Robert C. Elston

Q: What Schools Are Affiliated With Robert C. Elston

Robert C. Elston is affiliated with the following schools: Duke University, University of Southampton, University of Western Australia, University of Cambridge, University of Leicester, Institute of Cancer Research, University of Melbourne, Louisiana State University, Case Western Reserve University, Cornell University

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Robert C. Elston

Biology

#2274

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#3635

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#1019

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Genetics

#153

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#192

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#91

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Robert C. Elston

Mathematics

#3276

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#4870

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#1225

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Statistics

#148

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#193

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#63

USA Rank

mathematics Degrees

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Why Is Robert C. Elston Influential?

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According to Wikipedia, Robert C. Elston is a British born statistical geneticist and distinguished professor emeritus at Case Western Reserve University. He is one of the eponyms of the Elston–Stewart algorithm and Haseman–Elston regression.

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Robert C. Elston's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic dissection of complex traits. (1994) (1780)
Genetic dissection of complex traits (1996) (1711)
A general model for the genetic analysis of pedigree data. (1971) (1534)
The investigation of linkage between a quantitative trait and a marker locus (1972) (1374)
Natural selection on EPAS1 (HIF2α) associated with low hemoglobin concentration in Tibetan highlanders (2010) (671)
A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence. (2007) (547)
The mathematical theory of quantitative genetics (1982) (522)
A unified model for complex segregation analysis. (1983) (466)
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource (1985) (384)
Oral zinc in macular degeneration. (1988) (352)
Extensions to Pedigree Analysis (1975) (343)
Haseman and Elston revisited (2000) (324)
Skewness in commingled distributions. (1976) (324)
Evidence for mendelian inheritance in the pathogenesis of lung cancer. (1990) (278)
A quantitative-trait analysis of human plasma-dopamine beta-hydroxylase activity: evidence for a major functional polymorphism at the DBH locus. (2001) (277)
Transmission/disequilibrium tests for quantitative traits (2001) (268)
Increased familial risk for lung cancer. (1986) (263)
Linkage and association analysis of angiotensin I-converting enzyme (ACE)-gene polymorphisms with ACE concentration and blood pressure. (2001) (263)
Sibling correlations and segregation analysis of age‐related maculopathy: The beaver dam eye study (1994) (261)
A comparison of sib‐pair linkage tests for disease susceptibility loci (1985) (247)
Lifetime prevalence of uveal melanoma in white patients with oculo(dermal) melanocytosis. (1998) (232)
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis. (2004) (232)
A whole-genome scan for obstructive sleep apnea and obesity. (2003) (221)
The Meaning of Interaction (2010) (218)
Plasma Aldosterone Is Independently Associated With the Metabolic Syndrome (2006) (209)
Familial hyper-alpha-lipoproteinemia: studies in eighteen kindreds. (1975) (194)
An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland (1996) (192)
Dissection of genomewide-scan data in extended families reveals a major locus and oligogenic susceptibility for age-related macular degeneration. (2004) (192)
Ethnic- and gender-specific association of the nicotinic acetylcholine receptor alpha4 subunit gene (CHRNA4) with nicotine dependence. (2005) (188)
Testing for Hardy-Weinberg equilibrium in small samples (1977) (182)
Multiple phenotype modeling in gene-mapping studies of quantitative traits: power advantages. (1998) (171)
Changes in Human Immunodeficiency Virus Type 1 Gag at Positions L449 and P453 Are Linked to I50V Protease Mutants In Vivo and Cause Reduction of Sensitivity to Amprenavir and Improved Viral Fitness In Vitro (2002) (166)
Heritability of the severity of diabetic retinopathy: the FIND-Eye study. (2008) (163)
Optimal two‐stage genotyping in population‐based association studies (2003) (163)
Whole genome scan for obstructive sleep apnea and obesity in African-American families. (2004) (161)
A Weight-Free Index for the Purpose of Ranking or Selection with Respect to Several Traits at a Time (1963) (158)
Genomewide scan for prostate cancer-aggressiveness loci. (2000) (158)
Defining “mutation” and “polymorphism” in the era of personal genomics (2015) (158)
Sampling considerations in the gathering and analysis of pedigree data. (1979) (157)
A genome screen of multiplex sibships with prostate cancer. (2000) (157)
Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). II. Biomarker studies (1985) (157)
Estimation of Time-Response Curves and Their Confidence Bands (1962) (155)
On estimating the heterozygosity and polymorphism information content value. (2000) (152)
Genome-Wide Scans for Diabetic Nephropathy and Albuminuria in Multiethnic Populations (2007) (148)
Odds ratio based multifactor-dimensionality reduction method for detecting gene-gene interactions (2007) (147)
Linkage and association (1998) (143)
Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and reading. (2004) (143)
Testing the association between polymorphic markers and quantitative traits in pedigrees (1987) (143)
The collaborative Lipid Research Clinics family study: Biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins (1985) (143)
The genetic basis of complex traits: rare variants or "common gene, common disease"? (2007) (140)
EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and Humans (2009) (140)
Genetics of the apnea hypopnea index in Caucasians and African Americans: I. Segregation analysis (2002) (139)
Genetics of classic von Willebrand's disease. I. Phenotypic variation within families. (1979) (138)
Lods, wrods, and mods: The interpretation of lod scores calculated under different models (1994) (137)
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND) (2015) (135)
Familiality in Barrett's Esophagus, Adenocarcinoma of the Esophagus, and Adenocarcinoma of the Gastroesophageal Junction (2006) (130)
Genome Scan of M. tuberculosis Infection and Disease in Ugandans (2008) (129)
Detecting rare variants for complex traits using family and unrelated data (2010) (129)
Aerosol bronchodilator delivery methods. Relative impact on pulmonary function and cost of respiratory care. (1989) (127)
A unified association analysis approach for family and unrelated samples correcting for stratification. (2008) (127)
Sudden cardiac death, genes, and arrhythmogenesis: consideration of new population and mechanistic approaches from a National Heart, Lung, and Blood Institute workshop, Part II. (2001) (126)
Multifactorial qualitative traits: genetic analysis and prediction of recurrence risks. (1974) (126)
A subset of familial colorectal neoplasia kindreds linked to chromosome 9q22.2-31.2 (2003) (126)
Study of the genetic transmission of hypercholesterolemia and hypertriglyceridemia in a 195 member kindred (1975) (124)
Linkage Information Content of Polymorphic Genetic Markers (1999) (122)
A whole-genome screen of a quantitative trait of age-related maculopathy in sibships from the Beaver Dam Eye Study. (2003) (121)
Improved power by use of a weighted score test for linkage disequilibrium mapping. (2007) (117)
A more powerful robust sib‐pair test of linkage for quantitative traits (1989) (116)
Power and robustness of sib-pair linkage tests and extension to larger sibships (1982) (115)
Robust methods for the detection of genetic linkage for quantitative data from pedigrees (1989) (114)
Continuous mechanical turning of intensive care unit patients shortens length of stay in some diagnostic-related groups (1989) (112)
Genetic epidemiology of breast cancer and associated cancers in high-risk families. I. Segregation analysis. (1983) (111)
Segregation analysis of bronchial response to methacholine inhalation challenge in families with and without asthma. (1986) (111)
A powerful method of combining measures of association and Hardy–Weinberg disequilibrium for fine‐mapping in case‐control studies (2006) (108)
Efficiency and robustness of pedigree segregation analysis. (1978) (108)
Multilocus linkage tests based on affected relative pairs. (2000) (107)
Specificity of the clinical diagnosis of dementia (1975) (107)
Effect of IL28B genotype on early viral kinetics during interferon-free treatment of patients with chronic hepatitis C. (2012) (106)
Genetic models of reading disability (1980) (106)
Single- and multilocus allelic variants within the GABA(B) receptor subunit 2 (GABAB2) gene are significantly associated with nicotine dependence. (2005) (102)
Adding Further Power to the Haseman and Elston Method for Detecting Linkage in Larger Sibships: Weighting Sums and Differences (2003) (102)
Novel recurrently mutated genes in African American colon cancers (2015) (99)
Electrocardiographic Prediction of Abnormal Genotype in Congenital Long QT Syndrome: Experience in 101 Related Family Members (2001) (99)
The estimation of genetic variance from twin data (1970) (99)
Use of the robust sib-pair method to screen for single-locus, multiple-locus, and pleiotropic effects: application to traits related to hypertension. (1991) (98)
