Newton Morton

Q: What Schools Are Affiliated With Newton Morton

Newton Morton is affiliated with the following schools: University of Texas at Austin, Swarthmore College, University of Wisconsin–Madison, University of Southampton

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Newton Morton

Biology

#644

World Rank

#1132

Historical Rank

#358

USA Rank

Genetics

#43

World Rank

#68

Historical Rank

#30

USA Rank

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Biology

Why Is Newton Morton Influential?

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According to Wikipedia, Newton Ennis Morton was an American population geneticist and one of the founders of the field of genetic epidemiology. Early life and education Morton was born in Camden, New Jersey. When he was three months old, his family moved to New Haven, Connecticut. His interest in science started at an early age, when he would collect butterflies. Morton attended Hopkins School, later transferring to Swarthmore College for two years. He lost enthusiasm for entomology, so instead he decided to pursue a career in genetics after being inspired by Dobzhansky's book, Genetics and the Origin of Species.

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Newton Morton'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

Sequential tests for the detection of linkage. (1955) (1675)
Genetic Epidemiology of Hearing Impairment (1991) (933)
Lp(a) lipoprotein as a risk factor for myocardial infarction. (1986) (800)
AN ESTIMATE OF THE MUTATIONAL DAMAGE IN MAN FROM DATA ON CONSANGUINEOUS MARRIAGES. (1956) (697)
Analysis of family resemblance. 3. Complex segregation of quantitative traits. (1974) (583)
The neolithic transition and the genetics of populations in Europe. (1985) (549)
Von Hippel-Lindau disease: a genetic study. (1991) (548)
Parameters of the human genome. (1991) (545)
A unified model for complex segregation analysis. (1983) (466)
The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type. (1956) (439)
Genetic epidemiology (1997) (421)
Complex segregation analysis with pointers. (1981) (392)
The marker (X) syndrome: a cytogenetic and genetic analysis (1984) (381)
Extended tracts of homozygosity in outbred human populations. (2006) (368)
Skewness in commingled distributions. (1976) (324)
Report of the Committee on Methods of Linkage Analysis and Reporting. (1985) (314)
Genetic tests under incomplete ascertainment. (1959) (314)
Genetic epidemiology of single-nucleotide polymorphisms. (1999) (299)
MEASUREMENT OF GENE FREQUENCY DRIFT IN SMALL POPULATIONS (1955) (281)
A metric map of humans: 23,500 loci in 850 bands. (1996) (272)
Tests and estimates of allelic association in complex inheritance. (1998) (271)
Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness. (1996) (271)
Genetic Data Analysis. Methods for Discrete Population Genetic Data (1992) (226)
Analysis of family resemblance. II. A linear model for familial correlation. (1974) (211)
Racial admixture in north‐eastern Brazil (1965) (211)
The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis (2002) (197)
Formal genetics of muscular dystrophy. (1959) (179)
Fisher, the life of a scientist. (1979) (177)
Significance levels in complex inheritance. (1998) (172)
Mapping a disease locus by allelic association. (1998) (171)
The glutamine 27 beta2-adrenoceptor polymorphism is associated with elevated IgE levels in asthmatic families. (1997) (167)
Resolution of cultural and biological inheritance by path analysis. (1976) (164)
Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing. (1977) (163)
International system for human gene nomenclature (1979) ISGN (1979). (1979) (161)
A genetic study of immunoglobulin E. (1978) (158)
The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. (1994) (156)
Outline of Genetic Epidemiology (1982) (152)
Further segregation analysis of the fragile X syndrome with special reference to transmitting males (2004) (146)
Dominant genes for colorectal cancer are not rare (1992) (143)
Analysis of family resemblance. IV. Operational characteristics of segregation analysis. (1975) (140)
Guidelines for human gene nomenclature. An international system for human gene nomenclature (ISGN, 1987). (1987) (138)
Hardy–Weinberg quality control (1999) (138)
Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. (1995) (137)
The use of long PCR to confirm three common alleles at the CYP2A6 locus and the relationship between genotype and smoking habit (2000) (136)
Genetics of interracial crosses in Hawaii. (1967) (135)
The optimal measure of allelic association (2001) (131)
Revisiting Race in a Genomic Age (2009) (129)
Path analysis of qualitative data on pairs of relatives: application to schizophrenia. (1981) (129)
Reproductive and menstrual history of females with fragile X expansions (2000) (120)
Methods in Genetic Epidemiology (1983) (118)
Cultural and biological determinants of lipoprotein concentrations (1979) (116)
Bioassay of kinship. (1971) (115)
The effect of exposure to the atomic bombs on pregnancy termination in Hiroshima and Nagasaki: preliminary report. (1953) (114)
Non-disjunction of chromosome 18. (1998) (113)
A NOTE ON DEAF MUTISM (1959) (110)
Association between − 308 tumour necrosis factor promoter polymorphism and bronchial hyperreactivity in asthma (1999) (109)
Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus. (1992) (105)
Genetic studies on cystic fibrosis in Hawaii. (1968) (105)
