William A. Scaringe

944 citations

23 papers · 708 · h-index 15

Impact in

Cancer Research top 10%
- Cancer Genomics and Diagnostics
Molecular Biology
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Phosphodiesterase function and regulation
- RNA and protein synthesis mechanisms

Papers in

Molecular Biology 18
- CRISPR and Genetic Engineering 7
- Cancer-related gene regulation 6
- Genomics and Chromatin Dynamics 5
- Molecular Biology Techniques and Applications 3
- DNA Repair Mechanisms 2
Cancer Research 9
- Cancer Genomics and Diagnostics 7

Co-authors: Steve S. Sommer (20 shared papers)Kathleen A. Hill (13 shared papers)Jinong Feng (4 shared papers)Kelly Gonzalez (6 shared papers)Jicheng Wang (5 shared papers)Dongqing Gu (4 shared papers)Victoria L. Buettner (2 shared papers)Wenjia Song (2 shared papers)
Journals: Human Mutation (9 papers)Proceedings of the National Academy of Sciences (2 papers)Environmental and Molecular Mutagenesis (2 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (2 papers)Biochemical and Biophysical Research Communications (1 paper)
Partner nations: United States Canada China

In The Last Decade

William A. Scaringe

23 papers receiving 693 citations

Peers

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-authors

The 25 scholars most cited alongside William A. Scaringe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with William A. Scaringe Line = papers co-authored together William A. Scaringe links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Molecular Analysis of Microdissected Tumors and Preneoplastic Intraductal Lesions in Pancreatic Carcinoma American Journal Of Pathology ·Ernst Heinmöller, Wolfgang Dietmaier, Hubert Zirngibl, Petra Heinmöller, William A. Scaringe, K. W. Jauch, F Hofstädter, Josef Rüschoff	2000	96
2	Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia Biochemical and Biophysical Research Communications ·Wenjia Song, Wenyan Li, Jinong Feng, Leonard L. Heston, William A. Scaringe, Steve S. Sommer	2008	73
3	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 ·Kathleen A. Hill, Victoria L. Buettner, Asanga Halangoda, Makoto Kunishige, Stephen Moore, Jeff Longmate, William A. Scaringe, Steve S. Sommer	2004	56
4	Evidence for mutation showers Proceedings of the National Academy of Sciences ·Jicheng Wang, Kelly Gonzalez, William A. Scaringe, Kimberly Tsai, Ning Liu, Dongqing Gu, Wenyan Li, Kathleen A. Hill, Steve S. Sommer	2007	56
5	Frequency of recent retrotransposition events in the human factor IX gene Human Mutation ·Xuemin Li, William A. Scaringe, Kathleen A. Hill, Stacy Roberts, April Mengos, Diane Careri, Miguel Tezanos Pinto, Carol K. Kasper, Steve S. Sommer	2001	55
6	Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide Human Mutation ·Carolyn H. Buzin, Jinong Feng, Yan Jin, William A. Scaringe, Qiang Liu, Johan T. den Dunnen, Jerry R. Mendell, Steve S. Sommer	2005	47
7	Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature Human Mutation ·Dongqing Gu, William A. Scaringe, Kai Li, Juan‐Sebastian Saldivar, Kathleen A. Hill, Zhenbin Chen, Kelly Gonzalez, Steve S. Sommer	2007	45
8	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 ·Rhett P. Ketterling, Joni B. Drost, William A. Scaringe, Dong-zhou Liao, Jingzhong Liu, Carol K. Kasper, Steve S. Sommer	1999	41
9	Human germline mutation in the factor IX gene Mutation Research/DNA Repair ·Steve S. Sommer, William A. Scaringe, Kathleen A. Hill	2001	36
10	A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin Proceedings of the National Academy of Sciences ·Chunmei Yang, Jinong Feng, Wenjia Song, Jicheng Wang, Becky Pinjou Tsai, Yun‐wu Zhang, William A. Scaringe, Kathleen A. Hill, Paris Margaritis, Katherine A. High, Steve S. Sommer	2007	33
