James V. Neel

Q: What Schools Are Affiliated With James V. Neel

James V. Neel is affiliated with the following schools: Indiana University Bloomington, Emory University, Indiana University, College of Wooster, University of Michigan, University of California, San Diego, University of Rochester

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James V. Neel

Biology

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#151

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Genetics

#20

World Rank

#37

Historical Rank

#15

USA Rank

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Why Is James V. Neel Influential?

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According to Wikipedia, James Van Gundia Neel was an American geneticist who played a key role in the development of human genetics as a field of research in the United States. He made important contributions to the emergence of genetic epidemiology and pursued an understanding of the influence of environment on genes. In his early work, he studied sickle-cell disease and thalassemia conducted research on the effects of radiation on survivors of the Hiroshima atomic bombing.

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James V. Neel's Published Works

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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

Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"? (1962) (3264)
Asian affinities and continental radiation of the four founding Native American mtDNAs. (1993) (726)
A clinical, pathological, and genetic study of multiple neurofibromatosis (1956) (579)
Hypocatalasemia: a new genetic carrier state. (1960) (555)
Blood Pressure, Sodium Intake, and Sodium Related Hormones in the Yanomamo Indians, a “No‐salt” Culture (1975) (518)
Genetics of retinoblastoma. (1951) (352)
The "thrifty genotype" in 1998. (2009) (333)
The costs of human inbreeding and their implications for variations at the DNA level (1994) (298)
The Inheritance of Sickle Cell Anemia. (1949) (296)
A study of major congenital defects in Japanese infants. (1958) (294)
The genetics of diabetes mellitus. (1970) (277)
Genetic effects of the atomic bombs: a reappraisal. (1981) (256)
The genetic structure of a tribal population, the Yanomama Indians (1972) (256)
Between two worlds. (1966) (249)
The NAS-NRC twin panel: methods of construction of the panel, zygosity diagnosis, and proposed use. (1967) (246)
STUDIES ON THE XAVANTE INDIANS OF THE BRAZILIAN MATO GROSSO. (1964) (236)
JC virus DNA is present in the mucosa of the human colon and in colorectal cancers. (1999) (222)
The children of parents exposed to atomic bombs: estimates of the genetic doubling dose of radiation for humans. (1990) (216)
Evolutionary health promotion. (2002) (211)
Endemic human T cell lymphotropic virus type II infection among isolated Brazilian Amerindians. (1992) (206)
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America. (1994) (205)
Radiation effects. (1982) (195)
Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America. (1988) (167)
Lessons from a "primitive" people. (1970) (161)
The genetic structure of a tribal population, the Yanomama Indians. XII. Biodemographic studies. (1975) (160)
The effects of inbreeding on Japanese children (1965) (156)
The effects of parental consanguinity and inbreeding in Hirado, Japan. V. Summary and interpretation. (1972) (153)
Standard karyotype of the Norway rat, Rattus norvegicus. Committee for a standardized karyotype of rattus norvegicus. (1973) (151)
Diabetes mellitus: a "thrifty" genotype rendered detrimental by "progress"? 1962. (1999) (136)
Further studies on the Xavante Indians. X. Some hypotheses-generalizations resulting from these studies. (1967) (133)
Congenital malformations, stillbirths, and early mortality among the children of atomic bomb survivors: a reanalysis. (1990) (133)
Malignant tumors during the first 2 decades of life in the offspring of atomic bomb survivors. (1990) (127)
A new inherited abnormality of human hemoglobin. (1950) (122)
Search for mutations altering protein charge and/or function in children of atomic bomb survivors: final report. (1988) (121)
Children of incest. (1966) (116)
The effect of exposure to the atomic bombs on pregnancy termination in Hiroshima and Nagasaki: preliminary report. (1953) (114)
Virologic and genetic studies relate Amerind origins to the indigenous people of the Mongolia/Manchuria/southeastern Siberia region. (1994) (112)
Lessons from a (1970) (111)
The genetic structure of a tribal population, the Yanomama Indians. XV. Patterns inferred by autocorrelation analysis. (1986) (108)
Hypothesis: "Rogue cell"-type chromosomal damage in lymphocytes is associated with infection with the JC human polyoma virus and has implications for oncopenesis. (1996) (108)
Village and tribal genetic distances among American Indians, and the possible implications for human evolution. (1970) (108)
Radiation and the Sex Ratio in Man (1958) (107)
Microevolution in lower Central America: genetic characterization of the Chibcha-speaking groups of Costa Rica and Panama, and a consensus taxonomy based on genetic and linguistic affinity. (1990) (104)
Allelic disequilibrium and allele frequency distribution as a function of social and demographic history. (1997) (103)
"Private" genetic variants and the frequency of mutation among South American Indians. (1973) (98)
Notes on the effect of measles and measles vaccine in a virgin-soil population of South American Indians. (1970) (97)
Regional linguistic and genetic differences among Yanomama indians. (1974) (96)
The genetic structure of a tribal population, the Yanomama Indians. VI. Analysis by F-statistics (including a comparison with the Makiritare and Xavante). (1972) (93)
The comparative radiation genetics of humans and mice. (1990) (92)
The demography of two tribes of primitive, relatively unacculturated American Indians. (1968) (90)
Inbreeding estimation from population data: models, procedures and implications. (1977) (86)
