Anne V Hing
Impact in
- Genetics top 1%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Congenital Ear and Nasal Anomalies
- Developmental Biology top 2%
Papers in
- Genetics 82
- Craniofacial Disorders and Treatments 40
- Genomics and Rare Diseases 20
- Cleft Lip and Palate Research 15
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 8
- Congenital Ear and Nasal Anomalies 4
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- Congenital limb and hand anomalies 6
- Co-authors
- Michael L. Cunningham (26 shared papers)Carrie L. Heike (13 shared papers)Daniela V. Luquetti (7 shared papers)Timothy C. Cox (5 shared papers)Richard A. Hopper (5 shared papers)Helen Donis-Keller (4 shared papers)Kelly N. Evans (5 shared papers)Kathleen C.Y. Sie (4 shared papers)
- Journals
- Genetics in Medicine (14 papers)The American Journal of Human Genetics (13 papers)The Cleft Palate-Craniofacial Journal (6 papers)Human Molecular Genetics (4 papers)Genomics (3 papers)
- Partner nations
- United StatesAustraliaNetherlands
In The Last Decade
Anne V Hing
98 papers receiving 4.1k citations
Peers
Comparison fields: 5 of 107
- Genetics 2.3k
- Developmental Biology 138
- Genetics 273
- Pediatrics, Perinatology and Child Health 255
- Molecular Biology 926
Countries citing papers authored by Anne V Hing
This map shows the geographic impact of Anne V Hing'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 Anne V Hing with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anne V Hing more than expected).
Fields of papers citing papers by Anne V Hing
This network shows the impact of papers produced by Anne V Hing. 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 Anne V Hing. The network helps show where Anne V Hing may publish in the future.
Co-authors
The 25 scholars most cited alongside Anne V Hing, 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 101 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 539 | |
| 2 | 2011 | 333 | |
| 3 | 2011 | 226 | |
| 4 | 2010 | 179 | |
| 5 | 2009 | 165 | |
| 6 | 1999 | 162 | |
| 7 | 2008 | 155 | |
| 8 | 2021 | 139 | |
| 9 | 2009 | 134 | |
| 10 | 2018 | 101 | |
| 11 | 2007 | 92 | |
| 12 | 2009 | 82 | |
| 13 | 2013 | 79 | |
| 14 | 2012 | 75 | |
| 15 | 2006 | 74 | |
| 16 | 2007 | 73 | |
| 17 | 2010 | 69 | |
| 18 | 1999 | 63 | |
| 19 | 2021 | 62 | |
| 20 | 1992 | 61 |
About Anne V Hing
Anne V Hing is a scholar working on Genetics, Developmental Biology, Genetics, Molecular Biology and Cell Biology, having authored 101 papers that have together received 4.3k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (40 papers), Genomics and Rare Diseases (20 papers), Cleft Lip and Palate Research (15 papers), Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (8 papers), Congenital limb and hand anomalies (6 papers), Congenital Ear and Nasal Anomalies (4 papers) and Hereditary Neurological Disorders (3 papers). The work is most often cited by research in Genetics (2.3k citations), Developmental Biology (138 citations), Genetics (273 citations), Pediatrics, Perinatology and Child Health (255 citations) and Molecular Biology (926 citations). Anne V Hing has collaborated with scholars based in United States, Australia and Netherlands. Frequent co-authors include Michael L. Cunningham, Carrie L. Heike, Daniela V. Luquetti, Timothy C. Cox, Richard A. Hopper, Helen Donis-Keller, Kelly N. Evans, Kathleen C.Y. Sie, Cynthia Helms and Johanna M. Rommens. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, The Cleft Palate-Craniofacial Journal, Human Molecular Genetics and Genomics.
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.