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    1. 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
    2. 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
    3. 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
    4. Degn, B; Lundorf, MD; Wang, A; Vang, M; Mors, O; Kruse, TA; Ewald, H
      Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients fromthe Faroe Islands

      MOLECULAR PSYCHIATRY
    5. 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
    6. Kosaki, K; Suzuki, T; Kosaki, R; Yoshihashi, H; Itoh, M; Goto, Y; Matsuo, N
      Human homolog of the mouse imprinted gene Impact resides at the pericentric region of chromosome 18 within the critical region for bipolar affective disorder

      MOLECULAR PSYCHIATRY
    7. 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
    8. 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
    9. Ishibe, N; Sgambati, MT; Fontaine, L; Goldin, LR; Jain, N; Weissman, N; Marti, GE; Caporso, NE
      Clinical characteristics of familial B-CLL in the National Cancer Institute Familial Registry

      LEUKEMIA & LYMPHOMA
    10. Katzmarzyk, PT; Rankinen, T; Perusse, L; Rao, DC; Bouchard, C
      Familial risk of high blood pressure in the Canadian population

      AMERICAN JOURNAL OF HUMAN BIOLOGY
    11. Rijsdijk, FV; Hewitt, JK; Sham, PC
      Analytic power calculation for QTL linkage analysis of small pedigrees

      EUROPEAN JOURNAL OF HUMAN GENETICS
    12. Pong-Wong, R; George, AW; Woolliams, JA; Haley, CS
      A simple and rapid method for calculating identity-by-descent matrices using multiple markers

      GENETICS SELECTION EVOLUTION
    13. Fernandez, SA; Fernando, RL; Guldbrandtsen, B; Totir, LR; Carriquiry, AL
      Sampling genotypes in large pedigrees with loops

      GENETICS SELECTION EVOLUTION
    14. Choudhry, S; Mukerji, M; Srivastava, AK; Jain, S; Brahmachari, SK
      CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms

      HUMAN MOLECULAR GENETICS
    15. 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
    16. Amos, CI; de Andrade, M
      Genetic linkage methods for quantitative traits

      STATISTICAL METHODS IN MEDICAL RESEARCH
    17. Dogulu, CF; Kansu, T; Seyrantepe, V; Ozguc, M; Topaloglu, H; Johns, DR
      Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population

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

      ANNALS OF MEDICINE
    19. Uimari, P; Sillanpaa, MJ
      Bayesian oligogenic analysis of quantitative and qualitative traits in general pedigrees

      GENETIC EPIDEMIOLOGY
    20. Antoniou, AC; Pharoah, PDP; McMullan, G; Day, NE; Ponder, BAJ; Easton, D
      Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study

      GENETIC EPIDEMIOLOGY
    21. Atkinson, EJ; Hall, D; de Andrade, M
      A comparison of software packages that assess linkage using a variance components approach

      GENETIC EPIDEMIOLOGY
    22. Markianos, K; Carlson, S; Gibbs, M; Kruglyak, L
      A joint analysis of asthma affection status and IgE levels in multiple data sets collected for asthma

      GENETIC EPIDEMIOLOGY
    23. Bethony, J; Williams, JT; Almasy, L; Correa-Oliveira, R; Blangero, JC; Williams-Blangero, S
      Genetic analysis of quantitative traits in highly ascertained samples: Total serum IgE in families with asthma

      GENETIC EPIDEMIOLOGY
    24. Ziegler, A; Boddeker, IR; Geller, F
      A bivariate Haseman-Elston method and application to the analysis of asthma-related phenotypes on chromosome 5q

      GENETIC EPIDEMIOLOGY
    25. Zhang, SL; Zhang, K; Li, JM; Sun, FZ; Zhao, HY
      Test of association for quantitative traits in general pedigrees: The quantitative pedigree disequilibrium test

      GENETIC EPIDEMIOLOGY
    26. Yang, XH; Goldstein, AM; Chase, GA; Gastwirth, JL; Goldin, LR
      Use of weighted p-values in regional inference procedures

