Published in Am J Hum Genet on September 01, 1999
Genomewide linkage analysis of body mass index across 28 years of the Framingham Heart Study. Am J Hum Genet (2002) 4.07
Family-based tests of association in the presence of linkage. Am J Hum Genet (2000) 3.74
A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet (2001) 3.54
A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q. Am J Hum Genet (2001) 3.26
A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study. Am J Hum Genet (2005) 3.20
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder. Am J Hum Genet (2003) 3.02
Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. Am J Hum Genet (2003) 2.55
Deconstructing schizophrenia: an overview of the use of endophenotypes in order to understand a complex disorder. Schizophr Bull (2006) 2.46
Functional variants within the secreted frizzled-related protein 3 gene are associated with hip osteoarthritis in females. Proc Natl Acad Sci U S A (2004) 2.16
Whole-genome screening in ankylosing spondylitis: evidence of non-MHC genetic-susceptibility loci. Am J Hum Genet (2001) 1.82
Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. J Bone Miner Res (2007) 1.82
Genetics, transcriptomics, and proteomics of Alzheimer's disease. J Clin Psychiatry (2006) 1.81
The genetics of major depression. Neuron (2014) 1.80
Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects. J Med Genet (2005) 1.74
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet (2000) 1.68
A genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans. Am J Hum Genet (2006) 1.59
High-density genome scan in Crohn disease shows confirmed linkage to chromosome 14q11-12. Am J Hum Genet (2000) 1.52
Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in Sweden. Am J Hum Genet (2006) 1.50
Tests for genetic interactions in type 1 diabetes: linkage and stratification analyses of 4,422 affected sib-pairs. Diabetes (2011) 1.44
Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. Am J Hum Genet (2002) 1.44
Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22. Am J Hum Genet (2003) 1.40
Genetic insights into schizophrenia. Can J Psychiatry (2001) 1.38
Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis. PLoS Genet (2009) 1.36
Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q. Am J Hum Genet (2004) 1.32
Evidence for linkage of stature to chromosome 3p26 in a large U.K. Family data set ascertained for type 2 diabetes. Am J Hum Genet (2001) 1.32
A genome scan for renal function among hypertensives: the HyperGEN study. Am J Hum Genet (2000) 1.31
A genomewide search using an original pairwise sampling approach for large genealogies identifies a new locus for total and low-density lipoprotein cholesterol in two genetically differentiated isolates of Sardinia. Am J Hum Genet (2004) 1.24
Genetics and visceral leishmaniasis: of mice and man. Parasite Immunol (2009) 1.21
Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. Am J Hum Genet (2003) 1.19
A genomewide scan for type 1-diabetes susceptibility in Scandinavian families: identification of new loci with evidence of interactions. Am J Hum Genet (2001) 1.19
Replication study supports evidence for linkage to 9p24 in obsessive-compulsive disorder. Am J Hum Genet (2004) 1.13
Genetics of variation in serum uric acid and cardiovascular risk factors in Mexican Americans. J Clin Endocrinol Metab (2008) 1.13
Fine mapping of 10q and 18q for familial Alzheimer's disease in Caribbean Hispanics. Mol Psychiatry (2004) 1.13
Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women. Am J Hum Genet (2004) 1.04
A male-specific quantitative trait locus on 1p21 controlling human stature. J Med Genet (2005) 1.03
Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. Am J Med Genet B Neuropsychiatr Genet (2010) 1.01
A genome-wide linkage scan for bone mineral density in an extended sample: evidence for linkage on 11q23 and Xq27. J Med Genet (2004) 1.00
A comparison of selected quantitative trait loci associated with alcohol use phenotypes in humans and mouse models. Addict Biol (2010) 0.98
Genetic mapping of quantitative trait loci governing longevity of Caenorhabditis elegans in recombinant-inbred progeny of a Bergerac-BO x RC301 interstrain cross. Genetics (2001) 0.97
