Index to Volume 76 Abade, A., 431-453 anthropoid evolution, 921—935 Abe-Sandes, K., 77-86, 313-316 anthropological genetics, 801-804 ABO, 527-541 APOA4. See apolipoprotein A4 ABO-secretor locus, 789-795 APOE, 253-266, 267-275, 605-614 acid phosphatase (ACP 1), 289-297, 817- APOE genotypes, 615-621 835, 837-848 apolipoprotein Al (APOA1), 307-312 Acufia, M., 299-305 “Apolipoprotein Al Gene Polymorphisms admixture, in South America, 543-557 at the — 75 bp and + 83/84 bp Polymor- Adriatic islands, 15-31 phic Sites in Healthy Omanis Compared Adrien, L. R., 87-108 with World Populations,” 307-312 African populations, 87-108 apolipoprotein A4 (APOA4), 253-266 Afro-Brazilian populations, 77—86 “Apolipoprotein E Polymorphism and Its aging, 127-146 Association with Serum Lipid Levels in Al-Bahrani, A. 1., 307-312 Brazilian Children,” 267—275 Albania, 943-946 “Apolipoprotein E Polymorphism Is Re- Alexandrino, F., 313-316 lated to Plasma Lipids and Apolipoprot- Alfonso-Sanchez, M. A., 361-381 eins in Mexican Adolescents,” 605-614 Al-Kindi, M. N., 307-312 apolipoproteins, 605-614 “Allele Frequencies of D21S11, FGA, Arabs, 559-567 THO1, and VWA in Populations of the Arg972 polymorphism, 147-151 Balkans,” 943-946 Argentina, 413-429, 543-557 allele frequency, 153-159 Arnett, F. C., 591-604 Altai Republic, 109-125 Aromuns, 943-946 Altemani, C. M., 147-151 arteriosclerosis, 127-146 Alu insertion polymorphisms, 277-287 Assemblea dei Direttori dei Centri, Aluja, M. P., 431-453 455-467 Al-Yahyaee, S. A. S., 307-312 atherosclerosis, 267—275, 863-876 Amazon region, 643-646 Australia, 849-862 amelogenin, 15—31, 109-125 autosomes, 543-557 Amerindian admixture, 299-305 azoospermia, 469-478 Amerindians, 33-54, 413-429, 591-604, azoospermia factor (AZF), 469-478 723-730. See also Colombian Amerin- Azores, 431-453 dians AmpFLSTR loci, 569-590 Bahrain, 779-783 AmpliFLPs, 87-108 Balkan populations, 943—946 ancestral haplotype, 731-741 Baltic-speaking populations, 877—900 ancient DNA, 33-54, 109-125 Barrantes, R., 591-604 Anglés, N., 431-453 Basque population, 361-381, 731-741 antagonistic pleiotropy, 127-146 Bauer, M. J., 327-342 954 / Index to Volume 76 Ben Amor, M., 559-567 Bosnian mountain area, 15-31 Benavente, M., 615-621 Bossi, A., 455-467 Benevolenskaya, L., 591-604 Bottini, E., 289-297 Benin, 87—108 Bottini, M., 837-848 Berbers. 559-567 Bottini, N., 289-297 Bergamaschi, A., 289-297 Bourgeois, J., 109-125 Bertoni, B., 543-557 Brahmin population, 153-159 B-globin gene haplotypes, 765-778 Brazil, 147-151, 937-942 Bezerra, R. M. N., 147-151 Brazilian populations, 267—275, 313-316, Bezerra Alves, J. G., 267—275 643-646 Bharati, S., 211-228 Breece, K. E., 33-54 biallelic loci, 743-763 Brennecke, S. P., 849-862 biallelic marker, 77-86 Budilova, E. V., 623-641 Bianchi, N. O., 543-557 Budowle, B., 15-31 birth interval, 667—687 birth weight, 127-146, 327-342 BjelaSnica—Treskavica region, 15-31 Cai, G., 651-665 Blanco Villegas, M. J., 191-210 Calafell, F., 731-741 Blangero, J., 515—525, 651-665, 863-876 Calderon, R., 