William Byerley
Impact in
- Biological Psychiatry top 5%
- Psychiatry and Mental health top 2%
- Schizophrenia research and treatment
Papers in
- Genetics 36
- Genetic Associations and Epidemiology 24
- Genetics and Neurodevelopmental Disorders 15
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 11
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- Receptor Mechanisms and Signaling 9
- Co-authors
- Hilary Coon (34 shared papers)Marina Myles‐Worsley (29 shared papers)Robert Freedman (23 shared papers)Fred Reimherr (17 shared papers)John Holik (30 shared papers)Merilyne C. Waldo (9 shared papers)Paul H. Wender (15 shared papers)Mark Hoff (17 shared papers)
- Journals
- Psychiatric Genetics (14 papers)Schizophrenia Research (8 papers)Human Heredity (6 papers)Human Molecular Genetics (5 papers)Human Genetics (4 papers)
- Partner nations
- United StatesBelgiumCosta Rica
In The Last Decade
William Byerley
82 papers receiving 2.5k citations
Peers
Comparison fields: 5 of 111
- Biological Psychiatry 121
- Psychiatry and Mental health 568
- Cellular and Molecular Neuroscience 616
- Genetics 798
- Cognitive Neuroscience 445
Countries citing papers authored by William Byerley
This map shows the geographic impact of William Byerley'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 William Byerley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William Byerley more than expected).
Fields of papers citing papers by William Byerley
This network shows the impact of papers produced by William Byerley. 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 William Byerley. The network helps show where William Byerley may publish in the future.
Co-authors
The 25 scholars most cited alongside William Byerley, 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 83 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1996 | 214 | |
| 2 | 1994 | 183 | |
| 3 | 1994 | 132 | |
| 4 | 1994 | 104 | |
| 5 | 1991 | 103 | |
| 6 | 1999 | 94 | |
| 7 | Linkage analysis of schizophrenia with five dopamine receptor genes in nine pedigrees. | 1993 | 75 |
| 8 | Receptor alterations associated with serotonergic agents: an autoradiographic analysis. | 1987 | 73 |
| 9 | 2002 | 70 | |
| 10 | 1995 | 66 | |
| 11 | 1998 | 63 | |
| 12 | 1994 | 63 | |
| 13 | 1988 | 63 | |
| 14 | A genome-wide search for genes predisposing to manic-depression, assuming autosomal dominant inheritance. | 1993 | 61 |
| 15 | 1996 | 60 | |
| 16 | 1988 | 57 | |
| 17 | Sertraline, a selective inhibitor of serotonin uptake, for the treatment of outpatients with major depressive disorder. | 1988 | 53 |
| 18 | 1993 | 50 | |
| 19 | 1987 | 50 | |
| 20 | 1999 | 48 |
About William Byerley
William Byerley is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Cognitive Neuroscience and Cellular and Molecular Neuroscience, having authored 83 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (24 papers), Genetics and Neurodevelopmental Disorders (15 papers), Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (11 papers), Bipolar Disorder and Treatment (9 papers), Receptor Mechanisms and Signaling (9 papers), Schizophrenia research and treatment (8 papers) and Neurotransmitter Receptor Influence on Behavior (7 papers). The work is most often cited by research in Biological Psychiatry (121 citations), Psychiatry and Mental health (568 citations), Cellular and Molecular Neuroscience (616 citations), Genetics (798 citations) and Cognitive Neuroscience (445 citations). William Byerley has collaborated with scholars based in United States, Belgium and Costa Rica. Frequent co-authors include Hilary Coon, Marina Myles‐Worsley, Robert Freedman, Fred Reimherr, John Holik, Merilyne C. Waldo, Paul H. Wender, Mark Hoff, B.I. Grosser and Herbert T. Nagamoto. Their work appears in journals such as Psychiatric Genetics, Schizophrenia Research, Human Heredity, Human Molecular Genetics and 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.