William Byerley

35.1k total citations
83 papers, 2.6k citations indexed

About

William Byerley is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, William Byerley has authored 83 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 30 papers in Molecular Biology and 18 papers in Psychiatry and Mental health. Recurrent topics in William Byerley's work include Genetic Associations and Epidemiology (27 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genomic variations and chromosomal abnormalities (14 papers). William Byerley is often cited by papers focused on Genetic Associations and Epidemiology (27 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Genomic variations and chromosomal abnormalities (14 papers). William Byerley collaborates with scholars based in United States, Costa Rica and Belgium. William Byerley's 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 and has published in prestigious journals such as Nature, Journal of the American Statistical Association and Bioinformatics.

In The Last Decade

William Byerley

81 papers receiving 2.5k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
William Byerley 904 877 679 671 546 83 2.6k
Pippa A. Thomson 1.7k 1.9× 1.2k 1.3× 541 0.8× 472 0.7× 313 0.6× 63 3.2k
Göran C. Sedvall 727 0.8× 424 0.5× 1.3k 1.9× 862 1.3× 625 1.1× 47 2.9k
Sibylle G. Schwab 1.0k 1.1× 1.2k 1.4× 641 0.9× 473 0.7× 400 0.7× 62 2.7k
Nader D. Halim 882 1.0× 308 0.4× 752 1.1× 508 0.8× 635 1.2× 13 2.5k
Ronnen H. Segman 569 0.6× 721 0.8× 527 0.8× 757 1.1× 229 0.4× 40 2.1k
Younger W.‐Y. Yu 557 0.6× 369 0.4× 890 1.3× 753 1.1× 671 1.2× 59 2.5k
Yoko Kinoshita 715 0.8× 571 0.7× 616 0.9× 395 0.6× 224 0.4× 73 2.1k
Dieter B. Wildenauer 1.4k 1.6× 1.6k 1.8× 940 1.4× 590 0.9× 374 0.7× 79 3.4k
Michiko Fujimoto 1.2k 1.3× 382 0.4× 641 0.9× 521 0.8× 544 1.0× 72 2.7k
Terry Ritchie 787 0.9× 387 0.4× 1.3k 1.9× 589 0.9× 415 0.8× 46 2.8k

Countries citing papers authored by William Byerley

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of William Byerley

This figure shows the co-authorship network connecting the top 25 collaborators of William Byerley. A scholar is included among the top collaborators of William Byerley based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with William Byerley. William Byerley is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ryan, Niamh, et al.. (2024). Investigating copy number variants in schizophrenia pedigrees using a new consensus pipeline called PECAN. Scientific Reports. 14(1). 17518–17518.
2.
Song, Lei, Aiyi Liu, Jianxin Shi, et al.. (2019). SummaryAUC: a tool for evaluating the performance of polygenic risk prediction models in validation datasets with only summary level statistics. Bioinformatics. 35(20). 4038–4044. 16 indexed citations
3.
Ross, J Cosbie, Erika Gedvilaite, Judith A. Badner, et al.. (2016). A Rare Variant in <b><i>CACNA1D</i></b> Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree. PubMed. 2(3). 145–150. 15 indexed citations
4.
Greenwood, Tiffany A., Judith A. Badner, William Byerley, et al.. (2013). Heritability and linkage analysis of personality in bipolar disorder. Journal of Affective Disorders. 151(2). 748–755. 18 indexed citations
5.
Guella, Ilaria, Adolfo Sequeira, Brandi Rollins, et al.. (2013). Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex. Schizophrenia Research. 152(1). 111–116. 28 indexed citations
6.
Myles‐Worsley, Marina, Josepha Tiobech, Frank A. Middleton, et al.. (2011). Familial transmission of schizophrenia in Palau: A 20‐year genetic epidemiological study in three generations. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(3). 247–254. 5 indexed citations
7.
Sanders, Alan R., Douglas F. Levinson, Jubao Duan, et al.. (2010). The Internet-Based MGS2 Control Sample: Self Report of Mental Illness. American Journal of Psychiatry. 167(7). 854–865. 38 indexed citations
8.
Rodriguez, Carlos, et al.. (2005). Suggestive linkage of schizophrenia to 5p13 in Costa Rica. Molecular Psychiatry. 10(7). 651–656. 17 indexed citations
9.
DeLisi, Lynn E., et al.. (2002). Genome‐wide scan for linkage to schizophrenia in a Spanish‐origin cohort from Costa Rica. American Journal of Medical Genetics. 114(5). 497–508. 70 indexed citations
10.
Hoff, M., J. Rosenthal, Ming Zhao, et al.. (2000). Mutation screening of a neutral amino acid transporter, ASCT1, and its potential role in schizophrenia. Psychiatric Genetics. 10(2). 79–82. 4 indexed citations
11.
Myles‐Worsley, Marina, Hilary Coon, Josepha Tiobech, et al.. (1999). Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality. American Journal of Medical Genetics. 88(1). 4–10. 48 indexed citations
12.
Leonard, Sherry, Clifford A. Adams, Charles R. Breese, et al.. (1996). Nicotinic Receptor Function in Schizophrenia. Schizophrenia Bulletin. 22(3). 431–446. 214 indexed citations
13.
Byerley, William, Mark Hoff, John Holik, et al.. (1995). Linkage Analysis between Schizophrenia and Index Simple-Sequence Repeat Loci for Chromosome 21. Human Heredity. 45(1). 49–52. 6 indexed citations
14.
Coon, Hilary, John Holik, Mark Hoff, et al.. (1994). Analysis of chromosome 22 markers in nine schizophrenia pedigrees. American Journal of Medical Genetics. 54(1). 72–79. 104 indexed citations
15.
Gregor, Paul, Marina Myles‐Worsley, John Holik, et al.. (1994). Schizophrenia and glutamate receptor genes. Psychiatric Genetics. 4(3). 161–166. 5 indexed citations
16.
Byerley, William, M. Hoff, John Holik, & Hilary Coon. (1994). A linkage study with D5 dopamine and α2C-adrenergic receptor genes in six multiplex bipolar pedigrees. Psychiatric Genetics. 4(3). 121–124. 9 indexed citations
17.
Byerley, William, Mark Hoff, John Holik, Marc G. Caron, & Bruno Giros. (1993). VNTR polymorphism for the human dopamine transporter gene (DAT1). Human Molecular Genetics. 2(3). 335–335. 29 indexed citations
18.
Coon, Hilary, Mark Hoff, John Holik, et al.. (1993). C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families. American Journal of Medical Genetics. 48(1). 36–39. 8 indexed citations
19.
Jensen, Steven, R. Plaetke, John Holik, et al.. (1992). Linkage Analysis of the D1 Dopamine Receptor Gene and Manic Depression in Six Families. Human Heredity. 42(5). 269–275. 18 indexed citations
20.
Byerley, William, et al.. (1988). The effect of bright light on plasma prolactin. Biological Psychiatry. 24(7). 843–844. 4 indexed citations

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.

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