Catalogo Articoli (Spogli Riviste)

HELP
ATTENZIONE: attualmente gli articoli Current Contents (fonte ISI) a partire dall'anno 2002 sono consultabili sulla Risorsa On-Line

Le informazioni sugli articoli di fonte ISI sono coperte da copyright

La ricerca find articoli where authors phrase all words ' Lunetta, KL' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 28 riferimenti
Selezionare un intervallo

Per ulteriori informazioni selezionare i riferimenti di interesse.

    1. Robins, JM; Smoller, JW; Lunetta, KL
      On the validity of the TDT test in the presence of comorbidity and ascertainment bias

      GENETIC EPIDEMIOLOGY
    2. Krop, IE; Sgroi, D; Porter, DA; Lunetta, KL; LeVangie, R; Seth, P; Kaelin, CM; Rhei, E; Bosenberg, M; Schnitt, S; Marks, JR; Pagon, Z; Belina, D; Razumovic, J; Polyak, K
      HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    3. Wallace, SR; Oken, MM; Lunetta, KL; Panoskaitsis-Mortari, A; Masellis, AM
      Abnormalities of bone marrow mesenchymal cells in multiple myeloma patients

      CANCER
    4. Yeh, JJ; Lunetta, KL; van Orsouw, NJ; Moore, FD; Mutter, GL; Vijg, J; Dahia, PLM; Eng, C
      Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours

      ONCOGENE
    5. Smoller, JW; Lunetta, KL; Robins, J
      Implications of comorbidity and ascertainment bias for identifying diseasegenes

      AMERICAN JOURNAL OF MEDICAL GENETICS
    6. Seth, P; Lunetta, KL; Bell, DW; Gray, H; Nasser, SM; Rhei, E; Kaelin, CM; Iglehart, DJ; Marks, JR; Garber, JE; Haber, DA; Polyak, K
      Phenol sulfotransferases: Hormonal regulation, polymorphism, and age of onset of breast cancer

      CANCER RESEARCH
    7. Lunetta, KL; Faraone, SV; Biederman, J; Laird, NM
      Family-based tests of association and linkage that use unaffected sibs, covariates, and interactions

      AMERICAN JOURNAL OF HUMAN GENETICS
    8. Marsh, DJ; Kum, JB; Lunetta, KL; Bennett, MJ; Gorlin, RJ; Ahmed, SF; Bodurtha, J; Crowe, C; Curtis, MA; Dasouki, M; Dunn, T; Feit, H; Geraghty, MT; Graham, JM; Hodgson, SV; Hunter, A; Korf, BR; Manchester, D; Miesfeldt, S; Murday, VA; Nathanson, KL; Parisi, M; Pober, B; Romano, C; Tolmie, JL; Trembath, R; Winter, RM; Zackai, EH; Zori, RT; Weng, LP; Dahia, PLM; Eng, C
      PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

      HUMAN MOLECULAR GENETICS
    9. Lunetta, KL; Wilcox, M; Smoller, J; Neuberg, D
      Exploring linkage for alcoholism using affection status and quantitative event related potential phenotypes

      GENETIC EPIDEMIOLOGY
    10. Wilcox, MA; Smoller, JW; Lunetta, KL; Neuberg, D
      Using recursive partitioning for exploration and follow-up of linkage and association analyses

      GENETIC EPIDEMIOLOGY
    11. MARSH DJ; COULON V; LUNETTA KL; ROCCASERRA P; DAHIA PLM; ZHENG ZM; LIAW D; CARON S; DUBOUE B; LIN AY; RICHARDSON AL; BONNETBLANC JM; BRESSIEUX JM; CABARROTMOREAU A; CHOMPRET A; DEMANGE L; EELES RA; YAHANDA AM; FEARON ER; FRICKER JP; GORLIN RJ; HODGSON SV; HUSON S; LACOMBE D; LEPRAT F; ODENT S; TOULOUSE C; OLOPADE OI; SOBOL H; TISHLER S; WOODS CG; ROBINSON BG; WEBER HC; PARSONS R; PEACOCKE M; LONGY M; ENG C
      MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION

      Human molecular genetics
    12. LUNETTA KL; ROGUS JJ
      STRATEGY FOR MANNING MINOR HISTOCOMPATIBILITY GENES INVOLVED IN GRAFT-VERSUS-HOST DISEASE - A NOVEL APPLICATION OF DISCORDANT SIB PAIR METHODOLOGY

      Genetic epidemiology
    13. MARSH DJ; ROTH S; LUNETTA KL; HEMMINKI A; DAHIA PLM; SISTONEN P; ZHENG ZM; CARON S; VANORSOUW NJ; BODMER WF; COTTRELL SE; DUNLOP MG; ECCLES D; HODGSON SV; JARVINEN H; KELLOKUMPU I; MARKIE D; NEALE K; PHILLIPS R; ROZEN P; SYNGAL S; VIJG J; TOMLINSON IPM; AALTONEN LA; ENG C
      EXCLUSION OF PTEN AND 10Q22-24 AS THE SUSCEPTIBILITY LOCUS FOR JUVENILE POLYPOSIS SYNDROME

