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Items: 1 to 20 of 319

1.

Direct chromosome-length haplotyping by single-cell sequencing.

Porubský D, Sanders AD, van Wietmarschen N, Falconer E, Hills M, Spierings DC, Bevova MR, Guryev V, Lansdorp PM.

Genome Res. 2016 Nov;26(11):1565-1574.

PMID:
27646535
2.

Coding and noncoding variants in HFM1, MLH3, MSH4, MSH5, RNF212, and RNF212B affect recombination rate in cattle.

Kadri NK, Harland C, Faux P, Cambisano N, Karim L, Coppieters W, Fritz S, Mullaart E, Baurain D, Boichard D, Spelman R, Charlier C, Georges M, Druet T.

Genome Res. 2016 Oct;26(10):1323-1332.

PMID:
27516620
3.

Effect of manipulating recombination rates on response to selection in livestock breeding programs.

Battagin M, Gorjanc G, Faux AM, Johnston SE, Hickey JM.

Genet Sel Evol. 2016 Jun 22;48(1):44. doi: 10.1186/s12711-016-0221-1.

4.

Detecting Recombination Hotspots from Patterns of Linkage Disequilibrium.

Wall JD, Stevison LS.

G3 (Bethesda). 2016 Aug 9;6(8):2265-71. doi: 10.1534/g3.116.029587.

5.

High-Resolution Mapping of Crossover and Non-crossover Recombination Events by Whole-Genome Re-sequencing of an Avian Pedigree.

Smeds L, Mugal CF, Qvarnström A, Ellegren H.

PLoS Genet. 2016 May 24;12(5):e1006044. doi: 10.1371/journal.pgen.1006044.

6.

Setting up Multiplex Panels for Genetic Testing of Familial Hypertrophic Cardiomyopathy Based on Linkage Analysis.

Saghafi H, Haghjoo M, Sabbagh S, Samiee N, Vakilian F, Salehi Omran MT, Dadashi M, Amin A, Keramatipour M.

Iran J Public Health. 2016 Mar;45(3):329-39.

7.

The Genetic Architecture of Natural Variation in Recombination Rate in Drosophila melanogaster.

Hunter CM, Huang W, Mackay TF, Singh ND.

PLoS Genet. 2016 Apr 1;12(4):e1005951. doi: 10.1371/journal.pgen.1005951.

8.

Correlations between Synaptic Initiation and Meiotic Recombination: A Study of Humans and Mice.

Gruhn JR, Al-Asmar N, Fasnacht R, Maylor-Hagen H, Peinado V, Rubio C, Broman KW, Hunt PA, Hassold T.

Am J Hum Genet. 2016 Jan 7;98(1):102-15. doi: 10.1016/j.ajhg.2015.11.019.

9.

Introgression of Neandertal- and Denisovan-like Haplotypes Contributes to Adaptive Variation in Human Toll-like Receptors.

Dannemann M, Andrés AM, Kelso J.

Am J Hum Genet. 2016 Jan 7;98(1):22-33. doi: 10.1016/j.ajhg.2015.11.015. Erratum in: Am J Hum Genet. 2016 Feb 4;98(2):399.

10.

ARG-walker: inference of individual specific strengths of meiotic recombination hotspots by population genomics analysis.

Chen H, Yang P, Guo J, Kwoh CK, Przytycka TM, Zheng J.

BMC Genomics. 2015;16 Suppl 12:S1. doi: 10.1186/1471-2164-16-S12-S1.

11.

Construction of Ultradense Linkage Maps with Lep-MAP2: Stickleback F2 Recombinant Crosses as an Example.

Rastas P, Calboli FC, Guo B, Shikano T, Merilä J.

Genome Biol Evol. 2015 Dec 14;8(1):78-93. doi: 10.1093/gbe/evv250.

12.

No Evidence that Infection Alters Global Recombination Rate in House Mice.

Dumont BL, Devlin AA, Truempy DM, Miller JC, Singh ND.

PLoS One. 2015 Nov 9;10(11):e0142266. doi: 10.1371/journal.pone.0142266.

13.

Cattle Sex-Specific Recombination and Genetic Control from a Large Pedigree Analysis.

Ma L, O'Connell JR, VanRaden PM, Shen B, Padhi A, Sun C, Bickhart DM, Cole JB, Null DJ, Liu GE, Da Y, Wiggans GR.

PLoS Genet. 2015 Nov 5;11(11):e1005387. doi: 10.1371/journal.pgen.1005387.

14.

Fifteen years of genomewide scans for selection: trends, lessons and unaddressed genetic sources of complication.

Haasl RJ, Payseur BA.

Mol Ecol. 2016 Jan;25(1):5-23. doi: 10.1111/mec.13339. Review.

15.

Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration.

Iqbal Z, Püttmann L, Musante L, Razzaq A, Zahoor MY, Hu H, Wienker TF, Garshasbi M, Fattahi Z, Gilissen C, Vissers LE, de Brouwer AP, Veltman JA, Pfundt R, Najmabadi H, Ropers HH, Riazuddin S, Kahrizi K, van Bokhoven H.

Eur J Hum Genet. 2016 Mar;24(3):392-9. doi: 10.1038/ejhg.2015.148.

PMID:
26173967
16.

Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates.

Ottolini CS, Newnham LJ, Capalbo A, Natesan SA, Joshi HA, Cimadomo D, Griffin DK, Sage K, Summers MC, Thornhill AR, Housworth E, Herbert AD, Rienzi L, Ubaldi FM, Handyside AH, Hoffmann ER.

Nat Genet. 2015 Jul;47(7):727-35. doi: 10.1038/ng.3306.

17.

Genetic influences on response to novel objects and dimensions of personality in Papio baboons.

Johnson Z, Brent L, Alvarenga JC, Comuzzie AG, Shelledy W, Ramirez S, Cox L, Mahaney MC, Huang YY, Mann JJ, Kaplan JR, Rogers J.

Behav Genet. 2015 Mar;45(2):215-27. doi: 10.1007/s10519-014-9702-6.

18.

The landscape of human STR variation.

Willems T, Gymrek M, Highnam G; 1000 Genomes Project Consortium., Mittelman D, Erlich Y.

Genome Res. 2014 Nov;24(11):1894-904. doi: 10.1101/gr.177774.114.

19.

Resolution of genetic map expansion caused by excess heterozygosity in plant recombinant inbred populations.

Truong SK, McCormick RF, Morishige DT, Mullet JE.

G3 (Bethesda). 2014 Aug 15;4(10):1963-9. doi: 10.1534/g3.114.012468.

20.

Examining variation in recombination levels in the human female: a test of the production-line hypothesis.

Rowsey R, Gruhn J, Broman KW, Hunt PA, Hassold T.

Am J Hum Genet. 2014 Jul 3;95(1):108-12. doi: 10.1016/j.ajhg.2014.06.008.

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