Jennifer Boyle

558 total citations
16 papers, 404 citations indexed

About

Jennifer Boyle is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Jennifer Boyle has authored 16 papers receiving a total of 404 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Jennifer Boyle's work include DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (3 papers) and Genetic Syndromes and Imprinting (2 papers). Jennifer Boyle is often cited by papers focused on DNA Repair Mechanisms (5 papers), CRISPR and Genetic Engineering (3 papers) and Genetic Syndromes and Imprinting (2 papers). Jennifer Boyle collaborates with scholars based in United States, United Kingdom and Germany. Jennifer Boyle's co-authors include Sikandar G. Khan, Kenneth H. Kraemer, Rita A. Kandel, Tony F. Cruz, Kyoko Imoto, John J. DiGiovanna, Deborah Tamura, Takahiro Ueda, Kyu‐Seon Oh and J. Ross Hawkins and has published in prestigious journals such as SHILAP Revista de lepidopterología, Ophthalmology and Osteoarthritis and Cartilage.

In The Last Decade

Jennifer Boyle

15 papers receiving 399 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jennifer Boyle United States	11	245	114	68	65	52	16	404
Yoshifumi Ninomiya Japan	7	173 0.7×	62 0.5×	36 0.5×	73 1.1×	28 0.5×	7	416
Kate E. Gregory United States	7	187 0.8×	71 0.6×	102 1.5×	107 1.6×	28 0.5×	8	443
Ola Tingby Sweden	8	279 1.1×	47 0.4×	38 0.6×	76 1.2×	55 1.1×	8	451
Frédéric Kesteloot Belgium	5	170 0.7×	109 1.0×	36 0.5×	57 0.9×	37 0.7×	6	353
Ravikumar Rallapalli United States	10	433 1.8×	60 0.5×	67 1.0×	74 1.1×	30 0.6×	13	573
Y Takasaki Japan	5	224 0.9×	38 0.3×	30 0.4×	57 0.9×	32 0.6×	7	413
Yoshinari Saito Japan	9	156 0.6×	35 0.3×	148 2.2×	92 1.4×	33 0.6×	10	406
Harikiran Nistala United States	8	184 0.8×	66 0.6×	56 0.8×	218 3.4×	41 0.8×	11	375
Albane A. Bizet Canada	6	279 1.1×	55 0.5×	25 0.4×	56 0.9×	18 0.3×	8	427
A. M. Vagner‐Capodano France	14	245 1.0×	39 0.3×	28 0.4×	95 1.5×	49 0.9×	29	503

Countries citing papers authored by Jennifer Boyle

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Boyle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Boyle

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

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Connors, Dana E., Jeff Allen, Jennifer Boyle, et al.. (2020). International liquid biopsy standardization alliance white paper. Critical Reviews in Oncology/Hematology. 156. 103112–103112. 70 indexed citations

Hawkins, J. Ross, et al.. (2019). The Genomic Health of Human Pluripotent Stem Cells: Genomic Instability and the Consequences on Nuclear Organization. Frontiers in Genetics. 9. 623–623. 24 indexed citations

O’Connor, Daniel, Jenny Buckland, Neil Almond, et al.. (2019). Commonly setting biological standards in rare diseases. Expert Opinion on Orphan Drugs. 7(7-8). 305–314. 1 indexed citations

Chai, Hongyan, et al.. (2019). Integrated FISH, Karyotyping and aCGH Analyses for Effective Prenatal Diagnosis of Common Aneuploidies and Other Cytogenomic Abnormalities. SHILAP Revista de lepidopterología. 7(2). 16–16. 6 indexed citations

Boyle, Jennifer, et al.. (2017). Building a Research Community. ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam).

Brooks, Brian P., A. Thompson, Rachel Bishop, et al.. (2013). Ocular Manifestations of Xeroderma Pigmentosum. Ophthalmology. 120(7). 1324–1336. 57 indexed citations

Tamura, Deborah, Sikandar G. Khan, Melissa A. Merideth, et al.. (2012). Effect of mutations in XPD(ERCC2) on pregnancy and prenatal development in mothers of patients with trichothiodystrophy or xeroderma pigmentosum. European Journal of Human Genetics. 20(12). 1308–1310. 8 indexed citations

Zhou, Xiaolong, Sikandar G. Khan, Deborah Tamura, et al.. (2012). Abnormal XPD-induced nuclear receptor transactivation in DNA repair disorders: trichothiodystrophy and xeroderma pigmentosum. European Journal of Human Genetics. 21(8). 831–837. 18 indexed citations

Boyle, Jennifer, Malcolm Hawkins, David Barton, et al.. (2011). Establishment of the first WHO international genetic reference panel for Prader Willi and Angelman syndromes. European Journal of Human Genetics. 19(8). 857–864. 12 indexed citations

10.

Hawkins, Malcolm, Jennifer Boyle, Rob Elles, et al.. (2010). Preparation and validation of the first WHO international genetic reference panel for Fragile X syndrome. European Journal of Human Genetics. 19(1). 10–17. 20 indexed citations

11.

Khan, Sikandar G., Koji Yamanegi, Zhi‐Ming Zheng, et al.. (2009). XPCbranch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients. Human Mutation. 31(2). 167–175. 14 indexed citations

12.

Emmert, Steffen, Takahiro Ueda, Urs Zumsteg, et al.. (2008). Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2). Experimental Dermatology. 18(1). 64–68. 21 indexed citations

13.

Boyle, Jennifer, Takahiro Ueda, Kyoko Imoto, et al.. (2008). Persistence of repair proteins at unrepaired DNA damage distinguishes diseases withERCC2(XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy. Human Mutation. 29(10). 1194–1208. 57 indexed citations

14.

Oh, Kyu‐Seon, Kyoko Imoto, Jennifer Boyle, Sikandar G. Khan, & Kenneth H. Kraemer. (2007). Influence of XPB helicase on recruitment and redistribution of nucleotide excision repair proteins at sites of UV-induced DNA damage. DNA repair. 6(9). 1359–1370. 27 indexed citations

15.

Boyle, Jennifer, et al.. (1995). Characterization of proteoglycan accumulation during formation of cartilagenous tissue in vitro. Osteoarthritis and Cartilage. 3(2). 117–125. 66 indexed citations

16.

Boyle, Jennifer, et al.. (1995). OSTEOARTHRITIS and CARTILAGE Characterization of proteoglycan accumulation during formation - of cartilagenous tissue in vitro. 3 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.

Explore authors with similar magnitude of impact