Glen Brice

8.2k total citations · 1 hit paper
52 papers, 4.5k citations indexed

About

Glen Brice is a scholar working on Oncology, Molecular Biology and Surgery. According to data from OpenAlex, Glen Brice has authored 52 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Oncology, 18 papers in Molecular Biology and 16 papers in Surgery. Recurrent topics in Glen Brice's work include Lymphatic System and Diseases (25 papers), Skin and Cellular Biology Research (11 papers) and Vascular Malformations and Hemangiomas (10 papers). Glen Brice is often cited by papers focused on Lymphatic System and Diseases (25 papers), Skin and Cellular Biology Research (11 papers) and Vascular Malformations and Hemangiomas (10 papers). Glen Brice collaborates with scholars based in United Kingdom, United States and Canada. Glen Brice's 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 and has published in prestigious journals such as Science, Circulation and Nature Communications.

In The Last Decade

Glen Brice

51 papers receiving 4.3k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin

2002 844 citations Tayebeh Rezaie, Anne H. Child et al. Science profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Glen Brice United Kingdom	34	1.7k	1.5k	1.3k	819	795	52	4.5k
Dorit Shweiki Israel	7	3.7k 2.2×	764 0.5×	695 0.6×	597 0.7×	396 0.5×	13	5.9k
I G Rennie United Kingdom	29	831 0.5×	680 0.4×	1.8k 1.4×	152 0.2×	250 0.3×	136	2.8k
Injune Kim South Korea	40	4.4k 2.7×	1.0k 0.7×	173 0.1×	963 1.2×	406 0.5×	63	7.1k
Magali Saint‐Geniez United States	31	2.6k 1.6×	328 0.2×	1.9k 1.5×	355 0.4×	259 0.3×	67	5.0k
Per Levéen Sweden	19	2.7k 1.7×	608 0.4×	178 0.1×	645 0.8×	184 0.2×	26	4.5k
Itzhak Hemo Israel	19	2.4k 1.5×	357 0.2×	1.6k 1.3×	247 0.3×	133 0.2×	39	4.1k
Katri Pajusola Finland	23	4.0k 2.4×	3.3k 2.1×	106 0.1×	907 1.1×	729 0.9×	30	5.5k
Anne E. Hughes United Kingdom	26	1.0k 0.6×	574 0.4×	573 0.5×	198 0.2×	149 0.2×	59	3.0k
Mathias François Australia	37	1.7k 1.0×	1.3k 0.8×	99 0.1×	502 0.6×	343 0.4×	73	3.1k
Stephen X. Skapek United States	35	3.0k 1.8×	1.8k 1.2×	147 0.1×	462 0.6×	215 0.3×	97	5.5k

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 of co-authors of Glen Brice

This figure shows the co-authorship network connecting the top 25 collaborators of Glen Brice. A scholar is included among the top collaborators of Glen Brice 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 Glen Brice. Glen Brice 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

Joyce, Sarah, Kristiana Gordon, Glen Brice, et al.. (2015). The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome. European Journal of Human Genetics. 24(5). 690–696. 54 indexed citations

Brice, Glen, Pia Østergaard, Steve Jeffery, et al.. (2013). A novel mutation in GJA1 causing oculodentodigital syndrome and primary lymphoedema in a three generation family. Clinical Genetics. 84(4). 378–381. 58 indexed citations

Pink, Andrew, Michael A. Simpson, Glen Brice, et al.. (2011). Functional characterization of the regulatory mechanisms controlling HLA-C expression in psoriasis. British Journal of Dermatology. 164(4). 917–917. 1 indexed citations

Østergaard, Pia, Michael A. Simpson, Fiona Connell, et al.. (2011). Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). Nature Genetics. 43(10). 929–931. 348 indexed citations

Østergaard, Pia, Michael A. Simpson, Glen Brice, et al.. (2011). 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. 48(4). 251–255. 85 indexed citations

Bano, Gul, Sahar Mansour, Glen Brice, et al.. (2009). Pit-1 Mutation and Lipoedema in a Family. Experimental and Clinical Endocrinology & Diabetes. 118(6). 377–380. 26 indexed citations

Mellor, Russell H., et al.. (2007). Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb. Journal of Vascular Surgery. 46(3). 608–608. 6 indexed citations

Mellor, Russell H., Glen Brice, A.W.B. Stanton, et al.. (2007). Mutations in FOXC2 Are Strongly Associated With Primary Valve Failure in Veins of the Lower Limb. Circulation. 115(14). 1912–1920. 139 indexed citations

Ocaka, Louise, Neil D. Ebenezer, Glen Brice, et al.. (2007). Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel. Journal of Medical Genetics. 45(2). 87–92. 58 indexed citations

10.

Bloch‐Zupan, Agnès, S. L. Free, Pamela J. Thompson, et al.. (2006). A novel homeobox mutation in thePITX2gene in a family with Axenfeld‐Rieger syndrome associated with brain, ocular, and dental phenotypes. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(2). 184–191. 40 indexed citations

11.

Bell, Rachel E., Glen Brice, Sahar Mansour, et al.. (2005). Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations. Human Genetics. 117(2-3). 238–242. 35 indexed citations

12.

Brice, Glen, et al.. (2003). Case 2. Clinical and Experimental Dermatology. 28(4). 463–464. 1 indexed citations

13.

Rezaie, Tayebeh, Anne H. Child, Roger A. Hitchings, et al.. (2002). Adult-Onset Primary Open-Angle Glaucoma Caused by Mutations in Optineurin. Science. 295(5557). 1077–1079. 844 indexed citations breakdown →

14.

Child, Anne H., et al.. (2002). Identification of an OPA1 truncating mutation in a family with Optic Atrophy. Investigative Ophthalmology & Visual Science. 43(13). 2393–2393. 1 indexed citations

15.

Aung, Tin, Louise Ocaka, Neil D. Ebenezer, et al.. (2002). Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma. Human Genetics. 110(5). 513–514. 47 indexed citations

16.

Brice, Glen, Sahar Mansour, R. Bryan Bell, et al.. (2002). Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Journal of Medical Genetics. 39(7). 478–483. 194 indexed citations

17.

Aung, Tin, Louise Ocaka, Neil D. Ebenezer, et al.. (2001). A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene. Human Genetics. 110(1). 52–56. 106 indexed citations

18.

Mangion, Jonathan, Nazneen Rahman, Sahar Mansour, et al.. (1999). A Gene for Lymphedema-Distichiasis Maps to 16q24.3. The American Journal of Human Genetics. 65(2). 427–432. 64 indexed citations

19.

Stoilov, Ivaylo, Nurten Akarsu, Magda Barsoum‐Homsy, et al.. (1998). 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. 62(3). 573–584. 288 indexed citations

20.

Child, Anne H., et al.. (1997). Identification of a new ‘TIGR’ mutation in a family with juvenile-onset primary open angle glaucoma. Ophthalmic Genetics. 18(3). 109–118. 53 indexed citations

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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