A subroutine package for maximum likelihood estimation (MAXLIK) (1978) (98)
Genome-wide search for sarcoidosis susceptibility genes in African Americans (2005) (98)
A genome-wide scan to identify loci for smoking rate in the Framingham Heart Study population (2003) (97)
The Family Investigation of Nephropathy and Diabetes (FIND): design and methods. (2005) (96)
Two-marker association tests yield new disease associations for coronary artery disease and hypertension (2011) (95)
Higher offspring survival among Tibetan women with high oxygen saturation genotypes residing at 4,000 m. (2004) (93)
Emergence of Resistance to Protease Inhibitor Amprenavir in Human Immunodeficiency Virus Type 1-Infected Patients: Selection of Four Alternative Viral Protease Genotypes and Influence of Viral Susceptibility to Coadministered Reverse Transcriptase Nucleoside Inhibitors (2002) (93)
Pedigree analysis in human genetics. (1987) (92)
Genetic transmission of serum IgE Levels. (1981) (91)
A combinatorial approach to detecting gene-gene and gene-environment interactions in family studies. (2008) (91)
The structure of linkage disequilibrium at the DBH locus strongly influences the magnitude of association between diallelic markers and plasma dopamine beta-hydroxylase activity. (2003) (90)
The prior probability of autosomal linkage (1975) (90)
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction. (2007) (87)
Essentials of biostatistics (1988) (87)
Evidence for a major gene for cortical cataract. (1995) (86)
Ascertainment and age of onset in pedigree analysis. (1973) (85)
General models for segregation analysis. (1975) (85)
Man bites dog? The validity of maximizing lod scores to determine mode of inheritance. (1989) (85)
High Heritability of Ambulatory Blood Pressure in Families of East African Descent (2005) (84)
Choosing an optimal method to combine P‐values (2009) (84)
A test of transmission/disequilibrium for quantitative traits in pedigree data, by multiple regression. (1999) (83)
Log-linear model-based multifactor dimensionality reduction method to detect gene-gene interactions (2007) (82)
Extreme Selection Strategies in Gene Mapping Studies of Oligogenic Quantitative Traits Do Not Always Increase Power (1998) (81)
A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. (1998) (80)
Segregation analysis of physician-diagnosed asthma in Hispanic and non-Hispanic white families. A recessive component? (1996) (80)
Approaches to Gene Mapping in Complex Human Diseases. Edited by Jonathan L. Haines and Margaret A. Pericak Vance. John Wiley and Sons, New York, 1998. p. xxii + 434 pp., $69.95. (1999) (80)
Increased familial risk for non-lung cancer among relatives of lung cancer patients. (1987) (79)
Segregation analysis of non-insulin-dependent diabetes mellitus in Pima Indians: evidence for a major-gene effect. (1995) (78)
Genome scan for loci predisposing to anxiety disorders using a novel multivariate approach: strong evidence for a chromosome 4 risk locus. (2006) (78)
The identification of a conserved binding motif within human papillomavirus type 16 E6 binding peptides, E6AP and E6BP. (1998) (77)
Inhibition of papillomavirus protein function in cervical cancer cells by intrabody targeting. (2006) (77)
Genetic etiology of nuclear cataract: evidence for a major gene. (1993) (77)
Linkage and association analysis of candidate genes for TB and TNFα cytokine expression: evidence for association with IFNGR1, IL-10, and TNF receptor 1 genes (2007) (76)
Haplotype analysis indicates an association between the DOPA decarboxylase (DDC) gene and nicotine dependence. (2005) (74)
Linkage analysis of a complex disease through use of admixed populations. (2004) (74)
Extensions to pedigree analysis I. Likehood calculations for simple and complex pedigrees. (1975) (73)
Allele increasing susceptibility to human breast cancer may be linked to the glutamate-pyruvate transaminase locus. (1980) (73)
Linkage of a gene regulating dopamine-beta-hydroxylase activity and the ABO blood group locus. (1988) (73)
Apolipoprotein E and obstructive sleep apnea: evaluating whether a candidate gene explains a linkage peak (2006) (72)
The E1∧E4 Protein of Human Papillomavirus Type 16 Associates with a Putative RNA Helicase through Sequences in Its C Terminus (2000) (72)
GW433908/ritonavir once daily in antiretroviral therapy-naive HIV-infected patients: absence of protease resistance at 48 weeks (2004) (71)
In Silico Gene Prioritization by Integrating Multiple Data Sources (2011) (71)
A multivariate method for detecting genetic linkage, with application to a pedigree with an adverse lipoprotein phenotype. (1990) (71)
On the correlation between correlations (1975) (70)
Age of onset, age at examination, and other covariates in the analysis of family data (1989) (70)
A genomewide search finds major susceptibility loci for nicotine dependence on chromosome 10 in African Americans. (2006) (69)
Self-reported race and genetic admixture. (2006) (69)
Sudden cardiac death, genes, and arrhythmogenesis : consideration of new population and mechanistic approaches from a national heart, lung, and blood institute workshop, part I. (2001) (69)
Testing drug response in the presence of genetic information: sampling issues for clinical trials. (2000) (68)
Schizophrenia: Evidence for the major gene hypothesis (1970) (68)
The malignancy of dementias (1978) (68)
1046 FIRST-IN-MAN DEMONSTRATION OF POTENT ANTIVIRAL ACTIVITY WITH A NUCLEOSIDE POLYMERASE (R7128) AND PROTEASE (R7227/ITMN-191) INHIBITOR COMBINATION IN HCV: SAFETY, PHARMACOKINETICS, AND VIROLOGIC RESULTS FROM INFORM-1 (2009) (67)
On Fisher's Method of Combining p-Values (1991) (65)
Are Linkage Analysis and the Collection of Family Data Dead? Prospects for Family Studies in the Age of Genome-Wide Association (2007) (65)
Association of vitamin D receptor gene variants, adiposity and colon cancer. (2008) (65)
Methods of linkage analysis--and the assumptions underlying them [see comment]. (1998) (65)
A linkage study of panic disorder. (1987) (64)
Minimizing Resistance Consequences After Virologic Failure on Initial Combination Therapy: A Systematic Overview (2006) (64)
CYP3A5 and ABCB1 Genes Influence Blood Pressure and Response to Treatment, and Their Effect Is Modified by Salt (2007) (64)
Possible linkage relationships between certain blood groups and schizophrenia or other psychoses (1973) (64)
The analysis of quantitative traits for simple genetic models from parental, F 1 and backcross data. (1973) (64)
Using the optimal receiver operating characteristic curve to design a predictive genetic test, exemplified with type 2 diabetes. (2008) (64)
Segregation analysis of hereditary nonpolyposis colorectal cancer (1986) (64)
Biostatistical genetics and genetic epidemiology (2002) (63)
A faster and more general hidden Markov model algorithm for multipoint likelihood calculations. (1997) (63)
A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus. (1982) (63)
Heritability of renal function in hypertensive families of African descent in the Seychelles (Indian Ocean). (2005) (63)
The Elston-Stewart algorithm for continuous genotypes and environmental factors. (1992) (63)
A family with hereditary ataxia (1980) (63)
Ascertainment adjustment: where does it take us? (2000) (62)
Genome-Wide Scan for Estimated Glomerular Filtration Rate in Multi-Ethnic Diabetic Populations (2008) (61)
Familial correlations and heritability of maxillary midline diastema. (2003) (61)
Lung cancer detection and prevention: evidence for an interaction between smoking and genetic predisposition. (1992) (60)
Genetic etiology of gastric carcinoma: I. Chronic atrophic gastritis (1986) (60)
Gene-Gene Interactions Among CHRNA4, CHRNB2, BDNF, and NTRK2 in Nicotine Dependence (2008) (60)
Genetic-based prediction of disease traits: prediction is very difficult, especially about the future† (2014) (60)
Studies on blood and urine glucose in Seminole Indians: indications for segregation of a major gene. (1974) (59)
Ethnic differences in proximal and distal tubular sodium reabsorption are heritable in black and white populations (2009) (58)
Heritability analysis of cytokines as intermediate phenotypes of tuberculosis. (2003) (57)
Interaction of the E6 protein of human papillomavirus with cellular proteins. (1994) (57)
Segregation analysis of smoking-associated malignancies: evidence for Mendelian inheritance. (1994) (57)
Occurrence of branchial rickettsiales‐like infections in two bivalve molluscs, Tapes japonica and Patinopecten yessoensis, with comments on their significance (1986) (57)
The relationship between the sibling recurrence-risk ratio and genotype relative risk. (2000) (57)
Query: estimating "heritability" of a dichotomous trait. (1977) (56)
Complement factor H and hemicentin-1 in age-related macular degeneration and renal phenotypes. (2007) (56)
Genetic determinants of acute hypoxic ventilation: patterns of inheritance in mice. (2000) (55)
Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation (2015) (55)
The probabilistic determination of identity-by-descent sharing for pairs of relatives from pedigrees. (1990) (55)
HLA-DR, DQ genotypes of celiac disease patients and healthy subjects from the West of Ireland. (1996) (54)
Relationship of hassles, uplifts, and life events to psychological well-being of freshman medical students. (1989) (54)
The Hypotheses That Can be Tested When There are Interactions in an Analysis of Variance Model (1964) (53)
Association of CYP3A5 genotypes with blood pressure and renal function in African families (2006) (53)
Statistical modeling and analysis in human genetics. (1978) (53)