361-381 blood groups, 527-541 calpain mutations, 731-741 Boattini, A. 191-210 calpain-3 gene (CAPN3), 731-741 Boétsch, G., 527-541 Cameron, N., 127-146 Bonatto, S. L., 591-604 Cameroon, 87—108 Book reviews Cano, B., 615-621 The Delphic Boat (Danchin), 492-493 Cantos, M., 615-621 Human Biologists in the Archives (Her- CAPN-3, 731-741 ring and Swedlund, eds.), 163—165 cardiovascular disease, 615—621 Human Biology and History (Smith, ed.), Cardoso, G. L., 643-646 317-319 Cardoso-Saldafia, G. C., 605-614 Human Population Dynamics (Macbeth Carnese, F. R., 591-604 and Collinson, eds.), 161-163 Carvalhaes, F. A. P. L., 643-646 The Molecule Hunt (Jones), 489-491 Carvalho, C. M. B., 469-478 New Challenges to Health (Smith et al., Casazza, G., 455-467 eds.), 320-321 castes, 153-159 On Fertile Ground (Ellison), 947-951 CCR2, 643-646 Phylogenetic Analysis of Morphological CCRS, 643-646 Data (Wiens), 165—168 CD4, 229-251 Book reviewers Central Asia, 109-125 Chang, M. L., 165-168 Central Valley (California), 55-75 Fix, A. G., 161-163 CFTR, 455-467 Kaestle, F. A., 489-491 Little, M. A., 317-319 Chadid, T. T., 147-151 Palese, P., 320-321 Chakraborty, R., 401-412 Relethford, J. H., 492-493 Chakravorty, M., 153-159 Rockwell, L. C., 947-951 “Characteristic B-Globin Gene Cluster Stinson, S., 163-165 Haplotypes of Evenkis and Orogens in bootstrap analysis, 173-190 North China,” 765-778 Borg, A., 849-862 “Characterization of Admixture in an Index to Volume 76 / 955 Urban Sample from Buenos Aires, Ar- crude birth rate, 343-359 gentina, Using Uniparentally and Bipa- CSFI1PO, 15-31, 229-251, 723-730 rentally Inherited Genetic Markers,” cystic fibrosis, 455-467 543-557 cystic fibrosis incidence rate, 455-467 Chatters, J. C., 33-54 cystic fibrosis transmembrane regulator Chauhan, P. S., 743-763 gene (CFTR), 455-467 chemokine receptors, 643-646 cytokine, 153-159 Chiaroni, J., 527-541 cytokine variation, 515-525 Chilean population, 299-305 Czarny, J., 877-900 China, 765-778 Czerwinski, S. A., 863-876 cholesterol levels, 605—614, 863-876 Choudhury, A., 153-159 D1S80, 87-108 Cifuentes, L., 299-305 “D1S80 Single-Locus Discrimination coastal migration, 55-75 Among African Populations,” 87—108 Cobo, A. M., 731-741 D3S1358, 15-31, 109-125, 229-251, Colantonio, S. E., 1-14 569-590 Cole, S. A., 651-665 D5S818, 15-31, 109-125, 569-590, Colombian Amerindians, 765-778 723-730 Columbia Plateau, 55-75 D7S820, 15-31, 109-125, 569-590, “A Common Haplotype Associated with 723-730 the Basque 2362AG — TCATCT Muta- D8S1179, 15-31, 109-125, 569-590 tion in the Muscular Calpain-3 Gene,” D13S317, 15-31, 109-125, 569-590, 731-741 723-730 Comoros Islands, 527-541 D16S539, 15-31, 723-730 “Comparative Analysis of Dermatoglyphic D17S30, 785-788 Traits in Hungarian and Gypsy Popula- “D17S30 and TP53 VNTR Loci Polymor- tions,” 383-400 phisms in a Turkish Population” (brief “Comparative Study of Genetic Variation communication), 785—788 at 15 STR Loci in Three Isolated Popula- D18S5, 569-590 tions of the Bosnian Mountain Area,” D18S51, 