Alison J. Coffey

5.1k total citations
27 papers, 1.0k citations indexed

About

Alison J. Coffey is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Alison J. Coffey has authored 27 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Oncology. Recurrent topics in Alison J. Coffey's work include RNA Research and Splicing (6 papers), Muscle Physiology and Disorders (5 papers) and Drug Transport and Resistance Mechanisms (4 papers). Alison J. Coffey is often cited by papers focused on RNA Research and Splicing (6 papers), Muscle Physiology and Disorders (5 papers) and Drug Transport and Resistance Mechanisms (4 papers). Alison J. Coffey collaborates with scholars based in United Kingdom, United States and Netherlands. Alison J. Coffey's co-authors include David Bentley, Roland G. Roberts, Martin Bobrow, Munir Pirmohamed, Michael R. Johnson, Guy Leschziner, F. Giannelli, Rakesh Anand, David J. Balding and Jane Rogers and has published in prestigious journals such as Annals of Neurology, The Lancet Neurology and Human Molecular Genetics.

In The Last Decade

Alison J. Coffey

26 papers receiving 999 citations

Peers

Countries citing papers authored by Alison J. Coffey

Since Specialization

Citations

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

Fields of papers citing papers by Alison J. Coffey

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alison J. Coffey. 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 Alison J. Coffey. The network helps show where Alison J. Coffey may publish in the future.

