C.E. Browne

1.8k citations

15 papers · 1.1k indexed · h-index 11

Genetics top 2%
- Genomic variations and chromosomal abnormalities 11
- Genetic Syndromes and Imprinting 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
Pediatrics, Perinatology and Child Health top 5%
- Prenatal Screening and Diagnostics 6
Cognitive Neuroscience top 5%
Molecular Biology
- Chromatin Remodeling and Cancer 2
- Genomics and Chromatin Dynamics 2
Plant Science top 10%
- Chromosomal and Genetic Variations 5

Co-authors: P. A. Jacobs N. Simon Thomas Caroline Joyce Helen White N. Gregson N R Dennis Peter Strike P.A. Jacobs
Cited by: Genetics Pediatrics, Perinatology and Child Health Cognitive Neuroscience
Journals: Human Genetics (6 papers)Cytogenetic and Genome Research (2 papers)The American Journal of Human Genetics (1 paper)
Partner nations: United Kingdom Australia Greece

In The Last Decade

C.E. Browne

15 papers receiving 1.0k citations

Peers

Countries citing papers authored by C.E. Browne

Since Specialization

Citations

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

Fields of papers citing papers by C.E. Browne

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by C.E. Browne. 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 C.E. Browne. The network helps show where C.E. Browne may publish in the future.

Co-authorship network

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

All Works

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15 of 15 papers shown

#	Work
1	Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings Clinical Dysmorphology ·Helen Cox,Anneke Lucassen,Marlène Rio,C.E. Browne,Glenn L. Renforth,Lyndsey Craven,Malik Hasan Abdullah Ghali,David I. Wilson	2009	3
2	A complex medical phenotype in a patient with triplication of 2q12.3 to 2q13 characterized with oligonucleotide array CGH Cytogenetic and Genome Research ·Catherine L. Mercer,C.E. Browne,John Barber,V.K. Maloney,Shuwen Huang,N. Simon Thomas,Robert John Thornton	2009	8
3	X chromosome loss and ageing Cytogenetic and Genome Research ·Hadas Volkov,Peter Strike,C.E. Browne,P.A. Jacobs	2007	144
4	Chromosome 15q11-13 abnormalities and other medical conditions in individuals with autism spectrum disorders Psychiatric Genetics ·Patrick Bolton,Marijcke W. M. Veltman,Emma Weisblatt,Bertha María Estévez-Garrido,N. Simon Thomas,Sheila Youings,Russell Thompson,Siân E. Roberts,Nicholas R. Dennis,C.E. Browne,David Chiavacci,Vanessa Moore,Е.Б. Роева	2004	50
5	Characterisation of interstitial duplications and triplications of chromosome 15q11–q13 Human Genetics ·Siân E. Roberts,Nicholas R. Dennis,C.E. Browne,Lionel Willatt,Geoffrey Woods,I Cross,Patricia A. Jacobs,Simon Thomas	2002	71
6	Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH Human Genetics ·Samar M Emara,N R Dennis,G. W. Cowin,C.E. Browne	2001	90
7	The phenotypic manifestations of interstitial duplications of proximal 15q with special reference to the autistic spectrum disorders American Journal of Medical Genetics ·Patrick Bolton,N R Dennis,C.E. Browne,N. Simon Thomas,Marijcke W. M. Veltman,Russell Thompson,P. A. Jacobs	2001	155
8	Xp deletions associated with autism in three females Human Genetics ·N. Simon Thomas,Andrew J. Sharp,C.E. Browne,David Skuse,沈贻伟,Nicholas R. Dennis	1999	126
9	Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region Human Genetics ·N. Simon Thomas,C.E. Browne,Christine Oley,miaomiao Xi,John A. Crolla	1999	18
10	Investigation of a cryptic interstitial duplication involving the Prader-Willi/Angelman syndrome critical region Human Genetics ·N. Simon Thomas,C.E. Browne,Christine Oley,miaomiao Xi,John A. Crolla	1999	5
11	Anterior chamber eye anomalies, redundant skin and syndactyly-a new syndrome associated with breakpoints at 2q37.2 and 7q36.3 Clinical Dysmorphology ·I. Karen Temple,C.E. Browne,P R Hodgkins	1999	8
12	Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q Human Genetics ·John Barber,I E Cross,Mohammed C. Ashraf,James C. Nicholson,Kedibone Ramadie,C.E. Browne	1998	25
13	Inherited Interstitial Duplications of Proximal 15q: Genotype-Phenotype Correlations The American Journal of Human Genetics ·C.E. Browne,N R Dennis,E.R. Maher,Barbara B Mettelmaa,James C. Nicholson,James Sillibourne,John Barber	1997	143
14	Small terminal deletions of the long arm of chromosome 2: Two new cases American Journal of Medical Genetics ·Andrew Fisher,Dr. Madhu,C.E. Browne,John Barber,Margaret Barker,Colin Kennedy,B. Dinakar,Michael A. Patton	1994	23
15	Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding. Journal of Medical Genetics ·P. A. Jacobs,C.E. Browne,N. Gregson,Caroline Joyce,Helen White	1992	246

About C.E. Browne

C.E. Browne is a scholar working on Genetics, Developmental Biology, Pediatrics, Perinatology and Child Health, Plant Science and Molecular Biology, having authored 15 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (6 papers), Genetic Syndromes and Imprinting (5 papers), Chromosomal and Genetic Variations (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Chromatin Remodeling and Cancer (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Genetics (938 citations), Pediatrics, Perinatology and Child Health (324 citations), Cognitive Neuroscience (273 citations), Molecular Biology (415 citations) and Plant Science (186 citations). C.E. Browne has collaborated with scholars based in United Kingdom, Australia and Greece. Frequent co-authors include P. A. Jacobs, N. Simon Thomas, Caroline Joyce, Helen White, N. Gregson, N R Dennis, Peter Strike, P.A. Jacobs, Nicholas R. Dennis and John Barber. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, The American Journal of Human Genetics, Journal of Medical Genetics and Psychiatric 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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