      GENETIC EPIDEMIOLOGY
    27. Schmidt, S; Shao, YJ; Hauser, ER; Slifer, SH; Martin, ER; Scott, WK; Speer, MC; Pericak-Vance, MA
      Life after the screen: Making sense of many p-values

      GENETIC EPIDEMIOLOGY
    28. Amos, CI; Shete, S; Gu, XJ
      Variance components analysis for genetic linkage of time to onset for disease

      GENETIC EPIDEMIOLOGY
    29. Arya, R; Duggirala, R; Williams, JT; Almasy, L; Blangero, J
      Power to localize the major gene for disease liability is increased after accounting for the effects of related quantitative phenotypes

      GENETIC EPIDEMIOLOGY
    30. Pugh, EW; Papanicolaou, GJ; Justice, CM; Roy-Gagnon, MH; Sorant, AJM; Kingman, A; Wilson, AF
      Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers

      GENETIC EPIDEMIOLOGY
    31. Williams, JT; North, KE; Martin, LJ; Comuzzie, AG; Goring, HHH; Blangero, J
      Distribution of lod scores in oligogenic linkage analysis

      GENETIC EPIDEMIOLOGY
    32. Yoo, B; Pankratz, VS; de Andrade, M
      Practical application of residuals from survival models in quantitative trait linkage analysis

      GENETIC EPIDEMIOLOGY
    33. Shete, SS; Chen, JF; Zhou, XJ; Amos, CI
      Modeling agexmajor gene interaction by a variance component approach

      GENETIC EPIDEMIOLOGY
    34. Mathias, RA; Freidhoff, LR; Blumenthal, MN; Meyers, DA; Lester, L; King, R; Xu, JF; Solway, J; Barnes, KC; Pierce, J; Stine, OC; Togias, A; Oetting, W; Marshik, PL; Hetmanski, JB; Huang, SK; Ehrlich, E; Dunston, GM; Malveaux, F; Banks-Schlegel, S; Cox, NJ; Bleecker, E; Ober, C; Beaty, TH; Rich, SS
      Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic families

      GENETIC EPIDEMIOLOGY
    35. Opial, D; Boehnke, M; Tadesse, S; Lietz-Partzsch, A; Flammer, J; Munier, F; Mermoud, A; Hirano, M; Fluckiger, F; Mojon, DS
      Leber's hereditary optic neuropathy mitochondrial DNA mutations in normal-tension glaucoma

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    36. Brown, MD; Zhadanov, S; Allen, JC; Hosseini, S; Newman, NJ; Atamonov, VV; Mikhailovskaya, IE; Sukernik, RI; Wallace, DC
      Novel mtDNA mutations and oxidative phosphorylation dysfunction in RussianLHON families

      HUMAN GENETICS
    37. Murton, NJ; French, L; Toomes, C; Joseph, SS; Rehman, I; Hopkins, BL; Inglehearn, CF; Churchill, AJ
      A high-density transcript map of the human dominant optic atrophy OPA1 gene locus and re-evaluation of evidence for a founder haplotype

      CYTOGENETICS AND CELL GENETICS
    38. Watkins, SL; West, IC; Wilkinson, R; Thomas, TH
      Abnormal thiol reactivity of tropomyosin in essential hypertension and itsassociation with abnormal sodium-lithium countertransport kinetics

      JOURNAL OF HYPERTENSION
    39. Kammerer, CM; Cox, LA; Mahaney, MC; Rogers, J; Shade, RE
      Sodium-lithium countertransport activity is linked to chromosome 5 in baboons

      HYPERTENSION
    40. Foster, MW; Sharp, RR; Mulvihill, JJ
      Pharmacogenetics, race, and ethnicity: Social identities and individualized medical care

      THERAPEUTIC DRUG MONITORING
    41. Mead, PA; Wilkinson, R; Thomas, TH
      Na/Li countertransport abnormalities in type 1 diabetes with and without nephropathy are familial

      DIABETES CARE
    42. Freedman, R; Leonard, S
      Genetic linkage to schizophrenia at chromosome 15q14

