Peter Teague

1.9k total citations · 1 hit paper
21 papers, 1.5k citations indexed

About

Peter Teague is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Peter Teague has authored 21 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Peter Teague's work include Genomic variations and chromosomal abnormalities (4 papers), Retinal Development and Disorders (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Peter Teague is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Retinal Development and Disorders (4 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Peter Teague collaborates with scholars based in United Kingdom, Croatia and Denmark. Peter Teague's co-authors include Wendy A. Bickmore, Shelagh Boyle, Paul Perry, Joanna M. Bridger, Douglas Blackwood, Alan F. Wright, Walter Muir, David J. Porteous, Rebecca S. Devon and V. Murray and has published in prestigious journals such as The Journal of Cell Biology, Journal of Neurochemistry and The American Journal of Human Genetics.

In The Last Decade

Peter Teague

21 papers receiving 1.5k 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.

Differences in the Localization and Morphology of Chromosomes in the Human Nucleus

1999 724 citations Joanna M. Bridger, Shelagh Boyle et al. The Journal of Cell Biology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter Teague United Kingdom	15	1.1k	508	318	132	72	21	1.5k
Birger Voigt Japan	16	953 0.9×	482 0.9×	74 0.2×	121 0.9×	50 0.7×	35	1.3k
Christine Clemson United States	11	2.7k 2.4×	648 1.3×	202 0.6×	113 0.9×	46 0.6×	27	3.5k
Paul C. Lott United States	13	1.3k 1.2×	299 0.6×	111 0.3×	82 0.6×	49 0.7×	23	1.7k
Katherine Lachlan United Kingdom	19	869 0.8×	659 1.3×	84 0.3×	58 0.4×	69 1.0×	45	1.4k
Alix Weaver United States	5	825 0.7×	837 1.6×	181 0.6×	145 1.1×	99 1.4×	6	1.7k
Aparna Prasad United States	18	400 0.4×	493 1.0×	91 0.3×	75 0.6×	79 1.1×	44	1.0k
Karen Sperle United States	19	1.3k 1.2×	428 0.8×	270 0.8×	105 0.8×	55 0.8×	25	1.7k
Michele Pinelli Italy	19	745 0.7×	457 0.9×	59 0.2×	199 1.5×	99 1.4×	49	1.3k
Cécile Mignon‐Ravix France	15	475 0.4×	320 0.6×	72 0.2×	62 0.5×	81 1.1×	26	727
Britt‐Marie Anderlid Sweden	22	607 0.5×	813 1.6×	179 0.6×	51 0.4×	75 1.0×	56	1.3k

Countries citing papers authored by Peter Teague

Since Specialization

Citations

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

Fields of papers citing papers by Peter Teague

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Teague. 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 Peter Teague. The network helps show where Peter Teague may publish in the future.

Co-authorship network of co-authors of Peter Teague

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Teague. A scholar is included among the top collaborators of Peter Teague 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 Peter Teague. Peter Teague 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

Carothers, A D, Igor Rudan, Ivana Kolčić, et al.. (2006). Estimating Human Inbreeding Coefficients: Comparison of Genealogical and Marker Heterozygosity Approaches. Annals of Human Genetics. 70(5). 666–676. 66 indexed citations

Vitart, Véronique, Andrew D. Carothers, Caroline Hayward, et al.. (2005). Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design. The American Journal of Human Genetics. 76(5). 763–772. 21 indexed citations

Davidson, Donald J., Sheila Webb, Peter Teague, John R. W. Govan, & Julia R. Dorin. (2004). Lung Pathology in Response to Repeated Exposure to <i>Staphylococcus aureus</i> in Congenic Residual Function Cystic Fibrosis Mice Does Not Increase in Response to Decreased CFTR Levels or Increased Bacterial Load. Pathobiology. 71(3). 152–158. 11 indexed citations

Maratou, Klio, Thorsten Forster, Yael Costa, et al.. (2003). Expression profiling of the developing testis in wild‐type and Dazl knockout mice. Molecular Reproduction and Development. 67(1). 26–54. 42 indexed citations