Gene frequencies and microdifferentiation among the Makiritare Indians. IV. A comparison of a genetic network with ethnohistory and migration matrices; a new index of genetic isolation. (1970) (86)
Some further observations on the sex ratio among infants born to survivors of the atomic bombings of Hiroshima and Nagasaki. (1966) (84)
HEMATOLOGIC AND GENETIC STUDY OF THE TRANSMISSION OF THALASSEMIA: (COOLEY'S ANEMIA; MEDITERRANEAN ANEMIA) (1944) (84)
Genetics and the Epidemiology of Chronic Diseases. (1965) (81)
I. Demographic data on two additional villages: Genetic structure of the tribe. (1967) (81)
A new inherited abnormality of hemoglobin and its interaction with sickle cell hemoglobin. (1951) (79)
The rate with which spontaneous mutation alters the electrophoretic mobility of polypeptides. (1986) (78)
The incidence of consanguineous matings in Japan, with remarks on the estimation of comparative gene frequencies and the expected rate of appearance of induced recessive mutations. (1949) (78)
Intratribal genetic differentiation among the Yanomama Indians of southern Venezuela. (1967) (77)
THE CLINICAL DETECTION OF THE GENETIC CARRIERS OF INHERITED DISEASE (1947) (74)
Highly resolving two-dimensional gels for protein sequencing. (1991) (73)
Multivariate analysis of gametic disequilibrium in the Yanomama. (1977) (73)
The study of natural selection in primitive and civilized human populations. (1958) (71)
Cytogenetic "rogue" cells: what is their frequency, origin, and evolutionary significance? (1986) (70)
Search for mutations affecting protein structure in children of atomic bomb survivors: preliminary report. (1980) (70)
The hemoglobin genes: a remarkable example of the clustering of related genetic functions on a single mammalian chromosome. (1961) (70)
THE FREQUENCIES OF HAPTOGLOBIN TYPES IN FIVE POPULATIONS * (1958) (68)
The influence of cultural factors on the demography and pattern of gene flow from the Makiritare to the Yanomama Indians. (1970) (68)
The impact of random and lineal fission of the genetic divergence of small human groups: a case study among the Yanomama. (1981) (67)
The National Academy of Sciences--National Research Council Twin Registry: ten years of operation. (1978) (67)
Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait. (1951) (66)
The Children of atomic bomb survivors : a genetic study (1992) (65)
The inheritance of the sickling phenomenon, with particular reference to sickle cell disease. (1951) (65)
The genetic structure of a tribal population, the Yanomama indians. VII. Anthropometric differences among Yanomama villages. (1972) (64)
The population structure of an Amerindian tribe, the Yanomama. (1978) (64)
MATERNAL RADIATION AND MONGOLISM (1962) (62)
Human serum albumin: twenty‐three genetic variants and their population distribution (1973) (61)
The genetic structure of a tribal population, the Yanomama Indians. IX. Gene frequencies for 18 serum protein and erythrocyte enzyme systems in the Yanomama and five neighboring tribes: nine new variants. (1973) (61)
Genetic analysis of children of atomic bomb survivors. (1996) (60)
Endemic transmission of HTLV type II among Kayapo Indians of Brazil. (1994) (60)
The genetic structure of a tribal population, the Yanomama Indians XI. Gene frequencies for 10 blood groups and the ABH-Le secretor traits in the Yanomama and their neighbors; the uniqueness of the tribe. (1975) (60)
Mortality in the children of atomic bomb survivors and controls. (1974) (58)
Genetic studies on the Ticuna, an eniǵmatic tribe of Central Amazonas (1980) (57)
Demographic structure of a primitive population: a simulation. (1971) (57)
Genetic studies on the Ticuna, an eniǵmatic tribe of Central Amazonas (1980) (57)
Two-dimensional electrophoresis of plasma polypeptides reveals "high" heterozygosity indices. (1983) (57)
Genetic variants of human T-lymphotrophic virus type II in American Indian groups. (1996) (56)
Gene frequencies and microdifferentiation among the Makiritare Indians. I. Eleven blood group systems and the ABH-Le secretor traits: a note on Rh gene frequency determinations. (1970) (56)
Rate of spontaneous mutation at human loci encoding protein structure. (1980) (56)
Inheritance of arachnodactyly, ectopia lentis and other congenital anomalies (Marfan's syndrome) in the E. family. (1949) (56)
On Being Headman (1980) (56)
A cohort-type study of survival in the children of parents exposed to atomic bombings. (1966) (55)
The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia. (1950) (54)
Computer programs for adapting two-dimensional gels to the study of mutation. (1982) (54)
Multiple inherited erythrocyte abnormalities in an American Negro family: hereditary spherocytosis, sickling and thalassemia. (1959) (54)
Frequency of spontaneous and induced "point" mutations in higher eukaryotes. (1983) (53)
Diabetes Mellitus — A Geneticist’s Nightmare (1976) (52)
Genetic structure of a tribal population, the Yanomama Indians. XIII. Dental microdifferentiation. (1976) (52)
A Relation between Larval Nutrition and the Frequency of Crossing over in the Third Chromosome of Drosophila Melanogaster. (1941) (51)
The genetic structure of a tribal population, the Yanomama Indians: II. Eleven blood‐group systems and the ABH‐Le secretor traits * (1972) (49)
The frequency among Japanese of heterozygotes for deficiency variants of 11 enzymes. (1983) (49)
Further studies on hemoglobin C. II. The hematologic effects of hemoglobin C alone and in combination with sickle cell hemoglobin. (1953) (48)
Intra and intertribal genetic variation within a linguistic group: the Ge-speaking indians of Brazil. (1977) (48)
Genetic studies at the Atomic Bomb Casualty Commission-Radiation Effects Research Foundation: 1946-1997. (1998) (48)
Plaque, caries, periodontal diseases, and acculturation among Yanomamö Indians, Venezuela. (1977) (48)
Serum Protein Differences between Africans and Caucasians (1956) (48)
Epidemiologic studies among Amerindian populations of Amazonia. III. Intestinal parasitoses in newly contacted and acculturating villages. (1980) (47)