      AMERICAN JOURNAL OF MEDICAL GENETICS
    43. Xu, JZ; Pato, MT; Dalla Torre, C; Medeiros, H; Carvalho, C; Basile, VS; Bauer, A; Dourado, A; Valente, J; Soares, MJ; Macedo, AA; Coelho, I; Ferreira, CP; Azevedo, MH; Macciardi, F; Kennedy, JL; Pato, CN
      Evidence for linkage disequilibrium between the alpha 7-nicotinic receptorgene (CHRNA7) locus and schizophrenia in Azorean families

      AMERICAN JOURNAL OF MEDICAL GENETICS
    44. Freedman, R; Leonard, S; Olincy, A; Kaufmann, CA; Malaspina, D; Cloninger, CR; Svrakic, D; Faraone, SV; Tsuang, MT
      Evidence for the multigenic inheritance of schizophrenia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Dobrusin, M; Corbex, M; Kremer, I; Murad, I; Muhaheed, M; Bannoura, I; Muller, DJ; Schulze, TG; Reshef, A; Blanaru, M; Gathas, S; Rietschel, M; Belmaker, RH; Maier, W; Ebstein, RP
      No evidence for linkage by transmission disequilibrium test analysis of microsatellite marker D22S278 and schizophrenia in a Palestinian Arab and in a German population

      AMERICAN JOURNAL OF MEDICAL GENETICS
    46. Philibert, RA; Cheung, D; Welsh, N; Damschroder-Williams, P; Thiel, B; Ginns, EI; Gershenfeld, HK
      Absence of a significant linkage between Na+,K+-ATPase suburmit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish

      AMERICAN JOURNAL OF MEDICAL GENETICS
    47. Muir, WJ; Thomson, ML; McKeon, P; Mynett-Johnson, L; Whitton, C; Evans, KL; Porteous, DJ; Blackwood, DHR
      Markers close to the dopamine D5 receptor gene (DRD5) show significant association with schizophrenia but not bipolar disorder

      AMERICAN JOURNAL OF MEDICAL GENETICS
    48. Liu, JJ; Juo, SH; Terwilliger, JD; Grunn, A; Tong, XM; Brito, M; Loth, JE; Kanyas, K; Lerer, B; Endicott, J; Penchaszadeh, G; Gilliam, TC; Baron, M
      A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22

      AMERICAN JOURNAL OF MEDICAL GENETICS
    49. Escamilla, MA; McInnes, LA; Service, SK; Spesny, M; Reus, VI; Molina, J; Gallegos, A; Fournier, E; Batki, S; Neylan, T; Matthews, C; Vinogradov, S; Roche, E; Tyler, DJ; Shimayoshi, N; Mendez, R; Ramirez, R; Ramirez, M; Araya, C; Araya, X; Leon, PE; Sandkuijl, LA; Freimer, NB
      Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: A follow-up study on chromosome 18

      AMERICAN JOURNAL OF MEDICAL GENETICS
    50. Brown, MD; Allen, JC; Van Stavern, GP; Newman, NJ; Wallace, DC
      Clinical, genetic, and biochemical characterization of a leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations

      AMERICAN JOURNAL OF MEDICAL GENETICS
    51. Axenovich, TI; Zaidman, AM; Zorkoltseva, IV; Kalashnikova, EV; Borodin, PM
      Segregation analysis of Scheuermann disease in ninety families from Siberia

      AMERICAN JOURNAL OF MEDICAL GENETICS
    52. Jacobi, FK; Leo-Kottler, B; Mittelviefhaus, K; Zrenner, E; Meyer, J; Pusch, CM; Wissinger, B
      Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    53. Iwaki, T; Mastushita, T; Kobayashi, T; Yamamoto, Y; Nomura, Y; Kagami, K; Nakayama, T; Sugiura, I; Kojima, T; Takamatsu, J; Kanayama, N; Saito, H
      DNA sequence analysis of protein S deficiency - Identification of four point mutations in twelve Japanese subjects

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    54. Kelsoe, JR; Spence, MA; Loetscher, E; Foguet, M; Sadovnick, AD; Remick, RA; Flodman, P; Khristich, J; Mroczkowski-Parker, Z; Brown, JL; Masser, D; Ungerleider, S; Rapaport, MH; Wishart, WL; Luebbert, H
      A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    55. Deng, HW; Xu, FH; Conway, T; Deng, XT; Li, JL; Davies, KM; Deng, HY; Johnson, M; Recker, RR
      Is population bone mineral density variation linked to the marker D11S987 on chromosome 11q12-13?

