James L. Weber - Publications

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26/182 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
Low-probability matches
2015 Fisher OS, Liu W, Zhang R, Stiegler AL, Ghedia S, Weber JL, Boggon TJ. Structural basis for the disruption of the cerebral cavernous malformations 2 (CCM2) interaction with Krev interaction trapped 1 (KRIT1) by disease-associated mutations. The Journal of Biological Chemistry. 290: 2842-53. PMID 25525273 DOI: 10.1074/jbc.M114.616433  0.01
2014 Wu Y, Weber JL, Vladutiu GD, Tarnopolsky MA. Corrigendum to Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern [Mol. Genet. Metab. 104 (2011) 587-591] Molecular Genetics and Metabolism. 111: 539. DOI: 10.1016/j.ymgme.2014.02.006  0
2011 Wu Y, Weber JL, Vladutiu GD, Tarnopolsky MA. Six novel mutations in the myophosphorylase gene in patients with McArdle disease and a family with pseudo-dominant inheritance pattern. Molecular Genetics and Metabolism. 104: 587-91. PMID 21880526 DOI: 10.1016/j.ymgme.2011.08.012  0
2008 Ocaka L, Zhao C, Reed JA, Ebenezer ND, Brice G, Morley T, Mehta M, O'Dowd J, Weber JL, Hardcastle AJ, Child AH. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel. Journal of Medical Genetics. 45: 87-92. PMID 17932119 DOI: 10.1136/jmg.2007.051896  0
2008 Friedlaender JS, Friedlaender FR, Reed FA, Kidd KK, Kidd JR, Chambers GK, Lea RA, Loo J, Koki G, Hodgson JA, Merriwether DA, Weber JL. Correction: The Genetic Structure of Pacific Islanders Plos Genetics. 4. DOI: 10.1371/Annotation/Cbdd11A0-4A29-4E7C-9E4E-C00A184C7777  0
2006 Carothers AD, Rudan I, Kolcic I, Polasek O, Hayward C, Wright AF, Campbell H, Teague P, Hastie ND, Weber JL. Estimating human inbreeding coefficients: comparison of genealogical and marker heterozygosity approaches. Annals of Human Genetics. 70: 666-76. PMID 16907711 DOI: 10.1111/j.1469-1809.2006.00263.x  0
2006 Chudyk JP, Rusch TL, Fieweger KM, Dobrin SE, Weber JL. Automating Microsatellite Genotyping with Array Tape Jala - Journal of the Association For Laboratory Automation. 11: 260-267. DOI: 10.1016/j.jala.2006.05.007  0
2005 Giampietro PF, Raggio CL, Reynolds CE, Shukla SK, McPherson E, Ghebranious N, Jacobsen FS, Kumar V, Faciszewski T, Pauli RM, Rasmussen K, Burmester JK, Zaleski C, Merchant S, David D, Weber JL, et al. An analysis of PAX1 in the development of vertebral malformations. Clinical Genetics. 68: 448-53. PMID 16207213 DOI: 10.1111/j.1399-0004.2005.00520.x  0
2003 Rosenberg NA. Response to Comment on "Genetic Structure of Human Populations" Science. 300: 1877c-1877. DOI: 10.1126/Science.1084688  0
2003 Rusch TL, Dickinson W, Che J, Fieweger K, Chudyk J, Doktycz MJ, Yu A, Weber JL. Instrumentation for continuous array genotyping of short insertion/deletion polymorphisms Proceedings of Spie - the International Society For Optical Engineering. 4966: 138-145. DOI: 10.1117/12.483474  0
2003 Rusch TL, Dickinson W, Che J, Fieweger K, Chudyk J, Doktycz MJ, Yu A, Weber JL. Updated Instrumentation for Continuous Array Genotyping of Short Insertion/Deletion Polymorphisms Annual International Conference of the Ieee Engineering in Medicine and Biology - Proceedings. 4: 3582-3585.  0
2001 Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL. Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. American Journal of Medical Genetics. 105: 163-7. PMID 11304830 DOI: 10.1002/Ajmg.1192  0
2001 Yu A, Zhao C, Fan Y, Jang W, Mungall AJ, Deloukas P, Olsen A, Doggett NA, Ghebranious N, Broman KW, Weber JL. Comparison of human genetic and sequence-based physical maps. Nature. 409: 951-3. PMID 11237020 DOI: 10.1038/35057185  0
2001 Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T, Ohashi H, Voullaire L, Larizza D, Giorda R, Weber JL, Ledbetter DH, Zuffardi O. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. American Journal of Human Genetics. 68: 874-83. PMID 11231899 DOI: 10.1086/319506  0
2001 Weber JL, Broman KW. Genotyping for human whole-genome scans: past, present, and future. Advances in Genetics. 42: 77-96. PMID 11037315 DOI: 10.1016/S0065-2660(01)42016-5  0
2000 Matsumoto N, David DE, Johnson EW, Konecki D, Burmester JK, Ledbetter DH, Weber JL. Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndrome. European Journal of Human Genetics : Ejhg. 8: 875-83. PMID 11093278 DOI: 10.1038/Sj.Ejhg.5200549  0
