Published in Behav Genet on September 01, 1983
Linkage strategies for genetically complex traits. I. Multilocus models. Am J Hum Genet (1990) 19.91
Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: a twin and family history study of autism. Am J Hum Genet (1995) 2.94
IQ and schizophrenia in a Swedish national sample: their causal relationship and the interaction of IQ with genetic risk. Am J Psychiatry (2014) 2.05
Narrowing the boundaries of the genetic architecture of schizophrenia. Schizophr Bull (2009) 1.71
Reproductive fitness in familial schizophrenia. Schizophr Res (1996) 1.40
Segregation analysis of schizophrenia and related disorders. Am J Hum Genet (1984) 1.02
A comparison of linkage disequilibrium measures for fine-scale mapping. Genomics (1995) 11.58
Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet (1991) 7.87
Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med (1994) 7.47
A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet (1996) 6.58
Statistical analysis of multilocus recombination. Biometrics (1983) 6.49
An alternative model of recombination and interference. Ann Hum Genet (1979) 6.26
Assessing the role of HLA-linked and unlinked determinants of disease. Am J Hum Genet (1987) 5.47
Statistical evaluation of DNA fingerprinting: a critique of the NRC's report. Science (1993) 4.79
Autosomal dominant inheritance of early-onset breast cancer. Implications for risk prediction. Cancer (1994) 4.37
High-throughput genotyping with single nucleotide polymorphisms. Genome Res (2001) 3.55
Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups. Am J Hum Genet (2001) 3.51
Bayesian analysis of haplotypes for linkage disequilibrium mapping. Genome Res (2001) 3.49
No excess of homozygosity at loci used for DNA fingerprinting. Science (1990) 3.46
Diminished support for linkage between manic depressive illness and X-chromosome markers in three Israeli pedigrees. Nat Genet (1993) 3.40
A full genome search in multiple sclerosis. Nat Genet (1996) 2.96
Disequilibrium mapping: composite likelihood for pairwise disequilibrium. Genomics (1996) 2.90
Segregation analysis incorporating linkage markers. I. Single-locus models with an application to type I diabetes. Am J Hum Genet (1984) 2.74
Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet (1995) 2.72
An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. N Engl J Med (1993) 2.62
Genetic linkage between X-chromosome markers and bipolar affective illness. Nature (1987) 2.44
Spontaneous mutation and parental age in humans. Am J Hum Genet (1987) 2.37
Evaluating genetic association among ovarian, breast, and endometrial cancer: evidence for a breast/ovarian cancer relationship. Am J Hum Genet (1989) 2.37
Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes. Nat Genet (2001) 2.07
Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet Epidemiol (1996) 2.06
The relative power of family-based and case-control designs for linkage disequilibrium studies of complex human diseases. II. Individual genotyping. Genome Res (1999) 2.04
Application of a recombination model in calculating the variance of sib pair genetic identity. Ann Hum Genet (1979) 2.01
Idiopathic dystonia among Ashkenazi Jews: evidence for autosomal dominant inheritance. Ann Neurol (1989) 2.00
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nat Genet (1995) 1.90
Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34. Ann Neurol (1990) 1.89
A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet (1998) 1.87
The A1 allele at the D2 dopamine receptor gene and alcoholism. A reappraisal. JAMA (1993) 1.83
Male homosexuality: absence of linkage to microsatellite markers at Xq28. Science (1999) 1.78
A manic depressive history. Nat Genet (1996) 1.74
X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data. Ann Hum Genet (1982) 1.71
Mode of inheritance of nonsyndromic cleft lip with or without cleft palate: a reanalysis. Am J Hum Genet (1992) 1.66
Association between migraine and stroke in a large-scale epidemiological study of the United States. Arch Neurol (1997) 1.58
No association between an allele at the D2 dopamine receptor gene (DRD2) and alcoholism. JAMA (1991) 1.56
Estimation of morbid risk and age at onset with missing information. Am J Hum Genet (1991) 1.56
Diminished recall and the cohort effect of major depression: a simulation study. Psychol Med (1994) 1.53
Co-morbidity and familial aggregation of alcoholism and anxiety disorders. Psychol Med (1998) 1.52
Human gene for torsion dystonia located on chromosome 9q32-q34. Neuron (1989) 1.51
Lack of evidence for an association between alpha-adducin and blood pressure regulation in Asian populations. Am J Hypertens (2000) 1.51
The calculation of breast cancer risk for women with a first degree family history of ovarian cancer. Breast Cancer Res Treat (1993) 1.50
Relations of genetic and environmental factors in the etiology of epilepsy. Ann Neurol (1996) 1.47
Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews. Am J Hum Genet (1992) 1.46
Risk factors predicting the incidence of second primary breast cancer among women diagnosed with a first primary breast cancer. Am J Epidemiol (1992) 1.42
Autism and the X chromosome. Multipoint sib-pair analysis. Arch Gen Psychiatry (1996) 1.42
The relationship between maternal age and chromosome size in autosomal trisomy. Am J Hum Genet (1986) 1.40
