Shira Rockowitz

2.9k total citations
38 papers, 1.7k citations indexed

About

Shira Rockowitz is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Shira Rockowitz has authored 38 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Shira Rockowitz's work include Epigenetics and DNA Methylation (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Chromatin Dynamics (5 papers). Shira Rockowitz is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Genomics and Chromatin Dynamics (5 papers). Shira Rockowitz collaborates with scholars based in United States, Türkiye and Israel. Shira Rockowitz's co-authors include Deyou Zheng, Gang Greg Wang, Elaine Fuchs, Maria Nikolova, Amma Asare, Rene C. Adam, Meelis Kadaja, Samantha B. Larsen, Hanseul Yang and Daniel Oristian and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Shira Rockowitz

33 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Shira Rockowitz United States 17 1.3k 287 284 259 146 38 1.7k
Rebecca Haffner‐Krausz Israel 12 1.2k 1.0× 293 1.0× 115 0.4× 90 0.3× 139 1.0× 22 1.6k
Heinrich Schrewe Germany 28 1.5k 1.2× 373 1.3× 93 0.3× 221 0.9× 254 1.7× 46 2.2k
Kumi Kawai Japan 22 1.0k 0.8× 218 0.8× 104 0.4× 172 0.7× 350 2.4× 36 1.8k
Cecilia Bondjers Sweden 11 838 0.7× 181 0.6× 106 0.4× 171 0.7× 131 0.9× 11 1.3k
Brian Gavin United States 11 1.5k 1.2× 346 1.2× 144 0.5× 364 1.4× 212 1.5× 17 2.0k
Christophe Houbron France 16 1.4k 1.1× 299 1.0× 62 0.2× 133 0.5× 117 0.8× 24 2.0k
Emilia Vitale Italy 16 646 0.5× 762 2.7× 231 0.8× 240 0.9× 119 0.8× 38 1.6k
Deborah Lang United States 21 1.3k 1.0× 242 0.8× 158 0.6× 268 1.0× 381 2.6× 37 2.0k
Sylvie Taviaux France 21 992 0.8× 312 1.1× 102 0.4× 144 0.6× 213 1.5× 42 1.5k
Tommaso Pippucci Italy 23 708 0.6× 663 2.3× 81 0.3× 215 0.8× 93 0.6× 71 1.5k

Countries citing papers authored by Shira Rockowitz

Since Specialization
Citations

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

Fields of papers citing papers by Shira Rockowitz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shira Rockowitz

