William Byerley

6.0k total citations
15 papers, 327 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 15 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Psychiatry and Mental health. Recurrent topics in William Byerley's work include Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). William Byerley is often cited by papers focused on Genetic Associations and Epidemiology (10 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). William Byerley collaborates with scholars based in United States, Ireland and Costa Rica. William Byerley's co-authors include Hilary Coon, Marina Myles‐Worsley, Robert Freedman, Paul H. Wender, Fred Reimherr, John Holik, Brett A. Clementz, M. Hoff, Colleen A. Brenner and Mark Hoff and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biological Psychiatry and Molecular Psychiatry.

In The Last Decade

William Byerley

14 papers receiving 318 citations

Peers

William Byerley

GENET

PMH

PHEOH

M. J. Moses Australia

Amanda Elkin United Kingdom

Fiona Middle United Kingdom

Douglas F. Levinson United States

Teresa Escámez Spain

Diptendu Chatterjee India

Michael J. Owen United Kingdom

Jordan M. Ramsey United Kingdom

Jianxin Shi United States

Hannu Juvonen Finland

M. J. Moses Australia

William Byerley

173 ×0.9

GENET

143 ×1.2

157 ×1.9

PMH

32 ×0.8

PHEOH

21 ×0.6

Citations per year, relative to William Byerley William Byerley (= 1×) peers M. J. Moses

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

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15 of 15 papers shown

Ryan, Niamh, et al.. (2024). BICEP: Bayesian inference for rare genomic variant causality evaluation in pedigrees. Briefings in Bioinformatics. 26(1).

Ryan, Niamh, et al.. (2023). Ultrarare Missense Variants Implicated in Utah Pedigrees Multiply Affected With Schizophrenia. Biological Psychiatry Global Open Science. 3(4). 797–802. 4 indexed citations

Bodea, Corneliu, Frank A. Middleton, Nadine Melhem, et al.. (2016). Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31. PubMed. 2(4). 173–184. 1 indexed citations

Morgan, Ling, Brandi Rollins, Adolfo Sequeira, et al.. (2016). Quantitative Trait Locus and Brain Expression of HLA-DPA1 Offers Evidence of Shared Immune Alterations in Psychiatric Disorders. SHILAP Revista de lepidopterología. 5(1). 6–6. 22 indexed citations

Melhem, Nadine, Cong Lu, Frank A. Middleton, et al.. (2014). Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(6). 521–530. 6 indexed citations

Su, Shu-Yi, Jay Kasberger, Sergio E. Baranzini, et al.. (2012). Detection of identity by descent using next-generation whole genome sequencing data. BMC Bioinformatics. 13(1). 121–121. 11 indexed citations

Melhem, Nadine, Frank A. Middleton, Kathryn McFadden, et al.. (2011). Copy Number Variants for Schizophrenia and Related Psychotic Disorders in Oceanic Palau: Risk and Transmission in Extended Pedigrees. Biological Psychiatry. 70(12). 1115–1121. 23 indexed citations

Byerley, William & Judith A. Badner. (2010). Strategies to identify genes for complex disorders. Psychiatric Genetics. 21(4). 173–182. 7 indexed citations

Martin, Maureen V., Brandi Rollins, Adolfo Sequeira, et al.. (2009). Exon expression in lymphoblastoid cell lines from subjects with schizophrenia before and after glucose deprivation. BMC Medical Genomics. 2(1). 62–62. 18 indexed citations

10.

Payne, Jennifer L., Dean F. MacKinnon, Francis M. Mondimore, et al.. (2008). Familial aggregation of postpartum mood symptoms in bipolar disorder pedigrees. Bipolar Disorders. 10(1). 38–44. 43 indexed citations

11.

Devlin, Bernie, Silviu‐Alin Bacanu, Kathryn Roeder, et al.. (2002). Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau. Molecular Psychiatry. 7(7). 689–694. 50 indexed citations

12.

Bulayeva, Kazima, et al.. (2000). The ascertainment of multiplex schizophrenia pedigrees from Daghestan genetic isolates (Northern Caucasus, Russia). Psychiatric Genetics. 10(2). 67–72. 4 indexed citations

13.

Myles‐Worsley, Marina, Hilary Coon, Jennifer E. McDowell, et al.. (1999). Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families. American Journal of Medical Genetics. 88(5). 544–550. 76 indexed citations

14.

Myles‐Worsley, Marina, M. Hoff, John Holik, et al.. (1996). Anticipation in multiplex schizophrenia pedigrees. Psychiatric Genetics. 6(1). 7–12. 20 indexed citations

15.

Coon, Hilary, M. Hoff, John Holik, et al.. (1996). Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression. Biological Psychiatry. 39(8). 689–696. 42 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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