The population genetics of two inherited blood dyscrasias in man. (1950) (47)
Combinations of hemoglobin G, hemoglobin S and thalassemia occurring in one family. (1957) (47)
Maturation stage and proliferation-dependent expression of dUTPase in human T cells. (1993) (46)
Additional data on the population distribution of human serum albumin genes; three new variants (1973) (46)
Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin. (1953) (45)
The rate of mutation of the gene responsible for retinoblastoma in man. (1951) (45)
Genetic analysis of thirty-three platelet polypeptides detected in two-dimensional polyacrylamide gels. (1986) (45)
Further Studies on the Genetics of Thalassemia. (1947) (45)
THE GENETICS OF HUMAN HAEMOGLOBIN DIFFERENCES: PROBLEMS and PERSPECTIVES * (1956) (45)
The genetic structure of a tribal population, the Yanomama Indians: III. Seven serum protein systems * (1972) (44)
Genetic variation detected by quantitative analysis of end-labeled genomic DNA fragments. (1994) (44)
Rare variants, private polymorphisms, and locus heterozygosity in Amerindian populations. (1978) (44)
Hormonal Adaptation to the Stresses Imposed Upon Sodium Balance by Pregnancy and Lactation in the Yanomama Indians, A Culture Without Salt (1981) (44)
Mortality among the offspring (F1) of atomic bomb survivors, 1946-85. (1991) (44)
Huntington's chorea in Michigan. 2. Selection and mutation. (1959) (43)
A methylated human 9-kb repetitive sequence on acrocentric chromosomes is homologous to a subtelomeric repeat in chimpanzees. (1996) (42)
Identification of genetic variants in erythrocyte lysate by two-dimensional gel electrophoresis. (1984) (42)
Further studies of the Xavante Indians. IX. Immunologic status with respect to various diseases and organisms. (1968) (42)
Further studies on hemoglobin C. I. A description of three additional families segregating for hemoglobin C and sickle cell hemoglobin. (1953) (42)
"Rogue" lymphocytes among Ukrainians not exposed to radioactive fall-out from the Chernobyl accident: the possible role of this phenomenon in oncogenesis, teratogenesis, and mutagenesis. (1992) (41)
A PROSPECTUS FOR GENETIC STUDIES FOF THE AMERICAN INDIAN. (1964) (41)
Gene frequencies and microdifferentiation among the Makiritare Indians. II. Seven serum protein systems. (1970) (41)
Migration and genetic infrastructure of the Central American Guaymi and their affinities with other tribal groups. (1982) (41)
Probability of founder effect in a tribal population. (1978) (41)
Separation of allelic variants by two-dimensional electrophoresis. (1982) (41)
The frequency in Japanese of genetic variants of 22 proteins (1977) (41)
High yield of restriction fragment length polymorphisms in two-dimensional separations of human genomic DNA. (1995) (40)
CHAPTER 9 – Adapting Two-Dimensional Gel Electrophoresis to the Study of Human Germ-Line Mutation Rates* (1984) (40)
A Study of a Case of High Mutation Rate in Drosophila Melanogaster. (1942) (40)
Data base analysis of protein expression patterns during T-cell ontogeny and activation. (1993) (40)
Further studies of the Xavante Indians. 8. Some observations on blood, urine, and stool specimens. (1968) (39)
Identifying risk factors for diabetes in first degree relatives of non-insulin dependent diabetic patients. (1982) (39)
The Effect of Exposure to the Atomic Bombs on Pregnancy Termination in Hiroshima and Nagasaki: Preliminary Report (1953) (39)
The effect of inbreeding on mortality and morbidity in two Japanese cities. (1962) (38)
OBSERVATIONS ON THE NATURAL HISTORY OF HYPERURICEMIA AND GOUT. I. AN EIGHTEEN YEAR FOLLOW-UP OF NINETEEN GOUTY FAMILIES. (1964) (38)
The immunoglobulin allotypes (Gm and Km) of twelve Indian tribes of Central and South America. (1978) (38)
Further studies on the Xavante Indians. 3. Blood groups and ABH-Lea secretor types in the Simões Lopes and São Marcos Xavantes. (1967) (38)
Chromosome aberrations among the Yanomamma Indians. (1970) (37)
A genetic study of multiple polyposis of the colon with an appendix deriving a method of estimating relative fitness. (1955) (37)
Health and disease in unacculturated Amerindian populations. (1977) (37)
Hemagglutinins in uterine secretions. (1958) (37)
The genetic structure of a tribal population, the Yanomama Indians: IV. Eleven erythrocyte enzymes and summary of protein variants * (1972) (37)
Physician to the Gene Pool: Genetic Lessons and Other Stories (1994) (37)
Indirect estimates of mutation rates in tribal Amerindians. (1978) (37)
Description and validation of a method for simultaneous estimation of effective population size and mutation rate from human population data. (1989) (36)
The newly characterized colicin Y provides evidence of positive selection in pore-former colicin diversification. (2000) (36)
Multiple-locus departures from panmictic equilibrium within and between village gene pools of Amerindian tribes at different stages of agglomeration. (1983) (35)
Two-dimensional gel studies of genetic variation in the plasma proteins of Amerindians and Japanese (2004) (35)
The frequency in Japan of carriers of the rare "recessive" gene causing acatalasemia. (1961) (35)
Similarity of spontaneous germinal and in vitro somatic cell mutation rates in humans: implications for carcinogenesis and for the role of exogenous factors in "spontaneous" germinal mutagenesis. (1992) (35)
Amino acid substitutions in inherited albumin variants from Amerindian and Japanese populations. (1987) (35)
Albumin Yanomama‐2, a ‘private’ polymorphism of serum albumin (1974) (35)
Syndrome X: Is it for real? (1998) (35)
THE AUTOPSY FINDINGS (1956) (34)
The effects of parental consanguinity and inbreeding in Hirado, Japan. II. Physical development, tapping rate, blood pressure, intelligence quotient, and school performance. (1970) (34)
The genetic structure of a tribal population, the Yanomama Indians. XIV. Clines and their interpretation. (1976) (34)