A meta-analysis of the association of N-acetyltransferase 2 gene (NAT2) variants with breast cancer. (2007) (52)
DISCUSSION PAPER: LYONIZATION IN HEMOPHILIA: A CAUSE OF ERROR IN DIRECT DETECTION OF HETEROZYGOUS CARRIERS * (1975) (52)
The Collaborative Lipid Research Clinics Program Family Study. IV. Familial associations of plasma lipids and lipoproteins. (1984) (51)
Lung cancer histologic type and family history of cancer (1992) (51)
Genetic linkage analysis of sarcoidosis phenotypes: the sarcoidosis genetic analysis (SAGA) study (2007) (51)
Association of Specific Haplotypes of Neurotrophic Tyrosine Kinase Receptor 2 Gene (NTRK2) with Vulnerability to Nicotine Dependence in African-Americans and European-Americans (2007) (50)
Gene, pathway and network frameworks to identify epistatic interactions of single nucleotide polymorphisms derived from GWAS data (2012) (50)
Statistical validity of the Haseman‐Elston sib‐pair test in small samples (1993) (50)
Genomewide Linkage Scan for Diabetic Renal Failure and Albuminuria: The FIND Study (2011) (49)
A sarcoidosis genetic linkage consortium: the sarcoidosis genetic analysis (SAGA) study. (2005) (49)
1996 William Allan Award Address. Algorithms and inferences: the challenge of multifactorial diseases. (1997) (49)
Inhibition of E6-induced degradation of its cellular substrates by novel blocking peptides. (2004) (49)
Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS) (2011) (49)
Linkage and segregation analyses of apolipoproteins A1 and B, and lipoprotein cholesterol levels in a large pedigree with excess coronary heart disease: The Bogalusa heart study (1987) (49)
The Blau syndrome gene is not a major risk factor for sarcoidosis. (1999) (48)
Linkage analysis of plasma dopamine β-hydroxylase activity in families of patients with schizophrenia (2011) (48)
Genetic epidemiology of coronary heart disease. Past, present, and future. (1984) (48)
Familial uveal melanoma, III. Is the occurrence of familial uveal melanoma coincidental?. (1996) (47)
Confirmation of linkage to and localization of familial colon cancer risk haplotype on chromosome 9q22. (2010) (47)
Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis. (1983) (47)
Two‐stage global search designs for linkage analysis using pairs of affected relatives (1996) (47)
Genome-wide linkage scan for nicotine dependence in European Americans and its converging results with African Americans in the Mid-South Tobacco Family sample (2008) (47)
Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study. (2005) (47)
Potential role of an additive genetic component in the cause of amyotrophic lateral sclerosis and parkinsonism-dementia in the western Pacific. (1993) (46)
Age-of-onset heterogeneity in Huntington disease families. (1983) (45)
Assessment of Familiality, Obesity, and Other Risk Factors for Early Age of Cancer Diagnosis in Adenocarcinomas of the Esophagus and Gastroesophageal Junction (2009) (45)
On the relative sample size required for multiple comparisons. (2000) (45)
Evaluation of tuberculin reactivity in BCG-immunized siblings. (1994) (45)
A Segregation Analysis of Barrett's Esophagus and Associated Adenocarcinomas (2010) (45)
Familial anticardiolipin antibodies and C4 deficiency genotypes that coexist with MHC DQB1 risk factors. (1995) (45)
Regression Models for Linkage: Issues of Traits, Covariates, Heterogeneity, and Interaction (2003) (44)
Prolonged survival as a component of a hereditary breast and nonpolyposis colon cancer. (1981) (44)
Genetic mapping of complex traits. (1999) (44)
An efficient algorithm to compute the posterior genotypic distribution for every member of a pedigree without loops (1993) (44)
Genetic analysis workshop II: Sib pair screening tests for linkage (1984) (43)
Two‐level Haseman‐Elston regression for general pedigree data analysis (2005) (43)
Multifactorial genetic models for quantitative traits in humans. (1979) (43)
A partial least‐square approach for modeling gene‐gene and gene‐environment interactions when multiple markers are genotyped (2009) (42)
Robust asymptotic sampling theory for correlations in pedigrees (2003) (42)
A comparative study to screen dementia and APOE genotypes in an ageing East African population (2010) (42)
Causal analysis of academic performance (1977) (42)
Probabilistic classification of hemophilia A carriers by discriminant analysis. (1976) (42)
Multipoint linkage disequilibrium mapping with particular reference to the African‐American population (1999) (41)
The Seminole Indians of Florida: morphology and serology. (1970) (41)
Generalized modulus power transformations (1988) (41)
The transmission of manic depressive illness--II. Segregation analysis of three sets of family data. (1981) (41)
What is the significance of difference in phenotypic variability across SNP genotypes? (2013) (41)
Analysis pipeline for the epistasis search – statistical versus biological filtering (2014) (41)
Comparison of sarcoidosis phenotypes among affected African-American siblings. (2006) (41)
Improving power in contrasting linkage-disequilibrium patterns between cases and controls. (2007) (41)
Incidence of cytomegalovirus UL97 and UL54 amino acid substitutions detected after 100 or 200 days of valganciclovir prophylaxis. (2012) (41)
Structural equation model-based genome scan for the metabolic syndrome (2003) (40)
Linkage and association to genetic markers. (1995) (40)
Search for biological/genetic markers in a long-term epidemiological and morbid risk study of affective disorders. (1984) (40)
Comparison of microsatellites, single-nucleotide polymorphisms (SNPs) and composite markers derived from SNPs in linkage analysis (2005) (40)
Evidence for a Major Gene Influence on Tumor Necrosis Factor-α Expression in Tuberculosis: Path and Segregation Analysis (2005) (39)
The finite polygenic mixed model: An alternative formulation for the mixed model of inheritance (1994) (39)
Reproducibility of Results obtained with Indicator‐Dilution Technique for Estimating Cardiac Output in Man (1962) (39)
Statistical interaction in human genetics: how should we model it if we are looking for biological interaction? (2011) (39)
Melanocortin-3 receptor gene variants in a Maori kindred with obesity and early onset type 2 diabetes. (2002) (39)
Preventive allergy: genetics of IgE-mediated diseases. (1986) (38)
Familial dyslexia: genetic and medical findings in eleven three-generation families (1993) (38)
Examination of association with candidate genes for diabetic nephropathy in a Mexican American population. (2010) (38)
Family Aggregation of High Density Lipoprotein Cholesterol: Collaborative Lipid Research Clinics Program Family Study (1983) (37)
Identification of susceptibility genes for cancer in a genome-wide scan: results from the colon neoplasia sibling study. (2008) (37)
Discontinuity and quasi‐continuity: Alternative hypotheses of multifactorial inheritance (1970) (37)
Structure-function analysis of the ribosomal frameshifting signal of two human immunodeficiency virus type 1 isolates with increased resistance to viral protease inhibitors. (2007) (37)
Two-stage global search designs for linkage analysis using pairs of affected relatives. (1996) (37)
Mathematical assumptions versus biological reality: myths in affected sib pair linkage analysis. (2005) (37)
Neural tube defects in France: segregation analysis. (1982) (36)
Haseman and Elston revisited: The effects of ascertainment and residual familial correlations on power to detect linkage (2000) (36)
Relatives of probands: models for preliminary genetic analysis (1971) (36)
A review of the 'Statistical Analysis for Genetic Epidemiology' (SAGE) software package (2004) (36)
Identification of a major locus for age-related cortical cataract on chromosome 6p12-q12 in the Beaver Dam Eye Study (2004) (35)
A general transmission probability model for pedigree data. (1981) (35)
Familial risk of cancer among randomly selected cancer probands (1988) (35)
Genetic analysis of von Willebrand's disease in two large pedigrees: a multivariate approach. (1980) (35)
Linkage of multilocus components of variance to polymorphic markers (1997) (34)
Evidence for a possible major gene effect in absolute finger ridge count. (1973) (34)
'Twixt cup and lip: how intractable is the ascertainment problem? (1995) (34)
Heritability and intrafamilial aggregation of arterial characteristics (2007) (34)
A multivariate logistic model (MLM) for analyzing binary family data. (1998) (33)
Extensions to sib‐pair linkage tests applicable to disorders characterized by delayed onset (1990) (33)
Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees. (1989) (33)
Effect of cohort differences in smoking prevalence on models of lung cancer susceptibility (1992) (33)
Tuberculin reactivity after newborn BCG immunization in mono- and dizygotic twins. (1994) (32)
A genetic study of schizophrenia pedigrees. II. One-locus hypotheses. (1978) (32)
STATISTICAL GENETICS ’98 Methods of Linkage Analysis—and the Assumptions Underlying Them (1998) (32)
The genetics of sound induced seizure in inbred mice. (1966) (32)
The study of candidate genes in drug trials: sample size considerations. (1999) (32)
The Collaborative Lipid Research Clinics Program Family Study. III. Transformations and covariate adjustments of lipid and lipoprotein levels. (1984) (32)
Biometrical genetics with one or two loci: the inheritance of physiological characters in mice. (1973) (31)
The genetic analysis of quantitative trait differences between two homozygous lines. (1984) (31)
Age trends in human chiasma frequencies and recombination fractions. II. Method for analyzing recombination fractions and applications to the ABO:nail-patella linkage. (1976) (31)
Genetic characterization and fine mapping of susceptibility loci for sarcoidosis in African Americans on chromosome 5 (2006) (31)
