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William Scaringe

Research Profile

Chemicals & Drugs

Physiology

Living Beings

Disorders

Procedures

DNA Mutational Analysis

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Genes & Molecular Sequences

Genes, p53

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Publications

TOP 3
William A Scaringe; Kai Li; Dongqing Gu; Kelly D Gonzalez; Zhenbin Chen; Kathleen A Hill; Steve S Sommer
Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates.
Wenjia Song; Wenyan Li; Jinong Feng; Leonard L Heston; William A Scaringe; Steve S Sommer
Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.
Chunmei Yang; Jinong Feng; Wenjia Song; Jicheng Wang; Becky Tsai; Yunwu Zhang; William A Scaringe; Kathleen A Hill; Paris Margaritis; Katherine A High; Steve S Sommer
A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin.

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All Publications

2008: William A Scaringe; Kai Li; Dongqing Gu; Kelly D Gonzalez; Zhenbin Chen; Kathleen A Hill; Steve S Sommer
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 2008;17(18):2910-8.
2008: Wenjia Song; Wenyan Li; Jinong Feng; Leonard L Heston; William A Scaringe; Steve S Sommer
Identification of high risk DISC1 structural variants with a 2% attributable risk for schizophrenia.
Biochemical and biophysical research communications 2008;367(3):700-6.
2007: Chunmei Yang; Jinong Feng; Wenjia Song; Jicheng Wang; Becky Tsai; Yunwu Zhang; William A Scaringe; Kathleen A Hill; Paris Margaritis; Katherine A High; Steve S Sommer
A mouse model for nonsense mutation bypass therapy shows a dramatic multiday response to geneticin.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(39):15394-9.
2007: Dongqing Gu; William A Scaringe; Kai Li; Juan-Sebastian Saldivar; Kathleen A Hill; Zhenbin Chen; Kelly D Gonzalez; Steve S Sommer
Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature.
Human mutation 2007;28(8):760-70.
2007: Jicheng Wang; Kelly D Gonzalez; William A Scaringe; Kimberly Tsai; Ning Liu; Dongqing Gu; Wenyan Li; Kathleen A Hill; Steve S Sommer
Evidence for mutation showers.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(20):8403-8.
2007: Kelly D Gonzalez; Kathleen A Hill; Kai Li; Wenyan Li; William A Scaringe; Ji-Cheng Wang; Dongqing Gu; Steve S Sommer
Somatic microindels: analysis in mouse soma and comparison with the human germline.
Human mutation 2007;28(1):69-80.
2006: Kathleen A Hill; Victoria L Buettner; Analeah Heidt; Lin-Ling Chen; Wenyan Li; Kelly D Gonzalez; Ji-Cheng Wang; William A Scaringe; Steve S Sommer
Most spontaneous tumors in a mouse model of Li-Fraumeni syndrome do not have a mutator phenotype.
Carcinogenesis 2006;27(9):1860-6.
2006: Kathleen A Hill; Kelly D Gonzalez; William A Scaringe; Ji-Cheng Wang; Steve S Sommer
Preferential occurrence of 1-2 microindels.
Human mutation 2006;27(1):55-61.
2005: Kathleen A Hill; Asanga Halangoda; Petra W Heinmoeller; Kelly D Gonzalez; Chaniga Chitaphan; Jeff Longmate; William A Scaringe; Ji-Cheng Wang; Steve S Sommer
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 2005;45(5):442-54.
2005: Carolyn H Buzin; Jinong Feng; Jin Yan; William A Scaringe; Qiang Liu; Johan den Dunnen; Jerry R Mendell; Steve S Sommer
Mutation rates in the dystrophin gene: a hotspot of mutation at a CpG dinucleotide.
Human mutation 2005;25(2):177-88.
2004: Kathleen A Hill; Jicheng Wang; Kelly D Farwell; William A Scaringe; Steve S Sommer
Spontaneous multiple mutations show both proximal spacing consistent with chronocoordinate events and alterations with p53-deficiency.
Mutation research 2004;554(1-2):223-40.
2004: Jin Yan; Jinong Feng; Carolyn H Buzin; William A Scaringe; Qiang Liu; Jerry R Mendell; Johan den Dunnen; Steve S Sommer
Three-tiered noninvasive diagnosis in 96% of patients with Duchenne muscular dystrophy (DMD).
Human mutation 2004;23(2):203-4.
2004: Kathleen A Hill; Victoria L Buettner; Asanga Halangoda; Makoto Kunishige; Stephen R Moore; Jeff Longmate; William A Scaringe; Steve S Sommer
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 2004;43(2):110-20.
2002: Steve S Sommer; William A Scaringe; Kathleen A Hill
Is Alu-mediated recombination an important cause of hemophilia?
Thrombosis and haemostasis 2002;88(1):3-4.
2002: Jinong Feng; Joni B Drost; William A Scaringe; Qiang Liu; Steve S Sommer
Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations.
Human mutation 2002;19(1):49-57.
2001: Steve S Sommer; William A Scaringe; Kathleen A Hill
Human germline mutation in the factor IX gene.
Mutation research 2001;487(1-2):1-17.
2001: Xuemin Li; William A Scaringe; Kathleen A Hill; S Roberts; April Mengos; D Careri; M T Pinto; CK Kasper; Steve S Sommer
Frequency of recent retrotransposition events in the human factor IX gene.
Human mutation 2001;17(6):511-9.
2000: Victoria L Buettner; Kathleen A Hill; William A Scaringe; Steve S Sommer
Evidence that proximal multiple mutations in Big Blue transgenic mice are dependent events.
Mutation research 2000;452(2):219-29.
2000: Joni B Drost; William A Scaringe; Ana Rebeca Jaloma-Cruz; Xuemin Li; D F Ossa; CK Kasper; Steve S Sommer
Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene (F9) in Latin Americans.
Human mutation 2000;16(3):203-10.
2000: Qiang Liu; William A Scaringe; Steve S Sommer
Discrete mobility of single-stranded DNA in non-denaturing gel electrophoresis.
Nucleic acids research 2000;28(4):940-3.
2000: Ana Rebeca Jaloma-Cruz; William A Scaringe; Joni B Drost; S Roberts; Xuemin Li; Patricio Barros-Núñez; Luis Figuera; F Rivas; JM Cantú; Steve S Sommer
Nine independent F9 mutations in the Mexican hemophilia B population: nonrandom recurrences of point mutation events in the human germline.
Human mutation 2000;15(1):116-7.
1999: William A Scaringe; D Liao; Qiang Liu; Steve S Sommer
REF Select: expert system software for selecting restriction endonucleases for restriction endonuclease fingerprinting.
BioTechniques 1999;27(6):1188-90, 1192-4, 1196 passim.
1999: Jinong Feng; Carolyn H Buzin; Shih-Huey E Tang; William A Scaringe; Steve S Sommer
Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypes.
Human mutation 1999;14(2):175-80.
1999: Rhett P Ketterling; Joni B Drost; William A Scaringe; D Z Liao; J Z Liu; CK Kasper; Steve S Sommer
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 1999;13(3):221-31.