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    1. Nakajima, T; Jorde, LB; Ishigami, T; Umemura, S; Emi, M; Lalouel, JM; Inoue, I
      Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Currat, M; Trabuchet, G; Rees, D; Perrin, P; Harding, RM; Clegg, JB; Langaney, A; Excoffier, L
      Molecular analysis of the beta-globin gene cluster in the niokholo mandenka population reveals a recent origin of the beta(S) senegal mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    3. Wandstrat, A; Wakeland, E
      The genetics of complex autoimmune diseases: non-MHC susceptibility genes

      NATURE IMMUNOLOGY
    4. Scriver, CR
      Human genetics: Lessons from Quebec populations

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    5. Kere, J
      Human population genetics: Lessons from Finland

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    6. Thomson, G
      An overview of the genetic analysis of complex diseases, with reference totype I diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    7. Kelly, MA; Mijovic, CH; Barnett, AH
      Genetics of type I diabetes

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    8. Boutin, P; Froguel, P
      Genetics of human obesity

      BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM
    9. Park, Y; Eisenbarth, GS
      Genetic susceptibility factors of Type 1 diabetes in Asians

      DIABETES-METABOLISM RESEARCH AND REVIEWS
    10. Taylor, JG; Choi, EH; Foster, CB; Chanock, SJ
      Using genetic variation to study human disease

      TRENDS IN MOLECULAR MEDICINE
    11. Brookes, AJ
      Rethinking genetic strategies to study complex diseases

      TRENDS IN MOLECULAR MEDICINE
    12. Cardon, LR; Bell, JI
      Association study designs for complex diseases

      NATURE REVIEWS GENETICS
    13. Folstein, SE; Rosen-Sheidley, B
      Genetics of autism: Complex aetiology for a heterogeneous disorder

      NATURE REVIEWS GENETICS
    14. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    15. Mackay, TFC
      Quantitative trait loci in Drosophila

      NATURE REVIEWS GENETICS
    16. Palmer, LJ; Cookson, WOCM
      Using single nucleotide polymorphisms as a means to understanding the pathophysiology of asthma

      RESPIRATORY RESEARCH
    17. Ohashi, J; Tokunaga, K
      The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers

      JOURNAL OF HUMAN GENETICS
    18. Shinohara, Y; Ezura, Y; Iwasaki, H; Nakazawa, I; Ishida, R; Kodaira, M; Kajita, M; Shiba, T; Emi, M
      Linkage disequilibrium and haplotype analysis among ten single-nucleotide polymorphisms of interleukin 11 identified by sequencing of the gene

      JOURNAL OF HUMAN GENETICS
    19. Nakazawa, I; Nakajima, T; Ishigami, T; Umemura, S; Emi, M
      Linkage disequilibrium and haplotype analysis among eight novel single-nucleotide polymorphisms in the human tissue-type plasminogen activator (t-PA)gene

      JOURNAL OF HUMAN GENETICS
    20. Takashima, M; Ishikawa, K; Nagaoka, U; Shoji, S; Mizusawa, H
      A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in Japan

      JOURNAL OF HUMAN GENETICS
    21. Richter, B; Stegmann, K; Roper, B; Boddeker, I; Ngo, ETKM; Koch, MC
      Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population

      JOURNAL OF HUMAN GENETICS
    22. Ishida, R; Ezura, Y; Iwasaki, H; Nakazawa, I; Kajita, M; Kodaira, M; Ito, H; Emi, M
      Linkage disequilibrium and haplotype analysis among four novel single-nucleotide polymorphisms in the human leukemia inhibitory factor (LIF) gene

      JOURNAL OF HUMAN GENETICS
    23. Angerer, WP
      A note on the evaluation of fluctuation experiments

      MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    24. Carlson, CS; Newman, TL; Nickerson, DA
      SNPing in the human genome

      CURRENT OPINION IN CHEMICAL BIOLOGY
    25. Jannink, JL; Bink, MCAM; Jansen, RC
      Using complex plant pedigrees to map valuable genes

      TRENDS IN PLANT SCIENCE
    26. Zak, NB; Shifman, S; Shalom, A; Darvasi, A
      Population-based gene discovery in the post-genomic era

      DRUG DISCOVERY TODAY
    27. Kirov, G; Lowry, CA; Stephens, M; Oldfield, S; O'Donovan, MC; Lightman, SL; Owen, MJ
      Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder

      MOLECULAR PSYCHIATRY
    28. Curran, S; Mill, J; Tahir, E; Kent, L; Richards, S; Gould, A; Huckett, L; Sharp, J; Batten, C; Fernando, S; Ozbay, F; Yazgan, Y; Simonoff, E; Thompson, M; Taylor, E; Asherson, P
      Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples

