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    1. Kere, J
      Human population genetics: Lessons from Finland

      ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS
    2. Louis, ED; Ford, B; Frucht, S; Barnes, LF; Ming, XT; Ottman, R
      Risk of tremor and impairment from tremor in relatives of patients with essential tremor: A community-based family study

      ANNALS OF NEUROLOGY
    3. Auranen, M; Ala-Mello, S; Turunen, JA; Jarvela, I
      Further evidence for linkage of autosomal-dominant medullary cystic kidneydisease on chromosome 1q21

      KIDNEY INTERNATIONAL
    4. Susi, M; Holopainen, P; Mustalahti, K; Maki, M; Partanen, J
      Candidate gene region 15q26 and genetic susceptibility to coeliac disease in Finnish families

      SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
    5. Holopainen, P; Mustalahti, K; Uimari, P; Collin, P; Maki, M; Partanen, J
      Candidate gene regions and genetic heterogeneity in gluten sensitivity

      GUT
    6. Pastinen, T; Raitio, M; Lindroos, K; Tainola, P; Peltonen, L; Syvanen, AC
      A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays

      GENOME RESEARCH
    7. Varilo, T; Laan, M; Hovatta, I; Wiebe, V; Terwilliger, JD; Peltonen, L
      Linkage disequilibrium in isolated populations: Finland and a young sub-population of Kuusamo

      EUROPEAN JOURNAL OF HUMAN GENETICS
    8. Ilonen, J; Reijonen, H; Green, A; Reunanen, A; Knip, M; Simell, O; Akerblom, HK
      Geographical differences within Finland in the frequency of HLA-DQ genotypes associated with Type 1 diabetes susceptibility

      EUROPEAN JOURNAL OF IMMUNOGENETICS
    9. Alaejos, MS; Romero, FJD; Romero, CD
      Selenium and cancer: Some nutritional aspects

      NUTRITION
    10. Medica, I; Logar, N; Peterlin, B
      Characteristics of myotonic dystrophy in Istria: Molecular genetic approach. Part II: Analysis of genetic polymorphisms

      COLLEGIUM ANTROPOLOGICUM
    11. Levo, A; Kuismanen, K; Holopainen, P; Vahtera, E; Rasi, V; Krusius, T; Partanen, J
      Single founder mutation (W380G) in type II protein C deficiency in Finland

      THROMBOSIS AND HAEMOSTASIS
    12. Lee, YJ; Huang, FY; Wang, CH; Lo, FS; Tsan, KW; Hsu, CH; Huang, CY; Chang, SC; Chang, JG
      Polymorphism in the transmembrane region of the MICA gene and type 1 diabetes

      JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
    13. Koeleman, BPC; Dudbridge, F; Cordell, HJ; Todd, JA
      Adaptation of the extended transmission/disequilibrium test to distinguishdisease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test

      ANNALS OF HUMAN GENETICS
    14. Peltonen, L
      Positional cloning of disease genes: Advantages of genetic isolates

      HUMAN HEREDITY
    15. Mole, SE; Mitchison, HM; Munroe, PB
      Molecular basis of the neuronal ceroid lipofuscinoses: Mutations in CLN1, CLN2, CLN3, and CLN5

      HUMAN MUTATION
    16. Ohman, M; Oksanen, L; Kainulainen, K; Janne, OA; Kaprio, J; Koskenvuo, M; Mustajoki, P; Kontula, K; Peltonen, L
      Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs

      EUROPEAN JOURNAL OF HUMAN GENETICS
    17. Levo, A; Jaaskelainen, J; Sistonen, P; Siren, MK; Voutilainen, R; Partanen, J
      Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland

      EUROPEAN JOURNAL OF HUMAN GENETICS
    18. Timonen, TTT
      A hypothesis concerning deficiency of sunlight, cold temperature, and influenza epidemics associated with the onset of acute lymphoblastic leukemia in northern Finland