Multistage sampling for genetic studies. (2007) (30)
The genetic dissection of multifactorial traits (1995) (30)
Reduction of sample heterogeneity through use of population substructure: an example from a population of African American families with sarcoidosis. (2006) (30)
Segregation and Linkage Analyses of Dopamine-β-Hydroxylase Activity (1979) (30)
A cautionary note on the use of Mendelian randomization to infer causation in observational epidemiology. (2008) (30)
Long-term (120-Week) antiviral efficacy and tolerability of fosamprenavir/ritonavir once daily in therapy-naive patients with HIV-1 infection: an uncontrolled, open-label, single-arm follow-on study. (2006) (30)
Detecting genetic interactions for quantitative traits with U‐statistics (2011) (29)
A Randomized, Double‐Blind, Placebo‐Controlled, First‐Time‐in‐Human Study to Assess the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of GSK3389404 in Healthy Subjects (2019) (29)
Advances in statistical human genetics over the last 25 years (2006) (29)
Association between polymorphic blood markers and risk factors for cardiovascular disease in a large pedigree (1987) (29)
Genealogical and Genetic Structure. (1982) (29)
The phenotypic range of hemophilia A carriers. (1976) (29)
On the probability that a twin pair is monozygotic. (1969) (28)
Age trends in human chiasma frequencies and recombination fractions. I. Chiasma frequencies. (1975) (28)
Introduction and overview (2000) (28)
Bivariate analyses of cholesterol and triglyceride levels in families in which probands have type IIb lipoprotein phenotype. (1975) (28)
Restrictions on components of variance for epistatic models. (1998) (28)
Identification of gene‐gene interactions in the presence of missing data using the multifactor dimensionality reduction method (2009) (28)
Genetic studies in multiple myeloma 1. Association with HLA‐Cw5 (1983) (28)
Possible linkage between alcoholism and esterase-D. (1988) (27)
Genetic contributions to quantitative lipoprotein traits associated with coronary artery disease: analysis of a large pedigree from the Bogalusa Heart Study. (1993) (27)
The Pelvis and Beyond: Musculoskeletal Tender Points in Women With Chronic Pelvic Pain (2016) (27)
An approximation to the likelihood for a pedigree with loops (1996) (27)
Genetics of classic von Willebrand's disease. II. Optimal assignment of the heterozygous genotype (diagnosis) by discriminant analysis (1979) (27)
Mapping susceptibility loci for alcohol consumption using number of grams of alcohol consumed per day as a phenotype measure (2003) (26)
Genetic determinants of diabetic nephropathy: The family investigation of nephropathy and diabetes (FIND). (2003) (26)
Methodological issues in linkage analyses for psychiatric disorders: secular trends, assortative mating, bilineal pedigrees. Report of the MacArthur Foundation Network I Task Force on Methodological Issues. (1993) (26)
Haplotype-based quantitative trait mapping using a clustering algorithm (2006) (26)
An algorithm to approximate the likelihood for pedigree data with loops by cutting (1995) (26)
Linkage analysis of pure depressive disease. (1989) (26)
Adaptive Two-Stage Analysis of Genetic Association in Case-Control Designs (2007) (25)
In Vitro Development of Resistance to Human Immunodeficiency Virus Protease Inhibitor GW640385 (2006) (25)
A Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family Investigation of Nephropathy and Diabetes (FIND) (2013) (25)
Variation in Age at Cancer Diagnosis in Familial versus Nonfamilial Barrett's Esophagus (2011) (25)
Mathematical population genetics, Biomathematics. (1981) (25)
Deriving components of genetic variance for multilocus models (1997) (25)
A variance component based multi-marker association test using family and unrelated data (2013) (25)
Segregation analysis of congenital glaucoma: approach by two differential models. (1981) (25)
Working with schizophrenia: Experts' views on barriers and pathways to employment and job retention (2014) (25)
Genome-wide analyses demonstrate novel loci that predispose to drusen formation. (2005) (24)
Abnormal estrogen conjugation in women at risk for familial breast cancer at the periovulatory stage of the menstrual cycle. (1983) (24)
The transmission of manic depressive illness--I. Theory, description of the model and summary of results. (1981) (24)
An approach to the multivariate analysis of high‐density‐lipoprotein cholesterol in a large kindred: The Bogalusa Heart Study (1986) (24)
Phenotypic evaluation of previously uncharacterized cytomegalovirus DNA polymerase sequence variants detected in a valganciclovir treatment trial. (2014) (24)
Major gene model for the inheritance of catechol-O-methyltransferase activity in five large families. (1984) (24)
Models for Discrimination Between Alternative Modes of Inheritance (1990) (23)
INFLUENCE OF BREAST MILK, SOY OR TWO HYDROLYZED FORMULAS ON THE DEVELOPMENT OF ALLERGIC MANIFESTATIONS IN INFANTS AT RISK (1998) (23)
Genetic terminology. (2012) (23)
Recombinant Phenotyping of Cytomegalovirus Sequence Variants Detected After 200 or 100 Days of Valganciclovir Prophylaxis (2010) (23)
Fieller's theorem and linkage disequilibrium mapping (1999) (23)
Probability and paternity testing. (1986) (23)
Evaluation of removable statistical interaction for binary traits (2013) (23)
Fine Mapping Functional Sites or Regions from Case‐Control Data Using Haplotypes of Multiple Linked SNPs (2005) (23)
Segregation analysis. (1981) (23)
Infrequent detection of germline allele-specific expression of TGFBR1 in lymphoblasts and tissues of colon cancer patients. (2009) (23)
Testing for colon neoplasia susceptibility variants at the human COX2 locus. (2001) (23)
ONETOOL for the analysis of family-based big data (2018) (23)
On Additivity in the Analysis of Variance (1961) (23)
A Modified Revisited Haseman-Elston Method to Further Improve Power (2004) (22)
Cardiovascular risk factors from birth to 7 years of age: the Bogalusa Heart Study. Predictive value of parental measures in determining cardiovascular risk factor variables in early life. (1987) (22)
Probable linkage between essential familial hypercholesterolemia and third complement component (C3). (1976) (22)
A locus for generalized tonic‐clonic seizure susceptibility maps to chromosome 10q25‐q26 (2005) (22)
Resistance to the HIV Protease Inhibitor Amprenavir In Vitro and in Clinical Studies (2000) (22)
ABO associations with blood pressure, serum lipids and lipoproteins, and anthropometric measures. (1985) (22)
Single‐marker and two‐marker association tests for unphased case‐control genotype data, with a power comparison (2009) (22)
The Distribution of Long Range Admixture Linkage Disequilibrium in an African-American Population (2002) (22)
Segregation and linkage analysis. (2009) (22)
Association of ABCB1 genetic variants with renal function in Africans and in Caucasians (2008) (21)
Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHIT. (2005) (21)
Stepwise oligogenic segregation and linkage analysis illustrated with dopamine-beta-hydroxylase activity. (1990) (21)
Estimating haplotype frequencies in pooled DNA samples when there is genotyping error (2005) (21)
Genetic contributions to morphological and behavioral similarities among sibs and dizygotic twins: linkages and allelic differences. (1972) (21)
Genomic regions associated with susceptibility to Barrett’s esophagus and esophageal adenocarcinoma in African Americans: The cross BETRNet admixture study (2017) (21)
Two‐stage global search designs for linkage analysis I: Use of the mean statistic for affected sib pairs (2000) (21)
Genetic analysis workshop III: Sib pair analyses to determine linkage groups and to order loci (1985) (20)
A Genetic Study of Schizophrenia Pedigrees (1976) (20)
Variations in levels of blood clotting factors IX and X in a population of normal men: possible genetic polymorphisms. (1972) (20)
Genome-wide linkage scan for genes affecting longitudinal trends in systolic blood pressure (2003) (20)
Genetics of classic von Willebrand's disease. II. Optimal assignment of the heterozygous genotype (diagnosis) by discriminant analysis. (1979) (20)
Paternal age effect on age of onset in bipolar I disorder is mediated by sex and family history (2012) (20)
The analysis of quantitative inheritance simultaneously with twin and family data. (1968) (20)
The Seminole Indians of Oklahoma: morphology and serology. (1970) (20)
A Genetic Study of Schizophrenia Pedigrees (1976) (20)
Two‐stage global search designs for linkage analysis II: Including discordant relative pairs in the study (2000) (19)
Familial aggregation of allergen‐specific sensitization and asthma (2012) (19)
Evidence for possible linkage between genetic markers and affective disorders (1988) (19)
Pedigree discriminant analysis: a method to identify monogenic segregation. (1983) (19)
Statistical human genetics : methods and protocols (2012) (19)
A linkage study of depression spectrum disease: the use of the sib-pair method. (1976) (19)
Nonparametric disequilibrium mapping of functional sites using haplotypes of multiple tightly linked single-nucleotide polymorphism markers. (2003) (18)
Association Between Germline Mutation in VSIG10L and Familial Barrett Neoplasia. (2016) (18)
Segregation and linkage analyses of dopamine-beta-hydroxylase activity in a six-generation pedigree. (1987) (18)
A Likelihood Ratio‐Based Mann‐Whitney Approach Finds Novel Replicable Joint Gene Action for Type 2 Diabetes (2012) (18)
A Variable Age of Onset Segregation Model for Linkage Analysis, with Correction for Ascertainment, Applied to Glioma (2012) (18)
Effects of Misspecification of Allele Frequencies on the Type I Error Rate of Model-Free Linkage Analysis (1999) (18)