Genome-wide linkage analysis of population variation in high-density lipoprotein cholesterol. Hum Genet (2006) 0.92
Intracranial aneurysms in Finnish families: confirmation of linkage and refinement of the interval to chromosome 19q13.3. Am J Hum Genet (2004) 0.89
Tuberculin skin test negativity is under tight genetic control of chromosomal region 11p14-15 in settings with different tuberculosis endemicities. J Infect Dis (2014) 0.87
Comprehensive multi-stage linkage analyses identify a locus for adult height on chromosome 3p in a healthy Caucasian population. Hum Genet (2006) 0.85
Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome. J Med Genet (2006) 0.83
Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease. Neurogenetics (2008) 0.83
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases. J Med Genet (2006) 0.83
Identification of a major locus, TNF1, that controls BCG-triggered tumor necrosis factor production by leukocytes in an area hyperendemic for tuberculosis. Clin Infect Dis (2013) 0.83
A novel locus on the X chromosome regulates post-maturity bone density changes in mice. Bone (2006) 0.82
Linkage of atopic dermatitis to chromosomes 4q22, 3p24 and 3q21. Hum Genet (2009) 0.81
Genetic epidemiology. Approaches to the genetic analysis of rheumatoid arthritis. Arthritis Res (2001) 0.80
Functional polymorphisms of the coagulation factor II gene (F2) and susceptibility to systemic lupus erythematosus. J Rheumatol (2011) 0.80
Major Loci on Chromosomes 8q and 3q Control Interferon γ Production Triggered by Bacillus Calmette-Guerin and 6-kDa Early Secretory Antigen Target, Respectively, in Various Populations. J Infect Dis (2015) 0.79
Fine-mapping of candidate region in Amish and Ashkenazi families confirms linkage of refractive error to a QTL on 1p34-p36. Mol Vis (2009) 0.79
Meta-analyses of genome-wide linkage scans of anxiety-related phenotypes. Eur J Hum Genet (2012) 0.78
Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes. J Med Genet (2005) 0.76
A large-scale genome-wide linkage analysis to map loci linked to stature in Chinese population. J Clin Endocrinol Metab (2008) 0.76
Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3. BMC Med Genet (2014) 0.75
The genetics of eating disorders. Psychiatry (Edgmont) (2004) 0.75
Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. PLoS Genet (2016) 0.75
Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet (1995) 49.77
Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet (1995) 12.78
TESTING FOR HETEROGENEITY OF RECOMBINATION FRACTION VALUES IN HUMAN GENETICS. Ann Hum Genet (1963) 6.17
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nat Genet (1995) 5.87
Detecting marker-QTL linkage and estimating QTL gene effect and map location using a saturated genetic map. Genetics (1993) 5.24
Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet (1990) 4.54
Positional cloning moves from perditional to traditional. Nat Genet (1995) 3.37
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22. Nat Genet (1996) 3.00
Adequacy of single-locus approximations for linkage analyses of oligogenic traits. Genet Epidemiol (1992) 2.89
A search for type 1 diabetes susceptibility genes in families from the United Kingdom. Nat Genet (1998) 2.85
Evidence for two psoriasis susceptibility loci (HLA and 17q) and two novel candidate regions (16q and 20p) by genome-wide scan. Hum Mol Genet (1997) 2.48
A simple method to calculate resolving power and confidence interval of QTL map location. Behav Genet (1997) 2.37
An international two-stage genome-wide search for schizophrenia susceptibility genes. Nat Genet (1995) 2.26
Eye tracking dysfunction and schizophrenia: a critical perspective. Schizophr Bull (1993) 2.03
Further evidence for the increased power of LOD scores compared with nonparametric methods. Am J Hum Genet (1999) 1.96
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysis. Nat Genet (1995) 1.90
Linkage analysis under "random" and "genetic" reduced penetrance. Genet Epidemiol (1989) 1.77
Genomewide scan of multiple sclerosis in Finnish multiplex families. Am J Hum Genet (1997) 1.57
Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p. Am J Hum Genet (1997) 1.29
Evidence that a locus for familial psoriasis maps to chromosome 4q. Nat Genet (1996) 1.27
Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease. Am J Med Genet (1996) 1.23
