Michael E. Zwick

10.4k total citations
70 papers, 2.7k citations indexed

About

Michael E. Zwick is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Michael E. Zwick has authored 70 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 37 papers in Molecular Biology and 8 papers in Plant Science. Recurrent topics in Michael E. Zwick's work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Congenital heart defects research (9 papers). Michael E. Zwick is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Congenital heart defects research (9 papers). Michael E. Zwick collaborates with scholars based in United States, Germany and United Kingdom. Michael E. Zwick's co-authors include David J. Cutler, David T. Okou, Charles F. Aquadro, Thomas M. Boyce, David J. Cutler, Karyn Meltz Steinberg, Christina M. Middle, Thomas J. Albert, Jennifer G. Mullé and Aravinda Chakravarti and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Michael E. Zwick

67 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael E. Zwick United States 24 1.7k 1.2k 300 294 149 70 2.7k
Aaron K. Wong United States 26 2.1k 1.2× 1.2k 0.9× 163 0.5× 85 0.3× 180 1.2× 47 3.4k
Christopher Gregg United States 21 1.9k 1.1× 1.0k 0.8× 119 0.4× 170 0.6× 70 0.5× 35 2.6k
Jeremy Leipzig United States 25 2.3k 1.3× 1.0k 0.8× 234 0.8× 113 0.4× 305 2.0× 31 3.4k
Wen Huang United States 37 1.2k 0.7× 1.7k 1.4× 418 1.4× 281 1.0× 45 0.3× 114 3.4k
Yang Wu China 29 1.2k 0.7× 1.5k 1.2× 159 0.5× 188 0.6× 231 1.6× 115 3.4k
Jessica Severin Japan 17 2.0k 1.2× 661 0.5× 296 1.0× 88 0.3× 102 0.7× 25 2.8k
Jinyu Wu China 26 1.1k 0.6× 441 0.4× 344 1.1× 88 0.3× 116 0.8× 73 1.9k
Zhenglong Gu United States 29 2.9k 1.6× 923 0.8× 1.0k 3.4× 136 0.5× 160 1.1× 101 4.0k
Francisco J. Silva Spain 35 2.1k 1.2× 950 0.8× 1.0k 3.3× 431 1.5× 308 2.1× 104 4.9k
Chris C. A. Spencer United Kingdom 20 989 0.6× 1.3k 1.1× 174 0.6× 74 0.3× 216 1.4× 26 2.3k

Countries citing papers authored by Michael E. Zwick

Since Specialization
Citations

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

Fields of papers citing papers by Michael E. Zwick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael E. Zwick. 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 Michael E. Zwick. The network helps show where Michael E. Zwick may publish in the future.

Co-authorship network of co-authors of Michael E. Zwick

This figure shows the co-authorship network connecting the top 25 collaborators of Michael E. Zwick. A scholar is included among the top collaborators of Michael E. Zwick 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 Michael E. Zwick. Michael E. Zwick 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.
Yilmaz, Feyza, Gurusamy Umamaheswaran, Pille Hallast, et al.. (2023). High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing. Genome Medicine. 15(1). 35–35. 4 indexed citations
2.
Kozlova, Alena, Siwei Zhang, Hanwen Zhang, et al.. (2022). Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neurons. The American Journal of Human Genetics. 109(8). 1500–1519. 9 indexed citations
3.
Zwick, Michael E.. (2021). Organizing core facilities as force multipliers: strategies for research universities. Journal of Biomolecular Techniques JBT. jbt.2021–3202. 3 indexed citations
4.
Murphy, Melissa M., et al.. (2020). New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry. American Journal of Medical Genetics Part A. 182(5). 1152–1166. 9 indexed citations
5.
Ahern, Thomas P., Lindsay J. Collin, James W. Baurley, et al.. (2020). Metabolic Pathway Analysis and Effectiveness of Tamoxifen in Danish Breast Cancer Patients. Cancer Epidemiology Biomarkers & Prevention. 29(3). 582–590. 7 indexed citations
6.
Zwick, Michael E., et al.. (2018). Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale. Genome biology. 19(1). 14–14. 20 indexed citations
7.
Rambo‐Martin, Benjamin L., David J. Cutler, Lora Jh Bean, et al.. (2017). Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. G3 Genes Genomes Genetics. 8(1). 105–111. 11 indexed citations
8.
Rosenfeld, Jill A., et al.. (2016). Novel features of 3q29 deletion syndrome: Results from the 3q29 registry. American Journal of Medical Genetics Part A. 170(4). 999–1006. 59 indexed citations
9.
Mercer, Kristina B., et al.. (2015). New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings. European Journal of Medical Genetics. 58(12). 704–714. 28 indexed citations
10.
Locke, Adam E., Lora Jh Bean, Tracie C. Rosser, et al.. (2014). Contribution of copy-number variation to Down syndrome–associated atrioventricular septal defects. Genetics in Medicine. 17(7). 554–560. 20 indexed citations
11.
Ezewudo, Matthew & Michael E. Zwick. (2013). Evaluating Rare Variants in Complex Disorders Using Next-Generation Sequencing. Current Psychiatry Reports. 15(4). 349–349. 12 indexed citations
12.
Zwick, Michael E., Sandeep J. Joseph, Xavier Didelot, et al.. (2012). Genomic characterization of theBacillus cereussensu lato species: Backdrop to the evolution ofBacillus anthracis. Genome Research. 22(8). 1512–1524. 120 indexed citations
13.
Okou, David T., Archana Kumar, Cary G. Sauer, et al.. (2012). Common NOD2 risk variants in African Americans with Crohnʼs disease are due exclusively to recent Caucasian admixture. Inflammatory Bowel Diseases. 18(12). 2357–2359. 16 indexed citations
14.
He, Miao, Lisa E. Kratz, Joshua J. Michel, et al.. (2011). Mutations in the human SC4MOL gene encoding a methyl sterol oxidase cause psoriasiform dermatitis, microcephaly, and developmental delay. Journal of Clinical Investigation. 121(3). 976–984. 82 indexed citations
15.
Zwick, Michael E., et al.. (2010). Predicting Cache Contention with Setvectors. mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich). 2 indexed citations
16.
Mullé, Jennifer G., Viren Patel, Stephen T. Warren, et al.. (2010). Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays. PLoS ONE. 5(3). e9921–e9921. 15 indexed citations
17.
Collins, Stephen C., Paul J. Benke, Elizabeth Berry‐Kravis, et al.. (2010). Array-Based FMR1 Sequencing and Deletion Analysis in Patients with a Fragile X Syndrome–Like Phenotype. PLoS ONE. 5(3). e9476–e9476. 23 indexed citations
18.
Shetty, Amol C., Prashanth Athri, Kajari Mondal, et al.. (2010). SeqAnt: A web service to rapidly identify and annotate DNA sequence variations. BMC Bioinformatics. 11(1). 471–471. 27 indexed citations
19.
Passalacqua, Karla D., et al.. (2009). Structure and Complexity of a Bacterial Transcriptome. Journal of Bacteriology. 191(10). 3203–3211. 171 indexed citations
20.
Hegde, Madhuri, Ephrem Chin, Jennifer G. Mullé, et al.. (2008). Microarray-based mutation detection in thedystrophingene. Human Mutation. 29(9). 1091–1099. 75 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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