Alexander Gordon Bearn

Alexander Gordon Bearn's AcademicInfluence.com Rankings

Philosophy

#4394

World Rank

#6888

Historical Rank

Logic

#1885

World Rank

#2749

Historical Rank

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Philosophy

Alexander Gordon Bearn's Degrees

PhD Immunology University of Oxford

Why Is Alexander Gordon Bearn Influential?

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According to Wikipedia, Alexander Gordon Bearn informally Alick Bearn , a physician, scientist and author, was professor at Rockefeller University and Cornell University Medical College. He was a member of the National Academy of Sciences, and had been Executive Officer of the American Philosophical Society. He died Friday, May 15, 2009, in Philadelphia. Prior to his death Bearn was working on a family history that followed the Bearn family from Béarn, France to Angus, Scotland and finally to the United States.

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Alexander Gordon Bearn'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

Isolation and properties of a low molecular weight beta-2-globulin occurring in human biological fluids. (1968) (672)
The problem of chronic liver disease in young women. (1956) (260)
The effect of adrenaline and noradrenaline on hepatic blood flow and splanchnic carbohydrate metabolism in man (1951) (188)
Progress in Medical Genetics (1970) (175)
Localization of Lactic Acid Dehydrogenase Activity in Serum Fractions (1957) (174)
Hurler's syndrome. A genetic study in cell culture. (1966) (172)
STUDIES ON THE TRANSFERRINS OF ADULT SERUM, CORD SERUM, AND CEREBROSPINAL FLUID (1962) (132)
Isozymes of lactic dehydrogenase in human tissues. (1961) (132)
A Possible Experimental Approach to the Association of Hereditary α1-Antitrypsin Deficiency and Pulmonary Emphysema.∗ (1966) (126)
Abnormalities of copper metabolism in Wilson's disease and their relationship to the aminoaciduria. (1954) (125)
Localization of Cu64 in Serum Fractions Following Oral Administration (1954) (125)
Genetic and biochemical aspects of Wilson's disease. (1953) (122)
CYSTIC FIBROSIS OF THE PANCREAS (1969) (121)
A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration) (1959) (117)
Splanchnic blood flow in man by the bromsulfalein method: the relation of peripheral plasma bromsulfalein level to the calculated flow. (1950) (109)
The amino acid content of the blood and urine in Wilson's disease. (1954) (104)
Renal function in Wilson's disease. (1957) (102)
Wilson's disease; an inborn error of metabolism with multiple manifestations. (1957) (102)
A genetic cell marker in cystic fibrosis of the pancreas. (1968) (101)
Cystic fibrosis of the pancreas. A study in cell culture. (1969) (95)
Hepatic glucose output and hepatic insulin sensitivity in diabetes mellitus. (1951) (85)
HURLER'S SYNDROME: A GENETIC STUDY OF CLONES IN CELL CULTURE WITH PARTICULAR REFERENCE TO THE LYON HYPOTHESIS (1967) (77)
Hurler's Syndrome: Demonstration of an Inherited Disorder of Connective Tlssue in Cell Culture (1965) (77)
Haptoglobin and transferrin variation in humans and primates: two new transferrins in Chinese and Japanese populations (1962) (73)
Hurler's syndrome. Effect of retinol (vitamin A alcohol) on cellular mucopolysaccharides in cultured human skin fibroblasts. (1966) (72)