High titers of antibodies to two human polyomaviruses, JCV and BKV, correlate with increased frequency of chromosomal damage in human lymphocytes. (1996) (33)
The phylogenic relationships of some Indian tribes of Central and South America. (1969) (33)
Analysis of human peripheral blood T cells and single-cell-derived T cell clones uncovers extensive clonal CpG island methylation heterogeneity throughout the genome. (1999) (33)
Serum proteins, hemoglobins and erythrocyte enzymes of Brazilian Cayapo Indians. (1972) (33)
A two‐dimensional electrophoresis‐related laboratory information processing system: Spot matching (1991) (33)
Mathematical methods for population genetics (1950) (32)
Estimation of mutation rates based on the analysis of polypeptide constituents of cultured human lymphoblastoid cells. (1988) (32)
THE FREQUENCY OF THALASSEMIA (1945) (32)
The detection of the genetic carriers of hereditary disease. (1949) (32)
The genetic structure of a tribal population (1975) (32)
Myotonia. Thomsen's Disease (Myotonia Congenita), Paramyotonia, and Dystrophia Myotonica. A Clinical and Heredobiologic Investigation.Eivind Thomasen (1951) (32)
Gene frequencies and microdifferentiation among the Makiritare Indians. 3. Nine erythrocyte enzyme systems. (1970) (31)
STUDIES ON HYPERURICEMIA. II. A RECONSIDERATION OF THE DISTRIBUTION OF SERUM URIC ACID VALUES IN THE FAMILIES OF SMYTH, COTTERMAN, AND FREYBERG. (1965) (31)
Symphalangism and tarsal coalitions: a hereditary syndrome. A report on two families. (1969) (31)
Chromosomal breakage in leukocytes of South American Indians. (1973) (30)
Histocompatibility antigens in a genetically isolated American indian tribe. (1973) (30)
Two-dimensional electrophoretic analysis of erythrocyte membranes. (1982) (30)
Unusual blood genetic characteristics among the Ayoreo Indians of Bolivia and Paraguay. (1978) (29)
Quantitative and qualitative genetic variation in two‐dimensional DNA gels of human lymphocytoid cell lines (1995) (28)
Update on the genetic effects of ionizing radiation. (1991) (28)
A phylogeny for the principal alleles of the human phosphoglucomutase-1 locus. (1982) (28)
The frequency in Japanese of genetic variants of 22 proteins: V. Summary and comparison with data on Caucasians from the British Isles (1978) (28)
The genetic structure of a tribal population, the Yanomama Indians. 8. Dermatoglyphic differences among villages. (1973) (28)
The frequency of elevations in the A and fetal hemoglobin fractions in the natives of Liberia and adjacent regions, with data on haptoglobin and transferrin types. (1961) (28)
Founder effect and number of private polymorphisms observed in Amerindian tribes. (1978) (28)
Electrophoretic variants in three Amerindian tribes: the Baniwa, Kanamari, and Central Pano of western Brazil. (1979) (26)
Studies of the inheritance of human ribosomal DNA variants detected in two-dimensional separations of genomic restriction fragments. (1996) (26)
Further studies on the Xavante Indians. II. Some anthropometric, dermatoglyphic, and nonquantitative morphological traits of the Xavantes of Simões Lopes. (1967) (26)
Frequency of thermostability variants: estimation of total "rare" variant frequency in human populations. (1981) (26)
Familial factors in early deaths: Twins followed 30 years to ages 51–61 in 1978 (1981) (26)
Distribution of parasites in the red cells of sickle-cell trait carriers infected with Plasmodium falciparum. (1956) (26)
Implications of the Hiroshima-Nagasaki genetic studies for the estimation of the human "doubling dose" of radiation. (1989) (25)
Panel Discussion on Genetic and Environmental Factors in Human Hypertension (1958) (25)
The frequency in Japanese of genetic variants of 22 proteins (1977) (25)
Epidemiologic studies among Amerindian populations of Amazônia. I. Pyoderma: prevalence and associated pathogens. (1979) (25)
Further studies on the Xavante Indians. VI. The physical status of the Xavantes of Simões Lopes. (1967) (25)
Glucose tolerance in two unacculturated Indian tribes of Brazil (1982) (25)
Differential Fertility and Human Evolution (1972) (25)
The blood groups and secretor types in five potentially fatal diseases of Caucasian children. (1965) (24)
An association, in adult Japanese, between the occurrence of rogue cells among cultured lymphocytes (JC virus activity) and the frequency of "simple" chromosomal damage among the lymphocytes of persons exhibiting these rogue cells. (1998) (24)
Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency. (1960) (24)
Two-dimensional gel electrophoresis of cell proteins in childhood leukemia, with silver staining: a preliminary report. (1982) (24)
When some fine old genes meet a 'new' environment. (1999) (24)
Genetic Effects of the Atomic Bombs (1962) (24)
Changing perspectives on the genetic doubling dose of ionizing radiation for humans, mice, and Drosophila. (1999) (24)
Protein variants in Hiroshima and Nagasaki: tales of two cities. (1988) (23)
Mutation and disease in man. (1978) (23)
Two fast hemoglobin components in Liberian blood samples. (1956) (23)
A Genome Scanning Approach to Assess the Genetic Effects of Radiation in Mice and Humans (2004) (23)
Data pertaining to the population dynamics of sickle cell disease. (1953) (23)
Serum aldosterone and protein-binding variables in Yanomama Indians: a no-salt culture as compared to partially acculturated Guaymi Indians. (1985) (23)
A Second Study of the Survival of a Neutral Mutant in a Simulated Amerindian Population (1978) (23)
The distribution of several blood group genes in Liberia, the Ivory Coast and Upper Volta. (1960) (23)
CONCERNING THE INHERITANCE OF RED HAIR (1943) (22)
Two more "private" polymorphisms of Amerindian tribes: LDHb GUA-1 and ACP1 B GUA-1 in the Guaymi in Panama. (1977) (22)
Analytical Review: Perspectives in the Genetics of Sickle Cell Disease (1952) (22)
An algorithm for comparing two-dimensional electrophoretic gels, with particular reference to the study of mutation. (1986) (22)