2000 Witte JS, Goddard KA, Conti DV, Elston RC, Lin J, Suarez BK, Broman KW, Burmester JK, Weber JL, Catalona WJ. Genomewide scan for prostate cancer-aggressiveness loci. American Journal of Human Genetics. 67: 92-9. PMID 10825281 DOI: 10.1086/302960  0
2000 Broman KW, Weber JL. Characterization of human crossover interference. American Journal of Human Genetics. 66: 1911-26. PMID 10801387 DOI: 10.1086/302923  0
2000 Ehm MG, Karnoub MC, Sakul H, Gottschalk K, Holt DC, Weber JL, Vaske D, Briley D, Briley L, Kopf J, McMillen P, Nguyen Q, Reisman M, Lai EH, Joslyn G, et al. Genomewide search for type 2 diabetes susceptibility genes in four American populations. American Journal of Human Genetics. 66: 1871-81. PMID 10793009 DOI: 10.1086/302950  0
2000 Yuan B, Neuman R, Duan SH, Weber JL, Kwok PY, Saccone NL, Wu JS, Liu KY, Schonfeld G. Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22. American Journal of Human Genetics. 66: 1699-704. PMID 10762553 DOI: 10.1086/302904  0
2000 Suarez BK, Lin J, Burmester JK, Broman KW, Weber JL, Banerjee TK, Goddard KA, Witte JS, Elston RC, Catalona WJ. A genome screen of multiplex sibships with prostate cancer. American Journal of Human Genetics. 66: 933-44. PMID 10712208 DOI: 10.1086/302818  0
2000 Rosenberg MJ, Vaske D, Killoran CE, Ning Y, Wargowski D, Hudgins L, Tifft CJ, Meck J, Blancato JK, Rosenbaum K, Pauli RM, Weber J, Biesecker LG. Detection of chromosomal aberrations by a whole-genome microsatellite screen American Journal of Human Genetics. 66: 419-427. PMID 10677301 DOI: 10.1086/302743  0
1999 Broman KW, Weber JL. Long homozygous chromosomal segments in reference families from the centre d'Etude du polymorphisme humain. American Journal of Human Genetics. 65: 1493-500. PMID 10577902 DOI: 10.1086/302661  0
1999 Broman KW, Weber JL. Method for constructing confidently ordered linkage maps. Genetic Epidemiology. 16: 337-43. PMID 10207715 DOI: 10.1002/(Sici)1098-2272(1999)16:4<337::Aid-Gepi1>3.0.Co;2-T  0
1998 Broman KW, Weber JL. Estimation of pairwise relationships in the presence of genotyping errors. American Journal of Human Genetics. 63: 1563-4. PMID 9792888 DOI: 10.1086/302112  0
1998 Hizawa N, Collins G, Rafnar T, Huang SK, Duffy DL, Weber JL, Freidhoff LR, Ehrlich E, Marsh DG, Beaty TH, Barnes KC. Linkage analysis of Dermatophagoides pteronyssinus-specific IgE responsiveness with polymorphic markers on chromosome 6p21 (HLA-D region) in Caucasian families by the transmission/disequilibrium test. Collaborative Study on the Genetics of Asthma (CSGA). The Journal of Allergy and Clinical Immunology. 102: 443-8. PMID 9768586 DOI: 10.1016/S0091-6749(98)70133-2  0
1998 Hizawa N, Freidhoff LR, Chiu YF, Ehrlich E, Luehr CA, Anderson JL, Duffy DL, Dunston GM, Weber JL, Huang SK, Barnes KC, Marsh DG, Beaty TH. Genetic regulation of Dermatophagoides pteronyssinus-specific IgE responsiveness: a genome-wide multipoint linkage analysis in families recruited through 2 asthmatic sibs. Collaborative Study on the Genetics of Asthma (CSGA). The Journal of Allergy and Clinical Immunology. 102: 436-42. PMID 9768585 DOI: 10.1016/S0091-6749(98)70132-0  0
1998 Broman KW, Murray JC, Sheffield VC, White RL, Weber JL. Comprehensive human genetic maps: individual and sex-specific variation in recombination. American Journal of Human Genetics. 63: 861-9. PMID 9718341 DOI: 10.1086/302011  0
1998 Simonic I, Gericke GS, Ott J, Weber JL. Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. American Journal of Human Genetics. 63: 839-46. PMID 9718333 DOI: 10.1086/302002  0
1998 Fenske CD, Jeffery S, Weber JL, Houlston RS, Leonard JV, Lee PJ. Localisation of the gene for glycogen storage disease type 1c by homozygosity mapping to 11q. Journal of Medical Genetics. 35: 269-72. PMID 9598717 DOI: 10.1136/jmg.35.4.269  0
1998 Finckh U, Xu S, Kumaramanickavel G, Schürmann M, Mukkadan JK, Fernandez ST, John S, Weber JL, Denton MJ, Gal A. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3. Genomics. 48: 341-5. PMID 9545639 DOI: 10.1006/Geno.1997.5194  0
1998 Stone DL, Agarwala R, Schäffer AA, Weber JL, Vaske D, Oda T, Chandrasekharappa SC, Francomano CA, Biesecker LG. Genetic and physical mapping of the McKusick-Kaufman syndrome. Human Molecular Genetics. 7: 475-81. PMID 9467007 DOI: 10.1093/hmg/7.3.475  0
