Stephen P. Bryant

716 total citations
18 papers, 535 citations indexed

About

Stephen P. Bryant is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Stephen P. Bryant has authored 18 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Plant Science. Recurrent topics in Stephen P. Bryant's work include Logic, programming, and type systems (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Parallel Computing and Optimization Techniques (3 papers). Stephen P. Bryant is often cited by papers focused on Logic, programming, and type systems (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Parallel Computing and Optimization Techniques (3 papers). Stephen P. Bryant collaborates with scholars based in United States, United Kingdom and Germany. Stephen P. Bryant's co-authors include Nigel K. Spurr, David P. Kelsell, Frances J.D. Smith, I.M. Leigh, Gerhard Wiche, Jouni Uitto, J. F. Geddes, Katsushi Owaribe, E. Birgitte Lane and E.L. Rugg and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Human Molecular Genetics.

In The Last Decade

Stephen P. Bryant

18 papers receiving 510 citations

Peers

Countries citing papers authored by Stephen P. Bryant

Since Specialization

Citations

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

Fields of papers citing papers by Stephen P. Bryant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen P. Bryant. 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 Stephen P. Bryant. The network helps show where Stephen P. Bryant may publish in the future.

Co-authorship network of co-authors of Stephen P. Bryant

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

All Works

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18 of 18 papers shown

#	Work	Indexed citations
1	Genetic Analysis of Complex Traits 2003 ·Humana Press eBooks ·Stephen P. Bryant, Mathias Chiano	3
2	ICRF handbook of genome analysis 1998 ·Biodiversity Heritage Library (Smithsonian Institution) ·Nigel K. Spurr, Bryan D. Young, Stephen P. Bryant	8
3	Human 5-HT5AReceptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 7q34–q36 Using a Polymorphism in the 5′ Untranslated Region 1997 ·Biochemical and Biophysical Research Communications ·Daphne Shimron‐Abarbanell, Jeanette Erdmann, Ina R. Vogt, Stephen P. Bryant, Nigel K. Spurr, Michael Knapp, Peter Propping, Markus M. Nöthen	17
4	Construction of a Radiation Hybrid Map of Chromosome 9p 1996 ·Genomics ·Mark Bouzyk, Stephen P. Bryant, Karin Schmitt, Peter N. Goodfellow, Rosemary Ekong, Nigel K. Spurr	7
5	Software for genetic linkage analysis 1996 ·Molecular Biotechnology ·Stephen P. Bryant	1
6	Plectin deficiency results in muscular dystrophy with epidermolysis bullosa 1996 ·Nature Genetics ·Frances J.D. Smith, Robin A.J. Eady, I.M. Leigh, J. R. McMillan, E.L. Rugg, David P. Kelsell, Stephen P. Bryant, Nigel K. Spurr, J. F. Geddes, Gudula Kirtschig, Gabriella Milana, (unknown), Katsushi Owaribe, Gerhard Wiche, Lea Pulkkinen, Jouni Uitto, W.H. Irwin McLean, E. Birgitte Lane	299
7	Chromosomal Assignment of 79 cDNAs from a Range of Human Tissues 1996 ·Genomics ·Caroline A. Evans, Mark Bouzyk, (unknown), (unknown), Stephen P. Bryant, Nigel K. Spurr	2
8	Human Adenosine A1 Receptor Gene: Systematic Screening for DNA Sequence Variation and Linkage Mapping on Chromosome 1q31-32.1 Using a Silent Polymorphism in the Coding Region 1995 ·Biochemical and Biophysical Research Communications ·Jürgen Deckert, Markus M. Nöthen, Stephen P. Bryant, Huazhong Ren, Hans Wolf, Gary L. Stiles, Nigel K. Spurr, Peter Propping	5
9	Integrated genetic map of human chromosome 2 1995 ·Annals of Human Genetics ·(unknown), Stephen P. Bryant, Andrew Collins, Jean Weissenbach, Helen Donis-Keller, Bobby P. C. Koeleman, Alexander Steinkasserer, Nigel K. Spurr	4
10	Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneity 1995 ·Human Molecular Genetics ·David P. Kelsell, Howard P. Stevens, R. Ratnavel, Stephen P. Bryant, D. Timothy Bishop, Irene M. Leigh, Nigel K. Spurr	30
11	The 1994 Southern California Network Bulletin 1995 ·Seismological Research Letters ·Lisa A. Wald, K. Hafner, Stephen P. Bryant	2
12	European Gene Mapping Project(EUROGEM): Genetic Maps basedon the CEPH reference families 1994 ·European Journal of Human Genetics ·(unknown), Stephen P. Bryant, (unknown), Kevin G. Nyberg, (unknown), Anne M. Mills, Rasneer Sonia Bains, (unknown), (unknown), Sue Povey, (unknown), Jean Weissenbach, Howard M. Cann, Mark Lathrop, J Dausset, (unknown), Daniel Cohen	19
13	Localization of the CYP2D Gene Locus to Human Chromosome 22q13.1 by Polymerase Chain Reaction, in Situ Hybridization, and Linkage Analysis 1993 ·Genomics ·Alan C. Gough, Christopher A. Smith, Stephen H. Howell, C. Roland Wolf, Stephen P. Bryant, N.K. Spurr	51
14	The CEPH consortium linkage map of human chromosome 2 1992 ·Genomics ·(unknown), (unknown), Stephen P. Bryant, (unknown), ELIZABETH B. ROBSON, (unknown), (unknown), Trefor Jenkins, Jeffrey C. Murray, (unknown), Marshall Summar, Petros Tsipouras, A.E. Retief, (unknown), A. Bale, Gilles Vergnaud, James L. Weber, O. Wesley McBride, Helen Donis-Keller, R. White	5
15	A computer program to make linkage analysis with liped and linkage easier to perform and less prone to input errors 1988 ·Annals of Human Genetics ·(unknown), Stephen P. Bryant	65
16	The NYU Ada translator and interpreter 1980 ·ACM SIGPLAN Notices ·Robert Dewar, (unknown), Edmond Schonberg, (unknown), Stephen P. Bryant, (unknown), Michael Burke	5
17	The NYU Ada translator and interpreter 1980 ·Robert Dewar, (unknown), Edmond Schonberg, (unknown), Stephen P. Bryant, (unknown), Michael Burke	10
18	The NYU Ada translator and interpreter 1980 ·ACM SIGPLAN Notices ·Robert Dewar, (unknown), Edmond Schonberg, (unknown), Stephen P. Bryant, (unknown), Michael Burke	2

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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