Allison Werner‐Lin

1.7k total citations
61 papers, 1.0k citations indexed

About

Allison Werner‐Lin is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Sociology and Political Science. According to data from OpenAlex, Allison Werner‐Lin has authored 61 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Pediatrics, Perinatology and Child Health, 32 papers in Genetics and 22 papers in Sociology and Political Science. Recurrent topics in Allison Werner‐Lin's work include BRCA gene mutations in cancer (25 papers), Family Support in Illness (22 papers) and Childhood Cancer Survivors' Quality of Life (16 papers). Allison Werner‐Lin is often cited by papers focused on BRCA gene mutations in cancer (25 papers), Family Support in Illness (22 papers) and Childhood Cancer Survivors' Quality of Life (16 papers). Allison Werner‐Lin collaborates with scholars based in United States, Australia and Israel. Allison Werner‐Lin's co-authors include Barbara A. Bernhardt, Lindsey Hoskins, Mark H. Greene, Maya Doyle, Frances K. Barg, Sarah A. Walser, Judith L. M. McCoyd, Daniel S. Gardner, Jennifer L. Young and Shana L. Merrill and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Cancer.

In The Last Decade

Allison Werner‐Lin

55 papers receiving 940 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Allison Werner‐Lin United States 19 566 456 311 139 136 61 1.0k
Regina H. Kenen United States 21 640 1.1× 293 0.6× 447 1.4× 99 0.7× 101 0.7× 43 1.2k
Lieve Denayer Belgium 18 592 1.0× 285 0.6× 244 0.8× 84 0.6× 42 0.3× 25 923
Litanja Lodder Netherlands 8 681 1.2× 220 0.5× 332 1.1× 85 0.6× 32 0.2× 11 783
Stephanie A. Cohen United States 17 735 1.3× 238 0.5× 98 0.3× 134 1.0× 52 0.4× 42 1.1k
Tiffani A. DeMarco United States 26 1.5k 2.6× 502 1.1× 478 1.5× 178 1.3× 51 0.4× 56 1.8k
Clinton Finch United States 10 663 1.2× 167 0.4× 151 0.5× 105 0.8× 21 0.2× 11 772
Jonathon Gray United Kingdom 18 439 0.8× 116 0.3× 145 0.5× 75 0.5× 36 0.3× 41 897
Agnes Masny United States 12 625 1.1× 188 0.4× 237 0.8× 119 0.9× 20 0.1× 17 930
Evelyn Parsons United Kingdom 17 425 0.8× 245 0.5× 151 0.5× 194 1.4× 42 0.3× 33 933
Philip R. Reilly United States 14 348 0.6× 165 0.4× 103 0.3× 207 1.5× 46 0.3× 54 1.0k

Countries citing papers authored by Allison Werner‐Lin

Since Specialization
Citations

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

Fields of papers citing papers by Allison Werner‐Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allison Werner‐Lin. 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 Allison Werner‐Lin. The network helps show where Allison Werner‐Lin may publish in the future.