Familial analysis of qualitative traits under multifactorial inheritance (1985) (18)
Evidence for a dominant gene mechanism underlying coeliac disease in the West of Ireland (1991) (18)
Genetic Variation in 15-Hydroxyprostaglandin Dehydrogenase and Colon Cancer Susceptibility (2013) (18)
Association within twin pairs for a dichotomous trait (1996) (18)
Consortium approach to identifying genes for Barrett's esophagus and esophageal adenocarcinoma. (2007) (18)
Sampling Correction in Pedigree Analysis (2003) (17)
Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer (2014) (17)
Linkage analysis with an alternative formulation for the mixed model of inheritance: the finite polygenic mixed model. (1995) (17)
The Association of the Vanin-1 N131S Variant with Blood Pressure Is Mediated by Endoplasmic Reticulum-Associated Degradation and Loss of Function (2014) (17)
False discoveries in genome scanning (1997) (17)
Genetic markers of IgG influence the outcome of infection with hepatitis C virus. (2008) (17)
Commingling analysis of age-of-onset in bipolar I disorder and the morbid risk for major psychoses in first degree relatives of bipolar I probands. (2014) (17)
Meta-analysis for linkage to asthma and atopy in the chromosome 5q31-33 candidate region. (2001) (17)
Linkage studies of Usher syndrome: analysis of an Acadian kindred in Louisiana. (1988) (17)
Increase in power of transmission‐disequilibrium tests for quantitative traits (2002) (17)
Immunoglobulin allotypes influence IgG antibody responses to hepatitis C virus envelope proteins E1 and E2. (2008) (17)
Cellular genes in the mouse regulate in trans the expression of endogenous mouse mammary tumor viruses. (1985) (17)
Linkage analysis of depression spectrum disease (1989) (17)
Autonomic testing of women with interstitial cystitis/bladder pain syndrome (2014) (16)
Tapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case–control study (2005) (16)
An approach to the problem of whether clustering of functionally related genes occurs in higher organisms (1967) (16)
The power of independent types of genetic information to detect association in a case‐control study design (2008) (16)
Overview of model-free methods for linkage analysis. (2001) (16)
Path analysis under generalized marital resemblance: Evaluation of the assumptions underlying the mixed homogamy model by the Monte Carlo method (1989) (16)
A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI (2010) (16)
Evidence for a major gene effect in early-onset lung cancer. (1993) (16)
Interferon‐free regimens containing setrobuvir for patients with genotype 1 chronic hepatitis C: a randomized, multicenter study (2016) (15)
Alternative test for linkage between two loci (1997) (15)
Linkage Analysis of Alpha 1-Antitrypsin Deficiency: Lessons for Complex Diseases (2001) (15)
Linkage relationships between a major gene for catechol-o-methyltransferase activity and 25 polymorphic marker systems. (1984) (15)
Basic Biostatistics for Geneticists and Epidemiologists: A Practical Approach (2008) (15)
Functional Genomics of Lung Disease (2004) (15)
Capability of common SNPs to tag rare variants (2011) (15)
Segregation and linkage analysis of a large kindred of unipolar depression. (1981) (15)
Blood bank inventories. (1970) (15)
Confidence bands for the growth of head circumference in achondroplastic children during the first year of life. (1980) (15)
Hybridization modeling of oligonucleotide SNP arrays for accurate DNA copy number estimation (2009) (15)
Ascertainment: An Overwiew of the Classical Segregation Analysis Model for Independent Sibships (1991) (15)
Gene-Gene Interaction in Maternal and Perinatal Research (2010) (15)
The effect of multiple genetic variants in predicting the risk of type 2 diabetes (2009) (14)
Using the Optimal Robust Receiver Operating Characteristic (ROC) Curve for Predictive Genetic Tests (2010) (14)
Some Recent Developments in the Theoretical Aspects of Segregation Analysis (1993) (14)
A Framework for Structural Equation Models in General Pedigrees (2011) (14)
Mulitpoint admixture mapping (2000) (14)
203. Note: On Estimating Time-Response Curves (1964) (14)
A Non-Parametric Method for Building Predictive Genetic Tests on High-Dimensional Data (2011) (14)
Autosomal linkage scan for loci predisposing to comorbid dependence on multiple substances (2012) (14)
Polymorphism Information Content (2005) (14)
The Approximate Variance of a Function of Random Variables (1999) (14)
A bivariate problem in human genetics: ascertainment of families through a correlated trait. (1984) (14)
Sampling considerations in the design and analysis of family studies. (1984) (14)
Possible Linkage between α-Haptoglobin (Hp) and Depression Spectrum Disease (1979) (13)
Statistical Human Genetics (2012) (13)
Evidence of a major gene effect for angiotensinogen among Nigerians (1999) (13)
An LRP 8 Variant Is Associated with Familial and Premature Coronary Artery Disease and Myocardial Infarction (2007) (13)
Possible Linkage between α-Haptoglobin (Hp) and Depression Spectrum Disease (1979) (13)
Lack of association of genetic traits with alcoholism; C3, Ss and ABO systems. (1976) (13)
Linkage of chromosome 1 markers to alcoholism‐related phenotypes by sib pair linkage analysis of principal components (1999) (13)
On the Estimation of Heritability with Family-Based and Population-Based Samples (2015) (13)
Familial analysis of bipolar affective disorder using logistic models (1989) (13)
Evidence of genetic variation for alpha-N-acetyl-D-glucosaminidase in black and white populations: a new polymorphism. (1980) (13)
Heritability Estimation for Speech-Sound Traits with Developmental Trajectories (2011) (13)
Clinical, genetic, and biostatistical progress in the cancer family syndrome. (1979) (13)
Linkage studies of catechol-O-methyltransferase (COMT) and dopamine-beta-hydroxylase (DBH) cDNA expression levels (2007) (13)
Major locus analysis for quantitative traits. (1979) (13)
A linkage study of pure depressive disease: the use of the sib-pair method. (1976) (13)
Distribution and magnitude of type I error of model‐based multipoint lod scores: implications for multipoint mod scores (2006) (13)
The Current Status of Genetic Linkage Studies of Alcoholism and Unipolar Depression (1991) (12)
An examination of fundamental assumptions of the twin method. (1978) (12)
Is TGFBR1*6A a Susceptibility Allele for Nonsyndromic Familial Colorectal Neoplasia? (2007) (12)
A lyophilized human reference plasma for coagulation factors. Evidence for stability of factors I, II, V, and VII through XII. (1982) (12)
Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: The Bogalusa Heart Study (1986) (12)
The Collaborative Lipid Research Clinics Program Family Study. II. Response rates, representativeness of the sample, and stability of lipid and lipoprotein levels. (1984) (12)
Locating the Genes Underlying a Simulated Complex Disease by Discriminant Analysis (2001) (12)
Confidence limits based on the first occurrence of an event. (1993) (12)
New multivariate test for linkage, with application to pleiotropy: Fuzzy Haseman‐Elston (2003) (12)
A Generalized Genetic Random Field Method for the Genetic Association Analysis of Sequencing Data (2014) (12)
Statistical study of genotype assignment (carrier detection) in hemophilia B. (1979) (12)
Interstitial Cystitis – Elucidation of Psychophysiologic and Autonomic Characteristics (the ICEPAC Study): design and methods (2014) (12)
Power of Single‐ vs. Multi‐Marker Tests of Association (2012) (12)
Genetic analysis of serum lipid levels and blood pressure in a large kindred. (1987) (12)
Genetic association tests: a method for the joint analysis of family and case-control data (2009) (12)
Model‐free sib‐pair linkage analysis: Combining full‐sib and half‐sib pairs (2000) (11)
Pooling Data and Linkage Analysis in the Chromosome 5q Candidate Region for Asthma (2001) (11)
749 EARLY ON-TREATMENT RESPONSES DURING PEGYLATED IFN PLUS RIBAVIRIN ARE INCREASED FOLLOWING 13 DAYS OF COMBINATION NUCLEOSIDE POLYMERASE (RG7128) AND PROTEASE (RG7227) INHIBITOR THERAPY (INFORM-1) (2010) (11)
1323 THE EFFECT OF HOST IL28B GENOTYPE ON EARLY VIRAL KINETICS DURING INTERFERON-FREE TREATMENT IN PATIENTS WITH CHRONIC HEPATITIS C (CHC) (2011) (11)
The affected-/discordant-sib-pair design can guarantee validity of multipoint model-free linkage analysis of incomplete pedigrees when there is marker-marker disequilibrium. (2006) (11)
Computational aspects of fittlng a mixture of two normal distributions using maximum likelihood (1992) (11)
A Tournament of Linkage Tests in Complex Inheritance (2001) (11)
Polymorphism in the 5'-flanking region of the insulin gene and its potential relation to cardiovascular disease risk: observations in a biracial community. The Bogalusa Heart Study. (1989) (11)
A weighted U statistic for association analyses considering genetic heterogeneity (2015) (11)
One-stage versus two-stage strategies for genome scans. (2001) (10)
Predicting Barrett's Esophagus in Families: An Esophagus Translational Research Network (BETRNet) Model Fitting Clinical Data to a Familial Paradigm (2016) (10)
Segregation analyses of asthma and respiratory allergy: the Humboldt family study. (2001) (10)
Erratum: Sibling correlations and segregation analysis of age-related maculopathy: The beaver dam eye study (Genetic Epidemiology (1994) 11 (51- 67)) (1994) (10)
Regression toward the mean in 2 x 2 crossover designs with baseline measurements. (1992) (10)
Genetic etiology of gastric carcinoma: II. Segregation analysis of gastric pH, nitrate, and nitrite (1987) (10)
Segregation and linkage analyses of a large pedigree with hypertriglyceridemia. (1977) (10)
Possible linkage between Group‐Specific Component (Gc protein) and pure depressive disease (1977) (10)
