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    1. Alarcon, M; Cantor, RM; Liu, JJ; Gilliam, TC; Geschwind, DH
      Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. 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
    3. DeWan, AT; Parrado, AR; Matise, TC; Leal, SM
      The map problem: A comparison of genetic and sequence-based physical maps

      AMERICAN JOURNAL OF HUMAN GENETICS
    4. Haghighi, F; Hodge, SE
      Likelihood formulation of parent-of-origin effects on segregation analysis, including ascertainment

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Mayeux, R; Lee, JH; Romas, SN; Mayo, D; Santana, V; Williamson, J; Ciappa, A; Rondon, HZ; Estevez, P; Lantigua, R; Medrano, M; Torres, M; Stern, Y; Tycko, B; Knowles, JA
      Chromosome-12 mapping of late-onset Alzheimer disease among Caribbean Hispanics

      AMERICAN JOURNAL OF HUMAN GENETICS
    6. Tankersley, CG
      Physiological and Genomic Consequences of Intermittent hypoxia - Selected Contribution: Variation in acute hypoxic ventilatory response is linked to mouse chromosome 9

      JOURNAL OF APPLIED PHYSIOLOGY
    7. Kai, N; Suzuki, G; Watanabe, M; Isogai, A; Hinata, K
      Sequence comparisons among dispersed members of the Brassica S multigene family in an S-9 genome

      MOLECULAR GENETICS AND GENOMICS
    8. Mullerad, M; Falik, T; Madeb, R; Nativ, O
      Hereditary prostate cancer - the search for the gene

      ISRAEL MEDICAL ASSOCIATION JOURNAL
    9. Weetman, AP
      Determinants of autoimmune thyroid disease

      NATURE IMMUNOLOGY
    10. Lu, HH; Cox, AL; Zwaenepoel, W
      Contention elimination by replication of sequential sections in distributed shared memory programs

      ACM SIGPLAN NOTICES
    11. Hanson, RL; Imperatore, G; Narayan, KMV; Roumain, J; Fagot-Campagna, A; Pettitt, DJ; Bennett, PH; Knowler, WC
      Family and genetic studies of indices of insulin sensitivity and insulin secretion in Pima Indians

      DIABETES-METABOLISM RESEARCH AND REVIEWS
    12. Bray, NJ; Owen, MJ
      Searching for schizophrenia genes

      TRENDS IN MOLECULAR MEDICINE
    13. Ahmad, YA; Bruce, IN
      Genetic epidemiology - Systemic lupus erythematosus

      ARTHRITIS RESEARCH
    14. Jirholt, J; Lindqvist, AKB; Holmdahl, R
      The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genes

      ARTHRITIS RESEARCH
    15. Ikari, K; Onda, H; Furushima, K; Maeda, S; Harata, S; Takeda, J
      Establishment of an optimized set of 406 microsatellite markers covering the whole genome for the Japanese population

      JOURNAL OF HUMAN GENETICS
    16. Bethony, J; Williams, JT; Kloos, H; Blangero, J; Alves-Fraga, L; Buck, G; Michalek, A; Williams-Blangero, S; LoVerde, PT; Correa-Oliveira, R; Gazzinelli, A
      Exposure to Schistosoma mansoni infection in a rural area in Brazil. II: Household risk factors

      TROPICAL MEDICINE & INTERNATIONAL HEALTH
    17. Maziade, M; Roy, MA; Rouillard, E; Bissonnette, L; Fournier, JP; Roy, A; Garneau, Y; Montgrain, N; Potvin, A; Cliche, D; Dion, C; Wallot, H; Fournier, A; Nicole, L; Lavallee, JC; Merette, C
      A search for specific and, common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes

      MOLECULAR PSYCHIATRY
    18. Turecki, G; Grof, P; Grof, E; D'Souza, V; Lebuis, L; Marineau, C; Cavazzoni, P; Duffy, A; Betard, C; Zvolsky, P; Robertson, C; Brewer, C; Hudson, TJ; Rouleau, GA; Alda, M
      Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithium

      MOLECULAR PSYCHIATRY
    19. Badenhop, RF; Moses, MJ; Scimone, A; Mitchell, PB; Ewen, KR; Rosso, A; Donald, JA; Adams, LJ; Schofield, PR
      A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q

      MOLECULAR PSYCHIATRY
    20. Zubenko, GS; Hughes, HB; Stiffler, JS
      D10S1423 identifies a susceptibility locus for Alzheimer's disease in a prospective, longitudinal, double-blind study of asymptomatic individuals

      MOLECULAR PSYCHIATRY
    21. 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
    22. Van Agtmael, T; Forrest, SM; Williamson, R
      Genes for left-handedness: How to search for the needle in the haystack?

