Genetics of population isolates

Genetic isolates, as shown empirically by the Finnish, Old Order Amish, Hutterites, Sardinian and Jewish communities among others, represent a most important and powerful tool in genetically mapping inherited disorders. The main features associated with that genetic power are the existence of multigenerational pedigrees which are mostly descended from a small number of founders a short number of generations ago, environmental and phenotypic homogeneity, restricted geographical distribution, the presence of exhaustive and detailed records correlating individuals in very well ascertained pedigrees, and inbreeding as a norm. On the other hand, the presence of a multifounder effect or admixture among divergent populations in the founder time (e.g. the Finnish and the Paisa community from Colombia) will theoretically result in increased linkage disequilibrium among adjacent loci. The present review evaluates the historical context and features of some genetic isolates with emphasis on the basic population genetic concepts of inbreeding and genetic drift, and also the state‐of‐the‐art in mapping traits, both Mendelian and complex, on genetic isolates.

[1]  R. Norum,et al.  Blood groups in two Amish demes , 1967, Humangenetik.

[2]  J. Anaya,et al.  TAP, HLA-DQB1, and HLA-DRB1 polymorphism in Colombian patients with primary Sjögren's syndrome. , 2002, Seminars in arthritis and rheumatism.

[3]  J. Builes,et al.  Vitiligo: complex segregation and linkage disequilibrium analyses with respect to microsatellite loci spanning the HLA , 2002, Human Genetics.

[4]  J. Anaya,et al.  Rheumatoid arthritis association in Colombian population is restricted to HLA-DRB1*04 QRRAA alleles , 2002, Genes and Immunity.

[5]  Leena Peltonen,et al.  Identification of a variant associated with adult-type hypolactasia , 2002, Nature Genetics.

[6]  J D Terwilliger,et al.  Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q. , 2001, Human molecular genetics.

[7]  H. Coon,et al.  Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method. , 2001, American journal of human genetics.

[8]  D. Charlesworth,et al.  Breeding systems and genome evolution. , 2001, Current opinion in genetics & development.

[9]  N J Cox,et al.  The importance of genealogy in determining genetic associations with complex traits. , 2001, American journal of human genetics.

[10]  M S McPeek,et al.  The genetic dissection of complex traits in a founder population. , 2001, American journal of human genetics.

[11]  Bo Yuan,et al.  Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3. , 2001, American journal of human genetics.

[12]  A. Malandrini,et al.  Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1. , 2001, American journal of human genetics.

[13]  J. Molina,et al.  Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[14]  M. Rocchi,et al.  Novel X-linked mental retardation syndrome with short stature maps to Xq24. , 2001, American journal of medical genetics.

[15]  Tsviya Olender,et al.  The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy , 2001, Nature Genetics.

[16]  E. Trabetti,et al.  Linkage to atopy on chromosome 19 in north‐eastern Italian families with allergic asthma , 2001, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[17]  J. Carpten,et al.  Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23. , 2001, American journal of human genetics.

[18]  L. Peltonen,et al.  Genetic architecture of temperament. , 2001, The American journal of psychiatry.

[19]  Enrico Petretto,et al.  Archival, demographic and genetic studies define a Sardinian sub-isolate as a suitable model for mapping complex traits , 2001, Human Genetics.

[20]  J S Sinsheimer,et al.  Chromosome 1 loci in Finnish schizophrenia families. , 2001, Human molecular genetics.

[21]  L. Peltonen,et al.  Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups. , 2001, American journal of human genetics.

[22]  T. Beaty,et al.  Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. , 2001, American journal of human genetics.

[23]  R. Lifton,et al.  Mutations in the Na-Cl Cotransporter Reduce Blood Pressure in Humans , 2001, Hypertension.

[24]  E. Petretto,et al.  Identification of a new candidate locus for uric acid nephrolithiasis. , 2001, American journal of human genetics.

[25]  J. Terwilliger,et al.  Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21 , 2001, European Journal of Human Genetics.

[26]  Jurg Ott,et al.  Fine mapping of a gene responsible for regulating dietary cholesterol absorption; founder effects underlie cases of phytosterolaemia in multiple communities , 2001, European Journal of Human Genetics.

[27]  J. Ott,et al.  Identification of a novel common genetic risk factor for lumbar disk disease. , 2001, JAMA.

