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  • 1997
    J Ott 1997 Relationship estimation in affected sib pair analysis of late onset diseases European Journal of Human Genetics 5 2 69 77 abstract Medline entry F Haghighi W Li CSJ Fann 1997 Affected sibpair analysis of bipolar disorder using data on chromosome 18 Genetic Epidemiology 14 641 646 abstract Medline entry F Haghighi J Ott 1997 Estimating recessive disease allele frequency based on genetic maps European Journal of Human Genetics 5 4 203 205 abstract Medline entry SJ Jensen EP Sulman JM Marks TC Matise PJ Vojta JC Barrett GM Brodeur PS White 1997 An integrated transcript map of human chromosome 1p35 36 Genomics 42 1 126 136 abstract Medline entry SH Juo TH Beaty PO Kwiterovich Jr 1997 Etiologic heterogeneity of hyperapobetalipoproteinemia HyperapoB the results from segregation analysis in families enriched for coronary artery disease Arterioscler Thromb Vasc Biol 17 2729 2736 Medline entry SH Juo TH Beaty LD Duffy NE Maestri VL Prenger J Zeiger HH Lei J Coresh 1997 A comprehensive analysis of a common disease and its underlying traits Genetic Epidemiology 14 6 815 820 Medline entry M Karayiorgou M Altemus BL Galke D Goldman DL Murphy J Ott JA Gogos 1997 Genotype determining low catechol O methyltransferase activity as a risk factor for obsessive compulsive disorder Proceedings of National Academy of Sciences USA 94 9 4572 4575 abstract Medline entry Full Text PDF Full Text postscript Lazzarini A Schwarz KO Jiang S Stenroos ES T Lehner Johnson WG 1997 Pelizaeus Merzbacher like disease exclusion of the proteolipid protein locus and documentation of a new locus on Xq Neurology 49 3 824 832 SM Leal J Ott 1997 Analysis of two locus traits under heterogeneity for recessive versus dominant inheritance Genetic Epidemiology 14 1097 1100 abstract Medline entry A Lernmark G Eisenbarth L Ducat HA Erlich D Faustman J Ott MA Permutt RS Spielman J X She J Todd 1997 Family cell lines available for research an endangered resource American Journal of Human Genetics 61 3 778 779 W Li 1997 The study of correlation structures of DNA sequences a critical review Computer Chemistry special issue on open problems of computational biology 21 4 257 272 abstract Medline entry full text PDF W Li 1997 The Complexity of DNA the measure of compositional heterogeneity in DNA sequences and measures of complexity Complexity 3 2 33 37 full text PDF PR Lucek J Ott 1997 Neural network analysis of complex traits Genetic Epidemiology 14 1101 1106 abstract TL McGee M Devoto J Ott EL Berson TP Dryja 1997 Evidence that the penetrance of mutations at the RP11 locus causing dominant retinitis pigmentosa is influenced by a gene linked to the homologous RP11 allele American Journal of Human Genetics 61 5 1059 1066 abstract Medline entry full text PDF B Mulller Myhsok H J Heiland CR Mulller G Meng T Grimm J Ott 1997 Mapping undetected mutations within a gene evidence for two preferential regions in the DMD gene Human Heredity 47 61 65 J Ott Vital

    Original URL path: http://linkage.rockefeller.edu/pub/1997.html (2012-11-26)
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  • 1996

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    Original URL path: /pub/1996.html (2012-11-26)


