Jeannine Gerhardt

1.5k total citations
25 papers, 1.1k citations indexed

About

Jeannine Gerhardt is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Jeannine Gerhardt has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 4 papers in Cognitive Neuroscience. Recurrent topics in Jeannine Gerhardt's work include DNA Repair Mechanisms (13 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Epigenetics and DNA Methylation (9 papers). Jeannine Gerhardt is often cited by papers focused on DNA Repair Mechanisms (13 papers), Genetics and Neurodevelopmental Disorders (11 papers) and Epigenetics and DNA Methylation (9 papers). Jeannine Gerhardt collaborates with scholars based in United States, Germany and Israel. Jeannine Gerhardt's co-authors include Zev Rosenwaks, Nikica Zaninović, Dilek Colak, Samie R. Jaffrey, Matthew D. Disney, Michael S. Cohen, Advaitha Madireddy, Ellen Fanning, Carl L. Schildkraut and Zi Yan and has published in prestigious journals such as Science, Nature Communications and The Journal of Cell Biology.

In The Last Decade

Jeannine Gerhardt

25 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jeannine Gerhardt United States 16 808 412 180 141 114 25 1.1k
Alexei Stortchevoi United States 12 828 1.0× 335 0.8× 159 0.9× 115 0.8× 31 0.3× 18 988
Anna Marozzi Italy 21 778 1.0× 672 1.6× 47 0.3× 133 0.9× 33 0.3× 50 1.5k
Todor Dimitrov United States 12 716 0.9× 247 0.6× 159 0.9× 36 0.3× 84 0.7× 21 1.1k
Lionel A. Sanz United States 17 2.5k 3.0× 543 1.3× 178 1.0× 30 0.2× 68 0.6× 20 2.7k
Dennis Burian United States 12 412 0.5× 109 0.3× 95 0.5× 32 0.2× 22 0.2× 24 871
Ghazala Mirza United Kingdom 18 552 0.7× 714 1.7× 37 0.2× 38 0.3× 16 0.1× 20 1.1k
Elías Bechara France 12 837 1.0× 335 0.8× 54 0.3× 90 0.6× 29 0.3× 13 978
Wuzhou Yuan China 19 652 0.8× 131 0.3× 81 0.5× 11 0.1× 60 0.5× 73 909
Eric Karlins United States 12 266 0.3× 214 0.5× 88 0.5× 17 0.1× 75 0.7× 17 648
Zhihai Ma United States 10 664 0.8× 187 0.5× 88 0.5× 55 0.4× 15 0.1× 11 828

Countries citing papers authored by Jeannine Gerhardt

Since Specialization
Citations

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

Fields of papers citing papers by Jeannine Gerhardt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jeannine Gerhardt

