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1. Sieberts, SK; Wijsman, EM; Thompson, EA
   Relationship inference from trios of individuals, in the presence of typing error
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   S.K. Sieberts et al., "Relationship inference from trios of individuals, in the presence of typing error", AM J HU GEN, 70(1), 2002, pp. 170-180
2. Chapman, NH; Wijsman, EM
   Introduction: Linkage analyses in the Hutterites
   GENETIC EPIDEMIOLOGY
   
   N.H. Chapman e E.M. Wijsman, "Introduction: Linkage analyses in the Hutterites", GENET EPID, 21, 2001, pp. S222-S223
3. Chapman, NH; Leutenegger, AL; Badzioch, MD; Bogdan, M; Conlon, EM; Daw, EW; Gagnon, F; Li, N; Maia, JM; Wijsman, EM; Thompson, EA
   The importance of connections: Joining components of the Hutterite pedigree
   GENETIC EPIDEMIOLOGY
   
   N.H. Chapman et al., "The importance of connections: Joining components of the Hutterite pedigree", GENET EPID, 21, 2001, pp. S230-S235
4. Wijsman, EM; Almasy, L; Amos, CI; Borecki, IB; Falk, CT; King, TM; Martinez, MM; Meyers, D; Neuman, RJ; Olson, JM; Rich, S; Spence, MA; Thomas, DC; Vieland, VJ; Witte, JS; MacCluer, JW
   Analysis of complex genetic traits: Application to asthma and simulated data - Preface
   GENETIC EPIDEMIOLOGY
   
   E.M. Wijsman et al., "Analysis of complex genetic traits: Application to asthma and simulated data - Preface", GENET EPID, 21, 2001, pp. SXXXVIII-SXXXIX
5. Wijsman, EM; Nur, N
   On estimating the proportion of variance in a phenotypic trait attributable to a measured locus
   HUMAN HEREDITY
   
   E.M. Wijsman e N. Nur, "On estimating the proportion of variance in a phenotypic trait attributable to a measured locus", HUMAN HERED, 51(3), 2001, pp. 145-149
6. Daw, EW; Thompson, EA; Wijsman, EM
   Bias in multipoint linkage analysis arising from map misspecification
   GENETIC EPIDEMIOLOGY
   
   E.W. Daw et al., "Bias in multipoint linkage analysis arising from map misspecification", GENET EPID, 19(4), 2000, pp. 366-380
7. Wijsman, EM; Peterson, D; Leutenegger, AL; Thomson, JB; Goddard, KAB; Hsu, L; Berninger, VW; Raskind, WH
   Segregation analysis of phenotypic components of learning disabilities. I.Nonword memory and digit span
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   E.M. Wijsman et al., "Segregation analysis of phenotypic components of learning disabilities. I.Nonword memory and digit span", AM J HU GEN, 67(3), 2000, pp. 631-646
8. Daw, EW; Payami, H; Nemens, EJ; Nochlin, D; Bird, TD; Schellenberg, GD; Wijsman, EM
   The number of trait loci in late-onset Alzheimer disease
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   E.W. Daw et al., "The number of trait loci in late-onset Alzheimer disease", AM J HU GEN, 66(1), 2000, pp. 196-204
9. Hadley, EC; Rossi, WK; Albert, S; Bailey-Wilson, J; Baron, J; Cawthon, R; Christian, JC; Corder, EH; Franceschi, C; Kestenbaum, B; Kruglyak, L; Lauderdale, DS; Lubitz, J; Martin, GM; McClearn, GE; McGue, M; Miles, T; Mineau, G; Ouellett, G; Pedersen, NL; Preston, SH; Page, WF; Province, M; Schachter, F; Schork, NJ; Vaupel, JW; Vijg, J; Wallace, R; Wang, E; Wijsman, EM
   Genetic epidemiologic studies on age-specified traits
   AMERICAN JOURNAL OF EPIDEMIOLOGY
   
   E.C. Hadley et al., "Genetic epidemiologic studies on age-specified traits", AM J EPIDEM, 152(11), 2000, pp. 1003-1008
10. Raskind, WH; Hsu, L; Berninger, VW; Thomson, JB; Wijsman, EM
    Familial aggregation of dyslexia phenotypes
    BEHAVIOR GENETICS
    
    W.H. Raskind et al., "Familial aggregation of dyslexia phenotypes", BEHAV GENET, 30(5), 2000, pp. 385-396
11. Saavedra-Matiz, CA; Chapman, NH; Wijsman, EM; Horowitz, SH; Rosen, DR
    Linkage of hereditary distal myopathy with desmin accumulation to 2q
    HUMAN HEREDITY
    