Observations on the heterogeneity of malic and lactic dehydrogenase in human serum and red blood cells. (1958) (70)
Hereditary Deficiency of Serum α1-Antitrypsin (1964) (69)
Autosomal trisomy of a group 16–18 chromosome (1962) (69)
Variations in the Lactic Dehydrogenase of Vertebrate Erythrocytes (1962) (64)
Metabolic studies in Wilson's disease using Cu64. (1955) (62)
Effect of estrogens on copper metabolism in Wilson's disease. (1961) (58)
THE HETEROGENEITY OF LACTIC AND MALIC DEHYDROGENASE * (1958) (56)
Cystic fibrosis: fractionation of fibroblast media demonstrating ciliary inhibition. (1973) (53)
Roentgenographic abnormalities of the skeletal system in Wilson's disease (hepatolenticular degeneration). (1958) (52)
COMPARATIVE STUDIES OF THE ISOZYMES OF LACTIC DEHYDROGENASE IN RABBIT AND MAN (1962) (51)
The molecular structure of human ceruloplasmin: evidence for subunits. (1966) (51)
Isozymes of lactice dehydrogenase; their alterations in arthritic synovial fluid and sera. (1962) (51)
The response of the liver to insulin in normal subjects and in diabetes mellitus; hepatic vein catheterisation studies. (1952) (50)
A case of inherited deficiency of serum alpha-antitrypsin associated with pulmonary emphysema. (1966) (50)
Azure lunulae; an unusual change in the fingernails in two patients with hepatolenticular degeneration (Wilson's disease). (1958) (49)
TWO GENETIC VARIANTS OF THE GROUP-SPECIFIC COMPONENT OF HUMAN SERUM: GC CHIPPEWA AND GC ABORIGINE. (1963) (49)
CHARACTERIZATION OF CYSTIC FIBROSIS FACTOR AND ITS INTERACTION WITH HUMAN IMMUNOGLOBULIN (1973) (46)
CHROMOSOMAL ABNORMALITIES IN WALDENSTRÖM'S MACROGLOBULINÆMIA (1961) (45)
Cellular metachromasia, a genetic marker for studying the mucopolysaccharidoses. (1967) (45)
THE DISTRIBUTION OF HAPTOGLOBIN SUBTYPES IN VARIOUS POPULATIONS, INCLUDING SUBTYPE PATTERNS IN SOME NONHUMAN PRIMATES. (1964) (44)
DETERMINATION OF PHENOTYPES IN THE HUMAN GROUP-SPECIFIC COMPONENT (GC) SYSTEM BY STARCH GEL ELECTROPHORESIS. (1963) (43)
ISOLATION AND PARTIAL CHARACTERIZATION OF THE TWO PRINCIPAL INHERITED GROUP-SPECIFIC COMPONENTS OF HUMAN SERUM (1963) (41)
Haptoglobin and Transferrin Gene Frequencies in a Navajo Population: A New Transferrin Variant (1961) (41)
THE EXCRETION OF FIVE PLASMA PROTEINS PREVIOUSLY UNIDENTIFIED IN NORMAL HUMAN URINE. (1964) (41)
IMMUNOLOGICAL AND BIOCHEMICAL STUDIES ON SERUM HAPTOGLOBIN (1964) (41)
Site of Formation of the Group-Specific Component and Certain Other Serum Proteins.∗ (1964) (39)
OYSTER CILIARY INHIBITION BY CYSTIC FIBROSIS CULTURE MEDIUM (1972) (39)
Application of genetic regulatory mechanisms to human genetics. (1963) (39)
Some genetical implications of physical studies of human haptoglobins. (1958) (37)
Inherited Variations of Human Serum α1-Antitrypsin (1966) (36)
COMPARATIVE STUDIES ON THE PHYSICAL CHARACTERISTICS OF THE HERITABLE HAPTOGLOBIN GROUPS OF HUMAN SERUM (1959) (35)
Phospholipid Studies of Different Serum Lipoproteins Employing P32 (1954) (35)
Genetic aspects of Wilson's disease. (1959) (35)
Inheritance of an Abnormal Chromosome in Down's Syndrome (Mongolism) with Leukemia. (1962) (35)
ADDITIONAL STUDIES ON THE TRANSFERRINS OF CORD SERUM AND CEREBROSPINAL FLUID (1963) (34)
Boric Acid-induced Heterogeneity of Conalbumin by Starch-gel Electrophoresis (1963) (34)
AN INHERITED X-LINKED SERUM SYSTEM IN MAN (1966) (34)
