Barton Childs

Q: What Schools Are Affiliated With Barton Childs

Barton Childs is affiliated with the following schools: Williams College, Johns Hopkins University

Barton Childs's AcademicInfluence.com Rankings

Barton Childs

Biology

#4087

World Rank

#6144

Historical Rank

#1591

USA Rank

Genetics

#409

World Rank

#475

Historical Rank

#175

USA Rank

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Biology

Why Is Barton Childs Influential?

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According to Wikipedia, Barton Childs was an American pediatrician and geneticist. He was born in Chicago, Illinois, and graduated from Williams College in 1938. In 1942, he received his M.D. from Johns Hopkins University. Following military service in World War II, he returned to Johns Hopkins for a residency in pediatrics. After a fellowship at Boston Children's Hospital in Boston, he returned to Johns Hopkins University in 1949, where he remained until his retirement in 1981. He remained a professor emeritus in the Department of Pediatrics at The Johns Hopkins University School of Medicine until his death.

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Barton Childs'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

The human disease network (2007) (3010)
Mendelian inheritance of familial prostate cancer. (1992) (803)
Hereditary prostate cancer: epidemiologic and clinical features. (1993) (605)
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 (1998) (550)
Family history and the risk of prostate cancer (1990) (524)
Human disease genes (2001) (388)
Crohn's disease: influence of age at diagnosis on site and clinical type of disease. (1996) (346)
DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS. (1963) (333)
SEX DIFFERENCES IN SUSCEPTIBILITY TO INFECTIONS. (1965) (259)
Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism. I. (1961) (225)
Genetic heterogeneity. (1968) (199)
Genetic counseling: a consumers' view. (1972) (191)
X-Linked Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency: Heterozygote Has Two Clonal Populations (1968) (176)
Age at Onset and Causes of Disease (2015) (139)
A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism. (1958) (135)
The effect of Mendelian disease on human health: a measurement. (1985) (127)
Genetic susceptibility of benign prostatic hyperplasia. (1994) (110)
Preliminary evidence for genetic anticipation in Crohn's disease (1996) (108)
Clinical and genetic heterogeneity in idiopathic Addison's disease and hypoparathyroidism. (1968) (95)
Glucose-6-Phosphate Dehydrogenase in Drosophila: X-Linked Electrophoretic Variants (1964) (92)
Human Biology: An introduction to human evolution, variation, growth, and adaptability (1988) (87)
Glucuronic acid conjugation by patients with familial nonhemolytic jaundice and their relatives. (1959) (86)
Genetic Medicine: A Logic of Disease (1999) (85)
X-Linked 6-Phosphogluconate Dehydrogenase in Drosophila: Subunit Associations (1965) (78)
Schizophrenia: age at onset, gender and familial risk (1990) (76)
GENETIC ORIGIN OF SOME SEX DIFFERENCES AMONG HUMAN BEINGS. (1965) (74)
Idiopathic hyperglycinemia: a new disorder of amino acid metabolism. II. The concentrations of other amino acids in the plasma and their modification by the administration of leucine. (1961) (62)
A defect of glutathione metabolism in erythrocytes from patients with a naphthalene-induced hemolytic anemia. (1958) (61)
Risk Factors in Schizophrenia (1992) (59)
Risk Factors in Schizophrenia: Season of Birth in Maryland, USA (1983) (55)
Tay-Sachs screening: social and psychological impact. (1976) (55)
The association between season of birth and the risk for schizophrenia. (1981) (50)
The effect of Mendelian disease on human health. II: Response to treatment. (1985) (47)
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison. (1995) (46)
Familial nonhemolytic jaundice with kernicterus; a report of two cases without neurologic damage. (1956) (46)
Familial nonhemolytic jaundice with late onset of neurological damage. (1968) (42)
Coevolution: Genes, culture, and human diversity. (1992) (42)
Familial risk factors for prostate cancer. (1991) (41)
A science of the individual: implications for a medical school curriculum. (2005) (39)
Patterns of Alkaline Phosphatase in Developing Drosophila (1966) (37)
Genetics, biology and disease. (2000) (36)
The crystallization and properties of serum bilirubin. (1953) (35)
