My complex disease trait mapping, genome mapping, linkage analysis journal watch - year 2001 [ this week | 2004 | 2003 | 2002 | 2001 | 2000 | 1999 | 1998 ]

 Can't find the complex disease trait mapping, genome mapping or linkage analysis article published in 2001 in my site? 
Try a Google search!


Google
  1. Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajarvi R, Suokas J, Partonen T, Lonnqvist J, Meyer J, Peltonen L Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q. Human Mol Genet 2001 Dec 15; 10:3037-3048 [PubMed]
  2. Pastinen T, Perola M, Ignatius J, Sabatti C, Tainola P, Levander M, Syvanen AC, Peltonen L. Dissecting a population genome for targeted screening of disease mutations. Human Mol Genet 2001 Dec 15; 10:2961-2972 [PubMed]
  3. Wright AF, Van Heyningen V. Short cut to disease genes. Nature. 2001 Dec 13;414(6865):705-706. [PubMed]
  4. Challenges for the 21st Century. Nat Genet. 2001 Dec;29(4):353-354. [PubMed]
  5. Berger J, Suzuki T, Senti KA, Stubbs J, Schaffner G, Dickson BJ. Genetic mapping with SNP markers in Drosophila. Nat Genet. 2001 Dec;29(4):475-81. [PubMed][web supplement]
  6. Hoh J, Wille A, Ott J. Trimming, Weighting, and Grouping SNPs in Human Case-Control Association Studies. Genome Res. 2001 Dec; 11:2115-2119 [PubMed]
  7. Andolfatto P. Adaptive hitchhiking effects on genome variability. Curr Opin Genet Dev. 2001 Dec 11:635-641 [PubMed]
  8. Wall JD. Insights from linked single nucleotide polymorphisms: what we can learn from linkage disequilibrium. Curr Opin Genet Dev. 2001 Dec 11:647-651 [PubMed]
  9. Zavolan M, Kepler TB. Statistical inference of sequence-dependent mutation rates. Curr Opin Genet Dev. 2001 Dec;11(6):612-5. [PubMed]
  10. Wakeley J, Nielsen R, Liu-Cordero SN, Ardlie K. The Discovery of Single-Nucleotide Polymorphisms - and Inferences about Human Demographic History. Am J Hum Genet. 2001 Dec;69(6):1332-47 [PubMed]
  11. Goring HH, Terwilliger JD, Blangero J. Large Upward Bias in Estimation of Locus-Specific Effects from Genomewide Scans. Am J Hum Genet 2001 Dec;69(6):1357-69 [PubMed]
  12. Tsai HJ, Sun G, Weeks DE, Kaushal R, Wolujewicz M, McGarvey ST, Tufa J, Viali S, Deka R. Type 2 Diabetes and Three Calpain-10 Gene Polymorphisms in Samoans: No Evidence of Association. Am J Hum Genet. 2001 Dec;69(6):1236-44. [PubMed]
  13. European Consortium for IDDM Genome Studies. A Genomewide Scan for Type 1-Diabetes Susceptibility in Scandinavian Families: Identification of New Loci with Evidence of Interactions. Am J Hum Genet 2001 Dec;69(6):1301-1313 [PubMed]
  14. Xu X, Fang Z, Wang B, Chen C, Guang W, Jin Y, Yang J, Lewitzky S, Aelony A, Parker A, Meyer J, Weiss ST, Xu X. A Genomewide Search for Quantitative-Trait Loci Underlying Asthma. Am J Hum Genet 2001 Dec;69(6):1271-7 [PubMed]
  15. Matin A, Nadeau JH. Sensitized polygenic trait analysis. Trends Genet. 2001 Dec; 17:727-731. [PubMed]
  16. McCarthy LC, Hosford DA, Riley JH, Bird MI, White NJ, Hewett DR, Peroutka SJ, Griffiths LR, Boyd PR, Lea RA, Bhatti SM, Hosking LK, Hood CM, Jones KW, Handley AR, Rallan R, Lewis KF, Yeo AJ, Williams PM, Priest RC, Khan P, Donnelly C, Lumsden SM, O'Sullivan J, See CG, Smart DH, Shaw-Hawkins S, Patel J, Langrish TC, Feniuk W, Knowles RG, Thomas M, Libri V, Montgomery DS, Manasco PK, Xu CF, Dykes C, Humphrey PP, Roses AD, Purvis IJ. Single-Nucleotide Polymorphism Alleles in the Insulin Receptor Gene Are Associated with Typical Migraine. Genomics. 2001 Dec;78(3):135-149. [PubMed]
