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    1. Feitosa, MF; Borecki, IB; Rich, SS; Arnett, DK; Sholinsky, P; Myers, RH; Leppert, M; Province, MA
      Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: The National Heart, Lung, and Blood Institute Family Heart Study

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Johanneson, B; Alarcon-Riquelme, ME
      An update on the genetics of systemic lupus erythematosus

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    3. Ahmad, YA; Bruce, IN
      Genetic epidemiology - Systemic lupus erythematosus

      ARTHRITIS RESEARCH
    4. Graham, RR; Langefeld, CD; Gaffney, PM; Ortmann, WA; Selby, SA; Baechler, EC; Shark, KB; Ockenden, TC; Rohlf, KE; Moser, KL; Brown, WM; Gabriel, SE; Messner, RP; King, RA; Horak, P; Elder, JT; Stuart, PE; Rich, SS; Behrens, TW
      Genetic linkage and transmission disequilibrium of marker haplotypes at chromosome 1q41 in human systemic lupus erythematosus

      ARTHRITIS RESEARCH
    5. Field, M
      Tumour necrosis factor polymorphisms in rheumatic diseases

      QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS
    6. Cichon, S; Schmidt-Wolf, G; Schumacher, J; Muller, DJ; Hurter, M; Schulze, TG; Albus, M; Borrmann-Hassenbach, M; Franzek, E; Lanczik, M; Fritze, J; Kreiner, R; Weigelt, B; Minges, J; Lichtermann, D; Lerer, B; Kanyas, K; Strauch, K; Windemuth, C; Baur, MP; Wienker, TF; Maier, W; Rietschel, M; Propping, P; Nothen, MM
      A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26

      MOLECULAR PSYCHIATRY
    7. Kennedy, S; Bennett, S; Weeks, DE
      Genetics and infertility II - Affected sib-pair analysis in endometriosis

      HUMAN REPRODUCTION UPDATE
    8. Wakeland, EK; Liu, K; Graham, RR; Behrens, TW
      Delineating the genetic basis of systemic lupus erythematosus

      IMMUNITY
    9. Alcais, A; Abel, L
      Incorporation of covariates in multipoint model-free linkage analysis of binary traits: how important are unaffecteds?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    10. Dechairo, B; Dimon, C; van Heel, D; Mackay, I; Edwards, M; Scambler, P; Jewell, D; Cardon, L; Lench, N; Carey, A
      Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3)

      EUROPEAN JOURNAL OF HUMAN GENETICS
    11. Rijsdijk, FV; Hewitt, JK; Sham, PC
      Analytic power calculation for QTL linkage analysis of small pedigrees

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Lachmeijer, AMA; Arngrimsson, R; Bastiaans, EJ; Frigge, ML; Pals, G; Sigurdardottir, S; Stefansson, H; Palsson, B; Nicolae, D; Kong, A; Aarnoudse, JG; Gulcher, JR; Dekker, GA; ten Kate, LP; Stefansson, K
      A genome-wide scan for preeclampsia in the Netherlands

      EUROPEAN JOURNAL OF HUMAN GENETICS
    13. Palferman, S; Matthews, N; Turner, H; Moore, J; Hervas, A; Aubin, A; Wallace, S; Michelotti, J; Wainhouse, C; Paul, A; Thompson, E; Murin, M; Gupta, R; Garner, C; Pickles, A; Rutter, M; Bailey, A; Lamb, JA; Marlow, A; Scudder, P; Barnby, G; Monaco, AP; Baird, G; Cox, A; Docherty, Z; Warburton, P; Green, EP; Abbs, SJ; Le Couteur, A; McConachie, HR; Berney, T; Kelly, TP; De Vries, PJ; Bolton, P; Green, J; Gilchrist, A; Whittacker, J; Bolton, B; Packer, R; Maestrini, E; Van Engeland, H; De Jonge, MV; Kemner, C; Klauck, SM; Beyer, KS; Epp, S; Poustka, A; Benner, A; Poustka, F; Ruhl, D; Schmotzer, G; Bolte, S; Feineis-Matthews, S; Fombonne, E; Roge, B; Fremolle-Kruck, J; Pienkowski, C; Tauber, MT; Pedersen, L; Brondum-Nielsen, K; Eriksen, G; Haracopos, D; Cotterill, RMJ; Tsiantis, J; Papanikolaou, K; Lord, C; Corsello, C; Guter, S; Leventhal, B; Cook, E; Smalley, S; Bailey, J; Liu, A; Dedricks, M; Chrzanowski, L; Levitt, J; Pauls, D; Volkmar, F; Weeks, DE
      Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q