15-31, 109-125 15-31 D21S11, 15-31, 109-125, 569-590, complex segregation analysis, 401-412 943-946 compound haplotype systems, 277—287 Das, B., 743-763 Comuzzie, A. G., 651-665 Dash, S., 779-783 congenital deafness, 313-316 De Franga, E., 267-275 consanguineous marriage, |—14 Degioanni, A., 527-541 consanguinity degree, 1-14 Delaunay triangulation, 173-190 contraception, 711-722 Demarchi, D. A., 211-228, 413-429 Cooper, D. W., 849-862 Demerath, E. W., 127-146 Corella, D., 253-266 “Demographic Analysis of the Variation in coronary artery disease, 299-305 the Rates of Multiple Maternities in Corréa-Oliveira, R., 515-525 Sweden Since 1751,” 343-359 Corsica, 229-251 demographic factors, 1-14 Cosmi, E. V., 289-297 demographic history, 689-709 craniometrics, 499-513 demographic transition, 361-381 Crawford, M. H., 211-228, 805-815 Denisova, G., 877-900 Crow’s index, 361-381 de Oya, M., 615-621 Crubézy, E., 109-125 Derenko, M., 877-900 956 / Index to Volume 76 dermatoglyphics, 211-228, 383-400 Eriksson, A. W., 343-359 De Silvestri, A., 901-920 ESD, 479-488 “Determination of Human European Mito- Eshleman, J. A., 55-75 chondrial DNA Haplogroups by Means esterase D. See ESD of a Hierarchical Approach,” 431-453 Estonians, 877—900 Devor, E. J., 921-935 “Ethnic Differences in Allele Distribution DF1, 643-646 for the IL8 And ILIB Genes in Popula- DF508 mutation, 455-467 tions from Eastern India,” 153-159 “Differentiation of Mitochondrial DNA ethnic mixture, 77—86 and Y chromosomes in Russian Popula- “European ACP/*C Allele Has Recessive tions,” 877-900 Deleterious Effects on Early Life Viabil- disease registry, 455-467 ity,” 817-835 “Distribution of CCR5-A32, CCR2-641, European populations, 817—835. See also and SDF1-3’A Mutations in Populations specific countries and populations from the Brazilian Amazon Region” Evenkis, 765-778 (brief communication), 643-646 Everson, P. M., 667—687 diversifying selection, 921—935 “Evidence for a Major Gene Influence on DNA STR systems, 943-946 Persistent Developmental Stuttering,” DNA typing, 723-730 401-412 DR2DI, 543-557 evolution, 127-146 Drobnic, K., 15-31 extinction, 689-709 Dugoujon, J.-M., 559-567 Duncan, G., 87-108 FI3A1, 229-251 DYF155S2, 743-763 Fadhlaoui-Zid, K., 559-567 DYS19, 413-429, 743-763 fat intake, 253-266 DYS199, 413-429, 543-557 Feitosa, M. F., 937-942 DYS287, 743-763 Fellman, J., 343-359 DYS3891, 743-763 fertility, 667-687 DYS389II, 743-763 fertility transition, 711-722 DYS390, 413-429 FES, 229-251 DYS391, 413-429, 743-763 fetal growth retardation, 127-146 DYS392, 413-429 FGA, 15-31, 109-12, 569-590, 943-946 DYS393, 413-429, 743-763 fine mapping, 849-862 DYS437, 413-429 “Fine Mapping and SNP Analysis of Posi- DYS438, 413-429 tional Candidates at the Preeclampsia DYS439, 413-429 Susceptibility Locus (PREG!) on Chro- mosome 2,” 849-862 Eaton, L., 299-305 Finland, 343-359, 849-862. See also Ecuador, 723-730 Finns editorial, 801—804 Finno-Ugric-speaking populations, effective population size, 689-709 877-900 Efremovska, L., 943-946 