A deletion in the Hermansky–Pudlak syndrome 4 (Hps4) gene appears to be responsible for albinism in channel catfish

A genome-wide association study of heat stress-associated SNPs in catfish

(2016) Y. Jin et al.   ANIMAL GENETICS

Multiple across-strain and within-strain QTLs suggest highly complex genetic architecture for hypoxia tolerance in channel catfish

(2016) Xiaozhu Wang et al.   MOLECULAR GENETICS AND GENOMICS

GWAS analysis of QTL for enteric septicemia of catfish and their involved genes suggest evolutionary conservation of a molecular mechanism of disease resistance

(2016) Tao Zhou et al.   MOLECULAR GENETICS AND GENOMICS

The channel catfish genome sequence provides insights into the evolution of scale formation in teleosts

(2016) Zhanjiang Liu et al.   Nature Communications

How does agonistic behaviour differ in albino and pigmented fish?

(2016) Ondřej Slavík et al.   PeerJ

A genome-wide association study in catfish reveals the presence of functional hubs of related genes within QTLs for columnaris disease resistance

(2015) Xin Geng et al.   BMC GENOMICS

Ostracism of an Albino Individual by a Group of Pigmented Catfish

(2015) Ondřej Slavík et al.   PLoS One

A Comparative Transcriptome Analysis between Wild and Albino Yellow Catfish (Pelteobagrus fulvidraco)

(2015) Ming Zou et al.   PLoS One

A dominant mutation intyrp1Aleads to melanophore death in zebrafish

(2014) Jana Krauss et al.   Pigment Cell & Melanoma Research

Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism

(2013) Karen Grønskov et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Exome Sequencing Identifies SLC24A5 as a Candidate Gene for Nonsyndromic Oculocutaneous Albinism

(2013) Ai-Hua Wei et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Hermansky-Pudlak Syndrome: Health Care Throughout Life

(2013) S. L. Seward et al.   PEDIATRICS

oca2regulation of chromatophore differentiation and number is cell type specific in zebrafish

(2013) Alisha J. Beirl et al.   Pigment Cell & Melanoma Research

OCA5,a novel locus for non-syndromic oculocutaneous albinism, maps to chromosome 4q24

(2012) T Kausar et al.   CLINICAL GENETICS

Double heterozygous mutations ofMITFandPAX3result in Waardenburg syndrome with increased penetrance in pigmentary defects

(2012) T Yang et al.   CLINICAL GENETICS

BLOC-3 Mutated in Hermansky-Pudlak Syndrome Is a Rab32/38 Guanine Nucleotide Exchange Factor

(2012) Andreas Gerondopoulos et al.   CURRENT BIOLOGY

Slc45a2 and V-ATPase are regulators of melanosomal pH homeostasis in zebrafish, providing a mechanism for human pigment evolution and disease

(2012) Christopher M. Dooley et al.   Pigment Cell & Melanoma Research

Generation of genome-scale gene-associated SNPs in catfish for the construction of a high-density SNP array

(2011) Shikai Liu et al.   BMC GENOMICS

The Mon1-Ccz1 Complex Is the GEF of the Late Endosomal Rab7 Homolog Ypt7

(2010) Mirjana Nordmann et al.   CURRENT BIOLOGY

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

A Novel Role for Mc1r in the Parallel Evolution of Depigmentation in Independent Populations of the Cavefish Astyanax mexicanus

(2009) Joshua B. Gross et al.   PLoS Genetics

Lack of adequate sun protection for children with oculocutaneous albinism in South Africa

(2008) Patricia M Lund et al.   BMC PUBLIC HEALTH

Melanosomes at a glance

(2008) C. Wasmeier et al.   JOURNAL OF CELL SCIENCE