Michael A. Simpson

39.5k citations

167 papers · 6.6k · h-index 45

Impact in

Dermatology top 0.5%
- Dermatology and Skin Diseases
Immunology top 2%
- Psoriasis: Treatment and Pathogenesis

Papers in

Molecular Biology 51
- RNA regulation and disease 6
Genetics 34
- Genetic Associations and Epidemiology 6
- Genomics and Rare Diseases 6

Co-authors: Richard C. Trembath (17 shared papers)Andrew H. Crosby (17 shared papers)Catherine Smith (15 shared papers)John A. McGrath (28 shared papers)Francesca Capon (4 shared papers)Andrew Pink (4 shared papers)Dimitra Dafou (6 shared papers)Michael A. Patton (5 shared papers)
Journals: The American Journal of Human Genetics (11 papers)British Journal of Dermatology (10 papers)Journal of Investigative Dermatology (10 papers)Medical Teacher (5 papers)PLoS ONE (4 papers)
Partner nations: United Kingdom United States Australia

In The Last Decade

Michael A. Simpson

156 papers receiving 6.4k citations

Peers

Countries citing papers authored by Michael A. Simpson

Since Specialization

Citations

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

Fields of papers citing papers by Michael A. Simpson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael A. Simpson. 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 Michael A. Simpson. The network helps show where Michael A. Simpson may publish in the future.