1998 Gleeson CM, Sloan JM, McGuigan JA, Ritchie AJ, Weber JL, Russell SE. Barrett's oesophagus: microsatellite analysis provides evidence to support the proposed metaplasia-dysplasia-carcinoma sequence. Genes, Chromosomes & Cancer. 21: 49-60. PMID 9443041 DOI: 10.1002/(SICI)1098-2264(199801)21:1<49::AID-GCC7>3.0.CO;2-8  0
1998 Johnson EW, Dubovsky J, Rich SS, O'Donovan CA, Orr HT, Anderson VE, Gil-Nagel A, Ahmann P, Dokken CG, Schneider DT, Weber JL. Evidence for a novel gene for familial febrile convulsions, FEB2, linked to chromosome 19p in an extended family from the Midwest. Human Molecular Genetics. 7: 63-7. PMID 9384604 DOI: 10.1093/Hmg/7.1.63  0
1997 Gleeson CM, Sloan JM, McGuigan JA, Ritchie AJ, Weber JL, Russell SE. Allelotype analysis of adenocarcinoma of the gastric cardia. British Journal of Cancer. 76: 1455-65. PMID 9400942  0
1997 Weber JL, Myers EW. Human whole-genome shotgun sequencing. Genome Research. 7: 401-9. PMID 9149936 DOI: 10.1101/Gr.7.5.401  0
1997 Marsh DG, Maestri NE, Freidhoff LR, Barnes KC, Togias A, Ehrlich E, Beaty T, Duffy D, Rosenthal R, Imani F, Dunston G, Furbert-Harris P, Malveaux F, Ober C, Cox NJ, ... Weber JL, et al. A genome-wide search for asthma susceptibility loci in ethnically diverse populations Nature Genetics. 15: 389-392. PMID 9090385 DOI: 10.1038/Ng0497-389  0
1996 Mohrenweiser H, Olsen A, Archibald A, Beattie C, Burmeister M, Lamerdin J, Lennon G, Stewart E, Stubbs L, Weber JL, Johnson K. Report an abstracts of the third international workshop on human chromosome 19 mapping 1996. Cytogenetics and Cell Genetics. 74: 161-86. PMID 8941368 DOI: 10.1159/000134408  0
1996 Endo K, Sasaki H, Wakisaka A, Tanaka H, Saito M, Igarashi S, Takiyama Y, Sanpei K, Iwabuchi K, Suzuki Y, Onari K, Suzuki T, Weissenbach J, Weber JL, Nomura Y, et al. Strong linkage disequilibrium and haplotype analysis in Japanese pedigrees with Machado-Joseph disease. American Journal of Medical Genetics. 67: 437-44. PMID 8886159 DOI: 10.1002/(SICI)1096-8628(19960920)67:5<437::AID-AJMG1>3.0.CO;2-H  0
1996 Sunden SL, Businga T, Beck J, McClain A, Gastier JM, Pulido JC, Yandava CN, Brody T, Ghazizadeh J, Weber JL, Duyk GM, Murray JC, Buetow KH, Sheffield VC. Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2. Genomics. 32: 15-20. PMID 8786107 DOI: 10.1006/Geno.1996.0071  0
1996 Gil-Nagel A, Dubovsky J, Wilcox KJ, Stewart JM, Anderson VE, Leppik IE, Orr HT, Johnson EW, Weber JL, Rich SS. Familial cerebral cavernous angioma: a gene localized to a 15-cM interval on chromosome 7q. Annals of Neurology. 39: 807-10. PMID 8651655 DOI: 10.1002/Ana.410390619  0
1996 BLUMENTHAL MN, WANG Z, WEBER JL, RICH SS. Absence of linkage between 5q markers and serum IgE levels in four large atopic families Clinical Experimental Allergy. 26: 892-896. DOI: 10.1111/j.1365-2222.1996.tb00623.x  0
1996 Rusch TL, Petsinger J, Christensen C, Vaske DA, Brumley RL, Luckey JA, Weber JL. Scanning fluorescence detector for high-throughput DNA genotyping Proceedings of Spie - the International Society For Optical Engineering. 2680: 316-325.  0
1995 Johnson EW, Iyer LM, Rich SS, Orr HT, Gil-Nagel A, Kurth JH, Zabramski JM, Marchuk DA, Weissenbach J, Clericuzio CL, Davis LE, Hart BL, Gusella JF, Kosofsky BE, Louis DN, ... Weber JL, et al. Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig. Genome Research. 5: 368-80. PMID 8750196 DOI: 10.1101/Gr.5.4.368  0
1995 Sheffield VC, Weber JL, Buetow KH, Murray JC, Even DA, Wiles K, Gastier JM, Pulido JC, Yandava C, Sunden SL, Mattes G, Businga T, Mcclain A, Beck J, Scherpler T, et al. A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps Human Molecular Genetics. 4: 1837-1844. PMID 8595404 DOI: 10.1093/Hmg/4.10.1837  0
1995 Gastier JM, Pulido JC, Sunden S, Brody T, Buetow KH, Murray JC, Weber JL, Hudson TJ, Sheffield VC, Duyk GM. Survey of trinucleotide repeats in the human genome: Assessment of their utility as genetic markers Human Molecular Genetics. 4: 1829-1836. PMID 8595403 DOI: 10.1093/Hmg/4.10.1829  0
1995 Christodoulou K, Kyriakides T, Hristova AH, Georgiou DM, Kalaydjieva L, Yshpekova B, Ivanova T, Weber JL, Middleton LT. Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p. Human Molecular Genetics. 4: 1629-32. PMID 8541851 DOI: 10.1093/hmg/4.9.1629  0
1995 Arcot SS, Wang Z, Weber JL, Deininger PL, Batzer MA. Alu repeats: a source for the genesis of primate microsatellites. Genomics. 29: 136-44. PMID 8530063 DOI: 10.1006/Geno.1995.1224  0
