Patricia Bray‐Ward

5.9k citations

43 papers · 4.5k indexed · 3 hit papers · h-index 22

Co-authors: David C. Ward Paul M. Lizardi Xiaohua Huang Zhengrong Zhu David Thomas Jing Du Xiaohong Wu Seiyu Hosono
Topics: Genomic variations and chromosomal abnormalities (11 papers)Chromosomal and Genetic Variations (10 papers)Molecular Biology Techniques and Applications (7 papers)
Cited by: Hematology Molecular Biology Cancer Research
Journals: Proceedings of the National Academy of Sciences Journal of Biological Chemistry Nature Genetics
Partner nations: United States Germany Italy

In The Last Decade

Patricia Bray‐Ward

43 papers receiving 4.4k citations

Hit Papers

align trajectories

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.

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 →
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 →
Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

1995 604 citations Patricia Bray‐Ward et al. Proceedings of the National Academy of Sciences profile →

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder 2016 ·Frontiers in Neuroscience ·Anthony Torres,Thayne L. Sweeten,Randall C. Johnson,Dennis Odell,Jonna B. Westover,Patricia Bray‐Ward,David C. Ward,Christopher J. Davies,Aaron J. Thomas,Lisa Croen,Michael Benson	38
2	Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome 2010 ·PLoS ONE ·Ariel M. Pani,Holly H. Hobart,Colleen A. Morris,Carolyn Β. Mervis,Patricia Bray‐Ward,(unknown),(unknown),(unknown),(unknown),Gordon C. Gowans,Ronald G. Gregg	10
3	Serum protein markers for early detection of ovarian cancer 2005 ·Proceedings of the National Academy of Sciences ·Gil Mor,Irene Visintin,Yinglei Lai,Hongyu Zhao,Peter E. Schwartz,Thomas Rutherford,Yue Luo,Patricia Bray‐Ward,David C. Ward	357
4	Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies 2001 ·Laboratory Investigation ·Octavian Henegariu,Sevilhan Artan,John M. Greally,Xiao–Ning Chen,Julie R. Korenberg,Gail H. Vance,Lisa Stubbs,Patricia Bray‐Ward,David C. Ward	23
5	Assignment<footref rid="foot01"><sup>1</sup></footref> of SYNJ1 to human chromosome 21q22.2 and <i>Synj12</i> to the murine homologous region on chromosome 16C3–4 by in situ hybridization 2000 ·Cytogenetic and Genome Research ·Ottavio Cremona,Manjunath Nimmakayalu,Christof Haffner,Patricia Bray‐Ward,David C. Ward,Pietro De Camilli	20
6	Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization 1999 ·Genes Chromosomes and Cancer ·Sabrina Tosi,Giovanni De Giudici,Alessandro Rambaldi,Stephen W. Scherer,Patricia Bray‐Ward,(unknown),Andrea Biondi,Robert E. Kearney	35
7	Characteristics of Three Homologous 202 Genes (Ifi202a, Ifi202b, and Ifi202c) from the Murine Interferon-Activatable Gene 200 Cluster 1999 ·Genomics ·Hong Wang,Gouri Chatterjee,Jeffrey Meyer,Liu C,(unknown),Patricia Bray‐Ward,Péter Lengyel	53
8	Assignment<footref rid="foot01"><sup>1</sup></footref> of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1→p23.3 and murine 5B by in situ hybridization 1999 ·Cytogenetic and Genome Research ·(unknown),Patricia Bray‐Ward,Steven A. Goldstein,PG Gallagher	6
9	The HumanHNRPDLocus Maps to 4q21 and Encodes a Highly Conserved Protein 1998 ·Genomics ·Laurie A. Dempsey,Ming-Jie Li,Angela H. DePace,Patricia Bray‐Ward,Nancy Maizels	38
10	Mutation detection and single-molecule counting using isothermal rolling-circle amplificationbreakdown → 1998 ·Nature Genetics ·Paul M. Lizardi,Xiaohua Huang,Zhengrong Zhu,Patricia Bray‐Ward,David Thomas,David C. Ward	1147
