Gail P. Jarvik

45.3k total citations
264 papers, 11.1k citations indexed

About

Gail P. Jarvik is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Gail P. Jarvik has authored 264 papers receiving a total of 11.1k indexed citations (citations by other indexed papers that have themselves been cited), including 125 papers in Genetics, 42 papers in Molecular Biology and 38 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Gail P. Jarvik's work include Genomics and Rare Diseases (54 papers), BRCA gene mutations in cancer (52 papers) and Genetic Associations and Epidemiology (48 papers). Gail P. Jarvik is often cited by papers focused on Genomics and Rare Diseases (54 papers), BRCA gene mutations in cancer (52 papers) and Genetic Associations and Epidemiology (48 papers). Gail P. Jarvik collaborates with scholars based in United States, Canada and United Kingdom. Gail P. Jarvik's co-authors include Clement E. Furlong, Rebecca J. Richter, Wylie Burke, Thomas S. Hatsukami, Victoria H. Brophy, J. William Gaynor, Gil Wernovsky, Lucio G. Costa, Robert R. Clancy and Susan C. Nicolson and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Gail P. Jarvik

252 papers receiving 10.9k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Gail P. Jarvik 3.1k 2.1k 2.1k 1.8k 1.8k 264 11.1k
Barry I. Freedman 3.0k 1.0× 3.3k 1.5× 1.3k 0.6× 780 0.4× 1.7k 0.9× 420 16.3k
Alicia J. Jenkins 1.2k 0.4× 2.8k 1.3× 436 0.2× 2.1k 1.1× 1.6k 0.9× 420 14.4k
Florian Kronenberg 2.5k 0.8× 4.7k 2.2× 1.6k 0.8× 629 0.3× 2.2k 1.2× 380 20.4k
Peter J. Grant 858 0.3× 2.0k 0.9× 3.8k 1.8× 1.3k 0.7× 2.2k 1.2× 267 14.6k
François Cambien 3.1k 1.0× 3.9k 1.9× 1.7k 0.8× 491 0.3× 2.1k 1.2× 229 20.8k
Ada Hamosh 4.8k 1.5× 7.1k 3.4× 1.9k 0.9× 727 0.4× 535 0.3× 99 13.3k
Erwin P. Böttinger 1.8k 0.6× 9.6k 4.5× 1.6k 0.7× 791 0.4× 1.1k 0.6× 165 18.3k
Andrzej S. Królewski 3.2k 1.0× 3.1k 1.5× 675 0.3× 1.2k 0.7× 1.6k 0.9× 190 15.7k
H. A. W. Neil 1.2k 0.4× 2.6k 1.2× 545 0.3× 403 0.2× 1.6k 0.9× 113 17.4k
Thomas Illig 2.1k 0.7× 7.3k 3.4× 750 0.4× 377 0.2× 2.1k 1.2× 287 15.1k

Countries citing papers authored by Gail P. Jarvik

Since Specialization
Citations

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

Fields of papers citing papers by Gail P. Jarvik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gail P. Jarvik. 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 Gail P. Jarvik. The network helps show where Gail P. Jarvik may publish in the future.

