Murray H. Brilliant

6.4k total citations
79 papers, 3.6k citations indexed

About

Murray H. Brilliant is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Murray H. Brilliant has authored 79 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 37 papers in Genetics and 25 papers in Cell Biology. Recurrent topics in Murray H. Brilliant's work include melanin and skin pigmentation (24 papers), Biochemical Analysis and Sensing Techniques (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Murray H. Brilliant is often cited by papers focused on melanin and skin pigmentation (24 papers), Biochemical Analysis and Sensing Techniques (17 papers) and Genetics and Neurodevelopmental Disorders (14 papers). Murray H. Brilliant collaborates with scholars based in United States, Japan and United Kingdom. Murray H. Brilliant's co-authors include John M. Gardner, Richard A. King, Nobuko Hagiwara, Yoshimichi Nakatsu, Yoichi Gondo, Donna Durham‐Pierre, Eva M. Eicher, Mary F. Lyon, Orit Cohen‐Barak and Seth J. Orlow and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Murray H. Brilliant

79 papers receiving 3.5k citations

Peers

Countries citing papers authored by Murray H. Brilliant

Since Specialization

Citations

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

Fields of papers citing papers by Murray H. Brilliant

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Murray H. Brilliant. 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 Murray H. Brilliant. The network helps show where Murray H. Brilliant may publish in the future.

Co-authorship network of co-authors of Murray H. Brilliant

This figure shows the co-authorship network connecting the top 25 collaborators of Murray H. Brilliant. A scholar is included among the top collaborators of Murray H. Brilliant 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 Murray H. Brilliant. Murray H. Brilliant 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

