Hayley Archer

2.4k citations

17 papers · 1.1k indexed · h-index 14

Co-authors: Angus Clarke Julie Evans John Christodoulou Helen Leonard Sarah Williamson Jozef Gécz Julian R. Sampson Alison Kerr
Topics: Genetics and Neurodevelopmental Disorders (16 papers)Genomic variations and chromosomal abnormalities (7 papers)Autism Spectrum Disorder Research (7 papers)
Cited by: Genetics Cognitive Neuroscience Developmental Neuroscience
Journals: The American Journal of Human Genetics Journal of Medical Genetics European Journal of Human Genetics
Partner nations: United Kingdom Australia Denmark

In The Last Decade

Hayley Archer

16 papers receiving 1.1k citations

Peers

Countries citing papers authored by Hayley Archer

Since Specialization

Citations

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

Fields of papers citing papers by Hayley Archer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hayley Archer

This figure shows the co-authorship network connecting the top 25 collaborators of Hayley Archer. A scholar is included among the top collaborators of Hayley Archer 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 Hayley Archer. Hayley Archer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	Middle‐Aged Women With Rett Syndrome: Longitudinal Profile From the British Isles Rett Syndrome Survey and Suggestions for Care 2025 ·Journal of Applied Research in Intellectual Disabilities ·(unknown),(unknown),Hayley Archer,Angus Clarke	0
2	WDR 45 Mutation in Atypical Rett Syndrome with Brain Iron Accumulation 2015 ·Movement Disorders Clinical Practice ·Sarah Crisp,Esther Meyer,Allison Gregory,Hayley Archer,Susan J. Hayflick,Manju A. Kurian,Rajith de Silva	2
3	De Novo Loss-of-Function Mutations in SETD5, Encoding a Methyltransferase in a 3p25 Microdeletion Syndrome Critical Region, Cause Intellectual Disability 2014 ·The American Journal of Human Genetics ·Detelina Grozeva,Keren Carss,Olivera Spasić-Bošković,Michael Parker,Hayley Archer,Helen V. Firth,Soo‐Mi Park,Natalie Canham,Susan Holder,Meredith Wilson,Anna Hackett,Michael Field,James Floyd,Matthew E. Hurles,F. Lucy Raymond	89
4	Transcription Factor 4 and Myocyte Enhancer Factor 2C mutations are not common causes of Rett syndrome 2012 ·American Journal of Medical Genetics Part A ·(unknown),Hayley Archer,Angus Clarke,Pradeep Vasudevan,Christiane Zweier,Gladys Ho,Sarah Williamson,(unknown),Nan Yang,John Christodoulou	19
5	Epilepsy in Rett syndrome: Association between phenotype and genotype, and implications for practice 2011 ·Seizure ·(unknown),Angus Clarke,(unknown),Frances Gibbon,Phil E M Smith,Hayley Archer,(unknown),Mike Kerr	40
6	Epilepsy caused by CDKL5 mutations 2010 ·European Journal of Paediatric Neurology ·Maija L. Castrén,Eija Gaily,(unknown),Jaana Lähdetie,Hayley Archer,Sirpa Ala‐Mello	39
7	Two sisters with Rett syndrome and non-identical paternally-derived microdeletions in the MECP2 gene 2008 ·PubMed ·(unknown),Shane McKee,(unknown),Hayley Archer,James B. Hughes,Rachel Butler,Nadia Chuzhanova,D.N. Cooper,L. Lazarou	4
8	NTNG1 mutations are a rare cause of Rett syndrome 2006 ·American Journal of Medical Genetics Part A ·Hayley Archer,Julie Evans,David Millar,Peter Thompson,Alison Kerr,Helen Leonard,John Christodoulou,David Ravine,L. Lazarou,(unknown),Christopher Verity,Sharon D. Whatley,Daniela T. Pilz,Julian R. Sampson,Angus Clarke	38
