Stacey Hume

657 total citations
19 papers, 207 citations indexed

About

Stacey Hume is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Stacey Hume has authored 19 papers receiving a total of 207 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Stacey Hume's work include Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Stacey Hume is often cited by papers focused on Genomics and Rare Diseases (5 papers), Mitochondrial Function and Pathology (4 papers) and Metabolism and Genetic Disorders (3 papers). Stacey Hume collaborates with scholars based in Canada, United States and Belgium. Stacey Hume's co-authors include Margaret Lilley, Martin J. Somerville, Patrick Scott, Susan Christian, Steven C. Greenway, Aneal Khan, Christopher Newell, Ian M. MacDonald, Jane Shearer and Marsha Speevak and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Stacey Hume

18 papers receiving 205 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stacey Hume Canada 10 108 68 30 29 29 19 207
Lina Ghaloul‐Gonzalez United States 10 131 1.2× 58 0.9× 16 0.5× 52 1.8× 19 0.7× 29 254
Lee Zellmer United States 7 88 0.8× 203 3.0× 32 1.1× 22 0.8× 27 0.9× 8 257
Engela Honey South Africa 9 65 0.6× 38 0.6× 16 0.5× 24 0.8× 14 0.5× 25 168
Ana Vega Spain 8 140 1.3× 106 1.6× 8 0.3× 22 0.8× 26 0.9× 12 270
Karina Meden Sørensen Denmark 7 107 1.0× 60 0.9× 13 0.4× 7 0.2× 14 0.5× 9 185
William Lee Australia 7 261 2.4× 29 0.4× 34 1.1× 67 2.3× 46 1.6× 11 295
Joshua L. Deignan United States 7 79 0.7× 155 2.3× 15 0.5× 6 0.2× 68 2.3× 8 249
Pouria Mashouri Canada 6 118 1.1× 85 1.3× 5 0.2× 12 0.4× 26 0.9× 10 201
Olga Shamardina United Kingdom 3 56 0.5× 129 1.9× 32 1.1× 26 0.9× 24 0.8× 3 192

Countries citing papers authored by Stacey Hume

Since Specialization
Citations

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

Fields of papers citing papers by Stacey Hume

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stacey Hume

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

All Works

19 of 19 papers shown
1.
McDevitt, Trudi, Miranda Durkie, Norbert Arnold, et al.. (2024). EMQN best practice guidelines for genetic testing in hereditary breast and ovarian cancer. European Journal of Human Genetics. 32(5). 479–488. 5 indexed citations
2.
Walker, Christine, Stacey Hume, Jillian S. Parboosingh, et al.. (2023). Alberta Spinal Muscular Atrophy Newborn Screening—Results from Year 1 Pilot Project. International Journal of Neonatal Screening. 9(3). 42–42. 9 indexed citations
3.
Hume, Stacey, Xing‐Chang Wei, Christopher Newell, et al.. (2020). MITO-FIND: A study in 390 patients to determine a diagnostic strategy for mitochondrial disease. Molecular Genetics and Metabolism. 131(1-2). 66–82. 15 indexed citations
4.
Yarema, Mark, et al.. (2020). Identification of high-impact gene–drug pairs for pharmacogenetic testing in Alberta, Canada. Pharmacogenetics and Genomics. 31(2). 29–39. 6 indexed citations
5.
Kanji, Jamil N., Mathew Diggle, Dennis E. Bulman, et al.. (2020). Retrospective testing of respiratory specimens for COVID-19 to assess for earlier SARS-CoV-2 infections in Alberta, Canada. Journal of the Association of Medical Microbiology and Infectious Disease Canada. 6(1). 10–15. 6 indexed citations
6.
Banerjee, Mayukh, Denis Arutyunov, Hanna Kolski, et al.. (2019). The novel p.Ser263Phe mutation in the human high‐affinity choline transporter 1 (CHT1/ SLC5A7 ) causes a lethal form of fetal akinesia syndrome. Human Mutation. 40(10). 1676–1683. 14 indexed citations
7.
Newell, Christopher, Aneal Khan, David S. Sinasac, et al.. (2019). Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial disease. Neurology Genetics. 5(3). e336–e336. 4 indexed citations
8.
Hume, Stacey, Tanya N. Nelson, Marsha Speevak, et al.. (2019). CCMG practice guideline: laboratory guidelines for next-generation sequencing. Journal of Medical Genetics. 56(12). 792–800. 27 indexed citations
9.
Souza, Andrea de, Susan Christian, Stacey Hume, et al.. (2019). Newborn Screening: Current Status in Alberta, Canada. International Journal of Neonatal Screening. 5(4). 37–37. 9 indexed citations
10.
Newell, Christopher, et al.. (2018). Plasma-derived cell-free mitochondrial DNA: A novel non-invasive methodology to identify mitochondrial DNA haplogroups in humans. Molecular Genetics and Metabolism. 125(4). 332–337. 19 indexed citations
11.
Knoppers, Bartha Maria, Arthur Leader, Stacey Hume, et al.. (2017). Mitochondrial Replacement Therapy: The Road to the Clinic in Canada. Journal of Obstetrics and Gynaecology Canada. 39(10). 916–918. 6 indexed citations
12.
13.
Ma, Tianchi, Madeline Couse, Stacey Hume, et al.. (2014). An automated hand-held CMOS-based instrument for hand-held mutation detection via electrophoresis. 7. 8–12.
14.
Greenway, Steven C., Ross McLeod, Stacey Hume, et al.. (2013). Exome Sequencing Identifies a Novel Variant in ACTC1 Associated With Familial Atrial Septal Defect. Canadian Journal of Cardiology. 30(2). 181–187. 29 indexed citations
15.
Scott, Patrick, et al.. (2012). Toward Optimal Detection of the Common Prenatal Aneuploidies by Quantitative Fluorescent-Polymerase Chain Reaction: Comparison of Two Commercial Assays. Genetic Testing and Molecular Biomarkers. 16(8). 943–947. 1 indexed citations
16.
MacDonald, Ian M., et al.. (2012). Copy Number Variant Analysis in CHM to Detect Duplications Underlying Choroideremia. Ophthalmic Genetics. 34(4). 229–233. 12 indexed citations
17.
Christian, Susan, Margaret Lilley, Stacey Hume, Patrick Scott, & Martin J. Somerville. (2011). Defining the Role of Laboratory Genetic Counselor. Journal of Genetic Counseling. 21(4). 605–611. 25 indexed citations
18.
Gilchrist, Dawna, et al.. (2011). How Much Is Enough? Weighing the Evidence for Mutation Pathogenicity. Canadian Journal of Cardiology. 28(1). 119.e9–119.e9. 4 indexed citations
19.
Lilley, Margaret, Susan Christian, Stacey Hume, et al.. (2010). Newborn screening for cystic fibrosis in Alberta: Two years of experience. Paediatrics & Child Health. 15(9). 590–594. 15 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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Breakdown of academic impact, for papers by Lina Ghaloul‐Gonzalez Breakdown of academic impact, for papers by Lee Zellmer Breakdown of academic impact, for papers by Engela Honey Breakdown of academic impact, for papers by Ana Vega Breakdown of academic impact, for papers by Karina Meden Sørensen Breakdown of academic impact, for papers by William Lee Breakdown of academic impact, for papers by Joshua L. Deignan Breakdown of academic impact, for papers by Pouria Mashouri Breakdown of academic impact, for papers by Olga Shamardina
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