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Daniel Weeks - Publications

Affiliations: 
University of California, Los Angeles, Los Angeles, CA 
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38 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Weeks DE, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084  0.308
2021 Hindy G, Dornbos P, Chaffin MD, Liu DJ, Wang M, Selvaraj MS, Zhang D, Park J, Aguilar-Salinas CA, Antonacci-Fulton L, Ardissino D, Arnett DK, Aslibekyan S, Atzmon G, Ballantyne CM, ... ... Weeks DE, et al. Rare coding variants in 35 genes associate with circulating lipid levels-A multi-ancestry analysis of 170,000 exomes. American Journal of Human Genetics. PMID 34932938 DOI: 10.1016/j.ajhg.2021.11.021  0.434
2021 Kwong AM, Blackwell TW, LeFaive J, de Andrade M, Barnard J, Barnes KC, Blangero J, Boerwinkle E, Burchard EG, Cade BE, Chasman DI, Chen H, Conomos MP, Cupples LA, Ellinor PT, ... ... Weeks DE, et al. Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries. Genetics. PMID 33720349 DOI: 10.1093/genetics/iyab044  0.449
2021 Taliun D, Harris DN, Kessler MD, Carlson J, Szpiech ZA, Torres R, Taliun SAG, Corvelo A, Gogarten SM, Kang HM, Pitsillides AN, LeFaive J, Lee SB, Tian X, Browning BL, ... ... Weeks DE, et al. Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 590: 290-299. PMID 33568819 DOI: 10.1038/s41586-021-03205-y  0.472
2018 Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, et al. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genetic Epidemiology. PMID 30537345 DOI: 10.1002/Gepi.22177  0.519
2016 Chiu CY, Jung J, Chen W, Weeks DE, Ren H, Boehnke M, Amos CI, Liu A, Mills JL, Ting Lee ML, Xiong M, Fan R. Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models. European Journal of Human Genetics : Ejhg. PMID 28000696 DOI: 10.1038/Ejhg.2016.170  0.518
2016 Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genetic Epidemiology. PMID 27917525 DOI: 10.1002/Gepi.22014  0.51
2016 Fan R, Wang Y, Yan Q, Ding Y, Weeks DE, Lu Z, Ren H, Cook RJ, Xiong M, Swaroop A, Chew EY, Chen W. Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions. Genetic Epidemiology. PMID 26782979 DOI: 10.1002/Gepi.21947  0.304
2013 Fritsche LG, Chen W, Schu M, Yaspan BL, Yu Y, Thorleifsson G, Zack DJ, Arakawa S, Cipriani V, Ripke S, Igo RP, Buitendijk GH, Sim X, Weeks DE, Guymer RH, et al. Seven new loci associated with age-related macular degeneration. Nature Genetics. 45: 433-9, 439e1-2. PMID 23455636 DOI: 10.1038/Ng.2578  0.5
2011 Schäffer AA, Lemire M, Ott J, Lathrop GM, Weeks DE. Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees. Human Heredity. 71: 126-34. PMID 21734403 DOI: 10.1159/000324177  0.603
2011 He C, Weeks DE, Buyske S, Abecasis GR, Stewart WC, Matise TC. Enhanced genetic maps from family-based disease studies: population-specific comparisons. Bmc Medical Genetics. 12: 15. PMID 21247494 DOI: 10.1186/1471-2350-12-15  0.331
2008 Presson AP, Sobel EM, Pajukanta P, Plaisier C, Weeks DE, Aberg K, Papp JC. Merging microsatellite data: enhanced methodology and software to combine genotype data for linkage and association analysis. Bmc Bioinformatics. 9: 317. PMID 18644149 DOI: 10.1186/1471-2105-9-317  0.481
2007 Szatmari P, Paterson AD, Zwaigenbaum L, Roberts W, Brian J, Liu XQ, Vincent JB, Skaug JL, Thompson AP, Senman L, Feuk L, Qian C, Bryson SE, Jones MB, ... ... Weeks DE, et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics. 39: 319-28. PMID 17322880 DOI: 10.1038/Ng1985  0.306
2005 Barnby G, Abbott A, Sykes N, Morris A, Weeks DE, Mott R, Lamb J, Bailey AJ, Monaco AP. Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. American Journal of Human Genetics. 76: 950-66. PMID 15830322 DOI: 10.1086/430454  0.419
2005 Lamb JA, Barnby G, Bonora E, Sykes N, Bacchelli E, Blasi F, Maestrini E, Broxholme J, Tzenova J, Weeks D, Bailey AJ, Monaco AP. Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. Journal of Medical Genetics. 42: 132-7. PMID 15689451 DOI: 10.1136/Jmg.2004.025668  0.309
2004 Schmidt S, Scott WK, Postel EA, Agarwal A, Hauser ER, De La Paz MA, Gilbert JR, Weeks DE, Gorin MB, Haines JL, Pericak-Vance MA. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12. Bmc Genetics. 5: 18. PMID 15238159 DOI: 10.1186/1471-2156-5-18  0.307
2002 McGarvey S, Forrest W, Weeks D, Sun G, Smelser D, Tufa J, Viali S, Deka R. Human leptin locus (LEP) alleles and BMI in Samoans. International Journal of Obesity. 26: 783-788. PMID 12037648 DOI: 10.1038/Sj.Ijo.0801996  0.349