    C.A. Saavedra-Matiz et al., "Linkage of hereditary distal myopathy with desmin accumulation to 2q", HUMAN HERED, 50(3), 2000, pp. 166-170
12. Sjoberg, G; Saavedra-Matiz, CA; Rosen, DR; Wijsman, EM; Borg, K; Horowitz, SH; Sejersen, T
    A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filamentformation
    HUMAN MOLECULAR GENETICS
    
    G. Sjoberg et al., "A missense mutation in the desmin rod domain is associated with autosomal dominant distal myopathy, and exerts a dominant negative effect on filamentformation", HUM MOL GEN, 8(12), 1999, pp. 2191-2198
13. Daw, EW; Kumm, J; Snow, GL; Thompson, EA; Wijsman, EM
    Monte Carlo Markov chain methods for genome screening
    GENETIC EPIDEMIOLOGY
    
    E.W. Daw et al., "Monte Carlo Markov chain methods for genome screening", GENET EPID, 17, 1999, pp. S133-S138
14. Goldin, LR; Amos, CI; Chase, GA; Goldstein, AM; Jarvik, GP; Martinez, MM; Suarez, BK; Weeks, DE; Wijsman, EM; MacCluer, JW
    Genetic analysis workshop 11 - Analysis of genetic and environmental factors in common diseases - Preface
    GENETIC EPIDEMIOLOGY
    
    L.R. Goldin et al., "Genetic analysis workshop 11 - Analysis of genetic and environmental factors in common diseases - Preface", GENET EPID, 17, 1999, pp. SXXXI-SXXXII
15. Daw, EW; Heath, SC; Wijsman, EM
    Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    E.W. Daw et al., "Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees", AM J HU GEN, 64(3), 1999, pp. 839-851
16. Hokanson, JE; Brunzell, JD; Jarvik, GP; Wijsman, EM; Austin, MA
    Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    J.E. Hokanson et al., "Linkage of low-density lipoprotein size to the lipoprotein lipase gene in heterozygous lipoprotein lipase deficiency", AM J HU GEN, 64(2), 1999, pp. 608-618
17. WIJSMAN EM; BRUNZELL JD; JARVIK GP; AUSTIN MA; MOTULSKY AG; DEEB SS
    EVIDENCE AGAINST LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO THE APOLIPOPROTEIN AI-CIII-AIV GENE-COMPLEX
    Arteriosclerosis, thrombosis, and vascular biology
    
    E.M. Wijsman et al., "EVIDENCE AGAINST LINKAGE OF FAMILIAL COMBINED HYPERLIPIDEMIA TO THE APOLIPOPROTEIN AI-CIII-AIV GENE-COMPLEX", Arteriosclerosis, thrombosis, and vascular biology, 18(2), 1998, pp. 215-226
18. RASKIND WH; CONRAD EU; MATSUSHITA M; WIJSMAN EM; WELLS DE; CHAPMAN N; SANDELL LJ; WAGNER M; HOUCK J
    EVALUATION OF LOCUS HETEROGENEITY AND EXT1 MUTATIONS IN 34 FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES
    Human mutation
    
    W.H. Raskind et al., "EVALUATION OF LOCUS HETEROGENEITY AND EXT1 MUTATIONS IN 34 FAMILIES WITH HEREDITARY MULTIPLE EXOSTOSES", Human mutation, 11(3), 1998, pp. 231-239
19. SNOW GL; WIJSMAN EM
    PEDIGREE ANALYSIS PACKAGE (PAP) VS. MORGAN - MODEL SELECTION AND HYPOTHESIS-TESTING ON A LARGE PEDIGREE
    Genetic epidemiology
    
    G.L. Snow e E.M. Wijsman, "PEDIGREE ANALYSIS PACKAGE (PAP) VS. MORGAN - MODEL SELECTION AND HYPOTHESIS-TESTING ON A LARGE PEDIGREE", Genetic epidemiology, 15(4), 1998, pp. 355-369
20. LI HZ; THOMPSON EA; WIJSMAN EM
    SEMIPARAMETRIC ESTIMATION OF MAJOR GENE EFFECTS FOR AGE-OF-ONSET
    Genetic epidemiology
    
    H.Z. Li et al., "SEMIPARAMETRIC ESTIMATION OF MAJOR GENE EFFECTS FOR AGE-OF-ONSET", Genetic epidemiology, 15(3), 1998, pp. 279-298
21. Chapman, NH; Wijsman, EM
    Genome screens using linkage disequilibrium tests: Optimal marker characteristics and feasibility
    AMERICAN JOURNAL OF HUMAN GENETICS
    