  17. Sheffield LJ.  Strategies to find new genes involved in drug metabolism.  Curr Opin Mol Ther. 2001 Dec;3(6):579-84. [PubMed
  18. Kwok PY. Genetic association by whole-genome analysis? Science Nov 23; 294:1669-1670. [PubMed]
  19. Patil N, Berno AJ, Hinds DA, Barrett WA, Doshi JM, Hacker CR, Kautzer CR, Lee DH, Marjoribanks C, McDonough DP, Nguyen BT, Norris MC, Sheehan JB, Shen N, Stern D, Stokowski RP, Thomas DJ, Trulson MO, Vyas KR, Frazer KA, Fodor SP, Cox DR. Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science Nov 23; 294:1719-1723. [PubMed][web supplement]
  20. Cordell HJ, Clayton DG. A Unified Stepwise Regression Procedure for Evaluating the Relative Effects of Polymorphisms within a Gene Using Case/Control or Family Data: Application to HLA in Type 1 Diabetes. Am J Hum Genet. 2001 Nov 21 [epub ahead of print] [PubMed]
  21. Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D,  Mastaglia F, Laing NG, Stajich JM, Slotterbeck B, Booze MW, Ribble RC, Rampersaud E, West SG, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Vance JM, Pericak-Vance MA. Complete Genomic Screen in Parkinson Disease: Evidence for Multiple Genes. JAMA. 2001 Nov 14;286(18):2239-2244. [PubMed]
  22. Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Masterman D, Mastaglia F, Laing NG, Stajich JM, Ribble RC, Booze MW, Rogala A, Hauser MA, Zhang F, Gibson RA, Middleton LT, Roses AD, Haines JL, Scott BL, Pericak-Vance MA, Vance JM. Association of Single-Nucleotide Polymorphisms of the Tau Gene With Late-Onset Parkinson Disease. JAMA. 2001 Nov 14;286(18):2245-2250. [PubMed]
  23. DeWan AT, Parrado AR, Matise TC, Leal SM. The Map Problem: A Comparison of Genetic and Sequence-Based Physical Maps. Am J Hum Genet. 2001 Nov 9 [epub ahead of print] [PubMed]
  24. Nestler EJ. Psychogenomics: opportunities for understanding addiction . J Neurosci. 2001 Nov 1;21(21):8324-7. [PubMed]
  25. Brookes AJ. Rethinking genetic strategies to study complex diseases. Trends Mol Med. 2001 Nov;7(11):512-6. [PubMed]
  26. Newman DL, Abney M, McPeek MS, Ober C, Cox NJ. The Importance of Genealogy in Determining Genetic Associations with Complex Traits. Am. J. Hum. Genet. 2001 Nov; 69:1146-1148 [PubMed]
  27. Elston RC. Reporting of Linkage Results. Am. J. Hum. Genet.2001 Nov;  69:1149-1150 [PubMed]
  28. Ober C, Abney M, McPeek MS. The Genetic Dissection of Complex Traits in a Founder Population. Am. J. Hum. Genet.2001 Nov;  69:1068-1079. [PubMed]
  29. Altmuller J, Palmer LJ, Fischer G, Scherb H, Wjst M. Genomewide Scans of Complex Human Diseases: True Linkage Is Hard to Find. Am J Hum Genet. 2001 Nov;69(5):936-50. [ PubMed]
  30. Williams RW et al. The genetic structure of recombinant inbred mice: high-resolution consensus maps for complex trait analysis. Genome Biol. 2001 Nov; 11:0046 [PubMed][pdf]
  31. Ioannidis JP, Ntzani EE, Trikalinos TA, Contopoulos-Ioannidis DG. Replication validity of genetic association studies. Nat Genet. 2001 Nov;29(3):306-309. [PubMed][web supplement]
  32. Levy GG, Nichols WC, Lian EC, Foroud T, McClintick JN, McGee BM, Yang AY, Siemieniak DR, Stark KR, Gruppo R, Sarode R, Shurin SB, Chandrasekaran V,  Stabler SP, Sabio H, Bouhassira EE, Upshaw JD Jr, Ginsburg D, Tsai HM.  Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001 Oct 4;413(6855):488-94. [PubMed][web supplement]
