Weiya He
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Prenatal Screening and Diagnostics 2
- Co-authors
- Emily G. Allen (11 shared papers)Stephanie L. Sherman (11 shared papers)Krista Charen (6 shared papers)Celia E. Dominguez (2 shared papers)Chanley M. Small (1 shared paper)Michele Marcus (1 shared paper)Amy K. Sullivan (1 shared paper)Kira C. Taylor (1 shared paper)
- Journals
- Human Genetics (3 papers)Human Reproduction (2 papers)Genetics in Medicine (2 papers)Frontiers in Psychiatry (1 paper)Neuropeptides (1 paper)
- Partner nations
- United StatesChinaJapan
In The Last Decade
Weiya He
13 papers receiving 501 citations
Peers
Comparison fields: 5 of 44
- Genetics 400
- Cognitive Neuroscience 165
- Reproductive Medicine 26
- Molecular Biology 162
- Aging 4
Countries citing papers authored by Weiya He
This map shows the geographic impact of Weiya He'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 Weiya He with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Weiya He more than expected).
Fields of papers citing papers by Weiya He
This network shows the impact of papers produced by Weiya He. 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 Weiya He. The network helps show where Weiya He may publish in the future.
Co-authors
The 25 scholars most cited alongside Weiya He, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 170 | |
| 2 | 2004 | 100 | |
| 3 | 2008 | 64 | |
| 4 | 2009 | 52 | |
| 5 | 2020 | 37 | |
| 6 | 2021 | 32 | |
| 7 | 2015 | 17 | |
| 8 | 2015 | 17 | |
| 9 | 2018 | 8 | |
| 10 | 2021 | 6 | |
| 11 | 2017 | 4 | |
| 12 | 2020 | 1 | |
| 13 | 2007 | 1 | |
| 14 | 2025 | 0 |
About Weiya He
Weiya He is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience, Molecular Biology and Surgery, having authored 14 papers that have together received 509 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Autism Spectrum Disorder Research (3 papers), Prenatal Screening and Diagnostics (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Epigenetics and DNA Methylation (1 paper), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper), Family and Disability Support Research (1 paper) and Telomeres, Telomerase, and Senescence (1 paper). The work is most often cited by research in Genetics (400 citations), Cognitive Neuroscience (165 citations), Reproductive Medicine (26 citations), Molecular Biology (162 citations) and Aging (4 citations). Weiya He has collaborated with scholars based in United States, China and Japan. Frequent co-authors include Emily G. Allen, Stephanie L. Sherman, Krista Charen, Celia E. Dominguez, Chanley M. Small, Michele Marcus, Amy K. Sullivan, Kira C. Taylor, Michael P. Epstein and Heather S. Hipp. Their work appears in journals such as Human Genetics, Human Reproduction, Genetics in Medicine, Frontiers in Psychiatry and Neuropeptides.
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.