    N.H. Chapman e E.M. Wijsman, "Genome screens using linkage disequilibrium tests: Optimal marker characteristics and feasibility", AM J HU GEN, 63(6), 1998, pp. 1872-1885
22. WIJSMAN EM
    MONTE-CARLO MARKOV-CHAIN METHODS AND MODEL SELECTION IN GENETIC-ANALYSIS
    Animal biotechnology
    
    E.M. Wijsman, "MONTE-CARLO MARKOV-CHAIN METHODS AND MODEL SELECTION IN GENETIC-ANALYSIS", Animal biotechnology, 8(1), 1997, pp. 129-144
23. EDLAND SD; WIJSMAN EM; SCHODEREHRI GL; LEVERENZ JB
    LITTLE EVIDENCE OF REDUCED SURVIVAL TO ADULTHOOD OF APOE EPSILON-4 HOMOZYGOTES IN DOWNS-SYNDROME
    NeuroReport
    
    S.D. Edland et al., "LITTLE EVIDENCE OF REDUCED SURVIVAL TO ADULTHOOD OF APOE EPSILON-4 HOMOZYGOTES IN DOWNS-SYNDROME", NeuroReport, 8(16), 1997, pp. 3463-3465
24. WIJSMAN EM; AMOS CI
    GENETIC-ANALYSIS OF SIMULATED OLIGOGENIC TRAITS IN NUCLEAR AND EXTENDED PEDIGREES - SUMMARY OF GAW10 CONTRIBUTIONS
    Genetic epidemiology
    
    E.M. Wijsman e C.I. Amos, "GENETIC-ANALYSIS OF SIMULATED OLIGOGENIC TRAITS IN NUCLEAR AND EXTENDED PEDIGREES - SUMMARY OF GAW10 CONTRIBUTIONS", Genetic epidemiology, 14(6), 1997, pp. 719-735
25. GRAHAM J; CHAPMAN NH; GODDARD KAB; GOODE EL; WIJSMAN EM; JARVIK GP
    SEGREGATION AND LINKAGE ANALYSIS OF A QUANTITATIVE VERSUS A QUALITATIVE TRAIT IN LARGE PEDIGREES
    Genetic epidemiology
    
    J. Graham et al., "SEGREGATION AND LINKAGE ANALYSIS OF A QUANTITATIVE VERSUS A QUALITATIVE TRAIT IN LARGE PEDIGREES", Genetic epidemiology, 14(6), 1997, pp. 999-1004
26. HEATH SC; SNOW GL; THOMPSON EA; TSENG C; WIJSMAN EM
    MCMC SEGREGATION AND LINKAGE ANALYSIS
    Genetic epidemiology
    
    S.C. Heath et al., "MCMC SEGREGATION AND LINKAGE ANALYSIS", Genetic epidemiology, 14(6), 1997, pp. 1011-1016
27. BIRD TD; WIJSMAN EM; NOCHLIN D; LEEHEY M; SUMI SM; PAYAMI H; POORKAJ P; NEMENS E; RAFKIND M; SCHELLENBERG GD
    CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD
    Neurology
    
    T.D. Bird et al., "CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD", Neurology, 48(4), 1997, pp. 949-954
28. CHAPMAN NH; WIJSMAN EM
    OPTIMAL MARKER CHARACTERISTICS FOR GENOME SCREENS USING LINKAGE DISEQUILIBRIUM TESTS
    American journal of human genetics
    
    N.H. Chapman e E.M. Wijsman, "OPTIMAL MARKER CHARACTERISTICS FOR GENOME SCREENS USING LINKAGE DISEQUILIBRIUM TESTS", American journal of human genetics, 61(4), 1997, pp. 1576-1576
29. DAW EW; HEATH SC; WIJSMAN EM
    MULTIPOINT OLIGOGENIC ANALYSIS OF AGE-OF-ONSET DATA WITH APPLICATIONSTO LARGE ALZHEIMERS-DISEASE PEDIGREES
    American journal of human genetics
    
    E.W. Daw et al., "MULTIPOINT OLIGOGENIC ANALYSIS OF AGE-OF-ONSET DATA WITH APPLICATIONSTO LARGE ALZHEIMERS-DISEASE PEDIGREES", American journal of human genetics, 61(4), 1997, pp. 1588-1588
30. GODDARD KAB; WIJSMAN EM
    PEDIGREE SELECTION CRITERIA FOR GENOME SCREENING OF COMPLEX-MODELS
    American journal of human genetics
    