      LATERALITY
    23. Kennedy, S; Bennett, S; Weeks, DE
      Genetics and infertility II - Affected sib-pair analysis in endometriosis

      HUMAN REPRODUCTION UPDATE
    24. Oranwiroon, S; Akkarapatumwong, V; Pung-Amritt, P; Treesucon, A; Veerakul, G; Mahasandana, C; Panyim, S; Yenchitsomanus, P
      Determination of haemophilia A carrier status by mutation analysis

      HAEMOPHILIA
    25. Shahbazian, MD; Zoghbi, HY
      Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

      CURRENT OPINION IN NEUROLOGY
    26. Agui, T; Miyamoto, T; Tsumagari, T
      X-ray hypersensitivity in the LEA rat: Genetic linkage analysis of responsible loci

      EXPERIMENTAL ANIMALS
    27. Nelson, RG
      Diabetic renal disease in transitional and disadvantaged populations

      NEPHROLOGY
    28. Li, FY; Szobor, A; Croxen, R; Anselmo, V; Yuan, QP; Lindblad, K; Schalling, M; Komoly, S; Beeson, D; Larsson, C
      Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene loci

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    29. Tonini, GP; McConville, C; Cusano, R; Rees, SA; Dagnino, M; Longo, L; De Bernardi, B; Conte, M; Garaventa, A; Romeo, G; Devoto, M; Seri, M
      Exclusion of candidate genes and chromosomal regions in familial neuroblastoma

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    30. 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
    31. Kovach, MJ; Ruiz, J; Kimonis, K; Mueed, S; Sinha, S; Higgins, C; Elble, S; Elble, R; Kimonis, VE
      Genetic heterogeneity in autosomal dominant essential tremor

      GENETICS IN MEDICINE
    32. Martin, LJ; Blangero, J; Rogers, J; Mahaney, MC; Hixson, JE; Carey, KD; Morin, PA; Comuzzie, AG
      A quantitative trait locus influencing estrogen levels maps to a region homologous to human chromosome 20

      PHYSIOLOGICAL GENOMICS
    33. Tallal, P; Hirsch, LS; Realpe-Bonilla, T; Miller, S; Brzustowicz, LM; Bartlett, C; Flax, JF
      Familial aggregation in specific language impairment

      JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
    34. Li, JL; Deng, HY; Lai, DB; Xu, FH; Chen, J; Gao, GM; Recker, RR; Deng, HW
      Toward high-throughput genotyping: Dynamic and automatic software for manipulating large-scale genotype data using fluorescently labeled dinucleotidemarkers

      GENOME RESEARCH
    35. 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
    36. Wang, XL; Rainwater, DL; VandeBerg, JF; Mitchell, BD; Mahaney, MC
      Genetic contributions to plasma total antioxidant activity

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    37. Peacock, JM; Arnett, DK; Atwood, LD; Myers, RH; Coon, H; Rich, SS; Province, MA; Heiss, G
      Genome scan for quantitative trait loci linked to high-density lipoproteincholesterol - The NHLBI family heart study

      ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
    38. Schurmann, M; Reichel, P; Muller-Myhsok, B; Schlaak, M; Muller-Quernheim, J; Schwinger, E
      Results from a genome-wide search for predisposing genes in sarcoidosis

      AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
    39. He, X; Zhu, DL; Chu, SL; Jin, L; Xiong, MM; Wang, GL; Zhang, WZ; Zhou, HF; Mao, SY; Zhan, YM; Zhuang, QN; Liu, XM; Zhao, Y; Huang, W
      alpha-adducin gene and essential hypertension in China