A mapping function for man. (1977) (102)
Serum enzymes and genetic carriers in muscular dystrophy. (1960) (94)
Further scoring types in sequential linkage tests, with a critical review of autosomal and partial sex linkage in man. (1957) (92)
Path analysis under generalized assortative mating. I. Theory. (1979) (91)
Discrimination of genetic entities in muscular dystrophy. (1959) (88)
Genetic analysis of idiopathic hemochromatosis using both qualitative (disease status) and quantitative (serum iron) information. (1985) (87)
Genetic analysis of atopy and asthma as quantitative traits and ordered polychotomies (1994) (87)
A map of the human genome in linkage disequilibrium units. (2005) (86)
Genetics of spherocytosis. (1962) (85)
Analysis of family resemblance. V. Height and weight in northeastern Brazil. (1975) (83)
The mutational load due to detrimental genes in man. (1960) (82)
The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission. (1997) (82)
The Journey is Home (1985) (80)
Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores. (1998) (79)
Genetic structure of forensic populations. (1992) (79)
Oculoauriculovertebral anomaly: segregation analysis. (1992) (78)
Properties of linkage disequilibrium (LD) maps (2002) (78)
Genetic epidemiology of breast cancer in Britain (1991) (77)
Empirical risks in consanguineous marriages: birth weight, gestation time, and measurements of infants. (1958) (76)
Complex segregation analysis. (1971) (76)
Combined segregation and linkage analysis of Graves disease with a thyroid autoantibody diathesis. (1994) (75)
Microdeletions in FMR2 may be a significant cause of premature ovarian failure (1999) (73)
Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women. (1999) (71)
Allelic association between marker loci. (1999) (71)
A genetic study of cleft lip and palate in Hawaii. II. Complex segregation analysis and genetic risks. (1974) (71)
Error filtration, interference, and the human linkage map. (1991) (67)
Analysis of family resemblance. I. Introduction. (1974) (66)
Isolation by distance in human populations * (1977) (66)
The CEPH consortium primary linkage map of human chromosome 10. (1990) (63)
The effect of structural aberrations of the chromosomes on reproductive fitness in man (1975) (63)
GENETIC STUDIES OF NORTHEASTERN BRAZIL. (1964) (63)
Segregation analysis of peripheral neurofibromatosis (NF1). (1990) (62)
Bioassay of population structure under isolation by distance. (1968) (61)
Distance and kinship in northeastern Brazil. (1969) (61)
Isolation by distance in artificial populations. (1970) (61)
Origin of human trisomics and polyploids. (1977) (61)
Positional cloning by linkage disequilibrium. (2004) (60)
The contribution of injury severity, executive and implicit functions to awareness of deficits after traumatic brain injury (TBI) (2010) (60)
Genetics of the Lp lipoprotein in Japanese‐Americans (1985) (60)
Does haplotype diversity predict power for association mapping of disease susceptibility? (2004) (60)
Path analysis under generalized assortative mating. II. American I.Q. (1982) (60)
Genetic epidemiology of ovarian cancer: segregation analysis (1991) (59)
Genetic epidemiology of complex phenotypes (1991) (59)
Family resemblance for blood pressure. (1983) (59)
No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers. (2000) (58)
Estimation of myriad haplotype frequencies (1985) (58)
Variability of human linkage data. (1978) (58)
Combined analysis of genetic segregation and linkage under an oligogenic model. (1984) (56)
Guidelines for human linkage maps An International System for Human Linkage Maps (ISLM, 1990) (1991) (56)
Linkage disequilibrium maps and association mapping. (2005) (54)
Report of the committee on the genetic-constitution of chromosomes 1 and 2. (1987) (54)
RECESSIVE GENES IN SEVERE MENTAL DEFECT. (1965) (54)
Inheritance of acute appendicitis: familial aggregation and evidence of polygenic transmission. (1990) (54)
Segregation analysis in human genetics. (1958) (53)
Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps (2004) (53)
A first trial of retrospective collaboration for positional cloning in complex inheritance: assay of the cytokine region on chromosome 5 by the consortium on asthma genetics (COAG). (2000) (53)
Integration of gene maps: chromosome 21. (1992) (53)
A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency. (1988) (53)
MAP, an expert system for multiple pairwise linkage analysis (1989) (53)
Logarithm of odds (lods) for linkage in complex inheritance. (1996) (53)
Linkage map integration. (1996) (52)
Sinking pre-beta lipoprotein and coronary heart disease in Japanese-American men in Hawaii. (1978) (51)
Maternal age in trisomy (1988) (51)
Natural selection on polymorphisms in northeastern Brazil. (1966) (50)
Major loci for lipoprotein concentrations. (1978) (50)
The effect of structural aberrations of the chromosomes on reproductive fitness in man (1975) (50)
Further segregation analysis of the fragile X syndrome with special reference to transmitting males (2004) (50)
Effect of inbreeding on IQ and mental retardation. (1978) (49)
Algorithms for a location database (1992) (49)
Human Population Structure (1969) (48)
Multipoint linkage analysis. (1986) (47)
Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990). (1991) (47)
A maximum likelihood map of chromosome 1. (1979) (46)
Heterozygous expression of insulin-dependent diabetes mellitus (IDDM) determinants in the HLA system. (1983) (46)
