C. Coleman

发表

Single-molecule sequencing of long DNA molecules allows high contiguity de novo genome assembly for the fungus fly, Sciara coprophila

Susan J. Brown, A. Spradling, John M. Urban, 2020, bioRxiv.

Transcriptome Analysis of CD4+ T Cells in Coeliac Disease Reveals Imprint of BACH2 and IFNγ Regulation

R. McManus, E. Quinn, P. Cormican, 2015, PloS one.

The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

H. Kremer, J. Uitto, J. McGrath, 1999, American journal of human genetics.

A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

J. Uitto, C. Coleman, K. Mckenna, 1999, Experimental dermatology.

Novel keratin 17 mutations in pachyonychia congenita type 2.

R. Tenconi, C. Coleman, W. McLean, 2001, The Journal of investigative dermatology.

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

J. Uitto, C. Coleman, C. Munro, 1999, The British journal of dermatology.

A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.

J. Uitto, C. Coleman, F. Smith, 1998, Human molecular genetics.

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity

Matti Pirinen, Christian Gieger, Peter Donnelly, 2012 .

Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci

R. Anney, J. Conroy, S. Ennis, 2015, European Journal of Human Genetics.

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.

J. Uitto, C. Coleman, S. Hannush, 1999, American journal of ophthalmology.