      CLINICAL AND EXPERIMENTAL HYPERTENSION
    40. Yang, Y; Hentati, A; Deng, HX; Dabbagh, O; Sasaki, T; Hirano, M; Hung, WY; Ouahchi, K; Yan, JH; Azim, AC; Cole, N; Gascon, G; Yagmour, A; Ben-Hamida, M; Pericak-Vance, M; Hentati, F; Siddique, T
      The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

      NATURE GENETICS
    41. Date, H; Onodera, O; Tanaka, H; Iwabuchi, K; Uekawa, K; Igarashi, S; Koike, R; Hiroi, T; Yuasa, T; Awaya, Y; Sakai, T; Takahashi, T; Nagatomo, H; Sekijima, Y; Kawachi, I; Takiyama, Y; Nishizawa, M; Fukuhara, N; Saito, K; Sugano, S; Tsuji, S
      Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is causedby mutations in a new HIT superfamily gene

      NATURE GENETICS
    42. Wallace, RH; Marini, C; Petrou, S; Harkin, LA; Bowser, DN; Panchal, RG; Williams, DA; Sutherland, GR; Mulley, JC; Scheffer, IE; Berkovic, SF
      Mutant GABA(A) receptor gamma 2-subunit in childhood absence epilepsy and febrile seizures

      NATURE GENETICS
    43. Tavtigian, SV; Simard, J; Teng, DHF; Abtin, V; Baumgard, M; Beck, A; Camp, NJ; Carillo, AR; Chen, Y; Dayananth, P; Desrochers, M; Dumont, M; Farnham, JM; Frank, D; Frye, C; Ghaffari, S; Gupte, JS; Hu, R; Iliev, D; Janecki, T; Kort, EN; Laity, KE; Leavitt, A; Leblanc, G; McArthur-Morrison, J; Pederson, A; Penn, B; Peterson, KT; Reid, JE; Richards, S; Schroeder, M; Smith, R; Snyder, SC; Swedlund, B; Swensen, J; Thomas, A; Tranchant, M; Woodland, AM; Labrie, F; Skolnick, MH; Neuhausen, S; Rommens, J; Cannon-Albright, LA
      A candidate prostate cancer susceptibility gene at chromosome 17p

      NATURE GENETICS
    44. Ott, J; Hoh, J
      Statistical multilocus methods for disequilibrium analysis in complex traits

      HUMAN MUTATION
    45. Ban, Y; Taniyama, M; Tozaki, T; Yanagawa, T; Tomita, M; Ban, Y
      SEL1L microsatellite polymorphism in Japanese patients with autoimmune thyroid diseases

      THYROID
    46. Tomer, Y
      Unraveling the genetic susceptibility to autoimmune thyroid diseases: CTLA-4 takes the stage

      THYROID
    47. Dahan, K; Fuchshuber, A; Adamis, S; Smaers, M; Kroiss, S; Loute, G; Cosyns, JP; Hildebrandt, F; Verellen-Dumoulin, C; Pirson, Y
      Familial juvenile hyperuricemic nephropathy and autosomal dominant medullary cystic kidney disease type 2: Two facets of the same disease?

      JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
    48. Loughlin, J
      Genetic epidemiology of primary osteoarthritis

      CURRENT OPINION IN RHEUMATOLOGY
    49. Wesselkamper, SC; Chen, LC; Kleeberger, SR; Gordon, T
      Genetic variability in the development of pulmonary tolerance to inhaled pollutants in inbred mice

      AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY
    50. Castro, J; Telleria, JJ; Blanco-Quiros, A
      Susceptibility genes for asthma and allergy: Hits and questions

      JOURNAL OF INVESTIGATIONAL ALLERGOLOGY & CLINICAL IMMUNOLOGY
    51. 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
    52. Kitsos, G; Eiberg, H; Economou-Petersen, E; Wirtz, MK; Kramer, PL; Aspiotis, M; Tommerup, N; Petersen, MB; Psilas, K
      Genetic linkage of autosomal dominant primary open angle glaucoma to chromosome 3q in a Greek pedigree

      EUROPEAN JOURNAL OF HUMAN GENETICS
    53. Bonsch, D; Scheer, P; Neumann, C; Lang-Roth, R; Seifert, E; Storch, P; Weiller, C; Lamprecht-Dinnesen, A; Deufel, T
      A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus

      EUROPEAN JOURNAL OF HUMAN GENETICS
    54. Rosenberg, C; Wouters, CH; Szuhai, K; Dorland, R; Pearson, P; Poll-The, BT; Colombijn, RM; Bruning, M; Lindhout, D
      A Rett syndrome patient with a ring X chromosome: further evidence for skewing of X inactivation and heterogeneity in the aetiology of the disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    55. Abecasis, GR; Cherny, SS; Cardon, LR
      The impact of genotyping error on family-based analysis of quantitative traits

      EUROPEAN JOURNAL OF HUMAN GENETICS
    56. Cancel-Tassin, G; Latil, A; Valeri, A; Mangin, P; Fournier, G; Berthon, P; Cussenot, O
      PCAP is the major known prostate cancer predisposing locus in families from south and west Europe

      EUROPEAN JOURNAL OF HUMAN GENETICS
    57. Koillinen, H; Wong, FK; Rautio, J; Ollikainen, V; Karsten, A; Larson, O; Teh, BT; Huggare, J; Lahermo, P; Larsson, C; Kere, J
      Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34

      EUROPEAN JOURNAL OF HUMAN GENETICS
    58. Borglum, AD; Balslev, T; Haagerup, A; Birkebaek, N; Binderup, H; Kruse, TA; Hertz, JM
      A new locus for Seckel syndrome on chromosome 18p11.31-q11.2

      EUROPEAN JOURNAL OF HUMAN GENETICS
    59. 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
    60. Radhakrishna, U; Senol, S; Herken, H; Gucuyener, K; Gehrig, C; Blouin, JL; Akarsu, NA; Antonarakis, SE
      An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree

      EUROPEAN JOURNAL OF HUMAN GENETICS
    61. Cardaba, B; Moffatt, MF; Fernandez, E; Jurado, A; Rojo, M; Garcia, M; Ansotegui, IJ; Cortegano, I; Arrieta, I; Etxenagusia, MA; del Pozo, V; Urraca, J; Aceituno, E; Gallardo, S; Palomino, P; Cookson, W; Lahoz, C
      Allergy to dermatophagoides in a group of Spanish gypsies: Genetic restrictions

      INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY
    62. Zheng, Y; Qiu, CC; Hou, SQ; Zhu, XL; Zheng, HQ; Zhao, LJ; Li, GJ; Liu, Y; Liu, YW
      Evidence for association of D1S249 locus on human chromosome 1 with the susceptibility to essential hypertension in Han Chinese

      SCIENCE IN CHINA SERIES C-LIFE SCIENCES
    63. Fernandez, SA; Fernando, RL; Guldbrandtsen, B; Totir, LR; Carriquiry, AL
      Sampling genotypes in large pedigrees with loops

      GENETICS SELECTION EVOLUTION
    64. Nathanson, KL; Weber, BL
      'Other' breast cancer susceptibility genes: searching for more holy grail

      HUMAN MOLECULAR GENETICS
    65. Nwosu, V; Carpten, J; Trent, JM; Sheridan, R
      Heterogeneity of genetic alterations in prostate cancer: evidence of the complex nature of the disease

      HUMAN MOLECULAR GENETICS
    66. Alagramam, KN; Yuan, HJ; Kuehn, MH; Murcia, CL; Wayne, S; Srisailpathy, CRS; Lowry, RB; Knaus, R; Van Laer, L; Bernier, FP; Schwartz, S; Lee, C; Morton, CC; Mullins, RF; Ramesh, A; Van Camp, G; Hagemen, GS; Woychik, RP; Smith, RJH
      Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

      HUMAN MOLECULAR GENETICS
    67. Ekelund, J; Hovatta, I; Parker, A; Paunio, T; Varilo, T; Martin, R; Suhonen, J; Ellonen, P; Chan, GY; Sinsheimer, JS; Sobel, E; Juvonen, H; Arajarvi, R; Partonen, T; Suvisaari, J; Lonnqvist, J; Meyer, J; Peltonen, L
      Chromosome 1 loci in Finnish schizophrenia families

      HUMAN MOLECULAR GENETICS
    68. Pesch, UEA; Leo-Kottler, B; Mayor, S; Jurklies, B; Kellner, U; Apfelstedt-Sylla, E; Zrenner, E; Alexander, C; Wissinger, B
      OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance

      HUMAN MOLECULAR GENETICS
    69. Toomes, C; Marchbank, NJ; Mackey, DA; Craig, JE; Newbury-Ecob, RA; Bennett, CP; Vize, CJ; Desai, SP; Black, GCM; Patel, N; Teimory, M; Markham, AF; Inglehearn, CF; Churchill, AJ
      Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy

      HUMAN MOLECULAR GENETICS
    70. Sekine, M; Nagata, H; Tsuji, S; Hirai, Y; Fujimoto, S; Hatae, M; Kobayashi, I; Fujii, T; Nagata, I; Ushijima, K; Obata, K; Suzuki, M; Yoshinaga, M; Umesaki, N; Satoh, S; Enomoto, T; Motoyama, S; Tanaka, K
      Localization of a novel susceptibility gene for familial ovarian cancer tochromosome 3p22-p25

      HUMAN MOLECULAR GENETICS
    71. McKenzie, CA; Abecasis, GR; Keavney, B; Forrester, T; Ratcliffe, PJ; Julier, C; Connell, JMC; Bennett, F; McFarlane-Anderson, N; Lathrop, GM; Cardon, LR
      Trans-ethnic fine mapping of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE)

      HUMAN MOLECULAR GENETICS
    72. Shih, MC; Whittemore, AS
      Allele-sharing among affected relatives: non-parametric methods for identifying genes

      STATISTICAL METHODS IN MEDICAL RESEARCH
    73. Barhoumi, C; Amouri, R; Ben Hamida, C; Ben Hamida, M; Machghoul, S; Gueddiche, M; Hentati, F
      Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3

      NEUROMUSCULAR DISORDERS
    74. Peto, J; Houlston, RS
      Genetics and the common cancers

      EUROPEAN JOURNAL OF CANCER
    75. Poduslo, SE; Yin, X
      A new locus on chromosome 19 linked with late-onset Alzheimer's disease

      NEUROREPORT
    76. Venanzi, S; Malerba, G; Galavotti, R; Lauciello, MC; Trabetti, E; Zanoni, G; Pescollderungg, L; Martinati, LC; Boner, AL; Pignatti, PF
      Linkage to atopy on chromosome 19 in north-eastern Italian families with allergic asthma

      CLINICAL AND EXPERIMENTAL ALLERGY
    77. Schurmann, M; Reichel, P; Muller-Myhsok, B; Dieringer, T; Wurm, K; Schlaak, M; Muller-Quernheim, J; Schwinger, E
      Angiotensin-converting enzyme (ACE) gene polymorphisms and familial occurrence of sarcoidosis

      JOURNAL OF INTERNAL MEDICINE
    78. Takahashi, T; Yamaguchi, E; Furuya, K; Kawakami, Y
      The ACE gene polymorphism and cough threshold for capsaicin after cilazapril usage

      RESPIRATORY MEDICINE
    79. Khoo, SK; Bradley, M; Wong, FK; Hedblad, MA; Nordenskjold, M; Teh, BT
      Birt-Hogg-Dube syndrome: mapping of a novel hereditary neoplasia gene to chromosome 17p12-q11.2

      ONCOGENE
    80. Reed, DR; Nanthakumar, E; North, M; Bell, C; Price, RA
      A genome-wide scan suggests a locus on chromosome 1q21-q23 contributes to normal variation in plasma cholesterol concentration

      JOURNAL OF MOLECULAR MEDICINE-JMM
    81. Comuzzie, AG; Williams, JT; Martin, LJ; Blangero, J
      Searching for genes underlying normal variation in human adiposity

      JOURNAL OF MOLECULAR MEDICINE-JMM
    82. Omran, H; Haffner, KN; Burth, S; Ala-Mello, S; Antignac, C; Hildebrandt, F
      Evidence for further genetic heterogeneity in nephronophthisis

      NEPHROLOGY DIALYSIS TRANSPLANTATION
    83. Johansson, C; Jansson, M; Linner, L; Yuan, QP; Pedersen, NL; Blackwood, D; Barden, N; Kelsoe, J; Schalling, M
      Genetics of affective disorders

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    84. Jurewicz, I; Owen, RJ; O'Donovan, MC; Owen, MJ
      Searching for susceptibility genes in schizophrenia