Susceptibility to insulin-dependent diabetes mellitus maps to a locus (IDDM11) on human chromosome 14q24.3-q31. Genomics (1996) 1.10
Linkage analysis of putative schizophrenia gene candidate regions on chromosomes 3p, 5q, 6p, 8p, 20p and 22q in a population-based sampled Finnish family set. Mol Psychiatry (1998) 1.08
Cutting a Gordian knot in the linkage analysis of complex human traits. Am J Hum Genet (1990) 1.04
6p24-22 region and major psychoses in the Eastern Quebec population. Le Groupe IREP. Am J Med Genet (1997) 1.02
Non-parametric analysis of chromosome 6p24-22 marker data and schizophrenia in southern African Bantu-speaking families. Psychiatr Genet (1997) 0.83
Surgical emphysema as a complication of anaesthesia. Br Med J (1955) 0.82
Lifetime and 12-month prevalence of DSM-III-R psychiatric disorders in the United States. Results from the National Comorbidity Survey. Arch Gen Psychiatry (1994) 48.75
Genetic and environmental factors in relative body weight and human adiposity. Behav Genet (1997) 12.07
Analysis of family resemblance. 3. Complex segregation of quantitative traits. Am J Hum Genet (1974) 9.68
Genetic epidemiology of major depression: review and meta-analysis. Am J Psychiatry (2000) 9.02
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nat Genet (1995) 5.87
Childhood adversity and adult psychiatric disorder in the US National Comorbidity Survey. Psychol Med (1997) 5.53
A review and meta-analysis of the genetic epidemiology of anxiety disorders. Am J Psychiatry (2001) 4.55
Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet (1999) 4.54
What is a mental/psychiatric disorder? From DSM-IV to DSM-V. Psychol Med (2010) 4.33
Smoking and major depression. A causal analysis. Arch Gen Psychiatry (1993) 4.15
A population-based twin study in women of smoking initiation and nicotine dependence. Psychol Med (1999) 3.78
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia. Mol Psychiatry (2007) 3.49
Genetic and environmental contributions to alcohol abuse and dependence in a population-based sample of male twins. Am J Psychiatry (1999) 3.38
Illicit psychoactive substance use, heavy use, abuse, and dependence in a US population-based sample of male twins. Arch Gen Psychiatry (2000) 3.33
Stressful life events, genetic liability, and onset of an episode of major depression in women. Am J Psychiatry (1995) 3.22
The genetic epidemiology of smoking. Nicotine Tob Res (1999) 3.21
Multipoint linkage analysis. Am J Hum Genet (1986) 3.12
Model-fitting approaches to the analysis of human behaviour. Heredity (Edinb) (1978) 3.02
The power of the classical twin study to resolve variation in threshold traits. Behav Genet (1994) 2.97
A longitudinal twin study of personality and major depression in women. Arch Gen Psychiatry (1993) 2.97
Age at first drink and risk for alcoholism: a noncausal association. Alcohol Clin Exp Res (1999) 2.71
Major depression and generalized anxiety disorder. Same genes, (partly) different environments? Arch Gen Psychiatry (1992) 2.66
Genetics and developmental psychopathology: 2. The main effects of genes and environment on behavioral problems in the Virginia Twin Study of Adolescent Behavioral Development. J Child Psychol Psychiatry (1997) 2.65
The genetical analysis of covariance structure. Heredity (Edinb) (1977) 2.45
Genetic epidemiology of binging and vomiting. Br J Psychiatry (1998) 2.41
The family history method: whose psychiatric history is measured? Am J Psychiatry (1991) 2.39
Relating body mass index to figural stimuli: population-based normative data for Caucasians. Int J Obes Relat Metab Disord (2001) 2.36
Heritability of binge-eating and broadly defined bulimia nervosa. Biol Psychiatry (1998) 2.34
The structure of the genetic and environmental risk factors for six major psychiatric disorders in women. Phobia, generalized anxiety disorder, panic disorder, bulimia, major depression, and alcoholism. Arch Gen Psychiatry (1995) 2.30
A whole genome association study of neuroticism using DNA pooling. Mol Psychiatry (2007) 2.30
Models for the joint effect of genotype and environment on liability to psychiatric illness. Am J Psychiatry (1986) 2.29
A twin-family study of alcoholism in women. Am J Psychiatry (1994) 2.26
