Gail Norbury

1.4k citations

28 papers · 956 indexed · h-index 15

Molecular Biology
Surgery top 10%
Cellular and Molecular Neuroscience top 10%
Pediatrics, Perinatology and Child Health top 10%
Genetics

Co-authors: Steve E. Humphries Cathy Meaney David Craufurd Jayne Leggo Elisabeth Rosser David C. Rubinsztein Mathias Chiano Ian Tomlinson
Topics: Prenatal Screening and Diagnostics (7 papers)Lipoproteins and Cardiovascular Health (7 papers)Genetic factors in colorectal cancer (5 papers)
Cited by: Cellular and Molecular Neuroscience Cancer Research Pediatrics, Perinatology and Child Health
Journals: Proceedings of the National Academy of SciencesSHILAP Revista de lepidopterologíaNeurology
Partner nations: United Kingdom Denmark Italy

In The Last Decade

Gail Norbury

28 papers receiving 932 citations

Peers

Countries citing papers authored by Gail Norbury

Since Specialization

Citations

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

Fields of papers citing papers by Gail Norbury

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gail Norbury

This figure shows the co-authorship network connecting the top 25 collaborators of Gail Norbury. A scholar is included among the top collaborators of Gail Norbury 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 Gail Norbury. Gail Norbury 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	How many FH genetic tests were performed by the UK Genetic Laboratory Hubs in 2022? 2023 ·SHILAP Revista de lepidopterología ·Steve E. Humphries,Richard Challis,Kate Downes,(unknown),(unknown),(unknown),(unknown),(unknown),Daniel J. O’Sullivan,Alison Taylor‐Beadling,E. A. Thompson,(unknown),Gail Norbury	4
2	Cost Effectiveness of Using Array-CGH for Diagnosing Learning Disability 2015 ·Applied Health Economics and Health Policy ·Gurdeep S. Sagoo,Shehla Mohammed,(unknown),Gail Norbury,Joo Wook Ahn,Caroline Mackie Ogilvie,Mark Kroese	12
3	Non-invasive prenatal determination of fetal sex: translating research into clinical practice 2010 ·Clinical Genetics ·Melissa Hill,K. Finning,Peter Martin,(unknown),Cathy Meaney,Gail Norbury,Geoff Daniels,Lyn S. Chitty	124
4	Multiplex ligation‐dependent probe amplification analysis to screen for deletions and duplications of the LDLR gene in patients with familial hypercholesterolaemia 2009 ·Clinical Genetics ·Alison Taylor,(unknown),(unknown),Kavisha Patel,Steve E. Humphries,Gail Norbury	27
5	Noninvasive prenatal diagnosis of early onset primary dystonia I in maternal plasma 2009 ·Prenatal Diagnosis ·Cathy Meaney,Gail Norbury	21
6	Mutation detection rate and spectrum in familial hypercholesterolaemia patients in the UK pilot cascade project 2009 ·Clinical Genetics ·Alison Taylor,(unknown),Kavisha Patel,Ros Whittall,G M Wood,Matthew J. Farrer,(unknown),(unknown),D.R. Nair,Mahmoud Barbir,(unknown),Sarah J. Egan,(unknown),Yvette Lolin,(unknown),(unknown),S. G. Hadfield,Gail Norbury,Steve E. Humphries	148
7	What is the clinical utility of DNA testing in patients with familial hypercholesterolaemia? 2008 ·Current Opinion in Lipidology ·Steve E. Humphries,Gail Norbury,S. E. A. Leigh,S. G. Hadfield,(unknown)	53
8	Apert Syndrome: The Current Role of Prenatal Ultrasound and Genetic Analysis in Diagnosis and Counselling 2008 ·Fetal Diagnosis and Therapy ·A. Athanasiadis,Μenelaos Zafrakas,(unknown),(unknown),(unknown),Gail Norbury,J. Bontis	18
9	Non-invasive prenatal diagnosis of single gene disorders: How close are we? 2008 ·Seminars in Fetal and Neonatal Medicine ·Gail Norbury,Chris J. Norbury	28
