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La ricerca find articoli where authors phrase all words ' WIJSMAN EM' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 67 riferimenti
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    1. Sieberts, SK; Wijsman, EM; Thompson, EA
      Relationship inference from trios of individuals, in the presence of typing error

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Chapman, NH; Wijsman, EM
      Introduction: Linkage analyses in the Hutterites

      GENETIC EPIDEMIOLOGY
    3. Chapman, NH; Leutenegger, AL; Badzioch, MD; Bogdan, M; Conlon, EM; Daw, EW; Gagnon, F; Li, N; Maia, JM; Wijsman, EM; Thompson, EA
      The importance of connections: Joining components of the Hutterite pedigree

      GENETIC EPIDEMIOLOGY
    4. Wijsman, EM; Almasy, L; Amos, CI; Borecki, IB; Falk, CT; King, TM; Martinez, MM; Meyers, D; Neuman, RJ; Olson, JM; Rich, S; Spence, MA; Thomas, DC; Vieland, VJ; Witte, JS; MacCluer, JW
      Analysis of complex genetic traits: Application to asthma and simulated data - Preface

      GENETIC EPIDEMIOLOGY
    5. Wijsman, EM; Nur, N
      On estimating the proportion of variance in a phenotypic trait attributable to a measured locus

      HUMAN HEREDITY
    6. Daw, EW; Thompson, EA; Wijsman, EM
      Bias in multipoint linkage analysis arising from map misspecification

      GENETIC EPIDEMIOLOGY
    7. Wijsman, EM; Peterson, D; Leutenegger, AL; Thomson, JB; Goddard, KAB; Hsu, L; Berninger, VW; Raskind, WH
      Segregation analysis of phenotypic components of learning disabilities. I.Nonword memory and digit span

      AMERICAN JOURNAL OF HUMAN GENETICS
    8. Daw, EW; Payami, H; Nemens, EJ; Nochlin, D; Bird, TD; Schellenberg, GD; Wijsman, EM
      The number of trait loci in late-onset Alzheimer disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    9. Hadley, EC; Rossi, WK; Albert, S; Bailey-Wilson, J; Baron, J; Cawthon, R; Christian, JC; Corder, EH; Franceschi, C; Kestenbaum, B; Kruglyak, L; Lauderdale, DS; Lubitz, J; Martin, GM; McClearn, GE; McGue, M; Miles, T; Mineau, G; Ouellett, G; Pedersen, NL; Preston, SH; Page, WF; Province, M; Schachter, F; Schork, NJ; Vaupel, JW; Vijg, J; Wallace, R; Wang, E; Wijsman, EM
      Genetic epidemiologic studies on age-specified traits

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    10. Raskind, WH; Hsu, L; Berninger, VW; Thomson, JB; Wijsman, EM
      Familial aggregation of dyslexia phenotypes

      BEHAVIOR GENETICS
    11. Saavedra-Matiz, CA; Chapman, NH; Wijsman, EM; Horowitz, SH; Rosen, DR
      Linkage of hereditary distal myopathy with desmin accumulation to 2q

      HUMAN HEREDITY
    12. Sjoberg, G; Saavedra-Matiz, CA; Rosen, DR; Wijsman, EM; Borg, K; Horowitz, SH; Sejersen, T
      A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filamentformation

      HUMAN MOLECULAR GENETICS
    13. Daw, EW; Kumm, J; Snow, GL; Thompson, EA; Wijsman, EM
      Monte Carlo Markov chain methods for genome screening

      GENETIC EPIDEMIOLOGY
    14. Goldin, LR; Amos, CI; Chase, GA; Goldstein, AM; Jarvik, GP; Martinez, MM; Suarez, BK; Weeks, DE; Wijsman, EM; MacCluer, JW
      Genetic analysis workshop 11 - Analysis of genetic and environmental factors in common diseases - Preface

      GENETIC EPIDEMIOLOGY
    15. Daw, EW; Heath, SC; Wijsman, EM
      Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. Hokanson, JE; Brunzell, JD; Jarvik, GP; Wijsman, EM; Austin, MA
      Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency

      AMERICAN JOURNAL OF HUMAN GENETICS
    17. WIJSMAN EM; BRUNZELL JD; JARVIK GP; AUSTIN MA; MOTULSKY AG; DEEB SS
      EVIDENCE AGAINST LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO THE APOLIPOPROTEIN AI-CIII-AIV GENE-COMPLEX

