Wendy N. Cooper

5.5k total citations
34 papers, 2.3k citations indexed

About

Wendy N. Cooper is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Wendy N. Cooper has authored 34 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 13 papers in Pediatrics, Perinatology and Child Health and 8 papers in Genetics. Recurrent topics in Wendy N. Cooper's work include Epigenetics and DNA Methylation (16 papers), Genetic Syndromes and Imprinting (8 papers) and Birth, Development, and Health (7 papers). Wendy N. Cooper is often cited by papers focused on Epigenetics and DNA Methylation (16 papers), Genetic Syndromes and Imprinting (8 papers) and Birth, Development, and Health (7 papers). Wendy N. Cooper collaborates with scholars based in United Kingdom, Australia and South Sudan. Wendy N. Cooper's co-authors include Farida Latif, Luke B. Hesson, Angelo Agathanggelou, Eamonn R. Maher, Miguel Constância, Richard G. Grundy, Fiona MacDonald, Daniel Catchpoole, Nabeel A. Affara and David B. Dunger and has published in prestigious journals such as Cancer Research, Oncogene and Current Biology.

In The Last Decade

Wendy N. Cooper

34 papers receiving 2.3k citations

Peers

Countries citing papers authored by Wendy N. Cooper

Since Specialization

Citations

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

Fields of papers citing papers by Wendy N. Cooper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy N. Cooper. 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 Wendy N. Cooper. The network helps show where Wendy N. Cooper may publish in the future.