      HUMAN MOLECULAR GENETICS
    14. Amos, CI; de Andrade, M
      Genetic linkage methods for quantitative traits

      STATISTICAL METHODS IN MEDICAL RESEARCH
    15. Winterer, G; Egan, MF; Radler, T; Hyde, T; Coppola, R; Weinberger, DR
      An association between reduced interhemispheric EEG coherence in the temporal lobe and genetic risk for schizophrenia (vol 49, pg 129, 2001)

      SCHIZOPHRENIA RESEARCH
    16. Winterer, G; Egan, MF; Radler, T; Hyde, T; Coppola, R; Weinberger, DR
      An association between reduced interhemispheric EEG coherence in the temporal lobe and genetic risk for schizophrenia

      SCHIZOPHRENIA RESEARCH
    17. Boddeker, IR; Muller, HH; Kress, R; Geller, F; Ziegler, A; Schafer, H
      The use of sequential designs in genome scans for asthma susceptibility loci with affected sib pairs

      GENETIC EPIDEMIOLOGY
    18. Chang, CJ; Fann, CSJ
      Using data mining to address heterogeneity in the Southampton data

      GENETIC EPIDEMIOLOGY
    19. Rutherford, S; Johnson, MP; Curtain, RP; Griffiths, LR
      Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension

      HUMAN GENETICS
    20. John, S; Eyre, S; Myerscough, A; Barrett, J; Silman, A; Ollier, W; Worthington, J
      Linkage and association analysis of candidate genes in rheumatoid arthritis

      JOURNAL OF RHEUMATOLOGY
    21. Luft, FC
      Twins in cardiovascular genetic research

      HYPERTENSION
    22. Fouldrin, G; Jay, M; Bonnet-Brilhault, F; Menard, JF; Petit, M; Thibaut, F
      Concordance of deficit and non-deficit subtypes in siblings affected with schizophrenia

      PSYCHIATRY RESEARCH
    23. Holberg, CJ; Erickson, RP; Bernas, MJ; Witte, MH; Fultz, KE; Andrade, M; Witte, CL
      Segregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    24. Barrett, S; Beck, JC; Bernier, R; Bisson, E; Braun, TA; Casavant, TL; Childress, D; Folstein, SE; Garcia, M; Gardiner, MB; Gilman, S; Haines, JL; Hopkins, K; Landa, R; Meyer, NH; Mullane, JA; Nishimura, DY; Palmer, P; Piven, J; Purdy, J; Santangelo, SL; Searby, C; Sheffield, V; Singleton, J; Slager, S; Struchen, T; Svenson, S; Vieland, V; Wang, K; Winklosky, B
      An autosomal genomic screen for autism (vol 88, pg 609, 1999)

      AMERICAN JOURNAL OF MEDICAL GENETICS
    25. Mandal, DM; Wilson, AF; Bailey-Wilson, JE
      Effects of misspecification of allele frequencies on the power of Haseman-Elston sib-pair linkage method for quantitative traits

      AMERICAN JOURNAL OF MEDICAL GENETICS
    26. van Tilburg, J; van Haeften, TW; Pearson, P; Wijmenga, C
      Defining the genetic contribution of type 2 diabetes mellitus

      JOURNAL OF MEDICAL GENETICS
    27. Asherson, PJ; Curran, S
      Approaches to gene mapping in complex disorders and their application in child psychiatry and psychology

      BRITISH JOURNAL OF PSYCHIATRY
    28. Kaufman, KM; Kirby, MY; McClain, MT; Harley, JB; James, JA
      Lupus autoantibodies recognize the product of an alternative open reading frame of SmB/B '

