James L. Weber - Publications

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26 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
2011 Gallione CJ, Solatycki A, Awad IA, Weber JL, Marchuk DA. A founder mutation in the Ashkenazi Jewish population affecting messenger RNA splicing of the CCM2 gene causes cerebral cavernous malformations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 13: 662-6. PMID 21543988 DOI: 10.1097/GIM.0b013e318211ff8b  0.76
2009 Tishkoff SA, Reed FA, Friedlaender FR, Ehret C, Ranciaro A, Froment A, Hirbo JB, Awomoyi AA, Bodo JM, Doumbo O, Ibrahim M, Juma AT, Kotze MJ, Lema G, Moore JH, ... ... Weber JL, et al. The genetic structure and history of Africans and African Americans. Science (New York, N.Y.). 324: 1035-44. PMID 19407144 DOI: 10.1126/Science.1172257  0.76
2009 Raggio CL, Giampietro PF, Dobrin S, Zhao C, Dorshorst D, Ghebranious N, Weber JL, Blank RD. A novel locus for adolescent idiopathic scoliosis on chromosome 12p. Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society. 27: 1366-72. PMID 19340878 DOI: 10.1002/jor.20885  0.76
2009 Sammalisto S, Hiekkalinna T, Schwander K, Kardia S, Weder AB, Rodriguez BL, Doria A, Kelly JA, Bruner GR, Harley JB, Redline S, Larkin EK, Patel SR, Ewan AJ, Weber JL, et al. Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects. European Journal of Human Genetics : Ejhg. 17: 258-66. PMID 18781184 DOI: 10.1038/Ejhg.2008.152  0.76
2008 Payseur BA, Place M, Weber JL. Linkage disequilibrium between STRPs and SNPs across the human genome. American Journal of Human Genetics. 82: 1039-50. PMID 18423524 DOI: 10.1016/J.Ajhg.2008.02.018  0.76
2008 Rudan I, Carothers AD, Polasek O, Hayward C, Vitart V, Biloglav Z, Kolcic I, Zgaga L, Ivankovic D, Vorko-Jovic A, Wilson JF, Weber JL, Hastie N, Wright A, Campbell H. Quantifying the increase in average human heterozygosity due to urbanisation. European Journal of Human Genetics : Ejhg. 16: 1097-102. PMID 18322453 DOI: 10.1038/ejhg.2008.48  0.76
2008 Betanzos-Cabrera G, Harker BW, Doktycz MJ, Weber JL, Beattie KL. Channel glass-based detection of human short insertion/deletion polymorphisms by tandem hybridization. Molecular Biotechnology. 38: 145-53. PMID 18219594 DOI: 10.1007/s12033-007-9004-9  0.76
2008 Friedlaender JS, Friedlaender FR, Reed FA, Kidd KK, Kidd JR, Chambers GK, Lea RA, Loo JH, Koki G, Hodgson JA, Merriwether DA, Weber JL. The genetic structure of Pacific Islanders. Plos Genetics. 4: e19. PMID 18208337 DOI: 10.1371/Journal.Pgen.0040019  0.76
2008 Betanzos-Cabrera G, Harker BW, Doktycz MJ, Weber JL, Beattie KL. A comparison of hybridization efficiency between flat glass and channel glass solid supports. Molecular Biotechnology. 38: 71-80. PMID 18095192 DOI: 10.1007/s12033-007-9001-z  0.76
2007 Campbell H, Carothers AD, Rudan I, Hayward C, Biloglav Z, Barac L, Pericic M, Janicijevic B, Smolej-Narancic N, Polasek O, Kolcic I, Weber JL, Hastie ND, Rudan P, Wright AF. Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits. Human Molecular Genetics. 16: 233-41. PMID 17220173 DOI: 10.1093/hmg/ddl473  0.76
2006 Rosenberg NA, Mahajan S, Gonzalez-Quevedo C, Blum MG, Nino-Rosales L, Ninis V, Das P, Hegde M, Molinari L, Zapata G, Weber JL, Belmont JW, Patel PI. Low levels of genetic divergence across geographically and linguistically diverse populations from India. Plos Genetics. 2: e215. PMID 17194221 DOI: 10.1371/Journal.Pgen.0020215  0.76