      ANNALS OF HEMATOLOGY
    19. Kainulainen, K; Perola, M; Terwilliger, J; Kaprio, J; Koskenvuo, M; Syvanen, AC; Vartiainen, E; Peltonen, L; Kontula, K
      Evidence for involvement of the type 1 angiotensin II receptor locus in essential hypertension

      HYPERTENSION
    20. Kittles, RA; Long, JC; Bergen, AW; Eggert, M; Virkkunen, M; Linnoila, M; Goldman, D
      Cladistic association analysis of Y chromosome effects on alcohol dependence and related personality traits

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    21. Kittles, RA; Bergen, AW; Urbanek, M; Virkkunen, M; Linnoila, M; Goldman, D; Long, JC
      Autosomal, mitochondrial, and Y chromosome DNA variation in Finland: Evidence for a male-specific bottleneck

      AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY
    22. Lie, BA; Todd, JA; Pociot, F; Nerup, J; Akselsen, HE; Joner, G; Dahl-Jorgensen, K; Ronningen, KS; Thorsby, E; Undlien, DE
      The predisposition to type 1 diabetes linked to the human leukocyte antigen complex includes at least one non-class II gene

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. MITCHISON HM; HOFMANN SL; BECERRA CHR; MUNROE PB; LAKE BD; CROW YJ; STEPHENSON JBP; WILLIAMS RE; HOFMAN IL; TASCHNER PEM; MARTIN JJ; PHILIPPART M; ANDERMANN E; ANDERMANN F; MOLE SE; GARDINER RM; ORAWE AM
      MUTATIONS IN THE PALMITOYL-PROTEIN THIOESTERASE GENE (PPT, CLN1) CAUSING JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS WITH GRANULAR OSMIOPHILIC DEPOSITS

      Human molecular genetics
    24. Pekkarinen, P; Kestila, M; Paloneva, J; Terwilliger, J; Varilo, T; Jarvi, O; Hakola, P; Peltonen, L
      Fine-scale mapping of a novel dementia gene, PLOSL, by linkage disequilibrium

      GENOMICS
    25. VALLE T; EHNHOLM C; TUOMILEHTO J; BLASCHAK J; BERGMAN RN; LANGEFELD CD; GHOSH S; WATANABE RM; HAUSER ER; MAGNUSON V; ERIKSSON J; ALLY DS; NYLUND SJ; HAGOPIAN WA; KOHTAMAKI K; ROSS E; TOIVANEN L; BUCHANAN TA; VIDGREN G; COLLINS F; TUOMILEHTOWOLF E; BOEHNKE M
      MAPPING GENES FOR NIDDM - DESIGN OF THE FINLAND UNITED-STATES INVESTIGATION OF NIDDM GENETICS (FUSION) STUDY

      Diabetes care
    26. FAN RZ; LANGE K
      MODELS FOR HAPLOTYPE EVOLUTION IN A NONSTATIONARY POPULATION

      Theoretical population biology (Print)
    27. JARVELA I; ENATTAH NS; KOKKONEN J; VARILO T; SAVILAHTI E; PELTONEN L
      ASSIGNMENT OF THE LOCUS FOR CONGENITAL LACTASE DEFICIENCY TO 2Q21, INTHE VICINITY OF BUT SEPARATE FROM THE LACTASE-PHLORHIZIN HYDROLASE GENE

      American journal of human genetics
    28. UDD B; JUVONEN V; HAKAMIES L; NIEMINEN A; WALLGRENPETTERSSON C; CEDERQUIST K; SAVONTAUS ML
      HIGH PREVALENCE OF KENNEDYS-DISEASE IN WESTERN FINLAND - IS THE SYNDROME UNDERDIAGNOSED

      Acta neurologica Scandinavica
    29. BECKMAN L; SIKSTROM C; MIKELSAAR AV; KRUMINA A; AMBRASIENE D; KUCINSKAS V; BECKMAN G
      TRANSFERRIN VARIANTS AS MARKERS OF MIGRATIONS AND ADMIXTURE BETWEEN POPULATIONS IN THE BALTIC-SEA REGION

