Taila Hartley

4.3k total citations
54 papers, 1.2k citations indexed

About

Taila Hartley is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Taila Hartley has authored 54 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 27 papers in Molecular Biology and 8 papers in Cancer Research. Recurrent topics in Taila Hartley's work include Genomics and Rare Diseases (27 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Taila Hartley is often cited by papers focused on Genomics and Rare Diseases (27 papers), Genomic variations and chromosomal abnormalities (15 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Taila Hartley collaborates with scholars based in Canada, United States and United Kingdom. Taila Hartley's co-authors include Kym M. Boycott, Kristin D. Kernohan, Jacek Majewski, David A. Dyment, Najmeh Alirezaie, Toby Dylan Hocking, A. Micheil Innes, Martine Tétreault, David R. Adams and Heather Howley and has published in prestigious journals such as Cell, Brain and Neurology.

In The Last Decade

Taila Hartley

51 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Taila Hartley Canada	20	674	591	150	120	102	54	1.2k
Tommaso Pippucci Italy	23	663 1.0×	708 1.2×	215 1.4×	72 0.6×	167 1.6×	71	1.5k
Chandree L. Beaulieu Canada	20	459 0.7×	645 1.1×	93 0.6×	64 0.5×	127 1.2×	33	1.1k
Cuiping Hou United States	20	791 1.2×	740 1.3×	292 1.9×	97 0.8×	78 0.8×	39	1.6k
Kristin D. Kernohan Canada	18	584 0.9×	887 1.5×	105 0.7×	63 0.5×	52 0.5×	49	1.3k
Isabelle Thiffault United States	23	482 0.7×	822 1.4×	96 0.6×	85 0.7×	224 2.2×	65	1.4k
Karen Duran Netherlands	21	575 0.9×	755 1.3×	150 1.0×	136 1.1×	46 0.5×	28	1.4k
Joshua L. Deignan United States	18	753 1.1×	685 1.2×	289 1.9×	113 0.9×	145 1.4×	32	1.6k
Sarah L. Sawyer Canada	15	486 0.7×	589 1.0×	80 0.5×	49 0.4×	99 1.0×	37	1.0k
Steffen Uebe Germany	22	507 0.8×	819 1.4×	137 0.9×	55 0.5×	80 0.8×	58	1.3k
Matthew Hayden United Kingdom	5	511 0.8×	826 1.4×	97 0.6×	41 0.3×	55 0.5×	5	1.4k

Countries citing papers authored by Taila Hartley

Since Specialization

Citations

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

Fields of papers citing papers by Taila Hartley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Taila Hartley

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

All Works

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20 of 20 papers shown

Curtis, Meredith, Thomas Nalpathamkalam, Bhooma Thiruvahindrapuram, et al.. (2025). Leveraging cancer mutation data to inform the pathogenicity classification of germline missense variants. PLoS Genetics. 21(1). e1011540–e1011540.

Warman‐Chardon, Jodi, Taila Hartley, Aren E. Marshall, et al.. (2023). Biallelic SOX8 Variants Associated With Novel Syndrome With Myopathy, Skeletal Deformities, Intellectual Disability, and Ovarian Dysfunction. Neurology Genetics. 9(5). e200088–e200088. 2 indexed citations

Osmond, Matthew, Taila Hartley, Marta Gîrdea, et al.. (2022). PhenomeCentral: 7 years of rare disease matchmaking. Human Mutation. 43(6). 674–681. 11 indexed citations

Hayeems, Robin Z., François P. Bernier, Kym M. Boycott, et al.. (2022). Positioning whole exome sequencing in the diagnostic pathway for rare disease to optimise utility: a protocol for an observational cohort study and an economic evaluation. BMJ Open. 12(10). e061468–e061468. 3 indexed citations

Boycott, Kym M., Taila Hartley, Kristin D. Kernohan, et al.. (2022). Care4Rare Canada: Outcomes from a decade of network science for rare disease gene discovery. The American Journal of Human Genetics. 109(11). 1947–1959. 15 indexed citations

Backman, Keith, Wendy Mears, Joseph de Nanassy, et al.. (2021). A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia. European Journal of Medical Genetics. 64(5). 104193–104193. 5 indexed citations

Pratt, Misty, Chantelle Garritty, Micere Thuku, et al.. (2020). Application of exome sequencing for prenatal diagnosis: a rapid scoping review. Genetics in Medicine. 22(12). 1925–1934. 24 indexed citations

Marshall, Deborah A., Karen V. MacDonald, Sebastian Heidenreich, et al.. (2019). The value of diagnostic testing for parents of children with rare genetic diseases. Genetics in Medicine. 21(12). 2798–2806. 40 indexed citations

Alirezaie, Najmeh, Kristin D. Kernohan, Taila Hartley, Jacek Majewski, & Toby Dylan Hocking. (2018). ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants. The American Journal of Human Genetics. 103(4). 474–483. 141 indexed citations

10.

Hartley, Taila, Eric Bareke, Kym M. Boycott, et al.. (2017). Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1. Journal of Human Genetics. 62(6). 661–663. 11 indexed citations

11.

Johnstone, Devon L., Yoshiko Murakami, Kristin D. Kernohan, et al.. (2017). Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy. Human Molecular Genetics. 26(9). 1706–1715. 33 indexed citations

12.

Zambonin, Jessica L., David A. Dyment, Ryan E. Lamont, et al.. (2017). A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy. Neurogenetics. 19(1). 61–65. 11 indexed citations

13.

Kernohan, Kristin D., Taila Hartley, Najmeh Alirezaie, et al.. (2017). Evaluation of exome filtering techniques for the analysis of clinically relevant genes. Human Mutation. 39(2). 197–201. 13 indexed citations

14.

Nowaczyk, Małgorzata J.M., Lijia Huang, Mark A. Tarnopolsky, et al.. (2016). A novel multisystem disease associated with recessive mutations in the tyrosyl‐tRNA synthetase (YARS) gene. American Journal of Medical Genetics Part A. 173(1). 126–134. 31 indexed citations

15.

Brown, Alison, Martine Tétreault, David A. Dyment, et al.. (2016). Concordance between whole‐exome sequencing and clinical Sanger sequencing: implications for patient care. Molecular Genetics & Genomic Medicine. 4(5). 504–512. 25 indexed citations

16.

Stray‐Pedersen, Asbjørg, Jan-Maarten Cobben, Trine Prescott, et al.. (2015). Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. The American Journal of Human Genetics. 98(1). 202–209. 35 indexed citations

17.

Warman‐Chardon, Jodi, Chandree L. Beaulieu, Taila Hartley, Kym M. Boycott, & David A. Dyment. (2015). Axons to Exons: the Molecular Diagnosis of Rare Neurological Diseases by Next-Generation Sequencing. Current Neurology and Neuroscience Reports. 15(9). 64–64. 24 indexed citations

18.

Dyment, David A., Martine Tétreault, Chandree L. Beaulieu, et al.. (2014). Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study. Clinical Genetics. 88(1). 34–40. 64 indexed citations

19.

Hartley, Taila, Luca Cavallone, Nelly Sabbaghian, et al.. (2014). Mutation analysis of PALB2 in BRCA1 and BRCA2-negative breast and/or ovarian cancer families from Eastern Ontario, Canada. Hereditary Cancer in Clinical Practice. 12(1). 19–19. 18 indexed citations

20.

Aldinger, Kimberly A., Martine Tétreault, Jennifer C. Dempsey, et al.. (2014). Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy. The American Journal of Human Genetics. 95(2). 227–234. 78 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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