Major gene segregation of actinic prurigo among North American Indians in Saskatchewan. (2000) (10)
Familial lung cancer--correcting an error in calculation. (1986) (10)
Sex ratio in relatives of patients with affective disorder. (1973) (9)
Model‐free age‐of‐onset methods applied to the linkage of bipolar disorder (1997) (9)
On the Analysis of a Repeated Measure Design in Genome-Wide Association Analysis (2014) (9)
Calculating Asymptotic Significance Levels of the Constrained Likelihood Ratio Test with Application to Multivariate Genetic Linkage Analysis (2009) (9)
An approximation for the prior probability of autosomal linkage. (1975) (9)
Linkage analysis of alcohol dependence using both affected and discordant sib pairs (2005) (9)
Sampling correction in linkage analysis (2004) (9)
On analysis of path models by the multivariate normal model for pedigree analysis (1986) (9)
Ragweed sensitivity: segregation analysis and linkage to HLA-B. (1978) (9)
Effect of pH of Bupivacaine on Duration of Repeated Sciatic Nerve Blocks in the Albino Rat (1991) (9)
A NEW TEST OF ASSOCIATION FOR CONTINUOUS VARIABLES (1970) (9)
Power comparison of regression methods to test quantitative traits for association and linkage (2000) (9)
Joint modeling of longitudinal data and discrete-time survival outcome (2016) (9)
TUTORIAL IN BIOSTATISTICS GENETIC MAPPING OF COMPLEX TRAITS (1999) (9)
Evolution of resistance during first-line treatment with boosted fosamprenavir is associated with baseline mutations. (2006) (9)
Pedigree analysis to determine the mode of inheritance in a family with retinitis pigmentosa (1974) (9)
Differentiation of genotypic resistance profiles for amprenavir and lopinavir, a valuable aid for choice of therapy in protease inhibitor-experienced HIV-1-infected subjects. (2003) (9)
The Linkage Information Content Value of Polymorphism Genetic Markers in Model-Free Linkage Analysis (2002) (9)
A quantitative linkage score for an association study following a linkage analysis (2006) (9)
Disruption of sonic hedgehog signaling in Ellis-van Creveld dwarfism confers protection against bipolar affective disorder (2014) (9)
X-Linked Extension of the Revised Haseman-Elston Algorithm for Linkage Analysis in Sib Pairs (2003) (8)
Family‐Based Rare Variant Association Analysis: A Fast and Efficient Method of Multivariate Phenotype Association Analysis (2016) (8)
Immunoglobulin G genotypes and the risk of schizophrenia (2016) (8)
Linkage of serum leptin levels in families with sleep apnea (2005) (8)
Response of the hypothalamic-pituitary-adrenal axis to lumbar puncture induced stress. (2000) (8)
Interval Estimation of Familial Correlations from Pedigrees (2011) (8)
Genetic Analysis Workshop 6: Linkage analysis based on affected pedigree members. (1989) (8)
Introduction to Probability Theory and Statistics (2012) (8)
Multipoint mapping and linkage based upon affected pedigree members : Genetic Analysis Workshop 6, proceedings of a workshop held at Gulf Park, Long Beach, Mississippi, October 10-12, 1988 (1989) (8)
An in vitro test system for estimation of blood compatibility of biomaterials. (1974) (8)
Blood markers and depressive disorders: an association study. (1977) (8)
The HIV-1 protease substitution K55R: a protease-inhibitor-associated substitution involved in restoring viral replication. (2008) (8)
No fallacies in the formulation of the paternity index. (1986) (8)
A Note on Comparing the Power of Test Statistics at Low Significance Levels (2011) (8)
Plasma factor 8 activity in capillary and venous blood samples. (1968) (8)
Improvement of Mapping Accuracy by Unifying Linkage and Association Analysis (2006) (8)
Tests for a Disease-susceptibility Locus allowing for an Inbreeding Coefficient (F) (2003) (8)
Statistical validity for testing associations between genetic markers and quantitative traits in family data (1995) (7)
Measures of observer agreement when binomial data are collected in free operant situations (1982) (7)
A Novel Approach to Detect Parent‐of‐Origin Effects from Pedigree Data with Application to Beckwith‐Wiedemann Syndrome (2007) (7)
Some Capabilities for Model-Based and Model-Free Linkage Analysis using the Program Package S.A.G.E. (Statistical Analysis for Genetic Epidemiology) (2011) (7)
Comment on Dr. Robertson's communication (1974) (7)
Segregation analysis under an alternative formulation for the mixed model (1993) (7)
Extension of the Haseman-Elston Regression Model to Longitudinal Data (2006) (7)
Segregation and linkage analysis of α-N-acetyl-D-glucosaminidase (NAG) levels in a black family (1985) (7)
The Bias Introduced by Population Stratification in IBD Based Linkage Analysis (2006) (7)
Linkage between the APOB gene and serum apoB levels in a large pedigree from the Bogalusa heart study (1994) (7)
Prospects of admixture linkage disequilibrium mapping in the African-American genome. (2002) (7)
Bagging Optimal ROC Curve Method for Predictive Genetic Tests, with an Application for Rheumatoid Arthritis (2010) (7)
HLA and ragweed allergy. (1977) (7)
Linkage relationship between variable and constant region allotypic determinants of human immunoglobulin heavy chains (1980) (7)
Will Formal Genetics Become Dispensable? (2013) (7)
Integrated designs for gene discovery and characterization. (1999) (7)
Linkage and association analyses of alcoholism using a regression‐based transmission/disequilibrium test (1999) (7)
Applying family analyses to electronic health records to facilitate genetic research (2018) (7)
A major gene model for the familial aggregation of plasma IgA concentration (1987) (7)
Major gene analysis of quantitative variation in blood clotting factor X levels. (1979) (7)
Model‐free association analysis of a rare Disease (1995) (7)
Novel approaches to the analysis of family data in genetic epidemiology (2015) (7)
Coagulation factor XIII: A useful polymorphic genetic marker (2004) (7)
Resistance to HIV-1 Protease Inhibitors (2009) (7)
The collaborative lipid research clinics program family study: Detection of major genes influencing lipid levels by examination of heterogeneity of familial variances (1984) (7)
A polymorphism (D20S32e) close to the human melanocortin receptor 3 is associated with insulin resistance but not the metabolic syndrome. (2008) (7)
PGM1 null allele detected in a Caucasian mother-son pair. (1985) (7)
Lack of association between dermal arches and mitral valve prolapse: relation to anxiety. (1984) (7)
Likelihood models in human quantitative genetics. (1979) (6)
2nd International Conference on Progressive Multifocal Leukoencephalopathy (PML) 2015: JCV virology, progressive multifocal leukoencephalopathy pathogenesis, diagnosis and risk stratification, and new approaches to prevention and treatment (2015) (6)
A SIMPLE METHOD OF ESTIMATING RELATIVE POTENCY FROM TWO PARABOLAS (1965) (6)
Analysis of Swedish male breast cancer family data: A simple way to incorporate a common sibling effect (1998) (6)
Adding power to Haseman and Elston’s (1972) method (2000) (6)
Fine-mapping using the weighted average method for a case-control study (2005) (6)
Computers and blood bank control. (1966) (6)
Probable linkage between essential familial hypercholesterolemia and third complement component (C3). (1976) (6)
T cell receptor gamma gene polymorphisms and class II human lymphocyte antigen genotypes in patients with celiac disease from the west of Ireland. (1995) (6)
Testing Quantitative Traits for Association and Linkage in the Presence or Absence of Parental Data (2001) (6)
Inheritance of adrenal phenylethanolamine N-methyltransferase activity in the rat. (1984) (6)
PedWiz: a web-based tool for pedigree informatics (2013) (6)
Modeling age of onset and residual familial correlations for the linkage analysis of bipolar disorder (1997) (6)
What we know and what we need to know about familial gastroesophageal reflux disease and Barrett's esophagus. (2014) (5)
The HGAR1 familial hypercholesterolemia pedigree (1993) (5)
Discussion: Methodologies in human behavior genetics. (1973) (5)
Genetic epidemiology and the search for epilepsy genes. (1999) (5)
Reply to “message from a referee on the Elston method” (1973) (5)
Tuberculin reactivity in families of infants who failed to develop tuberculin reactivity after BCG immunization at birth. (1994) (5)
Linkage relations among 25 autosomal blood, urine, and saliva markers in two large multigenerational pedigrees. (1978) (5)
On testing whether one locus can account for the genetic difference in susceptibility between two homozygous lines. (1966) (5)
Segregation and linkage analyses of dopamine-beta-hydroxylase activity. (1979) (5)
Augmentation of the antibody response by hapten help. I. Dominant genetic control. (1982) (5)
Power comparison of regression methods to test quantitative traits for association and linkage. (2000) (5)
Local false discovery rate and minimum total error rate approaches to identifying interesting chromosomal regions (2005) (5)
A study of multiple biological markers in twins. (1985) (5)
Two-stage analysis strategy for identifying the IgM quantitative trait locus (2007) (5)
Adjustment for covariates using summary statistics of genome‐wide association studies (2018) (5)
Genome-wide association studies using an adaptive two-stage analysis for a case-control design (2007) (4)
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND) (2016) (4)
Statistical interactions and Bayes estimation of log odds in case-control studies (2017) (4)
Improving the power for disease locus detection in affected‐sib‐pair studies by using two‐locus analysis and multiple regression methods (1999) (4)
A method to correct for population structure using a segregation model (2009) (4)
