Patricia Bray‐Ward

5.9k total citations · 3 hit papers
43 papers, 4.5k citations indexed

About

Patricia Bray‐Ward is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Patricia Bray‐Ward has authored 43 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Molecular Biology, 17 papers in Genetics and 10 papers in Plant Science. Recurrent topics in Patricia Bray‐Ward's work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (10 papers) and Molecular Biology Techniques and Applications (7 papers). Patricia Bray‐Ward is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (10 papers) and Molecular Biology Techniques and Applications (7 papers). Patricia Bray‐Ward collaborates with scholars based in United States, Germany and Italy. Patricia Bray‐Ward's co-authors include David C. Ward, Paul M. Lizardi, Xiaohua Huang, David Thomas, Zhengrong Zhu, Zhenyu Sun, Stephen F. Kingsmore, Frank B. Dean, Seiyu Hosono and Mark D. Driscoll and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Patricia Bray‐Ward

43 papers receiving 4.4k citations

Hit Papers

Mutation detection and single-molecule counting using iso... 1995 2026 2005 2015 1998 2002 1995 250 500 750 1000
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Mutation detection and single-molecule counting using isothermal rolling-circle amplification
    1998 1.1k citations Paul M. Lizardi, Xiaohua Huang et al. Nature Genetics profile →
  2. Comprehensive human genome amplification using multiple displacement amplification
    2002 1.1k citations Patricia Bray‐Ward et al. Proceedings of the National Academy of Sciences profile →
  3. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.
    1995 604 citations Todd R. Golub, G. F. Barker et al. Proceedings of the National Academy of Sciences profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Patricia Bray‐Ward United States 22 3.2k 913 726 520 498 43 4.5k
Brigitte M. Jockusch Germany 50 4.3k 1.4× 407 0.4× 494 0.7× 176 0.3× 309 0.6× 134 8.0k
J. Wiegant Netherlands 42 4.4k 1.4× 1.8k 2.0× 222 0.3× 357 0.7× 630 1.3× 103 6.6k
Theresia E. B. Stradal Germany 46 3.5k 1.1× 483 0.5× 553 0.8× 176 0.3× 274 0.6× 111 7.6k
Nicholas E. Sherman United States 41 3.1k 1.0× 968 1.1× 291 0.4× 346 0.7× 308 0.6× 95 6.3k
Heidi Stuhlmann United States 34 3.8k 1.2× 1.3k 1.4× 242 0.3× 255 0.5× 382 0.8× 71 7.1k
Arnold Oliphant United States 28 2.1k 0.7× 1.3k 1.4× 186 0.3× 176 0.3× 388 0.8× 38 4.5k
M. van der Ploeg Netherlands 41 2.5k 0.8× 1.4k 1.5× 152 0.2× 217 0.4× 406 0.8× 102 4.9k
Edward R. LaVallie United States 32 3.0k 1.0× 730 0.8× 107 0.1× 505 1.0× 459 0.9× 54 5.3k
John O. Bishop United Kingdom 43 3.4k 1.1× 1.3k 1.4× 243 0.3× 134 0.3× 147 0.3× 124 6.0k
Jian‐Bing Fan United States 46 6.0k 1.9× 1.6k 1.8× 253 0.3× 320 0.6× 1.9k 3.9× 133 8.7k

Countries citing papers authored by Patricia Bray‐Ward

Since Specialization
Citations

This map shows the geographic impact of Patricia Bray‐Ward'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 Patricia Bray‐Ward with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patricia Bray‐Ward more than expected).

Fields of papers citing papers by Patricia Bray‐Ward

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patricia Bray‐Ward. 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 Patricia Bray‐Ward. The network helps show where Patricia Bray‐Ward may publish in the future.

