Glen Brice

8.2k citations

52 papers · 4.5k indexed · 1 hit paper · h-index 34

Ophthalmology top 0.5%
- Glaucoma and retinal disorders 9
- Retinal Diseases and Treatments 5
Oncology top 2%
- Lymphatic System and Diseases 25
Cell Biology top 2%
- Skin and Cellular Biology Research 11
Physiology top 2%
- Sympathectomy and Hyperhidrosis Treatments 5
Neurology top 5%
Surgery
- Vascular Malformations and Hemangiomas 10
Genetics
- Connective tissue disorders research 5
Molecular Biology
- Retinal Development and Disorders 4

Co-authors: Anne H. Child Peter Mortimer Steve Jeffery Sahar Mansour Mansoor Sarfarazi Pia Østergaard Ronald P. Crick Roger A. Hitchings
Cited by: Ophthalmology Oncology Cell Biology
Journals: Human Genetics (8 papers)Journal of Medical Genetics (5 papers)The American Journal of Human Genetics (4 papers)
Partner nations: United Kingdom United States Canada

In The Last Decade

Glen Brice

51 papers receiving 4.3k citations

Hit Papers

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Peers

Countries citing papers authored by Glen Brice

Since Specialization

Citations

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

Fields of papers citing papers by Glen Brice

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome European Journal of Human Genetics ·Sarah Joyce,Kristiana Gordon,Glen Brice,Pia Østergaard,Pierre Beltante,John Short,Sandra Moore,Peter Mortimer,Sahar Mansour	2015	54
2	Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis Nature Communications ·Elisavet Fotiou,Silvia Martin‐Almedina,Michael A. Simpson,Shin Lin,Kristiana Gordon,Glen Brice,Giles Atton,H. Lüdin,David C. Rees,Cyril Mignot,Julie Vogt,Tessa Homfray,M Snyder,Stanley G. Rockson,Steve Jeffery,Peter Mortimer,Sahar Mansour,Pia Østergaard	2015	223
3	A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family Clinical Genetics ·Glen Brice,Pia Østergaard,Steve Jeffery,Kristiana Gordon,P.S. Mortimer,Sahar Mansour	2013	58
4	Functional characterization of the regulatory mechanisms controlling HLA-C expression in psoriasis British Journal of Dermatology ·Andrew Pink,Michael A. Simpson,Glen Brice,Catherine Smith,Nemesha Desai,Peter Mortimer,Juliet N. Barker,Richard C. Trembath	2011	1
5	Primary lymphedema with coarctation of the aorta: Possible new syndrome or variant of Irons–Bianchi syndrome? American Journal of Medical Genetics Part A ·J. Scott Ferguson,S Schmidt,Glen Brice,Rob Hastings,Ruth Newbury‐Ecob,Peter Mortimer,Sahar Mansour	2011	1
6	Lipedema: An inherited condition American Journal of Medical Genetics Part A ·Anne H. Child,Kristiana Gordon,Ane Cecilie Duus,Glen Brice,Pia Østergaard,Steve Jeffery,Peter Mortimer	2010	184
7	Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas Human Genetics ·Fiona Connell,Pia Østergaard,Zofia Pawlaczyk,Glen Brice,Scripps In,Sahar Mansour,P.S. Mortimer,Steve Jeffery	2009	1
8	Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb Journal of Vascular Surgery ·Russell H. Mellor,Glen Brice,T. Carlyle	2007	6
9	The importance of mutation detection in Marfan syndrome and Marfan-related disorders: report of 193FBN1 mutations Human Mutation ·Paolo Comeglio,Philip H. Johnson,Gavin Arno,Glen Brice,Alison Evans,José Antonio Aragon-Martin,Jennifer Popies,Anatoli Kiotsekoglou,Anne H. Child	2007	76
10	Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations Human Genetics ·М В Штерншис,Rachel E. Bell,Glen Brice,Sahar Mansour,Mansoor Sarfarazi,Anne H. Child,Alberto Smith,Russell H. Mellor,K G Burnand,Peter Mortimer,Steve Jeffery	2005	35