A defense of path analysis in genetic epidemiology. (1983) (45)
Linkage disequilibrium in human populations (2003) (45)
The optimal measure of linkage disequilibrium reduces error in association mapping of affection status. (2005) (45)
Linkage studies in spinocerebellar ataxia (SCA). (1980) (45)
ESTIMATION OF PREVALENCE UNDER INCOMPLETE SELECTION. (1965) (45)
Origin of sex chromosome aneuploidy (1988) (45)
The detection of major genes under additive continuous variation. (1967) (45)
Radiation hybrid mapping. (1992) (45)
A Metric Linkage Disequilibrium Map of a Human Chromosome (2003) (44)
Major loci for atopy? (1992) (44)
Image transformation dissociated from visuospatial working memory (1995) (44)
Acrocentric chromosome associations in man. (1976) (44)
Segregation and linkage analyses of 72 leprosy pedigrees. (1985) (43)
Causal analysis of academic performance (1977) (42)
Segregation analysis of balanced pericentric inversions in pedigree data (1986) (42)
Suggestive evidence for genetic linkage between IgE phenotypes and chromosome 14q markers. (1999) (42)
Selection at the ABO locus. (1961) (41)
Demography of inbreeding in Switzerland. (1970) (41)
Standard maps of chromosome 10 (1990) (40)
Genetic structure of Switzerland. (1973) (39)
The Effect of Exposure to the Atomic Bombs on Pregnancy Termination in Hiroshima and Nagasaki: Preliminary Report (1953) (39)
International System for Human Gene Nomenclature (1979) ISGN (1979). (1980) (39)
Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy. (1983) (38)
Likelihood ratios for DNA identification. (1994) (38)
Population structure of Barra (Outer Hebrides) (1976) (38)
Kinship bioassay on hypervariable loci in blacks and Caucasians. (1993) (38)
Discontinuity and quasi‐continuity: Alternative hypotheses of multifactorial inheritance (1970) (37)
An n-allele model for progressive amplification in the FMR1 locus. (1995) (37)
Genetic studies of insulin-dependent diabetes mellitus: segregation and linkage analyses. (1982) (37)
Allelic association under map error and recombinational heterogeneity: a tale of two sites. (1998) (37)
Colchester revisited: a genetic study of mental defect. (1977) (37)
PTC TASTE SENSITIVITY AND ENDEMIC GOITER IN BRAZIL. (1965) (36)
Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis. (2009) (36)
Behavioral, social, and physiological determinants of lipoprotein concentrations. (1977) (36)
Genetic regulation of the kinetics of glucose‐induced insulin release in man Studies in families with diabetic and non‐diabetic probands (1985) (36)
Immunoglobulin E revisited. (1980) (35)
Allelic association with SNPs: Metrics, populations, and the linkage disequilibrium map (2001) (35)
Are the MN blood group maintained by selection? (1959) (33)
Chromosome anomalies as predictors of recurrence risk for spontaneous abortion. (1987) (33)
A chiasma map of man. (1977) (32)
Evidence for an autosomal recessive gene regulating the persistence of the insulin response to glucose in man (1982) (31)
Pingelap and Mokil Atolls: migration. (1971) (31)
Comparison of parametric and nonparametric methods to map oligogenes by linkage. (1997) (31)
Bioassay of Kinship in Populations of Middle Eastern Origin and Controls [and Comments and Replies] (1982) (30)
Blood Factor Association (1966) (30)
Genetic linkage and complex diseases: A comment (1990) (30)
Genetic epidemiology of Lesch-Nyhan disease. (1977) (30)
Investigating the ‘latent’ deficit hypothesis: Age at time of head injury, implicit and executive functions and behavioral insight (2010) (29)
Integration of gene maps: chromosome X. (1994) (29)
Pingelap and Mokil Atolls: achromatopsia. (1972) (29)
Analysis of crossingover in man. (1978) (29)
Linkage analysis of the 5q31–33 candidate region for asthma in 240 UK families (2001) (28)
Heterogeneity of insulin‐dependent diabetes–new evidence (1982) (28)
Pingelap and Mokil Atolls: historical genetics. (1972) (28)
Interaction between the ABO blood group and haptoglobin systems. (1970) (28)
Bioassay of kinship in Micronesia. (1973) (28)
Integration of gene maps: chromosome 1. (1992) (28)
LODs past and present. (1995) (27)
Genetic epidemiology of early onset breast cancer. (1994) (27)
A centromere map of the X chromosome from trisomies of maternal origin (1990) (27)
Population studies on the Aland Islands. II. Historical population structure: inference from bioassay of kinship and migration. (1973) (27)
Leukaemia and transient leukaemia in Down syndrome (1990) (27)
Path analysis of family resemblance in the presence of gene-environment interaction. (1974) (27)
Segregation Analysis of the NIMH Collaborative Study. Family Data on Bipolar Disorder (1992) (27)
Nonparametric tests for linkage with dependent sib pairs. (1995) (26)
Genetics of hyperuricemia in families with gout. (1979) (26)
Genetic epidemiology of hereditary non‐polyposis colorectal cancer syndromes in Modena, Italy: results of a complex segregation analysis (1994) (26)
Report of the Committee on the Genetic Constitution of Chromosome 1. (1978) (26)
Increased reliability for the determination of the carrier state in phenylketonuria. (1961) (26)
Family studies of non-insulin-dependent diabetes mellitus in South Indians (1994) (26)
Tables for Testing Significance in a 2 × 2 Contingency Table (1964) (26)
Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates. (1962) (26)
Resolution of linkage for irregular phenotype systems. (1981) (26)
Exclusion from proximal 11q of a common gene with megaphenic effect on atopy (1995) (25)
