Angela Barnicoat

5.1k citations

43 papers · 1.6k indexed · h-index 19

Genetics top 1%
Molecular Biology top 10%
Cognitive Neuroscience top 5%
Pediatrics, Perinatology and Child Health top 10%
Cellular and Molecular Neuroscience top 10%

Co-authors: Marcus Pembrey Martin Bobrow Mark C. Hirst Kay E. Davies Samantha J.L. Knight Louise J. Campbell A Flannery B. A. Oostra
Topics: Genomic variations and chromosomal abnormalities (15 papers)Genetics and Neurodevelopmental Disorders (12 papers)Autism Spectrum Disorder Research (7 papers)
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Nature Cell The Lancet
Partner nations: United Kingdom United States France

In The Last Decade

Angela Barnicoat

43 papers receiving 1.6k citations

Peers

Countries citing papers authored by Angela Barnicoat

Since Specialization

Citations

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

Fields of papers citing papers by Angela Barnicoat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angela Barnicoat

This figure shows the co-authorship network connecting the top 25 collaborators of Angela Barnicoat. A scholar is included among the top collaborators of Angela Barnicoat 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 Angela Barnicoat. Angela Barnicoat 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	Genetic and chemotherapeutic influences on germline hypermutation 2022 ·Nature ·Joanna Kaplanis,(unknown),Rashesh Sanghvi,Matthew D. C. Neville,Petr Danecek,Tim Coorens,Elena Prigmore,Patrick Short,Giuseppe Gallone,Jeremy F. McRae,Loukas Moutsianas,Chris A. Odhams,Jenny Carmichael,Angela Barnicoat,Helen V. Firth,Patrick O’Brien,Raheleh Rahbari,Matthew E. Hurles	49
2	AIFM1‐associated X‐linked spondylometaphyseal dysplasia with cerebral hypomyelination 2021 ·American Journal of Medical Genetics Part A ·(unknown),Angela Barnicoat,Amaka C Offiah,Alistair Calder,Kshitij Mankad,N. Simon Thomas,David J. Bunyan,Maggie Williams,(unknown),(unknown),Kayal Vijayakumar,Tom Hilliard,James Turner,Christine Burren,Fergal Monsell,Sarah Smithson	4
3	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome 2020 ·SHILAP Revista de lepidopterología ·Emma Wakeling,Meriel McEntagart,(unknown),Charles Shaw‐Smith,Karen Stals,Matthew N. Wakeling,Angela Barnicoat,Clare Beesley,Andrea Hanson‐Kahn,Mary K. Kukolich,David A. Stevenson,Philippe M. Campeau,Sian Ellard,Sarah H. Elsea,Xiang-Jiao Yang,Richard Caswell	11
4	EML1‐associated brain overgrowth syndrome with ribbon‐like heterotopia 2019 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Renske Oegema,George McGillivray,Richard J. Leventer,Anne‐Gaëlle Le Moing,Nadia Bahi‐Buisson,Angela Barnicoat,Simone Mandelstam,David Francis,Fiona Francis,Grazia M.S. Mancini,Sanne M. C. Savelberg,Gijs van Haaften,Kshitij Mankad,Maarten H. Lequin	17
5	Fragile X-associated conditions: implications for the whole family 2019 ·British Journal of General Practice ·Andrew G. McKechanie,Angela Barnicoat,Iris Trender‐Gerhard,(unknown),Andrew C. Stanfield	6
6	De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis 2017 ·SHILAP Revista de lepidopterología ·Angela Mauro,Ebun Omoyinmi,Neil J. Sebire,Angela Barnicoat,Paul Brogan	11
7	Sotos syndrome, infantile hypercalcemia, and nephrocalcinosis: a contiguous gene syndrome 2011 ·Pediatric Nephrology ·Janna Kenny,Melissa Lees,Susan Drury,Angela Barnicoat,William van’t Hoff,Rodger Palmer,Deborah Morrogh,Jonathan J. Waters,Nicholas Lench,Detlef Böckenhauer	24
8	Holistic management of DSD 2010 ·Best Practice & Research Clinical Endocrinology & Metabolism ·Caroline Brain,Sarah Creighton,Imran Mushtaq,Polly Carmichael,Angela Barnicoat,John W. Honour,Victor Larcher,John C. Achermann	73