    K.A.B. Goddard e E.M. Wijsman, "PEDIGREE SELECTION CRITERIA FOR GENOME SCREENING OF COMPLEX-MODELS", American journal of human genetics, 61(4), 1997, pp. 1613-1613
31. YU CE; OSHIMA J; WIJSMAN EM; NAKURA J; MIKI T; PIUSSAN C; MATTHEWS S; FU YH; MULLIGAN J; MARTIN GM; SCHELLENBERG GD; BURG G; EPSTEIN CJ; FISCHER W; FUJIWARA Y; FUKUCHI KI; HOEHN H; HURLIMANN AF; KISO S; MATTHEWS J; MELARAGNO MI; MURANO S; OUAIS S; POOT M; RIZZO M; SAIDA T; TANNOCK TCA; UYENO B
    MUTATIONS IN THE CONSENSUS HELICASE DOMAINS OF THE WERNER SYNDROME GENE
    American journal of human genetics
    
    C.E. Yu et al., "MUTATIONS IN THE CONSENSUS HELICASE DOMAINS OF THE WERNER SYNDROME GENE", American journal of human genetics, 60(2), 1997, pp. 330-341
32. NAKURA J; MIKI T; YE L; MITSUDA N; ZHAO Y; KIHARA K; YU CE; OSHIMA J; FUKUCHI K; WIJSMAN EM; SCHELLENBERG GD; MARTIN GM; MURANO S; HASHIMOTO K; FUJIWARA Y; OGIHARA T
    NARROWING THE POSITION OF THE WERNER SYNDROME LOCUS BY HOMOZYGOSITY ANALYSIS - EXTENSION OF HOMOZYGOSITY ANALYSIS
    Genomics
    
    J. Nakura et al., "NARROWING THE POSITION OF THE WERNER SYNDROME LOCUS BY HOMOZYGOSITY ANALYSIS - EXTENSION OF HOMOZYGOSITY ANALYSIS", Genomics, 36(1), 1996, pp. 130-141
33. OLSHEN AB; WIJSMAN EM
    PEDIGREE ANALYSIS PACKAGE VS MIXD - FITTING THE MIXED-MODEL ON A LARGE PEDIGREE
    Genetic epidemiology
    
    A.B. Olshen e E.M. Wijsman, "PEDIGREE ANALYSIS PACKAGE VS MIXD - FITTING THE MIXED-MODEL ON A LARGE PEDIGREE", Genetic epidemiology, 13(1), 1996, pp. 91-106
34. YU CE; OSHIMA J; FU YH; WIJSMAN EM; HISAMA F; ALISCH R; MATTHEWS S; NAKURA J; MIKI T; OUAIS S; MARTIN GM; MULLIGAN J; SCHELLENBERG GD
    POSITIONAL CLONING OF THE WARNERS SYNDROME GENE
    Science
    
    C.E. Yu et al., "POSITIONAL CLONING OF THE WARNERS SYNDROME GENE", Science, 272(5259), 1996, pp. 258-262
35. GODDARD KAB; YU CE; OSHIMA J; MIKI T; NAKURA J; PIUSSAN C; MARTIN GM; SCHELLENBERG GD; WIJSMAN EM; BROWN WT; BURG G; CERIMELE D; COTTINI F; EPSTEIN CJ; FISCHER W; FRACCARO M; FUJIWARA Y; FUKUCHI KI; HIWADA K; HOEHN H; HOSOKAWA Y; HURLIMANN AF; ISHAWATA H; KAMINO K; KIHARA K; KISO S; LIN Y; MAEDA T; MATTHEWS J; MATSUMURA T; MCKAY JE; MELARAGNO MI; MITSUDA M; MOTULSKY AG; MURAKAMI T; MURANO S; NIIKAWA N; POOT M; OGIHARA T; RIZZO M; SAIDA T; SCAPPATICCI S; TANNOK TCA; TAMAKI S; UTSU N; UYENO B; WAKAYAMA A; YANAGAWA M; YEVICH II; YOSHIDA S; ZIGRANG W
    TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS
    American journal of human genetics
    