Studies on genetic selection in a completely ascertained caucasian population. I. Frequencies, age and sex effects, and phenotype associations for 12 blood group systems. (1971) (22)
Evidence concerning the inadequacy of mutation as an explanation of the frequency of the sickle cell gene in the Belgian Congo. (1955) (22)
Esterase D in South American Indians. (1976) (22)
The JC and BK human polyoma viruses appear to be recent introductions to some South American Indian tribes: there is no serological evidence of cross-reactivity with the simian polyoma virus SV40. (1998) (21)
Thalassaemia in Liberia (1959) (21)
Date on the occurrence of hemoglobin C and other abnormal hemoglobins in some African populations. (1956) (21)
Approaches to Monitoring Human Populations for Mutation Rates and Genetic Disease (1973) (21)
Genetic demography of the amazonian Ticuna Indians (1980) (21)
Microevolution of the Chibcha-speaking peoples of lower Central America: rare genes in an Amerindian complex. (1992) (21)
Minority Populations as Genetic Isolates: The Interpretation of Inbreeding Results (1992) (21)
Studies on genetic selection in a completely ascertained caucasian population. II. Family analyses of 11 blood group systems. (1971) (21)
Human hemoglobin types; their epidemiologic implications. (1957) (21)
The detection of environmental mutagens. (1969) (21)
Genetic effects of atomic bombs. (1981) (21)
Hematologic studies in Hiroshima and a control city 2 years after the atomic bombing. (1949) (20)
The frequency in Japanese of genetic variants of 22 proteins III. Phosphoglucomutase‐1, phosphoglucomutase‐2, 6‐phosphogluconate dehydrogenase, adenylate kinase, and adenosine deaminase (1977) (20)
Gene flow across tribal barriers and its effect among the Amazonian Içana river Indians. (1986) (20)
On some pitfalls in developing an adequate genetic hypothesis. (1955) (20)
Development of molecular approaches to estimating germinal mutation rates. I. Detection of insertion/deletion/rearrangement variants in the human genome. (1989) (20)
Intragenic recombination at the human phosphoglucomutase 1 locus: predictions fulfilled. (1993) (19)
Two recent radiation-related genetic false alarms: leukemia in West Cumbria, England, and minisatellite mutations in Belarus. (1999) (19)
Contribution of familial factors to the occurrence of cancer before old age in twin veterans. (1982) (19)
A nationwide evaluation of multiple congenital abnormalities in Hungary (1988) (19)
The frequency of "rare" protein variants in Marshall islanders and other Micronesians. (1976) (19)
The various types of thyroid malfunction in cretinism and their relative frequency. (1961) (19)
Genetic studies on the congenitally hypothyroid. (1961) (19)
A STATISTICAL STUDY OF THE HEMATOLOGIC VARIABLES IN SUBJECTS WITH THALASSEMIA MINOR (1948) (18)
The Children of Atomic Bomb Survivors (1991) (18)
Cytogenetic Study of the Offspring of Atomic Bomb Survivors, Hiroshima and Nagasaki (1991) (18)
Germ-line gene therapy: another view. (1993) (17)
Reappraisal of studies concerning the genetic effects of the radiation of humans, mice, and Drosophila (1998) (17)
Epidemiologic studies among Amerindian populations of Amazonia. II. Prepvalence of Mansonella ozzardi. (1979) (17)
Is there a difference among human populations in the rate with which mutation produces electrophoretic variants? (1981) (17)
HARDY-WEINBERG EQUILIBRIUM AND PRIMITIVE POPULATIONS. (1965) (16)
Nonrandom distribution of structural mutants in ethylnitrosourea-treated cultured human lymphoblastoid cells. (1988) (16)
Sex linkage, inbreedng, and growth in childhood. (1963) (16)
The Major Ethnic Groups: Diversity in the Midst of Similarity (1981) (16)
Problem of “false positive” conclusions in genetic epidemiology: Lessons from the leukemia cluster near the sellafield nuclear installation (1994) (15)
The inheritance of spondylitis rhizomelique (ankylosing spondylitis) in the K. family. (1950) (15)
The Evolutionary Relationships of Two Populations: A Study of the Guaymi and the Yanomamal (1979) (15)
The Interrelations of Temperature, Body Size, and Character Expression in Drosophila Melanogaster. (1940) (15)
A SIMULATION OF THE FATE OF A MUTANT GENE OF NEUTRAL SELECTIVE VALUE IN A PRIMITIVE POPULATION (1974) (15)
Point substitutions in Japanese alloalbumins. (1989) (15)
THE ARTIFICIAL PRODUCTION AND SIGNIFICANCE OF TARGET CELLS: With Special Reference to Their Occurrence in Thalassemia (Cooley's Erythroblastic Anemia) (1945) (15)
GENETIC HETEROGENEITY IN HUMAN ACATALASIA. (1963) (15)
Frequency and distribution of rare electrophoretic mobility variants in a population of human newborns in Ann Arbor, Michigan (1987) (15)
Studies on the Interaction of Mutations Affecting the Chaetae of Drosophila Melanogaster. I. the Interaction of Hairy, Polychaetoid, and Hairy Wing. (1941) (14)
Familial factors in adenocarcinoma of the colon (1971) (14)
Genetic studies of quantitative variation in a component of human saliva (1963) (14)
Evaluation of the effects of chemical mutagens on man: the long road ahead. (1970) (14)
Children of the atomic bomb survivors: A genetic study (1994) (14)
Man in the tropics: the Yanomama Indians. (1977) (14)
The Pattern of Supernumerary Macrochaetae in Certain Drosophila Mutants. (1940) (14)
The Study of Human Mutation Rates (1952) (13)
Inherited electrophoretic variants detected in a Japanese population with two‐dimensional gels of erythrocyte lysates (1986) (13)
The Evolutionary Relationships of Two Populations: A Study of the Guaymi and the Yanomama [and Comments and Reply] (1979) (13)
Demographic and genetic relationships among Brazilian Wapishana Indians. (1980) (13)
Looking Ahead: Some Genetic Issues of the Future (1997) (13)
Racial studies: academy states position on call for new research. (1967) (13)
A revised estimate of the amount of genetic variation in human proteins: implications for the distribution of DNA polymorphisms. (1984) (13)
Problems in the estimation of the frequency of uncommon inherited traits. (1954) (13)
