina Talukdar and Leah Z. Rand and has published in prestigious journals such as Scientific Reports, Journal of Medical Genetics and Drug Safety.

In The Last Decade

Ingrid Slade

10 papers receiving 424 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingrid Slade United Kingdom	9	238	132	106	72	57	10	431
Nicholas Pachter Australia	14	210 0.9×	233 1.8×	67 0.6×	121 1.7×	72 1.3×	30	578
Sharon Sand United States	12	409 1.7×	164 1.2×	112 1.1×	138 1.9×	75 1.3×	26	583
Irène Feroce Italy	12	244 1.0×	152 1.2×	119 1.1×	101 1.4×	82 1.4×	33	521
Ryan Noss United States	10	182 0.8×	88 0.7×	60 0.6×	48 0.7×	37 0.6×	17	339
Jocelyne Chiquette Canada	14	350 1.5×	154 1.2×	184 1.7×	71 1.0×	65 1.1×	39	542
R Davidson United Kingdom	9	346 1.5×	159 1.2×	120 1.1×	45 0.6×	43 0.8×	12	511
Jeanna McCuaig Canada	14	320 1.3×	103 0.8×	158 1.5×	139 1.9×	45 0.8×	39	490
Gord Glendon Canada	12	435 1.8×	118 0.9×	203 1.9×	131 1.8×	70 1.2×	20	608
S Gershman Canada	4	409 1.7×	84 0.6×	107 1.0×	230 3.2×	59 1.0×	5	481
Veronica I. Lagos United States	8	420 1.8×	148 1.1×	91 0.9×	125 1.7×	37 0.6×	9	493

Countries citing papers authored by Ingrid Slade

Since Specialization

Citations

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

Fields of papers citing papers by Ingrid Slade

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ingrid Slade

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

All Works

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10 of 10 papers shown

1.

Rand, Leah Z., Michael Dunn, Ingrid Slade, Sheela Upadhyaya, & Mark Sheehan. (2019). Understanding and using patient experiences as evidence in healthcare priority setting. Cost Effectiveness and Resource Allocation. 17(1). 20–20. 54 indexed citations

2.

Briggs, Sarah & Ingrid Slade. (2019). Evaluating the Integration of Genomics into Cancer Screening Programmes: Challenges and Opportunities. PubMed. 7(2). 63–74. 7 indexed citations

3.

Johnson, Stephanie, Ingrid Slade, Alberto Giubilini, & Mackenzie Graham. (2019). Rethinking the ethical principles of genomic medicine services. European Journal of Human Genetics. 28(2). 147–154. 28 indexed citations

4.

Slade, Ingrid, Helen Hanson, Angela George, et al.. (2016). A cost analysis of a cancer genetic service model in the UK. Journal of Community Genetics. 7(3). 185–194. 29 indexed citations

5.

Slade, Ingrid, et al.. (2016). Genomics education for medical professionals – the current UK landscape. Clinical Medicine. 16(4). 347–352. 21 indexed citations

6.

George, Angela, Sheila Seal, Sabrina Talukdar, et al.. (2016). Implementing rapid, robust, cost-effective, patient-centred, routine genetic testing in ovarian cancer patients. Scientific Reports. 6(1). 29506–29506. 157 indexed citations

7.

Slade, Ingrid, et al.. (2015). Development of cancer genetic services in the UK: A national consultation. Genome Medicine. 7(1). 18–18. 30 indexed citations

8.

Slade, Ingrid, Anne R. Murray, Sandra Hanks, et al.. (2010). Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma. Familial Cancer. 10(2). 337–342. 47 indexed citations

9.

Erlewyn‐Lajeunesse, Michel, et al.. (2009). Diagnostic Utility of Two Case Definitions for Anaphylaxis. Drug Safety. 33(1). 57–64. 16 indexed citations

10.

Slade, Ingrid, Philip Stephens, Jenny Douglas, et al.. (2009). Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene. Journal of Medical Genetics. 47(5). 342–347. 42 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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