      Cancer research
    14. ROGUS JJ; LUNETTA KL
      ASYMPTOTIC PROPERTIES AND POWER OF LINKAGE TESTS FOR DISCORDANT AND TRANSPLANT SIB PAIRS

      American journal of human genetics
    15. LUNETTA KL
      EFFECT OF NON-AMPLIFYING (NULL) ALLELES ON AFFECTED AND DISCORDANT SIB PAIR LINKAGE ANALYSES

      American journal of human genetics
    16. NICHOLS WC; ANTIN JH; LUNETTA KL; TARRY VH; HERTEL CE; WHEATLEY MA; ARNOLD ND; SIEMIENIAK DR; BOEHNKE M; GINSBURG D
      POLYMORPHISM OF ADHESION MOLECULE CD31 IS NOT A SIGNIFICANT RISK FACTOR FOR GRAFT-VERSUS-HOST DISEASE

      Blood
    17. LUNETTA KL; BOEHNKE M; LANGE K; COX DR
      SELECTED LOCUS AND MULTIPLE PANEL MODELS FOR RADIATION HYBRID MAPPING

      American journal of human genetics
    18. HOU YC; RICHARDS JE; BINGHAM EL; PAWAR H; SCOTT K; SEGAL M; LUNETTA KL; BOEHNKE M; SIEVING PA
      LINKAGE STUDY OF BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) IN A LARGE NORTH-AMERICAN FAMILY

      Human heredity
    19. LANGE K; BOEHNKE M; COX DR; LUNETTA KL
      STATISTICAL-METHODS FOR POLYPLOID RADIATION HYBRID MAPPING

      PCR methods and applications
    20. LUNETTA KL; BOEHNKE M; LANGE K; COX DR
      EXPERIMENTAL-DESIGN AND ERROR-DETECTION FOR POLYPLOID RADIATION HYBRID MAPPING

      PCR methods and applications
    21. HOU YC; RICHARDS JE; BINGHAM E; PAWAR H; SCOTT K; SEGAL M; LUNETTA KL; BOEHNKE M; SIEVING PA
      BESTS VITELLIFORM MACULAR DYSTROPHY (VMD2) - LOCALIZATION BETWEEN D11S903 D11S956 AND ROM1 AND LIKELY EXCLUSION OF ROM1 AS CANDIDATE GENE/

      Investigative ophthalmology & visual science
    22. PAWAR HS; BINGHAM EL; LUNETTA KL; RICHARDS JE; BOEHNKE M; SIEVING PA
      JUVENILE RETINOSCHISIS (RS) - REFINED X-CHROMOSOME MAPPING

      Investigative ophthalmology & visual science
    23. NICHOLS WC; ANTIN JH; LUNETTA KL; MARTIN PJ; BLAZAR BR; CHAO NJ; SENITZER D; TAYLOR CA; TERRY VH; ARNOLD ND; SIEMIENIAK DR; BRUCK ME; MUHAMMAD SA; BOEHNKE M; GINSBURG D
      IDENTIFICATION OF NON-HLA LOCI CONTRIBUTING TO GRAFT-VERSUS-HOST DISEASE

      Blood
    24. LUNETTA KL; BOEHNKE M; LANGE K; COX DR
      EXPERIMENTAL-DESIGN CONSIDERATIONS FOR WHOLE-GENOME RADIATION HYBRIDS

      American journal of human genetics
    25. BOEHNKE M; COX DR; LUNETTA KL
      STATISTICAL-METHODS FOR POLYPLOID RADIATION HYBRID MAPPING

      American journal of human genetics
    26. PAWAR H; BINGHAM EL; LUNETTA KL; SEGAL M; RICHARDS JE; BOEHNKE M; SIEVING PA
      REFINED GENETIC-MAPPING OF JUVENILE X-LINKED RETINOSCHISIS

      Human heredity
    27. LUNETTA KL; BOEHNKE M
      MULTIPOINT RADIATION HYBRID MAPPING - COMPARISON OF METHODS, SAMPLE-SIZE REQUIREMENTS, AND OPTIMAL STUDY CHARACTERISTICS

      Genomics
    28. SIEYING PA; BINGHAM E; ZHUANG Z; RICHARDS JE; BOOMS P; WAPENAAR MC; DENDUNNEN JT; LUNETTA KL; BOEHNKE M
      GENETIC-LINKAGE AROUND X-LINKED RETINOSCHISIS (RS)

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 19:06:31