Published in Science on November 09, 1956
Blood groups and susceptibility to disease: a review. Br J Prev Soc Med (1957) 3.96
ABO blood groups and cancer of oesophagus, cancerof pancreas, and pituitary adenoma. Br Med J (1960) 1.57
Blood donor controls for blood group disease researches. Am J Hum Genet (1958) 1.42
Blood groups of gastric ulcer and carcinoma. Br Med J (1960) 1.34
Astrocytomas and the ABO blood groups. J Med Genet (1966) 0.80
The Implications of the Association between the ABO Blood Groups and Disease. J Coll Gen Pract Res Newsl (1959) 0.75
Distribution of ABO blood groups in children with embryonic tumours. Br Med J (1962) 0.75
The genetics and cytology of Chlamydomonas. Annu Rev Microbiol (1960) 6.34
Cause and effect in biology. Science (1961) 4.25
THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION. J Pediatr (1964) 4.12
A genetic analysis of linkage group I of Chlamydomonas reinhardi. Z Vererbungsl (1959) 3.84
Autoerythrocyte sensitization; a form of purpura producing painful bruising following autosensitization to red blood cells in certain women. Blood (1955) 3.69
THE PHOTOSYNTHETIC ELECTRON TRANSPORT CHAIN OF CHLAMYDOMONAS REINHARDI. I. TRIPHOSPHOPYRIDINE NUCLEOTIDE PHOTOREDUCTION IN WILD-TYPE AND MUTANT STRAINS. J Biol Chem (1963) 3.14
Anaphylactoid purpura in children (Schonlein-Henoch syndrome): review with a follow-up of the renal complications. AMA J Dis Child (1960) 3.04
Temporary remissions in acute leukemia in children produced by folic acid antagonist, 4-aminopteroyl-glutamic acid. N Engl J Med (1948) 2.81
THE PHOTOSYNTHETIC ELECTRON TRANSPORT CHAIN OF CHLAMYDOMONAS REINHARDI. II. COMPONENTS OF THE TRIPHOSPHOPYRIDINE NUCLEOTIDE-REDUCTIVE PATHWAY IN WILD-TYPE AND MUTANT STRAINS. J Biol Chem (1963) 2.80
A screening technique for photosynthetic mutants in unicellular algae. Nature (1960) 2.64
The relation of calcium and magnesium to crossing over in Chlamydomonas reinhardtii. Z Vererbungsl (1958) 2.62
Congenital (erythroid) hypoplastic anemia. A 25-year study. Am J Dis Child (1961) 2.61
Linkage maps in Chlamydomonas reinhardi. Genetics (1962) 2.50
Erythroblastosis fetalis. Pediatrics (1952) 2.36
Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus. N Engl J Med (1952) 2.23
SCHIZOPHRENIA AS A GENETIC MORPHISM. Nature (1964) 2.18
Coagulation defects with intrauterine death from Rh isosensitization. Am J Obstet Gynecol (1950) 1.90
Erythroblastosis fetalis; the value of blood from female donors for exchange transfusion. N Engl J Med (1949) 1.83
The nuclear cycle in Chlamydomonas reinhardi. Z Vererbungsl (1959) 1.77
Maternal afibrinogenemia associated with long-standing intrauterine fetal death. Am J Obstet Gynecol (1953) 1.68
Erythrocyte acid phosphomonesterase and glucose-6-phosphate dehydrogenase deficiency in Caucasians. Science (1963) 1.64
Effects of corticosteroids on coagulation of the blood. Nature (1962) 1.60
The diagnosis of thalassemia trait by starch block electrophoresis of the hemoglobin. Blood (1958) 1.57
In vitro erythrophagocytosis in acquired hemolytic anemia. Blood (1952) 1.57
Serum bilirubin levels in the newborn infant. J Pediatr (1953) 1.51
Prolonged obstructive jaundice in infancy. I. General survey of 156 cases. Pediatrics (1952) 1.42
Geographic blood group variability in the United States. J Am Med Assoc (1951) 1.41
Congenital afibrinogenemia; a study of some basic aspects of coagulation. Blood (1954) 1.41
Gene recombination in Chlamydomonas reinhardi. Cold Spring Harb Symp Quant Biol (1958) 1.40
Testosterone-induced remission in aplastic anemia of both acquired and congenital types. Further observations in 24 cases. N Engl J Med (1961) 1.39
Testosterone-induced remission in aplastic anemia. AMA J Dis Child (1959) 1.37
