Jo Peters

6.5k citations

66 papers · 3.8k indexed · 1 hit paper · h-index 31

Impact in

Genetics top 0.5%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Molecular Biology top 2%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- Genomics and Chromatin Dynamics

Papers in

Genetics 45
- Genetic Syndromes and Imprinting 32
- Genomic variations and chromosomal abnormalities 9
- Animal Genetics and Reproduction 6
Molecular Biology 51
- Epigenetics and DNA Methylation 26
- Genomics and Chromatin Dynamics 7
- DNA Repair Mechanisms 4

Co-authors: Steve D. M. Brown Elizabeth Fisher Derek C. Rogers Christine M. Williamson Simon Ball Joanne E. Martin Andrea Hunter Gavin Kelsey
Journals: Mammalian Genome (14 papers)Genomics (6 papers)Proceedings of the National Academy of Sciences (4 papers)Nature Genetics (4 papers)PLoS ONE (3 papers)
Partner nations: United Kingdom United States France

In The Last Decade

Jo Peters

64 papers receiving 3.8k citations

Hit Papers

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Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment 1997 · 605 citations

Peers

Countries citing papers authored by Jo Peters

Since Specialization

Citations

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

Fields of papers citing papers by Jo Peters

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jo Peters, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jo Peters Line = papers co-authored together Jo Peters links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The role of genomic imprinting in biology and disease: an expanding view Nature Reviews Genetics ·Jo Peters	2014	298
2	New Mutations at the Imprinted Gnas Cluster Show Gene Dosage Effects of Gs α in Postnatal Growth and Implicate XL α s in Bone and Fat Metabolism but Not in Suckling Molecular and Cellular Biology ·Sally A. Eaton, Christine M. Williamson, Simon Ball, C.V. Beechey, Lee Moir, Jessica K. Edwards, Lydia Teboul, Mark Maconochie, Jo Peters	2012	21
3	Loss of Gnas Imprinting Differentially Affects REM/NREM Sleep and Cognition in Mice PLoS Genetics ·Glenda Lassi, Simon Ball, Silvia Maggi, Giovanni Colonna, Thierry Nieus, Cheryl Cero, Alessandro Bartolomucci, Jo Peters, Valter Tucci	2012	37
4	Uncoupling Antisense-Mediated Silencing and DNA Methylation in the Imprinted Gnas Cluster PLoS Genetics ·Christine M. Williamson, Simon Ball, Claire Dawson, Stuti Mehta, C.V. Beechey, Martin Fray, Lydia Teboul, T. Neil Dear, Gavin Kelsey, Jo Peters	2011	79
5	MicroRNAs 296 and 298 are imprinted and part of the GNAS/Gnas cluster and miR-296 targets IKBKE and Tmed9 RNA ·Mahadi Misrun, Sally A. Eaton, Peter A. Underhill, Dedy Indarsyah, Jo Peters	2011	38
6	Imprinted noncoding RNAs Mammalian Genome ·Jo Peters, Mahadi Misrun	2008	56
7	Alternately spliced WT1 antisense transcripts interact with WT1 sense RNA and show epigenetic and splicing defects in cancer RNA ·Anthony R. Dallosso, Anne L. Hancock, Sally Malik, Ashreena Salpekar, Linda King‐Underwood, Kathy Pritchard‐Jones, Jo Peters, Kim Moorwood, Andrew Ward, Karim Malik, Keith Brown	2007	60
8	Interactions between imprinting effects: summary and review Cytogenetic and Genome Research ·B.M. Cattanach, C.V. Beechey, Jo Peters	2006	17
9	Three novel pigmentation mutants generated by genome‐wide random ENU mutagenesis in the mouse Comparative and Functional Genomics ·Vicky Tsipouri, John A. Curtin, Patrick M. Nolan, Lucie Vizor, Abderaouf M. Moustari, Carolyn Lacka, Bg Wallian, Noor Ullah Khan, Jo Martin, Jo Peters, A. Jackie Hunter, Derek C. Rogers, Sohaila Rastan, Steve D. M. Brown, Elizabeth Fisher, Nigel K. Spurr, Ian C. Gray	2004	2