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    29. Rao, SQ; Olson, JM; Moser, KL; Gray-McGuire, C; Bruner, GR; Kelly, J; Harley, JB
      Linkage analysis of human systemic lupus erythematosus-related traits - A principal component approach

      ARTHRITIS AND RHEUMATISM
    30. Nath, SK; Kelly, JA; Namjou, B; Lam, T; Bruner, GR; Scofield, RH; Aston, CE; Harley, JB
      Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in familieswith vitiligo-related systemic lupus erythematosus

      AMERICAN JOURNAL OF HUMAN GENETICS
    31. Cox, NJ; Wapelhorst, B; Morrison, VA; Johnson, L; Pinchuk, L; Spielman, RS; Todd, JA; Concannon, P
      Seven regions of the genome show evidence of linkage to type 1 diabetes ina consensus analysis of 767 multiplex families

      AMERICAN JOURNAL OF HUMAN GENETICS
    32. 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; Ryder, N; Cottington, E; Parr, J; Pickles, A; Rutter, M; Bailey, A; Barnby, G; Lamb, JA; Marlow, A; Scudder, P; Monaco, AP; Baird, G; Cox, A; Docherty, Z; Warburton, P; Green, EP; Abbs, SJ; Le Couteur, A; McConachie, HR; Berney, T; Kelly, TP; De Vries, PJ; Bolton, PF; Green, J; Gilchrist, A; Whittacker, J; Bolton, B; Packer, R; Maestrini, E; Blasi, F; Van Engeland, H; De Jonge, MV; Kemner, C; Klauck, SM; Beyer, KS; Epp, S; Poustka, A; Benner, A; Goethe, JW; Poustka, F; Ruhl, D; Schmotzer, G; Boolte, S; Feineis-Matthews, S; Fombonne, E; Rogee, B; Fremolle-Kruck, J; Pienkowski, C; Tauber, MT; Pedersen, L; Nielsen, KB; Eriksen, G; Haracopos, D; Cotterill, RMJ; Tsiantis, J; Papanikolaou, K; Lord, C; Corsello, C; Guter, S; Leventhal, B; Cook, E; Smalley, SL; Bailey, J; McGough, J; Levitt, J; Pauls, D; Volkmar, F; Weeks, DE
      A genomewide screen for autism: Strong evidence for linkage to chromosomes2q, 7q, and 16p

      AMERICAN JOURNAL OF HUMAN GENETICS
    33. Liu, JJ; Nyholt, DR; Magnussen, P; Parano, E; Pavone, P; Geschwind, D; Lord, C; Iversen, P; Hoh, J; Ott, J; Gilliam, TC
      A genomewide screen for autism susceptibility loci

      AMERICAN JOURNAL OF HUMAN GENETICS
    34. Hanson, RL; Kobes, S; Lindsay, RS; Knowler, WC
      Assessment of parent-of-origin effects in linkage analysis of quantitativetraits

      AMERICAN JOURNAL OF HUMAN GENETICS
    35. Marlow, AJ; Fisher, SE; Richardson, AJ; Francks, C; Talcott, JB; Monaco, AP; Stein, JF; Cardon, LR
      Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK

      BEHAVIOR GENETICS
    36. Gutknecht, L
      Full-genome scans with autistic disorder: A review

      BEHAVIOR GENETICS
    37. Zhang, W; Tapper, W; Collins, A; Jacobs, KB; Elston, RC; Morton, NE
      A tournament of linkage tests in complex inheritance

      HUMAN HEREDITY
    38. Purcell, S; Cherny, SS; Hewitt, JK; Sham, PC
      Optimal sibship selection for genotyping in quantitative trait locus linkage analysis

      HUMAN HEREDITY
    39. Forrest, WF
      Weighting improves the 'new Haseman-Elston' method