    K.A.B. Goddard et al., "TOWARD LOCALIZATION OF THE WERNER SYNDROME GENE BY LINKAGE DISEQUILIBRIUM AND ANCESTRAL HAPLOTYPING - LESSONS LEARNED FROM ANALYSIS OF 35 CHROMOSOME 8P11.1-21.1 MARKERS", American journal of human genetics, 58(6), 1996, pp. 1286-1302
36. PAYAMI H; ZAREPARSI S; MONTEE KR; SEXTON GJ; KAYE JA; BIRD TD; YU CE; WIJSMAN EM; HESTON LL; LITT M; SCHELLENBERG GD
    GENDER DIFFERENCE IN APOLIPOPROTEIN E-ASSOCIATED RISK FOR FAMILIAL ALZHEIMER-DISEASE - A POSSIBLE CLUE TO THE HIGHER INCIDENCE OF ALZHEIMER-DISEASE IN WOMEN
    American journal of human genetics
    
    H. Payami et al., "GENDER DIFFERENCE IN APOLIPOPROTEIN E-ASSOCIATED RISK FOR FAMILIAL ALZHEIMER-DISEASE - A POSSIBLE CLUE TO THE HIGHER INCIDENCE OF ALZHEIMER-DISEASE IN WOMEN", American journal of human genetics, 58(4), 1996, pp. 803-811
37. JARVIK GP; LARSON EB; GODDARD K; KUKULL WA; SCHELLENBERG GD; WIJSMAN EM
    INFLUENCE OF APOLIPOPROTEIN-E GENOTYPE ON THE TRANSMISSION OF ALZHEIMER-DISEASE IN A COMMUNITY-BASED SAMPLE
    American journal of human genetics
    
    G.P. Jarvik et al., "INFLUENCE OF APOLIPOPROTEIN-E GENOTYPE ON THE TRANSMISSION OF ALZHEIMER-DISEASE IN A COMMUNITY-BASED SAMPLE", American journal of human genetics, 58(1), 1996, pp. 191-200
38. GODDARD KAB; JARVIK GP; GRAHAM J; MCNENEY B; HSU L; SIEGMUND K; GROSSER S; OLSON J; WIJSMAN EM
    ANALYSIS OF QUANTITATIVE RISK-FACTORS FOR A COMMON OLIGOGENIC DISEASE
    Genetic epidemiology
    
    K.A.B. Goddard et al., "ANALYSIS OF QUANTITATIVE RISK-FACTORS FOR A COMMON OLIGOGENIC DISEASE", Genetic epidemiology, 12(6), 1995, pp. 759-764
39. SCHELLENBERG GD; SHARMA V; POORKAJ P; HISAMA F; WIJSMAN EM; WEISSMAN SM; BIRD TD
    THE CHROMOSOME-14 ALZHEIMERS-DISEASE LOCUS
    Journal of cellular biochemistry
    
    G.D. Schellenberg et al., "THE CHROMOSOME-14 ALZHEIMERS-DISEASE LOCUS", Journal of cellular biochemistry, 1995, pp. 86-86
40. LEVYLAHAD E; LAHAD A; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
    APOLIPOPROTEIN-E GENOTYPES AND AGE-OF-ONSET IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE
    Annals of neurology
    
    E. Levylahad et al., "APOLIPOPROTEIN-E GENOTYPES AND AGE-OF-ONSET IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE", Annals of neurology, 38(4), 1995, pp. 678-680
41. KOLLER WC; GLATT SL; HUBBLE JP; PAOLO A; TROSTER AI; HANDLER MS; HORVAT RT; MARTIN C; SCHMIDT K; KARST A; WIJSMAN EM; YU CE; SCHELLENBERG GD
    APOLIPOPROTEIN-E GENOTYPES IN PARKINSON DISEASE WITH AND WITHOUT DEMENTIA
    Annals of neurology
    
    W.C. Koller et al., "APOLIPOPROTEIN-E GENOTYPES IN PARKINSON DISEASE WITH AND WITHOUT DEMENTIA", Annals of neurology, 37(2), 1995, pp. 242-245
42. QUERFURTH HW; WIJSMAN EM; STGEORGEHYSLOP PH; SELKOE DJ
    BETA-APP MESSENGER-RNA TRANSCRIPTION IS INCREASED IN CULTURED FIBROBLASTS FROM THE FAMILIAL ALZHEIMERS DISEASE-1 FAMILY
    Molecular brain research
    
    H.W. Querfurth et al., "BETA-APP MESSENGER-RNA TRANSCRIPTION IS INCREASED IN CULTURED FIBROBLASTS FROM THE FAMILIAL ALZHEIMERS DISEASE-1 FAMILY", Molecular brain research, 28(2), 1995, pp. 319-337
43. PAYAMI H; MONTEE KR; KAYE JA; WIJSMAN EM; BIRD T; YU CE; HESTON LL; SCHELLENBERG GD
    THE APOLIPOPROTEIN-E E4 ALLELE AND SEX-SPECIFIC RISK OF ALZHEIMERS-DISEASE
    JAMA, the journal of the American Medical Association
    