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    56. Hasstedt, SJ; Ren, QF; Teng, K; Elbein, SC
      Effect of the peroxisome proliferator-activated receptor-gamma 2 Pro(12)Ala variant on obesity, glucose homeostasis, and blood pressure in members offamilial type 2 diabetic kindreds

      JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM
    57. Thallman, RM; Bennett, GL; Keele, JW; Kappes, SM
      Efficient computation of genotype probabilities for loci with many alleles: I. Allelic peeling

      JOURNAL OF ANIMAL SCIENCE
    58. Agarwala, R; Schaffer, AA; Tomlin, JF
      Towards a complete North American Anabaptist genealogy II. Analysis of inbreeding

      HUMAN BIOLOGY
    59. Yi, NJ; Xu, SZ
      Bayesian mapping of quantitative trait loci under complicated mating designs

      GENETICS
    60. McMahon, FJ; Simpson, SG; McInnis, MG; Badner, JA; MacKinnon, DF; DePaulo, JR
      Linkage of bipolar disorder to chromosome 18q and the validity of bipolar II disorder

      ARCHIVES OF GENERAL PSYCHIATRY
    61. Desautels, A; Turecki, G; Montplaisir, J; Sequeira, A; Verner, A; Rouleau, GA
      Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q

      AMERICAN JOURNAL OF HUMAN GENETICS
    62. Altmuller, J; Palmer, LJ; Fischer, G; Scherb, H; Wjst, M
      Genomewide scans of complex human diseases: True linkage is hard to find

      AMERICAN JOURNAL OF HUMAN GENETICS
    63. Hirschhorn, JN; Lindgren, CM; Daly, MJ; Kirby, A; Schaffner, SF; Burtt, NP; Altshuler, D; Parker, A; Rioux, JD; Platko, J; Gaudet, D; Hudson, TJ; Groop, LC; Lander, ES
      Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height

      AMERICAN JOURNAL OF HUMAN GENETICS
    64. Zhu, XF; Bouzekri, N; Southam, L; Cooper, RS; Adeyemo, A; McKenzie, CA; Luke, A; Chen, GJ; Elston, RC; Ward, R
      Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure

      AMERICAN JOURNAL OF HUMAN GENETICS
    65. Abney, M; McPeek, MS; Ober, C
      Broad and narrow heritabilities of quantitative traits in a founder population

      AMERICAN JOURNAL OF HUMAN GENETICS
    66. Garner, C; McInnes, LA; Service, SK; Spesny, M; Fournier, E; Leon, P; Freimer, NB
      Linkage analysis of a complex pedigree with severe bipolar disorder, usinga Markov chain Monte Carlo method

      AMERICAN JOURNAL OF HUMAN GENETICS
    67. Gurling, HMD; Kalsi, G; Brynjolfson, J; Sigmundsson, T; Sherrington, R; Mankoo, BS; Read, T; Murphy, P; Blaveri, E; McQuillin, A; Petursson, H; Curtis, D
      Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23

      AMERICAN JOURNAL OF HUMAN GENETICS
    68. Almasy, L; Porjesz, B; Blangero, J; Goate, A; Edenberg, HJ; Chorlian, DB; Kuperman, S; O'Connor, SJ; Rohrbaugh, J; Bauer, LO; Foroud, T; Rice, JP; Reich, T; Begleiter, H
      Genetics of event-related brain potentials in response to a semantic priming paradigm in families with a history of alcoholism

      AMERICAN JOURNAL OF HUMAN GENETICS
    69. Zhang, W; Tapper, W; Collins, A; Jacobs, KB; Elston, RC; Morton, NE
      A tournament of linkage tests in complex inheritance

