Linkage and association scan for tanning ability in an isolated Mongolian population

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses

(2011) R. R. Bellone et al.   Briefings in Functional Genomics

TRPM1: The endpoint of the mGluR6 signal transduction cascade in retinal ON-bipolar cells

(2010) Catherine W. Morgans et al.   BIOESSAYS

Regulation of Human Skin Pigmentation in situ by Repetitive UV Exposure: Molecular Characterization of Responses to UVA and/or UVB

(2010) Wonseon Choi et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry

(2009) Hongmei Nan et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

TRPM1 Forms Ion Channels Associated with Melanin Content in Melanocytes

(2009) E. Oancea et al.   Science Signaling

Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene

(2008) Manfred Kayser et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A genome-wide Asian genetic map and ethnic comparison: The GENDISCAN study

(2008) Young Ju et al.   BMC GENOMICS

Differential Gene Expression of TRPM1, the Potential Cause of Congenital Stationary Night Blindness and Coat Spotting Patterns (LP) in the Appaloosa Horse (Equus caballus)

(2008) R. R. Bellone et al.   GENETICS

Two newly identified genetic determinants of pigmentation in Europeans

(2008) Patrick Sulem et al.   NATURE GENETICS

A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation

(2008) Jiali Han et al.   PLoS Genetics