Finns, 877-900 Egypt, 87-108 fitness, 667—687 Elgaaied, A., 559-567 Fitzpatrick, E., 849-862 Elkhil, H. K., 559-567 Forrest, S., 849-862 Eller, E., 689-709 Francalacci, P., 431-453 endemic diseases, 837-848 Frassati, C., 527-541 epidemiology, 127-146 Freeland-Graves, J. H., 651—665 Index to Volume 76 / 957 Freitas, L. B., 591-604 “Genetic Diversity in Tunisia: A Study “Frequencies of Apolipoprotein A4 Gene Based on the GM Polymorphism of Polymorphisms and Association with Human Immunoglobulins,” 559-567 Serum Lipid Concentrations in Two “Genetic History of the Population of Cor- Healthy Spanish Populations.” 253-266 sica (Western Mediterranean) as Inferred “Frequency of the 35delG Mutation in the from Autosomal STR Analysis,” GJB2 Gene in Samples of European, 229-251 Asian, and African Brazilians,” genetic homogenization, 569-590 313-316 “Genetic Influences on Plasma Cytokine Fuster, V., 1-14 Variation in a Parasitized Population,” FUT2, 789-795 515-525 FY, 527-541 “Genetic Profile of the Kichwas (Qui- chuas) from Ecuador by Analysis of G6PD, 837-848 STR Loci,” 723-730 G6PD deficiency, 779-783 genetic structure, 173-190, 229-251 Gage, T. B., 327-342 of Sicily, 901-920 Galbraith, J. J., 921-935 “Genetic Structure and Gene Flow in Gran Gafian, A., 253-266 Chaco Populations of Argentina: Evi- Garcés, C., 615-621 dence from Y-Chromosome Markers,” Garo population, 569-590 413-429 Gaspar, P., 277-287 “Genetic Variants of the Paraoxonases gene X environment interaction, 863—876 (PON]! and PON2) in the Chilean Fopu- “Gene by Smoking Interaction: Evidence lation,” 299-305 for Effects on Low-Density Lipoprotein “Genetic Variation in a Compound Short Size and Plasma Levels of Triglyceride Tandem Repeat/Alu Haplotype System and High-Density Lipoprotein Choles- at the SB19.3 Locus: Properties and In- terol,” 863-876 terpretation,” 277-287 gene expression, 863—876 genomewide scan, 651—665 gene flow, 413-429, 499-513, 569-590 geographic factors, |—-14 gene geography, 173-190 “Geographic Patterns of (Genetic, Mor- “Genetic Analysis of a Scytho-Siberian phologic, Linguistic) Variation: How Skeleton and Its Implications for An- Barriers Can Be Detected by Using cient Central Asian Migrations,” Monmonier’s Algorithm,” 173-190 109-125 geohelminths, 515—525 genetic anthropology, 527-541 Germany, 479-488 genetic barriers, 173-190 Ghosh, A., 153-159 “Genetic Characterization of the Popula- Gibert, M., 527-541 tion of Grande Comore Island (Njazidja) Gillman, M. W., 127-146 According to Major Blood Groups,” GJB2, 313-316 527-541 “Global Patterns of Isolation by Distance genetic distance, 15-31 Based on Genetic and Morphological genetic diversity, 33-54, 77-86 Data,” 499-513 in North Africa, 559-567 Gloria-Bottini, F., 289-297, 837-848 of Spain, 615-621 glutathione S-transferase (GST), 937-942 “Genetic Diversity and Relationships “Glutathione S-Transferase M1 (GSTM1) among the Tribes of Meghalaya Com- and T1 (GSTT1) Polymorphisms in a pared to Other Indian and Continental Brazilian Mixed Population” (brief