Jamie Love‐Nichols
- Genetics top 10%
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 1
- Cognitive Neuroscience top 10%
-
- Epilepsy research and treatment 1
-
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Genomic variations and chromosomal abnormalities 1
-
- Renal and Vascular Pathologies 1
- Aortic aneurysm repair treatments 1
- Co-authors
- Wendy K. ChungHan G. BrunnerLisa M. ProckChrista Lese MartinRobin HansenDavid T. MillerMustafa ŞahinHelen V. Firth
- Partner nations
- United StatesNetherlandsCanada
In The Last Decade
Jamie Love‐Nichols
3 papers receiving 386 citations
Hit Papers
Peers
Comparison fields: 5 of 49
- Genetics 335
- Cognitive Neuroscience 113
- Pediatrics, Perinatology and Child Health 41
- Psychiatry and Mental health 31
- Genetics 15
Countries citing papers authored by Jamie Love‐Nichols
This map shows the geographic impact of Jamie Love‐Nichols'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 Jamie Love‐Nichols with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamie Love‐Nichols more than expected).
Fields of papers citing papers by Jamie Love‐Nichols
This network shows the impact of papers produced by Jamie Love‐Nichols. 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 Jamie Love‐Nichols. The network helps show where Jamie Love‐Nichols may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Jamie Love‐Nichols, 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 | 2022 | 14 | |
| 2 | 2020 | 7 | |
| 3 | Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disordersbreakdown → | 2019 | 367 |
About Jamie Love‐Nichols
Jamie Love‐Nichols is a scholar working on Genetics, Psychiatry and Mental health and Pulmonary and Respiratory Medicine, having authored 3 papers that have together received 388 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (1 paper), Renal and Vascular Pathologies (1 paper), Aortic aneurysm repair treatments (1 paper) and Epilepsy research and treatment (1 paper). The work is most often cited by research in Genetics (335 citations), Cognitive Neuroscience (113 citations) and Pediatrics, Perinatology and Child Health (41 citations). Jamie Love‐Nichols has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Wendy K. Chung, Han G. Brunner, Lisa M. Prock, Christa Lese Martin, Robin Hansen, David T. Miller, Mustafa Şahin, Helen V. Firth, Siddharth Srivastava and Kira A. Dies.
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.