-
1
-
-
0034837773
-
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations
-
Box, N.F., Duffy, D.L., Chen, W., et al. MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutations. Am J Hum Genet 69 (2001), 765–773.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 765-773
-
-
Box, N.F.1
Duffy, D.L.2
Chen, W.3
-
2
-
-
1242307966
-
Interactive effects of MC1R and OCA2 on melanoma risk phenotypes
-
Duffy, D.L., Box, N.F., Chen, W., et al. Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Hum Mol Genet 13 (2004), 447–461.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 447-461
-
-
Duffy, D.L.1
Box, N.F.2
Chen, W.3
-
3
-
-
0034641860
-
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation
-
Flanagan, N., Healy, E., Ray, A., et al. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation. Hum Mol Genet 9 (2000), 2531–2537.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2531-2537
-
-
Flanagan, N.1
Healy, E.2
Ray, A.3
-
4
-
-
0025336408
-
A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism
-
Giebel, L.B., Strunk, K.M., King, R.A., et al. A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism. Proc Natl Acad Sci USA 87 (1990), 3255–3258.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 3255-3258
-
-
Giebel, L.B.1
Strunk, K.M.2
King, R.A.3
-
5
-
-
0025729679
-
Tyrosinase gene mutations associated with type IB (“yellow”) oculocutaneous albinism
-
Giebel, L.B., Tripathi, R.K., Strunk, K.M., et al. Tyrosinase gene mutations associated with type IB (“yellow”) oculocutaneous albinism. Am J Hum Genet 48 (1991), 1159–1167.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 1159-1167
-
-
Giebel, L.B.1
Tripathi, R.K.2
Strunk, K.M.3
-
6
-
-
79955572378
-
Adaptations to climate-mediated selective pressures in humans
-
Hancock, A.M., Witonsky, D.B., Alkorta-Aranburu, G., et al. Adaptations to climate-mediated selective pressures in humans. PLoS Genet, 7, 2011, e1001375.
-
(2011)
PLoS Genet
, vol.7
, pp. e1001375
-
-
Hancock, A.M.1
Witonsky, D.B.2
Alkorta-Aranburu, G.3
-
7
-
-
0034712537
-
Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair
-
Healy, E., Flannagan, N., Ray, A., et al. Melanocortin-1-receptor gene and sun sensitivity in individuals without red hair. Lancet 355 (2000), 1072–1073.
-
(2000)
Lancet
, vol.355
, pp. 1072-1073
-
-
Healy, E.1
Flannagan, N.2
Ray, A.3
-
8
-
-
29144485743
-
SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans
-
Lamason, R.L., Mohideen, M.A., Mest, J.R., et al. SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans. Science 310 (2005), 1782–1786.
-
(2005)
Science
, vol.310
, pp. 1782-1786
-
-
Lamason, R.L.1
Mohideen, M.A.2
Mest, J.R.3
-
9
-
-
84886473302
-
-
Wiley-Blackwell Chichester, UK
-
Lamoreux, M.L., Delamas, V., Larue, L., et al. The Colors of Mice. A Model Genetic Network., 2010, Wiley-Blackwell, Chichester, UK.
-
(2010)
The Colors of Mice. A Model Genetic Network.
-
-
Lamoreux, M.L.1
Delamas, V.2
Larue, L.3
-
10
-
-
0030828856
-
Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene
-
Manga, P., Kromberg, J.G., Box, N.F., et al. Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene. Am J Hum Genet 61 (1997), 1095–1101.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1095-1101
-
-
Manga, P.1
Kromberg, J.G.2
Box, N.F.3
-
11
-
-
0034753365
-
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
-
Newton, J.M., Cohen-Barak, O., Hagiwara, N., et al. Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4. Am J of Hum Genet 69 (2001), 981–988.
-
(2001)
Am J of Hum Genet
, vol.69
, pp. 981-988
-
-
Newton, J.M.1
Cohen-Barak, O.2
Hagiwara, N.3
-
12
-
-
0003696452
-
The Pigmentary System
-
Blackwell Publishing USA
-
Nordlund, J.J., Boissy, R.E., Hearing, V.J., et al. The Pigmentary System. Mass, 2006, Blackwell Publishing, USA.
-
(2006)
Mass
-
-
Nordlund, J.J.1
Boissy, R.E.2
Hearing, V.J.3
-
13
-
-
66049157487
-
Signals of recent positive selection in a worldwide sample of human populations
-
Pickrell, J.K., Coop, G., Novembre, J., et al. Signals of recent positive selection in a worldwide sample of human populations. Genome Res 19 (2009), 826–837.
-
(2009)
Genome Res
, vol.19
, pp. 826-837
-
-
Pickrell, J.K.1
Coop, G.2
Novembre, J.3
-
14
-
-
76749097550
-
The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation
-
Pritchard, J.K., Pickrell, J.K., Coop, G., The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation. Curr Biol 20 (2010), R208–R215.
-
(2010)
Curr Biol
, vol.20
, pp. R208-R215
-
-
Pritchard, J.K.1
Pickrell, J.K.2
Coop, G.3
-
15
-
-
0027509280
-
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism
-
Rinchik, E.M., Bultman, S.J., Horsthemke, B., et al. A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism. Nature 361 (1993), 72–76.
-
(1993)
Nature
, vol.361
, pp. 72-76
-
-
Rinchik, E.M.1
Bultman, S.J.2
Horsthemke, B.3
-
16
-
-
0027413475
-
Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function
-
Robbins, L.S., Nadeau, J.H., Johnson, K.R., et al. Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell 72 (1993), 827–834.
-
(1993)
Cell
, vol.72
, pp. 827-834
-
-
Robbins, L.S.1
Nadeau, J.H.2
Johnson, K.R.3
-
17
-
-
35349012592
-
Genome-wide detection and characterization of positive selection in human populations
-
Sabeti, P.C., Varilly, P., Fry, B., et al. Genome-wide detection and characterization of positive selection in human populations. Nature 449 (2007), 913–918.
-
(2007)
Nature
, vol.449
, pp. 913-918
-
-
Sabeti, P.C.1
Varilly, P.2
Fry, B.3
-
18
-
-
7144254441
-
Melanocortin 1 receptor variants in an Irish population
-
Smith, R., Healy, E., Siddiqui, S., et al. Melanocortin 1 receptor variants in an Irish population. J Invest Dermatol, 111, 1998, 119.
-
(1998)
J Invest Dermatol
, vol.111
, pp. 119
-
-
Smith, R.1
Healy, E.2
Siddiqui, S.3
-
19
-
-
0028786945
-
Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans
-
Valverde, P., Healy, E., Jackson, I., et al. Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans. Nat Genet, 11, 1995, 328.
-
(1995)
Nat Genet
, vol.11
, pp. 328
-
-
Valverde, P.1
Healy, E.2
Jackson, I.3
-
20
-
-
33644981509
-
A map of recent positive selection in the human genome
-
Voight, B.F., Kudaravalli, S., Wen, X., et al. A map of recent positive selection in the human genome. PLoS Biol, 4, 2006, e72.
-
(2006)
PLoS Biol
, vol.4
, pp. e72
-
-
Voight, B.F.1
Kudaravalli, S.2
Wen, X.3
|