1995 Fossdal R, Magnússon L, Weber JL, Jensson O. Mapping the locus of atrophia areata, a helicoid peripapillary chorioretinal degeneration with autosomal dominant inheritance, to chromosome 11p15 Human Molecular Genetics. 4: 479-483. PMID 7795606 DOI: 10.1093/hmg/4.3.479  0
1995 Dubovsky J, Zabramski JM, Kurth J, Spetzler RF, Rich SS, Orr HT, Weber JL. A gene responsible for cavernous malformations of the brain maps to chromosome 7q. Human Molecular Genetics. 4: 453-8. PMID 7795602 DOI: 10.1093/Hmg/4.3.453  0
1995 Dubovsky J, Sheffield VC, Duyk GM, Weber JL. Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome Human Molecular Genetics. 4: 449-452. PMID 7795601 DOI: 10.1093/Hmg/4.3.449  0
1995 Morell R, Liang Y, Asher JH, Weber JL, Hinnant JT, Winata S, Arhya IN, Friedman TB. Analysis of short tandem repeat (STR) allele frequency distributions in a Balinese population Human Molecular Genetics. 4: 85-91. PMID 7711738  0
1995 Friedman TB, Liang Y, Weber JL, Hinnant JT, Barber TD, Winata S, Arhya IN, Asher JH. A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17 Nature Genetics. 9: 86-91. PMID 7704031 DOI: 10.1038/Ng0195-86  0
1995 Cox DW, Billingsley GD, Bale AE, Donis-Keller H, Edwards JH, Litt M, McBride W, Persichetti F, Spurr NK, Weber JL, Weissenbach J, White RL. CEPH consortium map of chromosome 14 Cytogenetic and Genome Research. 69: 175-178. PMID 7698005 DOI: 10.1159/000133955  0
1995 Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, et al. The CEPH Consortium Linkage Map of Human Chromosome 11 Genomics. 27: 101-112. PMID 7665156 DOI: 10.1006/Geno.1995.1011  0
1995 Levy-Lahad E, Wijsman EM, Nemens E, Anderson L, Goddard KA, Weber JL, Bird TD, Schellenberg GD. A familial Alzheimer's disease locus on chromosome 1. Science (New York, N.Y.). 269: 970-3. PMID 7638621 DOI: 10.1126/Science.7638621  0
1995 Leutelt J, Oehlmann R, Younus F, Van den Barn LI, Weber JL, Denton MJ, Mehdi SQ, Gal A. Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan Clinical Genetics. 47: 122-124. PMID 7634534  0
1994 Wang Z, Weber JL, Zhong G, Tanksley SD. Survey of plant short tandem DNA repeats. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. 88: 1-6. PMID 24185874 DOI: 10.1007/BF00222386  0
1994 Briggs MD, Rasmussen IM, Weber JL, Yuen J, Reinker K, Garber AP, Rimoin DL, Cohn DH. Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19. Genomics. 18: 656-60. PMID 8307576 DOI: 10.1016/S0888-7543(05)80369-6  0
1994 Wilkie PJ, Weber JL. Mapping of short tandem repeat polymorphisms on human chromosome 3. Genomics. 19: 167-9. PMID 8188221 DOI: 10.1006/GENO.1994.1030  0
1994 Buetow KH, Ludwigsen S, Scherpbier-Heddema T, Quillen J, Murray JC, Sheffield VC, Duyk GM, Weber JL, Weissenbach J, Gyapay G. Human genetic map. Genome maps V. Wall chart Science. 265: 2055-2070. PMID 8091228  0
1994 Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Sheffield VC, Sunden S, Duyk GM, Weissenbach J, Gyapay G, Dib C, Morrissette J, Lathrop GM, et al. A comprehensive human linkage map with centimorgan density Science. 265: 2049-2054. PMID 8091227 DOI: 10.1126/science.8091227  0
1994 Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Duyk GM, Sheffield VC, Wang Z, Murray JC. Integrated human genome−wide maps constructed using the CEPH reference panel Nature Genetics. 6: 391-393. PMID 8054980 DOI: 10.1038/Ng0494-391  0
1994 Pérez Jurado LA, Phillips JA, Summar ML, Mao J, Weber JL, Schaefer FV, Hazan J, Argente J. Genetic mapping of the human growth hormone-releasing factor gene (GHRF) using two intragenic polymorphisms detected by PCR amplification. Genomics. 20: 132-4. PMID 8020943 DOI: 10.1006/Geno.1994.1140  0
1994 Small KW, Weber J, Roses A, Pericak-Vance P. North Carolina macular dystrophy (MCDR1). A review and refined mapping to 6q14-q16.2. Ophthalmic Paediatrics and Genetics. 14: 143-50. PMID 8015785 DOI: 10.3109/13816819309042913  0
1994 Walker GJ, Nancarrow DJ, Walters MK, Palmer JM, Weber JL, Hayward NK. Linkage analysis in familial melanoma kindreds to markers on chromosome 6p International Journal of Cancer. 59: 771-775. PMID 7989117 DOI: 10.1002/ijc.2910590611  0
1994 Schwengel DA, Jedlicka AE, Nanthakumar EJ, Weber JL, Levitt RC. Comparison of fluorescence-based semi-automated genotyping of multiple microsatellite loci with autoradiographic techniques. Genomics. 22: 46-54. PMID 7959791 DOI: 10.1006/geno.1994.1344  0