Sir Archibald Garrod's conception of chemical individuality: a modern appreciation. (1970) (35)
ETIOLOGIC FACTORS IN SPORADIC CRETINISM. AN ANALYSIS OF NINETY CASES (1954) (34)
Tay-Sachs screening: motives for participating and knowledge of genetics and probability. (1976) (34)
Causes of essential hypertension. (1983) (33)
FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA. (1964) (32)
GENE MUTATION AS A CAUSE OF HUMAN DISEASE (1972) (31)
Genetic analysis of human behavior. (1972) (30)
Persistent echoes of the nature-nurture argument. (1977) (29)
Season of Birth of Siblings of Schizophrenic Patients (1992) (28)
Familial distributions of organ specific antibodies in the blood of patients with Addison's disease and hypoparathyroidism and their relatives. (1969) (28)
Human genetics teaching in U.S. Medical Schools (1982) (27)
HYPERGLYCINEMIA. V. THE MISCIBLE POOL AND TURNOVER RATE OF GLYCINE AND THE FORMATION OF SERINE. (1964) (26)
Genetic heterogeneity of α‐galactosidase in fabry's disease (1972) (25)
Comparison of Juvenile Diabetics with Positive and Negative Organ Specific Antibody Titers: Evidence for Genetic Heterogeneity (1973) (25)
Environmental Influences on Prenatal Development (1959) (23)
A survey of genetics as it applies to problems in medicine. (1957) (22)
Genetic variations in the quantitative control of erythrocyte glucose‐6‐phosphate dehydrogenase activity (1964) (20)
Glucose 6-phosphate dehydrogenase inDrosophila melanogaster: Starch gel electrophoretic variation due to molecular instability (1968) (19)
Genetic regulation of glucose 6-phosphate dehydrogenase activity in Drosophila melanogaster (1969) (19)
Genetics in the medical curriculum. (1982) (19)
Human behavioural genetics. (1976) (17)
Hybridization of mammalian somatic cells. (1970) (16)
Report of the Task Force on Teaching Human Genetics in North American Medical Schools. (1989) (15)
Perspectives in the teaching of human genetics. (1987) (15)
The William Allan Memorial Award Lecture. A place for genetics in health education, and vice versa. (1974) (13)
Why do some individuals have more infections than others? (2001) (11)
A logic of disease (2007) (11)
An electrophoretic method for detecting hypoxanthine-guanine phosphoribosyl transferase variants (1969) (10)
Genetic variation and nutrition. (1988) (10)
Genetic variations in man. (1963) (8)
Garrod, Galton, and clinical medicine. (1973) (8)
Dosage compensation in the regulation of erythrocyte glucose-6-phosphate dehydrogenase activity. (1963) (8)
Genetically determined variation in the immune system: implications for host defense (1989) (8)
Frontiers of psychiatric genetics. (1976) (8)
Genetics and child development. (1967) (8)
Molecular genetics in medicine (1988) (8)
Obstetricians' attitudes toward genetic screening. (1977) (7)
FAMILIAL NONHEMOLYTIC JAUNDICE WITH KERNICTERUS (1956) (6)
Primaquine sensitivity of erythrocytes. (1961) (5)
Genetics in pediatric disease. (1954) (5)
Science as a Way of Knowing: Human Genetics (1986) (5)
The personal impact of Tay-Sachs carrier screening. (1977) (5)
Electrophoretic study of human ribosomal core proteins: evidence for selection against variation. (1975) (4)
Genetic individuality and nutrition. (1990) (4)
Hereditary aspects of disease. (1959) (4)
Recombinant DNA analysis of multifactorial disease. (1988) (4)
Prenatal Diagnosis for Pediatricians (1980) (4)
GENETICS AND METABOLISM E. Mead Johnson Award Address (1960) (4)
Genetics and metabolism. (1956) (3)
Prospects for genetic screening. (1975) (3)
A note on Love's stress function. (1969) (3)
The metabolic basis of inherited disease. (1990) (3)
Medicine in a Genetic Context (2013) (3)
The entry of genetics into medicine (1999) (3)
Evolutionary genetics and environmental stress (1992) (3)
The impact of conversion from mycophenolate mofetil to mycophenolate sodium among renal transplant recipients on a sirolimus-based regimen. (2008) (3)
Genetic issues in pediatric and obstetric practice (1981) (2)
Edwards A. Park. (1994) (2)
Etiologic factors cases. (1954) (2)
Familial aspects of obesity. (1957) (2)
Why Study Human Genetics (1983) (2)
Methods in enzymology, Vol. 12: Nucleic acids (1968) (2)
Nephrogenic diabetes insipidus. A personal perspective. (1995) (1)
Genetics in medical education. (1993) (1)
Genetic heterogeneity of alpha-galactosidase in fabry's disease. (1972) (1)
Acceptance of the Howland Award (1989) (1)
Supporting Information on “ The Human Disease Network ” (2007) (1)
Harry Harris (1919-94): in memoriam. (1996) (1)