  33. Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP.  A forkhead-domain gene is mutated in a severe speech and language disorder. Nature. 2001 Oct 4;413(6855):519-23. [PubMed][web supplement]
  34. Pinker S. Talk of genetics and vice versa.  Nature. 2001 Oct 4;413(6855):465-6. [PubMed]
  35. Russo E. Population geneticists are in short supply, as the need to translate large data sets into disease-susceptibility traits grows. Naturejobs. 2001 Oct 4; 413: 4-5. [PubMed]
  36. Goodstadt L, Ponting CP. Sequence variation and disease in the wake of the draft human genome. Hum Mol Genet. 2001 Oct 1;10(20):2209-14. [PubMed]
  37. Jorde LB, Watkins WS, Bamshad MJ. Population genomics: a bridge from evolutionary history to genetic medicine. Hum Mol Genet. 2001 Oct 1;10(20):2199-207. [PubMed]
  38. Avner P, Bruls T, Poras I, Eley L, Gas S, Ruiz P, Wiles MV, Sousa-Nunes R, Kettleborough R, Rana A, Morissette J, Bentley L, Goldsworthy M, Haynes A, Herbert E, Southam  L, Lehrach H, Weissenbach J, Manenti G, Rodriguez-Tome P, Beddington R, Dunwoodie S, Cox RD.  A radiation hybrid transcript map of the mouse genome.  Nat Genet. 2001 Oct;29(2):194-200. [PubMed]
  39. Goldstein DB. Islands of linkage disequilibrium.  Nat Genet. 2001 Oct;29(2):109-11. [PubMed]
  40. Hudson TJ, Church DM, Greenaway S, Nguyen H, Cook A, Steen RG, Van Etten WJ, Castle AB, Strivens MA, Trickett P, Heuston C, Davison C, Southwell A, Hardisty R, Varela-Carver A, Haynes AR, Rodriguez-Tome P, Doi H, Ko MS, Pontius J, Schriml L, Wagner L, Maglott D, Brown SD, Lander ES, Schuler G, Denny P. A radiation hybrid map of mouse genes. Nat Genet. 2001 Oct;29(2):201-5. [PubMed]
  41. Daly MJ, Rioux JD, Schaffner SF, Hudson TJ, Lander ES. High-resolution haplotype structure in the human genome. Nat Genet. 2001 Oct;29(2):229-32. [PubMed]
  42. Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H,  Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA.  Haplotype tagging for the identification of common disease genes.  Nat Genet. 2001 Oct;29(2):233-7. [PubMed][web supplement]
  43. Cai WW, Chow CW, Damani S, Gregory SG, Marra M, Bradley A. An SSLP marker-anchored BAC framework map of the mouse genome. Nat Genet. 2001 Oct;29(2):133-4. [PubMed][web supplement]
  44. Nowotny P, Kwon JM, Goate AM. SNP analysis to dissect human traits. Curr Opin Neurobiol. 2001 Oct;11(5):637-41. [PubMed]
  45. Liu JS, Sabatti C, Teng J, Keats BJ, Risch N. Bayesian Analysis of Haplotypes for Linkage Disequilibrium Mapping.  Genome Res. 2001 Oct; 11:1716-1724 [PubMed]
  46. McInnes LA, Service SK, Reus VI, Barnes G, Charlat O, Jawahar S, Lewitzky S, Yang Q, Duong Q, Spesny M, Araya C, Araya X, Gallegos A, Meza L, Molina J, Ramirez R,  Mendez R, Silva S, Fournier E, Batki SL, Mathews CA, Neylan T, Glatt CE, Escamilla MA, Luo D, Gajiwala P, Song T, Crook S, Nguyen JB, Roche E, Meyer JM, Leon P, Sandkuijl LA, Freimer NB, Chen H. Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population.  Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11485-11490. [PubMed][pdf]
  47. Remington DL, Thornsberry JM, Matsuoka Y, Wilson LM, Whitt SR, Doebley J, Kresovich S, Goodman MM, Buckler ES IV. Structure of linkage disequilibrium and phenotypic associations in the maize genome.  Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11479-11484. [PubMed][pdf]