com- Populations,” 569-590 munication), 937-942 958 / Index to Volume 76 GM, 559-567 “Heterogeneity of the Y Chromosome in Goicoechea, A. S., 591-604 Afro-Brazilian Populations,” 77-86 Gonzalez-Andrade, F., 723-730 heterozygosity, 15-31 Goring, H. H. H., 849-862 Heyer, E., 173-190 Gran Chaco (Argentina), 413-429 “History of Human Biology (1929- Granizo, J. J., 615—621 2004), 805-815 Great Basin, 55—75 HIV-1, 643-646 Grimes, M., 667-687 Hokan, 55-75 growth, 127-146 hookworm, 515-525 Grzybowski, T., 877-900 host-defense mechanisms, 921—935 GSTM1, 937-942 HP, 289-297 GSTT1, 937-942 Huckenbeck, W., 943-946 Guegan, J.-F., 623-641 Human Biology (journal), 801-804 Guérard, E., 173-190 Human Genome Project, 801-804 Guerreiro, J. F, 643-646 “Human Genome Project and Advances in Guglielmino, C. R., 901-920 Anthropological Genetics, The” (edito- Guillén, M., 253-266 rial), 801-804 Giimiis, G., 785-788 Hungarian children, 383—400 Gypsy children, 383-400 Hutz, M. H., 267—275, 591-604 HV1 sequence, 109-125 hypertension, 127-146 Hackenberger, S. 33-54 hypervariable segment | (HVS1), 55-75 Hadziselimovic, R., 15-31 Hammer, M. F,, 817-835 Iceland, 849-862 Hamoy, I. G., 643-646 ILIB gene, 153-159 Hao, L., 765-778 IL8 gene, 153-159 haplogroups, 109-125, 431-453 Imanishi, T., 765-778 haplogroup screening, hierarchical ap- immunoglobulins, 559-567 proach to, 431—453 immunology, 515-525 haplotypes, 743-763 inbreeding, 1-14, 191-210 haplotype structure, 153-159 “Inbreeding Patterns in La Cabrera, Spain: haptoglobin development, 289-297 Dispensations, Multiple Consanguinity Harihara, S., 765-778 Analysis, and Isonymy,” 191-210 Hatagima, A., 937-942 Indakoetxea, B., 731-741 Hawks, J., 689-709 India, 153-159, 211-228, 569-590 heart disease, 127-146 Indian populations, 153—159, 743-763 Heffner, N., 327-342 “Ineffective Contraceptive Use and Its Heller, A. H., 591-604 Causes in a Natural Fertility Population Hellin’s law, 343-359 in Southern Jordan,” 711-722 Hembrum, J., 153-159 infant mortality, 327-342 hemoglobinopathies, 779-783 infectious disease, 361-381 “Hemoglobinopathies, G6PD Deficiency, Inga tribe, 765-778 and Hereditary Elliptocytosis in Bah- insulin resistance, 147-151 rain” (brief communication), 779-783 insulin resistance syndrome, 651—665 Henke, J., 479-488 interferon, 515-525 Henke, L., 479-488 interleukin, 515-525 hereditary elliptocytosis, 779-783 “Intra- and Intercontinental Molecular Herrera, R. J., 87-108 Variability of an Alu Insertion in the 3’ Index to Volume 76 / 959 Untranslated Region of the LDLR LDLR, 591-604 Gene,” 591-604 Lee, H. S., 401-412 Irizawa, Y., 479-488 life span, 623-641 IRS1I (insulin receptor substrate-1 gene), Lima, M., 431-453 147-151 limb-girdle muscular dystrophy type 2A ischemic heart disease, 615-621 (LGMD2A), 731-741 isolated population, 15-31 linguistic diversity, 55-75 isolation by distance, 499-513 linkage (genetic), 849-862 isonymy, 191-210 linkage disequilibrium, 789-795 Israel, 469-478 linkage simulation, 401-412 Italy, 455—467, 837-848 lipids, 253-266, 