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Items: 8

1.

A penile spine/vibrissa enhancer sequence is missing in modern and extinct humans but is retained in multiple primates with penile spines and sensory vibrissae.

Reno PL, McLean CY, Hines JE, Capellini TD, Bejerano G, Kingsley DM.

PLoS One. 2013 Dec 19;8(12):e84258. doi: 10.1371/journal.pone.0084258. eCollection 2013.

2.

Enhancers: five essential questions.

Pennacchio LA, Bickmore W, Dean A, Nobrega MA, Bejerano G.

Nat Rev Genet. 2013 Apr;14(4):288-95. doi: 10.1038/nrg3458. Review.

3.

PRISM offers a comprehensive genomic approach to transcription factor function prediction.

Wenger AM, Clarke SL, Guturu H, Chen J, Schaar BT, McLean CY, Bejerano G.

Genome Res. 2013 May;23(5):889-904. doi: 10.1101/gr.139071.112. Epub 2013 Feb 4.

4.

PESNPdb: a comprehensive database of SNPs studied in association with pre-eclampsia.

Tuteja G, Cheng E, Papadakis H, Bejerano G.

Placenta. 2012 Dec;33(12):1055-7. doi: 10.1016/j.placenta.2012.09.016. Epub 2012 Oct 18.

PMID:
23084601
5.

A "forward genomics" approach links genotype to phenotype using independent phenotypic losses among related species.

Hiller M, Schaar BT, Indjeian VB, Kingsley DM, Hagey LR, Bejerano G.

Cell Rep. 2012 Oct 25;2(4):817-23. doi: 10.1016/j.celrep.2012.08.032. Epub 2012 Sep 27.

6.

A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb.

Laurell T, Vandermeer JE, Wenger AM, Grigelioniene G, Nordenskjöld A, Arner M, Ekblom AG, Bejerano G, Ahituv N, Nordgren A.

Hum Mutat. 2012 Jul;33(7):1063-6. doi: 10.1002/humu.22097. Epub 2012 May 11.

7.

Human-specific loss of regulatory DNA and the evolution of human-specific traits.

McLean CY, Reno PL, Pollen AA, Bassan AI, Capellini TD, Guenther C, Indjeian VB, Lim X, Menke DB, Schaar BT, Wenger AM, Bejerano G, Kingsley DM.

Nature. 2011 Mar 10;471(7337):216-9. doi: 10.1038/nature09774.

8.

Forces shaping the fastest evolving regions in the human genome.

Pollard KS, Salama SR, King B, Kern AD, Dreszer T, Katzman S, Siepel A, Pedersen JS, Bejerano G, Baertsch R, Rosenbloom KR, Kent J, Haussler D.

PLoS Genet. 2006 Oct 13;2(10):e168. Epub 2006 Aug 23.

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