11	Evidence that proximal multiple mutations in Big Blue® transgenic mice are dependent events Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Victoria L. Buettner, Kathleen A. Hill, William A. Scaringe, Steve S. Sommer	2000	31
12	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 ·Kathleen A. Hill, Asanga Halangoda, Petra W. Heinmoeller, Kelly Gonzalez, Chaniga Chitaphan, Jeff Longmate, William A. Scaringe, Jicheng Wang, Steve S. Sommer	2005	29
13	Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiency Mutation research. Fundamental and molecular mechanisms of mutagenesis ·Kathleen A. Hill, Jicheng Wang, Kelly D. Farwell, William A. Scaringe, Steve S. Sommer	2004	22
14	A Streamlined Approach to Prader-Willi and Angelman Syndrome Molecular Diagnostics Frontiers in Genetics ·Samuel P. Strom, Waheeda A. Hossain, Melina Grigorian, Mickey Li, Joseph M. Fierro, William A. Scaringe, Hai-Yun Yen, Mirandy Teguh, Joanna Liu, Harry Gao, Merlin G. Butler	2021	18
15	Somatic microindels: analysis in mouse soma and comparison with the human germline Human Mutation ·Kelly Gonzalez, Kathleen A. Hill, Kai Li, Wenyan Li, William A. Scaringe, Jicheng Wang, Dongqing Gu, Steve S. Sommer	2006	15
16	The Value of Parental Testing by Next-Generation Sequencing Includes the Detection of Germline Mosaicism Journal of Molecular Diagnostics ·Casey Brewer, Meghan Gillespie, Joseph M. Fierro, William A. Scaringe, Jie Li, Che-yu Lee, Hai-Yun Yen, Hanlin Gao, Samuel P. Strom	2020	12
17	Nine independentF9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline Human Mutation ·Ana Rebeca Jaloma‐Cruz, William A. Scaringe, Joni B. Drost, Stacy Roberts, Xuemin Li, Patricio Barros-N��ez, Luis E. Figuera, Fernando Rivas, Jos� Mar�a Cant�, Steve S. Sommer	2000	11
18	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 ·William A. Scaringe, Kai Li, Dongqing Gu, Kelly Gonzalez, Zhenbin Chen, Kathleen A. Hill, Steve S. Sommer	2008	10
19	Preferential occurrence of 1-2 microindels Human Mutation ·Kathleen A. Hill, Kelly Gonzalez, William A. Scaringe, Jicheng Wang, Steve S. Sommer	2005	7
20	Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans Human Mutation ·Joni B. Drost, William A. Scaringe, Ana Rebeca Jaloma‐Cruz, Xuemin Li, Diego F. Ossa, Carol K. Kasper, Steve S. Sommer	2000	7

About William A. Scaringe

William A. Scaringe is a scholar working on Molecular Biology, Cancer Research, Hematology, Genetics and Genetics, having authored 23 papers that have together received 708 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (7 papers), CRISPR and Genetic Engineering (7 papers), Hemophilia Treatment and Research (6 papers), Cancer-related gene regulation (6 papers), Genomics and Chromatin Dynamics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Molecular Biology Techniques and Applications (3 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Cancer Research (146 citations), Molecular Biology (468 citations), Aging (11 citations), Genetics (166 citations) and Oncology (120 citations). William A. Scaringe has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Steve S. Sommer, Kathleen A. Hill, Jinong Feng, Kelly Gonzalez, Jicheng Wang, Dongqing Gu, Victoria L. Buettner, Wenjia Song, Carol K. Kasper and Ernst Heinmöller. Their work appears in journals such as Human Mutation, Proceedings of the National Academy of Sciences, Environmental and Molecular Mutagenesis, Mutation research. Fundamental and molecular mechanisms of mutagenesis and Biochemical and Biophysical Research Communications.

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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William A. Scaringe

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