Lambertus Klei
Impact in
- Cognitive Neuroscience top 2%
- Autism Spectrum Disorder Research
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic and phenotypic traits in livestock
- Genetic Mapping and Diversity in Plants and Animals
Papers in
- Genetics 25
- Genetic Associations and Epidemiology 15
- Genomic variations and chromosomal abnormalities 7
- Genetic and phenotypic traits in livestock 6
- Genetic Mapping and Diversity in Plants and Animals 5
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- Bioinformatics and Genomic Networks 4
- Congenital heart defects research 3
- Co-authors
- Bernie Devlin (38 shared papers)Kathryn Roeder (30 shared papers)Stephan Sanders (4 shared papers)Ann B. Lee (3 shared papers)Joseph D. Buxbaum (11 shared papers)Christina M. Hultman (8 shared papers)Sven Sandin (9 shared papers)Abraham Reichenberg (7 shared papers)
- Journals
- Molecular Autism (4 papers)Human Genetics (3 papers)Biological Psychiatry (3 papers)Schizophrenia Bulletin (3 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- United StatesSwedenCanada
In The Last Decade
Lambertus Klei
49 papers receiving 2.6k citations
Lambertus Klei's Hit Papers
Peers
Comparison fields: 5 of 129
- Cognitive Neuroscience 961
- Genetics 1.3k
- Molecular Biology 853
- Endocrine and Autonomic Systems 78
- Psychiatry and Mental health 158
Countries citing papers authored by Lambertus Klei
This map shows the geographic impact of Lambertus Klei'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 Lambertus Klei with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lambertus Klei more than expected).
Fields of papers citing papers by Lambertus Klei
This network shows the impact of papers produced by Lambertus Klei. 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 Lambertus Klei. The network helps show where Lambertus Klei may publish in the future.
Co-authors
The 25 scholars most cited alongside Lambertus Klei, 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 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Most genetic risk for autism resides with common variation Hit paper breakdown → | 2014 | 785 |
| 2 | 2015 | 215 | |
| 3 | 2012 | 171 | |
| 4 | 2012 | 123 | |
| 5 | 2007 | 116 | |
| 6 | 2005 | 113 | |
| 7 | 2014 | 89 | |
| 8 | 2014 | 89 | |
| 9 | 2012 | 76 | |
| 10 | 2009 | 70 | |
| 11 | 2008 | 70 | |
| 12 | 2003 | 65 | |
| 13 | 2018 | 56 | |
| 14 | 2010 | 50 | |
| 15 | 2009 | 49 | |
| 16 | 2017 | 49 | |
| 17 | 2018 | 49 | |
| 18 | 2009 | 44 | |
| 19 | 2017 | 32 | |
| 20 | 2020 | 31 |
About Lambertus Klei
Lambertus Klei is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Clinical Psychology and Physiology, having authored 50 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (15 papers), Autism Spectrum Disorder Research (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetic and phenotypic traits in livestock (6 papers), Obsessive-Compulsive Spectrum Disorders (5 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers), Bioinformatics and Genomic Networks (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Cognitive Neuroscience (961 citations), Genetics (1.3k citations), Molecular Biology (853 citations), Endocrine and Autonomic Systems (78 citations) and Psychiatry and Mental health (158 citations). Lambertus Klei has collaborated with scholars based in United States, Sweden and Canada. Frequent co-authors include Bernie Devlin, Kathryn Roeder, Stephan Sanders, Ann B. Lee, Joseph D. Buxbaum, Christina M. Hultman, Sven Sandin, Abraham Reichenberg, Yudi Pawitan and Jennifer Reichert. Their work appears in journals such as Molecular Autism, Human Genetics, Biological Psychiatry, Schizophrenia Bulletin and The American Journal of Human 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.