Transmission of breast cancer ‐ a controversy resolved (1992) (25)
Kinship, information and biological distance. (1975) (25)
The genetic susceptibility to insulin‐dependent diabetes mellitus: Combined segregation and linkage analysis (1985) (25)
Multilocus recombination frequencies. (1984) (25)
Mapping oligogenes for atopy and asthma by meta-analysis (2000) (25)
Bioassay of kinship in a South American Indian population. (1973) (24)
Estimation of demographic parameters from isolation by distance. (1982) (24)
Trials of the beta model for complex inheritance. (1996) (23)
Genetic Load Expressed as Fetal Death in Cattle (1963) (23)
Genetics of acheiropodia (the handless and footless families of Brazil). VI. Formal genetic analysis. (1975) (23)
Abstracts of workshop presentations (Part 13 of 13) (1985) (23)
Segregation and linkage analysis of 40 multiplex multiple sclerosis families. (1981) (23)
Into the post-HapMap era. (2008) (23)
A sequence-based integrated map of chromosome 22. (2001) (22)
Genes for intelligence on the X chromosome. (1992) (22)
Commingling in distributions of lipids and related variables. (1977) (22)
Recurrence risks in complex inheritance with special regard to pyloric stenosis. (1977) (22)
Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes (2007) (22)
ISOLATION BY DISTANCE IN NEW GUINEA AND MICRONESIA (1970) (22)
Neural tube malformations: complex segregation analysis and calculation of recurrence risks. (1979) (22)
Isolation by distance in Japan and Sweden compared with other countries. (1969) (21)
An Attempt to Map Two Genes for Tuberous Sclerosis Using Novel Two‐Point Methods a (1991) (21)
Large deviations in the distribution of rare genes. (1973) (21)
Alternative bioassays of kinship between loci. (1988) (21)
Multipoint mapping and the emperor's clothes (1988) (21)
Genetic markers in atherosclerosis: a review. (1976) (21)
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis (2000) (21)
Genetic and environmental determinants for lipoprotein concentrations in blood. (2009) (20)
Effects of single SNPs, haplotypes, and whole‐genome LD maps on accuracy of association mapping (2007) (20)
An Investigation of FRAXA Intermediate Allele Phenotype in A Longitudinal Sample (2006) (20)
Abstracts of workshop presentations (Part 2 of 16) (1987) (20)
Refined Association Mapping for a Quantitative Trait: Weight in the H19‐IGF2‐INS‐TH Region (2006) (20)
Significance of genetic factors for the plasma insulin response to glucose in healthy subjects (1976) (20)
Genome scanning by composite likelihood. (2007) (20)
Inter-rater reliability of the Dysexecutive Questionnaire (DEX): Comparative data from non-clinician respondents—all raters are not equal (2011) (20)
Bioassay of kinship in northwestern Europe* (1977) (20)
Estimation of haplotype frequencies. (2008) (19)
Abstracts of workshop presentations (Part 6 of 16) (1987) (19)
Problems and methods in the genetics of primitive groups. (1968) (19)
Mode of processing and hemisphere differences in the judgement of musical stimuli. (1989) (19)
The Genetic Load Due to Mother-Child Incompatibility (1960) (19)
Sequential test for linkage between cystic fibrosis of the pancreas and the MNS locus. (1956) (18)
The use of map functions in multipoint mapping. (1987) (18)
Reduction of physical assignments to a standard lod table: Chromosome 1 (1981) (18)
GENETICS OF INTERRACIAL CROSSES (1966) (18)
Genetic and environmental determinants of periodontal disease. (1979) (18)
THE RISK FACTORS FOR ARRHYTHMIC DEATH IN A SAMPLE OF MEN FOLLOWED FOR 20 YEARS (1988) (18)
Linkage analysis of markers on chromosome 11q13 with asthma and atopy in a United Kingdom population. (2000) (18)
Candidate Gene and Mutational Analysis in Asthma and Atopy (1999) (18)
FRAXA and FRAXE: evidence against segregation distortion and for an effect of intermediate alleles on learning disability. (1998) (17)
Surveillance of Down's syndrome as a paradigm of population monitoring. (1976) (17)
Population structure of the ABO blood groups in Switzerland. (1968) (17)
Analysis of family resemblance for immunoglobulin M, G and A levels. (1981) (17)
Achromatopsia in Pingelap Islanders. Study of a genetic isolate. (1971) (17)
GENETIC EPIDEMIOLOGY OF HEARING IMPAIRMENT IN GENETICS OF HEARING IMPAIRMENT (1991) (17)
Path Analysis of Quantitative Inheritance (1980) (16)
Determinants of blood pressure in Japanese-American families (1980) (16)
Tests of hypotheses on recombination frequencies. (1985) (16)
Topology of kinship in Micronesia. (1973) (16)
The risk factors for arrhythmic death in a sample of men followed for 20 years. (1988) (16)
Implicit cognition is impaired and dissociable in a head-injured group with executive deficits (2006) (16)
SMALLPOX AND THE ABO BLOOD GROUPS IN BRAZIL. (1964) (16)
Population genetics and disease control. (1971) (16)
Causal analysis of family resemblance. (1979) (16)
Evolutionary dynamics of the FMR1 locus (1995) (15)
The Lp lipoprotein in Japanese (1978) (15)
Clans as Genetic Barriers1 (1971) (15)
Pingelap and mokil atolls: genealogy. (1971) (15)
Toward positional cloning with SNPs. (2002) (14)
Heterogeneity between populations for multifactorial inheritance of plasma lipids. (1983) (14)
Efficiency of lod scores for representing multiple locus linkage data (1985) (14)
Genetic effects of cumulative x irradiation on the secondary sex ratio of the laboratory rat. (1968) (14)