    H. Payami et al., "THE APOLIPOPROTEIN-E E4 ALLELE AND SEX-SPECIFIC RISK OF ALZHEIMERS-DISEASE", JAMA, the journal of the American Medical Association, 273(5), 1995, pp. 374-374
44. LEVYLAHAD E; WIJSMAN EM; NEMENS E; ANDERSON L; GODDARD KAB; WEBER JL; BIRD TD; SCHELLENBERG GD
    A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-1
    Science
    
    E. Levylahad et al., "A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-1", Science, 269(5226), 1995, pp. 970-973
45. LEVYLAHAD E; WASCO W; POORKAJ P; ROMANO DM; OSHIMA J; PETTINGELL WH; YU CE; JONDRO PD; SCHMIDT SD; WANG K; CROWLEY AC; FU YH; GUENETTE SY; GALAS D; NEMENS E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD; TANZI RE
    CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS
    Science
    
    E. Levylahad et al., "CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS", Science, 269(5226), 1995, pp. 973-977
46. JARVIK GP; WIJSMAN EM; KUKULL WA; SCHELLENBERG GD; YU C; LARSON EB
    INTERACTIONS OF APOLIPOPROTEIN-E GENOTYPE, TOTAL CHOLESTEROL LEVEL, AGE, AND SEX IN PREDICTION OF ALZHEIMERS-DISEASE - A CASE-CONTROL STUDY
    Neurology
    
    G.P. Jarvik et al., "INTERACTIONS OF APOLIPOPROTEIN-E GENOTYPE, TOTAL CHOLESTEROL LEVEL, AGE, AND SEX IN PREDICTION OF ALZHEIMERS-DISEASE - A CASE-CONTROL STUDY", Neurology, 45(6), 1995, pp. 1092-1096
47. LEVYLAHAD E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
    ALZHEIMERS-DISEASE IN THE VOLGA GERMANS - PHENOCOPY ANALYSIS IN A COMMON, COMPLEX DISEASE
    American journal of human genetics
    
    E. Levylahad et al., "ALZHEIMERS-DISEASE IN THE VOLGA GERMANS - PHENOCOPY ANALYSIS IN A COMMON, COMPLEX DISEASE", American journal of human genetics, 57(4), 1995, pp. 184-184
48. JARVIK GP; LARSON EB; GODDARD K; SCHELLENBERG GD; WIJSMAN EM
    APOE GENOTYPE INFLUENCE IN ALZHEIMER-DISEASE TRANSMISSION
    American journal of human genetics
    
    G.P. Jarvik et al., "APOE GENOTYPE INFLUENCE IN ALZHEIMER-DISEASE TRANSMISSION", American journal of human genetics, 57(4), 1995, pp. 1406-1406
49. EVANS JP; PALMER S; SCHERER SM; KUKOLICH M; WIJSMAN EM; TSUI LC; STEPHENS K
    HETEROGENEITY OF THE AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION - REPLY
    American journal of human genetics
    
    J.P. Evans et al., "HETEROGENEITY OF THE AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION - REPLY", American journal of human genetics, 56(1), 1995, pp. 342-343
50. JARVIK GP; WIJSMAN EM
    ALZHEIMERS-DISEASE AND THE FAMILY EFFECT
    Nature genetics
    
    G.P. Jarvik e E.M. Wijsman, "ALZHEIMERS-DISEASE AND THE FAMILY EFFECT", Nature genetics, 8(2), 1994, pp. 115-115
51. NAKURA J; WIJSMAN EM; MIKI T; KAMINO K; YU CE; OSHIMA J; FUKUCHI K; WEBER JL; PIUSSAN C; MELARAGNO MI; EPSTEIN CJ; SCAPPATICCI S; FRACCARO M; FUJIWARA Y; MATSUMURA T; MURANO S; YOSHIDA S; SAIDA T; OGIHARA T; MARTIN GM; SCHELLENBERG GD
    HOMOZYGOSITY MAPPING OF THE WERNER SYNDROME LOCUS (WRN)
    Genomics
    
    J. Nakura et al., "HOMOZYGOSITY MAPPING OF THE WERNER SYNDROME LOCUS (WRN)", Genomics, 23(3), 1994, pp. 600-608
52. PALMER SE; DALE DC; LIVINGSTON RJ; WIJSMAN EM; STEPHENS K
    AUTOSOMAL-DOMINANT CYCLIC HEMATOPOIESIS - EXCLUSION OF LINKAGE TO THEMAJOR HEMATOPOIETIC REGULATORY GENE-CLUSTER ON CHROMOSOME-5
    Human genetics
    