Co-authorship network of co-authors of Alison J. Coffey

This figure shows the co-authorship network connecting the top 25 collaborators of Alison J. Coffey. A scholar is included among the top collaborators of Alison J. Coffey 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 Alison J. Coffey. Alison J. Coffey 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	A framework for the evaluation and reporting of incidental findings in clinical genomic testing 2024 ·European Journal of Human Genetics ·Carolyn M. Brown, Laura M. Amendola, Anjana Chandrasekhar, R. Tanner Hagelstrom, (unknown), (unknown), Erin Thorpe, Denise Perry, Ryan J. Taft, Alison J. Coffey	1
2	Expert Panel Curation of 113 Primary Mitochondrial Disease Genes for the Leigh Syndrome Spectrum 2023 ·Annals of Neurology ·Elizabeth M. McCormick, (unknown), Julie P. Taylor, Alison J. Coffey, Li Shen, Danuta Krotoski, Brian Harding, (unknown), Xiaowu Gai, Marni J. Falk, Zarazuela Zolkipli‐Cunningham, Shamima Rahman	23
3	Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome 2015 ·Journal of Molecular and Cellular Cardiology ·Konstantin Wemhöner, Corinna Friedrich, Birgit Stallmeyer, Alison J. Coffey, Andrew A. Grace, Sven Zumhagen, Guiscard Seebohm, (unknown), Susanne Rinné, Frank B. Sachse, Eric Schulze‐Bahr, Niels Decher	71
4	A detailed clinical and molecular survey of subjects with nonsyndromic USH2A retinopathy reveals an allelic hierarchy of disease-causing variants 2015 ·European Journal of Human Genetics ·Eva Lenassi, Ajoy Vincent, Zheng Li, Zubin Saihan, Alison J. Coffey, Heather B. Steele-Stallard, Anthony T. Moore, Karen P. Steel, Linda Luxon, Elise Héon, Maria Bitner‐Glindzicz, Andrew R. Webster	85
5	Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype 2013 ·Basic Research in Cardiology ·(unknown), Sven Zumhagen, Michael F. Netter, Alison J. Coffey, Andrew A. Grace, Jane Rogers, (unknown), Susanne Rinné, Birgit Stallmeyer, Niels Decher, Eric Schulze‐Bahr	18
6	Q8IYL2 is a candidate gene for the familial epilepsy syndrome of Partial Epilepsy with Pericentral Spikes (PEPS) 2011 ·Epilepsy Research ·Guy Leschziner, Alison J. Coffey, Toby Andrew, Sheila P. Gregório, Emmanuel Dias‐Neto, M Calafato, David Bentley, Lucy Kinton, Josemir W. Sander, Michael R. Johnson	15
7	Genetic and environmental factors determining clinical outcomes and cost of warfarin therapy: a prospective study 2009 ·Pharmacogenetics and Genomics ·Andrea Jorgensen, (unknown), (unknown), Andrew Keniry, Anita Hanson, Dyfrig Hughes, (unknown), Lisa Stevens, (unknown), Cheng‐Hong Toh, Farhad Kamali, Ann K. Daly, David Fitzmaurice, Alison J. Coffey, Paula Williamson, Brian Kevin Park, Panos Deloukas, Munir Pirmohamed	55
8	Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup‐shaped ears, congenital heart defect, and mental retardation—New MCA/MR syndrome in two affected sibs and a mildly affected mother? 2007 ·American Journal of Medical Genetics Part A ·Dagmar Wieczorek, Charles Shaw‐Smith, Jürgen Kohlhase, W Schmitt, Karin Buiting, Alison J. Coffey, Eleanor Howard, Ute Hehr, Gabriele Gillessen‐Kaesbach	12
9	Common ABCB1 polymorphisms are not associated with multidrug resistance in epilepsy using a gene-wide tagging approach 2007 ·Pharmacogenetics and Genomics ·Guy Leschziner, Toby Andrew, John Paul Leach, David Chadwick, Alison J. Coffey, David J. Balding, David Bentley, Munir Pirmohamed, Michael R. Johnson	40
10	Clinical factors and ABCB1 polymorphisms in prediction of antiepileptic drug response: a prospective cohort study 2006 ·The Lancet Neurology ·Guy Leschziner, Andrea Jorgensen, Munir Pirmohamed, Paula Williamson, Anthony G Marson, Alison J. Coffey, (unknown), Jane Rogers, David Bentley, David Chadwick, David J. Balding, Michael R. Johnson, Toby Andrew	58
11	Exon sequencing and high resolution haplotype analysis of ABC transporter genes implicated in drug resistance 2006 ·Pharmacogenetics and Genomics ·Guy Leschziner, Delilah Zabaneh, Munir Pirmohamed, Andrew Owen, Jane Rogers, Alison J. Coffey, David J. Balding, (unknown), Michael R. Johnson	58
12	Characterisation of a novel murine intestinal serine protease, DISP 2000 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Charles Shaw‐Smith, Alison J. Coffey, M. Leversha, Tom C. Freeman, D. R. Bentley, Julian R.F. Walters	9
13	Refined Mapping and YAC Contig Construction of the X-Linked Cleft Palate and Ankyloglossia Locus (CPX) Including the Proximal X–Y Homology Breakpoint within Xq21.3 1996 ·Genomics ·Simon Forbes, (unknown), Michael P. Richardson, Alison J. Coffey, Charlotte G. Cole, Simon G. Gregory, David Bentley, Steven Mumm, Gudrun E. Moore, Philip Stanier	26
14	A 6.5-Mb Yeast Artificial Chromosome Contig Incorporating 33 DNA Markers on the Human X Chromosome at Xq22 1994 ·Genomics ·David Vetrie, Elaine Kendall, Alison J. Coffey, Sheila Hassock, John Collins, Christopher D. Todd, Hans Lehrach, Martin Bobrow, (unknown), Ann Harris	22
15	Vertical Integration of Cosmid and YAC Resources for Interval Mapping on the X-Chromosome 1993 ·Genomics ·Jill Holland, Alison J. Coffey, F. Giannelli, (unknown)	10
16	Exon Structure of the Human Dystrophin Gene 1993 ·Genomics ·Roland G. Roberts, Alison J. Coffey, Martin Bobrow, David Bentley	126
17	Reconstruction of the 204 Mb human DMD-gene bhy homologous YAC recombination 1992 ·Human Molecular Genetics ·Johan T. den Dunnen, P.M. Grootscholten, J.G. Dauwerse, Alexander P. Walker, Anthony P. Monaco, Robin Butler, Rakesh Anand, Alison J. Coffey, D. R. Bentley, H. Yde Steensma, G.J.B. van Ommen	66
18	Determination of the exon structure of the distal portion of the dystrophin gene by vectorette PCR 1992 ·Genomics ·Roland G. Roberts, Alison J. Coffey, Martin Bobrow, David Bentley	81
19	Construction of a 2.6-Mb contig in yeast artificial chromosomes spanning the human dystrophin gene using an STS-based approach 1992 ·Genomics ·Alison J. Coffey, Roland G. Roberts, E D Green, (unknown), Rachel Butler, Rakesh Anand, F. Giannelli, (unknown)	83
20	Moderate haemophilia B in a female carrier caused by preferential inactivation of the paternal X chromosome 1991 ·European Journal Of Haematology ·(unknown), Alison J. Coffey, Rolf Ljung, Elsy Sjörin, Inga Marie Nilsson, Lars Holmberg, F. Giannelli	23

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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