Genetic epidemiology of an institutionalized cohort of mental retardates (1978) (14)
Segregation analysis of complex phenotypes: an application to schizophrenia and auditory P300 latency. (1994) (14)
Genetic linkage and spinocerebellar ataxia. (1978) (14)
Segregation analysis of colorectal cancer in Northern Ireland. (1995) (14)
The Evolutionary Relationships of Two Populations: A Study of the Guaymi and the Yanomama [and Comments and Reply] (1979) (13)
Segregation analysis of complex phenotypes: An application to schizophrenia and auditory P300 latency (1993) (13)
Family resemblance for fasting blood glucose in a population of Japanese Americans (1983) (13)
Malformations in northeastern Brazil. (1965) (13)
Genetic epidemiology of Menkes disease (1986) (13)
Kinship and Inbreeding in Populations of Middle Eastern Origin and Controls (1982) (13)
Abstracts of workshop presentations (Part 1 of 13) (1985) (13)
Transmission probabilities are not correctly implemented in the computer program POINTER. (1991) (13)
An integrated map of chromosome 9 (1995) (13)
Population structure of blood groups in Central and South American Indians. (1970) (13)
A retrospective collaboration on chromosome 5 by the International Consortium on Asthma Genetics (COAG) (2001) (13)
Studies on locus content mapping. (1996) (13)
Genetic epidemiology of coeliac disease (1984) (12)
Sex effect on intelligence and mental retardation (1974) (12)
HLA-linked and unlinked determinants of multiple sclerosis (2004) (12)
Data and theory for a revised chiasma map of man (2004) (12)
Cultural and biological inheritance of plasma lipids. (1983) (12)
THE EFFECT OF EXPOSURE OF PARENTS TO THE ATOMIC BOMBS ON THE FIRST GENERATION OFFSPRING IN HIROSHIMA AND NAGASAKI:PRELIMINARY REPORT (1953) (12)
Complex segregation analysis of diabetes mellitus. (1979) (12)
Inference in population structure studies. (1971) (12)
Gene maps and location databases (1991) (12)
Multiplex families with two or more probands. (1968) (11)
Meta-analysis and retrospective collaboration: two methods to map oligogenes for atopy and asthma. (1999) (11)
GENETIC EFFECTS OF CUMULATIVE IRRADIATION ON PRENATAL AND EARLY POSTNATAL SURVIVAL IN THE RAT. (1964) (11)
Cosmopolitan linkage disequilibrium maps (2005) (11)
A Study of the Su Alleles in Northeastern Brazil * (1966) (11)
Episodic memory dysfunction during sodium amytal testing of epileptic patients in relation to posterior cerebral artery perfusion. (1996) (11)
A Tournament of Linkage Tests in Complex Inheritance (2001) (11)
Data on linkage of ovalocytosis and blood groups. (1955) (11)
Genetic Evidence Confirming the Localization of Sutter in the Kell Blood‐Group System (1965) (10)
Cytogenetic surveillance of spontaneous abortions. (1983) (10)
Abstracts of workshop presentations (Part 9 of 13) (1985) (10)
Resolution of cultural and biological inheritance by path analysis: Corrigenda and reply to Goldberger letter. (1978) (10)
Impaired self-awareness after traumatic brain injury: inter-rater reliability and factor structure of the Dysexecutive Questionnaire (DEX) in patients, significant others and clinicians (2014) (10)
Haplotypic determinants of instability in the FRAX region: Concatenated mutation or founder effect? (2001) (10)
Recombination, interference and sequence: comparison of chromosomes 21 and 22 (2002) (10)
Abstracts of workshop presentations (Part 12 of 16) (1987) (10)
Statistical and genetic aspects of quality control for DNA identification (1995) (10)
Possible linkages (lod score over 1.5) and a tentative map of the Jk-Km linkage group. (1978) (10)
Genetic epidemiology, genetic maps and positional cloning. (2003) (10)
Linkage in man: Pelger's nuclear anomaly, taste, and blood groups. (1954) (10)
The J substance of cattle. VI. Multiple alleles at the J locus. (1962) (10)
An inferred chiasma map of Drosophila melanogaster (1976) (10)
DNA in Court (1993) (10)
Hippocratic or hypocritic: Birth pangs of an ethical code (1998) (10)
A cytogenetic study of 47, XXY males of known origin and their parents (1988) (10)
Abstracts of meeting presentations (Part 11 of 11) (1984) (10)
An exact linkage test for multiple case families. (1983) (9)
Genetic mapping of the 21-hydroxylase locus: estimation of small recombination frequencies. (1988) (9)
Determinants of plasma uric acid (1979) (9)
Relation between homozygous viability and average dominance in Drosophila melanogaster. (1968) (9)
Genetic counseling in sex linkage. (1979) (9)
A Comparison of Methods to Detect Recombination Hotspots (2008) (9)
Relation between homozygous viability and average dominance in Drosophila melanogaster. (1968) (9)
Physical mapping by multiple pairwise analysis. (1992) (9)
Trials of structural exploratory data analysis. (1982) (9)
Estimation of Gene Frequencies in the MN System (1968) (9)
Abstracts of workshop presentations (Part 12 of 13) (1985) (9)
Immunoglobulins in the Eastern Carolines. (1973) (9)
Pingelap and Mokil Atolls: anthropometrics. (1972) (8)
Microdeletions in FMR 2 may be a significant cause of premature ovarian failure (1999) (8)
Biological and cultural determinants of immunoglobulin levels in a Brazilian population with Chagas' disease (2004) (8)
A twin study of intelligence in Russia (1975) (8)
Integration of gene maps: updating chromosome 1 (1995) (8)
Erythrocyte catechol-O-methyltransferase activity: genetic analysis in nuclear families with one child affected by Down syndrome. (1985) (8)
Abstracts of workshop presentations (Part 15 of 16) (1987) (8)