9	Nasopharyngeal teratoma and diaphragmatic hernia: no longer a random association but a new syndrome? 2009 ·Clinical Dysmorphology ·Clare Turnbull,Deborah Ruddy,Angela Barnicoat	2
10	Transmitted duplication of 8p23.1–8p23.2 associated with speech delay, autism and learning difficulties 2008 ·European Journal of Human Genetics ·(unknown),Angela Barnicoat,(unknown),(unknown),(unknown),Shuwen Huang,Viv Maloney,N. Simon Thomas,David J. Bunyan,(unknown),John Barber	61
11	Duplications of proximal 16q flanked by heterochromatin are not euchromatic variants and show no evidence of heterochromatic position effect 2006 ·Cytogenetic and Genome Research ·John Barber,Shuai Zhang,(unknown),Amanda Collins,V.K. Maloney,Richard P. Hastings,Bernadette Farren,Angela Barnicoat,A. Polityko,(unknown),Heike Starke,Shu Ye	18
12	Midline cleft lip and nasal dermoids over five generations: a distinct entity or autosomal dominant Pai syndrome? 2006 ·Clinical Dysmorphology ·Melissa Lees,(unknown),Loshan Kangesu,Brian C. Sommerlad,Angela Barnicoat	13
13	Joint and skin laxity with Dandy-Walker malformation and contractures: a distinct recessive syndrome? 2001 ·Clinical Dysmorphology ·Shane McKee,Angela Barnicoat,Alan Fryer,Frances Flinter,(unknown),C McKeown	4
14	Disruption of the Bipartite Imprinting Center in a Family with Angelman Syndrome 2001 ·The American Journal of Human Genetics ·Karin Buiting,Angela Barnicoat,Christina Lich,Marcus Pembrey,Sue Malcolm,Bernhard Horsthemke	50
15	Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13) 2001 ·American Journal of Medical Genetics ·Bert B.A. de Vries,Melissa Lees,Samantha J.L. Knight,Regina Regan,(unknown),Jonathan Flint,Angela Barnicoat,Robin M. Winter	18
16	Diagnosis of fragile‐X syndrome: the experiences of parents 1999 ·Journal of Intellectual Disability Research ·Barbara A. Carmichael,Marcus Pembrey,G Turner,Angela Barnicoat	38
17	Clinical and genetic heterogeneity in Meckel syndrome 1997 ·Human Genetics ·Paulina Paavola,Riitta Salonen,Alessandra Baumer,Albert Schinzel,Patricia A. Boyd,S. Gould,(unknown),Romano Tenconi,Angela Barnicoat,Robin Winter,Laura‐Maria Peltonen	37
18	Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: clinical assessment 1996 ·Clinical Genetics ·Angela Barnicoat,(unknown),E. Boyd,Zoe Docherty,(unknown),J. L. Huret,Marissa King,Edna L. Maltby,(unknown),(unknown),(unknown),M Super,John Tolmie	11
19	The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXE 1993 ·Human Molecular Genetics ·Mark C. Hirst,Angela Barnicoat,Geraldine Flynn,(unknown),M. G. Daker,Veronica J. Buckle,Kay E. Davies,Martin Bobrow	55
20	Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation 1993 ·Cell ·Samantha J.L. Knight,A Flannery,Mark C. Hirst,Louise J. Campbell,Zóe Christodoulou,(unknown),J. J. Pointon,Helen Middleton‐Price,Angela Barnicoat,Marcus Pembrey,Jill Holland,B. A. Oostra,Martin Bobrow,Kay E. Davies	436

About Angela Barnicoat

Angela Barnicoat is a scholar working on Genetics, Developmental Biology and Cognitive Neuroscience, having authored 43 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Autism Spectrum Disorder Research (7 papers). The work is most often cited by research in Genetics (1.2k citations), Cognitive Neuroscience (469 citations) and Molecular Biology (947 citations). Angela Barnicoat has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Marcus Pembrey, Martin Bobrow, Mark C. Hirst, Kay E. Davies, Samantha J.L. Knight, Louise J. Campbell, A Flannery, B. A. Oostra, Helen Middleton‐Price and J. J. Pointon. Their work appears in journals such as Nature, Cell and The Lancet.

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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