      HUMAN HEREDITY
    40. Schwab, SG; Hallmayer, J; Albus, M; Lerer, B; Eckstein, GN; Borrmann, M; Segman, RH; Hanses, C; Freymann, J; Yakir, A; Trixler, M; Falkai, P; Rietschel, M; Maier, W; Wildenauer, DB
      A genome-wide autosomal screen for schizophrenia susceptibility loci in 71families with affected siblings: support for loci on chromosome 10p and 6

      MOLECULAR PSYCHIATRY
    41. Auranen, M; Nieminen, T; Majuri, S; Vanhala, R; Peltonen, L; Jarvela, I
      Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q,13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families

      MOLECULAR PSYCHIATRY
    42. Malerba, G; Lauciello, MC; Scherpbier, T; Trabetti, E; Galavotti, R; Cusin, V; Pescollderungg, L; Zanoni, G; Martinati, LC; Boner, AL; Levitt, RC; Pignatti, PF
      Linkage analysis of chromosome 12 markers in Italian families with atopic asthmatic children

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    43. Chatziplis, DG; Haley, CS
      Selective genotyping for QTL detection using sib pair analysis in outbred populations with hierarchical structures

      GENETICS SELECTION EVOLUTION
    44. Glenn, CL; Wang, WYS; Benjafield, AV; Morris, BJ
      Linkage and association of tumor necrosis factor receptor 2 locus with hypertension, hypercholesterolemia and plasma shed receptor

      HUMAN MOLECULAR GENETICS
    45. Elston, RC
      Introduction and overview

      STATISTICAL METHODS IN MEDICAL RESEARCH
    46. Curran, S; Taylor, EA
      Attention deficit-hyperactivity disorder: biological causes and treatments

      CURRENT OPINION IN PSYCHIATRY
    47. Elston, RC; Buxbaum, S; Jacobs, KB; Olson, JM
      Haseman and Elston revisited

      GENETIC EPIDEMIOLOGY
    48. Sham, PC; Zhao, JH; Cherny, SS; Hewitt, JK
      Variance-components QTL linkage analysis of selected and non-normal samples: Conditioning on trait values

      GENETIC EPIDEMIOLOGY
    49. Walder, K; Hanson, RL; Kobes, S; Knowler, WC; Ravussin, E
      An autosomal genomic scan for loci linked to plasma leptin concentration in Pima Indians

      INTERNATIONAL JOURNAL OF OBESITY
    50. Saccone, NL; Kwon, JM; Corbett, J; Goate, A; Rochberg, N; Edenberg, HJ; Foroud, T; Li, TK; Begleiter, H; Reich, T; Rice, JP
      A genome screen of maximum number of drinks as an alcoholism phenotype

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Rutter, M
      Genetic studies of autism: From the 1970s into the millennium

      JOURNAL OF ABNORMAL CHILD PSYCHOLOGY
    52. Xiong, MM; Guo, SW
      Multiple regression approach to mapping of quantitative trait loci (QTL) based on sib-pair data: A theoretical analysis

      ANNALS OF STATISTICS
    53. Petrucci, M; Scott, P; Ouimet, D; Trouve, ML; Proulx, Y; Valiquette, L; Guay, G; Bonnardeaux, A
      Evaluation of the calcium-sensing receptor gene in idiopathic hypercalciuria and calcium nephrolithiasis

      KIDNEY INTERNATIONAL
    54. Nemani, M; Sahbatou, M; Blanche, H; Thomas, G; Pascoe, L
      The efficiency of genetic analysis of DNA from aged siblings to detect chromosomal regions implicated in longevity

      MECHANISMS OF AGEING AND DEVELOPMENT
    55. Friedlander, Y; Talmud, PJ; Edwards, KL; Humphries, SE; Austin, MA
      Sib-pair linkage analysis of longitudinal changes in lipoprotein risk factors and lipase genes in women twins

      JOURNAL OF LIPID RESEARCH
    56. Otto, JM; Chandrasekeran, R; Vermes, C; Mikecz, K; Finnegan, A; Rickert, SE; Enders, JT; Glant, TT
      A genome scan using a novel genetic cross identifies new susceptibility loci and traits in a mouse model of rheumatoid arthritis

