Collette K. Hand

2.2k total citations
26 papers, 1.5k citations indexed

About

Collette K. Hand is a scholar working on Neurology, Neurology and Molecular Biology. According to data from OpenAlex, Collette K. Hand has authored 26 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 8 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in Collette K. Hand's work include Neurological diseases and metabolism (8 papers), Amyotrophic Lateral Sclerosis Research (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Collette K. Hand is often cited by papers focused on Neurological diseases and metabolism (8 papers), Amyotrophic Lateral Sclerosis Research (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Collette K. Hand collaborates with scholars based in Canada, Ireland and United Kingdom. Collette K. Hand's co-authors include Guy A. Rouleau, Denise A. Figlewicz, Rebecca S. Devon, Michael R. Hayden, Nollaig A. Parfrey, Yoshinori Okada, Jennifer Skaug, Jawad Khoris, Thomas A. Kwiatkowski and William Camu and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Annals of Neurology.

In The Last Decade

Collette K. Hand

26 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Collette K. Hand Canada 14 769 628 492 310 251 26 1.5k
Scott M. Gianino United States 21 742 1.0× 483 0.8× 435 0.9× 199 0.6× 298 1.2× 23 1.8k
Sylvie Tuffery‐Giraud France 26 444 0.6× 1.2k 2.0× 269 0.5× 111 0.4× 432 1.7× 72 2.0k
Adrian J. Waite United Kingdom 17 725 0.9× 643 1.0× 352 0.7× 146 0.5× 324 1.3× 20 1.3k
Dante J. Morassutti United States 11 193 0.3× 749 1.2× 243 0.5× 227 0.7× 675 2.7× 14 1.8k
Toby A. Ferguson United States 16 279 0.4× 382 0.6× 180 0.4× 92 0.3× 650 2.6× 32 1.2k
Giles D. Watts United States 16 983 1.3× 844 1.3× 232 0.5× 391 1.3× 358 1.4× 23 2.0k
James N. Sleigh United Kingdom 26 350 0.5× 1.3k 2.1× 661 1.3× 118 0.4× 695 2.8× 60 1.9k
Giorgia Dina Italy 21 376 0.5× 1.1k 1.7× 459 0.9× 513 1.7× 1.2k 4.6× 32 2.5k
Ritchie Ho United States 16 622 0.8× 1.2k 1.9× 380 0.8× 376 1.2× 351 1.4× 22 2.0k
Elizabeth B. Moloney Netherlands 14 343 0.4× 339 0.5× 129 0.3× 85 0.3× 322 1.3× 15 910

Countries citing papers authored by Collette K. Hand

Since Specialization
Citations

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

Fields of papers citing papers by Collette K. Hand

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Collette K. Hand. 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 Collette K. Hand. The network helps show where Collette K. Hand may publish in the future.

Co-authorship network of co-authors of Collette K. Hand

This figure shows the co-authorship network connecting the top 25 collaborators of Collette K. Hand. A scholar is included among the top collaborators of Collette K. Hand 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 Collette K. Hand. Collette K. Hand 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.
Hand, Collette K., et al.. (2024). Low incidence of BRAF and NRAS mutations in a population with a high incidence of melanoma. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 484(3). 475–479. 1 indexed citations
2.
Barrett, Maurice, Collette K. Hand, Fergus Shanahan, Thomas J. Murphy, & Paul W. O’Toole. (2020). Mutagenesis by Microbe: the Role of the Microbiota in Shaping the Cancer Genome. Trends in cancer. 6(4). 277–287. 64 indexed citations
3.
Hardiman, Orla, Donal Costigan, Bryan Lynch, et al.. (2014). Andersen–Tawil Syndrome With Early Fixed Myopathy. Journal of Clinical Neuromuscular Disease. 16(2). 79–82. 11 indexed citations
4.
Parfrey, Nollaig A., et al.. (2012). A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree. Neurogenetics. 13(2). 125–132. 8 indexed citations
5.
Hand, Collette K., Geneviève Bernard, Marie‐Pierre Dubé, Michael Shevell, & Guy A. Rouleau. (2012). A Novel PLP1 Mutation Further Expands the Clinical Heterogeneity at the Locus. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 39(2). 220–224. 4 indexed citations
6.
Hand, Collette K., et al.. (2007). A Novel ATP1A2 Gene Mutation in an Irish Familial Hemiplegic Migraine Kindred. Headache The Journal of Head and Face Pain. 48(1). 101–108. 29 indexed citations
7.
8.
Stefanelli, Mark, et al.. (2004). A founder effect in three large Newfoundland families with a novel clinically variable spastic ataxia and supranuclear gaze palsy. American Journal of Medical Genetics Part A. 131A(3). 249–254. 6 indexed citations
9.
Koenekoop, Robert K., Magali Loyer, Collette K. Hand, et al.. (2003). Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families. American Journal of Ophthalmology. 136(4). 678–687. 64 indexed citations
10.
Hand, Collette K., Rebecca S. Devon, François Gros‐Louis, et al.. (2003). Mutation Screening of the ALS2 Gene in Sporadic and Familial Amyotrophic Lateral Sclerosis. Archives of Neurology. 60(12). 1768–1768. 36 indexed citations
11.
Dupré, Nicolas, Dominique J. Verlaan, Collette K. Hand, et al.. (2003). Linkage to the CCM2 Locus and Genetic Heterogeneity in Familial Cerebral Cavernous Malformation. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 30(2). 122–128. 24 indexed citations
12.
Hand, Collette K., Jawad Khoris, François Salachas, et al.. (2002). A Novel Locus for Familial Amyotrophic Lateral Sclerosis, on Chromosome 18q. The American Journal of Human Genetics. 70(1). 251–256. 95 indexed citations
13.
Meijer, Inge A., et al.. (2002). A Locus for Autosomal Dominant Hereditary Spastic Ataxia, SAX1,Maps to Chromosome 12p13. The American Journal of Human Genetics. 70(3). 763–769. 20 indexed citations
14.
Hand, Collette K. & Guy A. Rouleau. (2002). Familial amyotrophic lateral sclerosis. Muscle & Nerve. 25(2). 135–159. 166 indexed citations
15.
Meijer, Inge A., Collette K. Hand, Patrick Cossette, Denise A. Figlewicz, & Guy A. Rouleau. (2002). Spectrum of SPG4 Mutations in a Large Collection of North American Families With Hereditary Spastic Paraplegia. Archives of Neurology. 59(2). 281–281. 61 indexed citations
16.
Hand, Collette K., et al.. (2001). Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family. Annals of Neurology. 49(2). 267–271. 59 indexed citations
17.
Dupré, Nicolas, et al.. (2001). A Founder Mutation in French-Canadian Families with X-linked Hereditary Neuropathy. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 28(1). 51–55. 5 indexed citations
18.
Lamartine, Jérôme, Zoha Kibar, Isabelle Lanneluc, et al.. (2000). Mutations in GJB6 cause hidrotic ectodermal dysplasia. Nature Genetics. 26(2). 142–144. 184 indexed citations
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20.

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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