11	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 1998 ·Somatic Cell and Molecular Genetics ·(unknown),(unknown),Patricia Bray‐Ward,Rajendra P. Kandpal	3
12	Pulsed-field gel electrophoresis and FISH mapping of chromosome 9q22: placement of a novel zinc finger gene within the NBCCS and ESS1 region 1997 ·Cytogenetic and Genome Research ·Sonja Levanat,Abirami Chidambaram,Carol Wicking,Patricia Bray‐Ward,C. Pressman,Rune Toftgård,(unknown),Jeanne C. Myers,Brandon J. Wainwright,Michael Dean,A. Bale	6
13	FISH-Mapped CEPH YACs Spanning 0 to 46 cM on Human Chromosome 6 1996 ·Genomics ·Patricia Bray‐Ward,Christopher L. Bowlus,(unknown),Denis Le Paslier,J. Weissenbach,Jeffrey R. Gruen	9
14	Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21 1996 ·Human Molecular Genetics ·(unknown),Johannes Wienberg,Angelika Köhler,Patricia Bray‐Ward,(unknown),William G. Wilson,(unknown),Robert Roger Lebel,Jeffrey R. Sawyer,Paul L. Campbell,David J. Aughton,Hope H. Punnett,Edward J. Lammer,Fa‐Ten Kao,David C. Ward,Maximilian Muenke	48
15	Region-specific YAC banding and painting probes for comparative genome mapping: implications for the evolution of human chromosome 2 1996 ·Chromosoma ·Thomas Haaf,Patricia Bray‐Ward	17
16	A Transcription Map of the Major Histocompatibility Complex (MHC) Class I Region 1996 ·Genomics ·Jeffrey R. Gruen,Srinivasa Nalabolu,(unknown),Christopher L. Bowlus,(unknown),(unknown),(unknown),(unknown),(unknown),Hongxia Xu,Satish Parimoo,Girish Nallur,Richard S. Ajioka,(unknown),Patricia Bray‐Ward,J. Pan,S M Weissman	36
17	Integration of the Cytogenetic, Genetic, and Physical Maps of the Human Genome by FISH Mapping of CEPH YAC Clones 1996 ·Genomics ·Patricia Bray‐Ward,Joan C. Menninger,(unknown),Trushna Desai,(unknown),Amy Banks,David C. Ward	92
18	CEPH viewer: a client-server database to browse and manipulate CEPH physical mapping and linkage data 1995 ·Genomics ·Prakash M. Nadkarni,Patricia Bray‐Ward	1
19	Internet-based Support for Bioscience Research: A Collaborative Genome center for Human Chromosome 12 1995 ·Journal of the American Medical Informatics Association ·Perry L. Miller,P. Nadkarni,Kenneth K. Kídd,Kei‐Hoi Cheung,David C. Ward,Amy Banks,Patricia Bray‐Ward,(unknown),(unknown),Ivonne Marondel,(unknown),Beatrice Renault,Sang-Heon Yoon,Kenneth Krauter,Raju Kucherlapati	11
20	Towards cloning the gene for holoprosencephaly on chromosome 2 1994 ·The American Journal of Human Genetics ·Patricia Bray‐Ward,Johannes Wienberg,David C. Ward	1

About Patricia Bray‐Ward

Patricia Bray‐Ward is a scholar working on Developmental Biology, Genetics and Developmental Neuroscience, having authored 43 papers that have together received 4.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (10 papers) and Molecular Biology Techniques and Applications (7 papers). The work is most often cited by research in Hematology (520 citations), Molecular Biology (3.2k citations) and Cancer Research (498 citations). Patricia Bray‐Ward has collaborated with scholars based in United States, Germany and Italy. Frequent co-authors include David C. Ward, Paul M. Lizardi, Xiaohua Huang, Zhengrong Zhu, David Thomas, Jing Du, Xiaohong Wu, Seiyu Hosono, A. Fawad Faruqi and Stephen F. Kingsmore. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature 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.

Explore authors with similar magnitude of impact