[28]  L. Peltonen,et al.  Secondary calpain3 deficiency in 2q-linked muscular dystrophy , 2001, Neurology.

[29]  J. Todd,et al.  Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1, -DRB1 disease loci. , 2001, Human molecular genetics.

[30]  A. Bentivoglio,et al.  Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36. , 2001, American journal of human genetics.

[31]  D. Landau,et al.  Clinical and genetic characterization of an autosomal dominant nephropathy. , 2001, American journal of medical genetics.

[32]  N. Freimer,et al.  Genome screening for linkage disequilibrium in a Costa Rican sample of patients with bipolar-I disorder: a follow-up study on chromosome 18. , 2001, American journal of medical genetics.

[33]  M. Wagner,et al.  Genome-wide scan of obesity in the Old Order Amish. , 2001, The Journal of clinical endocrinology and metabolism.

[34]  C Maayan,et al.  Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. , 2001, American journal of human genetics.

[35]  P. Tucker,et al.  Episodic evolution of pyrin in primates: human mutations recapitulate ancestral amino acid states , 2001, Nature Genetics.

[36]  N W Wood,et al.  DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13–36.32 in an Italian family with cranial‐cervical or upper limb onset , 2001, Annals of neurology.

[37]  B. Rubin,et al.  Familial dysautonomia is caused by mutations of the IKAP gene. , 2001, American journal of human genetics.

[38]  S. Lewitzky,et al.  A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population. , 2001, Diabetes.

[39]  Leena Peltonen,et al.  Dissecting Human Disease in the Postgenomic Era , 2001, Science.

[40]  G. Bedoya,et al.  A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia , 2001, Neuroscience Letters.

[41]  F. Lopera,et al.  [Analysis of complex segregation in a large family with hereditary cerebrovascular disease in Antioquia, Colombia]. , 2001, Revista de neurologia.

[42]  A. Chapelle,et al.  Mutations in the RNA Component of RNase MRP Cause a Pleiotropic Human Disease, Cartilage-Hair Hypoplasia , 2001, Cell.

[43]  G. Bertorelle,et al.  Genetics and the population history of Europe. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[44]  V A McKusick,et al.  Genomics and medicine. Dissecting human disease in the postgenomic era. , 2001, Science.

[45]  J. Todd,et al.  Confirmation of the DRB1-DQB1 loci as the major component of IDDM1 in the isolated founder population of Sardinia. , 2000, Human molecular genetics.

[46]  C. Philippe,et al.  A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15. , 2000, American journal of human genetics.

[47]  Kenneth Lange,et al.  Use of population isolates for mapping complex traits , 2000, Nature Reviews Genetics.

[48]  F. Lopera,et al.  [Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia]. , 2000, Revista de neurologia.

[49]  M. McCarthy,et al.  Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest Colombia. , 2000, American journal of human genetics.

[50]  M. Parra,et al.  Autosomal, mtDNA, and Y-chromosome diversity in Amerinds: pre- and post-Columbian patterns of gene flow in South America. , 2000, American journal of human genetics.

[51]  R. Ravazzolo,et al.  Localisation of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11–q13 , 2000, European Journal of Human Genetics.

[52]  A. Tsalenko,et al.  A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. , 2000, American journal of human genetics.

[53]  M. McCarthy,et al.  An association study of bipolar mood disorder (type I) with the 5-HTTLPR serotonin transporter polymorphism in a human population isolate from Colombia , 2000, Neuroscience Letters.

[54]  A A Schäffer,et al.  A novel nemaline myopathy in the Amish caused by a mutation in troponin T1. , 2000, American journal of human genetics.

[55]  T. Shohat,et al.  A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21. , 2000, American journal of human genetics.

[56]  D. Charlesworth,et al.  The effect of hitch-hiking on genes linked to a balanced polymorphism in a subdivided population. , 2000, Genetical research.

[57]  Ralf Krahe,et al.  Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor–vitamin B12 by cubilin , 2000 .

[58]  V. Nimgaonkar,et al.  Low prevalence of psychoses among the Hutterites, an isolated religious community. , 2000, The American journal of psychiatry.

[59]  S. Rosengren,et al.  Gene encoding a new RING-B-box-Coiled-coil protein is mutated in mulibrey nanism , 2000, Nature Genetics.

