Jonathan D. Picker
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
Papers in
- Genetics 30
- Genetics and Neurodevelopmental Disorders 21
- Genomic variations and chromosomal abnormalities 19
- Genomics and Rare Diseases 7
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- Congenital heart defects research 8
- Mitochondrial Function and Pathology 4
- RNA modifications and cancer 4
- Co-authors
- Amy Lawson‐Yuen (2 shared papers)Juan‐Sebastian Saldivar (1 shared paper)Steve S. Sommer (1 shared paper)Joseph T. Coyle (4 shared papers)Randi Jenssen Hagerman (2 shared papers)Elizabeth Berry-Kravis (2 shared papers)Walter E. Kaufmann (2 shared papers)Ave M. Lachiewicz (1 shared paper)
- Journals
- European Journal of Human Genetics (5 papers)PEDIATRICS (5 papers)Genetics in Medicine (3 papers)Journal of Child and Adolescent Psychopharmacology (2 papers)The Journal of Pediatrics (2 papers)
- Partner nations
- United StatesChinaCanada
In The Last Decade
Jonathan D. Picker
61 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 106
- Genetics 1.9k
- Cognitive Neuroscience 906
- Molecular Biology 1.3k
- Pediatrics, Perinatology and Child Health 286
- Cellular and Molecular Neuroscience 291
Countries citing papers authored by Jonathan D. Picker
This map shows the geographic impact of Jonathan D. Picker'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 Jonathan D. Picker with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jonathan D. Picker more than expected).
Fields of papers citing papers by Jonathan D. Picker
This network shows the impact of papers produced by Jonathan D. Picker. 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 Jonathan D. Picker. The network helps show where Jonathan D. Picker may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan D. Picker, 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 62 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 482 | |
| 2 | 2010 | 313 | |
| 3 | 2010 | 250 | |
| 4 | 2008 | 239 | |
| 5 | 2008 | 180 | |
| 6 | 2012 | 146 | |
| 7 | 2011 | 99 | |
| 8 | 2002 | 92 | |
| 9 | 2006 | 84 | |
| 10 | 2012 | 81 | |
| 11 | 2014 | 74 | |
| 12 | 2015 | 72 | |
| 13 | 2016 | 62 | |
| 14 | 2007 | 61 | |
| 15 | 2005 | 60 | |
| 16 | 2018 | 59 | |
| 17 | 2019 | 59 | |
| 18 | 2016 | 47 | |
| 19 | 2018 | 44 | |
| 20 | 2003 | 43 |
About Jonathan D. Picker
Jonathan D. Picker is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Genetics and Clinical Biochemistry, having authored 62 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (21 papers), Genomic variations and chromosomal abnormalities (19 papers), Autism Spectrum Disorder Research (10 papers), Congenital heart defects research (8 papers), Genomics and Rare Diseases (7 papers), Mitochondrial Function and Pathology (4 papers), RNA modifications and cancer (4 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Genetics (1.9k citations), Cognitive Neuroscience (906 citations), Molecular Biology (1.3k citations), Pediatrics, Perinatology and Child Health (286 citations) and Cellular and Molecular Neuroscience (291 citations). Jonathan D. Picker has collaborated with scholars based in United States, China and Canada. Frequent co-authors include Amy Lawson‐Yuen, Juan‐Sebastian Saldivar, Steve S. Sommer, Joseph T. Coyle, Randi Jenssen Hagerman, Elizabeth Berry-Kravis, Walter E. Kaufmann, Ave M. Lachiewicz, Michele Y. Ono and Louise W. Gane. Their work appears in journals such as European Journal of Human Genetics, PEDIATRICS, Genetics in Medicine, Journal of Child and Adolescent Psychopharmacology 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.