Report of a workshop on the application of molecular genetics to the study of mutation in the children of atomic bomb survivors (1993) (13)
Some further observations on the effect of inbreeding on mortality in Kure, Japan. (1966) (12)
Implications of some recent developments in hematological and serological genetics. (1954) (12)
THE EFFECT OF EXPOSURE OF PARENTS TO THE ATOMIC BOMBS ON THE FIRST GENERATION OFFSPRING IN HIROSHIMA AND NAGASAKI:PRELIMINARY REPORT (1953) (12)
Private polymorphisms: how many? How old? How useful for genetic taxonomies? (1996) (12)
New studies on the Macushi Indians of northern Brazil. (1984) (12)
Medicine's genetic horizons. (1958) (12)
Frequency of polymorphisms for alleles encoding for liver proteins of domesticated mice. (1985) (12)
Assigning a probability for paternity in apparent cases of mutation. (1981) (12)
Genetic studies of the Macushi and Wapishana Indians (2004) (11)
Congenital Aniridia. (1960) (11)
A pilot study of the use of placental cord blood samples in monitoring for mutational events. (1988) (11)
Control of disease among Amerindians in cultural transition. (1974) (11)
Characteristics of Escherichia coli Serotypes in the Yanomama, a Primitive Indian Tribe of South America (1971) (11)
The frequency in Japanese of genetic variants of 22 proteins: IV. Acid phosphatase, NADP‐isocitrate dehydrogenase, peptidase A, peptidase B and phosphohexose isomerase (1978) (11)
Perspectives in the genetics of sickle cell disease. (1952) (10)
Detection of human somatic cell structural gene mutations by two‐dimensional electrophoresis (1987) (10)
The inheritance and frequency of the MNS factors in the American Negro. (1951) (10)
Biochemical Approaches to Monitoring Human Populations for Germinal Mutation rates: I. Electrophoresis (1983) (10)
A revised indirect estimate of mutation rates in Amerindians. (1986) (10)
The genetic structure of a tribal population, the Yanomama Indians. 1. Introduction. (1972) (10)
The effects of parental consanguinity and inbreeding in Hirado, Japan. 3. Vision and hearing. (1970) (10)
Part 5: Infectious disease among Amerindians. (1982) (10)
The delayed effects of ionizing radiation. (1958) (10)
Genetic Effects of the Atomic Bombs in Hiroshima and Nagasaki (1991) (10)
Some Ethical Issues at the Population Level Raised by ‘Soft’ Eugenics, Euphenics, and Isogenics1 (1999) (10)
Developments in monitoring human populations for mutation rates. (1974) (9)
Bilirubin binding by variant albumins in Yanomama Indians. (1984) (9)
Towards a Better Understanding of the Genetic Basis of Diabetes Mellitus (1976) (9)
A pedigree of multiple polyposis of the colon. (1954) (9)
Social and Scientific Priorities in the Use of Genetic Knowledge (1973) (9)
Average locus differences in mutability related to protein "class": a hypothesis. (1990) (9)
The past and the future in the study of radiation‐induced mutation in the germ‐line of mice and humans (1989) (9)
A system of nomenclature for the varieties of human hemoglobin. (1953) (9)
Quantitative studies on the haptoglobin of apparently healthy adult male twins. (1962) (9)
Extraction of DNA from frozen red blood cells. (1993) (8)
SPECIAL PROBLEMS INHERENT IN THE STUDY OF HUMAN GENETICS WITH PARTICULAR REFERENCE TO THE EVALUATION OF RADIATION RISKS. (1957) (8)
Inherited thermostability variants of seven enzymes in a Japanese population (1985) (8)
Some applications of the principles of genetics to the practice of medicine. (1951) (8)
Approaches to DNA methods for the detection of heritable mutations in humans. (1990) (8)
The Colonel Harlan D. Sanders Award Address for 1998: JC virus and its possible role in oncogenesis. (1999) (8)
Outcome of pregnancy in women exposed to the atomic bomb in Nagasaki. Atomic bomb exposure and the pregnancies of biologically related parents. A prospective study of the genetic effects of ionizing radiation in man (1959) (8)
Dermatoglyphic characters and physique: a correlation study. (1982) (8)
Studies on the potential genetic effects of the atomic bombs. (1956) (8)
Phenotypic variability in mutant characters of Drosophila funebris (1937) (7)
A "disproportion" between the frequency of rare electropmorphs and enzyme deficiency variants in Amerindians. (1984) (7)
The genetics of blood. (1957) (7)
The genetics of juvenile-onset-type diabetes mellitus. (1977) (7)
The human gastrointestinal tract is a reservoir for JC virus infection (1998) (7)
The “ Thrifty Genotype ” in 1998 l (2008) (6)
INHERITED CATARACT IN THE B. GENEALOGY: OCCURRENCE OF DIVERSE TYPES OF CATARACT IN THE DESCENDANTS OF ONE PERSON (1945) (6)
New data on the vision of South American Indians. (1976) (6)
THE BLOOD GROUP POLYMORPHISMS: WHY ARE THEY THERE? (1970) (6)
Studies on the Interaction of Mutations Affecting the Chaetae of Drosophila Melanogaster. II. the Relation of Character Expression to Size in Flies Homozygous for Polychaetoid, Hairy, Hairy Wing, and the Combinations of These Factors. (1943) (6)
Genetic studies of the Macushi and Wapishana Indians (1977) (6)
Dipetalonema perstans and Mansonella ozzardi in Indians of southern Venezuela. (1976) (6)
The meaning of empiric risk figures for disease or defect (1958) (5)
Absence of linkage between the genes responsible for the sickling phenomenon, the MN blood types, and the S-agglutinogen. (1952) (5)
Thoughts on the future of human genetics. (1969) (5)
Are Genetic Factors Involved in Racial and Ethnic Differences in Late-Life Health? (1997) (5)
The Polymorph Mutant of Drosophila melanogaster (1942) (5)
Atomic bomb exposure and the pregnancies of biologically related parents. A prospective study of the genetic effects of ionizing radiation in man. (1960) (5)
Polydactyly of the Second Metatarsal with Associated Defects of the Feet: A New, Simply Inherited Skeletal Deformity. (1963) (5)
Our twenty-fifth. (1974) (5)
Should editorials also be peer-reviewed? (1988) (5)
Genetics and human congenital malformations. (1957) (5)
Failure to demonstrate mutations affecting protein structure or function in children with congenital defects or born prematurely. (1984) (4)