  • 1995
    318 CSJ Fann J Ott 1995 Parsimonious estimation of sex specific map distances by stepwise maximum likelihood regression Genomics 29 571 575 abstract Full Text postscript C Gambacorti Passerini J Ott A Bergen 1995 Human molecular genetics network correspondence New England Journal of Medicine 333 1573 H Kobayashi L Baumbach TC Matise A Schiavi F Greenberg E Hoffman 1995 A gene for a severe lethal form of X linked arthrogryposis X linked infantile spinal muscular atrophy maps to human chromosome Xp113 q112 Human Molecular Genetics 4 7 1213 1216 Medline entry A Lazzarini ES Stenroos T Lehner V McKoy B Gold MK McCormack CS Reid J Ott WG Johnson 1995 Short tandem repeat polymorphism linkage studies in a New England family with X linked mental retardation MRX20 American Journal of Medical Genetics 57 552 557 SM Leal J Ott 1995 Incorporating the variability of genotype specific penetrance probabilities in the calculation of risk support intervals Genetic Epidemiology 12 859 862 abstract TC Matise 1995 Genome scanning for complex disease genes using the transmission disequilibrium test and haplotype based haplotype relative risk Genetic Epidemiology 12 641 645 abstract Medline entry J Ott 1995 Linkage analysis with biological markers Human Heredity 45 169 174 abstract J Ott 1995 How do you compute a lod score news and views Nature Genetics 11 354 355 D Pauls J Ott S M Paul CR Allen CJ Fann JP Carulli KM Falls CA Bouthillier TC Gravius TP Keith JA Egeland EI Ginns 1995 Linkage analysis of chromosome 18 markers do not identify a major susceptibility locus for bipolar affected disorder in the old order Amish American Journal of Human Genetics 57 636 643 abstract AE Pulver Lasseter VK Kasch L Wolyniec PS Nestadt G Blouin JL Kimberland M Babb R Vourlis S Chen H Lalioti M

    Original URL path: http://linkage.rockefeller.edu/pub/1995.html (2012-11-26)
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  • 1994
    Dubay A Vignal M Agrapart T Imai Y Nakamura M Polymeropoulos J Weissenbach DR Cox GM Lathrop 1994 A radiation hybrid map of 506 STS markers spanning human chromosome 11 Nature Genetics 8 1 70 76 abstract Medline entry M Karayiorgou L Kasch VK Lasseter J Hwang R Elango DJ Bernardini M Kimberland R Babb CA Francomano PS Wolyniec M Lamacz G Nestadt D Meyers J Ott B Childs S Antonarakis HH Kazazian DE Housman AE Pulver 1994 Report from the Maryland epidemiology schizophrenia linkage study No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model American Journal of Medical Genetics 54 345 353 JA Knowles Y Shugart P Banerjee TC Gilliam CA Lewis SG Jacobson J Ott 1994 Identification of a locus distinct from RDS peripherin for autosomal recessive retinitis pigmentosa on chromosome 6p Human Molecular Genetics 3 1401 1403 abstract SM Leal J Ott 1994 A likelihood approach to calculating risk support intervals American Journal of Human Genetics 54 913 917 abstract C Magnani L Cremonesi E Belloni M Ferrari M Seia MP Russo M Devoto P Ronchetto G Romeo 1994 Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of CF in the Italian population Clinical Genetics 45 135 139 abstract C Merette LM Brzustowicz RJ Daniels KE Davies TC Gilliam J Melki A Munnich MA Pericak Vance T Siddique B Voosen B Wirth J Ott 1994 An Investigation of Genetic Heterogeneity and Linkage Disequilibrium with 161 families with Spinal Muscular Atrophy Genomics 21 27 33 abstract Medline entry J Ott H Donis Keller 1994 Statistical methods in genetic mapping Genomics 22 496 497 AE Pulver Karayiorgou M Wolyniec PS Lasseter VK Kasch L Nestadt G Antonarakis S Housman D Kazazian HH Meyers D J Ott