[60]  M. Wagner,et al.  QTL influencing blood pressure maps to the region of PPH1 on chromosome 2q31-34 in Old Order Amish. , 2000, Circulation.

[61]  G. Bouffard,et al.  Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome , 2000, Nature Genetics.

[62]  M. Wagner,et al.  Diabetes in the Old Order Amish: characterization and heritability analysis of the Amish Family Diabetes Study. , 2000, Diabetes care.

[63]  M. Polymeropoulos,et al.  Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis , 2000, Nature Genetics.

[64]  V. McKusick Ellis-van Creveld syndrome and the Amish , 2000, Nature Genetics.

[65]  G. Barbujani Geographic patterns: how to identify them and why. , 2000, Human biology.

[66]  M. Nordborg Linkage disequilibrium, gene trees and selfing: an ancestral recombination graph with partial self-fertilization. , 2000, Genetics.

[67]  J. Anaya,et al.  [Multiple sclerosis: epidemiological-genetic studies in the population of Antioquia, Colombia. Disequilibrium of HLA DQ alpha]. , 2000, Revista de neurologia.

[68]  A. de la Chapelle,et al.  Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. , 2000, Blood.

[69]  Peter J. van der Spek,et al.  A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases , 1999, Nature Genetics.

[70]  M. Alpers,et al.  Emergence of FY*A(null) in a Plasmodium vivax-endemic region of Papua New Guinea. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[71]  L. Peltonen,et al.  Genome scan for predisposing loci for distal interphalangeal joint osteoarthritis: evidence for a locus on 2q. , 1999, American journal of human genetics.

[72]  L. Peltonen,et al.  Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25. , 1999, American journal of human genetics.

[73]  J. Suvisaari,et al.  A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. , 1999, American journal of human genetics.

[74]  Leena Peltonen,et al.  Positional Cloning of Disease Genes: Advantages of Genetic Isolates , 1999, Human Heredity.

[75]  J. Kere,et al.  Gene Mapping in Isolated Populations: New Roles for Old Friends? , 1999, Human Heredity.

[76]  F. Lopera,et al.  Hallazgos neuropatológicos en la enfermedad de Alzheimer de inicio temprano (mutación E280A-PS1) , 1999 .

[77]  J. Anaya,et al.  Multiple Sclerosis: Association to HLA DQα in a Tropical Population , 1999, Experimental and Clinical Immunogenetics.

[78]  L. Kruglyak Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.

[79]  C. Ober,et al.  Ancestral and recombinant 16-locus HLA haplotypes in the Hutterites , 1999, Immunogenetics.

[80]  J. Sánchez,et al.  [Mode of inheritance of idiopathic generalized non-myoclonic epilepsy in families investigated by studying members with idiopathic epilepsy with tonic-clonic crises on waking. Antioquia, Colombia]. , 1999, Revista de neurologia.

[81]  J. Long,et al.  Autosomal, mitochondrial, and Y chromosome DNA variation in Finland: evidence for a male-specific bottleneck. , 1999, American journal of physical anthropology.

[82]  F. Lopera,et al.  [Discrimination between genetic factors in attention deficit]. , 1999, Revista de neurologia.

[83]  J. Long,et al.  Cladistic association analysis of Y chromosome effects on alcohol dependence and related personality traits. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[84]  S. Priori,et al.  Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome. , 1999, Circulation.

[85]  L Kruglyak,et al.  Genetic isolates: separate but equal? , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[86]  H. Coon,et al.  Genetic epidemiological study of schizophrenia in Palau, Micronesia: prevalence and familiality. , 1999, American journal of medical genetics.

[87]  F. Lopera,et al.  [Neuropathological findings in early-onset Alzheimer's disease (E280a-PS1 mutation)]. , 1999, Revista de neurologia.

[88]  T Varilo,et al.  Molecular genetics of the Finnish disease heritage. , 1999, Human molecular genetics.

[89]  A. Chapelle,et al.  Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping. , 1999, American journal of human genetics.

[90]  L. Peltonen,et al.  Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37. , 1998, American journal of human genetics.

[91]  H. Coon,et al.  Evidence for a chromosome 2p13–14 schizophrenia susceptibility locus in families from Palau, Micronesia , 1998, Molecular Psychiatry.

[92]  L. Peltonen,et al.  Assignment of the locus for congenital lactase deficiency to 2q21, in the vicinity of but separate from the lactase-phlorizin hydrolase gene. , 1998, American journal of human genetics.