    S.E. Palmer et al., "AUTOSOMAL-DOMINANT CYCLIC HEMATOPOIESIS - EXCLUSION OF LINKAGE TO THEMAJOR HEMATOPOIETIC REGULATORY GENE-CLUSTER ON CHROMOSOME-5", Human genetics, 93(2), 1994, pp. 195-197
53. SCHELLENBERG GD; BONNYCASTLE L; YU CE; WIJSMAN EM; BIRD TD
    THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE LOCUS
    Cytogenetics and cell genetics
    
    G.D. Schellenberg et al., "THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE LOCUS", Cytogenetics and cell genetics, 66(1), 1994, pp. 16-16
54. OLSON JM; WIJSMAN EM
    DESIGN AND SAMPLE-SIZE CONSIDERATIONS IN THE DETECTION OF LINKAGE DISEQUILIBRIUM WITH A DISEASE LOCUS
    American journal of human genetics
    
    J.M. Olson e E.M. Wijsman, "DESIGN AND SAMPLE-SIZE CONSIDERATIONS IN THE DETECTION OF LINKAGE DISEQUILIBRIUM WITH A DISEASE LOCUS", American journal of human genetics, 55(3), 1994, pp. 574-580
55. YU CE; OSHIMA J; GODDARD KAB; MIKI T; NAKURA J; OGIHARA T; POOT M; HOEHN H; FRACCARO M; PIUSSAN C; MARTIN GM; SCHELLENBERG GD; WIJSMAN EM
    LINKAGE DISEQUILIBRIUM AND HAPLOTYPE STUDIES OF CHROMOSOME-8P-11.1-21.1 MARKERS AND WERNER-SYNDROME
    American journal of human genetics
    
    C.E. Yu et al., "LINKAGE DISEQUILIBRIUM AND HAPLOTYPE STUDIES OF CHROMOSOME-8P-11.1-21.1 MARKERS AND WERNER-SYNDROME", American journal of human genetics, 55(2), 1994, pp. 356-364
56. PALMER SE; SCHERER SW; KUKOLICH M; WIJSMAN EM; TSUI LC; STEPHENS K; EVANS JP
    EVIDENCE FOR LOCUS HETEROGENEITY IN HUMAN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION
    American journal of human genetics
    
    S.E. Palmer et al., "EVIDENCE FOR LOCUS HETEROGENEITY IN HUMAN AUTOSOMAL-DOMINANT SPLIT HAND SPLIT FOOT MALFORMATION", American journal of human genetics, 55(1), 1994, pp. 21-26
57. YU CE; PAYAMI H; OLSON JM; BOEHNKE M; WIJSMAN EM; ORR HT; KUKULL WA; GODDARD KAB; NEMENS E; WHITE JA; ALONSO ME; TAYLOR TD; BALL MJ; KAYE J; MORRIS J; CHUI H; SADOVNICK AD; MARTIN GM; LARSON EB; HESTON LL; BIRD TD; SCHELLENBERG GD
    THE APOLIPOPROTEIN E CI/CII GENE-CLUSTER AND LATE-ONSET ALZHEIMER-DISEASE/
    American journal of human genetics
    
    C.E. Yu et al., "THE APOLIPOPROTEIN E CI/CII GENE-CLUSTER AND LATE-ONSET ALZHEIMER-DISEASE/", American journal of human genetics, 54(4), 1994, pp. 631-642
58. WIJSMAN EM
    GENETIC-ANALYSIS OF ALZHEIMERS-DISEASE - A SUMMARY OF CONTRIBUTIONS TO GAW8
    Genetic epidemiology
    
    E.M. Wijsman, "GENETIC-ANALYSIS OF ALZHEIMERS-DISEASE - A SUMMARY OF CONTRIBUTIONS TO GAW8", Genetic epidemiology, 10(6), 1993, pp. 349-360
59. WIJSMAN EM; BIRD TD; MARTIN GM; SCHELLENBERG GD
    THE SEATTLE ALZHEIMERS-DISEASE DATA SET
    Genetic epidemiology
    
    E.M. Wijsman et al., "THE SEATTLE ALZHEIMERS-DISEASE DATA SET", Genetic epidemiology, 10(6), 1993, pp. 365-369
60. THOMPSON EA; LIN S; OLSHEN AB; WIJSMAN EM
    MONTE-CARLO ANALYSIS ON A LARGE PEDIGREE
    Genetic epidemiology
    