      HUMAN HEREDITY
    70. Koch, R; Julius, U; Jaross, W; Schroder, HE
      Estimation of the heritability of latent variables which are included in astructural model for metabolic syndrome

      HUMAN HEREDITY
    71. Jorde, LB
      Consanguinity and prereproductive mortality in the Utah Mormon population

      HUMAN HEREDITY
    72. Amos, CI; de Andrade, M; Zhu, DK
      Comparison of multivariate tests for genetic linkage

      HUMAN HEREDITY
    73. Cook, CCH; Hope, L; Gurling, H
      Ascertainment of families for a linkage study of alcoholism

      ADDICTION BIOLOGY
    74. Schelhaas, HJ; Ippel, PF; Beemer, FA; Hageman, G
      Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxias

      EUROPEAN JOURNAL OF NEUROLOGY
    75. Duffy, A; Turecki, G; Grof, P; Cavazzoni, P; Grof, E; Joober, R; Ahrens, B; Berghofer, A; Muller-Oerlinghausen, B; Dvorakova, M; Libigerova, E; Vojtechovsky, M; Zvolsky, P; Nilsson, A; Licht, RW; Rasmussen, NA; Schou, M; Vestergaard, P; Holzinger, A; Schumann, C; Thau, K; Robertson, C; Rouleau, GA; Alda, M
      Association and linkage studies of candidate genes involved in GABAergic neurotransmission in lithium-responsive bipolar disorder

      JOURNAL OF PSYCHIATRY & NEUROSCIENCE
    76. Chen, AS; Kovach, MJ; Herman, K; Avakian, A; Frank, W; Forrester, S; Lin, JP; Kimonis, V
      Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families

      GENETICS IN MEDICINE
    77. Niculescu, AB; Segal, DS; Kuczenski, R; Barrett, T; Hauger, RL; Kelsoe, JR
      Identifying a series of candidate genes for mania and psychosis: a convergent functional genomics approach

      PHYSIOLOGICAL GENOMICS
    78. Mashima, Y; Kigasawa, K; Wakakura, M; Oguchi, Y
      Do idebenone and vitamin therapy shorten the time to achieve visual recovery in Leber hereditary optic neuropathy?

      JOURNAL OF NEURO-OPHTHALMOLOGY
    79. Williams, RR; Rao, DC; Ellison, RC; Arnett, DK; Heiss, G; Oberman, A; Eckfeldt, JH; Leppert, MF; Province, MA; Mokrin, SC; Hunt, SC
      NHLBI Family Blood Pressure Program: Methodology and recruitment in the HyperGEN network

      ANNALS OF EPIDEMIOLOGY
    80. Axenovich, TI; Svischeva, GR; Aulchenko, YS
      Mapping of quantitative trait loci in animals: Partitioning of variances

      RUSSIAN JOURNAL OF GENETICS
    81. Abecasis, GR; Cookson, WOC; Cardon, LR
      Pedigree tests of transmission disequilibrium

      EUROPEAN JOURNAL OF HUMAN GENETICS
    82. de Andrade, M; Amos, CI
      Ascertainment issues in variance components models

      GENETIC EPIDEMIOLOGY
    83. Daw, EW; Thompson, EA; Wijsman, EM
      Bias in multipoint linkage analysis arising from map misspecification

      GENETIC EPIDEMIOLOGY
    84. Deng, HW; Chen, WM; Conway, T; Zhou, Y; Davies, KM; Stegman, MR; Deng, HY; Recker, RR
      Determination of bone mineral density of the hip and spine in human pedigrees by genetic and life-style factors

      GENETIC EPIDEMIOLOGY
    85. Elston, RC; Buxbaum, S; Jacobs, KB; Olson, JM
      Haseman and Elston revisited

      GENETIC EPIDEMIOLOGY
    86. Schaid, DJ; Elston, RC; Tran, L; Wilson, AF
      Model-free sib-pair linkage analysis: Combining full-sib and half-sib pairs

      GENETIC EPIDEMIOLOGY
    87. Amos, CI; Gu, XJ; Chen, JF; Davis, BR
      Least squares estimation of variance components for linkage