      JOURNAL OF IMMUNOLOGY
    57. Blangero, J; Williams, JT; Almasy, L
      Quantitative trait locus mapping using human pedigrees

      HUMAN BIOLOGY
    58. Robinson, RL; Curran, JL; Ellis, FR; Halsall, PJ; Hall, WJ; Hopkins, PM; Iles, DE; West, SP; Shaw, MA
      Multiple interacting gene products may influence susceptibility to malignant hyperthermia

      ANNALS OF HUMAN GENETICS
    59. Ghosh, S; Watanabe, RM; Valle, TT; Hauser, ER; Magnuson, VL; Langefeld, CD; Ally, DS; Mohlke, KL; Silander, K; Kohtamaki, K; Chines, P; Balow, J; Birznieks, G; Chang, J; Eldridge, W; Erdos, MR; Karanjawala, ZE; Knapp, JI; Kudelko, K; Martin, C; Morales-Mena, A; Musick, A; Musick, T; Pfahl, C; Porter, R; Rayman, JB; Rha, D; Segal, L; Shapiro, S; Sharaf, R; Shurtleff, B; So, A; Tannenbaum, J; Te, C; Tovar, J; Unni, A; Welch, C; Whiten, R; Witt, A; Blaschak-Harvan, J; Douglas, JA; Duren, WL; Epstein, MP; Fingerlin, TE; Kaleta, HS; Lange, EM; Li, C; McEachin, RC; Stringham, HM; Trager, E; White, PP; Eriksson, J; Toivanen, L; Vidgren, G; Nylund, SJ; Tuomilehto-Wolf, E; Ross, EH; Demirchyan, E; Hagopian, WA; Buchanan, TA; Tuomilehto, J; Bergman, RN; Collins, FS; Boehnke, M
      The Finland-United States Investigation of Non-Insulin-Dependent Diabetes Mellitus Genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes

      AMERICAN JOURNAL OF HUMAN GENETICS
    60. Levinson, DF; Holmans, P; Straub, RE; Owen, MJ; Wildenauer, DB; Gejman, PV; Pulver, AE; Laurent, C; Kendler, KS; Walsh, D; Norton, N; Williams, NM; Schwab, SG; Lerer, B; Mowry, BJ; Sanders, AR; Antonarakis, SE; Blouin, JL; DeLeuze, JF; Mallet, J
      Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: Schizophrenia linkage collaborative group III

      AMERICAN JOURNAL OF HUMAN GENETICS
    61. Nyholt, DR
      All LODs are not created equal

      AMERICAN JOURNAL OF HUMAN GENETICS
    62. Dupuis, J; Van Eerdewegh, P
      Multipoint linkage analysis of the pseudoautosomal regions, using affectedsibling pairs

      AMERICAN JOURNAL OF HUMAN GENETICS
    63. Wilson, AF; Sorant, AJM
      Equivalence of single- and multilocus markers: Power to detect linkage with composite markers derived from biallelic loci

      AMERICAN JOURNAL OF HUMAN GENETICS
    64. Sham, PC; Cherny, SS; Purcell, S; Hewitt, JK
      Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

      AMERICAN JOURNAL OF HUMAN GENETICS
    65. Pratt, SC; Daly, MJ; Kruglyak, L
      Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components

      AMERICAN JOURNAL OF HUMAN GENETICS
    66. Knoblauch, H; Muller-Myhsok, B; Busjahn, A; Ben Avi, L; Bahring, S; Baron, H; Heath, SC; Uhlmann, R; Faulhaber, HD; Shpitzen, S; Aydin, A; Reshef, A; Rosenthal, M; Eliav, O; Muhl, A; Lowe, A; Schurr, D; Harats, D; Jeschke, E; Friedlander, Y; Schuster, H; Luft, FC; Leitersdorf, E
      A cholesterol-lowering gene maps to chromosome 13q

      AMERICAN JOURNAL OF HUMAN GENETICS
    67. Cardon, LR; Abecasis, GR
      Some properties of a variance components model for fine-mapping quantitative trait loci

      BEHAVIOR GENETICS
    68. Cardon, LR
      A sib-pair regression model of linkage disequilibrium for quantitative traits

      HUMAN HEREDITY
    69. Alcais, A; Abel, L
      Linkage analysis of quantitative trait loci: Sib pairs or sibships?

