William P. Bone

1.4k total citations
13 papers, 484 citations indexed

About

William P. Bone is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, William P. Bone has authored 13 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in William P. Bone's work include Genomics and Rare Diseases (5 papers), Genetic Associations and Epidemiology (4 papers) and Cancer Genomics and Diagnostics (3 papers). William P. Bone is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetic Associations and Epidemiology (4 papers) and Cancer Genomics and Diagnostics (3 papers). William P. Bone collaborates with scholars based in United States, Germany and Canada. William P. Bone's co-authors include Melissa Haendel, Peter N. Robinson, Orion J. Buske, Nicole Washington, Julius O.B. Jacobsen, Sebastian Köhler, Manuel Holtgrewe, Max Schubach, Marten Jäger and Enrico Siragusa and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Nature Genetics.

In The Last Decade

William P. Bone

13 papers receiving 475 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William P. Bone United States 10 291 276 79 33 21 13 484
Zachary Zappala United States 6 266 0.9× 244 0.9× 73 0.9× 16 0.5× 9 0.4× 6 420
Mi-Ryung Han South Korea 11 208 0.7× 104 0.4× 108 1.4× 62 1.9× 28 1.3× 24 409
Jorge Urresti United States 8 459 1.6× 240 0.9× 48 0.6× 32 1.0× 5 0.2× 12 659
Elizabeth Hynes United States 11 416 1.4× 293 1.1× 111 1.4× 20 0.6× 7 0.3× 16 876
Vicente A. Yépez Germany 11 396 1.4× 227 0.8× 69 0.9× 29 0.9× 6 0.3× 22 562
Janine Meienberg Switzerland 9 219 0.8× 327 1.2× 94 1.2× 13 0.4× 7 0.3× 12 512
Lisa Mahanta United States 11 235 0.8× 195 0.7× 73 0.9× 15 0.5× 8 0.4× 15 552
Philip M. Boone United States 15 211 0.7× 240 0.9× 55 0.7× 31 0.9× 5 0.2× 21 541
Sophie Tritschler Germany 12 505 1.7× 158 0.6× 94 1.2× 42 1.3× 22 1.0× 13 745
Sue Povey United Kingdom 4 301 1.0× 90 0.3× 62 0.8× 41 1.2× 19 0.9× 4 432

Countries citing papers authored by William P. Bone

Since Specialization
Citations

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

Fields of papers citing papers by William P. Bone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William P. Bone. 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 William P. Bone. The network helps show where William P. Bone may publish in the future.

Co-authorship network of co-authors of William P. Bone

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

All Works

13 of 13 papers shown
1.
Lazar, Nathan H., Safiye Çelik, Lu Chen, et al.. (2024). High-resolution genome-wide mapping of chromosome-arm-scale truncations induced by CRISPR–Cas9 editing. Nature Genetics. 56(7). 1482–1493. 19 indexed citations
2.
Gawronski, Katerina A.B., William P. Bone, YoSon Park, et al.. (2023). Evaluating the Contribution of Cell Type–Specific Alternative Splicing to Variation in Lipid Levels. Circulation Genomic and Precision Medicine. 16(3). 248–257. 2 indexed citations
3.
Chen, Brian Y., et al.. (2022). ColocQuiaL: a QTL-GWAS colocalization pipeline. Bioinformatics. 38(18). 4409–4411. 11 indexed citations
4.
Zhang, Xinyuan, Anastasia Lucas, Yogasudha Veturi, et al.. (2022). Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature Communications. 13(1). 3428–3428. 8 indexed citations
5.
Bone, William P., Katherine M. Siewert, Anupama Jha, et al.. (2021). Multi-trait association studies discover pleiotropic loci between Alzheimer’s disease and cardiometabolic traits. Alzheimer s Research & Therapy. 13(1). 34–34. 20 indexed citations
6.
Hu, Wenxiang, Angela H. Weller, Eric R. Chen, et al.. (2019). Natural human genetic variation determines basal and inducible expression of PM20D1 , an obesity-associated gene. Proceedings of the National Academy of Sciences. 116(46). 23232–23242. 29 indexed citations
7.
Pusey, Barbara N., David R. Adams, C. Christopher Lau, et al.. (2016). Explorations to improve the completeness of exome sequencing. BMC Medical Genomics. 9(1). 56–56. 7 indexed citations
8.
Smedley, Damian, Julius O.B. Jacobsen, Marten Jäger, et al.. (2015). Next-generation diagnostics and disease-gene discovery with the Exomiser. Nature Protocols. 10(12). 2004–2015. 228 indexed citations
9.
Buske, Orion J., Marta Gîrdea, Sergiu Dumitriu, et al.. (2015). PhenomeCentral: A Portal for Phenotypic and Genotypic Matchmaking of Patients with Rare Genetic Diseases. Human Mutation. 36(10). 931–940. 75 indexed citations
10.
Trehan, Aditi, Jacqueline M. Brady, Valerie V. Maduro, et al.. (2015). MED23‐associated intellectual disability in a non‐consanguineous family. American Journal of Medical Genetics Part A. 167(6). 1374–1380. 21 indexed citations
11.
Bhattacharyya, Nisan, Lynne A. Wolfe, William P. Bone, et al.. (2015). Impaired osteoblast and osteoclast function characterize the osteoporosis of Snyder - Robinson syndrome. Orphanet Journal of Rare Diseases. 10(1). 27–27. 27 indexed citations
12.
Davids, Mariska, Megan Kane, Miao He, et al.. (2015). Disruption of Golgi morphology and altered protein glycosylation in PLA2G6-associated neurodegeneration. Journal of Medical Genetics. 53(3). 180–189. 24 indexed citations
13.
Smedley, Damian, Sebastian Köhler, William P. Bone, et al.. (2014). Use of animal models for exome prioritization of rare disease genes. Orphanet Journal of Rare Diseases. 9(Suppl 1). O19–O19. 13 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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