Stephanie Greer

1.4k total citations
18 papers, 339 citations indexed

About

Stephanie Greer is a scholar working on Molecular Biology, Cancer Research and Pathology and Forensic Medicine. According to data from OpenAlex, Stephanie Greer has authored 18 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Cancer Research and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Stephanie Greer's work include Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (5 papers) and Genomics and Phylogenetic Studies (5 papers). Stephanie Greer is often cited by papers focused on Cancer Genomics and Diagnostics (9 papers), Genetic factors in colorectal cancer (5 papers) and Genomics and Phylogenetic Studies (5 papers). Stephanie Greer collaborates with scholars based in United States, Australia and South Korea. Stephanie Greer's co-authors include Hanlee P. Ji, Jiamin Chen, Susan M. Grimes, Matthew Kubit, John Bell, Lincoln Nadauld, Billy T. Lau, Noemi Andor, William A. Weiss and Grace Zheng and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Blood.

In The Last Decade

Stephanie Greer

17 papers receiving 338 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephanie Greer United States 9 229 90 62 58 49 18 339
Semyon Kolmykov Russia 9 384 1.7× 92 1.0× 78 1.3× 37 0.6× 54 1.1× 19 528
Hannah F. Almubarak Saudi Arabia 5 252 1.1× 110 1.2× 94 1.5× 60 1.0× 26 0.5× 7 371
Ashley Cass United States 8 319 1.4× 105 1.2× 48 0.8× 59 1.0× 60 1.2× 13 429
Yury V. Kondrakhin Russia 7 338 1.5× 74 0.8× 51 0.8× 34 0.6× 44 0.9× 12 446
Lydia Hopp Germany 15 316 1.4× 79 0.9× 48 0.8× 65 1.1× 53 1.1× 26 430
Zhenzhen Wen China 13 237 1.0× 147 1.6× 23 0.4× 63 1.1× 95 1.9× 26 476
Gergana Bounova Netherlands 7 307 1.3× 95 1.1× 32 0.5× 80 1.4× 34 0.7× 7 390
Austin J. Hepperla United States 12 419 1.8× 69 0.8× 32 0.5× 49 0.8× 32 0.7× 22 485
Sonal Datta India 9 284 1.2× 67 0.7× 51 0.8× 130 2.2× 29 0.6× 15 418
Yelena Chernyavskaya United States 9 403 1.8× 119 1.3× 38 0.6× 42 0.7× 53 1.1× 12 510

Countries citing papers authored by Stephanie Greer

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Greer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Greer

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

All Works

18 of 18 papers shown
1.
Zhou, Bo, Carolin Purmann, Hanmin Guo, et al.. (2024). Resolving the 22q11.2 deletion using CTLR-Seq reveals chromosomal rearrangement mechanisms and individual variance in breakpoints. Proceedings of the National Academy of Sciences. 121(31). e2322834121–e2322834121.
2.
Greer, Stephanie, et al.. (2023). Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic. Journal of Translational Medicine. 21(1). 378–378. 7 indexed citations
3.
Greer, Stephanie, Jiamin Chen, Margrét H. Ögmundsdóttir, et al.. (2022). Germline variants of ATG7 in familial cholangiocarcinoma alter autophagy and p62. Scientific Reports. 12(1). 10333–10333. 6 indexed citations
4.
Vogelaar, Ingrid P., Stephanie Greer, Fan Wang, et al.. (2022). Large Cancer Pedigree Involving Multiple Cancer Genes including Likely Digenic MSH2 and MSH6 Lynch Syndrome (LS) and an Instance of Recombinational Rescue from LS. Cancers. 15(1). 228–228. 2 indexed citations
5.
Pavlichin, Dmitri S., HoJoon Lee, Stephanie Greer, et al.. (2022). KmerKeys: a web resource for searching indexed genome assemblies and variants. Nucleic Acids Research. 50(W1). W448–W453. 2 indexed citations
6.
Zhao, Lan, Susan M. Grimes, Stephanie Greer, et al.. (2021). Characterization of the consensus mucosal microbiome of colorectal cancer. NAR Cancer. 3(4). zcab049–zcab049. 15 indexed citations
7.
Shin, Gi Won, Stephanie Greer, Erik Hopmans, et al.. (2021). Profiling diverse sequence tandem repeats in colorectal cancer reveals co-occurrence of microsatellite and chromosomal instability involving Chromosome 8. Genome Medicine. 13(1). 145–145. 8 indexed citations
8.
Hummelen, Paul Van, Matthew Kubit, HoJoon Lee, et al.. (2020). Whole genome analysis identifies the association of TP53 genomic deletions with lower survival in Stage III colorectal cancer. Scientific Reports. 10(1). 5009–5009. 6 indexed citations
9.
Shin, Gi Won, Stephanie Greer, HoJoon Lee, et al.. (2019). Targeted short read sequencing and assembly of re-arrangements and candidate gene loci provide megabase diplotypes. Nucleic Acids Research. 47(19). e115–e115. 8 indexed citations
10.
Zhou, Bo, Steve S. Ho, Stephanie Greer, et al.. (2019). Haplotype-resolved and integrated genome analysis of the cancer cell line HepG2. Nucleic Acids Research. 47(8). 3846–3861. 41 indexed citations
11.
Zhou, Bo, Steve S. Ho, Stephanie Greer, et al.. (2019). Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562. Genome Research. 29(3). 472–484. 60 indexed citations
12.
Greer, Stephanie, et al.. (2019). Structural variant analysis for linked-read sequencing data with gemtools. Bioinformatics. 35(21). 4397–4399. 8 indexed citations
13.
Sathe, Anuja, Billy T. Lau, Susan M. Grimes, Stephanie Greer, & Hanlee P. Ji. (2019). Abstract 2105: Single cell RNA sequencing reveals multiple adaptive resistance mechanisms to regorafenib in colon cancer. Cancer Research. 79(13_Supplement). 2105–2105. 1 indexed citations
14.
Andor, Noemi, Valeria Perrina, Darius Juškevičius, et al.. (2018). Exploring the spatiotemporal genetic heterogeneity in metastatic lung adenocarcinoma using a nuclei flow‐sorting approach. The Journal of Pathology. 247(2). 199–213. 7 indexed citations
15.
Andor, Noemi, Erin F. Simonds, Debra K. Czerwinski, et al.. (2018). Single-cell RNA-Seq of follicular lymphoma reveals malignant B-cell types and coexpression of T-cell immune checkpoints. Blood. 133(10). 1119–1129. 77 indexed citations
16.
Greer, Stephanie, Lincoln Nadauld, Billy T. Lau, et al.. (2017). Linked read sequencing resolves complex genomic rearrangements in gastric cancer metastases. Genome Medicine. 9(1). 57–57. 38 indexed citations
17.
Bell, John, Billy T. Lau, Stephanie Greer, et al.. (2017). Chromosome-scale mega-haplotypes enable digital karyotyping of cancer aneuploidy. Nucleic Acids Research. 45(19). e162–e162. 22 indexed citations
18.

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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