Co-authors

The 25 scholars most cited alongside Michael A. Simpson, 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 Michael A. Simpson Line = papers co-authored together Michael A. Simpson links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 167 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis The American Journal of Human Genetics ·Alexandros Onoufriadis, Michael A. Simpson, Andrew Pink, Paola Di Meglio, Catherine Smith, Venu Pullabhatla, Jo Knight, Sarah L. Spain, Frank O. Nestlé, A. David Burden, Francesca Capon, Richard C. Trembath, (unknown)	2011	369
2	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) Nature Genetics ·Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour	2011	350
3	Structural Insights into Histone Demethylation by JMJD2 Family Members Cell ·Zhongzhou Chen, Jianye Zang, Johnathan R. Whetstine, Xia Hong, Foteini Davrazou, Tatiana G. Kutateladze, Michael A. Simpson, Qilong Mao, Cheol‐Ho Pan, Shaodong Dai, James Hagman, Kirk C. Hansen, Yang Shi, Gongyi Zhang	2006	307
4	Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase Nature Genetics ·Michael A. Simpson, J. Helen Cross, Christos Proukakis, David A. Priestman, David C. A. Neville, Gabriele Reinkensmeier, Heng Wang, Max Wiznitzer, Kay Gurtz, Argyro Verganelaki, Anna Pryde, Michael A. Patton, Raymond A. Dwek, Terry D. Butters, Frances M. Platt, Andrew H. Crosby	2004	294
5	Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis Nature Communications ·Elisavet Fotiou, Silvia Martin‐Almedina, Michael A. Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, M Snyder, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard	2015	226
6	Mutations in NOTCH2 cause Hajdu-Cheney syndrome, a disorder of severe and progressive bone loss Nature Genetics ·Michael A. Simpson, Melita Irving, Esra Asilmaz, Mary Jane Gray, Dimitra Dafou, Frances Elmslie, Sahar Mansour, Sue Holder, Caroline Brain, Barbara K. Burton, Katherine H. Kim, Richard M. Pauli, Salim Aftimos, Helen Stewart, Chong Ae Kim, Muriel Holder‐Espinasse, Stephen P. Robertson, William Drake, Richard C. Trembath	2011	219
7	Novel Mutation in Desmoplakin Causes Arrhythmogenic Left Ventricular Cardiomyopathy Circulation ·Mark Norman, Michael A. Simpson, Jens Mogensen, A.O. Shaw, Siân Hughes, Petros Syrris, Srijita Sen‐Chowdhry, Edward Rowland, Andrew H. Crosby, William J. McKenna	2005	211
8	De Novo Mutations in MLL Cause Wiedemann-Steiner Syndrome The American Journal of Human Genetics ·Wendy D. Jones, Dimitra Dafou, Meriel McEntagart, Wesley J. Woollard, Frances Elmslie, Muriel Holder‐Espinasse, Melita Irving, Anand Saggar, Sarah Smithson, Richard C. Trembath, Charu Deshpande, Michael A. Simpson	2012	188
9	Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development The American Journal of Human Genetics ·Michael A. Simpson, Ray C. J. Hsu, Lindsay Keir, Jianjun Hao, G. Sivapalan, Linda M. Ernst, E H Zackai, L.I. Al-Gazali, Georg Hülskamp, Helen Kingston, Trine Prescott, Andra Ion, M Patton, Victoria Murday, Anne George, Andrew H. Crosby	2007	163
10	Germline FH Mutations Presenting With Pheochromocytoma The Journal of Clinical Endocrinology & Metabolism ·Graeme R. Clark, Marco Sciacovelli, Edoardo Gaude, Diana Walsh, Gail Kirby, Michael A. Simpson, Richard C. Trembath, Jonathan Berg, Emma R. Woodward, Esther Kinning, Patrick J. Morrison, Christian Frezza, Eamonn R. Maher	2014	137
11	AP1S3 Mutations Are Associated with Pustular Psoriasis and Impaired Toll-like Receptor 3 Trafficking The American Journal of Human Genetics ·Niovi Setta-Kaffetzi, Michael A. Simpson, Alexander A. Navarini, Varsha Patel, Hui‐Chun Lu, Michael H. Allen, Michael Duckworth, H. Bachelez, A. David Burden, Siew Eng Choon, C.E.M. Griffiths, Brian Kirby, Antonios G.A. Kolios, Marieke M.B. Seyger, Christa Prins, Asma Smahi, Richard C. Trembath, Franca Fraternali, Catherine Smith, (unknown), Francesca Capon	2014	137
12	Sequencing of human genomes with nanopore technology Nature Communications ·Rory Bowden, R. W. Davies, Andreas Heger, Alistair T. Pagnamenta, Mariateresa de Cesare, Laura Oikkonen, Duncan Parkes, Colin Freeman, Fatima Dhalla, Smita Y. Patel, Niko Popitsch, Camilla L. C. Ip, Hannah Roberts, Silvia Salatino, Helen Lockstone, Gerton Lunter, Jenny C. Taylor, David Buck, Michael A. Simpson, Peter Donnelly	2019	129
13	Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema Circulation Research ·Kristiana Gordon, Dörte Schulte, Glen Brice, Michael A. Simpson, M. Guy Roukens, Andreas van Impel, Fiona Connell, Kamini Kalidas, Steve Jeffery, Peter Mortimer, Sahar Mansour, Stefan Schulte‐Merker, Pia Østergaard	2013	126
14	Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron Degeneration The American Journal of Human Genetics ·Maria K. Tsaousidou, Karim Ouahchi, (unknown), Yi Yang, Michael A. Simpson, Nigel G. Laing, Philip A. Wilkinson, R. E. Madrid, Heema Patel, Fayçal Hentati, Michael A. Patton, Afif Hentati, P. Lamont, Teepu Siddique, Andrew H. Crosby	2008	119
15	γ-Secretase Mutations in Hidradenitis Suppurativa: New Insights into Disease Pathogenesis Journal of Investigative Dermatology ·Andrew Pink, Michael A. Simpson, Nemesha Desai, Richard C. Trembath, (unknown)	2012	116
16	Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia The American Journal of Human Genetics ·Michael A. Simpson, J. Helen Cross, Christos Proukakis, Anna Pryde, R. Jane Hershberger, Arnaud Chatonnet, Michael A. Patton, Andrew H. Crosby	2003	114
17	Psoriasis and Genetics Acta Dermato Venereologica ·Nick Dand, Satveer K. Mahil, Francesca Capon, Catherine Smith, Michael A. Simpson, Juliet N. Barker	2020	108
18	Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes Gut ·Katja Christodoulou, Anthony E. Wiskin, Jane Whitney Gibson, William Tapper, Claire Willis, Nadeem Afzal, Rosanna Upstill‐Goddard, John W. Holloway, Michael A. Simpson, R Mark Beattie, Andrew Collins, Sarah Ennis	2012	97
19	Mutations in FAM20C also identified in non‐lethal osteosclerotic bone dysplasia Clinical Genetics ·Michael A. Simpson, Angela E. Scheuerle, Jane A. Hurst, Patton Ma, Helen Stewart, Andrew H. Crosby	2009	90
20	Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype Journal of Medical Genetics ·Pia Østergaard, Michael A. Simpson, Glen Brice, Sahar Mansour, Fiona Connell, Alexandros Onoufriadis, A. H. Child, (unknown), Kamini Kalidas, Peter Mortimer, Richard C. Trembath, Steve Jeffery	2011	86

About Michael A. Simpson

Michael A. Simpson is a scholar working on Molecular Biology, Genetics, Cell Biology, Immunology and Surgery, having authored 167 papers that have together received 6.6k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (13 papers), Psoriasis: Treatment and Pathogenesis (9 papers), Hereditary Neurological Disorders (7 papers), Organ Transplantation Techniques and Outcomes (7 papers), RNA regulation and disease (6 papers), Genetic Associations and Epidemiology (6 papers), Genomics and Rare Diseases (6 papers) and Neurological diseases and metabolism (6 papers). The work is most often cited by research in Dermatology (590 citations), Immunology (933 citations), Cell Biology (654 citations), Hematology (418 citations) and Genetics (1.0k citations). Michael A. Simpson has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Richard C. Trembath, Andrew H. Crosby, Catherine Smith, John A. McGrath, Francesca Capon, Andrew Pink, Dimitra Dafou, Michael A. Patton, Peter Mortimer and Pia Østergaard. Their work appears in journals such as The American Journal of Human Genetics, British Journal of Dermatology, Journal of Investigative Dermatology, Medical Teacher 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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Michael A. Simpson

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