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23篇 您的检索式：作者名="PLAGNOL V"

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	题名	作者	年代	出处	被引量
1	Markov chain Monte Carlo without likelihoods显示文摘	Majoram P Molitor J Plagnol V	2003	Proc Natl Acad Sci2003，1，00：	1
2	Recombination and linkage disequilibrium in Arabidopsis thaliana显示文摘	KIM S PLAGNOL V HUT T	2007	Nat Genet2007，39，8：	1
3	Possible ancestral structure in human populations 显示文摘	Plagnol V Wall JD	2006	PLoS Genet2006，2，：	1
4	Imputation of sequence variants for identification of genetic risks for Parkinson's disease:a meta-analysis of genome-wide association studies显示文摘	Nalls MA Plagnol V Hernandez DG		0，，9766：	1
5	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: A recta-analysis of genome-wide association stud- ies显示文摘	International Parkinson Disease Genomics C Nails M A Plagnol V	2011	The Lancet2011，377，9766：	1
6	Imputation of sequence variants for identification of genetic risks for Parkinson' s disease: a meta-analysis of genome-wide association studies 显示文摘	International Parkinson Disease Genomics Consortium Nalls MA Plagnol V	2011	Lancet2011，377，9766：	1
7	Calculation of the population density in the low pressure mercury-argon discharge 显示文摘	Plagnol V Zissis G Bernat I	1993	J Phys Ⅲ1993，3，：	1
8	Imputation of sequence variants for identification of genetic risks for Parkinson's disease:a meta-analysis of genomewide association studies显示文摘	International Parkinson Disease Genomics Consortium Nalls MA Plagnol V	2011	Lancet2011，377，：	1
9	Use of targeted exome sequencing as diagnostic tool for familial hypereholesterolaemia 显示文摘	Futema M Plagnol V Whittall RA	2012	J Med Genet2012，49，10：	1
10	Mutations in ANO3 cause dominant craniocervical dystonia:ion channel implicated in pathogenesis显示文摘	Charlesworth G Plagnol V Holmstrom K M	2012	Am J Hum Genet2012，91，6：	1
11	Shared and distinct genetic variants in type I diabetes and celiac disease显示文摘	Smyth DJ Plagnol V Walker NM	2008	N Engl J Med2008，359，26：	1
12	Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21 显示文摘	Spencer CC Plagnol V Strange A	2011	HumMol Genet2011，20，2：	1
13	Shared and distinct genetic variants in type 1 diabetes and celiac disease显示文摘	Smyth DJ Plagnol V Walker NM		0，，26：	1
14	Biallelic mutations in the autophagy regulator DRAM2 cause retinal dystrophy with ear- ly macular involvement 显示文摘	EL-ASRAG ME SERGOUNIOTIS PI MCKIBBIN M PLAGNOL V SHERIDAN E WASEEM N	2015	Am J Hum Genet2015，96，6：	1
15	Dissection of the genetics of Parkinson's disease identifies an additional association 5 'of SNCA and multiple associated haplotypes at 17q21 显示文摘	Spencer CC Plagnol V Strange A	2011	Hum MolGenet2011，20，2：	1
16	A robust model for read count data in exome sequencing experiments and implications for copy number variant calling 显示文摘	Plagnol V Curtis J Epstein M	2012	Bioinformatics2012，28，21：	1
17	Targeted sequence capture and high throughput sequencing in the molecular diagnosis of ichthyosis and other skin diseases 显示文摘	SCOTT CA PLAGNOL V NITOIU D	2013	J Invest Dermato12013，133，2：	1
18	Use of larget<(J exome sequen-cing as diagnostic tool for familial hypercholesterola<mia 显示文摘	Futema M Plagnol V Whittall HA	2012	J Med( enet2012，49，10：	1
19	Imputation of sequence variants for identification of genetic risks for Parkinson's disease : a Meta-analysis of genome- wide association studies显示文摘	International Parkinson Disease Genomics Consortium Nails MA Plagnol V	2011	Lancet2011，377，：	1
20	Exome sequencing identifies MPL as a causative gene in familial aplastic anemia显示文摘	Walne AJ Dokal A Plagnol V	2012	Haematologica2012，97，：	1

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