267-275 Liria, Y. K., 605-614 Japan, 479-488 Lithuanians, 877—900 Japanese, 765-778, 789-795 Liu, H., 849-862 Jha, B. T, 515-525 Liu, Y. T., 643-646 Jin, F., 765-778 “LOC 390443 (RNase 9) on Chromosome Jirel population, 515-525 14q11.2 Is Related to the RNase A JK, 527-541 Superfamily and Contains a Unique Johnson, J. R., 55-75 Amino-Terminal Preproteinlike Se- Jordan, 711-722 quence,” 921-935 journal history, 805-815 “Local Extinction and Recolonization, Species Effective Population Size, and Kadikiran, A., 785-788 Modern Human Origins,” 689-709 Kaestle, F. A., 33-54, 55-75 LOD score, 849-862 Kamsa tribe, 765-778 L6pez de Munain, A., 731-741 Kansas, 667-687 Lorenz, J., 55-75 Kapur, L., 15-31 low-density lipoprotein receptor gene, Kayastha population, 153-159 591-604 KEL, 527-541 Ludes, B., 109-125 Kenya, 87-108 Lunkina, A., 877-900 Kerala population, 743-763 Lyngngam population, 569-590 Keyser-Tracqui, C., 109-125 Khasi subtribes, 569-590 MacCluer, J. W., 651-665, 863-876 Kichwas, 723-730 Macedonia, 943-946 Kimura, H., 789-795 Maciel-Guerra, A. T., 313-316 Kizil skeleton (95-KBI-52), 109-125 Magna, L. A., 313-316 Kleiman, S. E., 469-478 Magrini, A., 289-297 Koda, Y., 789-795 Mahaney, M. C., 863-876 Koreans, 765-778 Maharashtra population, 743-763 Krieger, H., 937-942 Mahishya population, 153-159 Krylov, M., 591-604 major dominant gene model with incom- Kumar, V., 211-228, 569-590 plete penetrance, 401-412 malaria, 837-848 “Lack of Arg972 Polymorphism in the male infertility, 469-478 IRS1 Gene in Parakana Brazilian Indi- Malgosa, A., 431-453 ans,” 147-151 Malhi, R. S., 33-54, 55-75 Langstieh, B. T., 569-590 Malyarchuk, B., 877-900 Latvians, 877-900 Manni, F., 173-190 960 / Index to Volume 76 Marjanovic, D., 15-31 Montiel, R., 431-453 Marques, C. F. S., 937-942 Morozova, I., 877-900 marriage dispensations, 191-210 mortality crisis, 361-381 Martinez Marignac, V. L., 543-557 mortality rate, 623-641 Marubayashi, A., 765-778 Moses, E. K., 849-862 maternal age, and multiple births, 343-359 mtDNA, 431-453, 877-900. See also mi- “Maternai Cigarette Smoking, Metabolic tochondrial DNA Enzyme Polymorphism, and Develop- mtDNA haplogroups, 543-557 mental Events in the Early Stages of Ex- multiple-birth rates, 343-359 trauterine Life,” 289-297 multiple consanguinity, 191-210 Medina-Urrutia, A. X., 605-614 multipoint linkage analysis, 651—665 Mediterranean basin populations, 229-251 Munkhbat, B., 591-604 Meghalaya populations, 569-590 Munkhtuvshin, N., 591—604 Menezes, R., 147-151 muscular dystrophy, 731-741 Mennonites, 667—687 mutation accumulation, 127-146 Mercier, P., 527-541 metabolic syndrome, 651-665 Nagy, A. S., 383-400 Mexican Americans, 651—665, 863-876 Native American genetics, 55—75 Mexican population, 605—614 Native Americans, 33-54 microdeletions, 469-478 natural fertility, 711-722 microevolution, 361-381 natural selection, 361-381, 817—835 microsatellite DNA, 499-513 Nepal, 515-525 microsatellite markers, 731-741 network analysis, 413—429 microsatellites, 413-429 networks, 