This figure shows the co-authorship network connecting the top 25 collaborators of Jeannine Gerhardt. A scholar is included among the top collaborators of Jeannine Gerhardt 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 Jeannine Gerhardt. Jeannine Gerhardt 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.
Zuccaro, Michael V., et al.. (2024). DNA replication in early mammalian embryos is patterned, predisposing lamina-associated regions to fragility. Nature Communications. 15(1). 5247–5247. 13 indexed citations
2.
Edwards, Matthew, Ning Wang, Ido Sagi, et al.. (2024). Parent-of-origin-specific DNA replication timing is confined to large imprinted regions. Cell Reports. 43(9). 114700–114700. 1 indexed citations
3.
Madireddy, Advaitha & Jeannine Gerhardt. (2023). Visualizing DNA replication by single-molecule analysis of replicated DNA. STAR Protocols. 4(4). 102721–102721. 1 indexed citations
4.
Deshpande, Madhura, Gouri J. Nanjangud, Amnon Koren, et al.. (2022). Error-prone repair of stalled replication forks drives mutagenesis and loss of heterozygosity in haploinsufficient BRCA1 cells. Molecular Cell. 82(20). 3781–3793.e7. 13 indexed citations
5.
Ding, Qiliang, Matthew Edwards, Ning Wang, et al.. (2021). The genetic architecture of DNA replication timing in human pluripotent stem cells. Nature Communications. 12(1). 6746–6746. 22 indexed citations
6.
Fan, Yilin, et al.. (2021). LRR1-mediated replisome disassembly promotes DNA replication by recycling replisome components. The Journal of Cell Biology. 220(8). 15 indexed citations
7.
Deshpande, Madhura & Jeannine Gerhardt. (2018). Break-induced replication sparks CGG-repeat instability. Nature Structural & Molecular Biology. 25(8). 643–644. 1 indexed citations
8.
Guler, Gulfem D., Zev Rosenwaks, & Jeannine Gerhardt. (2018). Human DNA Helicase B as a Candidate for Unwinding Secondary CGG Repeat Structures at the Fragile X Mental Retardation Gene. Frontiers in Molecular Neuroscience. 11. 138–138. 7 indexed citations
9.
Lekovich, Jovana P., Kangpu Xu, Chelsea M. Canon, et al.. (2017). CGG repeat length and AGG interruptions as indicators of fragile X–associated diminished ovarian reserve. Genetics in Medicine. 20(9). 957–964. 20 indexed citations
10.
Madireddy, Advaitha & Jeannine Gerhardt. (2017). Replication Through Repetitive DNA Elements and Their Role in Human Diseases. Advances in experimental medicine and biology. 1042. 549–581. 22 indexed citations
11.
Lekovich, Jovana P., et al.. (2017). Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations. Frontiers in Molecular Neuroscience. 10. 290–290. 47 indexed citations
12.
Reichman, David E., Laura Park, Raphaël Lis, et al.. (2016). Notch hyper-activation drives trans-differentiation of hESC-derived endothelium. Stem Cell Research. 17(2). 391–400. 11 indexed citations
13.
Gerhardt, Jeannine, Angela D. Bhalla, Jill Sergesketter Butler, et al.. (2016). Stalled DNA Replication Forks at the Endogenous GAA Repeats Drive Repeat Expansion in Friedreich’s Ataxia Cells. Cell Reports. 16(5). 1218–1227. 51 indexed citations
14.
Madireddy, Advaitha, Settapong T Kosiyatrakul, Emilia Herrera‐Moyano, et al.. (2016). FANCD2 Facilitates Replication through Common Fragile Sites. Molecular Cell. 64(2). 388–404. 132 indexed citations
15.
Gerhardt, Jeannine. (2015). Epigenetic modifications in human fragile X pluripotent stem cells; Implications in fragile X syndrome modeling. Brain Research. 1656. 55–62. 12 indexed citations
16.
Gerhardt, Jeannine, Gulfem D. Guler, & Ellen Fanning. (2015). Human DNA helicase B interacts with the replication initiation protein Cdc45 and facilitates Cdc45 binding onto chromatin. Experimental Cell Research. 334(2). 283–293. 16 indexed citations
17.
Colak, Dilek, Nikica Zaninović, Michael S. Cohen, et al.. (2014). Promoter-Bound Trinucleotide Repeat mRNA Drives Epigenetic Silencing in Fragile X Syndrome. Science. 343(6174). 1002–1005. 231 indexed citations
18.
Gerhardt, Jeannine, Mark Tomishima, Nikica Zaninović, et al.. (2013). The DNA Replication Program Is Altered at the FMR1 Locus in Fragile X Embryonic Stem Cells. Molecular Cell. 53(1). 19–31. 84 indexed citations
19.
Gray, Steven J., et al.. (2006). An Origin of DNA Replication in the Promoter Region of the Human Fragile X Mental Retardation (FMR1) Gene. Molecular and Cellular Biology. 27(2). 426–437. 39 indexed citations
20.
Gerhardt, Jeannine, et al.. (2006). Identification of New Human Origins of DNA Replication by an Origin-Trapping Assay. Molecular and Cellular Biology. 26(20). 7731–7746. 32 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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