The effect of inbreeding on mortality in Japan. (1962) (4)
Some hereditary diseases having subclinical manifestations in carriers. (1948) (4)
Accuracy of World War II blood typing. (1962) (4)
The natural history of serum uric acid levels in the relatives of patients suffering from gout (1962) (4)
Studies concerning a new inherited abnormality of hemoglobin. (1952) (4)
Unfolding perspectives on the genetic effects of human exposures to radiation. (1990) (3)
Isolation, Migration and Health: The distinction between primary and secondary isolates (1992) (3)
Symposium recent trends of bioanthropological research among lowland South American Indian populations, Miami FL, April 4-7, 1990 (1991) (3)
Hepatitis--Bs antigen in an isolated Indian population of southern Venezuela: a family study. (1979) (3)
Symposium on South American Indians: Introduction (1991) (3)
IV. The detection of carriers of “recessive” genes (1954) (3)
The functions of a department of genetics in a medical school. (1957) (3)
Diversity within an between South American Indian Tribes. (1973) (3)
The circumstances of human evolution. (1976) (3)
A geneticist looks at modern medicine. (1960) (3)
Genetic Structure of a Tribal Population: the Yaonmamo Indians (1974) (3)
Evolutionary perspectives and the new genetics. Proceedings of an international symposium honoring Dr. James V. Neel. Ann Arbor, Michigan, June 17-18, 1985. (1986) (3)
A PEDIGREE OF CLUBFOOT (1950) (3)
New approaches to evaluating the genetic effects of the atomic bombs. (1995) (3)
The Ecumenical Future of Human Genetics (1987) (3)
Microbiological Studies in a Primitive Society: Significance of Escherichia coli from Yanomamö Indians (1970) (2)
Heterozygosity and ethnic variation in Japanese platelet proteins (2004) (2)
The study of natural selection in primitive and civilized human populations. 1958. (1989) (2)
Opportunities for research in human genetics. (1959) (2)
ON EMPHASES IN HUMAN GENETICS (1974) (2)
Abnormal forms of hemoglobin from a genetic point of view. (1956) (2)
Leber's Disease. A Genealogic, Genetic and Clinical Study of 101 Cases of Retrobulbar Optic Neuritis in 20 Danish Familie. Opera Ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis. Volume 10.Ruth Lundsgaard (1950) (2)
Report of the committee on genetic effects of atomic radiation. (1956) (2)
Blood polymorphisms and morphological variability in Brazilian Indians (1994) (2)
The contribution of germinal mutation to human disease. (1979) (2)
REVIEW Evolutionary Health Promotion (2002) (2)
Delayed biomedical effects of the bombs (1985) (2)
Our atomic heritage (1951) (2)
A comparison of gene frequency and anthropometric distance matrices in seven villages of four Indian tribes. (1974) (2)
Some trends in the study of spontaneous and induced mutation in man. (1979) (2)
Analysis of Genetic Variation in Amerindian Sera by 2-D Page (1984) (2)
Some Genetic Aspects of Therapeutic Abortion (1967) (1)
International Commission for Protection against Environmental Mutagens and Carcinogens. Report of a workshop on the application of molecular genetics to the study of mutation in the children of atomic bomb survivors. (1993) (1)
Genetic effects of the atomic bombs. Rejoinder to Dr. de Bellefeuille. (1962) (1)
An open letter to The American Society of Human Genetics: the neglected genetic issue--the why and how of curbing population growth. (1995) (1)
Curt Stern: August 30, 1902-October 23, 1981. (1986) (1)
Guest Comment [on Last Issue's Stressing of Effects of Nuclear Warfare] (1982) (1)
The Yanomamo and the 1960s Measles Epidemic (2001) (1)
no serological evidence of cross-reactivity with the simian polyoma virus SV 40 (1998) (1)
A unified approach to the study of mutation, from bacteria to humans: Some potentialities of the new DNA technologies (1999) (1)
Human population genetics, 1961. (1962) (1)
Book Review:The Etiology of Deaf-Mutism, with Special Reference to Heredity. Harold Lindenov (1950) (1)
The coming of age of genetic counseling. (1973) (1)
Yanomamö : a multidisciplinary study (2009) (1)
How Would Haldane Have Viewed the Societal Implications of Today’s Genetic Knowledge? (1993) (1)
PROCEEDINGS OF THE THIRD INTERNATIONAL CONGRESS OF HUMAN GENETICS, HELD AT THE UNIVERSITY OF CHICAGO, SEPTEMBER 5--10, 1966. (1967) (1)
The Genetic Effects of Human Exposures to Ionizing Radiation (1995) (1)
Proceedings of the Third International Congress of Human Genetics, the University of Chicago, Illinois, U.S.A., September 5-10, 1966 (1967) (1)
GENETICS AND NUTRITION: AN EVOLUTIONARY PERSPECTIVE (1984) (1)
Human mutation rates. (1989) (1)
Prospects for research on schizophrenia. IV. Genetic and environmental factors. Parallels in medicine. (1972) (1)
Marfan's syndrome in the E. family. (1948) (1)
The Future of These Studies (1991) (1)
The feasibility and urgency of monitoring human populations for the genetic effects of radiation: the Hiroshima-Nagasaki experience. (1985) (1)
Symposium on intrauterine diagnosis; held at Indianapolis, Indiana, October 13 and 14, 1970. Introductory remarks. (1971) (0)
Consanguinity as a determinant of pre-productive mortality: A global perspective (1995) (0)
Letter from James V. Neel to Joshua Lederberg (1962) (0)
BLOOD PRESSURE IN THE YANOMAMO INDIANS Table 3 Body Weight , Twenty-four Hour Urine Volume and Excretion of Creatinine in Yanomamo Indians and Control Subjects Urine (0)
THE ANALYSIS OF THE BIRTHWEIGHT DATA (1956) (0)
Ankylosing spondylitis in the K. kindred and the question of an arthritic diathesis. (1948) (0)
Letter from James V. Neel to Walter F. Bodmer (1966) (0)
Physical Anthropology: Comparative Karyology of Primates. Brunetto Chiarelli, Ann L. Koen, and G. Ardito. (1981) (0)
A time of change. (1994) (0)
The study of human mutation rates. Progress report, 1989--1992 (1992) (0)
Models to man establishment of reference points for estimating genetic risk in man (1983) (0)
Twin Concordances in the United States for Early Mortality and Their Variation with Zygosity (1974) (0)
