Nicole Washington

15.6k total citations
43 papers, 1.8k citations indexed

About

Nicole Washington is a scholar working on Molecular Biology, Genetics and General Health Professions. According to data from OpenAlex, Nicole Washington has authored 43 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 20 papers in Genetics and 5 papers in General Health Professions. Recurrent topics in Nicole Washington's work include Genomics and Rare Diseases (15 papers), Bioinformatics and Genomic Networks (11 papers) and Biomedical Text Mining and Ontologies (8 papers). Nicole Washington is often cited by papers focused on Genomics and Rare Diseases (15 papers), Bioinformatics and Genomic Networks (11 papers) and Biomedical Text Mining and Ontologies (8 papers). Nicole Washington collaborates with scholars based in United States, United Kingdom and Germany. Nicole Washington's co-authors include Melissa Haendel, Chris Mungall, Sebastian Köhler, Simon Ward, Suzanna Lewis, Peter N. Robinson, Damian Smedley, Tomasz Żemojtel, Monte Westerfield and Michael Ashburner and has published in prestigious journals such as Nucleic Acids Research, Circulation and Nature Communications.

In The Last Decade

Nicole Washington

43 papers receiving 1.8k citations

Peers

Nicole Washington

GENET

AGING

James A. Kadin United States

Ruowang Li United States

David Mittelman United States

Jason A. Stewart United States

Alexis Battle United States

Guðmundur Á. Þórisson United Kingdom

Seth Carbon United States

Farhad Hormozdiari United States

Duygu Ucar United States

Peter Krawitz Germany

James A. Kadin United States

Nicole Washington

2.0k ×1.7

710 ×0.8

GENET

196 ×1.1

141 ×0.9

54 ×0.6

AGING

Citations per year, relative to Nicole Washington Nicole Washington (= 1×) peers James A. Kadin

Countries citing papers authored by Nicole Washington

Since Specialization

Citations

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

Fields of papers citing papers by Nicole Washington

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicole Washington. 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 Nicole Washington. The network helps show where Nicole Washington may publish in the future.

Co-authorship network of co-authors of Nicole Washington

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Telis, Natalie, Douglas Stoller, Christopher Chapman, et al.. (2025). P190: Scalable system-wide CYP2C19 pharmacogenomic testing reveals excess incidence of adverse events in metabolizers receiving inappropriate prescriptions. Genetics in Medicine Open. 3. 102155–102155. 1 indexed citations

Barrett, Kelly M. Schiabor, Natalie Telis, Lisa M. McEwen, et al.. (2024). Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetes. SHILAP Revista de lepidopterología. 4(1). 239–239. 1 indexed citations

Washington, Nicole, Natalie Telis, Daniel P. Judge, et al.. (2024). Abstract 4147064: Retrospective study shows pharmacogenomic testing could reduce adverse events associated with clopidogrel use by 38%. Circulation. 150(Suppl_1). 1 indexed citations

Bolze, Alexandre, Kelly M. Schiabor Barrett, Gai Elhanan, et al.. (2024). Combining rare and common genetic variants improves population risk stratification for breast cancer. SHILAP Revista de lepidopterología. 2. 101826–101826. 5 indexed citations

Cirulli, Elizabeth T., Kelly M. Schiabor Barrett, Alexandre Bolze, et al.. (2024). A power-based sliding window approach to evaluate the clinical impact of rare genetic variants in the nucleotide sequence or the spatial position of the folded protein. Human Genetics and Genomics Advances. 5(3). 100284–100284. 1 indexed citations

Washington, Nicole, et al.. (2023). Racial/ethnic differences in anorexia and bulimia diagnoses among U.S. college students. Eating Behaviors. 50. 101779–101779. 2 indexed citations

Barrett, Kelly M. Schiabor, Elizabeth T. Cirulli, Alexandre Bolze, et al.. (2023). Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation. Genetics in Medicine. 25(4). 100012–100012. 20 indexed citations

Jacobsen, Julius O.B., Christèle du Souich, Kent Shefchek, et al.. (2022). The Clinical Variant Analysis Tool: Analyzing the evidence supporting reported genomic variation in clinical practice. Genetics in Medicine. 24(7). 1512–1522. 3 indexed citations

Bolze, Alexandre, Iva Neveux, Kelly M. Schiabor Barrett, et al.. (2022). HLA-A∗03:01 is associated with increased risk of fever, chills, and stronger side effects from Pfizer-BioNTech COVID-19 vaccination. Human Genetics and Genomics Advances. 3(2). 100084–100084. 29 indexed citations

10.

Read, Robert W., Karen Schlauch, Vincent C. Lombardi, et al.. (2021). Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Frontiers in Genetics. 12. 639418–639418. 9 indexed citations

11.

Barrett, Kelly M. Schiabor, Alexandre Bolze, Yunyun Ni, et al.. (2021). Positive predictive value highlights four novel candidates for actionable genetic screening from analysis of 220,000 clinicogenomic records. Genetics in Medicine. 23(12). 2300–2308. 8 indexed citations

12.

Taylor, April, et al.. (2020). Pediatric Residents’ Sense of Meaning in Their Work: Is This Value Related to Higher Specialty Satisfaction and Reduced Burnout?. Academic Pediatrics. 21(3). 557–563. 9 indexed citations

13.

Dunaway, Keith W., Erick Loomis, Stephen Riffle, et al.. (2019). Genetic counseling, 2030: An on‐demand service tailored to the needs of a price conscious, genetically literate, and busy world. Journal of Genetic Counseling. 28(2). 456–465. 18 indexed citations

14.

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

15.

Haendel, Melissa, Nicole Vasilevsky, Matthew Brush, et al.. (2015). Disease insights through cross-species phenotype comparisons. Mammalian Genome. 26(9-10). 548–555. 16 indexed citations

16.

Groza, Tudor, Sebastian Köhler, Nicole Vasilevsky, et al.. (2015). The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease. The American Journal of Human Genetics. 97(1). 111–124. 150 indexed citations

17.

Bandrowski, Anita, Matthew Brush, Jeffrey S. Grethe, et al.. (2015). The Resource Identification Initiative: A Cultural Shift in Publishing. Neuroinformatics. 14(2). 169–182. 23 indexed citations

18.

Robinson, Peter N., Sebastian Köhler, Anika Oellrich, et al.. (2013). Improved exome prioritization of disease genes through cross-species phenotype comparison. Genome Research. 24(2). 340–348. 214 indexed citations

19.

Contrino, Sergio, Richard Smith, Daniela Butano, et al.. (2011). modMine: flexible access to modENCODE data. Nucleic Acids Research. 40(D1). D1082–D1088. 91 indexed citations

20.

Cutter, Asher D., James D. Wasmuth, & Nicole Washington. (2008). Patterns of Molecular Evolution in Caenorhabditis Preclude Ancient Origins of Selfing. Genetics. 178(4). 2093–2104. 79 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.

Explore authors with similar magnitude of impact