Medical genetics to genomic medicine. (2002) (1)
Genetics of Neurological Disorders (1985) (1)
Genetic heterogeneity. (1968) (1)
Human genetics: Problems and approaches (1988) (1)
???The Clinical Detection of the Genetic Carriers of Inherited Disease???: Context and Present-Day Perspectives (1992) (1)
Genomics, proteomics, and genetics in medicine. (2003) (1)
APPROACHES TO GENETIC COUNSELING * (1975) (1)
Book Review:Biochemical Disorders in Human Disease. R. H. S. Thompson, E. J. King (1958) (0)
Amino acid metabolism and genetic variation (1969) (0)
Counseling in Medical Genetics (1956) (0)
1996 ASHG Award for excellence in education. Remarks on receiving the ASHG award for education. (1997) (0)
Garrod's inborn factors in disease : including an annotated facsimile reprint of The inborn factors of disease by Archibald E. Garrod (1989) (0)
march of dimes/colonel harland sanders award (1999) (0)
INTRODUCTION OF BARTON CHILDS (1999) (0)
Genetic Mechanisms in Human Disease: Chromosomal Aberrations. M. F. A. Montague, Ed. Thomas, Springfield, Ill., 1961. xviii + 592 pp. Illus. $19.50 (1962) (0)
New Directions in Genetics (1963) (0)
Introduction to the Human Genetics Symposium (1990) (0)
Hereditary hyperbilirubinemias. (1980) (0)
Human Biochemical Genetics (1960) (0)
Genetic Screening... Potential and Pitfalls. (1976) (0)
An Outline of Chemical Genetics (1961) (0)
SYMPOSIUM ON CONGENITAL METABOLIC DISEASE (1958) (0)
Letter from Barton Childs to Joshua Lederberg (1986) (0)
A Place for Genetics in Health Education and Vice-Versa (2019) (0)
Molecular genetics in medicine. Introduction. (1988) (0)
GENETICS ,B IOLOGY AND DISEASE (2000) (0)
Transactions of the Society for Pediatric Research: Thirty-First Annual Meeting, Atlantic City, N.J., May 4-5, 1961 (1961) (0)
The Journal thanks the following consultants who, in addition to the members of the Editorial Board, gave their time to review manuscripts submitted in 1980. (1980) (0)
Presentation of the Howland Award to Harry H. Gordon (1976) (0)
SYMPOSIUM ON CONGENITAL METABOLIC DISEASE: GENETIC ASPECTS OF CONGENITAL METABOLIC DISEASE (1958) (0)
Book Review:The Metabolic Basis of Inherited Disease. John B. Stanbury, James B. Wyngaarden, Donald S. Frederickson (1961) (0)
Prospects for genetic screening. (1975) (0)
Public Attitudes Toward the Handicapped (1980) (0)
Blocking of the brachial plexus by the axillary perivascular technic in arteriography of the upper extremity (1974) (0)
I. Feature article: Genetics for medical students. (1987) (0)
The William Allan Memorial Award: presented to Charles R. Scriver, M.D. at the annual meeting of the American Society of Human Genetics, Vancouver, British Columbia, October 6, 1978. (1979) (0)
The effect of low doses of x-ray (diagnostic procedures) on the chromosomes of human infants (1964) (0)
On Reprinting: Genetic Mechanisms in Human Disease: Chromosomal Aberrations . M. F. A. Montague, Ed. Thomas, Springfield, Ill., 1961. xviii + 592 pp. Illus. $19.50. (1962) (0)
GENETIC IMPLICATIONS OF RARE DISEASES. (1964) (0)
Principles of human genetics (1974) (0)
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22 qll ( velocardiofacial syndrome / human / somatic cell hybrids / psychosis ) (2005) (0)
An Introduction to Human Biochemical Genetics . H. Harris. Eugenics Laboratory Memoirs, XXXVII. Cambridge Univ. Press, New York, 1953. 96 pp. Illus. $2.75. (1955) (0)
The Genetics of Primaquine Sensitivity of the Erythrocytes (2008) (0)
Genetic screening. (1975) (0)
Clinical Genetics.Arnold Sorsby (1954) (0)
Pediatrics: American Academy of Pediatrics: Placental Transfer, Fetal Susceptibility Studied by AAP (1961) (0)
SIROLIMUS DECREASES SERUM PSA POST- TRANSPLANT: 2131 (2008) (0)
329 Generation of patient-reported outcomes during early drug development (2015) (0)
Perspectives in medical genetics. (1977) (0)
Introductory Speech for Kurt Hirschhorn (2003) (0)
Exclusion of linkage between schizophrenia and some candidate genes (1993) (0)
Book Review:The New Genetics and Clinical Practice. D. J. Weatherall (1987) (0)
Research session: I. The influence of heredity on the health of the family (1955) (0)
Genetic aspects of congenital metabolic disease. (1958) (0)
A New View of Health: Genetics and Environment. (1978) (0)

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Other Resources About Barton Childs

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What Schools Are Affiliated With Barton Childs?

Barton Childs is affiliated with the following schools: