Robert C. Green

64.6k total citations · 3 hit papers
342 papers, 16.7k citations indexed

About

Robert C. Green is a scholar working on Genetics, Psychiatry and Mental health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Robert C. Green has authored 342 papers receiving a total of 16.7k indexed citations (citations by other indexed papers that have themselves been cited), including 167 papers in Genetics, 63 papers in Psychiatry and Mental health and 58 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Robert C. Green's work include BRCA gene mutations in cancer (105 papers), Genomics and Rare Diseases (91 papers) and Dementia and Cognitive Impairment Research (56 papers). Robert C. Green is often cited by papers focused on BRCA gene mutations in cancer (105 papers), Genomics and Rare Diseases (91 papers) and Dementia and Cognitive Impairment Research (56 papers). Robert C. Green collaborates with scholars based in United States, Canada and United Kingdom. Robert C. Green's co-authors include Amy L. McGuire, J. Scott Roberts, Andrew J. Saykin, Heidi L. Rehm, Michael W. Weiner, Clifford R. Jack, Arthur W. Toga, John Q. Trojanowski, Leslie M. Shaw and William J. Jagust and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Robert C. Green

331 papers receiving 16.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

2013 1.6k citations Robert C. Green, Amy L. McGuire et al. Genetics in Medicine profile →
The Alzheimer's Disease Neuroimaging Initiative: A review of papers published since its inception

2013 698 citations Robert C. Green et al. Alzheimer s & Dementia profile →
Understanding disease progression and improving Alzheimer's disease clinical trials: Recent highlights from the Alzheimer's Disease Neuroimaging Initiative

2018 324 citations Robert C. Green et al. Alzheimer s & Dementia profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Robert C. Green United States	62	5.8k	4.3k	3.9k	2.9k	2.4k	342	16.7k
Teri A. Manolio United States	86	6.1k 1.0×	3.4k 0.8×	2.1k 0.5×	5.7k 2.0×	2.8k 1.2×	215	37.6k
Cathie Sudlow United Kingdom	60	3.5k 0.6×	2.6k 0.6×	1.7k 0.4×	2.6k 0.9×	2.2k 0.9×	217	20.9k
Lindsay A. Farrer United States	71	4.4k 0.8×	7.2k 1.7×	4.3k 1.1×	7.4k 2.6×	1.3k 0.6×	425	23.6k
Rudi G. J. Westendorp Netherlands	92	1.7k 0.3×	6.2k 1.4×	3.4k 0.9×	4.0k 1.4×	1.8k 0.8×	577	30.7k
Alan B. Zonderman United States	85	1.8k 0.3×	4.5k 1.0×	4.5k 1.2×	3.1k 1.1×	3.0k 1.3×	450	27.0k
Walter A. Rocca United States	99	3.4k 0.6×	6.9k 1.6×	10.2k 2.6×	3.2k 1.1×	2.6k 1.1×	347	33.2k
Albert Hofman Netherlands	91	2.5k 0.4×	4.0k 0.9×	2.1k 0.5×	4.6k 1.6×	2.6k 1.1×	360	31.4k
Naomi E. Allen United Kingdom	50	5.8k 1.0×	3.8k 0.9×	1.1k 0.3×	3.7k 1.3×	4.2k 1.8×	134	23.0k
Cornelia M. van Duijn Netherlands	96	7.1k 1.2×	9.6k 2.2×	4.7k 1.2×	11.8k 4.1×	3.3k 1.4×	676	40.3k
M. Arfan Ikram Netherlands	96	1.4k 0.2×	6.4k 1.5×	6.5k 1.7×	3.5k 1.2×	3.4k 1.4×	837	34.1k

Countries citing papers authored by Robert C. Green

Since Specialization

Citations

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

Fields of papers citing papers by Robert C. Green

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert C. Green. 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 Robert C. Green. The network helps show where Robert C. Green may publish in the future.

Co-authorship network of co-authors of Robert C. Green

This figure shows the co-authorship network connecting the top 25 collaborators of Robert C. Green. A scholar is included among the top collaborators of Robert C. Green 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 Robert C. Green. Robert C. Green 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

Gold, Nina B., et al.. (2025). O35: A genotype-first approach among adults at risk for treatable monogenic disorders reveals underdiagnosis and incomplete penetrance. Genetics in Medicine Open. 3. 102111–102111. 1 indexed citations

Nathan, Aparna, Stuart R. Lipsitz, Satoshi Koyama, et al.. (2025). Nonadherence to guidelines for genetic testing in families with ovarian cancer shows racial bias. Genetics in Medicine. 27(7). 101444–101444. 1 indexed citations

Uveges, Melissa Kurtz, Hadley Stevens Smith, Stacey Pereira, et al.. (2024). Family genetic risk communication and reverse cascade testing in the BabySeq project. Genetics in Medicine. 27(3). 101350–101350.