10	Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouse: Short Communications Comparative and Functional Genomics ·Vicky Tsipouri, John A. Curtin, Patrick M. Nolan, Lucie Vizor, Abderaouf M. Moustari, Carolyn Lacka, Bg Wallian, Noor Ullah Khan, Jo Martin, Jo Peters, A. Jackie Hunter, Derek C. Rogers, Sohaila Rastan, Steve D. M. Brown, Elizabeth Fisher, Nigel K. Spurr, Ian C. Gray	2004	0
11	An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the ‘Legs at odd angles’ ( Loa ) mutation Gene ·Abi Witherden, Majid Hafezparast, Sharon J. Nicholson, Azlina Ahmad‐Annuar, Nessan Bermingham, Demet Araç, Joanna M. Rankin, Marjan Iravani, Simon Ball, Jo Peters, Joanne E. Martin, Derek Huntley, Holger Hummerich, Marek Sergot, Elizabeth Fisher	2002	5
12	Structural characterization of Rasgrf1 and a novel linked imprinted locus Gene ·Younghye Kim, Saveur-Michel Maira, Yue-Zhong Wu, Gustavo Leone, Jo Peters, Bong-June Yoon, Paul D. Soloway, Christoph Plass	2002	28
13	SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice Neuroscience Letters ·Derek C. Rogers, Jo Peters, Pauline N. Gitao, Simon Ball, Sharon J. Nicholson, Abi Witherden, Majid Hafezparast, Judy Latcham, T. L. Robinson, Aleksandr Nicolaichuk, Elizabeth Fisher	2001	145
14	Two imprinted gene mutations: three phenotypes Human Molecular Genetics ·B.M. Cattanach, Jo Peters, Simon Ball, C. Rasberry	2000	47
15	Combining mutagenesis and genomics in the mouse — closing the phenotype gap Trends in Genetics ·Steve D. M. Brown, Jo Peters	1996	81
16	Linkage Mapping around the Ragged (Ra) and Wasted (wst) Loci on Distal Mouse Chromosome 2 Genomics ·Catherine M. Abbott, Stavros Malas, Alison Pilz, Kiersten Mckoy, Robin R. Ali, Jo Peters	1994	16
17	Comparative mapping of mouse Chromosome 4 and human Chromosome 9: Lv, Orm, and Hxb are closely linked on mouse Chromosome 4 Mammalian Genome ·Alison Pilz, J.K. Vidanarachchi, Jo Peters, Catherine M. Abbott	1992	10
18	The gene for proliferating cell nuclear antigen (Pcna) maps to mouse Chromosome 2 Mammalian Genome ·Catherine M. Abbott, Alison Pilz, J.K. Vidanarachchi, Jo Peters	1992	7
19	Adenosine deaminase,Ada, is in mouse chromosome 2H3, and is not allelic with wasted,wst Biochemical Genetics ·Catherine M. Abbott, E.P. Evans, M. D. Burtenshaw, Simon Ball, C. J. Skidmore, J. B. Jones, Jo Peters	1991	7
20	Chromosome maps of man and mouse. IV Annals of Human Genetics ·A.G. Searle, Jo Peters, Mary F. Lyon, Judith G. Hall, E.P. Evans, J. H. Edwards, Veronica J. Buckle	1989	182

About Jo Peters

Jo Peters is a scholar working on Genetics, Molecular Biology, Cancer Research, Cell Biology and Physiology, having authored 66 papers that have together received 3.8k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (32 papers), Epigenetics and DNA Methylation (26 papers), Genomic variations and chromosomal abnormalities (9 papers), Genomics and Chromatin Dynamics (7 papers), Animal Genetics and Reproduction (6 papers), Pancreatic function and diabetes (6 papers), DNA Repair Mechanisms (4 papers) and Cancer-related molecular mechanisms research (4 papers). The work is most often cited by research in Genetics (2.0k citations), Molecular Biology (2.6k citations), Pediatrics, Perinatology and Child Health (537 citations), Cancer Research (323 citations) and Cellular and Molecular Neuroscience (355 citations). Jo Peters has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Steve D. M. Brown, Elizabeth Fisher, Derek C. Rogers, Christine M. Williamson, Simon Ball, Joanne E. Martin, Andrea Hunter, Gavin Kelsey, C.V. Beechey and Mary F. Lyon. Their work appears in journals such as Mammalian Genome, Genomics, Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

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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