[93]  R. Spritz,et al.  Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23. , 1998, American journal of human genetics.

[94]  E. Lander,et al.  Genome-Wide Search for Asthma Susceptibility Loci in a Founder Population , 1998 .

[95]  L. Peltonen,et al.  Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individuals. , 1998, American journal of human genetics.

[96]  C. Greenberg,et al.  A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus. , 1998, American journal of human genetics.

[97]  S. Scherer,et al.  Genetic variation in paraoxonase-1 and paraoxonase-2 is associated with variation in plasma lipoproteins in Alberta Hutterites. , 1998, Atherosclerosis.

[98]  E. Lander,et al.  CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis , 1998, Nature Genetics.

[99]  L. Peltonen,et al.  Dual origins of Finns revealed by Y chromosome haplotype variation. , 1998, American journal of human genetics.

[100]  T. Lehtimäki,et al.  Linkage of familial combined hyperlipidaemia to chromosome 1q21–q23 , 1998, Nature Genetics.

[101]  Cox,et al.  Mapping genes for complex traits in founder populations , 1998, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

[102]  L. Peltonen,et al.  Assignment of the tibial muscular dystrophy locus to chromosome 2q31. , 1998, American journal of human genetics.

[103]  L Peltonen,et al.  Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome. , 1998, Molecular cell.

[104]  L. Peltonen,et al.  Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13. , 1998, American journal of human genetics.

[105]  A. Ruiz-Linares,et al.  [Antiochian genealogies in which idiopathic epilepsy presents familial conglomeration. Simulations of power for the detection of genetic linkage]. , 1998, Revista de neurologia.

[106]  L. Pakarinen,et al.  [Finnish heredity even in hearing disorders?]. , 1998, Duodecim; laaketieteellinen aikakauskirja.

[107]  E. Lander,et al.  Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma. , 1998, Human molecular genetics.

[108]  L. Peltonen Molecular background of the Finnish disease heritage. , 1997, Annals of medicine.

[109]  G. Barbujani DNA variation and language affinities. , 1997, American journal of human genetics.

[110]  C. Greenberg,et al.  Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci. , 1997, American journal of medical genetics.

[111]  B. Lorenz,et al.  Positional cloning of the gene associated with X-linked juvenile retinoschisis , 1997, Nature Genetics.

[112]  L. Peltonen,et al.  Rare disease genes--lessons and challenges. , 1997, Genome research.

[113]  L. Peltonen,et al.  High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 by FISH. , 1997, Genome research.

[114]  A. Ruiz-Linares,et al.  Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation. , 1997, JAMA.

[115]  G Barbujani,et al.  An apportionment of human DNA diversity. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[116]  A. Ruiz-Linares,et al.  Clinical Features of Early-Onset Alzheimer Disease in a Large Kindred With an E280A Presenilin-1 Mutation , 1997 .

[117]  A. Myers,et al.  E280A PS‐1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles , 1997, Human mutation.

[118]  Shinsei Minoshima,et al.  Positional cloning of the APECED gene , 1997, Nature Genetics.

[119]  D. Gerhard,et al.  A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish. , 1996, American journal of human genetics.

[120]  D. Morton,et al.  Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the Amish. , 1996, American journal of human genetics.

[121]  Christer Holmberg,et al.  Mutations of the Down–regulated in adenoma (DRA) gene cause congenital chloride diarrhoea , 1996, Nature Genetics.

[122]  S. Pääbo,et al.  Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[123]  Leena Peltonen,et al.  A putative vulnerability locus to multiple sclerosis maps to 5p14–p12 in a region syntenic to the murine locus Eae2 , 1996, Nature Genetics.

[124]  A S Slutsky,et al.  Asthma on Tristan da Cunha: looking for the genetic link. The University of Toronto Genetics of Asthma Research Group. , 1996, American journal of respiratory and critical care medicine.

[125]  L. Peltonen,et al.  The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA. , 1996, American journal of human genetics.

[126]  N. Freimer,et al.  An approach to investigating linkage for bipolar disorder using large Costa Rican pedigrees. , 1996, American journal of medical genetics.

[127]  Bravo Ml,et al.  Polymorphisms and phyletic relationships of the Paisa community from Antioquia (Colombia). , 1996 .