1994 Weber JL. Know thy genome. Nature Genetics. 7: 343-4. PMID 7920648 DOI: 10.1038/ng0794-343  0
1994 Hughes AE, Shearman AM, Weber JL, Barr RJ, Wallace RG, Osterberg PH, Nevin NC, Mollan RA. Genetic linkage of familial expansile osteolysis to chromosome 18q. Human Molecular Genetics. 3: 359-61. PMID 7911698 DOI: 10.1093/hmg/3.2.359  0
1994 Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi Ki, Weber JL, Piussan C, Melaragno MI, Epstein CJ, Scappaticci S, Fraccaro M, Matsumura T, Murano S, et al. Homozygosity Mapping of the Werner Syndrome Locus (WRN) Genomics. 23: 600-608. PMID 7851888 DOI: 10.1006/Geno.1994.1548  0
1994 Bonnycastle LL, Yu CE, Hunt CR, Trask BJ, Clancy KP, Weber JL, Patterson D, Schellenberg GD. Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2). Genomics. 23: 85-93. PMID 7829106 DOI: 10.1006/Geno.1994.1462  0
1994 Oshima J, Yu CE, Boehnke M, Weber JL, Edelhoff S, Wagner MJ, Wells DE, Wood S, Disteche CM, Martin GM, Schellenberg GD. Integrated Mapping Analysis of the Werner Syndrome Region of Chromosome 8 Genomics. 23: 100-113. PMID 7829057 DOI: 10.1006/Geno.1994.1464  0
1993 Müller U, Warman ML, Mulliken JB, Weber JL. Assignment of a gene locus involved in craniosynostosis to chromosome 5qter. Human Molecular Genetics. 2: 119-22. PMID 8499900 DOI: 10.1093/Hmg/2.2.119  0
1993 Peltomäki P, Aaltonen LA, Sistonen P, Pylkkänen L, Mecklin JP, Järvinen H, Green JS, Jass JR, Weber JL, Leach FS. Genetic mapping of a locus predisposing to human colorectal cancer. Science (New York, N.Y.). 260: 810-2. PMID 8484120 DOI: 10.1126/Science.8484120  0
1993 Engelstein M, Hudson TJ, Lane JM, Lee MK, Leverone B, Landes GM, Peltonen L, Weber JL, Dracopoli NC. A PCR-based linkage map of human chromosome 1. Genomics. 15: 251-8. PMID 8449488 DOI: 10.1006/geno.1993.1054  0
1993 Wilkie PJ, Polymeropoulos MH, Trent JM, Small KW, Weber JL. Genetic and Physical Map of 11 Short Tandem Repeat Polymorphisms on Human Chromosome 6 Genomics. 15: 225-227. PMID 8432543 DOI: 10.1006/geno.1993.1042  0
1993 Müller U, Weber JL, Berry P, Kupke KG. Second polar body incorporation into a blastomere results in 46,XX/69,XXX mixoploidy. Journal of Medical Genetics. 30: 597-600. PMID 8411035 DOI: 10.1136/jmg.30.7.597  0
1993 Dawson E, Shaikh S, Weber JL, Wang Z, Weissenbach J, Powell JF, Gill M. A continuous linkage map of 22 short tandem repeat polymorphisms on human chromosome 12 Genomics. 17: 245-248. PMID 8406462 DOI: 10.1006/Geno.1993.1314  0
1993 Weber JL, Wong C. Mutation of human short tandem repeats. Human Molecular Genetics. 2: 1123-8. PMID 8401493 DOI: 10.1093/hmg/2.8.1123  0
1993 Litt M, Kramer P, Hauge XY, Weber JL, Wang Z, Wilkie PJ, Holt MS, Mishra S, Donis-Keller H, Warnich L. A microsatellite-based index map of human chromosome 11. Human Molecular Genetics. 2: 909-13. PMID 8364573 DOI: 10.1093/hmg/2.7.909  0
1993 Olson TM, Michels VV, Lindor NM, Pastores GM, Weber JL, Schaid DJ, Driscoll DJ, Feldt RH, Thibodeau SN. Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7. Human Molecular Genetics. 2: 869-73. PMID 8364568 DOI: 10.1093/hmg/2.7.869  0
1993 Graeber MB, Müller U, Monaco AP, Weber JL. Four dinucleotide repeat polymorphisms at the D7S804 locus. Human Molecular Genetics. 2: 2195. PMID 8111392 DOI: 10.1093/Hmg/2.12.2195  0
1993 Nancarrow DJ, Walker GJ, Weber JL, Walters MK, Palmer JM, Hayward NK. Linkage mapping of melanoma (MLM) using 172 microsatellite markers. Genomics. 14: 939-47. PMID 1478674 DOI: 10.1016/S0888-7543(05)80115-6  0
1993 Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nature Genetics. 2: 46-9. PMID 1303248 DOI: 10.1038/Ng0992-46  0
1992 Small KW, Weber JL, Hung WY, Vance J, Roses A, Pericak-Vance M. North Carolina macular dystrophy: exclusion map using RFLPs and microsatellites. Genomics. 11: 763-6. PMID 1685483 DOI: 10.1016/0888-7543(91)90087-U  0
1992 Small KW, Weber JL, Roses A, Lennon F, Vance JM, Pericak-Vance MA. North Carolina macular dystrophy is assigned to chromosome 6. Genomics. 13: 681-5. PMID 1639395 DOI: 10.1016/0888-7543(92)90141-E  0
1992 Wang Z, Weber JL. Continuous linkage map of human chromosome 14 short tandem repeat polymorphisms. Genomics. 13: 532-6. PMID 1639382 DOI: 10.1016/0888-7543(92)90121-8  0
1992 Purohit KR, Weber JL, Ward LJ, Keats BJB. The Kell blood group locus is close to the cystic fibrosis locus on chromosome 7 Human Genetics. 89: 457-458. PMID 1618496 DOI: 10.1007/BF00194323  0
