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Items: 7

1.

Family-based association tests for sequence data, and comparisons with population-based association tests.

Ionita-Laza I, Lee S, Makarov V, Buxbaum JD, Lin X.

Eur J Hum Genet. 2013 Oct;21(10):1158-62. doi: 10.1038/ejhg.2012.308.

2.

The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.

Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW; Autism Sequencing Consortium..

Neuron. 2012 Dec 20;76(6):1052-6. doi: 10.1016/j.neuron.2012.12.008.

3.

[Application of whole exome sequencing in the diagnosis of hereditary neurological diseases].

Ilinsky VV, Korneeva VA, Shatalov PA.

Zh Nevrol Psikhiatr Im S S Korsakova. 2015;115(1):45-52. Review. Russian.

PMID:
25909789
4.

Family-based methods for linkage and association analysis.

Laird NM, Lange C.

Adv Genet. 2008;60:219-52. doi: 10.1016/S0065-2660(07)00410-5. Review.

PMID:
18358323
5.

Using familial information for variant filtering in high-throughput sequencing studies.

Bahlo M, Tankard R, Lukic V, Oliver KL, Smith KR.

Hum Genet. 2014 Nov;133(11):1331-41. doi: 10.1007/s00439-014-1479-4. Review. Erratum in: Hum Genet. 2015 May;134(5):509.

6.

Revisiting Mendelian disorders through exome sequencing.

Ku CS, Naidoo N, Pawitan Y.

Hum Genet. 2011 Apr;129(4):351-70. doi: 10.1007/s00439-011-0964-2. Review.

PMID:
21331778
7.

Parental phenotypes in family-based association analysis.

Purcell S, Sham P, Daly MJ.

Am J Hum Genet. 2005 Feb;76(2):249-59. Review.

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