  48. Krebs S, Seichter D, Forster M. Genotyping of dinucleotide tandem repeats by MALDI mass spectrometry of ribozyme-cleaved RNA transcripts. Nat Biotechnol. 2001 Sep; 877-880. [PubMed]
  49. Konig IR, Schafer H, Muller HH, Ziegler A. Optimized Group Sequential Study Designs for Tests of Genetic Linkage and Association in Complex Diseases . Am. J. Hum. Genet. 2001 Sep;69(3):590-600. [PubMed]
  50. Sen S, Churchill GA. A statistical framework for quantitative trait mapping.  Genetics. 2001 Sep;159(1):371-87. [PubMed][pdf]
  51. Wakeland EK, Liu K, Graham RR, Behrens TW. Delineating the Genetic Basis of Systemic Lupus Erythematosus.  Immunity. 2001 Sep; 15:397-408 [PubMed]
  52. Reich DE, Lander ES. On the allelic spectrum of human disease . Trends Genet. 2001 Sep;17(9):502-10. [PubMed]
  53. Puca AA, Daly MJ, Brewster SJ, Matise TC, Barrett J, Shea-Drinkwater M, Kang S, Joyce E, Nicoli J, Benson E, Kunkel LM, Perls T. A genome-wide scan for linkage to human exceptional longevity identifies a locus on chromosome 4.  Proc Natl Acad Sci U S A. 2001 Aug 28;98(18):10505-10508. [PubMed][pdf]
  54. Wright AF, Hastie ND. Complex genetic diseases: controversy over the Croesus code. Genome Biol. 2001 Aug 1; 2(8): comment2007.1-2007.8 [PubMed]
  55. Weier HU. Dna fiber mapping techniques for the assembly of high-resolution physical maps.  J Histochem Cytochem. 2001 Aug;49(8):939-48. [PubMed]
  56. Sham P.  Shifting paradigms in gene-mapping methodology for complex traits.  Pharmacogenomics. 2001 Aug;2(3):195-202. [PubMed]
  57. Gura T. Can SNPs deliver on susceptibility genes? Science 2001 Jul 27; 293:593-595 [PubMed]
  58. Helmuth L. Map of the Human Genome 3.0. Science 2001 Jul 27; 293:538-585. [PubMed]
  59. Stephens JC, Schneider JA, Tanguay DA, Choi J, Acharya T, Stanley SE, Jiang R, Messer CJ, Chew A, Han JH, Duan J, Carr JL, Lee MS, Koshy B, Kumar AM, Zhang G, Newell WR, Windemuth A, Xu C, Kalbfleisch TS, Shaner SL, Arnold K, Schulz V, Drysdale CM, Nandabalan K, Judson RS, Ruano G, Vovis GF. Haplotype variation and linkage disequilibrium in 313 human genes.   Science. 2001 Jul 20;293(5529):489-93. [PubMed]
  60. Tishkoff SA, Varkonyi R, Cahinhinan N, Abbes S, Argyropoulos G, Destro-Bisol G, Drousiotou A, Dangerfield B, Lefranc G, Loiselet J, Piro A, Stoneking M, Tagarelli A, Tagarelli G, Touma EH, Williams SM, Clark AG. Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance. Science. 2001 Jul 20;293(5529):455-62. [PubMed][web supplement]
  61. Adam D. Genetics group targets disease markers in the human sequence.   Nature. 2001 Jul 12;412(6843):105. [PubMed]
  62. Ranade K, Chang MS, Ting CT, Pei D, Hsiao CF, Olivier M, Pesich R, Hebert J, Chen YD, Dzau VJ, Curb D, Olshen R, Risch N, Cox DR, Botstein D. High-throughput genotyping with single nucleotide polymorphisms. Genome Res. 2001 Jul;11(7):1262-8. [PubMed]
  63. Pritchard JK. Are rare variants responsible for susceptibility to complex diseases?  Am J Hum Genet. 2001 Jul;69(1):124-37. [PubMed]
  64. Bihoreau MT, Sebag-Montefiore L, Godfrey RF, Wallis RH, Brown JH, Danoy PA, Collins SC, Rouard M, Kaisaki PJ, Lathrop M, Gauguier D. A High-Resolution Consensus Linkage Map of the Rat, Integrating Radiation Hybrid and Genetic Maps.  Genomics. 2001 Jul;75(1/3):57-69. [PubMed]