    E.A. Thompson et al., "MONTE-CARLO ANALYSIS ON A LARGE PEDIGREE", Genetic epidemiology, 10(6), 1993, pp. 677-682
61. OLSON JM; WIJSMAN EM
    LINKAGE BETWEEN QUANTITATIVE TRAIT AND MARKER LOCI - METHODS USING ALL RELATIVE PAIRS
    Genetic epidemiology
    
    J.M. Olson e E.M. Wijsman, "LINKAGE BETWEEN QUANTITATIVE TRAIT AND MARKER LOCI - METHODS USING ALL RELATIVE PAIRS", Genetic epidemiology, 10(2), 1993, pp. 87-102
62. BONNYCASTLE LLC; YU CE; WIJSMAN EM; ORR HT; PATTERSON D; CLANCY KP; GODDARD KAB; ALONSO ME; NEMENS E; WHITE JA; HESTON LL; MARTIN GM; BIRD TD; SCHELLENBERG GD
    THE C-FOS GENE AND EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE
    Neuroscience letters
    
    L.L.C. Bonnycastle et al., "THE C-FOS GENE AND EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE", Neuroscience letters, 160(1), 1993, pp. 33-36
63. NAKURA J; MIKI T; NAGANO K; KIHARA K; YE L; KAMINO K; FUJIWARA Y; YOSHIDA S; MURANO S; FUKUCHI K; WIJSMAN EM; MARTIN GM; SCHELLENBERG GD; OGIHARA T
    CLOSE LINKAGE OF THE GENE FOR WERNER SYNDROME TO ANK1 AND D8S87 ON THE SHORT ARM OF CHROMOSOME-8
    Gerontology
    
    J. Nakura et al., "CLOSE LINKAGE OF THE GENE FOR WERNER SYNDROME TO ANK1 AND D8S87 ON THE SHORT ARM OF CHROMOSOME-8", Gerontology, 39, 1993, pp. 11-15
64. STEPHENS K; SYBERT VP; WIJSMAN EM; EHRLICH P; SPENCER A
    A KERATIN-14 MUTATIONAL HOT-SPOT FOR EPIDERMOLYSIS-BULLOSA SIMPLEX, DOWLING-MEARA - IMPLICATIONS FOR DIAGNOSIS
    Journal of investigative dermatology
    
    K. Stephens et al., "A KERATIN-14 MUTATIONAL HOT-SPOT FOR EPIDERMOLYSIS-BULLOSA SIMPLEX, DOWLING-MEARA - IMPLICATIONS FOR DIAGNOSIS", Journal of investigative dermatology, 101(2), 1993, pp. 240-243
65. SCHELLENBERG GD; WIJSMAN EM; PAYAMI H; BOEHNKE M; OLSON JM; YU C; ORR HT; KUKULL WA; HESTON LL; LARSON EB; BIRD TD
    FAMILIAL ALZHEIMERS-DISEASE AND GENETIC-HETEROGENEITY
    American journal of human genetics
    
    G.D. Schellenberg et al., "FAMILIAL ALZHEIMERS-DISEASE AND GENETIC-HETEROGENEITY", American journal of human genetics, 53(3), 1993, pp. 135-135
66. PALMER SE; DALE DC; LIVINGSTON RJ; WIJSMAN EM; STEPHENS K
    ROLE OF PLEIOTROPIC CYTOKINE SIGNAL TRANSDUCERS IN AUTOSOMAL-DOMINANTCYCLIC HEMATOPOIESIS
    American journal of human genetics
    
    S.E. Palmer et al., "ROLE OF PLEIOTROPIC CYTOKINE SIGNAL TRANSDUCERS IN AUTOSOMAL-DOMINANTCYCLIC HEMATOPOIESIS", American journal of human genetics, 53(3), 1993, pp. 1747-1747
67. SCHELLENBERG GD; PAYAMI H; WIJSMAN EM; ORR HT; GODDARD KAB; ANDERSON L; NEMENS E; WHITE JA; ALONSO ME; BALL MJ; KAYE J; MORRIS JC; CHUI H; SADOVNICK AD; HESTON LL; MARTIN GM; BIRD TD
    CHROMOSOME-14 AND LATE-ONSET FAMILIAL ALZHEIMER-DISEASE (FAD)
    American journal of human genetics
    
    G.D. Schellenberg et al., "CHROMOSOME-14 AND LATE-ONSET FAMILIAL ALZHEIMER-DISEASE (FAD)", American journal of human genetics, 53(3), 1993, pp. 619-628