      Arteriosclerosis, thrombosis, and vascular biology
    18. RASKIND WH; CONRAD EU; MATSUSHITA M; WIJSMAN EM; WELLS DE; CHAPMAN N; SANDELL LJ; WAGNER M; HOUCK J
      EVALUATION OF LOCUS HETEROGENEITY AND EXT1 MUTATIONS IN 34 FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES

      Human mutation
    19. SNOW GL; WIJSMAN EM
      PEDIGREE ANALYSIS PACKAGE (PAP) VS. MORGAN - MODEL SELECTION AND HYPOTHESIS-TESTING ON A LARGE PEDIGREE

      Genetic epidemiology
    20. LI HZ; THOMPSON EA; WIJSMAN EM
      SEMIPARAMETRIC ESTIMATION OF MAJOR GENE EFFECTS FOR AGE-OF-ONSET

      Genetic epidemiology
    21. Chapman, NH; Wijsman, EM
      Genome screens using linkage disequilibrium tests: Optimal marker characteristics and feasibility

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. WIJSMAN EM
      MONTE-CARLO MARKOV-CHAIN METHODS AND MODEL SELECTION IN GENETIC-ANALYSIS

      Animal biotechnology
    23. EDLAND SD; WIJSMAN EM; SCHODEREHRI GL; LEVERENZ JB
      LITTLE EVIDENCE OF REDUCED SURVIVAL TO ADULTHOOD OF APOE EPSILON-4 HOMOZYGOTES IN DOWNS-SYNDROME

      NeuroReport
    24. WIJSMAN EM; AMOS CI
      GENETIC-ANALYSIS OF SIMULATED OLIGOGENIC TRAITS IN NUCLEAR AND EXTENDED PEDIGREES - SUMMARY OF GAW10 CONTRIBUTIONS

      Genetic epidemiology
    25. GRAHAM J; CHAPMAN NH; GODDARD KAB; GOODE EL; WIJSMAN EM; JARVIK GP
      SEGREGATION AND LINKAGE ANALYSIS OF A QUANTITATIVE VERSUS A QUALITATIVE TRAIT IN LARGE PEDIGREES

      Genetic epidemiology
    26. HEATH SC; SNOW GL; THOMPSON EA; TSENG C; WIJSMAN EM
      MCMC SEGREGATION AND LINKAGE ANALYSIS

      Genetic epidemiology
    27. BIRD TD; WIJSMAN EM; NOCHLIN D; LEEHEY M; SUMI SM; PAYAMI H; POORKAJ P; NEMENS E; RAFKIND M; SCHELLENBERG GD
      CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD

      Neurology
    28. CHAPMAN NH; WIJSMAN EM
      OPTIMAL MARKER CHARACTERISTICS FOR GENOME SCREENS USING LINKAGE DISEQUILIBRIUM TESTS

      American journal of human genetics
    29. DAW EW; HEATH SC; WIJSMAN EM
      MULTIPOINT OLIGOGENIC ANALYSIS OF AGE-OF-ONSET DATA WITH APPLICATIONSTO LARGE ALZHEIMERS-DISEASE PEDIGREES

      American journal of human genetics
    30. GODDARD KAB; WIJSMAN EM
      PEDIGREE SELECTION CRITERIA FOR GENOME SCREENING OF COMPLEX-MODELS

      American journal of human genetics
    31. YU CE; OSHIMA J; WIJSMAN EM; NAKURA J; MIKI T; PIUSSAN C; MATTHEWS S; FU YH; MULLIGAN J; MARTIN GM; SCHELLENBERG GD; BURG G; EPSTEIN CJ; FISCHER W; FUJIWARA Y; FUKUCHI KI; HOEHN H; HURLIMANN AF; KISO S; MATTHEWS J; MELARAGNO MI; MURANO S; OUAIS S; POOT M; RIZZO M; SAIDA T; TANNOCK TCA; UYENO B
      MUTATIONS IN THE CONSENSUS HELICASE DOMAINS OF THE WERNER SYNDROME GENE