      HUMAN HEREDITY
    70. Siegmund, KD; Todorov, AA
      Linkage analysis for diseases with variable age of onset

      HUMAN HEREDITY
    71. Mandal, DM; Wilson, AF; Elston, RC; Weissbecker, K; Keats, BJ; Bailey-Wilson, JE
      Effects of misspecification of allele frequencies on the type I error rateof model-free linkage analysis

      HUMAN HEREDITY
    72. Nothen, MM; Cichon, S; Rohleder, H; Hemmer, S; Franzek, E; Fritze, J; Albus, M; Borrmann-Hassenbach, M; Kreiner, R; Weigelt, B; Minges, J; Lichtermann, D; Maier, W; Craddock, N; Fimmers, R; Holler, T; Baur, MP; Rietschel, M; Propping, P
      Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families

      MOLECULAR PSYCHIATRY
    73. Knoblauch, H; Busjahn, A; Muller-Myhsok, B; Faulhaber, HD; Schuster, H; Uhlmann, R; Luft, FC
      Peroxisome proliferator-activated receptor gamma gene locus is related to body mass index and lipid values in healthy nonobese subjects

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    74. Ziegler, A
      Sampling strategies for model free linkage analyses of quantitative traits: Implications for sib pair studies of reading and spelling disabilities tominimize the total study cost

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    75. Fisher, SE; Stein, JF; Monaco, AP
      A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia)

      EUROPEAN CHILD & ADOLESCENT PSYCHIATRY
    76. Shugart, YY; Goldgar, DE
      Multipoint genomic scanning for quantitative loci: effects of map density,sibship size and computational approach

      EUROPEAN JOURNAL OF HUMAN GENETICS
    77. Martinez, ML; Vukasinovic, N; Freeman, G
      Random model approach for QTL mapping in half-sib families

      GENETICS SELECTION EVOLUTION
    78. Kehoe, P; Wavrant-De Vrieze, F; Crook, R; Wu, WS; Holmans, P; Fenton, I; Spurlock, G; Norton, N; Williams, H; Williams, N; Lovestone, S; Perez-Tur, J; Hutton, M; Chartier-Harlin, MC; Shears, S; Roehl, K; Booth, J; Van Voorst, W; Ramic, D; Williams, J; Goate, A; Hardy, J; Owen, MJ
      A full genome scan for late onset Alzheimer's disease

      HUMAN MOLECULAR GENETICS
    79. Aita, VM; Christiano, AM; Gilliam, TC
      Mapping complex traits in diseases of the hair and skin

      EXPERIMENTAL DERMATOLOGY
    80. Goldin, LR; Chase, GA; Wilson, AF
      Regional inference with averaged P values increases the power to detect linkage

      GENETIC EPIDEMIOLOGY
    81. Alcais, A; Abel, L
      Maximum-likelihood-binomial method for genetic model-free linkage analysisof quantitative traits in sibships

      GENETIC EPIDEMIOLOGY
    82. Feakes, R; Sawcer, S; Chataway, J; Coraddu, F; Broadley, S; Gray, J; Jones, HB; Clayton, D; Goodfellow, PN; Compston, A
      Exploring the dense mapping of a region of potential linkage in complex disease: An example in multiple sclerosis

      GENETIC EPIDEMIOLOGY
    83. de Andrade, M; Amos, CI; Thiel, TJ
      Methods to estimate genetic components of variance for quantitative traitsin family studies

      GENETIC EPIDEMIOLOGY
    84. Goldin, LR; Chase, GA
      Comparison of two linkage inference procedures for genes related to the P300 component of the event related potential

      GENETIC EPIDEMIOLOGY
    85. Wyszynski, DF; Panhuysen, CIM
      Parental sex effect in families with alcoholism

      GENETIC EPIDEMIOLOGY
    86. Bailey, JN; Suchard, MA; Smalley, SL; Sinsheimer, JS
      Search for a genexenvironment interaction: GxE hunt

