Anna L. Mitchell
Impact in
- Genetics top 5%
- Connective tissue disorders research
- Cleft Lip and Palate Research
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Dermatological and Skeletal Disorders
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 5
- Genomics and Rare Diseases 4
- Dermatological and Skeletal Disorders 3
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- Prenatal Screening and Diagnostics 2
- Co-authors
- Laura L. Konczal (1 shared paper)Marilyn C. Jones (1 shared paper)Kosuke Izumi (1 shared paper)Peter H. Byers (3 shared papers)Ulrike Schwarze (2 shared papers)Mitchell L. Drumm (4 shared papers)Lisa Joy Martin (1 shared paper)Sarah L. Zimmerman (1 shared paper)
- Journals
- Journal of Cystic Fibrosis (3 papers)The American Journal of Human Genetics (3 papers)Clinical Genetics (2 papers)Human Mutation (2 papers)Genetics in Medicine (2 papers)
- Partner nations
- United StatesFranceNew Zealand
In The Last Decade
Anna L. Mitchell
25 papers receiving 718 citations
Peers
Comparison fields: 5 of 73
- Genetics 448
- Developmental Biology 10
- Pharmacy 15
- Periodontics 23
- Pediatrics, Perinatology and Child Health 35
Countries citing papers authored by Anna L. Mitchell
This map shows the geographic impact of Anna L. Mitchell'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 Anna L. Mitchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna L. Mitchell more than expected).
Fields of papers citing papers by Anna L. Mitchell
This network shows the impact of papers produced by Anna L. Mitchell. 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 Anna L. Mitchell. The network helps show where Anna L. Mitchell may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna L. Mitchell, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 113 | |
| 2 | 2012 | 94 | |
| 3 | 2016 | 93 | |
| 4 | 2012 | 69 | |
| 5 | 2018 | 61 | |
| 6 | 2003 | 42 | |
| 7 | 2009 | 37 | |
| 8 | 2016 | 31 | |
| 9 | 2019 | 28 | |
| 10 | 2015 | 26 | |
| 11 | 2020 | 25 | |
| 12 | 2013 | 20 | |
| 13 | 2018 | 18 | |
| 14 | 2012 | 16 | |
| 15 | 2005 | 15 | |
| 16 | 2013 | 13 | |
| 17 | 2020 | 12 | |
| 18 | 2016 | 11 | |
| 19 | 2015 | 9 | |
| 20 | 2011 | 8 |
About Anna L. Mitchell
Anna L. Mitchell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine, Developmental Biology and Demography, having authored 25 papers that have together received 755 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Connective tissue disorders research (5 papers), Genomics and Rare Diseases (4 papers), Dermatological and Skeletal Disorders (3 papers), Cystic Fibrosis Research Advances (3 papers), Prenatal Screening and Diagnostics (2 papers), Congenital limb and hand anomalies (1 paper) and RNA Research and Splicing (1 paper). The work is most often cited by research in Genetics (448 citations), Developmental Biology (10 citations), Pharmacy (15 citations), Periodontics (23 citations) and Pediatrics, Perinatology and Child Health (35 citations). Anna L. Mitchell has collaborated with scholars based in United States, France and New Zealand. Frequent co-authors include Laura L. Konczal, Marilyn C. Jones, Kosuke Izumi, Peter H. Byers, Ulrike Schwarze, Mitchell L. Drumm, Lisa Joy Martin, Sarah L. Zimmerman, Carlos Enrique Prada and Lauren E. Grote. Their work appears in journals such as Journal of Cystic Fibrosis, The American Journal of Human Genetics, Clinical Genetics, Human Mutation and Genetics in Medicine.
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.