Nancy A. Kramer
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
-
- Chromatin Remodeling and Cancer
- Hedgehog Signaling Pathway Studies
- PI3K/AKT/mTOR signaling in cancer
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 3
- Genetic and Kidney Cyst Diseases 2
- Genetic Syndromes and Imprinting 2
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- Congenital heart defects research 3
- Hedgehog Signaling Pathway Studies 2
- RNA modifications and cancer 2
- Co-authors
- John M. Graham (8 shared papers)Thane S. Pittman (1 shared paper)Karen Webster Gripp (2 shared papers)William B. Dobyns (1 shared paper)Tally Lerman‐Sagie (1 shared paper)Elizabeth Hopkins (1 shared paper)Linda S. deVries (1 shared paper)Ghayda Mirzaa (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)European Journal of Medical Genetics (2 papers)Journal of the American College of Cardiology (1 paper)Mammalian Genome (1 paper)Nature Genetics (1 paper)
- Partner nations
- United StatesNetherlandsUnited Kingdom
In The Last Decade
Nancy A. Kramer
18 papers receiving 1.3k citations
Nancy A. Kramer's Hit Papers
Peers
Comparison fields: 5 of 108
- Genetics 529
- Molecular Biology 650
- Genetics 85
- Pediatrics, Perinatology and Child Health 146
- Applied Psychology 39
Countries citing papers authored by Nancy A. Kramer
This map shows the geographic impact of Nancy A. 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 A. 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 A. Kramer more than expected).
Fields of papers citing papers by Nancy A. Kramer
This network shows the impact of papers produced by Nancy A. 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 A. Kramer. The network helps show where Nancy A. Kramer may publish in the future.
Co-authors
The 25 scholars most cited alongside Nancy A. 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 | 577 |
| 2 | 2013 | 177 | |
| 3 | 2012 | 160 | |
| 4 | 1980 | 136 | |
| 5 | 2013 | 67 | |
| 6 | 2015 | 54 | |
| 7 | 1996 | 47 | |
| 8 | 2016 | 37 | |
| 9 | 2011 | 37 | |
| 10 | 2015 | 32 | |
| 11 | 2014 | 30 | |
| 12 | 2009 | 26 | |
| 13 | 2013 | 19 | |
| 14 | 1998 | 17 | |
| 15 | 2012 | 13 | |
| 16 | 1977 | 6 | |
| 17 | 2013 | 1 | |
| 18 | The effects of an embodied conversationational agent's subtle nonverbal behavior on user's evaluation and behavioral mimicry | 2007 | 1 |
| 19 | 1979 | 1 |
About Nancy A. Kramer
Nancy A. Kramer is a scholar working on Genetics, Molecular Biology, Genetics, Pathology and Forensic Medicine and Occupational Therapy, having authored 19 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Congenital heart defects research (3 papers), Hedgehog Signaling Pathway Studies (2 papers), RNA modifications and cancer (2 papers), Genetic and Kidney Cyst Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Vascular Procedures and Complications (1 paper). The work is most often cited by research in Genetics (529 citations), Molecular Biology (650 citations), Genetics (85 citations), Pediatrics, Perinatology and Child Health (146 citations) and Applied Psychology (39 citations). Nancy A. Kramer has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include John M. Graham, Thane S. Pittman, Karen Webster Gripp, William B. Dobyns, Tally Lerman‐Sagie, Elizabeth Hopkins, Linda S. deVries, Ghayda Mirzaa, Dawn H. Siegel and Dorit Lev. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Medical Genetics, Journal of the American College of Cardiology, Mammalian Genome 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.