Significance of maximal lods (1991) (7)
Abstracts of workshop presentations (Part 10 of 16) (1987) (7)
Human X-Chromosome Arm Ratios and Percentages of Total Complement Length. (1961) (7)
A formal genetic analysis of the HL-A system. (1973) (7)
A multimetric approach to analysis of genome-wide association by single markers and composite likelihood (2008) (7)
Fifty years of genetic epidemiology, with special reference to Japan (2006) (7)
Race, height, and blood pressure in Northeastern Brazil. (1983) (7)
Abstracts of meeting presentations (Part 2 of 11) (1982) (6)
Origin of teratomas and twins (1986) (6)
Heterogeneity in nonsyndromal congenital glaucoma. (1982) (6)
APC intragenic haplotypes in familial adenomatous polyposis (1996) (6)
A genetics program library (1969) (6)
Genetic epidemiology of duchenne muscular dystrophy in Japan: Classical segregation analysis (1987) (6)
Kinship and inbreeding on Namu Atoll (Marshall Islands). (1972) (6)
Allelic association discriminates draft orders (2001) (6)
Kinship mapping of multilocus systems (2004) (6)
International Genetic Epidemiology Society: Commentary on Darkness in El Dorado by Patrick Tierney (2001) (6)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
A linkage tournament: affection status, parametric analysis, multivariate traits, and enhancements to variance components and relative pairs (2002) (6)
Hybridity effect on mortality. (1974) (6)
Counting algorithms for linkage (1990) (6)
Segregation and linkage analysis. (1982) (6)
Limb Girdle Muscular Dystrophy Type 2A (CAPN3): Mapping Using Allelic Association (1998) (6)
Population structure and historical genetics of isolates. (1973) (6)
Discussion Session 4 (1998) (6)
Mapping a gene for rheumatoid arthritis on chromosome 18q21 (2007) (6)
Diseases determined by major genes. (1979) (6)
Genetic aspects of population policy (1999) (5)
Unsolved Problems in Genetic Epidemiology (1999) (5)
Ahaptoglobinemia in northeastern Brazil. (1969) (5)
Meta‐analysis in complex diseases (1995) (5)
Familial determinants of blood pressure in Northeastern Brazil (1980) (5)
Likely linkage: Inv with Jk (1977) (5)
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2. (1985) (5)
Quantitative scores for asthma and atopy (1998) (5)
Association of the Gln 27 beta 2-adrenoceptor polymorphism and IgE variability in asthmatic families. (1997) (5)
Estimation of polymorphism in quantitative measurements on homologous pairs of human chromosomes. (1978) (5)
Abstracts of meeting presentations (Part 8 of 11) (1984) (5)
Quantitative hemagglutination in the ABO system. (1969) (5)
Segregation analysis of ovarian cancer using diathesis to include other cancers (1997) (5)
Abstracts of meeting presentations (Part 10 of 11) (1984) (5)
Transition matrices with mutation. (1980) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Combination of Linkage Evidence in Complex Inheritance (2001) (4)
Blood groups and haptoglobins in the Eastern Carolines. (1973) (4)
The future of genetic epidemiology. (1992) (4)
Positive association in the absence of linkage suggests a minor role for the glucokinase gene in the pathogenesis of Type 2 (non-insulin-dependent) diabetes mellitus amongst South Indians (1993) (4)
History of genetic mapping (2004) (4)
Pingelap and Mokil Atolls: clans and cognate frequencies. (1972) (4)
Residual family resemblance for PTC taste sensitivity (1977) (4)
Pingelap eye disease. (1970) (4)
Molecular biology and human diversity: Kinship, inbreeding, and matching probabilities (1996) (4)
Abstracts of workshop presentations (Part 3 of 16) (1987) (4)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
Cosmopolitan linkage disequilibrium (2005) (4)
Isolation by Distance (2001) (4)
Stability and haplotype analysis of the FRAXE region (2000) (4)
Mapping quantitative effects of oligogenes by allelic association (2002) (4)
Prediction of genetic risks from segregation analyses of morbid risks. (1994) (4)
The AD1 locus in familial Alzheimer disease (1992) (4)
Methods in Genetic Epidemiology (Contributions to Epidemiology and Biostatistics). (1985) (4)
Blocks of Limited Haplotype Diversity (2007) (4)
Epidemiology and genetics of endemic goiter. II. Genetic aspects. (1982) (4)
Abstracts of workshop presentations (Part 1 of 16) (1987) (4)
Genetic linkage analysis of atopic disease (1994) (4)
Abstracts of workshop presentations (Part 7 of 16) (1987) (4)
Genetic aspects of hemophilias A and B in Rio Grande do Sul, Brazil. (1971) (4)
Individual disease risk and multimetric analysis of Crohn disease (2008) (4)
Academic performance in Hawaii. (1976) (3)
Abstracts of workshop presentations (Part 11 of 13) (1985) (3)
Evidence against the reported linkage of phosphoglucomutase (PGM) and phenylthiocarbamide-tasting (PTC). (1968) (3)
Abstracts of workshop presentations (Part 8 of 16) (1987) (3)
Disomic locus content mapping. (1994) (3)
A Study of the S^u Alleles in Northeastern Brazil (1966) (3)
Genetic structure of northeastern brazilian populations (1971) (3)
Complete abolition of reading and writing ability with a third ventricle colloid cyst: implications for surgical intervention and proposed neural substrates of visual recognition and visual imaging ability (2013) (3)
DNA IDENTIFICATION. AUTHORS' REPLY (1996) (3)
Estimation of the inbreeding coefficient from ABO blood-group gene frequencies. (1970) (3)
Effects of inbreeding on mortality. (1966) (3)
4. Pairs of Relatives (1982) (3)
Abstracts of workshop presentations (Part 4 of 16) (1987) (3)