1992 Beckman JS, Weber JL. Survey of human and rat microsatellites. Genomics. 12: 627-31. PMID 1572635 DOI: 10.1016/0888-7543(92)90285-Z  0
1992 Wilkie PJ, Krizman DB, Weber JL. Linkage map of human chromosome 9 microsatellite polymorphisms. Genomics. 12: 607-9. PMID 1559711 DOI: 10.1016/0888-7543(92)90456-3  0
1992 Mills KA, Buetow KH, Xu Y, Weber JL, Altherr MR, Wasmuth JJ, Murray JC. Genetic and physical maps of human chromosome 4 based on dinucleotide repeats. Genomics. 14: 209-19. PMID 1427835 DOI: 10.1016/S0888-7543(05)80208-3  0
1992 Schellenberg GD, Bird TD, Wijsman EM, Orr HT, Anderson L, Nemens E, White JA, Bonnycastle L, Weber JL, Alonso ME. Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14. Science (New York, N.Y.). 258: 668-71. PMID 1411576 DOI: 10.1126/Science.1411576  0
1992 Weber JL. Human DNA polymorphisms and methods of analysis. Current Opinion in Biotechnology. 1: 166-71. PMID 1367853 DOI: 10.1016/0958-1669(90)90026-H  0
1992 Westbrook CA, Neuman WL, McPherson J, Camper S, Wasmuth J, Plaetke R, Williamson R. Report of the second international workshop on human chromosome 5 mapping. Cytogenetics and Cell Genetics. 61: 225-31. PMID 1362532 DOI: 10.1159/000133415  0
1992 Decker RA, Moore J, Ponder B, Weber JL. Linkage mapping of human chromosome 10 microsatellite polymorphisms. Genomics. 12: 604-6. PMID 1348490 DOI: 10.1016/0888-7543(92)90455-2  0
1992 Kandt RS, Haines JL, Smith M, Northrup H, Gardner RJ, Short MP, Dumars K, Roach ES, Steingold S, Wall S. Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney disease. Nature Genetics. 2: 37-41. PMID 1303246 DOI: 10.1038/Ng0992-37  0
1992 Decker RA, Ponder BA, Mole SE, Weber JL. Dinucleotide repeat polymorphisms at the D10S183 and D10S245 loci. Human Molecular Genetics. 1: 777. PMID 1302619 DOI: 10.1093/Hmg/1.9.777  0
1991 Ning Y, Weber JL, Killary AM, Ledbetter DH, Smith JR, Pereira-Smith OM. Genetic analysis of indefinite division in human cells: evidence for a cell senescence-related gene(s) on human chromosome 4. Proceedings of the National Academy of Sciences of the United States of America. 88: 5635-9. PMID 2062841 DOI: 10.1073/Pnas.88.13.5635  0
1991 Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA. Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization. Genomics. 9: 570-5. PMID 2037288 DOI: 10.1016/0888-7543(91)90348-I  0
1991 Weber JL, Kwitek AE, May PE, Zoghbi HY. Dinucleotide repeat polymorphism at the D6S105 locus. Nucleic Acids Research. 19: 968. PMID 2017389 DOI: 10.1093/nar/19.4.968  0
1991 Petersen MB, Weber JL, Slaugenhaupt SA, Kwitek AE, McInnis MG, Chakravarti A, Antonarakis SE. Linkage mapping of D21S171 to the distal long arm of human chromosome 21 using a polymorphic (AC)n dinucleotide repeat. Human Genetics. 87: 401-4. PMID 1879826 DOI: 10.1007/Bf00197156  0
1991 Weber JL, Polymeropoulos MH, May PE, Kwitek AE, Xiao H, McPherson JD, Wasmuth JJ. Mapping of human chromosome 5 microsatellite DNA polymorphisms. Genomics. 11: 695-700. PMID 1774070 DOI: 10.1016/0888-7543(91)90077-R  0
1991 Wang Jabs E, Li X, Coss CA, Taylor EW, Meyers DA, Weber JL. Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3 Genomics. 11: 193-198. DOI: 10.1016/0888-7543(91)90118-X  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D15S87 locus. Nucleic Acids Research. 18: 4640. PMID 2388866 DOI: 10.1093/nar/18.15.4640  0
1990 Weber JL, Kappel C, May PE, Kwitek AE. Dinucleotide repeat polymorphism at the D19S75 locus. Nucleic Acids Research. 18: 4639. PMID 2388864 DOI: 10.1093/nar/18.15.4639  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D13S71 locus. Nucleic Acids Research. 18: 4638. PMID 2388862 DOI: 10.1093/nar/18.15.4638  0
1990 Weber JL, Kwitek AE, May PE, Polymeropoulos M. Dinucleotide repeat polymorphism at the D12S43 locus. Nucleic Acids Research. 18: 4637. PMID 2388861 DOI: 10.1093/Nar/18.15.4637-A  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D10S89 locus. Nucleic Acids Research. 18: 4637. PMID 2388860 DOI: 10.1093/nar/18.15.4637  0
1990 Weber JL, Kwitek AE, May PE, Killary AM. Dinucleotide repeat polymorphism at the D4S174 locus. Nucleic Acids Research. 18: 4636. PMID 2388858 DOI: 10.1093/Nar/18.15.4636  0
1990 Weber JL, May PE, Patterson D, Drabkin H, Killary AM. Dinucleotide repeat polymorphism at the D3S196 locus. Nucleic Acids Research. 18: 4635. PMID 2388857 DOI: 10.1093/nar/18.15.4635  0
