Jonathan Picker
Impact in
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 22
- Genetics and Neurodevelopmental Disorders 16
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 5
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- Congenital heart defects research 5
- Epigenetics and DNA Methylation 3
- 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)Walter E. Kaufmann (2 shared papers)Randi J. Hagerman (2 shared papers)Elizabeth Berry‐Kravis (2 shared papers)Rebecca Kronk (1 shared paper)
- Journals
- European Journal of Human Genetics (4 papers)PEDIATRICS (4 papers)Genetics in Medicine (3 papers)Annals of Neurology (2 papers)Journal of Child and Adolescent Psychopharmacology (2 papers)
- Partner nations
- United StatesChinaUnited Kingdom
In The Last Decade
Jonathan Picker
47 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 97
- Genetics 1.3k
- Cognitive Neuroscience 602
- Clinical Biochemistry 104
- Molecular Biology 952
- Pediatrics, Perinatology and Child Health 222
Countries citing papers authored by Jonathan Picker
This map shows the geographic impact of Jonathan 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 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 Picker more than expected).
Fields of papers citing papers by Jonathan Picker
This network shows the impact of papers produced by Jonathan 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 Picker. The network helps show where Jonathan Picker may publish in the future.
Co-authors
The 25 scholars most cited alongside Jonathan 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 476 | |
| 2 | 2008 | 227 | |
| 3 | 2008 | 163 | |
| 4 | 2012 | 130 | |
| 5 | 2011 | 93 | |
| 6 | 2002 | 85 | |
| 7 | 2006 | 84 | |
| 8 | 2012 | 76 | |
| 9 | Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency | 2014 | 71 |
| 10 | 2014 | 65 | |
| 11 | 2007 | 61 | |
| 12 | 2005 | 60 | |
| 13 | 2016 | 55 | |
| 14 | 2016 | 46 | |
| 15 | 2019 | 44 | |
| 16 | 2003 | 40 | |
| 17 | 2016 | 40 | |
| 18 | 2018 | 39 | |
| 19 | 2014 | 35 | |
| 20 | 2015 | 32 |
About Jonathan Picker
Jonathan Picker is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Genetics and Cellular and Molecular Neuroscience, having authored 49 papers that have together received 2.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (14 papers), Autism Spectrum Disorder Research (8 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (5 papers), Metabolism and Genetic Disorders (4 papers), Epigenetics and DNA Methylation (3 papers) and Folate and B Vitamins Research (3 papers). The work is most often cited by research in Genetics (1.3k citations), Cognitive Neuroscience (602 citations), Clinical Biochemistry (104 citations), Molecular Biology (952 citations) and Pediatrics, Perinatology and Child Health (222 citations). Jonathan Picker has collaborated with scholars based in United States, China and United Kingdom. Frequent co-authors include Amy Lawson‐Yuen, Juan‐Sebastian Saldivar, Steve S. Sommer, Joseph T. Coyle, Walter E. Kaufmann, Randi J. Hagerman, Elizabeth Berry‐Kravis, Rebecca Kronk, Louise W. Gane and Carol Delahunty. Their work appears in journals such as European Journal of Human Genetics, PEDIATRICS, Genetics in Medicine, Annals of Neurology and Journal of Child and Adolescent Psychopharmacology.
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.