Emma Wakeling
Impact in
- Genetics top 2%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 43
- Genetic Syndromes and Imprinting 21
- Genetics and Neurodevelopmental Disorders 5
- Connective tissue disorders research 5
- Genomic variations and chromosomal abnormalities 4
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- Epigenetics and DNA Methylation 9
- RNA regulation and disease 5
- Co-authors
- Gudrun E. Moore (11 shared papers)Philip Stanier (10 shared papers)Sayeda Abu‐Amero (8 shared papers)Deborah Mackay (9 shared papers)Michael A. Preece (5 shared papers)I. Karen Temple (9 shared papers)Susan Holder (5 shared papers)David Monk (2 shared papers)
- Journals
- Journal of Medical Genetics (8 papers)European Journal of Human Genetics (5 papers)Archives of Disease in Childhood (4 papers)The Journal of Clinical Endocrinology & Metabolism (2 papers)Clinical Genetics (2 papers)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Emma Wakeling
67 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 75
- Genetics 905
- Pediatrics, Perinatology and Child Health 457
- Molecular Biology 759
- Developmental Biology 18
- Endocrinology, Diabetes and Metabolism 110
Countries citing papers authored by Emma Wakeling
This map shows the geographic impact of Emma Wakeling'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 Emma Wakeling with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emma Wakeling more than expected).
Fields of papers citing papers by Emma Wakeling
This network shows the impact of papers produced by Emma Wakeling. 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 Emma Wakeling. The network helps show where Emma Wakeling may publish in the future.
Co-authors
The 25 scholars most cited alongside Emma Wakeling, 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 70 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 141 | |
| 2 | 2000 | 115 | |
| 3 | 2018 | 91 | |
| 4 | 2001 | 88 | |
| 5 | 2000 | 82 | |
| 6 | 2010 | 78 | |
| 7 | 1996 | 78 | |
| 8 | 2008 | 71 | |
| 9 | 2013 | 59 | |
| 10 | 2009 | 59 | |
| 11 | 2011 | 53 | |
| 12 | 2006 | 46 | |
| 13 | 1999 | 43 | |
| 14 | 2015 | 36 | |
| 15 | 2015 | 25 | |
| 16 | 2020 | 22 | |
| 17 | 1998 | 22 | |
| 18 | 2022 | 21 | |
| 19 | 1998 | 20 | |
| 20 | 2006 | 19 |
About Emma Wakeling
Emma Wakeling is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Genetics and Surgery, having authored 70 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (21 papers), Prenatal Screening and Diagnostics (11 papers), Epigenetics and DNA Methylation (9 papers), RNA regulation and disease (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Connective tissue disorders research (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (905 citations), Pediatrics, Perinatology and Child Health (457 citations), Molecular Biology (759 citations), Developmental Biology (18 citations) and Endocrinology, Diabetes and Metabolism (110 citations). Emma Wakeling has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Gudrun E. Moore, Philip Stanier, Sayeda Abu‐Amero, Deborah Mackay, Michael A. Preece, I. Karen Temple, Susan Holder, David Monk, Megan P. Hitchins and Margaret Lever. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Archives of Disease in Childhood, The Journal of Clinical Endocrinology & Metabolism and Clinical Genetics.
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.