Gillian W. Hooker

2.0k total citations
55 papers, 1.5k citations indexed

About

Gillian W. Hooker is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Gillian W. Hooker has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Genetics, 13 papers in Pediatrics, Perinatology and Child Health and 11 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Gillian W. Hooker's work include BRCA gene mutations in cancer (43 papers), Genomics and Rare Diseases (19 papers) and Cancer Genomics and Diagnostics (9 papers). Gillian W. Hooker is often cited by papers focused on BRCA gene mutations in cancer (43 papers), Genomics and Rare Diseases (19 papers) and Cancer Genomics and Diagnostics (9 papers). Gillian W. Hooker collaborates with scholars based in United States, Canada and Iceland. Gillian W. Hooker's co-authors include G. Shirleen Roeder, Barbara B. Biesecker, Patricia A. Deverka, Michael P. Douglas, Kathryn A. Phillips, Leslie G. Biesecker, James A. Langeland, Adam Neidert, Jing Li and Beth N. Peshkin and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and SHILAP Revista de lepidopterología.

In The Last Decade

Gillian W. Hooker

51 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gillian W. Hooker United States	24	947	386	296	242	143	55	1.5k
Christine Patch United Kingdom	24	1.1k 1.1×	257 0.7×	293 1.0×	419 1.7×	85 0.6×	80	1.6k
Leigh Jackson United Kingdom	20	549 0.6×	270 0.7×	270 0.9×	171 0.7×	92 0.6×	47	1.2k
Chris Jacobs Australia	19	1.0k 1.1×	343 0.9×	254 0.9×	196 0.8×	290 2.0×	95	1.7k
Stephanie A. Cohen United States	17	735 0.8×	134 0.3×	183 0.6×	238 1.0×	214 1.5×	42	1.1k
Vickie L. Venne United States	15	536 0.6×	153 0.4×	138 0.5×	155 0.6×	135 0.9×	27	848
Clinton Finch United States	10	663 0.7×	105 0.3×	114 0.4×	167 0.7×	155 1.1×	11	772
Katie L. Lewis United States	21	591 0.6×	99 0.3×	242 0.8×	116 0.5×	77 0.5×	49	1.0k
Joseph D. McInerney United States	13	641 0.7×	207 0.5×	218 0.7×	210 0.9×	68 0.5×	55	1.0k
Petra G. Frets Netherlands	20	879 0.9×	212 0.5×	138 0.5×	388 1.6×	62 0.4×	32	1.4k
Beverly M. Yashar United States	24	561 0.6×	1.1k 2.9×	151 0.5×	183 0.8×	68 0.5×	67	2.1k

Countries citing papers authored by Gillian W. Hooker

Since Specialization

Citations

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

Fields of papers citing papers by Gillian W. Hooker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gillian W. Hooker. 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 Gillian W. Hooker. The network helps show where Gillian W. Hooker may publish in the future.

Co-authorship network of co-authors of Gillian W. Hooker

This figure shows the co-authorship network connecting the top 25 collaborators of Gillian W. Hooker. A scholar is included among the top collaborators of Gillian W. Hooker 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 Gillian W. Hooker. Gillian W. Hooker 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

Williams, Zachary J., et al.. (2024). Attitudes of autistic adults toward genetic testing for autism. Journal of Genetic Counseling. 34(1). e1918–e1918. 5 indexed citations

Mittendorf, Kathleen F., Harris T. Bland, Gillian W. Hooker, et al.. (2024). Family history and cancer risk study (FOREST): A clinical trial assessing electronic patient-directed family history input for identifying patients at risk of hereditary cancer. Contemporary Clinical Trials. 148. 107714–107714.

Hooker, Gillian W., et al.. (2023). Development and validation of the Vanderbilt PRS-KS, an instrument to quantify polygenic risk score knowledge. SHILAP Revista de lepidopterología. 1(1). 100822–100822.