Hemoglobin Binding Capacity of Isolated Haptoglobin Polypeptide Chains.∗ (1966) (33)
Cell culture and the Chediak-Higashi syndrome. (1967) (33)
Wilson's disease. (1961) (33)
GENE MUTATION AS A CAUSE OF HUMAN DISEASE (1972) (31)
Hepatic blood flow and carbohydrate changes in man during fainting (1951) (31)
THE PRESENCE OF SUBUNITS IN THE INHERITED GROUP-SPECIFIC PROTEIN OF HUMAN SERUM. (1965) (30)
Cystic fibrosis: distribution of mucopolysaccharides in fibroblast cultures. (1969) (30)
FURTHER STUDIES ON METACHROMASIA IN CULTURED HUMAN FIBROBLASTS (1970) (29)
Gaucher's Disease: A Genetic Disease Detected in Skin Fibroblast Cultures (1968) (29)
Localization of the thyroxine-binding protein of serum by starch gel electrophoresis. (1958) (28)
Additional Genetic Variation of Human Serum Transferrin (1962) (28)
Cystic fibrosis: current concepts. (1974) (28)
Isolation and partial characterization of the polypeptide chains in human ceruloplasmin. (1969) (27)
The electrophoretic patterns of normal and variant phenotypes of the group specific (Gc) components in human serum. (1966) (25)
Genetic studies in relation to kuru. 3. Distribution of the inherited serum group-specific protein (Ge) phenotypes in New Guineans: an association of kuru and the Gc Ab phenotype. (1972) (24)
Localization of a Lactic Dehydrogenase Isozyme in Nuclei of Young Cells in the Erythrocyte Series.∗ (1962) (22)
Heterogeneity of ceruloplasmin. (1962) (22)
Antibodies to inherited &‐lipoprotein antigens in the serum of multiply transfused patients (1970) (22)
Studies on the "group specific component" of human serum. Gene frequencies in several populations. (1961) (21)
THE DISTRIBUTION OF THE TRANSFERRIN VARIANTS D-1 AND D-CHI IN VARIOUS POPULATIONS. (1964) (21)
INHERITED VARIATIONS IN HUMAN SERUM PROTEINS: STUDIES ON THE GROUP‐SPECIFIC COMPONENT * (1961) (20)
An Improved Method of Preparing Haptoglobin Polypeptide Chains Using Guanidine Hydrochloride∗ (1968) (19)
ANTERIOR UVEITIS AND ALPHA-1-ANTITRYPSIN (1979) (19)
Distribution of Serum Group-specific Components (Gc) in Afghanistan, Korean, Nigerian and Israeli Populations (1964) (18)
HETEROGENEITY OF THE INHERITED GROUP-SPECIFIC COMPONENT OF HUMAN SERUM (1964) (18)
Correction of celluar metachromasia in cultured fibroblasts in several inherited mucopolysaccharidoses. (1970) (18)
HEREDITARY DEFICIENCY OF SERUM ALPHA-L-ANTITRYPSIN. (1964) (17)
White Blood Cell Cultures in Genetic Studies on the Human Mucopolysaccharidoses (1969) (16)
The use of preparative polyacrylamide-column electrophoresis in isolation of electrophoretically distinguishable components of the serum group-specific protein. (1967) (16)
THE DISTRIBUTION OF GC-TYPES IN SERA FROM AUSTRALIAN ABORIGINES. (1963) (16)
THE DISTRIBUTION OF THE GROUP SPECIFIC COMPONENT (GC) IN SELECTED POPULATIONS IN SOUTH EAST ASIA AND OCEANIA. (1963) (16)
Distribution of the Serum Group-Specific Components in Israel (1962) (15)
The effect of retinol (vitamin-A alcohol) on urinary excretion of mucopolysaccharides in the Hurler syndrome. (1967) (15)
The place of bal in the therapy of Wilson's disease (1956) (14)
Genetic Study of Cystic Fibrosis of the Pancreas using White Blood Cell Cultures (1969) (14)
Comparison of the tryptic peptides and amino acid composition of the beta polypeptide chains of the three common haptoglobin phenotypes. (1967) (14)
Excretion of Haptoglobin in Normal Urine (1962) (14)