Co-authorship network of co-authors of Allison Werner‐Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Allison Werner‐Lin. A scholar is included among the top collaborators of Allison Werner‐Lin 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 Allison Werner‐Lin. Allison Werner‐Lin 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.
Rising, Camella J., et al.. (2024). Defining the complex needs of families with rare diseases—the example of telomere biology disorders. European Journal of Human Genetics. 32(12). 1615–1623. 1 indexed citations
2.
Rising, Camella J., William M. P. Klein, Alix G. Sleight, et al.. (2024). Diet and physical activity behaviors: how are they related to illness perceptions, coping, and health-related quality of life in young people with hereditary cancer syndromes?. Journal of Behavioral Medicine. 47(4). 707–720. 2 indexed citations
3.
Pearce, Emily, Camella J. Rising, Melissa B. Gilkey, et al.. (2024). “Crying in the Wilderness”—The Use of Web-Based Support in Telomere Biology Disorders: Thematic Analysis. JMIR Formative Research. 8. e64343–e64343.
4.
Pearce, Emily, Camella J. Rising, Allison Werner‐Lin, et al.. (2024). A “rotating menu” of medical uncertainty for families affected by telomere biology disorders: A qualitative interview study. SHILAP Revista de lepidopterología. 6. 100486–100486.
5.
Rising, Camella J., Alix G. Sleight, Patrick Boyd, et al.. (2024). Relating to the Body Under Chronic Cancer Threat: Implications for Psychosocial Health Among Adolescents and Young Adults with Cancer Predisposition Syndromes. Journal of Adolescent and Young Adult Oncology. 14(2). 151–159.
6.
Werner‐Lin, Allison, et al.. (2022). Posttraumatic Growth Following Adverse Childhood Experiences: “My Creative Arts Teacher Got Me Through It”. Psychology and Behavioral Sciences. 11(4). 105–115.
7.
Sleight, Alix G., et al.. (2022). “I can control what I do with my daily life”: Occupational experiences of adolescents and young adults with Li-Fraumeni Syndrome. Journal of Occupational Science. 30(4). 661–672. 6 indexed citations
8.
Werner‐Lin, Allison, Camella J. Rising, Patrick Boyd, et al.. (2022). How do young people with a hereditary cancer predisposition syndrome understand and experience cancer survivorship? “With Li‐Fraumeni syndrome, it’s just an intermission”. Psycho-Oncology. 32(3). 375–382. 4 indexed citations
9.
Werner‐Lin, Allison, et al.. (2022). Embodied risk for families with Li-Fraumeni syndrome: Like electricity through my body. Social Science & Medicine. 301. 114905–114905. 5 indexed citations
10.
Werner‐Lin, Allison, et al.. (2020). Waiting and “weighted down”: the challenge of anticipatory loss for individuals and families with Li-Fraumeni Syndrome. Familial Cancer. 19(3). 259–268. 16 indexed citations
11.
Werner‐Lin, Allison, et al.. (2020). “I need to know if I’m going to die young”: Adolescent and young adult experiences of genetic testing for Li–Fraumeni syndrome. Journal of Psychosocial Oncology. 39(1). 54–73. 16 indexed citations
12.
Werner‐Lin, Allison, Judith L. M. McCoyd, & Barbara A. Bernhardt. (2019). Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable. The Hastings Center Report. 49(S1). S61–S71. 17 indexed citations
13.
Werner‐Lin, Allison, Shana L. Merrill, & Amanda Brandt. (2018). Talking with Children About Adult‐Onset Hereditary Cancer Risk: A Developmental Approach for Parents. Journal of Genetic Counseling. 27(3). 533–548. 23 indexed citations
14.
Werner‐Lin, Allison, et al.. (2018). Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results. American Journal of Medical Genetics Part A. 176(3). 578–588. 21 indexed citations
15.
Lewis, Alexandra, et al.. (2018). A Systematic Review of How Young People Live with Inherited Disease: What Can We Learn for Li-Fraumeni Syndrome?. Journal of Adolescent and Young Adult Oncology. 7(5). 525–545. 24 indexed citations
16.
Werner‐Lin, Allison, Sarah A. Walser, Frances K. Barg, & Barbara A. Bernhardt. (2016). “They Can't Find Anything Wrong with Him, Yet”: Mothers’ experiences of parenting an infant with a prenatally diagnosed copy number variant (CNV). American Journal of Medical Genetics Part A. 173(2). 444–451. 40 indexed citations
17.
Werner‐Lin, Allison, Judith L. M. McCoyd, Maya Doyle, & Sarah Gehlert. (2016). Leadership, Literacy, and Translational Expertise in Genomics: Challenges and Opportunities for Social Work. Health & Social Work. 41(3). e52–e59. 11 indexed citations
18.
Werner‐Lin, Allison, et al.. (2015). Couple’s Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results. Qualitative Health Research. 26(14). 1975–1987. 62 indexed citations
19.
Hoskins, Lindsey, Allison Werner‐Lin, & Mark H. Greene. (2014). In Their Own Words: Treating Very Young BRCA1/2 Mutation-Positive Women with Care and Caution. PLoS ONE. 9(2). e87696–e87696. 27 indexed citations
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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