743-763 migration, 109-125 newborns, 289-297 Mikerezi, I., 943-946 New Zealand, 849-862 Milani, S., 455-467 92R7, 743-763 “Minimal Sharing of Y-Chromosome STR North Africa, 559-567 Haplotypes Among Five Endogamous northern Hungary, 383-400 Population Groups from Western and “A Novel Tetrameric Short Tandem Repeat Southwestern India,” 743-763 Located in the 3’ Flanking Region of the Miscicka-Sliwka, D., 877-900 Human ABO-Secretor Gene (FUT2) and Mitchell, R. J., 413-429 Association Between FUT2 and FUT2/ mitochondrial DNA, 33-54, 55-75, 543- 01 Loci” (brief communication), 557. See also mtDNA 789-795 “Mitochondrial DNA and Prehistoric Set- tlements: Native Migrations on the West- obesity, 651-665 ern Edge of North America,” 55-75 OCA2, 543-557 MNS, 527-541 Ohtsuka, R., 711-722 modern human origins, 689-709 oligozoospermia, 469—478 Moffat-Wilson, K. A., 921-935 Oliveira, C. A., 313-316 molecular archeology, 109-125 Omani population, 307-312 “Molecular Basis of ESD*5 and ESD*7 Omoto, K., 765-778 and Haplotype Analysis with New Poly- “Opportunity for Natural Selection in a morphisms in Introns” (brief communi- Basque Population and Its Secular cation), 479-488 Trend: Evolutionary Implications of Epi- Mongolians, 591—604 demic Mortality,” 361-381 Monmonier’s algorithm, 173-190 optimum family size, 667—687 Index to Volume 76 / 961 Oraon population, 153-159 of Japanese, 789-795 Ordovas, J. M., 253-266 of Kichwas, 723-730 Orogens, 765-778 population structure, 413-429 overdominance, 817-835 of Comoros Islands, 527-541 population subdivision. of Sicily, 901-920 Padoan, R., 455-467 Portugal, 277-287 palmar interdigital ridge counts, 211—228 Posadas-Romero, C., 605-614 Pang, H., 789-795 Poza, J. J., 731-741 Paoli, G., 229-251 preeclampsia, 849-862 Pap, M., 383-400 preeclampsia susceptibility locus, 849-862 Paraguay, 543-557 PREGI, 849-862 Parakana Indians, 147-151 primates, 921—935 paraoxonase, 299-305 “Principal Component for Metabolic Syn- parasitology, 515-525 drome Risk Maps to Chromosome 4p in parity, 343-359 Mexican Americans: The San Antonio Parra, E. J., 543-557 Family Heart Study,” 651-665 “Patterns of Ethnic, Linguistic, and Geo- principal components analysis, 211-228 graphic Heterogeneity of Palmar Inter- Prussia, 667—687 digital Ridge Counts in the Indian PV92, 543-557 Subcontinent,” 211-228 “Patterns of mtDNA Diversity in North- Quichuas, 723-730 western North America,” 33-54 Paz, G., 469-478 Rai, D. R., 515-525 PCR, 87-108 Rainwater, D. L., 863-876 pediatric paradox, 327-342 recolonization, 689-709 “Pediatric Paradox: Heterogeneity in the red blood cell polymorphisms, 499-513 Birth Cohort,” 327-342 Reddy, B. M., 211-228, 569-590 Pefia, J. A., 361-381 regression, 667—687 Pena, S. D. J., 469-478 Relethford, J. H., 499-513, 689-709 Penta D, 15-31 repeated pairs, 191-210 Penta E, 15-31 repeat polymorphism, 479-488 Penutian, 33-54, 55-75 replicative senescence, 127-146 peopling, 229-251 “Reproductive Measures, Fitness, and Mi- persistent developmental stuttering, grating Mennonites: An Evolutionary 401-412 Analysis,” 667-687 Pettener, D., 191-210 reproductive norm, 711-722 phylogenetic analysis, 87-108 reproductive span, 667—687 phylogeography, 877—900 reproductive success, 667—687 Pima Indians, 147-151 Reviron, D., 527-541 Pocovi, M., 253-266 RFLPs, 431-453 Pojskic, N., 15-31 RH, 527-541 Poles, 877-900 ribonucleases, 921—935 PON 1, 299-305 Ricaut, F-X., 109-125 PON2, 299-305 RNase A superfamily, 921-935 population-associated alleles (PAAs), Rocha, J. L. , 277-287, 469-478 543-557 Rodriguez Otero, H., 191-210 population differentiation, 689-709 roundworm, 515-525 population genetics, 87-108 Roychoudhury, S., 153-159 962 / Index to Volume 76 Ruiz, L. M., 87-108 Sicily, 901-920 Russia, 667—687 Siervogel, R. M., 127-146 Russian populations, 877-900 Silva, W. A., Jr., 77-86, 313-316 Rustamov, A., 785-788 Singh, L., 569-590 Rwanda, 87-108 single nucleotide polymorphism (SNP), Rychkov, S., 877-900 153-159, 277-287, 479-488, 849-862 Smith, D. G., 33-54, 55-75 Saad, M. J. A., 147-151 smoking, 289-297, 863-876 Saad, S. T. O., 147-151 Soares, M. C. P., 147-151 Saenz, A., 731-741 “Socioeconomic, Demographic, and Geo- Sales, T. S. I., 147-151 graphic Variables Affecting the Diverse Salishan, 33-54 Degrees of Consanguineous Marriages Salzano, F. M., 591-604 in Spain,” 1-14 Sanabria, N. Y., 87-108 socioeconomic factors, 1-14 San Antonio Family Heart Study, 651—665 Soejima, M., 789-795 Sanchez, D., 723-730 South America, 543-557 Sanchez-Mazas, A., 559-567 Spain, 1-14, 191-210, 253-26, 615-621 Santhal population, 153-159 spatial autocorrelation, 21 1—228 Santos, C., 431-453 spontaneous abortion, 817—835 Santos, F. R., 469-478 Stefanini, L., 289-297 Santra, A., 153-159 Stern, M. P., 863-876 Sao Tomé, 277-287 Stevenson, J. C., 667-687 Sardinia, 837-848 STR. See short tandem repeat (STR) Sartorato, E. L., 313-316 Stratton, H., 327-342 SB19.3, 543-557 stuttering, 401—412 Scheil, H.-G., 943-946 Subedi, J., 515-525 Schmidt, H. D., 943-946 Sueyoshi, S., 711-722 Scythian population, 109-125 Sunguroglu, A., 785-788 seasonal diseases, 837-848 surnames, 901-920 seasonal fertility, 837-848 Sweden, 343-359 “Seasonal Variation of Genotype-Specific Fertility and Adaptation to Endemic Dis- TACR 1, 849-862 eases: A Study in Past Malarial Areas of Taglioli, L., 229-251 Italy,” 837-848 TCF7LI1, 849-862 Seixas, S., 277-287 telomerase, 127-146 selective pressure, 361-381 telomere, 127-146 sequence-tagged site (STS), 469-478 telomere attrition, 127-146 Seshadri, M., 743-763 “Telomeres and Telomerase in the Fetal Or- sexual dimorphism, 623-641 igins of Cardiovascular Disease: A Re- Shimizu, K., 765-778 view,” 127-146 Shook, B. A. S., 33-54 Teriokhin, A. T., 623-641 short tandem repeat (STR), 15-31, 109- THO1, 15—31, 229-251, 723-730, 125, 229-251, 277-287, 723-730, 943-946 789-795 Thangaraj, K., 569-590 Siberians, 591-604 Thomas, F., 623-641 “Sicilian Provinces: Population Subdivi- Tofanelli, S. 229-251 sions Revealed by Surname Frequen- Tokimasa, K., 765-778 cies,” 901-920 Touinssi, M., 527-541