Co-authorship network of co-authors of Gail P. Jarvik

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

All Works

20 of 20 papers shown
1.
Stanaway, Ian B., Simon Davies, Jeffrey Perl, et al.. (2025). Genetic Variation and Ultrafiltration with Peritoneal Dialysis. Journal of the American Society of Nephrology. 37(1). 49–66.
2.
Moonesinghe, Ramal, Lu Shi, Gail P. Jarvik, et al.. (2025). Association of HFE genotypes with hemochromatosis-related phenotypes in the All of Us research program. Genetics in Medicine Open. 3. 101959–101959.
3.
Venner, Eric, Karynne Patterson, Divya Kalra, et al.. (2024). The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities. Communications Biology. 7(1). 174–174. 25 indexed citations
4.
Rosenthal, Elisabeth A., Li Hsu, Minta Thomas, et al.. (2024). Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score. Genetic Epidemiology. 49(1). e22590–e22590.
5.
Hui, Daniel, Scott Dudek, Krzysztof Kiryluk, et al.. (2023). Risk factors affecting polygenic score performance across diverse cohorts. eLife. 12.
6.
Manolio, Teri A., Carol J. Bult, Rex L. Chisholm, et al.. (2023). Genomic medicine year in review: 2023. The American Journal of Human Genetics. 110(12). 1992–1995. 1 indexed citations
7.
Crosslin, David R., Sean D. Mooney, Eric D. Morrell, et al.. (2023). Evaluating construct validity of computable acute respiratory distress syndrome definitions in adults hospitalized with COVID-19: an electronic health records based approach. BMC Pulmonary Medicine. 23(1). 292–292. 6 indexed citations
8.
Shadrina, Alexandra S., Ian B. Stanaway, Gail P. Jarvik, et al.. (2022). Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities. PLoS ONE. 17(5). e0268725–e0268725. 2 indexed citations
9.
Amendola, Laura M., Tia L. Kauffman, Kathleen F. Mittendorf, et al.. (2022). Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience. Human Genetics and Genomics Advances. 3(3). 100120–100120. 6 indexed citations
10.
Liles, Elizabeth, Michael C. Leo, Amanda S. Freed, et al.. (2022). ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial. Genetics in Medicine. 24(8). 1664–1674. 2 indexed citations
11.
Henrikson, Nora B., James D. Ralston, Kathleen A. Leppig, et al.. (2022). Implementation matters: How patient experiences differ when genetic counseling accompanies the return of genetic variants of uncertain significance. PubMed Central.
12.
Amendola, Laura M., et al.. (2021). ShareDNA: a smartphone app to facilitate family communication of genetic results. BMC Medical Genomics. 14(1). 10–10. 7 indexed citations
13.
Rope, Alan F., Tia L. Kauffman, Laura M. Amendola, et al.. (2018). A case for expanding carrier testing to include actionable X‐linked disorders. Clinical Case Reports. 6(11). 2092–2095. 2 indexed citations
14.
Amendola, Laura M., Martha Horike‐Pyne, Susan Brown Trinidad, et al.. (2017). Discordance in selected designee for return of genomic findings in the event of participant death and estate executor. Molecular Genetics & Genomic Medicine. 5(2). 172–176. 6 indexed citations
15.
Dorschner, Michael O., Laura M. Amendola, Brian H. Shirts, et al.. (2014). Refining the structure and content of clinical genomic reports. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 166(1). 85–92. 30 indexed citations
16.
Bielinski, Suzette J., Jyotishman Pathak, Hongfang Liu, et al.. (2012). Using Electronic Health Records to Identify Heart Failure Cohorts with Differentiation for Preserved and Reduced Ejection Fraction.. AMIA. 1 indexed citations
17.
Rosenthal, Elisabeth A., James Ronald, Joseph H. Rothstein, et al.. (2011). Linkage and association of phospholipid transfer protein activity to LASS4. Journal of Lipid Research. 52(10). 1837–1846. 16 indexed citations
18.
Johnson, Andrew D., Emelia J. Benjamin, Caroline S. Fox, et al.. (2009). Abstract 1806: Notifiable Genetic Variants on Commercially Available SNP Arrays: Implications for Research Participants in Genome-wide Association Studies for Cardiovascular Disease. Circulation. 120. 1 indexed citations
19.
Crawford, Dana C., Alex S. Nord, Michael D. Badzioch, et al.. (2007). A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk. Journal of Lipid Research. 49(3). 588–596. 22 indexed citations
20.
Rozek, Laura S., Thomas S. Hatsukami, Rebecca J. Richter, et al.. (2005). The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status. Journal of Lipid Research. 46(9). 1888–1895. 46 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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