Julie Evans

3.7k citations

27 papers · 2.1k indexed · h-index 20

Co-authors: Timothy M. Frayling Hayley Archer Angus Clarke Andrew T. Hattersley Sian Ellard John Christodoulou Lisa I.S. Allen Helen Leonard
Topics: Genetics and Neurodevelopmental Disorders (7 papers)Calpain Protease Function and Regulation (4 papers)Genomic variations and chromosomal abnormalities (4 papers)
Cited by: Genetics Dermatology Cognitive Neuroscience
Journals: Journal of Clinical Investigation The Journal of Clinical Endocrinology & Metabolism Neurology
Partner nations: United Kingdom Australia United States

In The Last Decade

Julie Evans

26 papers receiving 2.1k citations

Peers

Countries citing papers authored by Julie Evans

Since Specialization

Citations

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

Fields of papers citing papers by Julie Evans

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julie Evans

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Conclusion of diagnostic odysseys due to inversions disrupting GLI3 and FBN1 2022 ·Journal of Medical Genetics ·Alistair T. Pagnamenta,Jing Yu,Julie Evans,Philip Twiss,(unknown),Amaka C Offiah,(unknown),Sarju Mehta,(unknown),Sarah Smithson,Jenny C. Taylor	9
2	Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features 2013 ·Epilepsia ·Johanna Uusimaa,Vasantha Gowda,(unknown),Conrad Smith,Julie Evans,(unknown),(unknown),A O'Rourke,Yusuf A. Rajabally,Tammy Hedderly,Frances M. Cowan,Carl Fratter,Joanna Poulton	34
3	Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations 2012 ·Journal of Neurology Neurosurgery & Psychiatry ·Robert D. S. Pitceathly,Susan E Tomlinson,Iain P. Hargreaves,(unknown),Janice L. Holton,Jasper M. Morrow,Julie Evans,Conrad Smith,Carl Fratter,Cathy E. Woodward,Mary G. Sweeney,Shamima Rahman,Michael G. Hanna	13
4	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
5	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
6	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
7	The Major Psoriasis Susceptibility Locus PSORS1 Is not a Risk Factor for Late-Onset Psoriasis 2005 ·Journal of Investigative Dermatology ·Michael H. Allen,(unknown),Colin Veal,Julie Evans,(unknown),Alexander Marsland,A. David Burden,C.E.M. Griffiths,Richard C. Trembath,Juliet N. Barker	77
8	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
9	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
10	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
11	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
12	Genetic Analysis of PSORS1 Distinguishes Guttate Psoriasis and Palmoplantar Pustulosis 2003 ·Journal of Investigative Dermatology ·Kati Asumalahti,Mahreen Ameen,Sari Suomela,Eva Hagforsen,G Michaëlsson,Julie Evans,(unknown),Colin Veal,Michael Allen,Joyce Leman,A. David Burden,Brian Kirby,Maureen Connolly,C.E.M. Griffiths,Richard C. Trembath,Juha Kere,Ulpu Saarialho‐Kere,Juliet N. Barker	156
13	Meta-Analysis and a Large Association Study Confirm a Role for Calpain-10 Variation in Type 2 Diabetes Susceptibility 2003 ·The American Journal of Human Genetics ·Michael N. Weedon,Peter E. H. Schwarz,Yukio Horikawa,Naoko Iwasaki,Thomas Illig,Rolf Holle,Wolfgang Rathmann,(unknown),Jan Schulze,(unknown),Julie Evans,Laura del Bosque‐Plata,G. A. Hitman,Mark Walker,J Lévy,Mike Sampson,Graeme I. Bell,Mark I. McCarthy,Andrew T. Hattersley,Timothy M. Frayling	136
14	Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome 2002 ·The Journal of Clinical Endocrinology & Metabolism ·Lema Haddad,Julie Evans,Neda Gharani,(unknown),(unknown),Steven Wiltshire,Timothy M. Frayling,Terence J. Wilkin,Andrew G. Demaine,Ann Millward,Andrew T. Hattersley,Gerry Conway,Nancy J. Cox,Graeme I. Bell,Steve Franks,Mark I. McCarthy	60
15	Family-Based Analysis Using a Dense Single-Nucleotide Polymorphism–Based Map Defines Genetic Variation at PSORS1, the Major Psoriasis-Susceptibility Locus 2002 ·The American Journal of Human Genetics ·Colin Veal,Francesca Capon,Michael H. Allen,Emma Heath,Julie Evans,(unknown),(unknown),David Burden,David M. Tillman,Juliet N. Barker,Richard C. Trembath	117
16	Variation in the Calpain-10 Gene Affects Blood Glucose Levels in the British Population 2002 ·Diabetes ·Stephen Lynn,Julie Evans,Chris White,Timothy M. Frayling,Andrew T. Hattersley,Douglass M. Turnbull,Yukio Horikawa,Nancy J. Cox,Graeme I. Bell,Mark Walker	67
17	beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors. 2001 ·Diabetes ·Timothy M. Frayling,Julie Evans,M. Bulman,Ewan R. Pearson,Lisa I.S. Allen,Katharine R. Owen,Coralie Bingham,Michael Hannemann,Maggie Shepherd,Sian Ellard,Andrew T. Hattersley	202
18	Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31 2000 ·Human Genetics ·Julie Evans,Timothy M. Frayling,Sian Ellard,Nick Gutowski	38
19	Confirmation of linkage of Duane's syndrome and refinement of the disease locus to an 8.8-cM interval on chromosome 2q31 2000 ·Human Genetics ·Julie Evans,Timothy M. Frayling,Sian Ellard,Nick Gutowski	10
20	Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes 1999 ·Journal of Clinical Investigation ·Wendy M. Macfarlane,Timothy M. Frayling,Sian Ellard,Julie Evans,Lisa I.S. Allen,Michael Bulman,Susan Ayres,Maggie Shepherd,Penny Clark,Ann Millward,Andrew Demaine,Terence J. Wilkin,Kevin Docherty,Andrew T. Hattersley	201

About Julie Evans

Julie Evans is a scholar working on Clinical Biochemistry, Genetics and Animal Science and Zoology, having authored 27 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Calpain Protease Function and Regulation (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (1.2k citations), Dermatology (171 citations) and Cognitive Neuroscience (293 citations). Julie Evans has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Timothy M. Frayling, Hayley Archer, Angus Clarke, Andrew T. Hattersley, Sian Ellard, John Christodoulou, Lisa I.S. Allen, Helen Leonard, Maggie Shepherd and Jozef Gécz. Their work appears in journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism 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.

Explore authors with similar magnitude of impact