      Human heredity
    30. WEINBERG CR; WILCOX AJ; LIE RT
      A LOG-LINEAR APPROACH TO CASE-PARENT-TRIAD DATA - ASSESSING EFFECTS OF DISEASE GENES THAT ACT EITHER DIRECTLY OR THROUGH MATERNAL EFFECTS AND THAT MAY BE SUBJECT TO PARENTAL IMPRINTING

      American journal of human genetics
    31. LAAN M; PAABO S
      DEMOGRAPHIC HISTORY AND LINKAGE DISEQUILIBRIUM IN HUMAN-POPULATIONS

      Nature genetics
    32. LEVO A; PARTANEN J
      MUTATION-HAPLOTYPE ANALYSIS OF STEROID 21-HYDROXYLASE (CYP21) DEFICIENCY IN FINLAND - IMPLICATIONS FOR THE POPULATION HISTORY OF DEFECTIVE ALLELES

      Human genetics
    33. RANTALA M; SAVOLAINEN MJ; KERVINEN K; KESANIEMI YA
      APOLIPOPROTEIN-E PHENOTYPE AND DIET-INDUCED ALTERATION IN BLOOD-PRESSURE

      The American journal of clinical nutrition
    34. ROSTEDT I; LALU K; LUKKA M; SAJANTILA A
      GENOTYPING OF 5 SHORT TANDEM REPEAT LOCI VIA TRIPLEX AND DUPLEX PCR

      Forensic science international
    35. PIETINEN P; VARTIAINEN E; MANNISTO S
      TRENDS IN BODY-MASS INDEX AND OBESITY AMONG ADULTS IN FINLAND FROM 1972 TO 1992

      International journal of obesity
    36. HODGE AM; DOWSE GK; GAREEBOO H; TUOMILEHTO J; ALBERTI KGMM; ZIMMET PZ
      INCIDENCE, INCREASING PREVALENCE, AND PREDICTORS OF CHANGE IN OBESITYAND FAT DISTRIBUTION OVER 5 YEARS IN THE RAPIDLY DEVELOPING POPULATION OF MAURITIUS

      International journal of obesity
    37. KRAVCHUK OI; SPITSYN VA; GINTER EK; MAKAROV SV
      POPULATION GENETIC-CHARACTERISTICS OF HIG HLAND AND MEADOW MARI - GENETIC-MARKERS

      Genetika
    38. SIREN MK; SARENEVA H; LOKKI ML; KOSKIMIES S
      UNIQUE HLA-ANTIGEN FREQUENCIES IN THE FINNISH POPULATION

      Tissue antigens
    39. KEKOMAKI S; PARTANEN J; KEKOMAKI R
      PLATELET ALLOANTIGENS HPA-1, HPA-2, HPA-3, HPA-5 AND HPA-6B IN FINNS

      TRANSFUSION MEDICINE
    40. LOUHIJA J; MIETTINEN HE; KONTULA K; TIKKANEN MJ; MIETTINEN TA; TILVIS RS
      AGING AND GENETIC-VARIATION OF PLASMA APOLIPOPROTEINS - RELATIVE LOSSOF THE APOLIPOPROTEIN E4 PHENOTYPE IN CENTENARIANS

      Arteriosclerosis and thrombosis
    41. HELLSTEN E; VESA J; SPEER MC; MAKELA TP; JARVELA I; ALITALO K; OTT J; PELTONEN L
      REFINED ASSIGNMENT OF THE INFANTILE NEURONAL CEROID-LIPOFUSCINOSIS (INCL, CLN1) LOCUS AT 1P32 - INCORPORATION OF LINKAGE DISEQUILIBRIUM IN MULTIPOINT ANALYSIS

      Genomics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/06/20 alle ore 03:19:51