1990 Lewis JG, Weber JL, Petersen MB, Slaugenhaupt SA, Kwitek A, May PE, Warren AC, Chakravarti A, Antonarakis SE. Linkage mapping of the highly informative DNA marker D21S156 to human chromosome 21 using a polymorphic GT dinucleotide repeat. Genomics. 8: 400-2. PMID 1979059 DOI: 10.1016/0888-7543(90)90300-J  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D18S35 locus. Nucleic Acids Research. 18: 6465. PMID 1978751 DOI: 10.1093/nar/18.21.6465-a  0
1990 Wijmenga C, Frants RR, Brouwer OF, Moerer P, Weber JL, Padberg GW. Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. Lancet (London, England). 336: 651-3. PMID 1975852 DOI: 10.1016/0140-6736(90)92148-B  0
1990 Weber JL. Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms. Genomics. 7: 524-30. PMID 1974878 DOI: 10.1016/0888-7543(90)90195-Z  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphisms at the D7S435 and D7S440 loci. Nucleic Acids Research. 18: 4039. PMID 1973841 DOI: 10.1093/nar/18.13.4039  0
1990 Weber JL, Kwitek AE, May PE, Patterson D, Drabkin H. Dinucleotide repeat polymorphisms at the D8S85, D8S87, and D8S88 loci. Nucleic Acids Research. 18: 4038. PMID 1973840 DOI: 10.1093/nar/18.13.4038  0
1990 Weber JL, Kwitek AE, May PE, Polymeropoulos MH, Ledbetter S. Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci. Nucleic Acids Research. 18: 4037. PMID 1973839 DOI: 10.1093/Nar/18.13.4037  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci. Nucleic Acids Research. 18: 4036. PMID 1973838 DOI: 10.1093/nar/18.13.4036  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphisms at the D5S107, D5S108, D5S111, D5S117 and D5S118 loci. Nucleic Acids Research. 18: 4035. PMID 1973837 DOI: 10.1093/nar/18.13.4035  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266, and D16S267 loci. Nucleic Acids Research. 18: 4034. PMID 1973836 DOI: 10.1093/nar/18.13.4034  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D18S34 locus. Nucleic Acids Research. 18: 3431. PMID 1972571 DOI: 10.1093/nar/18.11.3431-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D19S76 locus. Nucleic Acids Research. 18: 2835. PMID 1971100 DOI: 10.1093/nar/18.9.2835  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D1S102 locus. Nucleic Acids Research. 18: 2199. PMID 1970878 DOI: 10.1093/nar/18.8.2199  0
1990 Weber JL, May PE, Kappel C. Dinucleotide repeat polymorphism at the D19S49 locus. Nucleic Acids Research. 18: 1927. PMID 1970869 DOI: 10.1093/nar/18.7.1927  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D1S104 locus Nucleic Acids Research. 18: 2835-2835. DOI: 10.1093/nar/18.9.2835-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D2S71 locus Nucleic Acids Research. 18: 2203-2203. DOI: 10.1093/nar/18.8.2203-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D9S43 locus Nucleic Acids Research. 18: 2203-2203. DOI: 10.1093/nar/18.8.2203  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D4S171 locus Nucleic Acids Research. 18: 2202-2202. DOI: 10.1093/nar/18.8.2202-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D20S27 locus Nucleic Acids Research. 18: 2202-2202. DOI: 10.1093/nar/18.8.2202  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D3S240 locus Nucleic Acids Research. 18: 2201-2201. DOI: 10.1093/nar/18.8.2201-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D18S34 locus Nucleic Acids Research. 18: 2201-2201. DOI: 10.1093/nar/18.8.2201  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D2S72 locus Nucleic Acids Research. 18: 2200-2200. DOI: 10.1093/nar/18.8.2200-a  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the PENK locus Nucleic Acids Research. 18: 2200-2200. DOI: 10.1093/nar/18.8.2200  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D1S103 locus Nucleic Acids Research. 18: 2199-2199. DOI: 10.1093/nar/18.8.2199-a  0
1990 Weber JL, Kwitek AE, May PE, Wallance MR, Collins FS, Ledbetter DH. Dinucleotide repeat polymorphisms at the D17S250 and D17S261 loci Nucleic Acids Research. 18: 4640-4640. DOI: 10.1093/Nar/18.15.4640-A  0
1990 Weber JL, May PE. Dinucleotide repeat polymorphism at the D22S156 locus Nucleic Acids Research. 18: 4639-4639. DOI: 10.1093/nar/18.15.4639-a  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D14S34 locus Nucleic Acids Research. 18: 4638-4638. DOI: 10.1093/nar/18.15.4638-a  0
