Glen Brice

8.2k citations

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

Impact in

Ophthalmology top 0.5%
- Glaucoma and retinal disorders
- Retinal Diseases and Treatments
Oncology top 2%
- Lymphatic System and Diseases

Papers in

Oncology 25
- Lymphatic System and Diseases 25
Molecular Biology 18
- Retinal Development and Disorders 4

Co-authors: Anne H. Child (19 shared papers)Peter Mortimer (25 shared papers)Steve Jeffery (20 shared papers)Sahar Mansour (22 shared papers)Mansoor Sarfarazi (8 shared papers)Pia Østergaard (15 shared papers)Ronald P. Crick (4 shared papers)Roger A. Hitchings (5 shared papers)
Journals: Human Genetics (8 papers)Journal of Medical Genetics (5 papers)The American Journal of Human Genetics (4 papers)European Journal of Human Genetics (3 papers)Human Mutation (3 papers)
Partner nations: United Kingdom United States Canada

In The Last Decade

Glen Brice

51 papers receiving 4.3k citations

Glen Brice's Hit Papers

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Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin 2002 · 844 citations

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-authors

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

Showing the 20 most-cited of 52 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin 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 Hit paper breakdown →	2002	844
2	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) Nature Genetics ·Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour	2011	348
3	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, Ihuoma Alozie, Anne Child, 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
4	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, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, M Snyder, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard	2015	223
5	Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24 Journal of Medical Genetics ·Glen Brice, Sahar Mansour, R. Bryan Bell, J. R. O. Collin, Anne H. Child, A. F. Brady, M. Sarfarazi, K G Burnand, Steven Jeffery, Peter Mortimer, Victoria A. Murday	2002	194
6	Lipedema: An inherited condition American Journal of Medical Genetics Part A ·Anne H. Child, Kristiana Gordon, Pip Sharpe, Glen Brice, Pia Østergaard, Steve Jeffery, Peter Mortimer	2010	184
7	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, Diliana Stoilova, Glen Brice, Trushna Desai, Ovidiu C. Trifan, Darmalingum Poinoosawmy, Ronald P. Crick	1998	178
8	Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype Stroke ·Poneh Adib‐Samii, Glen Brice, Roswell Martin, Hugh S. Markus	2010	155
9	Mutations in FOXC2 Are Strongly Associated With Primary Valve Failure in Veins of the Lower Limb Circulation ·Russell H. Mellor, Glen Brice, A.W.B. Stanton, Jane O. French, Alberto Smith, Steve Jeffery, J. R. Levick, K G Burnand, Peter Mortimer	2007	139
10	Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema Circulation Research ·Kristiana Gordon, Dörte Schulte, Glen Brice, Michael A. Simpson, M. Guy Roukens, Andreas van Impel, Fiona Connell, Kamini Kalidas, Steve Jeffery, Peter Mortimer, Sahar Mansour, Stefan Schulte‐Merker, Pia Østergaard	2013	125
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	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
13	The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings Clinical Genetics ·FC Connell, Kristiana Gordon, Glen Brice, Vaughan Keeley, Steve Jeffery, P.S. Mortimer, Sahar Mansour, Pia Østergaard	2013	105
14	Clinical Features and Course of Patients with Glaucoma with the E50K Mutation in the Optineurin Gene Investigative Ophthalmology & Visual Science ·Tin Aung, Tayebeh Rezaie, Koji Okada, Ananth C. Viswanathan, Anne H. Child, Glen Brice, Shomi S. Bhattacharya, Ordan J. Lehmann, Mansoor Sarfarazi, Roger A. Hitchings	2005	100
15	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, C. Sandy, J R O Collin, Angela F. Brady, David F. Callen, K G Burnand, Peter Mortimer, Steve Jeffery	2001	96
16	Mapping of Primary Congenital Lymphedema to the 5q35.3 Region The American Journal of Human Genetics ·Alison Evans, Glen Brice, Vihra N. Sotirova, Peter Mortimer, Joseph Beninson, K G Burnand, Jane L. Rosbotham, Anne H. Child, Mansoor Sarfarazi	1999	90
17	Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype Journal of Medical Genetics ·Pia Østergaard, Michael A. Simpson, Glen Brice, Sahar Mansour, Fiona Connell, Alexandros Onoufriadis, A. H. Child, Jun‐Eul Hwang, Kamini Kalidas, Peter Mortimer, Richard C. Trembath, Steve Jeffery	2011	85
18	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, Filipe Pereira da Silva, Anatoli Kiotsekoglou, Anne H. Child	2007	76
19	Analysis of the coding regions of VEGFR3 and VEGFC in Milroy disease and other primary lymphoedemas Human Genetics ·Fiona Connell, Pia Østergaard, Charles Carver, Glen Brice, N. Williams, Sahar Mansour, Peter Mortimer, Steve Jeffery	2008	68
20	Linkage and sequence analysis indicate that CCBE1 is mutated in recessively inherited generalised lymphatic dysplasia Human Genetics ·Fiona Connell, Kamini Kalidas, Pia Østergaard, Glen Brice, Tessa Homfray, Lesley Roberts, David J. Bunyan, Sally G. Mitton, Sahar Mansour, Peter Mortimer, Steve Jeffery	2009	67

About Glen Brice

Glen Brice is a scholar working on Oncology, Molecular Biology, Surgery, Cell Biology and Ophthalmology, 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), Cell Biology (737 citations), Physiology (795 citations) and Neurology (211 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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