[128]  J. Weissenbach,et al.  A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish , 1996, Nature Genetics.

[129]  Len A. Pennacchio,et al.  Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1) , 1996, Science.

[130]  Identification of Disease Genes in Genetic Isolates , 1996, Methods.

[131]  R. Hegele,et al.  Genetic and biochemical factors associated with variation in blood pressure in a genetic isolate. , 1996, Hypertension.

[132]  C. Newbold,et al.  High incidence of malaria in alpha-thalassaemic children. , 1996, Nature.

[133]  J. Sánchez,et al.  Idiopathic epilepsy with generalized tonic clonic seizures in Antioquia, Colombia: is the joint Amerindian and Negroid racial admixture the cause of its high prevalence? , 1996, Biological research.

[134]  C. Ober Current topic: HLA and reproduction: lessons from studies in the Hutterites. , 1996, Placenta.

[135]  L. Peltonen,et al.  Messages from an isolate: lessons from the Finnish gene pool. , 1995, Biological chemistry Hoppe-Seyler.

[136]  J. Beckmann,et al.  β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12 , 1995, Nature Genetics.

[137]  C. Ober Current topic: HLA and reproduction: Lessons from studies in the Hutterites , 1995 .

[138]  J. Weissenbach,et al.  Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage. , 1995, American journal of human genetics.

[139]  L. Peltonen,et al.  The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21–q24 , 1995, Nature Genetics.

[140]  A. Chapelle,et al.  Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure , 1995, Cell.

[141]  R. Hegele,et al.  Genetic variation on chromosome 1 associated with variation in body fat distribution in men. , 1995, Circulation.

[142]  L. Peltonen,et al.  Mutations in the palmitoyl protein thioesterase gene causing infantile neuronal ceroid lipofuscinosis , 1995, Nature.

[143]  E. Torrey Prevalence of psychosis among the Hutterites: a reanalysis of the 1950–1953 study , 1995, Schizophrenia Research.

[144]  L. Peltonen,et al.  Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locus. , 1995, American journal of human genetics.

[145]  R. Cann The history and geography of human genes , 1995, The Journal of Asian Studies.

[146]  J. Weissenbach,et al.  Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis. , 1995, Genomics.

[147]  Do Basque- and Caucasian-Speaking Populations Share Non-Indo-European Ancestors? , 1995, European journal of human genetics : EJHG.

[148]  J. Stephens,et al.  Mapping by admixture linkage disequilibrium in human populations: limits and guidelines. , 1994, American journal of human genetics.

[149]  Eric S. Lander,et al.  The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping , 1994, Cell.

[150]  J. Weissenbach,et al.  The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[151]  C. Ober,et al.  Analysis of HLA haplotype segregation in the Schmiedeleut Hutterites of South Dakota. , 1994, Human heredity.

[152]  L. Peltonen,et al.  The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6. , 1994, American journal of human genetics.

[153]  D. Charlesworth Plant Self-Incompatibility: The key to specificity , 1994, Current Biology.

[154]  J. Weissenbach,et al.  Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis , 1994, Nature Genetics.

[155]  L. Excoffier,et al.  New data for AG haplotype frequencies in Caucasoid populations and selective neutrality of the AG polymorphism. , 1994, Human biology.

[156]  A. Chapelle,et al.  Disease gene mapping in isolated human populations: the example of Finland. , 1993, Journal of medical genetics.

[157]  M. Nei,et al.  Evolutionary relationships of human populations on a global scale. , 1993, Molecular biology and evolution.

[158]  A. Piazza,et al.  Human Genomic Diversity in Europe: A Summary of Recent Research and Prospects for the Future , 1993, European journal of human genetics : EJHG.

[159]  K. Narisawa,et al.  Identification of a common mutation in Finnish patients with nonketotic hyperglycinemia. , 1992, The Journal of clinical investigation.

[160]  L. Peltonen,et al.  DNA profiling in a genetically isolated population using three hypervariable DNA markers. , 1992, Human Heredity.

[161]  A. Chapelle,et al.  Aberrant splicing of the CHM gene is a significant cause of choroideremia , 1992, Nature Genetics.

[162]  L. Cavalli-Sforza Genes, peoples and languages. , 1991, Scientific American.

[163]  M. Kimura The neutral theory of molecular evolution: a review of recent evidence. , 1991, Idengaku zasshi.

