William A. Scaringe

822 total citations
22 papers, 609 citations indexed

About

William A. Scaringe is a scholar working on Molecular Biology, Cancer Research and Hematology. According to data from OpenAlex, William A. Scaringe has authored 22 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Cancer Research and 7 papers in Hematology. Recurrent topics in William A. Scaringe's work include CRISPR and Genetic Engineering (7 papers), Cancer Genomics and Diagnostics (7 papers) and Hemophilia Treatment and Research (6 papers). William A. Scaringe is often cited by papers focused on CRISPR and Genetic Engineering (7 papers), Cancer Genomics and Diagnostics (7 papers) and Hemophilia Treatment and Research (6 papers). William A. Scaringe collaborates with scholars based in United States, Canada and China. William A. Scaringe's co-authors include Steve S. Sommer, Kathleen A. Hill, Jinong Feng, Kelly Gonzalez, Jicheng Wang, Victoria L. Buettner, Dongqing Gu, Wenjia Song, Carol K. Kasper and Leonard L. Heston and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Biochemical and Biophysical Research Communications and Human Molecular Genetics.

In The Last Decade

William A. Scaringe

22 papers receiving 599 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
William A. Scaringe United States	14	468	169	126	72	66	22	609
Daniel Savic United States	13	708 1.5×	230 1.4×	118 0.9×	38 0.5×	80 1.2×	26	981
Walter Zumkeller Germany	11	228 0.5×	218 1.3×	60 0.5×	24 0.3×	38 0.6×	17	497
Kevin Iori United States	7	354 0.8×	155 0.9×	72 0.6×	33 0.5×	37 0.6×	8	579
Lidia Lopez‐Serra Spain	12	776 1.7×	194 1.1×	64 0.5×	87 1.2×	68 1.0×	12	861
Lijun Xiong China	12	869 1.9×	207 1.2×	79 0.6×	87 1.2×	30 0.5×	16	1.0k
Karin Segers Belgium	15	565 1.2×	533 3.2×	122 1.0×	27 0.4×	25 0.4×	29	835
Daniel Biggs United Kingdom	9	428 0.9×	132 0.8×	64 0.5×	100 1.4×	16 0.2×	15	782
Mizuyo Kojima Japan	13	514 1.1×	130 0.8×	63 0.5×	16 0.2×	51 0.8×	16	597
Kulwant Singh Canada	8	510 1.1×	70 0.4×	75 0.6×	25 0.3×	30 0.5×	14	612
Rubén Agrelo Spain	12	696 1.5×	214 1.3×	153 1.2×	33 0.5×	104 1.6×	17	879

Countries citing papers authored by William A. Scaringe

Since Specialization

Citations

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

Fields of papers citing papers by William A. Scaringe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William A. Scaringe

This figure shows the co-authorship network connecting the top 25 collaborators of William A. Scaringe. A scholar is included among the top collaborators of William A. Scaringe 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 A. Scaringe. William A. Scaringe 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

Strom, Samuel P., Waheeda A. Hossain, Melina Grigorian, et al.. (2021). A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics. Frontiers in Genetics. 12. 608889–608889. 17 indexed citations

Brewer, Casey, William A. Scaringe, Jie Li, et al.. (2020). The Value of Parental Testing by Next-Generation Sequencing Includes the Detection of Germline Mosaicism. Journal of Molecular Diagnostics. 22(5). 670–678. 11 indexed citations

Scaringe, William A., Kai Li, Dongqing Gu, et al.. (2008). Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates. Human Molecular Genetics. 17(18). 2910–2918. 10 indexed citations

Song, Wenjia, Wenyan Li, Jinong Feng, et al.. (2008). Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia. Biochemical and Biophysical Research Communications. 367(3). 700–706. 73 indexed citations

Wang, Jicheng, Kelly Gonzalez, William A. Scaringe, et al.. (2007). Evidence for mutation showers. Proceedings of the National Academy of Sciences. 104(20). 8403–8408. 56 indexed citations

Gu, Dongqing, William A. Scaringe, Kai Li, et al.. (2007). Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature. Human Mutation. 28(8). 760–770. 46 indexed citations

Gonzalez, Kelly, Kathleen A. Hill, Kai Li, et al.. (2006). Somatic microindels: analysis in mouse soma and comparison with the human germline. Human Mutation. 28(1). 69–80. 15 indexed citations

Hill, Kathleen A., Kelly Gonzalez, Jeff Longmate, et al.. (2005). Tissue-specific time courses of spontaneous mutation frequency and deviations in mutation pattern are observed in middle to late adulthood in Big Blue mice. Environmental and Molecular Mutagenesis. 45(5). 442–454. 29 indexed citations

Hill, Kathleen A., Kelly Gonzalez, William A. Scaringe, Jicheng Wang, & Steve S. Sommer. (2005). Preferential occurrence of 1-2 microindels. Human Mutation. 27(1). 55–61. 7 indexed citations

10.

Buzin, Carolyn H., Jinong Feng, Yan Jin, et al.. (2005). Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide. Human Mutation. 25(2). 177–188. 45 indexed citations

11.

Hill, Kathleen A., Jicheng Wang, Kelly D. Farwell, William A. Scaringe, & Steve S. Sommer. (2004). Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiency. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 554(1-2). 223–240. 22 indexed citations

12.

Hill, Kathleen A., Victoria L. Buettner, Makoto Kunishige, et al.. (2004). Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue‐specific time courses of mutation frequency but similar mutation types. Environmental and Molecular Mutagenesis. 43(2). 110–120. 56 indexed citations

13.

Li, Xuemin, William A. Scaringe, Kathleen A. Hill, et al.. (2001). Frequency of recent retrotransposition events in the human factor IX gene. Human Mutation. 17(6). 511–519. 55 indexed citations

14.

Feng, Jinong, Joni B. Drost, William A. Scaringe, Qiang Liu, & Steve S. Sommer. (2001). Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations. Human Mutation. 19(1). 49–57. 4 indexed citations

15.

Sommer, Steve S., William A. Scaringe, & Kathleen A. Hill. (2001). Human germline mutation in the factor IX gene. Mutation Research/DNA Repair. 487(1-2). 1–17. 36 indexed citations

16.

Drost, Joni B., William A. Scaringe, Ana Rebeca Jaloma‐Cruz, et al.. (2000). Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans. Human Mutation. 16(3). 203–210. 7 indexed citations

17.

Jaloma‐Cruz, Ana Rebeca, William A. Scaringe, Joni B. Drost, et al.. (2000). Nine independentF9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline. Human Mutation. 15(1). 116–117. 11 indexed citations

18.

Buettner, Victoria L., Kathleen A. Hill, William A. Scaringe, & Steve S. Sommer. (2000). Evidence that proximal multiple mutations in Big Blue® transgenic mice are dependent events. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 452(2). 219–229. 31 indexed citations

19.

Ketterling, Rhett P., Joni B. Drost, William A. Scaringe, et al.. (1999). Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutations. Human Mutation. 13(3). 221–231. 41 indexed citations

20.

Scaringe, William A., et al.. (1999). REF Select: Expert System Software for Selecting Restriction Endonucleases for Restriction Endonuclease Fingerprinting. BioTechniques. 27(6). 1188–1201. 2 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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