11	Milroy disease and the VEGFR-3 mutation phenotype Journal of Medical Genetics ·Glen Brice,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	2005	115
12	Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurinbreakdown → Science ·Tayebeh Rezaie,Anne H. Child,Roger A. Hitchings,Glen Brice,Lauri Miller,Miguel Coca‐Prados,Elise Héon,Theodore Krupin,Robert Ritch,Donald L. Kreutzer,Ronald P. Crick,Mansoor Sarfarazi	2002	844
13	Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma Human Genetics ·Tin Aung,Louise Ocaka,Neil D. Ebenezer,Alex Morris,Glen Brice,Anne H. Child,Roger A. Hitchings,Ordan J. Lehmann,Shomi S. Bhattacharya	2002	47
14	Detection of six novel FBN1 mutations in British patients affected by Marfan syndrome Human Mutation ·Paolo Comeglio,Alison Evans,Glen Brice,Anne H. Child	2001	12
15	A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene Human Genetics ·Tin Aung,Louise Ocaka,Neil D. Ebenezer,Alex Morris,Michael Krawczak,Dawn L. Thiselton,Christiane Alexander,Marcela Votruba,Glen Brice,Anne H. Child,Peter J. Francis,Roger A. Hitchings,Ordan J. Lehmann,Shomi S. Bhattacharya	2001	106
16	Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene Human Genetics ·Rachel E. Bell,Glen Brice,Anne H. Child,V Murday,Sahar Mansour,Xiao Zhi-gao,J R O Collin,Angela F. Brady,David F. Callen,K G Burnand,Peter Mortimer,Steve Jeffery	2001	96
17	Distichiasis-lymphoedema: clinical features, venous function and lymphoscintigraphy British Journal of Dermatology ·Jane L. Rosbotham,Glen Brice,Anne H. Child,T. O. NUNAN,P.S. Mortimer,K G Burnand	2000	22
18	A Gene for Lymphedema-Distichiasis Maps to 16q24.3 The American Journal of Human Genetics ·Jonathan Mangion,Nazneen Rahman,Sahar Mansour,Glen Brice,Jane L. Rosbotham,Anne H. Child,Victoria A. Murday,Peter Mortimer,Rita Barfoot,A Sigurdsson,Sarah Edkins,M. Sarfarazi,K G Burnand,Alison Evans,T. O. NUNAN,Michael R. Stratton,Steve Jeffery	1999	64
19	Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1 The American Journal of Human Genetics ·Ivaylo Stoilov,Nurten Akarsu,Thais R. Arroio,Giovanni Perin,Magda Barsoum‐Homsy,M. Erol Turaçlı,Meral Or,Richard A. Lewis,Nusret Özdemir,Glen Brice,Sedat Aktan,Line Chevrette,Miguel Coca‐Prados,Mansoor Sarfarazi	1998	288
20	Localization of the Fourth Locus (GLC1E) For Adult-Onset Primary Open-Angle Glaucoma to the 10p15-p14 Region The American Journal of Human Genetics ·Mansoor Sarfarazi,Anne H. Child,J. M. Synge,Glen Brice,Trushna Desai,Ovidiu C. Trifan,N. Lenz,Ronald P. Crick	1998	178

About Glen Brice

Glen Brice is a scholar working on Ophthalmology, Oncology and Cell Biology, having authored 52 papers that have together received 4.5k indexed citations. Recurring topics across this work include Lymphatic System and Diseases (25 papers), Skin and Cellular Biology Research (11 papers), Vascular Malformations and Hemangiomas (10 papers), Glaucoma and retinal disorders (9 papers), Retinal Diseases and Treatments (5 papers), Connective tissue disorders research (5 papers), Sympathectomy and Hyperhidrosis Treatments (5 papers) and Retinal Development and Disorders (4 papers). The work is most often cited by research in Ophthalmology (1.3k citations), Oncology (1.5k citations) and Cell Biology (737 citations). Glen Brice has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Anne H. Child, Peter Mortimer, Steve Jeffery, Sahar Mansour, Mansoor Sarfarazi, Pia Østergaard, Ronald P. Crick, Roger A. Hitchings, Miguel Coca‐Prados and Kristiana Gordon. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics and Human Mutation.

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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