1990 Weber JL, Kwitek AE, May PE. Dinucleotide repeat polymorphism at the D6S87 locus Nucleic Acids Research. 18: 4636-4636. DOI: 10.1093/nar/18.15.4636-a  0
1990 Weber JL, May PE, Patterson D, Drabkin H, Killary AM. Dinucleotide repeat polymorphism at the D3S196 locus Nucleic Acids Research. 18: 4635-4635. DOI: 10.1093/Nar/18.15.4635-A  0
1988 Weber JL, Sim BK, Lyon JA, Wolff R. Merozoite surface protein sequence from the Camp strain of the human malaria parasite Plasmodium falciparum. Nucleic Acids Research. 16: 1206. PMID 3278296 DOI: 10.1093/nar/16.3.1206  0
1988 Weber JL. Interspersed repetitive DNA from Plasmodium falciparum. Molecular and Biochemical Parasitology. 29: 117-24. PMID 2842673 DOI: 10.1016/0166-6851(88)90066-7  0
1988 Weber JL. Plasmodium falciparum: mapping genes to nine parasite chromosomes. Experimental Parasitology. 65: 148-53. PMID 2828102 DOI: 10.1016/0014-4894(88)90117-8  0
1988 Weber JL, Lyon JA, Wolff RH, Hall T, Lowell GH, Chulay JD. Primary structure of a Plasmodium falciparum malaria antigen located at the merozoite surface and within the parasitophorous vacuole. Journal of Biological Chemistry. 263: 11421-11425. DOI: 10.1016/s0021-9258(18)37973-0  0
1987 Weber JL, Egan JE, Lyon JA, Wirtz RA, Charoenvit Y, Maloy WL, Hockmeyer WT. Plasmodium berghei: cloning of the circumsporozoite protein gene. Experimental Parasitology. 63: 295-300. PMID 3556207 DOI: 10.1016/0014-4894(87)90176-7  0
1987 Egan JE, Weber JL, Ballou WR, Hollingdale MR, Majarian WR, Gordon DM, Maloy WL, Hoffman SL, Wirtz RA, Schneider I. Efficacy of murine malaria sporozoite vaccines: implications for human vaccine development. Science (New York, N.Y.). 236: 453-6. PMID 3551073 DOI: 10.1126/SCIENCE.3551073  0
1987 Weber JL. Analysis of sequences from the extremely A + T-rich genome of Plasmodium falciparum. Gene. 52: 103-9. PMID 3297924 DOI: 10.1016/0378-1119(87)90399-4  0
1986 Weber JL, Leininger WM, Lyon JA. Variation in the gene encoding a major merozoite surface antigen of the human malaria parasite Plasmodium falciparum. Nucleic Acids Research. 14: 3311-23. PMID 3517809 DOI: 10.1093/NAR/14.8.3311  0
1986 Lyon JA, Geller RH, Haynes JD, Chulay JD, Weber JL. Epitope map and processing scheme for the 195,000-dalton surface glycoprotein of Plasmodium falciparum merozoites deduced from cloned overlapping segments of the gene. Proceedings of the National Academy of Sciences of the United States of America. 83: 2989-93. PMID 2422662 DOI: 10.1073/pnas.83.9.2989  0
1985 Weber JL, Durrin LK, Gorski J. Repetitive DNA sequences within and around the rat prolactin gene. Molecular and Cellular Biochemistry. 65: 171-9. PMID 3982398 DOI: 10.1007/Bf00221100  0
1985 Weber JL, Hockmeyer WT. Structure of the circumsporozoite protein gene in 18 strains of Plasmodium falciparum. Molecular and Biochemical Parasitology. 15: 305-16. PMID 3897857 DOI: 10.1016/0166-6851(85)90092-1  0
1984 Dame JB, Williams JL, McCutchan TF, Weber JL, Wirtz RA, Hockmeyer WT, Maloy WL, Haynes JD, Schneider I, Roberts D. Structure of the gene encoding the immunodominant surface antigen on the sporozoite of the human malaria parasite Plasmodium falciparum. Science (New York, N.Y.). 225: 593-9. PMID 6204383 DOI: 10.1126/science.6204383  0
1984 Durrin LK, Weber JL, Gorski J. Chromatin structure, transcription, and methylation of the prolactin gene domain in pituitary tumors of Fischer 344 rats. Journal of Biological Chemistry. 259: 7086-7093. DOI: 10.1016/S0021-9258(17)39841-1  0
1983 Schuler LA, Weber JL, Gorski J. Polymorphism near the rat prolactin gene caused by insertion of an Alu-like element. Nature. 305: 159-60. PMID 6310412 DOI: 10.1038/305159A0  0
1982 Weber JL, Cole RD. Chromatin fragments containing bovine 1.715 g ml-1 satellite DNA. Nucleosome structure and protein composition. Journal of Biological Chemistry. 257: 11784-11790. DOI: 10.1016/s0021-9258(18)33832-8  0
1982 Weber JL, Cole RD. Chromatin fragments containing bovine 1.715 g ml-1 satellite DNA. Purification by chromatography on malachite green DNA affinity resin. Journal of Biological Chemistry. 257: 11774-11783. DOI: 10.1016/s0021-9258(18)33831-6  0
1977 Milman G, Anton DL, Weber JL. Chinese hamster purine-nucleoside phosphorylase: purification, structural, and catalytic properties. Biochemistry. 15: 4967-73. PMID 825137 DOI: 10.1021/BI00668A004  0
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