Co-authorship network of co-authors of Patricia Bray‐Ward

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Bray‐Ward. A scholar is included among the top collaborators of Patricia Bray‐Ward 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 Patricia Bray‐Ward. Patricia Bray‐Ward 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.
Torres, Anthony, Thayne L. Sweeten, Randall C. Johnson, et al.. (2016). Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder. Frontiers in Neuroscience. 10. 463–463. 38 indexed citations
2.
Pani, Ariel M., Holly H. Hobart, Colleen A. Morris, et al.. (2010). Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome. PLoS ONE. 5(8). e12349–e12349. 10 indexed citations
3.
Hobart, Holly H., Colleen A. Morris, Carolyn Β. Mervis, et al.. (2010). Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 154C(2). 220–228. 43 indexed citations
4.
Mor, Gil, Irene Visintin, Yinglei Lai, et al.. (2005). Serum protein markers for early detection of ovarian cancer. Proceedings of the National Academy of Sciences. 102(21). 7677–7682. 357 indexed citations
5.
6.
Henegariu, Octavian, Sevilhan Artan, John M. Greally, et al.. (2001). Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies. Laboratory Investigation. 81(4). 483–491. 23 indexed citations
7.
8.
Wang, Hong, Gouri Chatterjee, Jeffrey Meyer, et al.. (1999). Characteristics of Three Homologous 202 Genes (Ifi202a, Ifi202b, and Ifi202c) from the Murine Interferon-Activatable Gene 200 Cluster. Genomics. 60(3). 281–294. 53 indexed citations
9.
Dempsey, Laurie A., Ming-Jie Li, Angela H. DePace, Patricia Bray‐Ward, & Nancy Maizels. (1998). The HumanHNRPDLocus Maps to 4q21 and Encodes a Highly Conserved Protein. Genomics. 49(3). 378–384. 38 indexed citations
10.
Bray‐Ward, Patricia, et al.. (1998). Molecular Cloning of a Zinc Finger Gene eZNF from a Human Inner Ear cDNA Library, and In Situ Expression Pattern of Its Mouse Homologue In Mouse Inner Ear. Somatic Cell and Molecular Genetics. 24(2). 121–129. 3 indexed citations
11.
Lizardi, Paul M., Xiaohua Huang, Zhengrong Zhu, et al.. (1998). Mutation detection and single-molecule counting using isothermal rolling-circle amplification. Nature Genetics. 19(3). 225–232. 1147 indexed citations breakdown →
12.
Levanat, Sonja, Abirami Chidambaram, Carol Wicking, et al.. (1997). Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region. Cytogenetic and Genome Research. 76(3-4). 208–213. 6 indexed citations
13.
Bray‐Ward, Patricia, et al.. (1996). FISH-Mapped CEPH YACs Spanning 0 to 46 cM on Human Chromosome 6. Genomics. 36(1). 104–111. 9 indexed citations
14.
Gruen, Jeffrey R., Srinivasa Nalabolu, Christopher L. Bowlus, et al.. (1996). A Transcription Map of the Major Histocompatibility Complex (MHC) Class I Region. Genomics. 36(1). 70–85. 36 indexed citations
15.
Bray‐Ward, Patricia, et al.. (1996). Integration of the Cytogenetic, Genetic, and Physical Maps of the Human Genome by FISH Mapping of CEPH YAC Clones. Genomics. 32(1). 1–14. 92 indexed citations
16.
Nalabolu, Srinivasa, Charles A. Bowles, Haiyan Wei, et al.. (1996). A transcription map of the Major Histocompatibility Complex (MHC) Class I region. Human Immunology. 47(1-2). 64–64. 3 indexed citations
17.
Stegmaier, Kimberly, Shona Pendse, G. F. Barker, et al.. (1995). Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood. Blood. 86(1). 38–44. 101 indexed citations
18.
Nadkarni, Prakash M. & Patricia Bray‐Ward. (1995). CEPH viewer: a client-server database to browse and manipulate CEPH physical mapping and linkage data. Genomics. 25(1). 318–320. 1 indexed citations
19.
Golub, Todd R., G. F. Barker, Stefan K. Bohlander, et al.. (1995). Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.. Proceedings of the National Academy of Sciences. 92(11). 4917–4921. 604 indexed citations breakdown →
20.
Bray‐Ward, Patricia, Johannes Wienberg, & David C. Ward. (1994). Towards cloning the gene for holoprosencephaly on chromosome 2. The American Journal of Human Genetics. 55. 1 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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