Adele Schneider
Impact in
- Genetics top 2%
- Ocular Disorders and Treatments
- Congenital Ear and Nasal Anomalies
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 46
- Ocular Disorders and Treatments 36
- Congenital Ear and Nasal Anomalies 24
- Genomic variations and chromosomal abnormalities 6
- Craniofacial Disorders and Treatments 5
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- Retinal Development and Disorders 8
- Hedgehog Signaling Pathway Studies 5
- Co-authors
- Tanya Bardakjian (27 shared papers)Anthony R. Gregg (3 shared papers)Linda M. Reis (10 shared papers)Elena V. Semina (9 shared papers)Rebecca C. Tyler (4 shared papers)David Fitzpatrick (6 shared papers)Veronica van Heyningen (4 shared papers)Kathleen A. Williamson (4 shared papers)
- Journals
- Human Molecular Genetics (4 papers)Clinical Genetics (4 papers)European Journal of Human Genetics (2 papers)Genetics in Medicine (2 papers)American Journal of Obstetrics and Gynecology (2 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Adele Schneider
63 papers receiving 2.1k citations
Peers
Comparison fields: 5 of 100
- Genetics 502
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 366
- Ophthalmology 159
- Molecular Biology 908
Countries citing papers authored by Adele Schneider
This map shows the geographic impact of Adele Schneider'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 Adele Schneider with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Adele Schneider more than expected).
Fields of papers citing papers by Adele Schneider
This network shows the impact of papers produced by Adele Schneider. 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 Adele Schneider. The network helps show where Adele Schneider may publish in the future.
Co-authors
The 25 scholars most cited alongside Adele Schneider, 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 67 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2015 | 247 | |
| 2 | 2004 | 237 | |
| 3 | 2013 | 173 | |
| 4 | 2005 | 160 | |
| 5 | 2006 | 158 | |
| 6 | 2011 | 87 | |
| 7 | 2009 | 86 | |
| 8 | 2006 | 70 | |
| 9 | 2011 | 65 | |
| 10 | 2011 | 59 | |
| 11 | 2015 | 58 | |
| 12 | 2013 | 57 | |
| 13 | 2011 | 56 | |
| 14 | 2010 | 44 | |
| 15 | 2010 | 40 | |
| 16 | 2014 | 40 | |
| 17 | 2013 | 38 | |
| 18 | 1981 | 37 | |
| 19 | 2010 | 29 | |
| 20 | Identification of novel mutations and sequence variants in the SOX2 and CHX10 genes in patients with anophthalmia/microphthalmia. | 2008 | 26 |
About Adele Schneider
Adele Schneider is a scholar working on Genetics, Genetics, Molecular Biology, Surgery and Pediatrics, Perinatology and Child Health, having authored 67 papers that have together received 2.2k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (36 papers), Congenital Ear and Nasal Anomalies (24 papers), Reconstructive Facial Surgery Techniques (14 papers), Retinal Development and Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers), Prenatal Screening and Diagnostics (6 papers), Craniofacial Disorders and Treatments (5 papers) and Hedgehog Signaling Pathway Studies (5 papers). The work is most often cited by research in Genetics (502 citations), Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (366 citations), Ophthalmology (159 citations) and Molecular Biology (908 citations). Adele Schneider has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Tanya Bardakjian, Anthony R. Gregg, Linda M. Reis, Elena V. Semina, Rebecca C. Tyler, David Fitzpatrick, Veronica van Heyningen, Kathleen A. Williamson, Ronald J. Wapner and Roger V. Lebo. Their work appears in journals such as Human Molecular Genetics, Clinical Genetics, European Journal of Human Genetics, Genetics in Medicine and American Journal of Obstetrics and Gynecology.
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.