    Original URL path: http://linkage.rockefeller.edu/pub/1994.html (2012-11-26)
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  • 1993
    MJ Denton A Gal 1993 Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant Retinitis Pigmentosa Genomics 17 230 233 abstract B Casey M Devoto KL Jones A Ballabio 1993 Mapping of a gene for familial situs abnormalities to human chromosome Xq24 q271 Nature Genetics 5 403 407 abstract A Dobin WJ Kimberling W Pettinger JE Bailey Wilson YY Shugart P Gabow 1993 Segregation analysis of autosomal dominant polycystic kidney disease Genetic Epidemiology 10 189 200 abstract R Gabizon H Rosenman Z Meiner I Kahana E Kahana Y Shugart J Ott SB Prusiner 1993 Mutation and polymorphism of the prion protein gene in Lybian Jews with Creutzfeldt Jacob disease American Journal of Human Genetics 53 828 835 abstract E Hellsten J Vesa MC Speer TP Makela I Jarvela K Alit J Ott L Peltonen 1993 Refined assignment of the Infantile Neuronal Ceroid Lipofuscinosis INCL CLN1 locus at 1p32 incorporation of linkage disequilibrium in multipoint analysis Genomics 16 720 725 abstract SM Leal J Ott 1993 A bootstrap approach to estimating power for linkage heterogeneity Genetic Epidemiology 10 465 470 abstract MM LeBeau J Overhauser RE Straub G Silverman TC Gilliam J Ott P O Connell U Francke A Geurts van Kessel 1993 Report of the first international workshop on human chromosome 18 mapping Cytogenetics and Cell Genetics 63 78 95 Y Luo I Ceccherini B Pasini I Matera MP Bicocchi V Barone R Bocciardi H Kaariainen D Weber M Devoto G Romeo 1993 Close linkage with the RET proto oncogene and deletion mutations in autosomal dominant Hirschsprung disease Hum Molec Genet 2 1803 1808 abstract C Merette T Lehner J Ott 1993 Two new approaches toward linkage heterogeneity of FAD Two locus models and age of onset as a discriminator Genetic Epidemiology 10 455 459 abstract J Ott 1993 Detecting marker inconsistencies in human gene mapping Human Heredity 43 25 30 abstract J Ott C Merette 1993 Is there heterogeneity of age at onset for breast cancer Letter to the Editor American Journal of Human Genetics 52 3 627 630 K Petrukhin SG Fischer M Pirastu RE Tanzi I Chernov M Devoto LM Brzustowicz E Cayanis E Vitale J Russo D Matseoane B Boukhgalter W Wasco AL Figus J Loudianos A Cao I Sternlieb G Evgrafov E Parano L Pavone D Warburton J Ott G Penchaszadeh IH Scheinberg TC Gilliam 1993 Mapping cloning and genetic characterization of the region containing the Wilson disease gene Nature Genetics 5 338 343 abstract Medline entry KE Petrukhin MC Speer E Cayanis M de Fatima Bonaldo U Tantravahi MB Soares SG Fischer D Warburton TC Gilliam J Ott 1993 A microsatellite genetic linkage map of human chromosome 13 Genomics 15 76 85 abstract NJ Schork M Boehnke JD Terwilliger J Ott 1993 Two trait locus linkage analysis a powerful strategy for mapping complex genetic traits American Journal of Human Genetics 53 1127 1136 abstract Medline entry MA Spence DT Bishop M Boehnke RC Elston C Falk SE Hodge J

    Original URL path: http://linkage.rockefeller.edu/pub/1993.html (2012-11-26)
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  • 1992
    M Anvret AK Percy J Ott H Zoghbi 1992 Examination of X chromosome markers in Rett syndrome exclusion mapping with a novel variation on multilocus linkage analysis American Journal of Human Genetics 50 278 287 abstract M Maziade MA Roy JP Fournier D Cliche C Merette C Caron Y Garneau M Montgrain C Shriqui C Dion et al 1992 Reliability of best estimate diagnosis in genetic linkage studies of major psychoses results from the Quebec pedigree studies American Journal of Psychiatry 149 12 1674 1686 1992 abstract R Medori H J Tritschler A LeBlanc F Villare V Manetto HY Chen R Xue S Leal P Montagna P Cortelli P Tinuper P Avoni M Mochi A Baruzzi JJ Hauw J Ott E Lugaresi L Autilio Gambetti P Gambetti 1992 Fatal familial insomnia a prion disease with a mutation at codon 178 of the prion protein gene New England Journal of Medicine 326 444 449 abstract C Merette M C King J Ott 1992 Heterogeneity analysis of breast cancer families by using age at onset as a covariate American Journal of Human Genetics 50 515 519 abstract HW Moser AB Moser KD Smith A Bergin J Boral J Shankroff OC Stine C Merette J Ott W Krivit E Shapiro 1992 Adreno leukodystrophy Phenotypic variability implications for therapy Journal of Inher Metab Dis 15 645 664 abstract J Ott 1992 Strategies for characterizing highly polymorphic markers in human gene mapping American Journal of Human Genetics 51 283 290 abstract J Ott 1992 Introductory remarks genetic models and statistical approaches Ann Med 24 375 377 J Ott 1992 The future of multilocus linkage analysis Ann Med 24 401 403 abstract RB Petersen M Tabaton L Berg B Schrank RM Torack S Leal J Julien C Vital B Deleplanque WW Pendlebury D Drachman TW Smith

