Nancy Kramer
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and rare skin diseases.
- Developmental Neuroscience top 10%
Papers in
- Genetics 11
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 4
- Genomic variations and chromosomal abnormalities 3
- Genetic Mapping and Diversity in Plants and Animals 1
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- Metabolism and Genetic Disorders 2
- Co-authors
- John M. Graham (8 shared papers)Karen Webster Gripp (2 shared papers)Linda S. de Vries (1 shared paper)Robert L. Conway (1 shared paper)Ghayda Mirzaa (1 shared paper)Dawn H. Siegel (1 shared paper)Tally Lerman‐Sagie (1 shared paper)Dorit Lev (1 shared paper)
- Journals
- European Journal of Medical Genetics (2 papers)The American Journal of Human Genetics (2 papers)Mammalian Genome (1 paper)Human Mutation (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Nancy Kramer
13 papers receiving 1.2k citations
Nancy Kramer's Hit Papers
Peers
Comparison fields: 5 of 64
- Genetics 611
- Developmental Neuroscience 51
- Pediatrics, Perinatology and Child Health 194
- Developmental Biology 30
- Psychiatry and Mental health 90
Countries citing papers authored by Nancy Kramer
This map shows the geographic impact of Nancy Kramer'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 Nancy Kramer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nancy Kramer more than expected).
Fields of papers citing papers by Nancy Kramer
This network shows the impact of papers produced by Nancy Kramer. 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 Nancy Kramer. The network helps show where Nancy Kramer may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy Kramer, 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 | De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes Hit paper breakdown → | 2012 | 581 |
| 2 | 2013 | 177 | |
| 3 | 2012 | 161 | |
| 4 | 2013 | 71 | |
| 5 | 2015 | 54 | |
| 6 | 2016 | 38 | |
| 7 | 2011 | 37 | |
| 8 | 2015 | 34 | |
| 9 | 2014 | 30 | |
| 10 | 2009 | 26 | |
| 11 | 2013 | 19 | |
| 12 | 1998 | 17 | |
| 13 | 2012 | 13 |
About Nancy Kramer
Nancy Kramer is a scholar working on Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health, Developmental Biology and Molecular Biology, having authored 13 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Metabolism and Genetic Disorders (2 papers), Fetal and Pediatric Neurological Disorders (2 papers), Protein Tyrosine Phosphatases (1 paper), Congenital limb and hand anomalies (1 paper) and Genetic Mapping and Diversity in Plants and Animals (1 paper). The work is most often cited by research in Genetics (611 citations), Developmental Neuroscience (51 citations), Pediatrics, Perinatology and Child Health (194 citations), Developmental Biology (30 citations) and Psychiatry and Mental health (90 citations). Nancy Kramer has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include John M. Graham, Karen Webster Gripp, Linda S. de Vries, Robert L. Conway, Ghayda Mirzaa, Dawn H. Siegel, Tally Lerman‐Sagie, Dorit Lev, William B. Dobyns and Elizabeth Hopkins. Their work appears in journals such as European Journal of Medical Genetics, The American Journal of Human Genetics, Mammalian Genome, Human Mutation and Nature 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.