The incidence of cystic fibrosis in Hawaii. (1968) (3)
Epidemiology and genetics of endemic goiter. I. Epidemiological aspects. (1983) (3)
Characteristics of a linkage heterogeneity test. (1978) (3)
Analysis of family resemblance and group differences. (1975) (3)
Genome-wide association mapping under the Malecot model and composite likelihood (2007) (3)
Genetics and social structure: Mathematical structuralism in population genetics and social theory. (1975) (3)
Empirical recurrence risks in facial clefts. (1975) (3)
Genetics without frontiers (1998) (2)
Abstracts of workshop presentations (Part 11 of 16) (1987) (2)
Linkage disequilibrium in human populations (vol 100, pg 6069, 2003) (2003) (2)
Chapter 10 – Human Behavioral Genetics (1972) (2)
Hardy-Weinberg quality control. (1999) (2)
Pitfalls and Prospects in Genetic Epidemiology of Cancer (1991) (2)
Darkness in El Dorado: Human genetics on trial (2001) (2)
DNA Forensic Science 1995 (1995) (2)
Abstracts of workshop presentations (Part 14 of 16) (1987) (2)
Recollections of James Neel. (2003) (2)
Abstracts of workshop presentations (Part 4 of 13) (1985) (2)
A New Rh Allele, ryn (R‐1,2,w3,w4) (1967) (2)
Hereditary genius: a centennial problem in resolution of cultural and biological inheritance. (1980) (2)
Abstracts of workshop presentations (Part 5 of 16) (1987) (2)
5. Outbreeding Indicators Not Responsive to Inbreeding (1967) (2)
Allelic association in the FRAX region (2000) (2)
Foundations of genetic epidemiology (1986) (2)
Mapping quantitative effects of oligogenes by allelic association. (2002) (2)
The future of gene mapping. (1997) (2)
Genetics of interracial crosses in Hawaii. (1967) (2)
[Segregation analysis of myotonia atrophica]. (1970) (2)
10. Genetic Risks (1982) (1)
Abstracts of workshop presentations (Part 7 of 13) (1985) (1)
Genetics laboratory exercises. (1956) (1)
Alternative approaches to population structure (2005) (1)
Human genetics. A selection of insights (1980) (1)
Complex segregation analysis of the locus for beta-aminoisobutyric acid excretion (BAIB) (1981) (1)
Refined association mapping of a causal site for a quantitative trait: weight in the H19-IGF2-INS-TH region (2006) (1)
Susceptibility Loci Regulating Total Serum IgE Levels , Bronchial Hyperresponsiveness , and Clinical Asthma Map to Chromosome 5 q * (1)
Abstracts of workshop presentations (Part 9 of 16) (1987) (1)
Genetic structure of forensic populations. (1992) (1)
Linkage and Allelic Association (2004) (1)
[Genetic factors involved in asthma and atopy. Studies in British families]. (2000) (1)
Fundamentals of genetic epidemiology, M. J. Khoury, T. H. Beaty, and B. H. Cohen, New York: Oxford University Press, 1993, 383 pages, $55.00 (1994) (1)
Genetic analysis workshop II: Combined segregation, linkage, and association analysis (1984) (1)
Applicability of the Rao mapping function. (1995) (1)
Linkage and association. (1984) (1)
Genetic epidemiology in pedigrees kinship and path analysis (1979) (1)
Abstracts of meeting presentations (Part 6 of 11) (1984) (1)
Genetic studies on atopy and asthma in Wessex (1995) (1)
Abstracts of workshop presentations (Part 6 of 13) (1985) (1)
Bivalent alleles. (1966) (1)
Abstracts of workshop presentations (Part 5 of 13) (1985) (1)
Abstracts of workshop presentations (Part 2 of 13) (1985) (1)
The future of human population genetics. (1972) (1)
Abstracts of workshop presentations (Part 16 of 16) (1987) (1)
The genetic structure of populations (1973) (1)
Abstracts of meeting presentations (Part 9 of 11) (1984) (1)
Recent Developments in Genetic Epidemiology (1993) (1)
Familial cancer control (ESO monographs), W. Weber (Ed.). Springer-Verlag, Berlin Heidelberg New York (1992), ISBN: 3-540-55570-60 (1993) (1)
Dominant spinocerebellar ataxia: genetic counseling. (1983) (1)
Genetic analysis workshop III: Construction of genetic maps using two‐point lod tables (1985) (1)
Commentary: Growth of beanbag genetics. (2008) (1)
Monomorphism and heterozygosity (1975) (1)
Biology of Brain Dysfunction (1974) (1)
Complex inheritance: the 21st century. (2001) (1)
Editorial: Executive Function(s): Conductor, Orchestra or Symphony? Towards a Trans-Disciplinary Unification of Theory and Practice Across Development, in Normal and Atypical Groups (2018) (1)
Shared environment and cultural inheritance (1987) (1)
Appendix : Statistical Methods / Subject Index (1982) (1)
GENES FOR INTELLIGENCE ON THE X CHROMOSOME. REPLY (1992) (1)
Genetic markers in atherosclerosis : a review complete penetrance (0)
Symposium summaries from cold spring harbor (1964) (0)
Subject Index, Vol. 29, 1979 (1979) (0)
Integration of gene maps: mouse chromosome X (1995) (0)
Genetic epidemiology. (1997) (0)
Quantitative hemagglutination in the ABO system. (1969) (0)
A Genetic StudyofCleft LipandPalate inHawaii. II.ComplexSegregation Analysis andGenetic Risks (1974) (0)
Subject Index, Vol. 31, 1981 (1981) (0)
Letter: Controversial issues in human population genetics. (1974) (0)
MINISTRY AND THE RETARDED (1965) (0)
Computer applications in population studies (1971) (0)
Memorandum from Newton E. Morton (on outline of a program in medical genetics, with special reference to the first year, 1956-57) (1956) (0)
Extension of the association probability to a quantitative trait. The 55rd Annual Meeting of The American Society of Human Genetics (2005) (0)
3. Sociological Factors (1967) (0)
Acknowledgement to the Reviews (1998) (0)