Bickmore, Wendy A. & Peter Teague. (2002). Influences of chromosome size, gene density and nuclear position on the frequency of constitutional translocations in the human population. Chromosome Research. 10(8). 707–715. 62 indexed citations

Devon, Rebecca S., S.I. Anderson, Peter Teague, et al.. (2001). Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder. Psychiatric Genetics. 11(2). 71–78. 95 indexed citations

Devon, Rebecca S., Susan M. Anderson, Peter Teague, et al.. (2001). The genomic organisation of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia. Molecular Psychiatry. 6(3). 311–314. 69 indexed citations

Miano, Maria Giuseppina, Samuel G. Jacobson, Andrew D. Carothers, et al.. (2000). Pitfalls in Homozygosity Mapping. The American Journal of Human Genetics. 67(5). 1348–1351. 10 indexed citations

Hodge, P. J., Peter Teague, Alan F. Wright, & Denis F. Kinane. (2000). Clinical and Genetic Analysis of a Large North European Caucasian Family Affected by Early-onset Periodontitis. Journal of Dental Research. 79(3). 857–863. 37 indexed citations

10.

Battersby, S., Alan D. Ogilvie, Douglas Blackwood, et al.. (1999). Presence of Multiple Functional Polyadenylation Signals and a Single Nucleotide Polymorphism in the 3′ Untranslated Region of the Human Serotonin Transporter Gene. Journal of Neurochemistry. 72(4). 1384–1388. 84 indexed citations

11.

Vogel, Tanja, R.M. Speed, Peter Teague, & Howard J. Cooke. (1999). Mice with Y chromosome deletion and reduced Rbm genes on a heterozygous Dazl1 null background mimic a human azoospermic factor phenotype. Human Reproduction. 14(12). 3023–3029. 17 indexed citations

12.

Heyman, Isobel, Ian Frampton, Veronica van Heyningen, et al.. (1999). Psychiatric disorder and cognitive function in a family with an inherited, novel mutation of the developmental control gene PAX6. Psychiatric Genetics. 9(2). 85–90. 40 indexed citations

13.

Bridger, Joanna M., et al.. (1999). Differences in the Localization and Morphology of Chromosomes in the Human Nucleus. The Journal of Cell Biology. 145(6). 1119–1131. 724 indexed citations breakdown →

14.

Bruford, Elspeth A., Ruth Riise, Peter Teague, et al.. (1997). Linkage Mapping in 29 Bardet–Biedl Syndrome Families Confirms Loci in Chromosomal Regions 11q13, 15q22.3–q23, and 16q21. Genomics. 41(1). 93–99. 96 indexed citations

15.

He, Lin, A D Carothers, Douglas Blackwood, et al.. (1996). Recombination patterns around the breakpoints of a balanced 1;11 autosomal translocation associated with major mental illness. Psychiatric Genetics. 6(4). 201–208. 3 indexed citations

16.

Mansfield, David, Peter Teague, & Alison G. Barber. (1994). Genetic linkage studies in autosomal recessive retinitis pigmentosa. The American Journal of Human Genetics. 55. 3 indexed citations

17.

Teague, Peter, Micheala A. Aldred, Marcelle Jay, et al.. (1994). Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.. PubMed. 55(1). 105–11. 56 indexed citations

18.

Aldred, Micheala A., Peter Teague, Marcelle Jay, et al.. (1994). Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.. Journal of Medical Genetics. 31(11). 848–852. 6 indexed citations

19.

Wright, Alan F., Peter Teague, Patricia Pignatelli, et al.. (1993). A study of genetic linkage heterogeneity in 35 adult-onset polycystic kidney disease families. Human Genetics. 90(5). 569–571. 19 indexed citations

20.

Aldred, Micheala A., Katherine L. Dry, Dianne Sharp, et al.. (1992). Linkage analysis in X-linked congenital stationary night blindness. Genomics. 14(1). 99–104. 16 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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