Wenli Gu
Impact in
- Genetics top 1%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Developmental Neuroscience top 5%
Papers in
-
- Congenital heart defects research 7
- Hedgehog Signaling Pathway Studies 4
- Ion channel regulation and function 4
- Genetics 13
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- James R. Lupski (12 shared papers)Feng Zhang (2 shared papers)Matthew E. Hurles (1 shared paper)Peihua Lu (2 shared papers)Ortrud K. Steinlein (9 shared papers)Eylert Brodtkorb (3 shared papers)Melanie Lacaria (5 shared papers)Christian Derst (2 shared papers)
- Journals
- Genetics in Medicine (2 papers)JAMA Network Open (1 paper)Human Molecular Genetics (1 paper)Adipocyte (1 paper)European Journal of Preventive Cardiology (1 paper)
- Partner nations
- ChinaUnited StatesGermany
In The Last Decade
Wenli Gu
44 papers receiving 2.6k citations
Wenli Gu's Hit Papers
Peers
Comparison fields: 5 of 116
- Genetics 1.3k
- Developmental Neuroscience 151
- Cellular and Molecular Neuroscience 372
- Molecular Biology 1.4k
- Cell Biology 302
Countries citing papers authored by Wenli Gu
This map shows the geographic impact of Wenli Gu'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 Wenli Gu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wenli Gu more than expected).
Fields of papers citing papers by Wenli Gu
This network shows the impact of papers produced by Wenli Gu. 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 Wenli Gu. The network helps show where Wenli Gu may publish in the future.
Co-authors
The 25 scholars most cited alongside Wenli Gu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 47 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Copy Number Variation in Human Health, Disease, and Evolution Hit paper breakdown → | 2009 | 869 |
| 2 | 2008 | 443 | |
| 3 | [Chondroitin sulfate proteoglycans in neural development and regeneration]. | 2007 | 195 |
| 4 | 2007 | 118 | |
| 5 | 2002 | 113 | |
| 6 | 2002 | 88 | |
| 7 | 2022 | 88 | |
| 8 | 2010 | 71 | |
| 9 | 2002 | 63 | |
| 10 | 2016 | 59 | |
| 11 | 2008 | 54 | |
| 12 | 2002 | 51 | |
| 13 | 2012 | 46 | |
| 14 | 2012 | 36 | |
| 15 | 2014 | 33 | |
| 16 | 2019 | 31 | |
| 17 | 2008 | 30 | |
| 18 | 2011 | 25 | |
| 19 | 2012 | 25 | |
| 20 | 2013 | 22 |
About Wenli Gu
Wenli Gu is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Cell Biology and Neurology, having authored 47 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Congenital heart defects research (7 papers), Neuroscience and Neuropharmacology Research (4 papers), Hedgehog Signaling Pathway Studies (4 papers), Chromosomal and Genetic Variations (4 papers), Ion channel regulation and function (4 papers), Autoimmune Neurological Disorders and Treatments (4 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Genetics (1.3k citations), Developmental Neuroscience (151 citations), Cellular and Molecular Neuroscience (372 citations), Molecular Biology (1.4k citations) and Cell Biology (302 citations). Wenli Gu has collaborated with scholars based in China, United States and Germany. Frequent co-authors include James R. Lupski, Feng Zhang, Matthew E. Hurles, Peihua Lu, Ortrud K. Steinlein, Eylert Brodtkorb, Melanie Lacaria, Christian Derst, Sai‐Li Fu and Pei‐Hua Lu. Their work appears in journals such as Genetics in Medicine, JAMA Network Open, Human Molecular Genetics, Adipocyte and European Journal of Preventive Cardiology.
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.