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Nat Genet (1997) 1.39
Estimation of allele frequencies for VNTR loci. Am J Hum Genet (1991) 1.38
Relationship between breast histopathology and family history of breast cancer. Cancer (1993) 1.38
The genetics of infantile hypertrophic pyloric stenosis. A reanalysis. Am J Dis Child (1993) 1.25
Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients. Canadian Collaborative Study Group. Neurology (2000) 1.23
Ethnic differentiation at VNTR loci, with special reference to forensic applications. Am J Hum Genet (1992) 1.23
Clinical indicators of genetic susceptibility to epilepsy. Epilepsia (1996) 1.23
Familial aggregation of absolute pitch. Am J Hum Genet (2000) 1.20
Are generalized and localization-related epilepsies genetically distinct? Arch Neurol (1998) 1.20
Comments on lack of interference in the four strand model of crossing over. J Math Biol (1977) 1.15
Diagnostic criteria for dystonia in DYT1 families. Neurology (2002) 1.12
Estimating morbidity risks with variable age of onset: review of methods and a maximum likelihood approach. Biometrics (1983) 1.10
HLA-DQB1*0602 homozygosity increases relative risk for narcolepsy but not disease severity in two ethnic groups. US Modafinil in Narcolepsy Multicenter Study Group. Tissue Antigens (1998) 1.10
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations. Am J Hum Genet (2000) 1.09
Tay-Sachs screening in the Jewish Ashkenazi population: DNA testing is the preferred procedure. Am J Med Genet (2001) 1.07
Birth cohort and familial risk of epilepsy: the effect of diminished recall in studies of lifetime prevalence. Am J Epidemiol (1995) 1.07
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. Am J Med Genet (1999) 1.06
Minimum incidence of primary cervical dystonia in a multiethnic health care population. Neurology (2007) 1.05
Mapping quantitative-trait loci in humans by use of extreme concordant sib pairs: selected sampling by parental phenotypes. Am J Hum Genet (1996) 1.03
Physical properties of VNTR data, and their impact on a test of allelic independence. Am J Hum Genet (1993) 1.03
A note on Hardy-Weinberg equilibrium of VNTR data by using the Federal Bureau of Investigation's fixed-bin method. Am J Hum Genet (1992) 1.02
Gene loss and gain in the evolution of the vertebrates. Dev Suppl (1994) 1.02
The effects of reduced fertility, method of ascertainment, and a second unlinked locus on affected sib-pair marker allele sharing. Am J Med Genet (1983) 1.02
Segregation analysis of schizophrenia and related disorders. Am J Hum Genet (1984) 1.02
The genetic epidemiology of second primary breast cancer. Am J Epidemiol (1992) 1.01
Genetic analyses of complex behavioral disorders. Proc Natl Acad Sci U S A (1997) 1.01
Assessing the role of X-linked inheritance in bipolar-related major affective disorder. J Psychiatr Res (1986) 0.99
Male sexual orientation and genetic evidence. Science (1993) 0.98
Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis. Am J Hum Genet (2001) 0.97
Response. Science (1991) 0.95
Genetic variation in aldosterone synthase predicts plasma glucose levels. Proc Natl Acad Sci U S A (2001) 0.95
Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. Clin Pharmacol Ther (2015) 0.93
Response:interpretations of multiregional evolution. Science (1996) 0.92
The glycine allele of a glycine/arginine polymorphism in the beta2-adrenergic receptor gene is associated with essential hypertension in a population of Chinese origin. Am J Hypertens (2001) 0.92
Lack of association of the angiotensinogen-6 polymorphism with blood pressure levels in the comprehensive NHLBI Family Blood Pressure Program. National Heart, Lung and Blood Institute. J Hypertens (2000) 0.91
Inheritance of idiopathic torsion dystonia among Ashkenazi Jews. Adv Neurol (1988) 0.91
A multigenerational family with multiple sclerosis. Brain (2002) 0.89
Influence of dietary fat, apolipoprotein E phenotype, and sex on plasma lipoprotein levels. Circulation (1992) 0.89
Corrections to "Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs". Am J Hum Genet (1992) 0.87
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibrium. Genome Res (1997) 0.87
Genetic variation in the human urea transporter-2 is associated with variation in blood pressure. Hum Mol Genet (2001) 0.87
Segregation analysis of cryptogenic epilepsy and an empirical test of the validity of the results. Am J Hum Genet (1997) 0.86
Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+. Neurology (2009) 0.86
Bacteriochlorophyll cs, a new bacteriochlorophyll from Chloroflexus aurantiacus. Arch Microbiol (1978) 0.85
Haemochromatosis, HFE and genetic complexity. Nat Genet (1997) 0.85
Birth order effects on nonverbal IQ scores in autism multiplex families. J Autism Dev Disord (2001) 0.85
Age at onset in bipolar-related major affective illness: clinical and genetic implications. J Psychiatr Res (1983) 0.84
Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nat Genet (1995) 0.84
The spectrum concept of schizophrenia: evidence for a genetic-environmental continuum. J Psychiatr Res (1987) 0.82
NRC report on DNA typing. Science (1993) 0.81
Feasibility of half-sibling designs for detecting a genetic component to a disease. Genet Epidemiol (1994) 0.81