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Results: 1 to 20 of 36

1.

A genome scan conducted in a multigenerational pedigree with convergent strabismus supports a complex genetic determinism.

Georges A, Cambisano N, Ahariz N, Karim L, Georges M.

PLoS One. 2013 Dec 23;8(12):e83574. doi: 10.1371/journal.pone.0083574. eCollection 2013.

PMID:
24376720
[PubMed - in process]
Free PMC Article
2.

HapFABIA: identification of very short segments of identity by descent characterized by rare variants in large sequencing data.

Hochreiter S.

Nucleic Acids Res. 2013 Dec;41(22):e202. doi: 10.1093/nar/gkt1013. Epub 2013 Oct 29.

PMID:
24174545
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

A population-based analysis of clustering identifies a strong genetic contribution to lethal prostate cancer.

Nelson Q, Agarwal N, Stephenson R, Cannon-Albright LA.

Front Genet. 2013 Aug 20;4:152. doi: 10.3389/fgene.2013.00152. eCollection 2013.

PMID:
23970893
[PubMed]
Free PMC Article
4.

IBD-Groupon: an efficient method for detecting group-wise identity-by-descent regions simultaneously in multiple individuals based on pairwise IBD relationships.

He D.

Bioinformatics. 2013 Jul 1;29(13):i162-70. doi: 10.1093/bioinformatics/btt237.

PMID:
23812980
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Identity by descent: variation in meiosis, across genomes, and in populations.

Thompson EA.

Genetics. 2013 Jun;194(2):301-26. doi: 10.1534/genetics.112.148825. Review.

PMID:
23733848
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Identifying bipolar disorder susceptibility loci in a densely affected pedigree.

Collins AL, Kim Y, Szatkiewicz JP, Bloom RJ, Hilliard CE, Quackenbush CR, Meier S, Rivas F, Mayoral F, Cichon S, Nöthen MM, Rietschel M, Sullivan PF.

Mol Psychiatry. 2013 Dec;18(12):1245-6. doi: 10.1038/mp.2012.176. Epub 2012 Dec 18. No abstract available.

PMID:
23247078
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Pairwise shared genomic segment analysis in three Utah high-risk breast cancer pedigrees.

Cai Z, Thomas A, Teerlink C, Farnham JM, Cannon-Albright LA, Camp NJ.

BMC Genomics. 2012 Nov 28;13:676. doi: 10.1186/1471-2164-13-676.

PMID:
23190577
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.

Arrington CB, Bleyl SB, Matsunami N, Bowles NE, Leppert TI, Demarest BL, Osborne K, Yoder BA, Byrne JL, Schiffman JD, Null DM, DiGeronimo R, Rollins M, Faix R, Comstock J, Camp NJ, Leppert MF, Yost HJ, Brunelli L.

Am J Med Genet A. 2012 Dec;158A(12):3137-47. doi: 10.1002/ajmg.a.35664. Epub 2012 Nov 19.

PMID:
23165927
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A system for exact and approximate genetic linkage analysis of SNP data in large pedigrees.

Silberstein M, Weissbrod O, Otten L, Tzemach A, Anisenia A, Shtark O, Tuberg D, Galfrin E, Gannon I, Shalata A, Borochowitz ZU, Dechter R, Thompson E, Geiger D.

Bioinformatics. 2013 Jan 15;29(2):197-205. doi: 10.1093/bioinformatics/bts658. Epub 2012 Nov 18. Erratum in: Bioinformatics.2013 Mar 1;29(5):669.

PMID:
23162081
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort.

Browning SR, Browning BL.

Hum Genet. 2013 Feb;132(2):129-38. doi: 10.1007/s00439-012-1230-y. Epub 2012 Sep 29. Erratum in: Hum Genet. 2013 Aug;132(8):957-8.

PMID:
23052944
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Shared genomic segment analysis: the power to find rare disease variants.

Knight S, Abo RP, Abel HJ, Neklason DW, Tuohy TM, Burt RW, Thomas A, Camp NJ.

Ann Hum Genet. 2012 Nov;76(6):500-9. doi: 10.1111/j.1469-1809.2012.00728.x. Epub 2012 Sep 19.

PMID:
22989048
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.

Cannon-Albright LA, Teerlink CC, Farnham JM, Thomas AW, Zone JJ, Leachman SA.

J Invest Dermatol. 2013 Jan;133(1):128-34. doi: 10.1038/jid.2012.271. Epub 2012 Sep 6.

PMID:
22951724
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

The role of large pedigrees in an era of high-throughput sequencing.

Wijsman EM.

Hum Genet. 2012 Oct;131(10):1555-63. doi: 10.1007/s00439-012-1190-2. Epub 2012 Jun 20. Review.

PMID:
22714655
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Detection of identity by descent using next-generation whole genome sequencing data.

Su SY, Kasberger J, Baranzini S, Byerley W, Liao W, Oksenberg J, Sherr E, Jorgenson E.

BMC Bioinformatics. 2012 Jun 6;13:121. doi: 10.1186/1471-2105-13-121.

PMID:
22672699
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Optimized selection of unrelated subjects for whole-genome sequencing studies of rare high-penetrance alleles.

Edwards TL, Li C.

Genet Epidemiol. 2012 Jul;36(5):472-9. doi: 10.1002/gepi.21641. Epub 2012 May 23.

PMID:
22623060
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Rule-based induction method for haplotype comparison and identification of candidate disease loci.

Karinen S, Saarinen S, Lehtonen R, Rastas P, Vahteristo P, Aaltonen LA, Hautaniemi S.

Genome Med. 2012 Mar 19;4(3):21.

PMID:
22429919
[PubMed]
Free PMC Article
17.

Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.

Cai Z, Knight S, Thomas A, Camp NJ.

BMC Proc. 2011 Nov 29;5 Suppl 9:S9. doi: 10.1186/1753-6561-5-S9-S9.

PMID:
22373081
[PubMed]
Free PMC Article
18.

Detecting rare variant associations by identity-by-descent mapping in case-control studies.

Browning SR, Thompson EA.

Genetics. 2012 Apr;190(4):1521-31. doi: 10.1534/genetics.111.136937. Epub 2012 Jan 20.

PMID:
22267498
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis.

Marchani EE, Wijsman EM.

Hum Hered. 2011;72(4):289-97. doi: 10.1159/000334083. Epub 2011 Dec 23.

PMID:
22189471
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Quality control issues and the identification of rare functional variants with next-generation sequencing data.

Hemmelmann C, Daw EW, Wilson AF.

Genet Epidemiol. 2011;35 Suppl 1:S22-8. doi: 10.1002/gepi.20645.

PMID:
22128054
[PubMed - indexed for MEDLINE]
Free PMC Article

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