A novel method to detect rare variants using both family and unrelated case-control data (2011) (4)
Linkage Disequilibrium Mapping of Complex Genetic Diseases Using Multiallelic Markers (2001) (4)
Segregation and linkage analysis of alpha-N-acetyl-D-glucosaminidase (NAG) levels in a black family. (1985) (4)
Parametric linkage analysis. (2002) (4)
Prediction of Empirical p Values from Asymptotic p Values for Conditional Logistic Affected Relative Pair Linkage Analysis (2006) (4)
Linkage and related analyses of Barrett's esophagus and its associated adenocarcinomas (2016) (4)
The use of polymorphic markers to detect genetic variability. (1988) (4)
A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis (2011) (4)
On the distribution of the likelihood ratio test statistic for a mixture of two normal distributions (1996) (4)
Effect of age on the gm:pi linkage. (1976) (4)
Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17 (2011) (4)
Blood compatibility of biomaterials: further evaluation of the Lindholm test. (1974) (4)
A multivariate analysis of familial associations of lipoprotein levels in the Lipid Research Clinics Collaborative Family Study: I. Familial correlation and regression analyses (1985) (4)
Using family history information to distinguish true and false positive model‐free linkage results (1998) (4)
Estimation of time, age, and cohort effects (1963) (4)
Linkage relationships of Lp and Ag serum lipoproteins with 25 polymorphic markers (1977) (4)
The estimation of genetic gain in milk yield due to sire selection over a period of time. (1960) (4)
Estimating heritability using family and unrelated individuals data (2011) (4)
Types of disease and models for their genetic analysis. (1980) (4)
The Laws of Probability (2008) (3)
Interrogating population structure and its impact on association tests (2011) (3)
A method to assess the environment for genetic studies: the Common Environment Index and the Household Relationships Interview. (1985) (3)
Haseman-Elston weighted by marker informativity (2005) (3)
A genetic linkage study in support of the concept of depression spectrum disease. (1977) (3)
Letter: Estimation of nonpaternity for X-linked trait. (1975) (3)
A General Linkage Method for the Detection of Major Genes (1990) (3)
Finding Genetic Mechanisms in Syndromes of Sleep Disordered Breathing: Report to the RNS Assembly and the ATS Board from the ad hoc Committee on Inheritance and Ventilatory Control; Approved by the ATS Board of Directors July 11, 1999 (1999) (3)
Bayesian intervals for linkage locations (2009) (3)
Populations, Samples, and Study Design (2008) (3)
Modeling Genetic and Environmental Factors in Biological Systems Using Structural Equation Modeling: An Application to Energy Balance (2009) (3)
Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4 (2007) (3)
HLA in breast cancer-prone families and the cancer family syndrome. (1977) (3)
Localization of the Q1 Mutation by Cladistic Analysis (2001) (3)
Testing gene-environment interactions in gene-based association studies (2011) (3)
Enhancing the Power to Detect Low-Frequency Variants in Genome-Wide Screens (2014) (3)
Gametic equilibrium between 24 polymorphic markers (1990) (3)
The Genetic Epidemiology of Age-Related Maculopathy (2001) (3)
Fisher’s influence on me (2018) (3)
Response to Epstein et al. (2002) (3)
A comparison of some sib-pair linkage methods and multiple locus extensions. (1989) (3)
Association and linkage analysis of ICD‐10 diagnosis for alcoholism (1999) (3)
The effect of some common environmental factors on the level of blood clotting factor X. (1978) (3)
Pedigree discriminant analysis of two French Canadian Tay‐Sachs families (1987) (3)
Statistical Genetic Terminology. (2017) (3)
Determination of the order of loci on the short arm of chromosome 11 using two and three locus linkage analyses of pedigree and sib pair data (1986) (3)
Critique of a published analysis of the Jacobsen data (1986) (3)
Statistical Human Genetics (2017) (3)
Genometric analysis of mental diseases (1991) (3)
Combining two‐point genetic linkage analyses using mapping functions (1994) (3)
Local Ancestry Inference in Large Pedigrees (2020) (3)
Effects of marker information on sib‐pair linkage analysis of a rare disease (1995) (3)
Gene-Gene Interactions (2012) (3)
Genetic Analysis Workshop 6: Multipoint mapping of loci in the region of cystic fibrosis. (1989) (2)
Testing specific hypotheses by fitting underlying distributions to categorical data. (1994) (2)
Comparison of a unified analysis approach for family and unrelated samples with the transmission-disequilibrium test to study associations of hypertension in the Framingham Heart Study (2009) (2)
Segregation Analysis of Asthma and Respiratory Allergy in Population‐Based Samples of Families (2001) (2)
Linkage mapping methods applied to the COGA data set: Presentation Group 4 of Genetic Analysis Workshop 14 (2005) (2)
Genetic analysis of white cell blood groups. (1967) (2)
Association and linkage between genetic markers and morphological and behavioral attributes in dizygotic twins. (1977) (2)
A Century of Biometrical Genetics (2000) (2)
Putative Linkage Signals Identified for Breast Cancer in African American Families (2014) (2)
Quantitative Effects of the Reaction between Factor VIII and Factor VIII Inhibitors (1971) (2)
GENETIC DETERMINANTS OF DIABETIC NEPHROPATHY (2003) (2)
PW01-12 - Two or Three Age-of-Onset Groups in Bipolar I Disorder? Findings of Commingling Analysis in Romanian and German Bipolar I Patients (2010) (2)
The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutations. (1991) (2)
Linkage relationships of biochemical markers to Q- and C-band variants in a large black kindred (2004) (2)
A statistical model of tracking (1989) (2)
The null distribution of likelihood-ratio statistics in the conditional-logistic linkage model (2013) (2)
Reporting of linkage results. (2001) (2)
Integrals of products of multinormal mixtures (1985) (2)
Developmental expression of tyrosyl kinase activity in human serum. (1987) (2)
Genetic analysis of multivariate traits. (1991) (2)
Genetic linkage with HLA in spinocerebellar ataxia. (1979) (2)
Oral combination therapy: Future hepatitis C virus treatment? (2011) (2)
A genetic study of schizophrenia pedigree. I. Demographic studies: sample description, age of onset, ascertainment and classification. (1976) (2)
Likelihood calculation conditional on observed pedigree structure. (1998) (2)
A logistic mixture model for a family-based association study (2007) (2)
Model Free Linkage Analysis in Extended Families Confirms a Susceptibility Locus for Age Related Macular Degeneration (ARMD) on 1q31 (2003) (2)
Likelihood Models for Multivariate Traits in Human Genetics1 (1985) (2)
Impact of Preadjusting a Quantitative Phenotype Prior to Sib‐Pair Linkage Analysis when Gene×Environment Interaction Exists (2001) (2)
A new test statistic for linkage applied to bipolar disorder and marker D18S41 (1997) (2)
Multivariate analyses of anthropometric and psychometric variables in probands with affective disorders and their families. (1975) (2)
Segregation Analysis of Gastric Cancer in a Japanese Population (2001) (2)
Phase uncertainty in case‐control association studies (2009) (2)
Factors contributing to the variability in serum lipid levels and blood pressure in a large kindred. (1983) (2)
How Consistent are Genetic Factors in Explaining Leisure-Time Physical Activity and Sport Participation? The Portuguese Healthy Families Study (2018) (2)
Response to letter by Veronica J. Vieland and Susan E. Hodge (2005) (1)
118 Identification of a Novel Germ-Line Variant in an Uncharacterized Gene, FBE-1, and Its Putative Role in Familial Barrett's Esophagus (2015) (1)
Examinations of Methylenetetrahydrofolate Reductase C 677 T and A 1298 C Mutations — and In Utero Viability (2007) (1)
Treatment of Uninformative Families in Mean Allele Sharing Tests for Linkage (2006) (1)
A case study of high strain rate effects in glass filled thermoplastic materials (1998) (1)
Lack of evidence for segregation of a single dominant major gene as the cause of the difference in egg weight between two highly inbred lines of chickens (2004) (1)
Linkage-disequilibrium-based binning misleads the interpretation of genome-wide association studies. (2012) (1)
Correlation and Regression (2008) (1)
Subject Index Vol. 52, 2001 (2001) (1)
Probabilities of identity‐by‐descent patterns in sibships when the parents are not genotyped (1997) (1)
Possible linkage between alpha-haptoglobin (Hp) and depression spectrum disease. (1979) (1)
The E1 (cid:217) E4 Protein of Human Papillomavirus Type 16 Associates with a Putative RNA Helicase through Sequences in Its C Terminus (2000) (1)
Errata Sheet (1988) (1)
The Probability of Paternity (1990) (1)
Reply to Ashktorab et al.: Mutational landscape of colon cancers in African Americans (2015) (1)
Bivariate Analyses ofCholesterol andTriglyceride Levels in Families inWhichProbands HaveTypeTIb Lipoprotein Phenotype (1975) (1)
Erratum to: Segregation Analysis (1981) (1)
Information for detecting linkage when sampling affected individuals. (1989) (1)
Reciprocal causal influences among malnutrition, growth retardation, and diarrhea in preschool children (1990) (1)
Resolution of genetic and environmental influences. (1982) (1)
Optimizing the evidence for linkage by permuting marker order (2005) (1)
A Germline Variant on Chromosome 4q31.1 Associates with Susceptibility to Developing Colon Cancer Metastasis (2016) (1)
Familial Segregation of Venous Thromboembolism in Sweden: A Nationwide Family Study of Heritability and Complex Segregation Analysis (2021) (1)
A genome-wide scan for age-related maculopathy and other ocular phenotypes in a sample from the Beaver Dam Eye Study (BDES) (2002) (1)