Multivariate multipoint linkage analysis of quantitative trait loci. Behav Genet (1996) 2.24
The power of the classical twin study. Heredity (Edinb) (1978) 2.23
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder. Mol Psychiatry (2010) 2.21
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Mol Psychiatry (2012) 2.20
Joint linkage of multiple loci for a complex disorder. Am J Hum Genet (1993) 2.20
A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. Am J Hum Genet (1999) 2.15
Models of comorbidity for multifactorial disorders. Am J Hum Genet (1995) 2.10
Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. Mol Psychiatry (2009) 2.09
Meta-analysis of 32 genome-wide linkage studies of schizophrenia. Mol Psychiatry (2008) 2.07
Analyzing twin resemblance in multisymptom data: genetic applications of a latent class model for symptoms of conduct disorder in juvenile boys. Behav Genet (1993) 2.07
Depression and parental bonding: cause, consequence, or genetic covariance? Genet Epidemiol (1994) 2.05
A test of the equal-environment assumption in twin studies of psychiatric illness. Behav Genet (1993) 2.03
Neuroticism, major depression and gender: a population-based twin study. Psychol Med (2002) 2.01
The heritability of body mass index among an international sample of monozygotic twins reared apart. Int J Obes Relat Metab Disord (1996) 1.98
The Virginia Twin Study of Adolescent Behavioral Development. Influences of age, sex, and impairment on rates of disorder. Arch Gen Psychiatry (1997) 1.97
Tobacco, alcohol and drug use in eight- to sixteen-year-old twins: the Virginia Twin Study of Adolescent Behavioral Development. J Stud Alcohol (1999) 1.97
A population-based twin study of alcoholism in women. JAMA (1992) 1.97
Latent class analysis of lifetime depressive symptoms in the national comorbidity survey. Am J Psychiatry (1998) 1.95
Genetic and environmental influences on drug use and abuse/dependence in male and female twins. Drug Alcohol Depend (1998) 1.91
Identification of genetically mediated cortical networks: a multivariate study of pediatric twins and siblings. Cereb Cortex (2008) 1.89
The genetics of smoking initiation and quantity smoked in Dutch adolescent and young adult twins. Behav Genet (1999) 1.88
Differential heritability of adult and juvenile antisocial traits. Arch Gen Psychiatry (1995) 1.88
The prediction of major depression in women: toward an integrated etiologic model. Am J Psychiatry (1993) 1.87
Support for a possible schizophrenia vulnerability locus in region 5q22-31 in Irish families. Mol Psychiatry (1997) 1.87
The lifetime history of major depression in women. Reliability of diagnosis and heritability. Arch Gen Psychiatry (1993) 1.87
The resolution of cultural and biological inheritance: informativeness of different relationships. Behav Genet (1985) 1.86
Generalized anxiety disorder in women. A population-based twin study. Arch Gen Psychiatry (1992) 1.85
Endophenotype: a conceptual analysis. Mol Psychiatry (2010) 1.82
Assortative mating for major psychiatric diagnoses in two population-based samples. Psychol Med (1998) 1.80
Susceptibility genes for nicotine dependence: a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further study. Mol Psychiatry (1999) 1.79
Major depressive disorder. Neuron (2000) 1.79
Anorexia nervosa and major depression: shared genetic and environmental risk factors. Am J Psychiatry (2000) 1.78
Serum cholesterol and hemorrhagic stroke in the Honolulu Heart Program. Stroke (1989) 1.76
Symptoms of anxiety and symptoms of depression. Same genes, different environments? Arch Gen Psychiatry (1987) 1.75
Multivariate assessment of factors influencing illicit substance use in twins from female-female pairs. Am J Med Genet (2000) 1.74
The incidence and prognosis of unrecognized myocardial infarction in the Honolulu, Hawaii, Heart Program. Arch Intern Med (1989) 1.74
Sex differences in the sources of genetic liability to alcohol abuse and dependence in a population-based sample of U.S. twins. Alcohol Clin Exp Res (1999) 1.71
Psychiatric 'diseases' versus behavioral disorders and degree of genetic influence. Psychol Med (2010) 1.69
Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. Am J Hum Genet (2000) 1.68
Analysis of family resemblance. V. Height and weight in northeastern Brazil. Am J Hum Genet (1975) 1.67