      American journal of human genetics
    32. NAKURA J; MIKI T; YE L; MITSUDA N; ZHAO Y; KIHARA K; YU CE; OSHIMA J; FUKUCHI K; WIJSMAN EM; SCHELLENBERG GD; MARTIN GM; MURANO S; HASHIMOTO K; FUJIWARA Y; OGIHARA T
      NARROWING THE POSITION OF THE WERNER SYNDROME LOCUS BY HOMOZYGOSITY ANALYSIS - EXTENSION OF HOMOZYGOSITY ANALYSIS

      Genomics
    33. OLSHEN AB; WIJSMAN EM
      PEDIGREE ANALYSIS PACKAGE VS MIXD - FITTING THE MIXED-MODEL ON A LARGE PEDIGREE

      Genetic epidemiology
    34. YU CE; OSHIMA J; FU YH; WIJSMAN EM; HISAMA F; ALISCH R; MATTHEWS S; NAKURA J; MIKI T; OUAIS S; MARTIN GM; MULLIGAN J; SCHELLENBERG GD
      POSITIONAL CLONING OF THE WARNERS SYNDROME GENE

      Science
    35. GODDARD KAB; YU CE; OSHIMA J; MIKI T; NAKURA J; PIUSSAN C; MARTIN GM; SCHELLENBERG GD; WIJSMAN EM; BROWN WT; BURG G; CERIMELE D; COTTINI F; EPSTEIN CJ; FISCHER W; FRACCARO M; FUJIWARA Y; FUKUCHI KI; HIWADA K; HOEHN H; HOSOKAWA Y; HURLIMANN AF; ISHAWATA H; KAMINO K; KIHARA K; KISO S; LIN Y; MAEDA T; MATTHEWS J; MATSUMURA T; MCKAY JE; MELARAGNO MI; MITSUDA M; MOTULSKY AG; MURAKAMI T; MURANO S; NIIKAWA N; POOT M; OGIHARA T; RIZZO M; SAIDA T; SCAPPATICCI S; TANNOK TCA; TAMAKI S; UTSU N; UYENO B; WAKAYAMA A; YANAGAWA M; YEVICH II; YOSHIDA S; ZIGRANG W
      TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS

      American journal of human genetics
    36. PAYAMI H; ZAREPARSI S; MONTEE KR; SEXTON GJ; KAYE JA; BIRD TD; YU CE; WIJSMAN EM; HESTON LL; LITT M; SCHELLENBERG GD
      GENDER DIFFERENCE IN APOLIPOPROTEIN E-ASSOCIATED RISK FOR FAMILIAL ALZHEIMER-DISEASE - A POSSIBLE CLUE TO THE HIGHER INCIDENCE OF ALZHEIMER-DISEASE IN WOMEN

      American journal of human genetics
    37. JARVIK GP; LARSON EB; GODDARD K; KUKULL WA; SCHELLENBERG GD; WIJSMAN EM
      INFLUENCE OF APOLIPOPROTEIN-E GENOTYPE ON THE TRANSMISSION OF ALZHEIMER-DISEASE IN A COMMUNITY-BASED SAMPLE

      American journal of human genetics
    38. GODDARD KAB; JARVIK GP; GRAHAM J; MCNENEY B; HSU L; SIEGMUND K; GROSSER S; OLSON J; WIJSMAN EM
      ANALYSIS OF QUANTITATIVE RISK-FACTORS FOR A COMMON OLIGOGENIC DISEASE

      Genetic epidemiology
    39. SCHELLENBERG GD; SHARMA V; POORKAJ P; HISAMA F; WIJSMAN EM; WEISSMAN SM; BIRD TD
      THE CHROMOSOME-14 ALZHEIMERS-DISEASE LOCUS

      Journal of cellular biochemistry
    40. LEVYLAHAD E; LAHAD A; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
      APOLIPOPROTEIN-E GENOTYPES AND AGE-OF-ONSET IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE

      Annals of neurology
    41. KOLLER WC; GLATT SL; HUBBLE JP; PAOLO A; TROSTER AI; HANDLER MS; HORVAT RT; MARTIN C; SCHMIDT K; KARST A; WIJSMAN EM; YU CE; SCHELLENBERG GD
      APOLIPOPROTEIN-E GENOTYPES IN PARKINSON DISEASE WITH AND WITHOUT DEMENTIA