Neural tubemalformations: complex segregation analysis andcalculation ofrecurrencerisks1 (1979) (0)
Honolulu Heart Study: discussion. (1984) (0)
[Untitled Newton E. Morton lab notebook] (pages 43-70) (1956) (0)
Infectious Disease and Host–Pathogen Evolution: Genetic Epidemiology of Infectious Diseases: The First Half-Century (2004) (0)
10. References / Monographs In Human Genetics (1967) (0)
Title Page / Contents / Preface (1982) (0)
Computer applications in genetics : proceedings of a conference (1969) (0)
Contents, Vol. 15, 1965 (1965) (0)
Catalog of mapped human gene markers. (1980) (0)
Letter from Newton E. Morton to Ira. R. Telford (1958) (0)
Title Page / Index / Acknowledgments (1967) (0)
The genetics of asthma. Quantitative scores for asthma and atopy. (1998) (0)
[Untitled Newton E. Morton lab notebook] (pages 18-42) (1956) (0)
Response to Carothers' letter. (1979) (0)
Atopy phenotype. (1998) (0)
Letter to the Editors: Tests of order in multipoint linkage (1987) (0)
A history of association mapping. (2007) (0)
Abstracts of workshop presentations (Part 13 of 16) (1987) (0)
A CombinedSegregation andLinkageAnalysis ofInsulin-dependent Diabetes Mellitus (1987) (0)
Phenodeviants and Genetic Homeostasis. (1961) (0)
Likelihood ratios forDNA identification (population structure/DNA typing/forensic science) (1994) (0)
Chapter VIII Genetics of Muscular Dystrophy (1963) (0)
Brief Communication Immunoglobulin E Revisited (2006) (0)
SNP-based haplotypes and LD blocks in the fragile X region (2003) (0)
Abstracts of workshop presentations (Part 8 of 13) (1985) (0)
Population genetics of mental illness. (1967) (0)
8. Congenital Malformations (1967) (0)
Index rerum ad. Vol. 19 (1969) (0)
Left lip and palate-recurrence risk and genetic counseling. (1973) (0)
Professor Cedric B. Smith, pioneer in statistical genetics: Died January 10, 2002, at the age of 84 (2002) (0)
7. Population Structure (1982) (0)
3. Genes in Individuals (1982) (0)
Contents, Vol. 46, 1987/ Title Page / Table of Contents (1987) (0)
Optimal use of linkage disequilibrium, haplotypes, and integrated maps for positional cloning (2004) (0)
From Molecular Science to the Treatment of Allergy (1999) (0)
James Van Gundia Neel, papers, ca. 1935-1999 (2014) (0)
An Introduction to Probability and its Applications (1958) (0)
Statistics and truth (1991) (0)
Meta‐analysis for complex inheritance. (1998) (0)
Abstracts of meeting presentations (Part 1 of 11) (1982) (0)
Index rerum ad Vol. 15 (1965) (0)
Abstracts of meeting presentations (Part 7 of 11) (1984) (0)
9. Recapitulation and Conclusions (1967) (0)
8. Frequency, Fitness and Mutation (1982) (0)
4. Medical Factors (1967) (0)
A new Rh allele, gamma-yn (R-1,2,w3,w4). (1967) (0)
GENETIC EFFECTS OF CUMULATIVE IRRADIATION IN RATS. Technical Progress Report, 1960 (1959) (0)
A SEARCH FOR NATURAL SELECTION. MAGNITUDE OF NONBINOMIAL VARIATION IN FAMILY DATA. (1965) (0)
Natural Selection onPolymorphisms in Northeastern Brazil (1966) (0)
ATOPY PHENOTYPE. AUTHOR'S REPLY (1998) (0)
Contents, Vol. 23, 1973 (1973) (0)
A Unified ModelforComplexSegregation Analysis (1983) (0)
Head Injury Rates in a UK Prison Population : A Cause for Concern (2005) (0)
Inference in population structure studies. (1971) (0)
Emotion recognition and eye tracking of static and dynamic facial affect: A comparison of individuals with and without traumatic brain injury (2022) (0)
LD, FRAX and sequence-based maps (2001) (0)
Investigating visual strategies during the recognition of static and dynamic facial affect in TBI and control cohorts (2018) (0)
Implicit Cognition is Impaired and Dissociable after Frontal Head-injury (2005) (0)
Subject index Vol. 46, 1987 (1987) (0)
Contents, Vol. 37, 1984 (1984) (0)
Contents, Vol. 19, 1969 (1969) (0)
Genetic variants at chromosome 5q15 associated with immune-mediated diseases influence ERAP1 and ERAP2 function, expression and isoform profile (2018) (0)
Heritability of IQ. (1976) (0)
2. MATERIAL AND METHODS (1983) (0)
Exploring fixation patterns and social cognition after traumatic brain injury (2018) (0)
Mapping genetic systems by the supratype method (2004) (0)
Theoretical aspects of population genetics (1972) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Contributors and Participants (1982) (0)
Studies on locus content mapping ( radiation hybrids / genetic mapping / map integration / human genome ) (2005) (0)
The likely region of overlap (LRO) method for physical assignment of loci (1979) (0)
Subject Index Vol. 45, 1995 (2004) (0)
Untitled Newton E. Morton lab notebook (1956) (0)
Recurrence risks incomplex inheritance withspecial regard topyloric stenosis1 (1977) (0)
Tests of order in multipoint linkage. (1987) (0)
2. The Genetic Material (1982) (0)
Conference consternation (1997) (0)
Subject index Vol. 40, 1985 (1985) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Contents, Vol. 29, 1979 (1979) (0)
Report of the Committee on the Genetic Constitution of Chromosomes 1 and 2. (1975) (0)
Index autonun ad. Vol. 19 (2004) (0)
Abstracts of meeting presentations (Part 4 of 11) (1979) (0)
Editorial help (2004) (0)
DNA identification. (1996) (0)
Abstracts of workshop presentations (Part 10 of 13) (1985) (0)
The use of SNP-based haplotypes and LD blocks to positionally clone modifying determinants of expansion of the Fragile X triplet repeat (2003) (0)
Book Review:Les Methodes en Genetique Generale et en Genetique Humaine. Roger Huron, Jacques Ruffie (1960) (0)

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