#	Work	Indexed citations
1	Quantitative Foveal Structural Metrics as Predictors of Visual Acuity in Human Albinism 2024 ·Investigative Ophthalmology & Visual Science ·(unknown), (unknown), (unknown), Sergey Tarima, (unknown), Murray H. Brilliant, (unknown), Deborah M. Costakos, C. Gail Summers, (unknown), Arlene V. Drack, Joseph Carroll	3
2	Advancing artificial intelligence-assisted pre-screening for fragile X syndrome 2022 ·BMC Medical Informatics and Decision Making ·(unknown), David Page, Murray H. Brilliant, Marsha R. Mailick	10
3	The effect of college degree attainment on neurodegenerative symptoms in genetically at-risk women 2022 ·SSM - Population Health ·Jinkuk Hong, (unknown), Leann Smith DaWalt, Murray H. Brilliant, Elizabeth Berry‐Kravis, Marsha R. Mailick	5
4	Artificial intelligence–assisted phenotype discovery of fragile X syndrome in a population-based sample 2021 ·Genetics in Medicine ·(unknown), David Page, (unknown), Jinkuk Hong, Leann Smith DaWalt, (unknown), Ron Stewart, Murray H. Brilliant, Marsha R. Mailick	14
5	Data-driven phenotype discovery of FMR1 premutation carriers in a population-based sample 2019 ·Science Advances ·(unknown), David Page, Murray H. Brilliant, Mei Baker, Jan S. Greenberg, Jinkuk Hong, Leann Smith DaWalt, Krishanu Saha, (unknown), Ron Stewart, Elizabeth Berry‐Kravis, Marsha R. Mailick	26
6	Applying family analyses to electronic health records to facilitate genetic research 2017 ·Bioinformatics ·(unknown), Robert C. Elston, Guilherme J. M. Rosa, John Mayer, Zhan Ye, Terrie Kitchner, Murray H. Brilliant, David Page, Scott J. Hebbring	6
7	Posterior staphyloma in oculocutaneous albinism: another possible cause of reduced visual acuity 2015 ·Journal of American Association for Pediatric Ophthalmology and Strabismus ·Susan Lee, Lisa A. Schimmenti, Richard A. King, Murray H. Brilliant, Jennifer L. Anderson, (unknown), C. Gail Summers	8
8	Phenome-wide association studies (PheWASs) for functional variants 2014 ·European Journal of Human Genetics ·Zhan Ye, John Mayer, Lynn Ivacic, Zhiyi Zhou, Min He, Steven J. Schrodi, David Page, Murray H. Brilliant, Scott J. Hebbring	35
9	A polymorphism in HLA-G modifies statin benefit in asthma 2014 ·The Pharmacogenomics Journal ·D Naidoo, Andy Wu, Murray H. Brilliant, Joshua C. Denny, C.D. Ingram, (unknown), James G. Linneman, Michael J. McGeachie, Dan M. Roden, Christian M. Shaffer, Anushi Shah, Peter Weeke, ST Weiss, (unknown), Marisa W. Medina	18
10	Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections 2014 ·Frontiers in Genetics ·Zhan Ye, Daniel A. Vasco, Tonia C. Carter, Murray H. Brilliant, Steven J. Schrodi, Sanjay K. Shukla	33
11	The Mouse p (pink‐eyed dilution) and Human P Genes, Oculocutaneous Albinism Type 2 (OCA2), and Melanosomal pH 2001 ·Pigment Cell Research ·Murray H. Brilliant	144
12	Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4 2001 ·The American Journal of Human Genetics ·J.M. Newton, Orit Cohen‐Barak, Nobuko Hagiwara, John M. Gardner, Muriel T. Davisson, Richard A. King, Murray H. Brilliant	254
13	Identification of a Novel Transcript Produced by the Gene Responsible for the Hermansky–Pudlak Syndrome in Puerto Rico 1998 ·Journal of Investigative Dermatology ·Scott C. Wildenberg, James P. Fryer, John M. Gardner, Murray H. Brilliant, William S. Oetting, Richard A. King	9
14	The γ-aminobutyric acid receptor γ3 subunit gene (GABRG3) is tightly linked to the α5 subunit gene (GABRA5) on human chromosome 15q11–q13 and is transcribed in the same orientation 1995 ·Genomics ·Valerie Greger, Joan H.M. Knoll, Elizabeth A. Woolf, Karen A. Glatt, Rachel F. Tyndale, Timothy M. DeLorey, R. W. Olsen, Allan J. Tobin, James M. Sikela, Yoshimichi Nakatsu, Murray H. Brilliant, Paul J. Whiting, M. Lalande	57
15	Theoretical basis of one‐dimensional genome scanning: A direct method to identify the site of a mutation 1995 ·Electrophoresis ·Yoichi Gondo, Murray H. Brilliant	1
16	Melanosomal Tyrosine Transport in Normal and Pink‐eyed Dilution Murine Melanocytes 1995 ·Pigment Cell Research ·William A. Gahl, (unknown), Donna Durham‐Pierre, Murray H. Brilliant, Vincent J. Hearing	38
17	Genome scanning detects genetic alterations in human ovarian carcinoma 1994 ·Human Mutation ·Anthony Magliocco, Murray H. Brilliant	4
18	The Mouse Pink‐Eyed Dilution Gene: Association with Hypopigmentation in Prader‐Willi and Angelman Syndromes and with Human OCA2 1994 ·Pigment Cell Research ·Murray H. Brilliant, Richard A. King, Uta Francke, Simone Schuffenhauer, Thomas Meitinger, John M. Gardner, Donna Durham‐Pierre, Yoshimichi Nakatsu	23
19	A cluster of three GABAA receptor subunit genes is deleted in a neurological mutant of the mouse p locus 1993 ·Nature ·Yoshimichi Nakatsu, Rachel F. Tyndale, Timothy M. DeLorey, Donna Durham‐Pierre, John M. Gardner, (unknown), (unknown), Joseph Wagstaff, (unknown), James M. Sikela, (unknown), Allan J. Tobin, Murray H. Brilliant	83
20	The mouse pink-eyed dilution locus: a model for aspects of Prader-Willi syndrome, Angelman syndrome, and a form of hypomelanosis of Ito 1992 ·Mammalian Genome ·Murray H. Brilliant	32

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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