      Annals of neurology
    42. QUERFURTH HW; WIJSMAN EM; STGEORGEHYSLOP PH; SELKOE DJ
      BETA-APP MESSENGER-RNA TRANSCRIPTION IS INCREASED IN CULTURED FIBROBLASTS FROM THE FAMILIAL ALZHEIMERS DISEASE-1 FAMILY

      Molecular brain research
    43. PAYAMI H; MONTEE KR; KAYE JA; WIJSMAN EM; BIRD T; YU CE; HESTON LL; SCHELLENBERG GD
      THE APOLIPOPROTEIN-E E4 ALLELE AND SEX-SPECIFIC RISK OF ALZHEIMERS-DISEASE

      JAMA, the journal of the American Medical Association
    44. LEVYLAHAD E; WIJSMAN EM; NEMENS E; ANDERSON L; GODDARD KAB; WEBER JL; BIRD TD; SCHELLENBERG GD
      A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-1

      Science
    45. LEVYLAHAD E; WASCO W; POORKAJ P; ROMANO DM; OSHIMA J; PETTINGELL WH; YU CE; JONDRO PD; SCHMIDT SD; WANG K; CROWLEY AC; FU YH; GUENETTE SY; GALAS D; NEMENS E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD; TANZI RE
      CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS

      Science
    46. JARVIK GP; WIJSMAN EM; KUKULL WA; SCHELLENBERG GD; YU C; LARSON EB
      INTERACTIONS OF APOLIPOPROTEIN-E GENOTYPE, TOTAL CHOLESTEROL LEVEL, AGE, AND SEX IN PREDICTION OF ALZHEIMERS-DISEASE - A CASE-CONTROL STUDY

      Neurology
    47. LEVYLAHAD E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
      ALZHEIMERS-DISEASE IN THE VOLGA GERMANS - PHENOCOPY ANALYSIS IN A COMMON, COMPLEX DISEASE

      American journal of human genetics
    48. JARVIK GP; LARSON EB; GODDARD K; SCHELLENBERG GD; WIJSMAN EM
      APOE GENOTYPE INFLUENCE IN ALZHEIMER-DISEASE TRANSMISSION

      American journal of human genetics
    49. EVANS JP; PALMER S; SCHERER SM; KUKOLICH M; WIJSMAN EM; TSUI LC; STEPHENS K
      HETEROGENEITY OF THE AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION - REPLY

      American journal of human genetics
    50. JARVIK GP; WIJSMAN EM
      ALZHEIMERS-DISEASE AND THE FAMILY EFFECT

      Nature genetics
    51. NAKURA J; WIJSMAN EM; MIKI T; KAMINO K; YU CE; OSHIMA J; FUKUCHI K; WEBER JL; PIUSSAN C; MELARAGNO MI; EPSTEIN CJ; SCAPPATICCI S; FRACCARO M; FUJIWARA Y; MATSUMURA T; MURANO S; YOSHIDA S; SAIDA T; OGIHARA T; MARTIN GM; SCHELLENBERG GD
      HOMOZYGOSITY MAPPING OF THE WERNER SYNDROME LOCUS (WRN)

      Genomics
    52. PALMER SE; DALE DC; LIVINGSTON RJ; WIJSMAN EM; STEPHENS K
      AUTOSOMAL-DOMINANT CYCLIC HEMATOPOIESIS - EXCLUSION OF LINKAGE TO THEMAJOR HEMATOPOIETIC REGULATORY GENE-CLUSTER ON CHROMOSOME-5

      Human genetics
    53. SCHELLENBERG GD; BONNYCASTLE L; YU CE; WIJSMAN EM; BIRD TD
      THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE LOCUS

      Cytogenetics and cell genetics
    54. OLSON JM; WIJSMAN EM
      DESIGN AND SAMPLE-SIZE CONSIDERATIONS IN THE DETECTION OF LINKAGE DISEQUILIBRIUM WITH A DISEASE LOCUS

      American journal of human genetics
    55. YU CE; OSHIMA J; GODDARD KAB; MIKI T; NAKURA J; OGIHARA T; POOT M; HOEHN H; FRACCARO M; PIUSSAN C; MARTIN GM; SCHELLENBERG GD; WIJSMAN EM
      LINKAGE DISEQUILIBRIUM AND HAPLOTYPE STUDIES OF CHROMOSOME-8P-11.1-21.1 MARKERS AND WERNER-SYNDROME