This figure shows the co-authorship network connecting the top 25 collaborators of Shira Rockowitz. A scholar is included among the top collaborators of Shira Rockowitz 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 Shira Rockowitz. Shira Rockowitz 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.
Genetti, Casie A., Tanya Logvinenko, Leslie H. Hayes, et al.. (2025). Retrospective Cohort Analysis of Clinical, Molecular, and Histopathologic Characteristics of 275 Patients With Nemaline Myopathy. Neurology Genetics. 11(4). e200277–e200277.
2.
Arnett, Anne B., Ryan Koesterer, Han Zhang, et al.. (2025). Common and rare genetic variants explain distinct diagnostic variance in pediatric attention deficit hyperactivity disorder. Genetics in Medicine. 27(12). 101598–101598.
3.
Kane, Jennifer, Ashish Jain, Liang Sun, et al.. (2024). Basophils Play a Protective Role in the Recovery of Skin Barrier Function from Mechanical Injury in Mice. Journal of Investigative Dermatology. 144(8). 1784–1797.e4. 5 indexed citations
4.
Tindula, Gwen, Biju Issac, Liang Sun, et al.. (2024). Genome‐wide analysis of spina bifida risk variants in a case–control study from Bangladesh. Birth Defects Research. 116(3). e2331–e2331. 2 indexed citations
5.
D’Gama, Alissa M., Wanqing Shao, Lacey Smith, et al.. (2024). Genome Sequencing After Exome Sequencing in Pediatric Epilepsy. JAMA Neurology. 81(12). 1316–1316. 2 indexed citations
6.
Dias, Caroline, Alisa Mo, Chunhui Cai, et al.. (2024). Cell-type-specific effects of autism-associated 15q duplication syndrome in the human brain. The American Journal of Human Genetics. 111(8). 1544–1558. 6 indexed citations
7.
Fligor, Scott C., Savas T. Tsikis, Ashish Jain, et al.. (2024). Inflammation drives pathogenesis of early intestinal failure-associated liver disease. Scientific Reports. 14(1). 4240–4240. 8 indexed citations
8.
Hojlo, Margaret A., Casie A. Genetti, Richard S. Smith, et al.. (2023). Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes. 14(4). 779–779. 5 indexed citations
9.
Rockowitz, Shira, Ted Lee, Bo Zhang, et al.. (2023). Toward representative genomic research: the children’s rare disease cohorts experience. PubMed. 4. 921091166–921091166. 3 indexed citations
10.
Nguyen, Alan A., Saddiq Habiballah, Megan Day‐Lewis, et al.. (2023). Rethinking Immunological Risk: A Retrospective Cohort Study of Severe SARS-Cov-2 Infections in Individuals With Congenital Immunodeficiencies. The Journal of Allergy and Clinical Immunology In Practice. 11(11). 3391–3399.e3. 5 indexed citations
11.
Shubina-Oleinik, Olga, Carl Nist-Lund, Courtney E. French, et al.. (2021). Dual-vector gene therapy restores cochlear amplification and auditory sensitivity in a mouse model of DFNB16 hearing loss. Science Advances. 7(51). eabi7629–eabi7629. 48 indexed citations
12.
Cao, Chang, Miguel A. Prado, Liang Sun, et al.. (2021). Maternal Iron Deficiency Modulates Placental Transcriptome and Proteome in Mid-Gestation of Mouse Pregnancy. Journal of Nutrition. 151(5). 1073–1083. 15 indexed citations
13.
French, Courtney E., et al.. (2021). Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings. Human Genetics. 141(3-4). 387–400. 16 indexed citations
14.
Lu, Rui, Ping Wang, Trevor Parton, et al.. (2016). Epigenetic Perturbations by Arg882-Mutated DNMT3A Potentiate Aberrant Stem Cell Gene-Expression Program and Acute Leukemia Development. Cancer Cell. 30(1). 92–107. 116 indexed citations
15.
Rockowitz, Shira & Deyou Zheng. (2015). Significant expansion of the REST/NRSF cistrome in human versus mouse embryonic stem cells: potential implications for neural development. Nucleic Acids Research. 43(12). 5730–5743. 32 indexed citations
16.
Sun, Jian, Shira Rockowitz, Qing Xie, et al.. (2015). Identification ofin vivoDNA-binding mechanisms of Pax6 and reconstruction of Pax6-dependent gene regulatory networks during forebrain and lens development. Nucleic Acids Research. 43(14). 6827–6846. 82 indexed citations
17.
Adam, Rene C., Hanseul Yang, Shira Rockowitz, et al.. (2015). Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice. Nature. 521(7552). 366–370. 291 indexed citations
18.
Rockowitz, Shira, Wen‐Hui Lien, Erika Pedrosa, et al.. (2014). Comparison of REST Cistromes across Human Cell Types Reveals Common and Context-Specific Functions. PLoS Computational Biology. 10(6). e1003671–e1003671. 29 indexed citations
19.
Chen, Yu, Ping Chi, Shira Rockowitz, et al.. (2013). ETS factors reprogram the androgen receptor cistrome and prime prostate tumorigenesis in response to PTEN loss. Nature Medicine. 19(8). 1023–1029. 196 indexed citations
20.
Cai, Ling, Scott B. Rothbart, Rui Lu, et al.. (2012). An H3K36 Methylation-Engaging Tudor Motif of Polycomb-like Proteins Mediates PRC2 Complex Targeting. Molecular Cell. 49(3). 571–582. 181 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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