      GENETIC EPIDEMIOLOGY
    87. Greenwood, CMT; Brewer, CG; Morgan, K
      Validation of linkage by sampling based on environmental exposures

      GENETIC EPIDEMIOLOGY
    88. Mandal, DM; Sorant, AJM; Pugh, EW; Marcus, SE; Klein, AP; Mathias, RA; O'Neill, J; Temiyakarn, LF; Wilson, AF; Bailey-Wilson, JE
      Environmental covariates: Effects on the power of sib-pair linkage methods

      GENETIC EPIDEMIOLOGY
    89. Saccone, NL; Downey, TJ; Meyer, DJ; Neuman, RJ; Rice, JP
      Mapping genotype to phenotype for linkage analysis

      GENETIC EPIDEMIOLOGY
    90. McPeek, MS
      Optimal allele-sharing statistics for genetic mapping using affected relatives

      GENETIC EPIDEMIOLOGY
    91. Williams, JT; Blangero, J
      Comparison of variance components and sibpair-based approaches to quantitative trait linkage analysis in unselected samples

      GENETIC EPIDEMIOLOGY
    92. Wavrant-DeVrieze, F; Rudrasingham, V; Lambert, JC; Chakraverty, S; Kehoe, P; Crook, R; Amouyel, P; Wu, W; Holmans, P; Rice, F; Perez-Tur, J; Frigard, B; Morris, JC; Carty, S; Cottel, D; Tunstall, N; Lovestone, S; Petersen, RC; Chartier-Harlin, MC; Goate, A; Owen, MJ; Williams, J; Hardy, J
      No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease

      NEUROSCIENCE LETTERS
    93. Busjahn, A; Aydin, A; von Treuenfels, N; Faulhaber, HD; Gohlke, HR; Knoblauch, H; Schuster, H; Luft, FC
      Linkage but lack of association for blood pressure and the alpha-adducin locus in normotensive twins

      JOURNAL OF HYPERTENSION
    94. Barrett, S; Beck, JC; Bernier, R; Bisson, E; Braun, TA; Casavant, TL; Childress, D; Folstein, SE; Garcia, M; Gardiner, MB; Gilman, S; Haines, JL; Hopkins, K; Landa, R; Meyer, NH; Mullane, JA; Nishimura, DY; Palmer, P; Piven, J; Purdy, J; Santangelo, SL; Searby, C; Sheffield, V; Singleton, J; Slager, S; Struchen, T; Svenson, S; Vieland, V; Wang, K; Winklosky, B
      An autosomal genomic screen for autism

      AMERICAN JOURNAL OF MEDICAL GENETICS
    95. Saccone, NL; Rice, JP; Rochberg, N; Goate, A; Reich, T; Shears, S; Wu, W; Nurnberger, JI; Foroud, T; Edenberg, HJ; Li, TK
      Genome screen for platelet monoamine oxidase (MAO) activity

      AMERICAN JOURNAL OF MEDICAL GENETICS
    96. Rogers, J; Mahaney, MC; Almasy, L; Comuzzie, AG; Blangero, J
      Quantitative trait linkage mapping in anthropology

      YEARBOOK OF PHYSICAL ANTHROPOLOGY 1999, VOL 42
    97. Dudoit, S; Speed, TP
      A score test for linkage using identity by descent data from sibships

      ANNALS OF STATISTICS
    98. Maier, W; Lichtermann, D; Rietschel, M; Held, T; Falkai, P; Wagner, M; Schwab, S
      Genetics of schizophrenic disorders. Newer concepts and findings

      NERVENARZT
    99. Gessler, DDG; Xu, SZ
      Multipoint genetic mapping of quantitative trait loci with dominant markers in outbred populations

      GENETICA
    100. Busjahn, A; Knoblauch, H; Faulhaber, HD; Boeckel, T; Rosenthal, M; Uhlmann, R; Hoehe, M; Schuster, H; Luft, FC
      QT interval is linked to 2 long-QT syndrome loci in normal subjects

      CIRCULATION


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 02:55:34