Control gene mutation as a possible explanation of certain haptoglobin phenotypes. (1963) (13)
Chromosomal studies of three hermaphrodites. (1962) (13)
Variations in Heterozygous Expression at the Haptoglobin Locus. (1965) (13)
Pharmacogenetics. Heredity and the Response to Drugs (2015) (12)
A genetic study of cystic fibrosis of the pancreas in cell culture. (1969) (11)
Metachromasia and skin-fibroblast cultures in juvenile familial amaurotic idiocy. (1968) (11)
A CRITICAL EXAMINATION OF SOME REPORTED BIOCHEMICAL ABNORMALITIES IN MONGOLISM * (1970) (11)
Alterations in Sialic Acid Content of Human Transferrin (1961) (11)
GENETIC AND BIOCHEMICAL CONSIDERATIONS OF THE SERUM GROUP-SPECIFIC COMPONENT. (1964) (11)
The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome). (1968) (11)
Wilson's Disease (1956) (11)
Chromosomes and disease. (1961) (10)
Genetic aspects of diseases of complement: an explosion. (1975) (10)
Human Serum Protein Polymorphisms (1968) (9)
Cystic fibrosis: an improved method for studying white blood-cells in culture. (1969) (9)
Localisation of the cystic-fibrosis gene. (1968) (9)
A New Variant of Human Transferrin in a Venezuelan Family (1962) (9)
THE HURLER SYNDROME: A STUDY OF CULTURED LYMPHOID CELL LINES (1972) (8)
Control Gene Mutations in the Human Haptoglobin System (1963) (8)
Studies of polymorphic traits for the characterization of populations. General introduction. (1973) (8)
Quantitative Determination of the Group Specific Protein in Normal Human Serum.∗ (1965) (7)
BIOASSAYS OF CYSTIC-FIBROSIS FACTOR (1974) (7)
Inherited variations of human serum alpha-1-antitrypsin. (1966) (6)
alpha-1-antitrypsin and disease. (1977) (5)
Some observations on transferrin (1964) (5)
PSYCHOLOGICAL IMPAIRMENT IN WILSON'S DISEASE (1956) (5)
Minor hemoglobin components of normal human blood. (1957) (4)
Henry G. Kunkel 1916-1983. An appreciation of the man and his scientific contributions & a bibliography of his research papers (1985) (4)
TRANSFERRIN D-WIGAN. (1964) (4)
An Introduction to Medical Genetics (1967) (3)
A common X-linked serum marker and its relation to other loci on the X chromosome. (1966) (3)
WILSON’S DISEASE: IS THE PRIMARY INHERITED DEFECT ONE OF COPPER OR AMINO ACID METABOLISM? (1957) (2)
[Wilson's disease]. (1956) (2)
Blood groups, serum proteins and enzymes of the Ainu of Hokkaido. (1978) (2)
Genetics, the Axial Thread of Biology (1962) (2)
Structural determinants of disease and their contribution to clinical and scientific progress. (1976) (2)
STUDYING THE MUCOPOLYSACCHARIDOSES (1967) (2)
THE SERUM GROUP SPECIFIC COMPONENT IN NONHUMAN PRIMATES. (1965) (2)
Alpha-1-antitrypsin deficiency: a biological enigma. (1978) (1)
The Aging process : therapeutic implications : Merck, Sharp & Dohme International Medical Advisory Council, Santiago de Compostela, Spain, June 25-26, 1984 (1985) (1)
The effect of insulin on hepatic carbohydrate metabolism and splanchnic blood flow in man. (1951) (1)
Clinical aspects of disarranged chromosomal structure. (1960) (1)
Genetics of Neurological Disorders (1985) (1)
Professor Tage Kemp (1964) (1)
Response of the Liver to Insulin; Hepatic Vein Catheterization Studies in Man (2008) (1)
Dr. William Harvey (1578-1657) and the Harvey Society of New York (2015) (1)
The Chemistry of Hereditary Disease (1956) (1)
HURLER'S SYNDROME (1966) (1)