Co-authorship network of co-authors of Wendy N. Cooper

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy N. Cooper. A scholar is included among the top collaborators of Wendy N. Cooper 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 Wendy N. Cooper. Wendy N. Cooper 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	Characteristics, origin, and potential for cancer diagnostics of ultrashort plasma cell-free DNA 2021 ·Genome Research ·Irena Hudecova, Christopher G. Smith, Robert Hänsel‐Hertsch, Chandra Sekhar Reddy Chilamakuri, James A. Morris, (unknown), Katrin Heider, Dineika Chandrananda, Wendy N. Cooper, Davina Gale, Javier García-Corbacho, Simon Pacey, Richard D. Baird, Nitzan Rosenfeld, Florent Moulière	58
2	Detection of ctDNA from Dried Blood Spots after DNA Size Selection 2020 ·Clinical Chemistry ·Katrin Heider, Jonathan C. M. Wan, James Hall, Jelena Belic, (unknown), Irena Hudecova, Davina Gale, Wendy N. Cooper, Pippa Corrie, James D. Brenton, Christopher G. Smith, Nitzan Rosenfeld	36
3	Mesenchyme-derived IGF2 is a major paracrine regulator of pancreatic growth and function 2020 ·PLoS Genetics ·(unknown), Ionel Sandovici, Gemma V. Brierley, Nicola M. Smith, Warren E. Zimmer, Ilona Zvetkova, Haydn M. Prosser, Yoichi Sekita, Brian Lam, Marcella Ma, Wendy N. Cooper, Antonio Vidal‐Puig, Susan E. Ozanne, Gema Medina‐Gómez, Miguel Constância	13
4	Adipose tissue dysfunction as a central mechanism leading to dysmetabolic obesity triggered by chronic exposure to p,p’-DDE 2017 ·Scientific Reports ·Diogo Pestana, Diana Teixeira, Manuela Meireles, Cláudia Marques, Sónia Norberto, (unknown), Virgínia Cruz Fernandes, Luísa Correia‐Sá, Ana Faria, Luísa Guardão, João Tiago Guimarães, Wendy N. Cooper, Ionel Sandovici, Valentina F. Domingues, Cristina Delerue‐Matos, Rosário Monteiro, Miguel Constância, Conceição Calhau	34
5	Ageing is associated with molecular signatures of inflammation and type 2 diabetes in rat pancreatic islets 2015 ·Diabetologia ·Ionel Sandovici, (unknown), Wendy N. Cooper, Noel H. Smith, Jane L. Tarry‐Adkins, Benjamin J. Dunmore, Julien Bauer, Simon Andrews, Giles S.H. Yeo, Susan E. Ozanne, Miguel Constância	21
6	Periconceptional maternal micronutrient supplementation is associated with widespread gender related changes in the epigenome: a study of a unique resource in the Gambia 2012 ·Human Molecular Genetics ·Batbayar Khulan, Wendy N. Cooper, Benjamin M. Skinner, Julien Bauer, Stephen Owens, Andrew M. Prentice, Gusztáv Bélteki, Miguel Constância, David B. Dunger, Nabeel A. Affara	116
7	The RASSF8 candidate tumor suppressor inhibits cell growth and regulates the Wnt and NF-κB signaling pathways 2010 ·Oncogene ·Frances E. Lock, (unknown), Thomas L. Dunwell, David Matallanas, Wendy N. Cooper, Luke B. Hesson, (unknown), Andrew Ward, Pavlova Tv, Eugene R. Zabarovsky, Melissa M. Grant, Eamonn R. Maher, Andrew D. Chalmers, Walter Kölch, Farida Latif	68
8	How genome-wide approaches can be used to unravel the remaining secrets of the imprintome 2010 ·Briefings in Functional Genomics ·Wendy N. Cooper, Miguel Constância	10
9	RASSF2 associates with and stabilizes the proapoptotic kinase MST2 2009 ·Oncogene ·Wendy N. Cooper, Luke B. Hesson, David Matallanas, Ashraf Dallol, Alex von Kriegsheim, Robyn L. Ward, Walter Kölch, Farida Latif	71
10	The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias 2009 ·Molecular Cancer ·Luke B. Hesson, Thomas L. Dunwell, Wendy N. Cooper, Daniel Catchpoole, A.T. Brini, Raffaella Chiaramonte, Mike Griffiths, Andrew D. Chalmers, Eamonn R. Maher, Farida Latif	94
11	RAN GTPase Is a RASSF1A Effector Involved in Controlling Microtubule Organization 2009 ·Current Biology ·Ashraf Dallol, Luke B. Hesson, David Matallanas, Wendy N. Cooper, Eric O’Neill, Eamonn R. Maher, Walter Kölch, Farida Latif	30
12	Beckwith Weidemann syndrome: A behavioral phenotype–genotype study 2008 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Lindsey Kent, Sarah Bowdin, Gail Kirby, Wendy N. Cooper, Eamonn R. Maher	53
13	Depletion of the Ras Association Domain Family 1, Isoform A–Associated Novel Microtubule-Associated Protein, C19ORF5/MAP1S, Causes Mitotic Abnormalities 2007 ·Cancer Research ·Ashraf Dallol, Wendy N. Cooper, Fahd Al‐Mulla, Angelo Agathanggelou, Eamonn R. Maher, Farida Latif	42
14	Mitotic recombination and uniparental disomy in Beckwith–Wiedemann syndrome 2007 ·Genomics ·Wendy N. Cooper, (unknown), Fiona MacDonald, Eamonn R. Maher	34
15	Epigenetic regulation of the ras effector/tumour suppressor RASSF2 in breast and lung cancer 2007 ·Oncogene ·Wendy N. Cooper, (unknown), Ashraf Dallol, Elvira V. Grigorieva, Pavlova Tv, Luke B. Hesson, Ivan Bièche, Massimo Broggini, Eamonn R. Maher, Eugene R. Zabarovsky, Geoffrey Clark, Farida Latif	41
16	The Role of RASSF1A Methylation in Cancer 2007 ·Disease Markers ·Luke B. Hesson, Wendy N. Cooper, Farida Latif	166
17	Evaluation of the 3p21.3 tumour-suppressor gene cluster 2007 ·Oncogene ·Luke B. Hesson, Wendy N. Cooper, Farida Latif	136
18	Epigenetic analysis of HIC1, CASP8, FLIP, TSP1, DCR1, DCR2, DR4, DR5, KvDMR1, H19 and preferential 11p15.5 maternal-allele loss in von Hippel-Lindau and sporadic phaeochromocytomas 2005 ·Endocrine Related Cancer ·(unknown), Dewi Astuti, Dean Gentle, Wendy N. Cooper, Alberto Cascón, Daniel Catchpoole, Mercedes Robledo, Hartmut P.H. Neumann, Farida Latif, Eamonn R. Maher	55
19	Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma 2003 ·Oncogene ·Mark R. Morris, Luke B. Hesson, Kate Wagner, Neil V. Morgan, Dewi Astuti, (unknown), Wendy N. Cooper, (unknown), Dean Gentle, Fiona MacDonald, Takeshi Kishida, Richard G. Grundy, Masahiro Yao, Farida Latif, Eamonn R. Maher	87
20	Mapping the multiple self-healing squamous epithelioma (MSSE) gene and investigation of xeroderma pigmentosum group A (XPA) and PATCHED (PTCH) as candidate genes 1997 ·Human Genetics ·Frances M. Richards, (unknown), Wendy N. Cooper, (unknown), Inês Barroso, Carol Wicking, Brandon J. Wainwright, M.A. Ferguson‐Smith	33

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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