Symposium No. 1: Genetics and society. Introduction by the Chairman. On emphases in human genetics. (1974) (0)
A COMPARISON OF HIROSHIMA AND NAGASAKI (1991) (0)
ANALYSIS OF THE STILLBIRTH DATA (1991) (0)
THE CRITERIA OF RADIATION EMPLOYED IN THE STUDY (1991) (0)
The Biochemistry of Genetics (1955) (0)
Area program in population genetics. Final report, November 1, 1975-August 31, 1982 (1982) (0)
The heredity clinic of the department of human genetics. (1967) (0)
Evaluation oftheEffects ofChemicalMutagensonMan: TheLongRoadAhead* (1970) (0)
Thoughts on the future of human genetics. (1969) (0)
The Children of the Atomic Bomb Survivors: A Genetic Study. James V. Neel , William J. Schull (1991) (0)
Approaches to the genetic analysis of mammalian cells : Michigan conference on genetics (1962) (0)
Heritable Disorders of Connective Tissue (1957) (0)
On Brace's Notion of "Hominid Catastrophism" (1973) (0)
On Brace's Notion of "Hominid Catastrophism" (1973) (0)
Letter from James V. Neel to Ann Landers (1979) (0)
Symposium summaries from cold spring harbor (1964) (0)
The HEMOGLOBINOPATHIES: A Model Genetic System (1965) (0)
Chairman's comments: symposium on environmental mutagenesis. (1982) (0)
[GENETIC HETEROGENITY IN HUMAN ACATALASIA]. (1964) (0)
PROCEDURE FOR CODING GENETICS SHORT-FORM QUESTIONNAIRES (1991) (0)
日本人における22種の蛋白質の遺伝的変異体とその頻度-5-総括および英国白人に関する資料との比較 (1979) (0)
Workshop on genetics of diabetes. (1982) (0)
Biomedical Progenitor: Archibald Garrod and the Individuality of Man . Alexander G. Bearn. Oxford University Press, New York, 1993. xviii, 227 pp., illus. $49.95 or £35. (1994) (0)
[THE FREQUENCY IN JAPAN OF CARRIERS OF THE RARE 'RECESSIVE' GENE CAUSING ACATALASEMIA]. (1963) (0)
Response : Radiation Effects (1982) (0)
Studies of human mutation rates. Progress report, November 1, 1993--October 31, 1994 (1993) (0)
Presidential address: the wonder of our presence here. (1982) (0)
In the beginning... (2000) (0)
Some genetic aspects of therapeutic abortion. (1967) (0)
Some Ethical Problems Created by Advances in Human Genetics. (1973) (0)
The applications of genetics to human problems. (1954) (0)
ANALYSIS OF THE MALFORMATION DATA (1956) (0)
Identification of a DNA fragment which escaped methylation inactivation on the X chromosome by two-dimensional electrophoresis of human genomic DNA (1996) (0)
The Children of Atomic Bomb Survivors. A Genetic Study (1993) (0)
Index rerum ad Vol. 15 (1965) (0)
Genetics and the epidemiology of chronic diseases : A simposium June 17-19, 1963, Ann Arbor Michigan (1965) (0)
Area program in population genetics (1973) (0)
Is there a PGM1 4 allele specific to Amerindian populations? (1980) (0)
Studies of human mutation. Final report, [November 1, 1987--May 31, 1996] (1996) (0)
James Van Gundia Neel 1915. The clinical detection of the genetic carriers of inherited disease. 1947. (1992) (0)
How Much Progress this Time (1983) (0)
Warren Spencer (1898-1969). (1975) (0)
Reviewers of Manuscripts and Books (1970) (0)
Variants of red cell enzymes found in Japanese of Hiroshima and Nagasaki. (1980) (0)
Contents, Vol. 15, 1965 (1965) (0)
The doubling dose of ionizing radiation for drosophilia, mice, and humans (1997) (0)
James Van Gundia Neel 1915 (1992) (0)
Computer algorithms for the detection of mutational events affecting the polypeptides visualized with 2-D polyacrylamide gels. (1985) (0)
Letter from James V. Neel to Arno G. Motulsky (1968) (0)
Studies of human mutation rates (1990) (0)
Hardy-Weinberg Equilibrium and Primitive Populations. (1965) (0)
THE ANALYSIS OF THE ANTHROPOMETRIC DATA (1956) (0)
THE COMPARABILITY OF IRRADIATION SUBCLASSES (1956) (0)
Brief Communication: Extraction of DNA from Frozen Red Blood Cells (1993) (0)
Inferences concerning evolutionary forces from genetic data. (1973) (0)
Biomedical Progenitor. (Book Reviews: Archibald Garrod and the Individuality of Man.) (1994) (0)
Symposium: The genetics of various constitutional defects. (1952) (0)
How Can We Best Evaluate, and Compensate for, Genetic Hazards in the Environment and Workplace (1985) (0)
Opportunities for Research in Human Genetics. (1959) (0)
Biomedical progenitor. (1994) (0)
Editorial (0)
The “eugenic dilemma” revisited (1986) (0)
Further on Population Control (1997) (0)
The Immunoglobulin Allotypes ( Grn and Km ) of Twelve Indian Tribes of Central and South America (2005) (0)
Preventive Medicine (1946) (0)
ANALYSIS OF THE DATA CONCERNING DEATH DURING THE NINE-MONTH PERIOD FOLLOWING DELIVERY (1956) (0)
BloodPressure, SodiumIntake, andSodiumRelated HormonesintheYanomamoIndians, a "No-salt" Culture (1975) (0)
General Considerations on the Distribution of Haemoglobin in Africa. (1958) (0)
Data on the Occurrence of Hemoglobin C and Other Abnormal Hemoglobins in Some African Populations1 (2006) (0)
Book Review:Chondrodystrophic Dwarfs in Denmark. Supplemented with Investigations from Sweden and Norway with Special Reference to the Inheritance of Chondrodystrophy. Ernst Trier Morch (1949) (0)
A NEWINHERITED ABNORMALITY OFHUMAN HEMOGLOBIN* (2005) (0)
Book Review:Heredity in Human Leukemia and Its Relation to Cancer. A Genetic and Clinical Study of 209 Probands. Aage Videbaek (1950) (0)
On Guaymi in Costa Rica and Panama (1983) (0)
Book Review:Inheritance of Harelip and Cleft Palate. Contribution to the Elucidation of the Etiology of the Congenital Clefts of the Face. Poul Fogh-Andersen (1949) (0)
Abnormal hemoglobins. (1956) (0)
Book Review:Radiation, Genes, and Man. Bruce Wallace, Th. Dobzhansky (1960) (0)
Hemolytic anemia presumably due to coexistence of the genes for thalassemia and sickling. (1952) (0)
A System of Nomenclature for the Varieties of Human Hemoglobin (1953) (0)
Book Review:Heredity in Graves' Disease. With Remarks on Heredity in Toxic Adenoma in the Thyroid, Non-Toxic Goitre, and Myxoedema. Erik D. Bartels (1949) (0)
Book Review:Heredity in Essential Hypertension and Nephrosclerosis. A Genetic-Clinical Study of 200 Propositi Suffering from Nephrosclerosis. Paul Sobye (1951) (0)

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