H E T E R O G E N E I T Y of T H E I N H E R I T E D Group-specific Component of Human Serum* (2003) (1)
Electrophoretic separation of human serum in the lithium borate buffer sys- tem resulted in a greatly improved resolution of proteins (2003) (0)
Book ReviewGenetic Screening: Programs, principles, and research. (1976) (0)
Metachromasia elaborated. (1970) (0)
An I N H E R I T E D X -l I N K E D S E R U M System I N M a N T~e Xh S Y S ~ (0)
Some studies on inherited disease using the techniques of cell culture. (1968) (0)
Book Review:Genes, Enzymes, and Inherited Diseases. H. Eldon Sutton (1961) (0)
The Haptoglobin Groups in Man. R. L. Kirk. Karger, Basel, 1968 (U. S. distributor, Phiebig, White Plains, N. Y.). vi + 77 pp., illus. $4.80. Monographs in Human Genetics, vol. 4 (1969) (0)
OYSTER C ILIARY I NHIBITION B Y C YSTIC F IBROSIS CULTURE M EDIUM (1972) (0)
Innovation and acceleration in clinical drug development : Merck Sharp & Dohme International Medical Advisory Council, Siena, Italy, June 9-10, 1986 (1986) (0)
The genetic secrets of the humble fibroblast. (1970) (0)
Diseases of the gastrointestinal tract (liver). (1955) (0)
Alpha-1 antitrypsin deficiency. (1969) (0)
F U R T H E R STUDIES ON METACHROMASIA I N CULTURED HUMAN FIBROBLASTS STAINING OF GLYCOSAMINOGLYCANS (MucoPoLYSACCIIARIDES) BY ALCIAN BLUE IN SALT SOLUTIONS* BY B. SHANNON (1970) (0)
HURLER'S SYNDROME (1966) (0)
An Outline of Chemical Genetics (2015) (0)
The Prevalence of Humbug and Other Essays by Max Black (review) (2015) (0)
Genetic and cellular bases of congenital renal dysfunction. Introductory remarks on Session 1. Structural defects. (1970) (0)
Blood Protein: The Haptoglobin Groups in Man . R. L. Kirk. Karger, Basel, 1968 (U. S. distributor, Phiebig, White Plains, N. Y.). vi + 77 pp., illus. $4.80. Monographs in Human Genetics, vol. 4. (1969) (0)
IIURLER'S SYNDROME E~ECT O~ RE~rlNOL (VITAm~ A ALCOHOL) ON CELLULAR MUCOPOLYSAC- (1966) (0)
THE AMINO ACID CONTENTOF THE BLOODANDURINE IN WILSON'S DISEASE (2013) (0)
Medac medical advisory council series innovation and acceleration in clinical drug development (1987) (0)
Antibiotics in the management of infections : outlook for the 1980s : Merck Sharp & Dohme International Medical Advisory Council, Paris, France, June 14-15, 1982 (1982) (0)
Genetical variations in the serum proteins of man. (1961) (0)
The expression of inherited metabolic disease in cultured cells. (1974) (0)
An inherited α1-antitrypsin variant (1967) (0)
Medical genetics 1958–1960. An annotated review: By Victor A. McKusick, Professor of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland. C. V. Mosby Company, St. Louis, Mo., 1961. 534 pp. Price $14.50 (1962) (0)
RENAL FUNCTION IN WILSON'S DISEASEI (2013) (0)
James Van Gundia Neel, papers, ca. 1935-1999 (2014) (0)
Liver cell culture: current status and prospects for the study of inherited diseases. (1980) (0)
MUTAGEN-INDUCED HYBRIDIZATION OF SALMONELLA TYPHIMURIUM LT2 X ESCHERICHIA COLI K12 Hfr* (0)
PROGRESS IN MEDICAL GENETICS. VOLUME II (1966) (0)
Hereditary variations in synthesis of serum proteins in health and disease. (1960) (0)
A Gei, Retic Study in Cell Culture* (0)
Book Review:Papers on Human Genetics. Samuel H. Boyer, IV (1964) (0)
Letter: Bioassays of cystic-fibrosis factor. (1974) (0)

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