W. Roy Breg

2.5k total citations · 1 hit paper
26 papers, 2.0k citations indexed

About

W. Roy Breg is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, W. Roy Breg has authored 26 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in W. Roy Breg's work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). W. Roy Breg is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers). W. Roy Breg collaborates with scholars based in United States and Taiwan. W. Roy Breg's co-authors include O. J. Miller, S S Wachtel, Kirby D. Smith, J.M. Rary, Louis M. Kunkel, Samuel H. Boyer, Digamber S. Borgaonkar, Michael S. Watson, Mark Rabin and Orlando J. Miller and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.

In The Last Decade

W. Roy Breg

26 papers receiving 1.9k 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.

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

1977 1.3k citations S S Wachtel, O. J. Miller et al. Proceedings of the National Academy of Sciences profile →

Peers

Countries citing papers authored by W. Roy Breg

Since Specialization

Citations

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

Fields of papers citing papers by W. Roy Breg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by W. Roy Breg. 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 W. Roy Breg. The network helps show where W. Roy Breg may publish in the future.

Co-authorship network of co-authors of W. Roy Breg

This figure shows the co-authorship network connecting the top 25 collaborators of W. Roy Breg. A scholar is included among the top collaborators of W. Roy Breg 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 W. Roy Breg. W. Roy Breg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype 1994 ·Nature Genetics ·Bruce T. Lahn, (unknown), W. Roy Breg, Robert F. Stratton, Urvashi Surti, David C. Page	51
2	Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome 1993 ·Clinical Genetics ·Merlin G. Butler, Riccardo Pratesi, Michael S. Watson, W. Roy Breg, (unknown)	21
3	Fetal blood sampling and cytogenetic abnormalities 1993 ·Prenatal Diagnosis ·Jui‐Der Liou, Chih‐Ping Chen, W. Roy Breg, (unknown), (unknown), Teresa L. Yang‐Feng	18
4	Anthropometric comparison of mentally retarded males with and without the fragile X syndrome 1991 ·American Journal of Medical Genetics ·Merlin G. Butler, Geoffrey Allen, (unknown), (unknown), Michael S. Watson, W. Roy Breg	30
5	Duplication of euchromatin without phenotypic effects: A variant of chromosome 16 1990 ·American Journal of Medical Genetics ·Christine R. Bryke, W. Roy Breg, Venkateswara R. Potluri, Teresa L. Yang‐Feng	14
6	A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism 1987 ·Journal of Autism and Developmental Disorders ·Rhea Paul, Elizabeth Dykens, James F. Leckman, Michael S. Watson, W. Roy Breg, Donald J. Cohen	57
7	<i>NRAS </i>transforming gene maps to region p11→p13 on chromosome 1 by in situ hybridization 1984 ·Cytogenetic and Genome Research ·Mark Rabin, M. Watson, P E Barker, James C. Ryan, W. Roy Breg, F.H. Ruddle	51
8	Fragile X Syndrome 1984 ·Journal of Speech and Hearing Disorders ·Rhea Paul, Donald J. Cohen, W. Roy Breg, Michael S. Watson, Steven D. Herman	43
9	Human c-fos oncogene mapped within chromosomal region 14q21----q31. 1984 ·Proceedings of the National Academy of Sciences ·P E Barker, Mark Rabin, M. Watson, W. Roy Breg, F.H. Ruddle, Inder M. Verma	47
10	Tandem dup(1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies 1984 ·American Journal of Medical Genetics ·B. Rafael Elejalde, John M. Opitz, Maria Mercedes de Elejalde, Enid F. Gilbert, (unknown), Lorraine F. Meisner, Robert Roger Lebel, (unknown), W. Roy Breg	35
11	Evidence for methylation of inactive human rRNA genes in amplified regions 1981 ·Human Genetics ·Umadevi Tantravahi, W. Roy Breg, (unknown), Bernard F. Erlanger, Orlando J. Miller	40
12	Distribution of sex chromosome complements in 651 patients with turners syndrome 1980 ·The American Journal of Human Genetics ·R.E. Magenis, W. Roy Breg, (unknown), ErnestB. Hook, Catherine G. Palmer, László Pásztor, Robert L. Summitt, (unknown)	21
13	Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasia 1979 ·Blood ·(unknown), (unknown), (unknown), W. Roy Breg	2
14	Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasia 1979 ·Blood ·Barry Cooper, (unknown), L. Atkins, W. Roy Breg	12
15	Chromosome 3 duplication q/deletion p syndrome. 1978 ·PubMed ·Robert M. Fineman, Frederick Hecht, Ronald C. Ablow, Rufus O. Howard, W. Roy Breg	40
16	Regulation of rRNA gene expression in a human familial 14p+ marker chromosome 1978 ·Human Genetics ·Dorothy A. Miller, W. Roy Breg, Dorothy Warburton, (unknown), Orlando J. Miller	54
17	Mapping the locus of the H-Y antigen 1976 ·Cytogenetic and Genome Research ·G C Koo, S S Wachtel, W. Roy Breg, O. J. Miller	19
18	A Case of Mongolism in DZ Female Twins Studied at 10 and then at 43 Years of Age 1975 ·Acta geneticae medicae et gemellologiae ·William Greulich, W. Roy Breg, (unknown), Chris C. Plato, Herman Yannet	2
19	Partial deletion of the short arm of chromosome No. 4(4p-): Clinical studies in five unrelated patients 1970 ·The Journal of Pediatrics ·Orlando J. Miller, W. Roy Breg, Dorothy Warburton, Dorothy A. Miller, (unknown), P. W. Allderdice, Jessica G. Davis, H.P. Klinger, (unknown), Fred H. Allen	49
20	Non-Random Distribution of Chromosomes in Metaphase Figures from Cultured Human Leucocytes. II. The Peripheral Location of Chromosomes 13, 17–18 and 21 1963 ·Cytogenetic and Genome Research ·O. J. Miller, W. Roy Breg, Barid B. Mukherjee, (unknown), (unknown)	58

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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