Murray H. Brilliant - Concepedia

Author

Murray H. Brilliant

Also Known As

Donald W. Bowden, Hauser, Michael A., M Brilliant, M H Brilliant, M. H. Brilliant, M.H. Brilliant, MURRAY BRILLIANT, MURRAY H. BRILLIANT, Murray Brilliant, Murray H Brilliant

112

Publications

6.4K

Citations

H-Index

112

Concepts

All Affiliations

Marshfield Clinic Fox Chase Cancer Center University of Minnesota University of Arizona University of Wisconsin–Madison

About

Murray H. Brilliant is an author at Marshfield Clinic specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	37	2.7K
2	Public Health	8	8	365
3	Natural Sciences	5	5	328
4	Social Sciences	5	5	281
5	Health Sciences	2	2	477

Murray H. Brilliant

Publications

5.4K

Citations

H-Index

Page 1

	Year	Citations
Rare and low-frequency coding variants alter human adult height Eirini Marouli, Mariaelisa Graff, Carolina Medina‐Gómez, Nature Allelic VariantGeneticsStatistical GeneticsVariant InterpretationHuman Adult Height	2017	647
Mice devoid of γ-aminobutyrate type A receptor β3 subunit have epilepsy, cleft palate, and hypersensitive behavior Gregg E. Homanics, Timothy M. DeLorey, Leonard L. Firestone, Proceedings of the National Academy of Sciences	1997	476
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Valérie Turcot, Yingchang Lu, Heather M. Highland, Nature Genetics ObesityMetabolic SyndromeNutritionEnergy HomeostasisMetabolic Disorder	2017	420
Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4 J.M. Newton, Orit Cohen‐Barak, Nobuko Hagiwara, The American Journal of Human Genetics Knockout MouseOculocutaneous AlbinismAllelic VariantDevelopmental BiologyGenetic Disorder	2001	355
Usefulness of alkaline hydrogen peroxide oxidation to analyze eumelanin and pheomelanin in various tissue samples: application to chemical analysis of human hair melanins Shosuke Ito, Yukiko Nakanishi, Robert K. Valenzuela, Pigment Cell & Melanoma Research	2011	242
The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes John M. Gardner, Yoshimichi Nakatsu, Yoichi Gondo, Science	1992	232
Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3 Yong‐hui Jiang, Yanzhen Pan, Li Zhu, PLoS ONE	2010	172
Aberrant pH of Melanosomes in Pink-Eyed Dilution (p) Mutant Melanocytes Neelu Puri, John M. Gardner, Murray H. Brilliant Journal of Investigative Dermatology Cell BiologyPigmentMolecular BiologyAberrant Ph	2000	172
Identification of a melanosomal membrane protein encoded by the pink-eyed dilution (type II oculocutaneous albinism) gene. Susana Rosemblat, Donna Durham‐Pierre, John M. Gardner, Proceedings of the National Academy of Sciences Laboratory ImmunologyGeneticsImmunologyMolecular BiologyMolecular Genetics	1994	145
The mouse pale ear ( <i>ep</i> ) mutation is the homologue of human Hermansky–Pudlak syndrome John M. Gardner, Scott C. Wildenberg, Natalie M. Keiper, Proceedings of the National Academy of Sciences ChromatinHps GeneDevelopmental BiologyMendelian DisorderGenetic Disorder	1997	133

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