      MOLECULAR PSYCHIATRY
    29. Tordjman, S; Gutknecht, L; Carlier, M; Spitz, E; Antoine, C; Slama, F; Carsalade, V; Cohen, DJ; Ferrari, P; Roubertoux, PL; Anderson, GM
      Role of the serotonin transporter gene in the behavioral expression of autism

      MOLECULAR PSYCHIATRY
    30. Hattori, E; Ebihara, M; Yamada, K; Ohba, H; Shibuya, H; Yoshikawa, T
      Identification of a compound short tandem repeat stretch in the 5 '-upstream region of the cholecystokinin gene, and its association with panic disorder but not with schizophrenia

      MOLECULAR PSYCHIATRY
    31. Persico, AM; D'Agruma, L; Maiorano, N; Totaro, A; Militerni, R; Bravaccio, C; Wassink, TH; Schneider, C; Melmed, R; Trillo, S; Montecchi, F; Palermo, M; Pascucci, T; Puglisi-Allegra, S; Reichelt, KL; Conciatori, M; Marino, R; Quattrocchi, CC; Baldi, A; Zelante, L; Gasparini, P; Keller, F
      Reelin gene alleles and haplotypes as a factor predisposing to autistic disorder

      MOLECULAR PSYCHIATRY
    32. Veenstra-VanderWeele, J; Kim, SJ; Gonen, D; Hanna, GL; Leventhal, BL; Cook, EH
      Genomic organization of the SLC1A1/EAAC1 gene and mutation screening in early-onset obsessive-compulsive disorder

      MOLECULAR PSYCHIATRY
    33. Yoshikawa, T; Kikuchi, M; Saito, K; Watanabe, A; Yamada, K; Shibuya, H; Nankai, M; Kurumaji, A; Hattori, E; Ishiguro, H; Shimizu, H; Okubo, Y; Toru, M; Detera-Wadleigh, SD
      Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples

      MOLECULAR PSYCHIATRY
    34. Ohtsuki, T; Sakurai, K; Dou, H; Toru, M; Yamakawa-Kobayashi, K; Arinami, T
      Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia

      MOLECULAR PSYCHIATRY
    35. Iwata, N; Ozaki, N; Inada, T; Goldman, D
      Association of a 5-MT5A receptor polymorphism, Pro15Ser, to schizophrenia

      MOLECULAR PSYCHIATRY
    36. Semwal, P; Prasad, S; Bhatia, T; Deshpande, SN; Wood, J; Nimgaonkar, VL; Thelma, BK
      Family-based association studies of monoaminergic gene polymorphisms amongNorth Indians with schizophrenia

      MOLECULAR PSYCHIATRY
    37. Tan, Z; Jiang, SS; Lin, ZX; Zhang, BF; Yu, J; Feng, GY; He, L
      Identification of SNPs in human gamma aminobutyric acid A receptor gamma 2gene

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    38. Bykhovskaya, Y; Yang, HY; Taylor, K; Hang, T; Tun, RYM; Estivill, X; Casano, RAMS; Majamaa, K; Shohat, M; Fischel-Ghodsian, N
      Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness

      GENETICS IN MEDICINE
    39. Mathews, DJ; Kashuk, C; Brightwell, G; Eichler, EE; Chakravarti, A
      Sequence variation within the fragile x locus

      GENOME RESEARCH
    40. Lai, E
      Application of SNP technologies in medicine: Lessons learned and future challenges

      GENOME RESEARCH
    41. 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 RESEARCH
    42. Sachot, S; Moirand, R; Jouanolle, AM; Mosser, J; Fergelot, P; Deugnier, Y; Brissot, P; le Gall, JY; David, V
      Low penetrant hemochromatosis phenotype in eight families: No evidence of modifiers in the MHC region

      BLOOD CELLS MOLECULES AND DISEASES
    43. Sklar, P
      The genomic approach to candidate genes

      HARVARD REVIEW OF PSYCHIATRY
    44. Da Silveira, LA; Ribeiro, WL; Kirchgatter, K; Wunderlich, G; Matsuoka, H; Tanabe, K; Ferreira, MU
      Sequence diversity and linkage disequilibrium within the merozoite surfaceprotein-1 (Msp-1) locus of Plasmodium falciparum: A longitudinal study in Brazil

      JOURNAL OF EUKARYOTIC MICROBIOLOGY
    45. Jeffreys, AJ; Kauppi, L; Neumann, R
      Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