9	CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patients 2006 ·Journal of Medical Genetics ·Hayley Archer,Julie Evans,Stuart W. Edwards,James Colley,Ruth Newbury‐Ecob,Finbar O’Callaghan,(unknown),M O'Regan,John Tolmie,Julian R. Sampson,Angus Clarke,J. P. Osborne	149
10	Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation 2006 ·Journal of Medical Genetics ·Hayley Archer,Julie Evans,Helen Leonard,Lyn Colvin,David Ravine,John Christodoulou,Sarah Williamson,Tony Charman,Mark E.S. Bailey,Julian R. Sampson,Nicholas de Klerk,Angus Clarke	79
11	Early onset seizures and Rett-like features associated with mutations in CDKL5 2005 ·European Journal of Human Genetics ·Julie Evans,Hayley Archer,James Colley,Kirstine Ravn,Jytte Bieber Nielsen,Alison Kerr,Elizabeth Williams,John Christodoulou,Jozef Gécz,Philip Jardine,Michael Wright,Daniela T. Pilz,L. Lazarou,D.N. Cooper,Julian R. Sampson,Rachel Butler,Sharon D. Whatley,Angus Clarke	135
12	Dimensional phenotypic analysis and functional categorisation of mutations reveal novel genotype–phenotype associations in Rett syndrome 2005 ·European Journal of Human Genetics ·Tony Charman,(unknown),(unknown),Hayley Archer,Mary Gardiner,Gun Peggy Knudsen,Aoibhinn McDonnell,Jacqueline Perry,Sharon D. Whatley,David J. Bunyan,Kirstine Ravn,Rebecca H. Mount,Richard P. Hastings,Maj Hultén,Karen Helene Ørstavik,Sheena Reilly,Hilary Cass,Angus Clarke,Alison Kerr,Mark E.S. Bailey	48
13	People withMECP2mutation‐positive Rett disorder who converse 2005 ·Journal of Intellectual Disability Research ·Alison Kerr,Hayley Archer,Julie Evans,R.J. Prescott,Frances Gibbon	34
14	p.R270X MECP2 mutation and mortality in Rett syndrome 2005 ·European Journal of Human Genetics ·Le Jian,Hayley Archer,David Ravine,Alison Kerr,Nicholas de Klerk,John Christodoulou,Mark E.S. Bailey,Crystal L. Laurvick,Helen Leonard	29
15	Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3‐pter 2005 ·American Journal of Medical Genetics Part A ·Hayley Archer,(unknown),Stuart Enoch,Peter Thompson,Anthony W. Rowbottom,(unknown),Stephen T. Warren,David Johnson,David H. Ledbetter,(unknown),P. Gail Williams,Daniela T. Pilz	34
16	Variation in exon 1 coding region and promoter of MECP2 in Rett syndrome and controls 2004 ·European Journal of Human Genetics ·Julie Evans,Hayley Archer,Sharon D. Whatley,Alison Kerr,Angus Clarke,Rachel Butler	29
17	Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation 2004 ·The American Journal of Human Genetics ·Linda S. Weaving,John Christodoulou,Sarah Williamson,K. Friend,(unknown),Hayley Archer,Julie Evans,Angus Clarke,Gregory J. Pelka,Patrick Tam,Catherine M. Watson,Hooshang Lahooti,Carolyn Ellaway,Bruce Bennetts,Helen Leonard,Jozef Gécz	375

About Hayley Archer

Hayley Archer is a scholar working on Genetics, Cognitive Neuroscience and Developmental Neuroscience, having authored 17 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (7 papers) and Autism Spectrum Disorder Research (7 papers). The work is most often cited by research in Genetics (1.0k citations), Cognitive Neuroscience (407 citations) and Developmental Neuroscience (40 citations). Hayley Archer has collaborated with scholars based in United Kingdom, Australia and Denmark. Frequent co-authors include Angus Clarke, Julie Evans, John Christodoulou, Helen Leonard, Sarah Williamson, Jozef Gécz, Julian R. Sampson, Alison Kerr, Carolyn Ellaway and Catherine M. Watson. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics and European Journal of Human Genetics.

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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