On the association analysis of CNV data: a fast and robust family-based association method (2017) (1)
Analysis of Family Data (2012) (1)
2010 William Allan Award introduction: Jürg Ott. (2011) (1)
Significance Tests and Tests of Hypotheses (2008) (1)
A note on estimation using self-contained subsets (1988) (1)
Program Update and Novel Use of the DESPAIR Program to Design a Genome-Wide Linkage Study Using Relative Pairs (2009) (1)
Model‐based and model‐free multipoint genome‐wide linkage analysis of alcoholism (1999) (1)
Pedigree with an Adverse Lipoprotein Phenotype (2006) (1)
Use of Electronic Health Record to Predict Family Relationships for Phenome-wide Research (2018) (0)
Genome-Wide Search for Linkage of Estimated Glomerular Filtration Rate (eGFR) in the Family and Diabetes (2013) (0)
THE IMPACT STUDY: PHENOTYPIC ANALYSIS OF PREVIOUSLY UNCHARACTERIZED CYTOMEGALOVIRUS UL54 AND UL97 AMINO ACID SUBSTITUTIONS DETECTED IN VIRUS FROM PATIENTS RECEIVING 200 OR 100 DAYS OF VALGANCICLOVIR (VALCYTE®) PROPHYLAXIS: 1099 (2010) (0)
Identification of a major locus and other oligogenic loci for age related macular degeneration in extended families (2004) (0)
Recent Developments in Statistics. (1978) (0)
Applied mathematical models of etiology: critique II. (1980) (0)
Gene-Environment Interactions (2007) (0)
Resistance to HIV Non-Nucleoside Reverse Transcriptase Inhibitors (2009) (0)
Guides to a Critical Evaluation of Published Reports (2008) (0)
Subject Index Vol. 53, 2002 (2002) (0)
Subject Index Vol. 2, 1976 (1976) (0)
Stability Over Time of the Heterozygous VWD Phenotype (1979) (0)
MARVIN ZELEN LEADERSHIP AWARD IN STATISTICAL SCIENCE AWARDEES (2013) (0)
On the association analysis of CNV data: a fast and robust family-based association method (2017) (0)
Fundamentals of Biostatistics: by Stanley S. Schor, Ph.D., Professor and Chairman, Department of Biometrics, Temple University of the Commonwealth System of Higher Education, School of Medicine, Philadelphia. 312 pages. G. P. Putnam's Sons, New York, N. Y., 1968. $8.95 (1969) (0)
Arevie wo fthe 'Statistica lAnalysi sfor Genetic Epidemiology' (SAGE) softwar epackage (2004) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Power and Sample Size Calculations (2012) (0)
Identification of Heterozygotes for Hemophilia B and VWD by Discriminant Analysis (1979) (0)
Correcting for Ascertainment. (2017) (0)
Defining “mutation” and “polymorphism” in the era of personal genomics (2015) (0)
MajorLocusAnalysis forQuantitative Traits (1979) (0)
Sex role stereotypes in freshman medical students' perceptions of self and physicians. (1987) (0)
Comments on behavioral genetic methodology (1986) (0)
Likelihood Modelling: Genetic Mapping of Complex Traits (2005) (0)
47 Relationship of the immune response to purified ragweed antigens and the HLA-Dr system (1983) (0)
MajorGeneAnalysis ofQuantitative Variation inBloodClotting Factor X Levels (1979) (0)
Answers to Odd‐Numbered Problems (2008) (0)
Analysis of human genetic linkage. Jurg Ott. Baltimore: The Johns Hopkins University Press, 1985, 238 pp, $35.00 (1986) (0)
Subject Index Vol. 70, 2010 (2011) (0)
Contents Vol. 52, 2001 (2001) (0)
Estimating titres and their approximate standard errors in complement fixation tests (1965) (0)
Some Specialized Techniques (2008) (0)
Newton E. Morton (1929-2018). (2018) (0)
05.02: HERITABILITY AND INTRAFAMILIAL AGGREGATION OF ARTERIAL CHARACTERISTICS HERITABILITY AND INTRAFAMILIAL AGGREGATION (0)
Editorial help (2004) (0)
Case Comprehensive Cancer Center (2020) (0)
INVITEDEDITORIAL 'Twixt CupandLip: How Intractable Is theAscertainment Problem? (1995) (0)
Future trends in genetic analysis methodology. (1984) (0)
Contents Vol. 72, 2011 (2011) (0)
Models for ascertainment (1984) (0)
Contents Vol. 70, 2010 (2011) (0)
Contents, Vol. 2, 1976 (1976) (0)
Subject Index Vol. 51, 2001 (2001) (0)
STATISTICAL MODELING AND ANAL YSIS IN HUMAN GENETICS (1978) (0)
A Genome–Wide Linkage Analysis for Geographic Atrophy Suggests Linkage to Multiple Chromosomes (2005) (0)
An approximation for the prior probability of autosomal linkage. (1975) (0)
Genetical Statistics (1963) (0)
Comment [1] (multiple letters) (2002) (0)
Contents Vol. 63, 2007 (2007) (0)
No evidence of linkage with chromosome 1 markers for age-related maculopathy phenotypes The Beaver Dam Eye Study (2000) (0)
Genome-Wide Scan for Estimated GFR in Multi-Ethnic Diabetic Populations: The Family Investigation of Nephropathy and Diabetes of Nephropathy (2007) (0)
Model-Dependent Versus Model-Free Versus Nonparametric Tests (2012) (0)
Correcting for ascertainment. (2012) (0)
Authors' reply: Confidence limits based on the first occurrence of an event. V.T. George and R.C. Elton. Statistics in Medicine, 12, 685–690 (1993) (1998) (0)
Random Variables and Distributions (2008) (0)
Introductory genetics for statisticians (2004) (0)
Subject Index Vol. 63, 2007 (2007) (0)
Regression-based linkage analysis methods (2007) (0)
Single-Marker Analysis for Matched Case-Control Data (2012) (0)
Erratum: 'Statistical Analysis for Genetic Epidemiology' (S.A.G.E.) software package' (Human Genomics vol. 1 (6) (456-459)) (2005) (0)
815 MEDICAL FACTORS ARE POOR PREDICTORS OF PERCEPTION OF PAIN AND URGENCY IN INTERSTITIAL CYSTITIS (IC) (2011) (0)
229 Effect of early feeding of soy (SF), extensively-hydrolyzed casein (EHCF), and partially-hydrolyzed whey (PHWF) formula on the development of allergic manifestations in children during the second year of life (1996) (0)
Mo1853 Genetic Linkage Predisposing to Familial Barrett's Esophagus (FBE) (2013) (0)
Preface (0)
Bayes Factors for Case-Control Association Studies (2012) (0)
An Accidental Genetic Epidemiologist. (2020) (0)
Model‐Free Tests for Genetic Linkage (2001) (0)
A PROBLEM IN ASCERTAINMENT (2001) (0)
The Many Uses of Chi‐Square (2008) (0)
Books received (2007) (0)
Panel Discussion on Genes, Environment and Disease (1993) (0)
Sa1826 Predicting Barrett's Esophagus in Families of Patients With Barrett's Esophagus: A BETRNet Model Fitting Clinical Data to a Genetic Paradigm (2014) (0)
Analysis of Variance and Linear Models (2008) (0)
Meeting Summary Genetic Epidemiology of Coronary Heart Disease Past, Present, and Future (2005) (0)
Introduction to Genetic Epidemiology (2012) (0)
Estimates and Confidence Limits (2008) (0)
Linkage analysis for large pedigrees under mixed inheritance (1994) (0)
CRS of Two Seismic Lines in Rich County (1992) (0)
Appendix: Additional Notes and Computational Formulas (2008) (0)
Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND) (2016) (0)
Contents, Vol. 21, 1971 (1971) (0)
Arevie wo fthe 'StatisticalAnal ysisfor Genetic Epidemiology' (SAGE) softwarepacka ge (2004) (0)
T1924 Familiality, Obesity, and Other Risk Factors for Early Age of Cancer Diagnosis in Adenocarcinomas of the Esophagus and Gastro-Esophageal Junction (2009) (0)
Introduction: Linkage Analyses of Single Regions (2001) (0)
Genotype (2019) (0)
THEIR CONFIDENCE BANDS1 (2016) (0)
The HIV-1 protease mutation K55R is associated with the presence of the M461/L mutation (2003) (0)
16 A Segregation Analysis of Barrett's Esophagus and Associated Adenocarcinomas (2010) (0)
Identification of Genomic Regions Associated with Susceptibility to Barrett’s Esophagus and Esophageal Adenocarcinoma in African Americans: The Cross Betrnet Admixture Study (2017) (0)
An Introduction to Medical Statistics.@@@Essentials of Biostatistics. (1989) (0)
Detection and Estimation of Linkage, Especially Multipoint Mapping (1987) (0)
Comparison of Marker Intervals and Number of Sib Pairs Used for Linkage Analysis on Simulated Nuclear Family Data (2001) (0)
Hyperlipoproteinemia--a difference of opinion. (1968) (0)
Effect of age on the Gm:Pi linkage. (1976) (0)
Likelihood Ratios, Bayesian Methods and Multiple Hypotheses (2008) (0)
Letter: Comment on Dr. Robertson's communication. (1974) (0)
Linkage-Disequilibrium-BasedBinningMisleadsthe Interpretation of Genome-wide Association Studies (2012) (0)
The Analysis of Quantitative Inheritance Simul-taneously from Twin and Family Data (2006) (0)
Genetic Analysis ofWhiteCellBloodGroups (1967) (0)
Local Ancestry Inference in Large Pedigrees (2020) (0)
Workshop 8: Data analysis (1986) (0)
INVESTIGATING THE VALIDITY OF OBSERVATIONAL STUDY BASED ON ELECTRONIC MEDICAL RECORDS AND THE EFFECTIVENESS OF PERIOPERATIVE BETA-ADRENOCEPTOR THERAPY TO REDUCE POSTOPERATIVE CARDIAC EVENTS IN PATIENTS UNDERGOING MAJOR NON-CARDIAC SURGERY by XUEBEI AN Submitted in partial fulfillment of the requirem (2012) (0)
Subject Index Vol. 21 (1971) (0)
Evidence for a Dominant Gene Mechanism in Coeliac Disease (1991) (0)
Behavior Genetics Comes of Age. (1980) (0)
Jane M. Olson (December 6, 1952–May 2, 2004) (2004) (0)
Haplotype Analysis for Case-Control Data (2012) (0)
Cellular Genes in T H E Mouse Regulate in Trans T H E Expression of Endogenous Mouse Mammary T U M O R Viruses (0)
What is the Heritability of Ability and Personality (1984) (0)
840 Combining GWAS With Linkage Analysis Identifies a SNP Associated With Barrett's Esophagus And Esophageal Adenocarcinoma (2016) (0)
Contents Vol. 53, 2002 (2002) (0)
A non-parametric method finds genetic etiology of nicotine dependence differs in males and females (2015) (0)
Introduction: The Role and Relevance of Statistics, Genetics and Epidemiology in Medicine (2008) (0)
A variance component based multi-marker association test using family and unrelated data (2013) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Immunoglobulin G genotypes and the risk of schizophrenia (2016) (0)
Search for Distant Star Forming Galaxies (1988) (0)
Contents Vol. 51, 2001 (2001) (0)
References to the committee reports (1975) (0)
Elston–Stewart Algorithm (2005) (0)

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