Visscher PM - Search Results

1

Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.

Yap CX, Alvares GA, Henders AK, Lin T, Wallace L, Farrelly A, McLaren T, Berry J, Vinkhuyzen AAE, Trzaskowski M, Zeng J, Yang Y, Cleary D, Grove R, Hafekost C, Harun A, Holdsworth H, Jellett R, Khan F, Lawson L, Leslie J, Levis Frenk M, Masi A, Mathew NE, Muniandy M, Nothard M, Visscher PM, Dawson PA, Dissanayake C, Eapen V, Heussler HS, Whitehouse AJO, Wray NR, Gratten J. Yap CX, et al. Among authors: visscher pm. Mol Autism. 2021 Feb 10;12(1):12. doi: 10.1186/s13229-020-00407-5. Mol Autism. 2021. PMID: 33568206 Free PMC article.

2

Conventional multipoint nonparametric linkage analysis is not necessarily inherently biased.

Visscher PM, Wray NR. Visscher PM, et al. Am J Hum Genet. 2004 Oct;75(4):718-20; author reply 723-7. doi: 10.1086/424755. Am J Hum Genet. 2004. PMID: 15338458 Free PMC article. No abstract available.

3

Genetic and phenotypic stability of measures of neuroticism over 22 years.

Wray NR, Birley AJ, Sullivan PF, Visscher PM, Martin NG. Wray NR, et al. Among authors: visscher pm. Twin Res Hum Genet. 2007 Oct;10(5):695-702. doi: 10.1375/twin.10.5.695. Twin Res Hum Genet. 2007. PMID: 17903109

4

Highly cost-efficient genome-wide association studies using DNA pools and dense SNP arrays.

Macgregor S, Zhao ZZ, Henders A, Nicholas MG, Montgomery GW, Visscher PM. Macgregor S, et al. Among authors: visscher pm. Nucleic Acids Res. 2008 Apr;36(6):e35. doi: 10.1093/nar/gkm1060. Epub 2008 Feb 14. Nucleic Acids Res. 2008. PMID: 18276640 Free PMC article.

5

Heritability in the genomics era--concepts and misconceptions.

Visscher PM, Hill WG, Wray NR. Visscher PM, et al. Nat Rev Genet. 2008 Apr;9(4):255-66. doi: 10.1038/nrg2322. Epub 2008 Mar 4. Nat Rev Genet. 2008. PMID: 18319743 Review.

6

Genome-wide linkage analysis of multiple measures of neuroticism of 2 large cohorts from Australia and the Netherlands.

Wray NR, Middeldorp CM, Birley AJ, Gordon SD, Sullivan PF, Visscher PM, Nyholt DR, Willemsen G, de Geus EJ, Slagboom PE, Montgomery GW, Martin NG, Boomsma DI. Wray NR, et al. Among authors: visscher pm. Arch Gen Psychiatry. 2008 Jun;65(6):649-58. doi: 10.1001/archpsyc.65.6.649. Arch Gen Psychiatry. 2008. PMID: 18519823 Free PMC article.

7

The use of common mitochondrial variants to detect and characterise population structure in the Australian population: implications for genome-wide association studies.

Byrne EM, McRae AF, Zhao ZZ, Martin NG, Montgomery GW, Visscher PM. Byrne EM, et al. Among authors: visscher pm. Eur J Hum Genet. 2008 Nov;16(11):1396-403. doi: 10.1038/ejhg.2008.117. Epub 2008 Jul 9. Eur J Hum Genet. 2008. PMID: 18612324

8

Prediction of individual genetic risk of complex disease.

Wray NR, Goddard ME, Visscher PM. Wray NR, et al. Among authors: visscher pm. Curr Opin Genet Dev. 2008 Jun;18(3):257-63. doi: 10.1016/j.gde.2008.07.006. Epub 2008 Aug 28. Curr Opin Genet Dev. 2008. PMID: 18682292 Review.

9

Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.

Benyamin B, McRae AF, Zhu G, Gordon S, Henders AK, Palotie A, Peltonen L, Martin NG, Montgomery GW, Whitfield JB, Visscher PM. Benyamin B, et al. Among authors: visscher pm. Am J Hum Genet. 2009 Jan;84(1):60-5. doi: 10.1016/j.ajhg.2008.11.011. Epub 2008 Dec 11. Am J Hum Genet. 2009. PMID: 19084217 Free PMC article.

10

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk.

Evans DM, Visscher PM, Wray NR. Evans DM, et al. Among authors: visscher pm. Hum Mol Genet. 2009 Sep 15;18(18):3525-31. doi: 10.1093/hmg/ddp295. Epub 2009 Jun 24. Hum Mol Genet. 2009. PMID: 19553258

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