2001 Palferman S, Matthews N, Turner M, Moore J, Hervas A, Aubin A, Wallace S, Michelotti J, Wainhouse C, Paul A, Thompson E, Gupta R, Garner C, Murin M, Freitag C, ... ... Weeks D, et al. A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q and 16p American Journal of Human Genetics. 69: 570-581. PMID 11481586 DOI: 10.1086/323264  0.381
1999 Schaid DJ, Buetow K, Weeks DE, Wijsman E, Guo SW, Ott J, Dahl C. Discovery of cancer susceptibility genes: study designs, analytic approaches, and trends in technology. Journal of the National Cancer Institute. Monographs. 1-16. PMID 10854480 DOI: 10.1093/Oxfordjournals.Jncimonographs.A024219  0.453
1999 Marinov M, Matise TC, Lathrop GM, Weeks DE. A comparison of two algorithms, MultiMap and gene mapping system, for automated construction of genetic linkage maps. Genetic Epidemiology. 17: S649-54. PMID 10597508 DOI: 10.1002/Gepi.13701707106  0.505
1997 Julier C, Delépine M, Keavney B, Terwilliger J, Davis S, Weeks DE, Bui T, Jeunemaître X, Velho G, Froguel P, Ratcliffe P, Corvol P, Soubrier F, Lathrop GM. Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10. Human Molecular Genetics. 6: 2077-85. PMID 9328471 DOI: 10.1093/Hmg/6.12.2077  0.638
1997 Terwilliger JD, Shannon WD, Lathrop GM, Nolan JP, Goldin LR, Chase GA, Weeks DE. True and false positive peaks in genomewide scans: applications of length-biased sampling to linkage mapping. American Journal of Human Genetics. 61: 430-8. PMID 9311749 DOI: 10.1086/514855  0.666
1996 O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nature Genetics. 11: 402-8. PMID 7493020 DOI: 10.1038/ng1295-402  0.32
1995 Weeks DE, Nygaard TG, Neystat M, Harby LD, Wilhelmsen KC. A high-resolution genetic linkage map of the pericentromeric region of the human X chromosome Genomics. 26: 39-46. PMID 7782084 DOI: 10.1016/0888-7543(95)80080-6  0.301
1994 Weeks DE, Ott J, Lathrop GM. Detection of genetic interference: simulation studies and mouse data. Genetics. 136: 1217-26. PMID 8005426  0.609
1994 Weeks DE, Lange K. Trials, tribulations, and triumphs of the EM algorithm in pedigree analysis. Ima Journal of Mathematics Applied in Medicine and Biology. 6: 209-32. PMID 2577997 DOI: 10.1093/imammb/6.4.209  0.483
1993 Weeks DE, Lathrop GM, Ott J. Multipoint mapping under genetic interference. Human Heredity. 43: 86-97. PMID 8359820  0.638
1993 Nygaard TG, Wilhelmsen KC, Risch NJ, Brown DL, Trugman JM, Gilliam TC, Fahn S, Weeks DE. Linkage mapping of dopa-responsive dystonia (DRD) to chromosome 14q. Nature Genetics. 5: 386-91. PMID 8298648 DOI: 10.1038/ng1293-386  0.514
1992 Weeks DE, Lehner T, Ott J. Preliminary ranking procedures for multilocus ordering based on radiation hybrid data. Cytogenetics and Cell Genetics. 59: 125-7. PMID 1737477 DOI: 10.1159/000133222  0.383
1991 Weeks DE, Paterson MC, Lange K, Andrais B, Davis RC, Yoder F, Gatti RA. Assessment of Chronic γ Radiosensitivity as an in Vitro Assay for Heterozygote Identification of Ataxia-Telangiectasia Radiation Research. 128: 90. DOI: 10.2307/3578071  0.428
1990 Charmley P, Foroud T, Wei S, Concannon P, Weeks DE, Lange K, Gatti RA. A primary linkage map of the human chromosome 11q22-23 region Genomics. 6: 316-323. PMID 2307473 DOI: 10.1016/0888-7543(90)90572-C  0.561
1990 Weeks DE, Lehner T, Squires-Wheeler E, Kaufmann C, Ott J. Measuring the inflation of the lod score due to its maximization over model parameter values in human linkage analysis. Genetic Epidemiology. 7: 237-43. PMID 2227370 DOI: 10.1002/Gepi.1370070402  0.497
1990 Lange K, Weeks DE. Linkage methods for identifying genetic risk factors. World Review of Nutrition and Dietetics. 63: 236-49. PMID 2197801 DOI: 10.1159/000418512  0.502
1990 Weeks DE, Brzustowicz L, Squires-Wheeler E, Cornblatt B, Lehner T, Stefanovich M, Bassett A, Gilliam TC, Ott J, Erlenmeyer-Kimling L. Report of a workshop on genetic linkage studies in schizophrenia. Schizophrenia Bulletin. 16: 673-86. PMID 2077644 DOI: 10.1093/Schbul/16.4.673  0.439
1989 Lange K, Weeks D, Boehnke M. Programs for Pedigree Analysis: MENDEL, FISHER, and dGENE. Genetic Epidemiology. 5: 471-2. PMID 3061869 DOI: 10.1002/Gepi.1370050611  0.57
1989 Weeks DE, Ott J. Risk calculations under heterogeneity. American Journal of Human Genetics. 45: 819-21. PMID 2816945  0.355
1989 Lange K, Weeks DE. Efficient computation of lod scores: genotype elimination, genotype redefinition, and hybrid maximum likelihood algorithms. Annals of Human Genetics. 53: 67-83. PMID 2729896 DOI: 10.1111/j.1469-1809.1989.tb01122.x  0.531
1988 Weeks DE, Lange K. Preliminary ranking procedures for multilocus ordering. Genomics. 1: 236-42. PMID 3446584 DOI: 10.1016/0888-7543(87)90050-4  0.471
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