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6. Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Zheng HF; Forgetta V; Hsu YH; Estrada K; Rosello-Diez A; Leo PJ; Dahia CL; Park-Min KH; Tobias JH; Kooperberg C; Kleinman A; Styrkarsdottir U; Liu CT; Uggla C; Evans DS; Nielson CM; Walter K; Pettersson-Kymmer U; McCarthy S; Eriksson J; Kwan T; Jhamai M; Trajanoska K; Memari Y; Min J; Huang J; Danecek P; Wilmot B; Li R; Chou WC; Mokry LE; Moayyeri A; Claussnitzer M; Cheng CH; Cheung W; Medina-Gómez C; Ge B; Chen SH; Choi K; Oei L; Fraser J; Kraaij R; Hibbs MA; Gregson CL; Paquette D; Hofman A; Wibom C; Tranah GJ; Marshall M; Gardiner BB; Cremin K; Auer P; Hsu L; Ring S; Tung JY; Thorleifsson G; Enneman AW; van Schoor NM; de Groot LC; van der Velde N; Melin B; Kemp JP; Christiansen C; Sayers A; Zhou Y; Calderari S; van Rooij J; Carlson C; Peters U; Berlivet S; Dostie J; Uitterlinden AG; Williams SR; Farber C; Grinberg D; LaCroix AZ; Haessler J; Chasman DI; Giulianini F; Rose LM; Ridker PM; Eisman JA; Nguyen TV; Center JR; Nogues X; Garcia-Giralt N; Launer LL; Gudnason V; Mellström D; Vandenput L; Amin N; van Duijn CM; Karlsson MK; Ljunggren Ö; Svensson O; Hallmans G; Rousseau F; Giroux S; Bussière J; Arp PP; Koromani F; Prince RL; Lewis JR; Langdahl BL; Hermann AP; Jensen JE; Kaptoge S; Khaw KT; Reeve J; Formosa MM; Xuereb-Anastasi A; Åkesson K; McGuigan FE; Garg G; Olmos JM; Zarrabeitia MT; Riancho JA; Ralston SH; Alonso N; Jiang X; Goltzman D; Pastinen T; Grundberg E; Gauguier D; Orwoll ES; Karasik D; Davey-Smith G; ; Smith AV; Siggeirsdottir K; Harris TB; Zillikens MC; van Meurs JB; Thorsteinsdottir U; Maurano MT; Timpson NJ; Soranzo N; Durbin R; Wilson SG; Ntzani EE; Brown MA; Stefansson K; Hinds DA; Spector T; Cupples LA; Ohlsson C; Greenwood CM; ; Jackson RD; Rowe DW; Loomis CA; Evans DM; Ackert-Bicknell CL; Joyner AL; Duncan EL; Kiel DP; Rivadeneira F; Richards JB Nature; 2015 Oct; 526(7571):112-7. PubMed ID: 26367794 [TBL] [Abstract][Full Text] [Related]
7. Sequencing and imputation in GWAS: Cost-effective strategies to increase power and genomic coverage across diverse populations. Quick C; Anugu P; Musani S; Weiss ST; Burchard EG; White MJ; Keys KL; Cucca F; Sidore C; Boehnke M; Fuchsberger C Genet Epidemiol; 2020 Sep; 44(6):537-549. PubMed ID: 32519380 [TBL] [Abstract][Full Text] [Related]
8. Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies. Joshi PK; Prendergast J; Fraser RM; Huffman JE; Vitart V; Hayward C; McQuillan R; Glodzik D; Polašek O; Hastie ND; Rudan I; Campbell H; Wright AF; Haley CS; Wilson JF; Navarro P PLoS One; 2013; 8(7):e68604. PubMed ID: 23874685 [TBL] [Abstract][Full Text] [Related]
9. Improving power of association tests using multiple sets of imputed genotypes from distributed reference panels. Zhou W; Fritsche LG; Das S; Zhang H; Nielsen JB; Holmen OL; Chen J; Lin M; Elvestad MB; Hveem K; Abecasis GR; Kang HM; Willer CJ Genet Epidemiol; 2017 Dec; 41(8):744-755. PubMed ID: 28861891 [TBL] [Abstract][Full Text] [Related]
10. Unique roles of rare variants in the genetics of complex diseases in humans. Momozawa Y; Mizukami K J Hum Genet; 2021 Jan; 66(1):11-23. PubMed ID: 32948841 [TBL] [Abstract][Full Text] [Related]
11. Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers. Sidore C; Busonero F; Maschio A; Porcu E; Naitza S; Zoledziewska M; Mulas A; Pistis G; Steri M; Danjou F; Kwong A; Ortega Del Vecchyo VD; Chiang CWK; Bragg-Gresham J; Pitzalis M; Nagaraja R; Tarrier B; Brennan C; Uzzau S; Fuchsberger C; Atzeni R; Reinier F; Berutti R; Huang J; Timpson NJ; Toniolo D; Gasparini P; Malerba G; Dedoussis G; Zeggini E; Soranzo N; Jones C; Lyons R; Angius A; Kang HM; Novembre J; Sanna S; Schlessinger D; Cucca F; Abecasis GR Nat Genet; 2015 Nov; 47(11):1272-1281. PubMed ID: 26366554 [TBL] [Abstract][Full Text] [Related]
12. Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Wood AR; Perry JR; Tanaka T; Hernandez DG; Zheng HF; Melzer D; Gibbs JR; Nalls MA; Weedon MN; Spector TD; Richards JB; Bandinelli S; Ferrucci L; Singleton AB; Frayling TM PLoS One; 2013; 8(5):e64343. PubMed ID: 23696881 [TBL] [Abstract][Full Text] [Related]
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14. Whole-genome sequence variation, population structure and demographic history of the Dutch population. Genome of the Netherlands Consortium Nat Genet; 2014 Aug; 46(8):818-25. PubMed ID: 24974849 [TBL] [Abstract][Full Text] [Related]
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16. Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation. Gilly A; Ritchie GR; Southam L; Farmaki AE; Tsafantakis E; Dedoussis G; Zeggini E Hum Mol Genet; 2016 Jun; 25(11):2360-2365. PubMed ID: 27146844 [TBL] [Abstract][Full Text] [Related]
17. Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Nagy R; Boutin TS; Marten J; Huffman JE; Kerr SM; Campbell A; Evenden L; Gibson J; Amador C; Howard DM; Navarro P; Morris A; Deary IJ; Hocking LJ; Padmanabhan S; Smith BH; Joshi P; Wilson JF; Hastie ND; Wright AF; McIntosh AM; Porteous DJ; Haley CS; Vitart V; Hayward C Genome Med; 2017 Mar; 9(1):23. PubMed ID: 28270201 [TBL] [Abstract][Full Text] [Related]
18. Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations. Xue Y; Mezzavilla M; Haber M; McCarthy S; Chen Y; Narasimhan V; Gilly A; Ayub Q; Colonna V; Southam L; Finan C; Massaia A; Chheda H; Palta P; Ritchie G; Asimit J; Dedoussis G; Gasparini P; Palotie A; Ripatti S; Soranzo N; Toniolo D; Wilson JF; Durbin R; Tyler-Smith C; Zeggini E Nat Commun; 2017 Jun; 8():15927. PubMed ID: 28643794 [TBL] [Abstract][Full Text] [Related]
19. Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. Deelen P; Menelaou A; van Leeuwen EM; Kanterakis A; van Dijk F; Medina-Gomez C; Francioli LC; Hottenga JJ; Karssen LC; Estrada K; Kreiner-Møller E; Rivadeneira F; van Setten J; Gutierrez-Achury J; Westra HJ; Franke L; van Enckevort D; Dijkstra M; Byelas H; van Duijn CM; ; de Bakker PI; Wijmenga C; Swertz MA Eur J Hum Genet; 2014 Nov; 22(11):1321-6. PubMed ID: 24896149 [TBL] [Abstract][Full Text] [Related]
20. Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging. Surakka I; Kristiansson K; Anttila V; Inouye M; Barnes C; Moutsianas L; Salomaa V; Daly M; Palotie A; Peltonen L; Ripatti S Genome Res; 2010 Oct; 20(10):1344-51. PubMed ID: 20810666 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]