2006 Doggett NA, Xie G, Meincke LJ, Sutherland RD, Mundt MO, Berbari NS, Davy BE, Robinson ML, Rudd MK, Weber JL, Stallings RL, Han C. A 360-kb interchromosomal duplication of the human HYDIN locus. Genomics. 88: 762-71. PMID 16938426 DOI: 10.1016/j.ygeno.2006.07.012  0.76
2006 Weber JL. Clinical applications of Genome Polymorphism Scans. Biology Direct. 1: 16. PMID 16756678 DOI: 10.1186/1745-6150-1-16  0.76
2006 Xiao P, Liu P, Weber JL, Papasian CJ, Recker RR, Deng HW. Paternal uniparental isodisomy of the entire chromosome 3 revealed in a person with no apparent phenotypic disorders. Human Mutation. 27: 133-7. PMID 16429396 DOI: 10.1002/humu.20302  0.76
2006 Su Z, Li Y, James JC, McDuffie M, Matsumoto AH, Helm GA, Weber JL, Lusis AJ, Shi W. Quantitative trait locus analysis of atherosclerosis in an intercross between C57BL/6 and C3H mice carrying the mutant apolipoprotein E gene. Genetics. 172: 1799-807. PMID 16387874 DOI: 10.1534/Genetics.105.051912  0.76
2004 Niemann S, Zhao C, Pascu F, Stahl U, Aulepp U, Niswander L, Weber JL, Müller U. Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family. American Journal of Human Genetics. 74: 558-63. PMID 14872406 DOI: 10.1086/382196  0.76
2003 Horton R, Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW. Read all about it: The Lancet's Paper of the Year, 2003. Lancet. 362: 2101-3. PMID 14697815  0.76
2003 Ghebranious N, Vaske D, Yu A, Zhao C, Marth G, Weber JL. STRP screening sets for the human genome at 5 cM density. Bmc Genomics. 4: 6. PMID 12600278 DOI: 10.1186/1471-2164-4-6  0.76
2003 Ruf R, Rensing C, Topaloglu R, Guay-Woodford L, Klein C, Vollmer M, Otto E, Beekmann F, Haller M, Wiedensohler A, Leumann E, Antignac C, Rizzoni G, Filler G, Brandis M, ... Weber JL, et al. Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis. Pediatric Nephrology (Berlin, Germany). 18: 105-9. PMID 12579397 DOI: 10.1007/s00467-002-1018-8  0.76
2002 Rosenberg NA, Pritchard JK, Weber JL, Cann HM, Kidd KK, Zhivotovsky LA, Feldman MW. Genetic structure of human populations. Science (New York, N.Y.). 298: 2381-5. PMID 12493913 DOI: 10.1126/Science.1078311  0.76
2002 Collins-Schramm HE, Kittles RA, Operario DJ, Weber JL, Criswell LA, Cooper RS, Seldin MF. Markers that discriminate between European and African ancestry show limited variation within Africa. Human Genetics. 111: 566-9. PMID 12436248 DOI: 10.1007/S00439-002-0818-Z  0.76
2002 Weber JL, David D, Heil J, Fan Y, Zhao C, Marth G. Human diallelic insertion/deletion polymorphisms. American Journal of Human Genetics. 71: 854-62. PMID 12205564 DOI: 10.1086/342727  0.76
2002 Rosenberg MJ, Agarwala R, Bouffard G, Davis J, Fiermonte G, Hilliard MS, Koch T, Kalikin LM, Makalowska I, Morton DH, Petty EM, Weber JL, Palmieri F, Kelley RI, Schäffer AA, et al. Mutant deoxynucleotide carrier is associated with congenital microcephaly. Nature Genetics. 32: 175-9. PMID 12185364 DOI: 10.1038/Ng948  0.76
2002 Weber JL. The Iceland map. Nature Genetics. 31: 225-6. PMID 12053179 DOI: 10.1038/ng920  0.76
2002 Cann HM, de Toma C, Cazes L, Legrand MF, Morel V, Piouffre L, Bodmer J, Bodmer WF, Bonne-Tamir B, Cambon-Thomsen A, Chen Z, Chu J, Carcassi C, Contu L, Du R, ... ... Weber JL, et al. A human genome diversity cell line panel. Science (New York, N.Y.). 296: 261-2. PMID 11954565 DOI: 10.1126/Science.296.5566.261B  0.76
2002 Collins-Schramm HE, Phillips CM, Operario DJ, Lee JS, Weber JL, Hanson RL, Knowler WC, Cooper R, Li H, Seldin MF. Ethnic-difference markers for use in mapping by admixture linkage disequilibrium. American Journal of Human Genetics. 70: 737-50. PMID 11845411 DOI: 10.1086/339368  0.76
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