[164]  A. Aguirre,et al.  Are the Basques a single and a unique population? , 1991, American journal of human genetics.

[165]  K K Kidd,et al.  Drift, admixture, and selection in human evolution: a study with DNA polymorphisms. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[166]  L. Peltonen,et al.  Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease. , 1991, The EMBO journal.

[167]  J. Ghiso,et al.  Mutation in gelsolin gene in Finnish hereditary amyloidosis , 1990, The Journal of experimental medicine.

[168]  M. Feldman,et al.  Spatial subdivision of populations and estimates of genetic variation. , 1990, Theoretical population biology.

[169]  K. Kidd,et al.  Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish , 1989, Nature.

[170]  C. Ober,et al.  Genetic analysis of HLA in the U.S. Schmiedenleut Hutterites. , 1989, American journal of human genetics.

[171]  C. Obie,et al.  At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[172]  K. Weiss,et al.  Admixture as a tool for finding linked genes and detecting that difference from allelic association between loci. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[173]  P. Smouse,et al.  Recombination of haplotypes leads to biased estimates of admixture proportions in human populations. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[174]  M. Ruhlen A Guide to the World’s Languages , 1987 .

[175]  M. Khoury,et al.  Inbreeding and prereproductive mortality in the Old Order Amish. I. Genealogic epidemiology of inbreeding. , 1987, American journal of epidemiology.

[176]  K. Kidd,et al.  Searching for a major genetic locus for affective disorder in the Old Order Amish. , 1987, Journal of psychiatric research.

[177]  B. Weir,et al.  Estimation of inbreeding parameters in stratified populations , 1986, Annals of human genetics.

[178]  L. Cavalli-Sforza,et al.  Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. , 1986, American journal of human genetics.

[179]  J. Hostetler,et al.  History and relevance of the Hutterite population for genetic studies. , 1985, American journal of medical genetics.

[180]  E. Wijsman,et al.  Surnames in Sardinia II. Computation of migration matrices from surname distributions in different periods , 1984, Annals of human genetics.

[181]  W. Hauck,et al.  Shared HLA antigens and reproductive performance among Hutterites. , 1983, American journal of human genetics.

[182]  L L Cavalli-Sforza,et al.  Surnames as neutral alleles: observations in Sardinia. , 1983, Human biology.

[183]  I. Barrai,et al.  [Segregation analysis program for personal computers and microcomputers]. , 1983, Pathologica.

[184]  L. Cavalli-Sforza,et al.  The genetic origin of the Jews: a multivariate approach. , 1979, Human biology.

[185]  C. Valenzuela,et al.  Socioeconomic assortative mating in Santiago, Chile: a demonstration using stochastic matrices of mother-child relationships applied to ABO blood groups. , 1977, Social biology.

[186]  R. Chakraborty,et al.  Estimation of race admixture--a new method. , 1975, American journal of physical anthropology.

[187]  Mckusick Va Genetic studies in American inbred populations with particular reference to the Old Order Amish. , 1973 .

[188]  J. Perheentupa,et al.  Hereditary diseases in Finland; rare flora in rare soul. , 1973, Annals of clinical research.

[189]  Valenzuela Cy Block mating selection model in a random mating population , 1973 .

[190]  V. McKusick Genetic studies in American inbred populations with particular reference to the Old Order Amish. , 1973, Israel journal of medical sciences.

[191]  C. Valenzuela [Block mating selection model in a random mating population]. , 1973, Revista medica de Chile.

[192]  H. Nevanlinna The Finnish population structure. A genetic and genealogical study. , 2009, Hereditas.

[193]  B. Weir,et al.  Group inbreeding with two linked loci. , 1969, Genetics.

[194]  C. Cockerham,et al.  VARIANCE OF GENE FREQUENCIES , 1969, Evolution; international journal of organic evolution.

[195]  M. Kimura Genetic variability maintained in a finite population due to mutational production of neutral and nearly neutral isoalleles. , 1968, Genetical research.

[196]  J. J. Parsons,et al.  Antioqueno Colonization in Western Colombia. , 1950 .

[197]  S WRIGHT,et al.  Genetical Structure of Populations , 1950, British medical journal.

[198]  G. Dahlberg,et al.  Genetics of human populations. , 1948, Advances in genetics.