      GENETIC EPIDEMIOLOGY
    88. Blangero, J; Williams, JT; Almasy, L
      Robust LOD scores for variance component-based linkage analysis

      GENETIC EPIDEMIOLOGY
    89. Sham, PC; Zhao, JH; Cherny, SS; Hewitt, JK
      Variance-components QTL linkage analysis of selected and non-normal samples: Conditioning on trait values

      GENETIC EPIDEMIOLOGY
    90. Feng, XM; Pu, W; Gao, DW; Isashiki, Y; Ohba, N
      Diagnostic potential of mitochondrial DNA assessment in patients with optic neuropathy

      CHINESE MEDICAL JOURNAL
    91. Vanopdenbosch, L; Dubois, B; D'Hooghe, MB; Meire, F; Carton, H
      Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis

      JOURNAL OF NEUROLOGY
    92. Sheehan, NA
      On the application of Markov chain Monte Carlo methods to genetic analyseson complex pedigrees

      INTERNATIONAL STATISTICAL REVIEW
    93. Bailer, U; Leisch, F; Meszaros, K; Lenzinger, E; Willinger, U; Strobl, R; Gebhardt, C; Gerhard, E; Fuchs, K; Sieghart, W; Kasper, S; Hornik, K; Aschauer, HN
      Genome scan for susceptibility loci for schizophrenia

      NEUROPSYCHOBIOLOGY
    94. Vilchis, F; Mendez, JP; Canto, P; Lieberman, E; Chavez, B
      Identification of missense mutations in the SRD5A2 gene from patients withsteroid 5 alpha-reductase 2 deficiency

      CLINICAL ENDOCRINOLOGY
    95. Do, KA; Broom, BM; Kuhnert, P; Duffy, DL; Todorov, AA; Treloar, SA; Martin, NG
      Genetic analysis of the age at menopause by using estimating equations andBayesian random effects models

      STATISTICS IN MEDICINE
    96. Kotchen, TA; Kotchen, JM; Grim, CE; George, V; Kaldunski, ML; Cowley, AW; Hamet, P; Chelius, TH
      Genetic determinants of hypertension - Identification of candidate phenotypes

      HYPERTENSION
    97. Kornberg, JR; Brown, JL; Sadovnick, AD; Remick, RA; Keck, PE; McElroy, SL; Rapaport, MH; Thompson, PM; Kaul, JB; Vrabel, CM; Schommer, SC; Wilson, T; Pizzuco, D; Jameson, S; Schibuk, L; Kelsoe, JR
      Evaluating the parent-of-origin effect in bipolar affective disorder - Is a more penetrant subtype transmitted paternally?

      JOURNAL OF AFFECTIVE DISORDERS
    98. Ohtsuki, T; Ishiguro, H; Yoshikawa, T; Arinami, T
      WFS1 gene mutation search in depressive patients: detection of five missense polymorphisms but no association with depression or bipolar affective disorder

      JOURNAL OF AFFECTIVE DISORDERS
    99. Serretti, A; Macciardi, F; Cusin, C; Lattuada, E; Souery, D; Lipp, O; Mahieu, B; Van Broeckhoven, C; Blackwood, D; Muir, W; Aschauer, HN; Heiden, AM; Ackenheil, M; Fuchshuber, S; Raeymaekers, P; Verheyen, G; Kaneva, R; Jablensky, A; Papadimitriou, GN; Dikeos, DG; Stefanis, CN; Smeraldi, E; Mendlewicz, J
      Linkage of mood disorders with D2, D3 and TH genes: a multicenter study

      JOURNAL OF AFFECTIVE DISORDERS
    100. Murphy, VE; Mynett-Johnson, LA; Claffey, E; Bergin, P; McAuliffe, M; Kealey, C; McKeon, P
      Search for bipolar disorder susceptibility loci: The application of a modified genome scan concentrating on gene-rich regions

      AMERICAN JOURNAL OF MEDICAL GENETICS


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Documento generato il 29/10/20 alle ore 11:27:35