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Items: 16


Leveraging Multi-ethnic Evidence for Risk Assessment of Quantitative Traits in Minority Populations.

Coram MA, Fang H, Candille SI, Assimes TL, Tang H.

Am J Hum Genet. 2017 Oct 5;101(4):638. doi: 10.1016/j.ajhg.2017.09.005. No abstract available.


Leveraging Multi-ethnic Evidence for Risk Assessment of Quantitative Traits in Minority Populations.

Coram MA, Fang H, Candille SI, Assimes TL, Tang H.

Am J Hum Genet. 2017 Aug 3;101(2):218-226. doi: 10.1016/j.ajhg.2017.06.015. Epub 2017 Jul 27. Erratum in: Am J Hum Genet. 2017 Oct 5;101(4):638.


Systematic design and comparison of expanded carrier screening panels.

Beauchamp KA, Muzzey D, Wong KK, Hogan GJ, Karimi K, Candille SI, Mehta N, Mar-Heyming R, Kaseniit KE, Kang HP, Evans EA, Goldberg JD, Lazarin GA, Haque IS.

Genet Med. 2018 Jan;20(1):55-63. doi: 10.1038/gim.2017.69. Epub 2017 Jun 22.


Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans.

Cenik C, Cenik ES, Byeon GW, Grubert F, Candille SI, Spacek D, Alsallakh B, Tilgner H, Araya CL, Tang H, Ricci E, Snyder MP.

Genome Res. 2015 Nov;25(11):1610-21. doi: 10.1101/gr.193342.115. Epub 2015 Aug 21.


Leveraging Multi-ethnic Evidence for Mapping Complex Traits in Minority Populations: An Empirical Bayes Approach.

Coram MA, Candille SI, Duan Q, Chan KH, Li Y, Kooperberg C, Reiner AP, Tang H.

Am J Hum Genet. 2015 May 7;96(5):740-52. doi: 10.1016/j.ajhg.2015.03.008. Epub 2015 Apr 16.


Variation and genetic control of protein abundance in humans.

Wu L, Candille SI, Choi Y, Xie D, Jiang L, Li-Pook-Than J, Tang H, Snyder M.

Nature. 2013 Jul 4;499(7456):79-82. doi: 10.1038/nature12223. Epub 2013 May 15.


Genetic architecture of skin and eye color in an African-European admixed population.

Beleza S, Johnson NA, Candille SI, Absher DM, Coram MA, Lopes J, Campos J, Araújo II, Anderson TM, Vilhjálmsson BJ, Nordborg M, Correia E Silva A, Shriver MD, Rocha J, Barsh GS, Tang H.

PLoS Genet. 2013 Mar;9(3):e1003372. doi: 10.1371/journal.pgen.1003372. Epub 2013 Mar 21.


Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.

Candille SI, Absher DM, Beleza S, Bauchet M, McEvoy B, Garrison NA, Li JZ, Myers RM, Barsh GS, Tang H, Shriver MD.

PLoS One. 2012;7(10):e48294. doi: 10.1371/journal.pone.0048294. Epub 2012 Oct 31.


Human genetic variation altering anthrax toxin sensitivity.

Martchenko M, Candille SI, Tang H, Cohen SN.

Proc Natl Acad Sci U S A. 2012 Feb 21;109(8):2972-7. doi: 10.1073/pnas.1121006109. Epub 2012 Feb 6.


Molecular and evolutionary history of melanism in North American gray wolves.

Anderson TM, vonHoldt BM, Candille SI, Musiani M, Greco C, Stahler DR, Smith DW, Padhukasahasram B, Randi E, Leonard JA, Bustamante CD, Ostrander EA, Tang H, Wayne RK, Barsh GS.

Science. 2009 Mar 6;323(5919):1339-43. doi: 10.1126/science.1165448. Epub 2009 Feb 5.


New ligands for melanocortin receptors.

Kaelin CB, Candille SI, Yu B, Jackson P, Thompson DA, Nix MA, Binkley J, Millhauser GL, Barsh GS.

Int J Obes (Lond). 2008 Dec;32 Suppl 7:S19-27. doi: 10.1038/ijo.2008.234. Review.


A -defensin mutation causes black coat color in domestic dogs.

Candille SI, Kaelin CB, Cattanach BM, Yu B, Thompson DA, Nix MA, Kerns JA, Schmutz SM, Millhauser GL, Barsh GS.

Science. 2007 Nov 30;318(5855):1418-23. Epub 2007 Oct 18.


Linkage and segregation analysis of black and brindle coat color in domestic dogs.

Kerns JA, Cargill EJ, Clark LA, Candille SI, Berryere TG, Olivier M, Lust G, Todhunter RJ, Schmutz SM, Murphy KE, Barsh GS.

Genetics. 2007 Jul;176(3):1679-89. Epub 2007 May 4.


Dorsoventral patterning of the mouse coat by Tbx15.

Candille SI, Van Raamsdonk CD, Chen C, Kuijper S, Chen-Tsai Y, Russ A, Meijlink F, Barsh GS.

PLoS Biol. 2004 Jan;2(1):E3. Epub 2004 Jan 20.


Identification of the gene and the mutation responsible for the mouse nob phenotype.

Gregg RG, Mukhopadhyay S, Candille SI, Ball SL, Pardue MT, McCall MA, Peachey NS.

Invest Ophthalmol Vis Sci. 2003 Jan;44(1):378-84.


Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome.

Candille SI, Pardue MT, McCall MA, Peachey NS, Gregg RG.

Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2748-51.


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