Christopher Cunniff
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
-
- Muscle Physiology and Disorders 25
- Genetics 37
- Genetics and Neurodevelopmental Disorders 12
- Genomic variations and chromosomal abnormalities 11
- Craniofacial Disorders and Treatments 7
- Co-authors
- Russell S. Kirby (10 shared papers)Laura A. Schieve (7 shared papers)Marilyn C. Jones (5 shared papers)Kenneth Lyons Jones (7 shared papers)Catherine E. Rice (6 shared papers)Maureen S. Durkin (9 shared papers)Lisa A. Miller (10 shared papers)Nathan A. Ellis (2 shared papers)
- Journals
- PEDIATRICS (7 papers)Journal of Child Neurology (5 papers)Birth Defects Research (5 papers)Birth Defects Research Part A Clinical and Molecular Teratology (3 papers)The Journal of Pediatrics (3 papers)
- Partner nations
- United StatesUnited KingdomAustralia
In The Last Decade
Christopher Cunniff
119 papers receiving 5.0k citations
Peers
Comparison fields: 5 of 137
- Genetics 1.4k
- Cognitive Neuroscience 979
- Pediatrics, Perinatology and Child Health 642
- Psychiatry and Mental health 406
- Molecular Biology 2.0k
Countries citing papers authored by Christopher Cunniff
This map shows the geographic impact of Christopher Cunniff'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 Christopher Cunniff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Cunniff more than expected).
Fields of papers citing papers by Christopher Cunniff
This network shows the impact of papers produced by Christopher Cunniff. 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 Christopher Cunniff. The network helps show where Christopher Cunniff may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher Cunniff, 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 120 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 372 | |
| 2 | 2008 | 321 | |
| 3 | 1997 | 300 | |
| 4 | 2003 | 249 | |
| 5 | 1997 | 196 | |
| 6 | 2016 | 183 | |
| 7 | 2015 | 182 | |
| 8 | 2009 | 182 | |
| 9 | 2014 | 160 | |
| 10 | Clinical and molecular characterization of patients with distal 11q deletions. | 1995 | 144 |
| 11 | 2009 | 120 | |
| 12 | 2013 | 106 | |
| 13 | 1992 | 104 | |
| 14 | 1990 | 101 | |
| 15 | 2006 | 94 | |
| 16 | Prevalence of Duchenne/Becker muscular dystrophy among males aged 5-24 years–Four states, 2007 | 2009 | 92 |
| 17 | 2017 | 85 | |
| 18 | 1991 | 76 | |
| 19 | 1990 | 75 | |
| 20 | 2012 | 72 |
About Christopher Cunniff
Christopher Cunniff is a scholar working on Molecular Biology, Genetics, Surgery, Pediatrics, Perinatology and Child Health and Cognitive Neuroscience, having authored 120 papers that have together received 5.3k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (25 papers), Autism Spectrum Disorder Research (12 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers), Craniofacial Disorders and Treatments (7 papers), Congenital Diaphragmatic Hernia Studies (6 papers) and Neonatal Respiratory Health Research (5 papers). The work is most often cited by research in Genetics (1.4k citations), Cognitive Neuroscience (979 citations), Pediatrics, Perinatology and Child Health (642 citations), Psychiatry and Mental health (406 citations) and Molecular Biology (2.0k citations). Christopher Cunniff has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Russell S. Kirby, Laura A. Schieve, Marilyn C. Jones, Kenneth Lyons Jones, Catherine E. Rice, Maureen S. Durkin, Lisa A. Miller, Nathan A. Ellis, Jennifer A. Bassetti and Emma Ciafaloni. Their work appears in journals such as PEDIATRICS, Journal of Child Neurology, Birth Defects Research, Birth Defects Research Part A Clinical and Molecular Teratology and The Journal of Pediatrics.
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.