Bland, Harris T., Marian J. Gilmore, Gillian W. Hooker, et al.. (2023). Conducting inclusive research in genetics for transgender, gender‐diverse, and sex‐diverse individuals: Case analyses and recommendations from a clinical genomics study. Journal of Genetic Counseling. 33(4). 772–785. 5 indexed citations

Beskow, Laura M., et al.. (2023). Stigma manifestations in cardiomyopathy care impact outcomes for black patients: a qualitative study. BMC Cardiovascular Disorders. 23(1). 553–553. 1 indexed citations

Deverka, Patricia A., Janis Geary, Charles Mathews, et al.. (2023). Payer reimbursement practices and incentives for improving interpretation of germline genetic testing. Journal of Law and the Biosciences. 10(2). lsad020–lsad020. 4 indexed citations

Cragun, Deborah, Jason W. Beckstead, Meagan Farmer, et al.. (2021). IMProving care After inherited Cancer Testing (IMPACT) study: protocol of a randomized trial evaluating the efficacy of two interventions designed to improve cancer risk management and family communication of genetic test results. BMC Cancer. 21(1). 1099–1099. 5 indexed citations

Peshkin, Beth N., Claudine Isaacs, Shawna C. Willey, et al.. (2020). Predictors of contralateral prophylactic mastectomy in genetically high risk newly diagnosed breast cancer patients. Breast Cancer Research and Treatment. 180(1). 177–185. 9 indexed citations

Popejoy, Alice B., Kristy Crooks, Stephanie M. Fullerton, et al.. (2020). Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures. The American Journal of Human Genetics. 107(1). 72–82. 50 indexed citations

10.

Turbitt, Erin, et al.. (2017). Adaptation of couples living with a high risk of breast/ovarian cancer and the association with risk-reducing surgery. Familial Cancer. 17(4). 485–493. 6 indexed citations

11.

Jacobs, Aryana, Marc D. Schwartz, Heiðdís Valdimarsdóttir, et al.. (2016). Patient and genetic counselor perceptions of in-person versus telephone genetic counseling for hereditary breast/ovarian cancer. Familial Cancer. 15(4). 529–539. 25 indexed citations

12.

Hooker, Gillian W., et al.. (2016). Engagement and communication among participants in the ClinSeq Genomic Sequencing Study. Genetics in Medicine. 19(1). 98–103. 4 indexed citations

13.

Lewis, Katie L., et al.. (2015). Participant use and communication of findings from exome sequencing: a mixed-methods study. Genetics in Medicine. 18(6). 577–583. 50 indexed citations

14.

Lewis, Katie L., Paul K. J. Han, Gillian W. Hooker, et al.. (2015). Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology. PLoS ONE. 10(7). e0132690–e0132690. 39 indexed citations

15.

Abrams, Leah, Colleen M. McBride, Gillian W. Hooker, Joseph N. Cappella, & Laura M. Koehly. (2015). The Many Facets of Genetic Literacy: Assessing the Scalability of Multiple Measures for Broad Use in Survey Research. PLoS ONE. 10(10). e0141532–e0141532. 37 indexed citations

16.

Rodriguez, Sally, Debra Roter, Carlos Castillo‐Salgado, Gillian W. Hooker, & Lori H. Erby. (2015). Translation and validation of a Spanish-language genetic health literacy screening tool.. Health Psychology. 34(2). 120–129. 11 indexed citations

17.

Graves, Kristi D., Rachel Nusbaum, Gillian W. Hooker, et al.. (2013). Behavioral and psychosocial responses to genomic testing for colorectal cancer risk. Genomics. 102(2). 123–130. 31 indexed citations

18.

Sapp, Julie C., Dan Dong, Catherine Stark, et al.. (2013). Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children. Clinical Genetics. 85(2). 120–126. 99 indexed citations

19.

Lewis, Katie L., et al.. (2013). Preferences for results delivery from exome sequencing/genome sequencing. Genetics in Medicine. 16(6). 442–447. 51 indexed citations

20.

Peay, Holly L., Gillian W. Hooker, Layla Kassem, & Barbara B. Biesecker. (2009). Family risk and related education and counseling needs: Perceptions of adults with bipolar disorder and siblings of adults with bipolar disorder. American Journal of Medical Genetics Part A. 149A(3). 364–371. 29 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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