Sheila Dodge

University of California, Santa Cruz — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index9.4kcitations19works1.02yr avg
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Research Topics

Genomics and Rare Diseases(7), Cancer Genomics and Diagnostics(5), Genomics and Phylogenetic Studies(4), Autism Spectrum Disorder Research(3), Genetic Associations and Epidemiology(3)

Publications18 total

Using the linear references from the pangenome to discover missing autism variants
Nature Communications·2026· 1 citedOpen Access
Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility
Nature Genetics·2022· 175 citedOpen Access
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Nature Genetics·2022· 564 citedOpen Access
Cost-efficient whole genome-sequencing using novel mostly natural sequencing-by-synthesis chemistry and open fluidics platform
2022· 72 citedOpen Access
Rare coding variants in ten genes confer substantial risk for schizophrenia
Nature·2022· 823 citedOpen Access
Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism
2021· 35 citedOpen Access
Neptune: an environment for the delivery of genomic medicine
Genetics in Medicine·2021· 7 citedOpen Access
Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility
2021· 11 citedOpen Access
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations
The American Journal of Human Genetics·2021· 104 citedOpen Access
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations
2020· 11 citedOpen Access
Cómo resolver los atascos en el trabajo cognitivo
Harvard-Deusto business review·2019
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
BMC Genomics·2018· 280 citedOpen Access
Additional file 3: of Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
Figshare·2018Open Access
Additional file 2: of Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
Figshare·2018Open Access
Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platforms
2017· 10 citedOpen Access
Erratum to “Pathogen discovery from human tissue by sequence-based computational subtraction”
Genomics·2003
Pathogen discovery from human tissue by sequence-based computational subtraction
Genomics·2003· 42 cited
Initial sequencing and comparative analysis of the mouse genome
Nature·2002· 7.2k citedOpen Access

Frequent Co-authors

Stacey Gabriel(9), Steven Ferriera(6), Timothy DeSmet(6), Christine Stevens(5), Yossi Farjoun(5), Tom Howd(5), Wendy Brodeur(5), Niall J. Lennon(5), Aarno Palotie(4), Maura Costello(4), Mark Fleharty(4), Justin Abreu(4), Laurie Holmes(4), Tamara Mason(4), Gina Vicente(4), Michael Dasilva(4), Bruce W. Birren(3), Robert David(3), Karen Foley(3), Richard A. Gibbs(3)