  65. Jansen RC, Nap JP. Genetical genomics: the added value from segregation. Trends Genet. 2001 Jul;17(7):388-91. [PubMed]
  66. Grupe A, Germer S, Usuka J, Aud D, Belknap JK, Klein RF, Ahluwalia MK, Higuchi R, Peltz G. In silico mapping of complex disease-related traits in mice. Science. 2001 Jun 8;292(5523):1915-8. [PubMed]
  67. Gulcher JR, Kong A, Stefansson K. The role of linkage studies for common diseases. Curr Opin Genet Dev. 2001 Jun; 11:264-267. [PubMed]
  68. Meltzer PS. Spotting the target: microarrays for disease gene discovery. Curr Opin Genet Dev. 2001 Jun; 11: 258-263. [PubMed]
  69. McCarthy JJ. Characterizing patterns of genetic variations. Trends Biotechnol. 2001 Jun; 19:202 [PubMed]
  70. Xu J, Meyers DA, Ober C, Blumenthal MN, Mellen B, Barnes KC, King RA, Lester LA, Howard TD, Solway J, Langefeld CD, Beaty TH, Rich SS, Bleecker ER, Cox NJ. Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three US populations: collaborative study on the genetics of asthma. Am. J. Hum. Genet. 2001 Jun;68(6):1437-46. [PubMed]
  71. Lai E. Application of snp technologies in medicine: lessons learned and future challenges. Genome Res. 2001 Jun;11(6):927-9. [PubMed]
  72. Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, Almer S, Tysk C, O'Morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, Gower-Rousseau C, Macry J, Colombel JF, Sahbatou M, Thomas G. Association of  leucine-rich repeat variants with susceptibility to Crohn's disease. Nature. 2001 May 31;411(6837):599-603. [PubMed]
  73. Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, Britton H, Moran T, Karaliuskas R, Duerr RH, Achkar JP, Brant SR,  Bayless TM, Kirschner BS, Hanauer SB, Nunez G, Cho JH. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001 May 31;411(6837):603-6. [PubMed]
  74. Todd JA. Human genetics. Tackling common disease.  Nature. 2001 May 31;411(6837):537, 539. [PubMed]
  75. Reich DE, Cargill M, Bolk S, Ireland J, Sabeti PC, Richter DJ, Lavery T, Kouyoumjian R, Farhadian SF, Ward R, Lander ES.  Linkage disequilibrium in the human genome. Nature. 2001 May 10;411(6834):199-204. [PubMed]
  76. Longmate JA. Complexity and power in case-control association studies. Am J Hum Genet 2001 May;68(5):1229-37 [PubMed]
  77. Mathew C. Postgenomic technologies: hunting the genes for common disorders. BMJ. 2001 Apr 28;322(7293):1031-1034. [PubMed]
  78. Rohde K, Fuerst R. Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information. Hum Mutat. 2001 Apr;17(4):289-95. [PubMed]
  79. Ott J, Hoh J.  Statistical multilocus methods for disequilibrium analysis in complex traits. Hum Mutat. 2001 Apr;17(4):285-8. [PubMed]
  80. Bray MS, Boerwinkle E, Doris PA. High-throughput multiplex SNP genotyping with MALDI-TOF mass spectrometry: Practice, problems and promise . Hum Mutat. 2001 Apr;17(4):296-304 [PubMed]
  81. Lehnert V, Holzwarth J, Ott M, Thompson A, Demmak S, Foernzler D. A semi-automated system for analysis and storage of SNPs.  Hum Mutat. 2001 Apr;17(4):243-54. [PubMed]
  82. Collins A, Ennis S, Taillon-Miller P, Kwok PY, Morton NE.  Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map.  Hum Mutat. 2001 Apr;17(4):255-62. [PubMed]
  83. Wang Z, Moult J.  SNPs, protein structure, and disease. Hum Mutat. 2001 Apr;17(4):263-70. [PubMed]