      American journal of human genetics
    56. PALMER SE; SCHERER SW; KUKOLICH M; WIJSMAN EM; TSUI LC; STEPHENS K; EVANS JP
      EVIDENCE FOR LOCUS HETEROGENEITY IN HUMAN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION

      American journal of human genetics
    57. YU CE; PAYAMI H; OLSON JM; BOEHNKE M; WIJSMAN EM; ORR HT; KUKULL WA; GODDARD KAB; NEMENS E; WHITE JA; ALONSO ME; TAYLOR TD; BALL MJ; KAYE J; MORRIS J; CHUI H; SADOVNICK AD; MARTIN GM; LARSON EB; HESTON LL; BIRD TD; SCHELLENBERG GD
      THE APOLIPOPROTEIN E CI/CII GENE-CLUSTER AND LATE-ONSET ALZHEIMER-DISEASE/

      American journal of human genetics
    58. WIJSMAN EM
      GENETIC-ANALYSIS OF ALZHEIMERS-DISEASE - A SUMMARY OF CONTRIBUTIONS TO GAW8

      Genetic epidemiology
    59. WIJSMAN EM; BIRD TD; MARTIN GM; SCHELLENBERG GD
      THE SEATTLE ALZHEIMERS-DISEASE DATA SET

      Genetic epidemiology
    60. THOMPSON EA; LIN S; OLSHEN AB; WIJSMAN EM
      MONTE-CARLO ANALYSIS ON A LARGE PEDIGREE

      Genetic epidemiology
    61. OLSON JM; WIJSMAN EM
      LINKAGE BETWEEN QUANTITATIVE TRAIT AND MARKER LOCI - METHODS USING ALL RELATIVE PAIRS

      Genetic epidemiology
    62. BONNYCASTLE LLC; YU CE; WIJSMAN EM; ORR HT; PATTERSON D; CLANCY KP; GODDARD KAB; ALONSO ME; NEMENS E; WHITE JA; HESTON LL; MARTIN GM; BIRD TD; SCHELLENBERG GD
      THE C-FOS GENE AND EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE

      Neuroscience letters
    63. NAKURA J; MIKI T; NAGANO K; KIHARA K; YE L; KAMINO K; FUJIWARA Y; YOSHIDA S; MURANO S; FUKUCHI K; WIJSMAN EM; MARTIN GM; SCHELLENBERG GD; OGIHARA T
      CLOSE LINKAGE OF THE GENE FOR WERNER SYNDROME TO ANK1 AND D8S87 ON THE SHORT ARM OF CHROMOSOME-8

      Gerontology
    64. STEPHENS K; SYBERT VP; WIJSMAN EM; EHRLICH P; SPENCER A
      A KERATIN-14 MUTATIONAL HOT-SPOT FOR EPIDERMOLYSIS-BULLOSA SIMPLEX, DOWLING-MEARA - IMPLICATIONS FOR DIAGNOSIS

      Journal of investigative dermatology
    65. SCHELLENBERG GD; WIJSMAN EM; PAYAMI H; BOEHNKE M; OLSON JM; YU C; ORR HT; KUKULL WA; HESTON LL; LARSON EB; BIRD TD
      FAMILIAL ALZHEIMERS-DISEASE AND GENETIC-HETEROGENEITY

      American journal of human genetics
    66. PALMER SE; DALE DC; LIVINGSTON RJ; WIJSMAN EM; STEPHENS K
      ROLE OF PLEIOTROPIC CYTOKINE SIGNAL TRANSDUCERS IN AUTOSOMAL-DOMINANTCYCLIC HEMATOPOIESIS

      American journal of human genetics
    67. SCHELLENBERG GD; PAYAMI H; WIJSMAN EM; ORR HT; GODDARD KAB; ANDERSON L; NEMENS E; WHITE JA; ALONSO ME; BALL MJ; KAYE J; MORRIS JC; CHUI H; SADOVNICK AD; HESTON LL; MARTIN GM; BIRD TD
      CHROMOSOME-14 AND LATE-ONSET FAMILIAL ALZHEIMER-DISEASE (FAD)

      American journal of human genetics


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Documento generato il 24/01/21 alle ore 01:12:33