      NATURE GENETICS
    46. Daly, MJ; Rioux, JD; Schaffner, SE; Hudson, TJ; Lander, ES
      High-resolution haplotype structure in the human genome

      NATURE GENETICS
    47. Johnson, GCL; Esposito, L; Barratt, BJ; Smith, AN; Heward, J; Di Genova, G; Ueda, H; Cordell, HJ; Eaves, IA; Dudbridge, F; Twells, RCJ; Payne, F; Hughes, W; Nutland, S; Stevens, H; Carr, P; Tuomilehto-Wolf, E; Tuomilehto, J; Gough, SCL; Clayton, DG; Todd, JA
      Haplotype tagging for the identification of common disease genes

      NATURE GENETICS
    48. Shifman, S; Darvasi, A
      The value of isolated populations

      NATURE GENETICS
    49. Laitinen, T; Daly, MJ; Rioux, JD; Kauppi, P; Laprise, C; Petays, T; Green, T; Cargill, M; Haahtela, T; Lander, ES; Laitinen, LA; Hudson, TJ; Kere, J
      A susceptibility locus for asthma-related traits on chromosome 7 revealed by genome-wide scan in a founder population

      NATURE GENETICS
    50. Kruglyak, L; Nickerson, DA
      Variation is the spice of life

      NATURE GENETICS
    51. Watanabe, Y; Murray, JC; Bjork, BC; Bird, CP; Chiang, PW; Gregory, SG; Kurnit, DM; Schutte, BC
      Matroshka and ectopic polymorphisms: Two new classes of DNA sequence variation identified at the Van der Woude syndrome locus on 1q32-q41

      HUMAN MUTATION
    52. Rannala, B; Bertorelle, G
      Using linked markers to infer the age of a mutation

      HUMAN MUTATION
    53. Collins, A; Ennis, S; Taillon-Miller, P; Kwok, PY; Morton, NE
      Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map

      HUMAN MUTATION
    54. Ott, J; Hoh, J
      Statistical multilocus methods for disequilibrium analysis in complex traits

      HUMAN MUTATION
    55. Rohde, K; Fuerst, R
      Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information

      HUMAN MUTATION
    56. Cook, EH
      Genetics of autism

      CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA
    57. Yoshida, K; Hamajima, N; Kozaki, K; Saito, H; Maeno, K; Sugiura, T; Ookuma, K; Takahashi, T
      Association between the dopamine D2 receptor A2/A2 genotype and smoking behavior in the Japanese

      CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION
    58. Beaty, TH; Wang, H; Hetmanski, JB; Fan, YT; Zeiger, JS; Liang, KY; Chiu, YF; Vanderkolk, CA; Seifert, KC; Wulfsberg, EA; Raymond, G; Panny, SR; McIntosh, I
      A case-control study of nonsyndromic oral clefts in Maryland

      ANNALS OF EPIDEMIOLOGY
    59. Hohler, T; Marker-Hermann, E
      Psoriatic arthritis: clinical aspects, genetics, and the role of T cells

      CURRENT OPINION IN RHEUMATOLOGY
    60. Tetushkin, EY
      Genetics and the origin of human "races"

      RUSSIAN JOURNAL OF GENETICS
    61. Vorechovsky, I; Kralovicova, J; Laycock, MD; Webster, ADB; Marsh, SGE; Madrigal, A; Hammarstrom, L
      Short tandem repeat (STR) haplotypes in HLA: an integrated 50-kb STR/linkage disequilibrium/gene map between the RING3 and HLA-B genes and identification of STR haplotype diversification in the class III region

      EUROPEAN JOURNAL OF HUMAN GENETICS
    62. Pan, HC; Lin, HM; Ku, WY; Li, TC; Li, SY; Lin, CC; Hsiao, KM
      Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan:implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1

      EUROPEAN JOURNAL OF HUMAN GENETICS
    63. Verpillat, P; Bouley, S; Campion, D; Hannequin, D; Dubois, B; Belliard, S; Puel, M; Thomas-Anterion, C; Agid, Y; Brice, A; Clerget-Darpoux, F
      Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population

      EUROPEAN JOURNAL OF HUMAN GENETICS
    64. Lee, MH; Gordon, D; Ott, J; Lu, KM; Ose, L; Miettinen, T; Gylling, H; Stalenhoef, AF; Pandya, A; Hidaka, H; Brewer, B; Kojima, H; Sakuma, N; Pegoraro, R; Salen, G; Patel, SB
      Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities

      EUROPEAN JOURNAL OF HUMAN GENETICS
    65. Akey, J; Jin, L; Xiong, MM
      Haplotypes vs single marker linkage disequilibrium tests: what do we gain?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    66. Horvath, S; Xu, X; Laird, NM
      The family based association test method: strategies for studying general genotype-phenotype associations

      EUROPEAN JOURNAL OF HUMAN GENETICS
    67. Zouali, H; Chamaillard, M; Lesage, S; Cezard, JP; Colombel, JF; Belaiche, J; Almer, S; Tysk, C; Montague, S; Gassull, M; Christensen, S; Finkel, Y; Gower-Rousseau, C; Modigliani, R; Macry, J; Selinger-Leneman, H; Thomas, G; Hugot, JP
      Genetic refinement and physical mapping of a chromosome 16q candidate region for inflammatory bowel disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    68. Bergman, A; Einbeigi, Z; Olofsson, U; Taib, Z; Wallgren, A; Karlsson, P; Wahlstrom, J; Martinsson, T; Nordling, M
      The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation

      EUROPEAN JOURNAL OF HUMAN GENETICS
    69. Tao, SH; Liu, XM; Chu, JH; Zhang, RM; Du, LP; Luo, ZW
      Rate of decay in admixture linkage disequilibrium and its implication in gene mapping

      CHINESE SCIENCE BULLETIN
    70. Tao, SH; Zhang, RM; Chu, JH; Liu, XM; Du, LP; Qi, QY; Luo, ZW
      A population genetics model of linkage disequilibrium in admired populations

      CHINESE SCIENCE BULLETIN
    71. Ogorelkova, M; Kraft, HG; Ehnholm, C; Utermann, G
      Single nucleotide polymorphisms in exons of the apo(a) kringles IV types 6to 10 domain affect Lp(a) plasma concentrations and have different patterns in Africans and Caucasians

      HUMAN MOLECULAR GENETICS
    72. Miller, RD; Kwok, PY
      The birth and death of human single-nucleotide polymorphisms: new experimental evidence and implications for human history and medicine

      HUMAN MOLECULAR GENETICS
    73. Jorde, LB; Watkins, WS; Bamshad, MJ
      Population genomics: a bridge from evolutionary history to genetic medicine

      HUMAN MOLECULAR GENETICS
    74. van den Oord, EJCG
      Estimating effects of latent and measured genotypes in multilevel models

      STATISTICAL METHODS IN MEDICAL RESEARCH
    75. Walton, C; Handley, JM; Collins, FH; Baimai, V; Harbach, RE; Deesin, V; Butlin, RK
      Genetic population structure and introgression in Anopheles dirus mosquitoes in South-east Asia

      MOLECULAR ECOLOGY
    76. Moxley, G; Han, J
      HLA DMA and DMB show no association with rheumatoid arthritis in US Caucasians

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    77. Nowotny, P; Kwon, JM; Goate, AM
      SNP analysis to dissect human traits

      CURRENT OPINION IN NEUROBIOLOGY
    78. Aquadro, CF; DuMont, VB; Reed, FA
      Genome-wide variation in the human and fruitfly: a comparison

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    79. Huang, JB; Hsieh, TF; Chastagner, GA; Hsiang, T
      Clonal and sexual propagation in Botrytis elliptica

      MYCOLOGICAL RESEARCH
    80. Malhotra, AK
      The genetics of schizophrenia

      CURRENT OPINION IN PSYCHIATRY
    81. Frossard, PM; Malloy, MJ; Lestringant, GG; Kane, JP
      Haplotypes of the human renin gene associated with essential hypertension and stroke

      JOURNAL OF HUMAN HYPERTENSION
    82. Ma, X; Yang, K; Lindblad, P; Egevad, L; Hemminki, K
      VHL gene alterations in renal cell carcinoma patients: novel hotspot or founder mutations and linkage disequilibrium

      ONCOGENE
    83. Simo, JM; Joven, J; Vilella, E; Ribas, M; Figuera, L; Virgos, C; Sundaram, IM; Hoover-Plow, J
      Polymorphisms in human apolipoprotein(a) kringle IV-10 and coronary arterydisease: relationship to allele size, plasma lipoprotein(a) concentration,and lysine binding site activity

      JOURNAL OF MOLECULAR MEDICINE-JMM
    84. Heaton, MP; Chitko-McKown, CG; Grosse, WM; Keele, JW; Keen, JE; Laegreid, WW
      Interleukin-8 haplotype structure from nucleotide sequence variation in commercial populations of US beef cattle

      MAMMALIAN GENOME
    85. Samils, B; Stepien, V; Lagercrantz, U; Lascoux, M; Gullberg, U
      Genetic diversity in relation to sexual and asexual reproduction in populations of Melampsora larici-epitea