10	Prospective Register of Outcomes of Free-fetal DNA testing (PROOF) - results of the first year's audit 2007 ·UCL Discovery (University College London) ·Lyn S. Chitty,Geoff Daniels,K. Finning,(unknown),(unknown),Peter Martin,Christopher Meaney,Gail Norbury,(unknown)	11
11	A functional mutation in the LDLR promoter (−139C>G) in a patient with familial hypercholesterolemia 2007 ·European Journal of Human Genetics ·Andrew J. Smith,(unknown),Devi R Nair,(unknown),(unknown),Alison Taylor,Gail Norbury,Steve E. Humphries	23
12	Multiplex ARMS analysis to detect 13 common mutations in familial hypercholesterolaemia 2007 ·Clinical Genetics ·Alison Taylor,(unknown),(unknown),Mert Sozen,(unknown),Ros Whittall,Steve E. Humphries,Gail Norbury	25
13	DNA analysis: what and when to request? 2006 ·Archives of Disease in Childhood ·Gail Norbury	5
14	Carrier Frequency of a Nonsense Mutation in the Adenosine Deaminase (ADA) Gene Implies a High Incidence of ADA‐deficient Severe Combined Immunodeficiency (SCID) in Somalia and a Single, Common Haplotype Indicates Common Ancestry 2006 ·Annals of Human Genetics ·Juan José Martínez Sánchez,Gemma Monaghan,Claus Børsting,Gail Norbury,Niels Morling,H. Bobby Gaspar	34
15	Novel phenotype of craniosynostosis and ocular anterior chamber dysgenesis with a fibroblast growth factor receptor 2 mutation 2005 ·American Journal of Medical Genetics Part A ·Emma McCann,Stephen B. Kaye,William G. Newman,Gail Norbury,Graeme C. Black,(unknown)	10
16	Homozygous hypercholesterolaemia and ezetimibe: a case report 2004 ·Acta Paediatrica ·Christian J. Hendriksz,Gail Norbury,(unknown),Alison Taylor,Steve E. Humphries	2
17	The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation 2003 ·Clinical Dysmorphology ·Massimiliano Rossi,Rachel L. Jones,Gail Norbury,Agnès Bloch‐Zupan,Robin M. Winter	30
18	Contribution of cyclin d1 (CCND1) and E-cadherin (CDH1) polymorphisms to familial and sporadic colorectal cancer 2002 ·Oncogene ·(unknown),Frances M. Richards,Richard S. Houlston,D. Gareth Evans,Janusz Jankowski,Fiona MacDonald,Gail Norbury,Stewart J. Payne,(unknown),Ian Tomlinson,Eamonn R. Maher	87
19	Genetic Pathways of Colorectal Carcinogenesis Rarely Involve thePTEN and LKB1 Genes Outside the Inherited Hamartoma Syndromes 1998 ·American Journal Of Pathology ·(unknown),(unknown),Michael Churchman,Gail Norbury,Ian Tomlinson	64
20	Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease 1997 ·Proceedings of the National Academy of Sciences ·David C. Rubinsztein,Jayne Leggo,Mathias Chiano,(unknown),Gail Norbury,Elisabeth Rosser,David Craufurd	181

About Gail Norbury

Gail Norbury is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Pathology and Forensic Medicine, having authored 28 papers that have together received 956 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (7 papers), Lipoproteins and Cardiovascular Health (7 papers) and Genetic factors in colorectal cancer (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (189 citations), Cancer Research (154 citations) and Pediatrics, Perinatology and Child Health (183 citations). Gail Norbury has collaborated with scholars based in United Kingdom, Denmark and Italy. Frequent co-authors include Steve E. Humphries, Cathy Meaney, David Craufurd, Jayne Leggo, Elisabeth Rosser, David C. Rubinsztein, Mathias Chiano, Ian Tomlinson, Alison Taylor and S. G. Hadfield. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and Neurology.

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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