    Original URL path: http://linkage.rockefeller.edu/pub/1992.html (2012-11-26)
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  • 1991
    PP Green J Ott 1991 Guidelines for human linkage maps An International System for Human Linkage Maps ISLM 1990 Annals of Human Genetics 55 Pt 1 1 6 BJB Keats SL Sherman NE Morton EB Robson KH Buetow PE Cartwright A Chakravarti U Francke PP Green J Ott 1991 Guidelines for Human Linkage Maps An International System for Human Linkage Maps ISLM 1990 Meeting Report Genomics 9 557 560 S P Kwan T Lehner T Hagemann B Lu M Blaese H Ochs R Wedgwood J Ott IW Craig FS Rosen 1991 Localization of the gene for the Wiskott Aldrich syndrome between two flanking markers TIMP and DXS255 on Xp1122 Xp113 Genomics 10 29 33 abstract A Lernmark L Ducat G Eisenbarth J Ott MA Perlmutt P Rubinstein R Spielman 1991 Human cell lines from families available for diabetes research Letter to the Editor Diabetologia 34 61 C Merette T Lehner J Ott 1991 Interpreting nonsignificant outcomes of heterogeneity tests in gene mapping Letter to the Editor American Journal of Human Genetics 49 1381 1384 MR Passos Bueno B Byth D Love J Terwilliger J Ott D Rapaport M Vainzof M Zatz KE Davies 1991 Exclusion of the gene responsible for

    Original URL path: http://linkage.rockefeller.edu/pub/1991.html (2012-11-26)
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  • 1990
    chronic forms of spinal muscular atrophy Nature 345 823 825 E Ikonen J Palo J Ott J Gusella H Somer L Karila A Palotie L Peltonen 1990 Huntington disease in Finland Linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus American Journal of Human Genetics 46 5 11 abstract Medline entry BJB Keats SL Sherman J Ott 1990 Human Gene Mapping 105 Report of the committee on linkage and gene order Cytogenetics and Cell Genetics 55 387 94 S P Kwan J Terwilliger R Parmley G Raghu LA Sandkuyl J Ott H Ochs R Wedgwood F Rosen 1990 Identification of a closely linked DNA marker DXS178 to further refine the X linked agammaglobulinemia locus Genomics 6 238 242 abstract Medline entry MA Musarella L Anson Cartwright SM Leal LD Gilbert RG Worton GA Fishman J Ott 1990 Multipoint linkage analysis and heterogeneity testing in 20 X linked retinitis pigmentosa families Genomics 8 286 296 abstract Medline entry J Ott 1990 Genetic linkage and complex diseases A comment Genetic Epidemiology 7 35 36 J Ott 1990 Invited editorial Cutting a Gordian knot in the linkage analysis of complex human traits American Journal of Human Genetics 46 219 221 J Ott S Bhattacharya JD Chen MJ Denton J Donald C Dubay GJ Farrar GA Fishman D Frey A Gal P Humphries B Jay M Jay M Litt M Machler M Musarella M Neugebauer RL Nussbaum JD Terwilliger GG Weleber B Wirth F Wong RG Worton AF Wright 1990 Localizing multiple X chromosome linked retinitis pigmentosa loci using multilocus homogeneity tests Proceedings of National Academy of Sciences 87 701 704 abstract Medline entry J Ott J Caesar M Machler A Schinzel W Schmid 1990 Presymptomatic exclusion of myotonic dystrophy in a one generation

    Original URL path: http://linkage.rockefeller.edu/pub/1990.html (2012-11-26)
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