      EUROPEAN JOURNAL OF PLANT PATHOLOGY
    86. Li, T; Underhill, J; Liu, XH; Sham, PC; Donaldson, P; Murray, RM; Wright, P; Collier, DA
      Transmission disequilibrium analysis of HLA class II DRB1, DQA1, DQB1 and DPB1 polymorphisms in schizophrenia using family trios from a Han Chinese population

      SCHIZOPHRENIA RESEARCH
    87. Dubertret, C; Gorwood, P; Gouya, L; Deybach, JC; Ades, J
      Association and excess of transmission of a DRD2 haplotype in a sample of French schizophrenic patients.

      SCHIZOPHRENIA RESEARCH
    88. Mundo, E; Zai, G; Lee, L; Parikh, SV; Kennedy, JL
      The 5HT1D beta receptor gene in Bipolar Disorder: A family-based association study

      NEUROPSYCHOPHARMACOLOGY
    89. Olivier, M; Bustos, VI; Levy, MR; Smick, GA; Moreno, I; Bushard, JM; Almendras, AA; Sheppard, K; Zierten, DL; Aggarwal, A; Carlson, CS; Foster, BD; Vo, N; Kelly, L; Liu, X; Cox, DR
      Complex high-resolution linkage disequilibrium and haplotype patterns of single-nucleotide polymorphisms in 2.5 Mb of sequence on human chromosome 21

      GENOMICS
    90. Kauppi, P; Lindblad-Toh, K; Sevon, P; Toivonen, HTT; Rioux, JD; Villapakkam, A; Laitinen, LA; Hudson, TJ; Kere, J; Laitinen, T
      Second-generation association study of the 5q31 cytokine gene cluster and the interleukin-4 receptor in asthma

      GENOMICS
    91. Nurmi, EL; Bradford, Y; Chen, YH; Hall, J; Arnone, B; Gardiner, MB; Hutcheson, HB; Gilbert, JR; Pericak-Vance, MA; Copeland-Yates, SA; Michaelis, RC; Wassink, TH; Santangelo, SL; Sheffield, VC; Piven, J; Folstein, SE; Haines, JL; Sutcliffe, JS
      Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families

      GENOMICS
    92. Sanders, AR; Cao, QH; Taylor, J; Levin, TE; Badner, JA; Cravchik, A; Comeron, JM; Naruya, S; Del Rosario, A; Salvi, DA; Walczyk, KA; Mowry, BJ; Levinson, DF; Crowe, RR; Silverman, JM; Gejman, PV
      Genetic diversity of the human serotonin receptor 1B (HTR1B) gene

      GENOMICS
    93. Ota, M; Katsuyama, Y; Kimura, A; Tsuchiya, K; Kondo, M; Naruse, T; Mizuki, N; Itoh, K; Sasazuki, T; Inoko, H
      A second susceptibility gene for developing rheumatoid arthritis in the human MHC is localized within a 70-kb interval telomeric of the TNF genes in the HLA class III region

      GENOMICS
    94. Beck, TW; Menninger, J; Voigt, G; Newman, K; Nishigaki, Y; Nash, WG; Stephens, RM; Wang, Y; de Jong, PJ; O'Brien, SJ; Yuhki, N
      Comparative feline genomics: A BAC/PAC contig map of the major histocompatibility complex class II region

      GENOMICS
    95. Burrow, HM; Moore, SS; Johnston, DJ; Barendse, W; Bindon, BM
      Quantitative and molecular genetic influences on properties of beef: a review

      AUSTRALIAN JOURNAL OF EXPERIMENTAL AGRICULTURE
    96. Davies, W; Isles, AR; Wilkinson, LS
      Imprinted genes and mental dysfunction

      ANNALS OF MEDICINE
    97. Jones, I; Craddock, N
      Candidate gene studies of bipolar disorder

      ANNALS OF MEDICINE
    98. Devlin, B; Roeder, K; Bacanu, SA
      Unbiased methods for population-based association studies

      GENETIC EPIDEMIOLOGY
    99. Deng, HW; Li, J; Recker, RR
      Effect of polygenes on Xiong's transmission disequilibrium test of a QTL in nuclear families with multiple children

      GENETIC EPIDEMIOLOGY
    100. Chen, WM; Deng, HW
      A general and accurate approach for computing the statistical power of thetransmission disequilibrium test for complex disease genes

      GENETIC EPIDEMIOLOGY


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Documento generato il 27/05/20 alle ore 03:45:47