Fieg, Elizabeth L., Natasha Y. Frank, Robert C. Green, et al.. (2024). Processes and outcomes from a clinical genetics e-consultation service managed by a primary care physician champion. SHILAP Revista de lepidopterología. 2. 101831–101831.

Green, Robert C., et al.. (2024). Genetic counselors’ perspectives on genomic screening of apparently healthy newborns in the United States. SHILAP Revista de lepidopterología. 2. 101885–101885. 1 indexed citations

Gold, Jessica I., Sarina Madhavan, Joseph Park, et al.. (2023). Phenotypes of undiagnosed adults with actionable OTC and GLA variants. Human Genetics and Genomics Advances. 4(4). 100226–100226. 2 indexed citations

Zawatsky, Carrie L. Blout, et al.. (2023). Attitudes about Pharmacogenomic Testing Vary by Healthcare Specialty. Pharmacogenomics. 24(10). 539–549. 11 indexed citations

Lewis, Anna, Emma Perez, Anya E. R. Prince, et al.. (2022). Patient and provider perspectives on polygenic risk scores: implications for clinical reporting and utilization. Genome Medicine. 14(1). 114–114. 32 indexed citations

Kaur, Hundeep, Roman P. Jakob, Jan K. Marzinek, et al.. (2021). The antibiotic darobactin mimics a β-strand to inhibit outer membrane insertase. Nature. 593(7857). 125–129. 155 indexed citations

10.

Rehm, Heidi L., et al.. (2021). Primary care providers’ responses to unsolicited Lynch syndrome secondary findings of varying clinical significance. Genetics in Medicine. 23(10). 1977–1983. 5 indexed citations

11.

Lewis, Anna, Bartha Maria Knoppers, & Robert C. Green. (2021). An international policy on returning genomic research results. Genome Medicine. 13(1). 115–115. 21 indexed citations

12.

Schwartz, Talia S., Kurt D. Christensen, Melissa Kurtz Uveges, et al.. (2021). Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. Journal of Genetic Counseling. 31(1). 218–229. 7 indexed citations

13.

Lane, William J., Nicholas Gleadall, Sunitha Vege, et al.. (2020). Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry. Transfusion. 60(6). 1294–1307. 10 indexed citations

14.

Lane, William J., Sunitha Vege, Helen Mah, et al.. (2019). Automated typing of red blood cell and platelet antigens from whole exome sequences. Transfusion. 59(10). 3253–3263. 29 indexed citations

15.

Ziniel, Sonja I., Sarah Savage, Kurt D. Christensen, et al.. (2018). Enhancing Autonomy in Biobank Decisions: Too Much of a Good Thing?. Journal of Empirical Research on Human Research Ethics. 13(2). 125–138. 5 indexed citations

16.

Guan, Yue, Debra Roter, Lori H. Erby, et al.. (2018). Communication Predictors of Patient and Companion Satisfaction with Alzheimer’s Genetic Risk Disclosure. Journal of Health Communication. 23(8). 807–814. 8 indexed citations

17.

Christensen, Kurt D., Sarah Savage, Noelle Huntington, et al.. (2016). Family health history reporting is sensitive to small changes in wording. Genetics in Medicine. 18(12). 1308–1311. 6 indexed citations

18.

Christensen, Kurt D., Dmitry Dukhovny, Uwe Siebert, & Robert C. Green. (2015). Assessing the Costs and Cost-Effectiveness of Genomic Sequencing. Journal of Personalized Medicine. 5(4). 470–486. 77 indexed citations

19.

Peterson, David B., Chris Corcoran, Carlos Cruchaga, et al.. (2013). Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: The Cache County Dementia Progression Study. Alzheimer s & Dementia. 10(3). 366–371. 28 indexed citations

20.

Fanshawe, Thomas, A Toby Prevost, J. Scott Roberts, et al.. (2008). Explaining Behavior Change after Genetic Testing: The Problem of Collinearity between Test Results and Risk Estimates. Genetic Testing. 12(3). 381–386. 20 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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