      EUROPEAN NEUROPSYCHOPHARMACOLOGY
    85. Garver, DL; Holcomb, J; Mapua, FM; Wilson, R; Barnes, B
      Schizophrenia spectrum disorders: an autosomal-wide scan in multiplex pedigrees

      SCHIZOPHRENIA RESEARCH
    86. Fournie, GJ; Mas, M; Cautain, B; Savignac, M; Subra, JF; Pelletier, L; Saoudi, A; Lagrange, D; Calise, M; Druet, P
      Induction of autoimmunity through bystander effects. Lessons from immunological disorders induced by heavy metals

      JOURNAL OF AUTOIMMUNITY
    87. Vainzof, M; Anderson, LVB; McNally, EM; Davis, DB; Faulkner, G; Valle, G; Moreira, ES; Pavanello, RCM; Passos-Bueno, MR; Zatz, M
      Dysferlin protein analysis in limb-girdle muscular dystrophies

      JOURNAL OF MOLECULAR NEUROSCIENCE
    88. Murdoch, JN; Rachel, RA; Shah, S; Beermann, F; Stanier, P; Mason, CA; Copp, AJ
      Circletail, a new mouse mutant with severe neural tube defects: Chromosomal localization and interaction with the loop-tail mutation

      GENOMICS
    89. Xiao, SX; Bu, L; Zhu, LQ; Zheng, GY; Yang, MH; Qian, MQ; Hu, LD; Liu, J; Zhao, GP; Kong, XY
      A new locus for hereditary gingival fibromatosis (GINGF2) maps to 5q13-q22

      GENOMICS
    90. Fuchshuber, A; Kroiss, S; Karle, S; Berthold, S; Huck, K; Burton, C; Rahman, N; Koptides, M; Deltas, C; Otto, E; Ruschendorf, F; Feest, T; Hildebrandt, F
      Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region

      GENOMICS
    91. Behnam, JT; Hamer, C; Spalton, D; Johnston, R; Seller, MJ
      Physical and transcript map of the dominant optic atrophy (OPA1) gene critical region at 3q28-q29

      GENOMICS
    92. Sugiyama, F; Churchill, GA; Higgins, DC; Johns, C; Makaritsis, KP; Gavras, H; Paigen, B
      Concordance of murine quantitative trait loci for salt-induced hypertension with rat and human loci

      GENOMICS
    93. Good, D; Busfield, F; Duffy, D; Lovelock, PK; Kesting, JB; Cameron, DP; Shaw, JTE
      Familial Paget's disease of bone: Nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigree

      JOURNAL OF BONE AND MINERAL RESEARCH
    94. Tanck, MWT; Palstra, AP; van de Weerd, M; Leffering, CP; van der Poel, JJ; Bovenhuis, H; Komen, J
      Segregation of microsatellite alleles and residual heterozygosity at single loci in homozygous androgenetic common carp (Cyprinus carpio L.)

      GENOME
    95. Prathikanti, S; McMahon, FJ
      Genome scans for susceptibility genes in bipolar affective disorder

      ANNALS OF MEDICINE
    96. Ekstrom, CT
      Power of multipoint identity-by-descent methods to detect linkage using variance component models

      GENETIC EPIDEMIOLOGY
    97. Greenberg, DA; Abreu, PC
      Determining trait locus position from multipoint analysis: Accuracy and power of three different statistics

      GENETIC EPIDEMIOLOGY
    98. Uimari, P; Sillanpaa, MJ
      Bayesian oligogenic analysis of quantitative and qualitative traits in general pedigrees

      GENETIC EPIDEMIOLOGY
    99. Chatterjee, N; Shih, J; Hartge, P; Brody, L; Tucker, M; Wacholder, S
      Association and aggregation analysis using kin-cohort designs with applications to genotype and family history data from the Washington Ashkenazi Study

      GENETIC EPIDEMIOLOGY
    100. Ertekin-Taner, N; Graff-Radford, N; Younkin, LH; Eckman, C; Adamson, J; Schaid, DJ; Blangero, J; Hutton, M; Younkin, SG
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      GENETIC EPIDEMIOLOGY


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/02/20 alle ore 09:28:28