  84. Ye F, Li MS, Taylor JD, Nguyen Q, Colton HM, Casey WM, Wagner M, Weiner MP, Chen J. Fluorescent microsphere-based readout technology for multiplexed human single nucleotide polymorphism analysis and bacterial identification .  Hum Mutat. 2001 Apr;17(4):305-16. [PubMed]
  85. Lessem JL, Cherny SS. DeFries-Fulker multiple regression analysis of sibship QTL data: a SAS((R))macro.  Bioinformatics. 2001 Apr;17(4):371-372. [PubMed]
  86. Marth G, Yeh R, Minton M, Donaldson R, Li Q, Duan S, Davenport R, Miller RD, Kwok PY. Single-nucleotide polymorphisms in the public domain: how useful are they?  Nat Genet. 2001 Apr;27(4):371-2. [PubMed]
  87. Stephens M, Smith NJ, Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet. 2001 Apr;68(4):978-89. [PubMed]
  88. Weatherall DJ. Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias. Nat Rev Genet. 2001 Apr;2(4):245-55. [PubMed]
  89. Little P. The end of all human DNA maps? Nat Genet 2001. Mar; 27:229-230 [PubMed][pdf]
  90. Antonarakis SE. BACking up the promises. Nat Genet 2001. Mar; 27:230-232 [PubMed][pdf]
  91. Scheetz TE, Raymond MR, Nishimura DY, McClain A, Roberts C, Birkett C, Gardiner J, Zhang J, Butters N, Sun C,  Kwitek-Black A, Jacob H, Casavant TL, Soares MB, Sheffield VC. Generation of a High-Density rat EST map.  Genome Res 2001. Mar; 11:497-502 [PubMed]
  92. Almind K, Doria A, Kahn CR. Putting the genes for type II diabetes on the map. Nat Med 2001. Mar; 7:277 [PubMed]
  93. Komajda M, Charron P. The heart of genomics. Nat Med 2001. Mar; 7:287-288 [PubMed]
  94. Service SK, Ophoff RA, Freimer NB.  The genome-wide distribution of background linkage disequilibrium in a population isolate.  Hum Mol Genet. 2001 Mar 1;10(5):545-551. [PubMed]
  95. Human Genome Project Publications:
  96. Deutsch S, Iseli C, Bucher P, Antonarakis SE, Scott HS. A cSNP map and database for human chromosome 21. Genome Res. 2001 Feb 11: 300-307. [PubMed]
  97. Buetow KH, Edmonson M, MacDonald R, Clifford R, Yip P, Kelley J, Little DP, Strausberg R, Koester H, Cantor CR, Braun A. High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.  Proc Natl Acad Sci U S A 2001 Jan 16;98(2):581-4[PubMed][pdf]
  98. Ott J. Neural networks and disease asociation studies. Am J Med Genet. 2001 Jan 8;105(1):60-1. [PubMed]
  99. Fallin D, Cohen A, Essioux L, Chumakov I, Blumenfeld M, Cohen D, Schork NJ. Genetic analysis of case/ control data using estimated haplotype frequencies: application to APOE locus variation and alzheimer's disease. Genome Res. 2001 Jan; 11: 143-151.  [PubMed]
  100. Nelson DL. SNPs, linkage disequilibrium, human genetic variation and native american culture. Trends Genet. 2001 Jan; 17(1): 15-16 [PubMed]
  101. Pruitt KD, Maglott DR. RefSeq and LocusLink: NCBI gene-centered resources. Nucleic Acids Res. 2001 Jan 1;29(1):137-40. [PubMed]
  102. Bourgain C, Genin E, Holopainen P, Mustalahti K, Maki M, Partanen J, Clerget-Darpoux F. Use of Closely Related Affected Individuals for the Genetic Study of Complex Diseases in Founder Populations. Am J Hum Genet. 2001 Jan;68(1):154-159. [PubMed]
  103. Cherny SS, Abecasis GR, Cookson WO, Sham PC, Cardon LR. The effect of genotype and pedigree error on linkage analysis: analysis of three asthma genome scans. Genet Epidemiol. 2001;21 Suppl 1:S117-22. [PubMed]
  104. Collier DA. Sudden impact? The human genome sequence and the pace of gene discovery in complex diseases. Pharmacogenomics J. 2001;1(1):9-11. [PubMed]

last updated: 5 May 2002
home