Erythroblastosis fetalis. II. Prognosis in relation to history, maternal titer and length of fetal gestation. Pediatrics (1950) 1.36
A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with thalassemia trait. Blood (1958) 1.32
Congenital (erythroid) hypoplastic anemia: cortisone treated. Am J Dis Child (1961) 1.27
Erythroblastosis fetalis. IX. The problems of stillbirth. N Engl J Med (1954) 1.25
CHLORAMPHENICOL IN BLOOD: SIMPLE CHEMICAL ESTIMATIONS IN PATIENTS RECEIVING MULTIPLE ANTIBIOTICS. Science (1964) 1.25
Erythroblastosis fetalis. VII. Treatment with exchange transfusion. N Engl J Med (1951) 1.25
Purpura in infants and children; its natural history. AMA Am J Dis Child (1953) 1.24
Medicolegal applications of blood grouping. N Engl J Med (1954) 1.23
On the inheritance of the antigen f of the Rh complex. Am J Hum Genet (1954) 1.22
Erythroblastosis fetalis. VI. Prevention of kernicterus. AMA Am J Dis Child (1950) 1.22
Enzyme deficiency in erythrocytes in congenital nonspherocytic hemolytic anemia. Pediatrics (1959) 1.20
"Enclosed" hemorrhage and neonatal jaundice. Am J Dis Child (1961) 1.18
Rh and other blood groups. N Engl J Med (1949) 1.17
The pathway of triphosphopyridine nucleotide photoreduction in Chlamydomonas reinhardi. Proc Natl Acad Sci U S A (1962) 1.17
THE GASTROINTESTINAL EFFECTS OF IRON-DEFICIENCY ANEMIA. Pediatrics (1964) 1.14
The effect of adrenocorticotrophic hormone (ACTH) in idiopathic acquired hemolytic anemia as related to the hemolytic mechanisms. J Lab Clin Med (1951) 1.11
Leukocytic inclusions--Dohle bodies--associated with platelet abnormality (the May-Hegglin anomaly). Report of a family and review of the literature. Blood (1962) 1.10
Report of a second example of the Rh agglutinogen cv, with some comments on its relation to the agglutinogen f. Science (1953) 1.09
EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. I. MORPHOLOGY, ERYTHROKINETICS AND FAMILY ENZYME STUDIES. N Engl J Med (1964) 1.08
Erythroblastosis fetalis. I. Problems in the interpretation of changing mortality in erythroblastosis fetalis. Pediatrics (1950) 1.06
Erythroblastosis fetalis. IV. Further observations on kernicterus. Pediatrics (1950) 1.04
An investigation of electron spin resonance in wild type Chlamydomonas reinhardi and mutant strains having impaired photosynthesis. Biophys J (1962) 1.02
Fetomaternal transfusion. AMA J Dis Child (1959) 1.02
Haemophilia and related haemorrhagic disorders. Practitioner (1957) 1.01
Erythroblastosis foetalis or haemolytic disease of the newborn. Proc R Soc Med (1947) 1.00
Use of the plasma acid phosphatase value in the differentiation of thrombocytopenic states. N Engl J Med (1963) 1.00
Chromosome organization and gene recombination. Cold Spring Harb Symp Quant Biol (1956) 0.99
Anemia associated with protein deficiency. A study of 2 cases with cystic fibrosis. J Pediatr (1961) 0.96
Hemoglobin M. Science (1957) 0.96
Treatment of classic hemophilia: the use of fibrinogen rich in factor VIII for hemorrhage and for surgery. N Engl J Med (1961) 0.95
Observations on the new Rh agglutinin anti-f. Blood (1954) 0.95
ERYTHROCYTE PYRUVATE KINASE DEFICIENCY RESULTING IN CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA. N Engl J Med (1963) 0.95
Erythroblastosis fetalis. N Engl J Med (1957) 0.94
Erythroblastosis fetalis. III. Prognosis in relation to clinical and serologic manifestations at birth. Pediatrics (1950) 0.93
Haptoglobin patterns in cord blood serums. Nature (1961) 0.91
Alkali-resistant hemoglobin in aplastic anemia of both acquired and congenital types. N Engl J Med (1962) 0.91
Vitamin B12 deficiency associated with disease of the small intestine. Observations on an infant following extensive small bowel resection. J Pediatr (1960) 0.91
Genetical evidence for synthesis of transferrin in the foetus. Nature (1961) 0.89
Portal hypertension a complication of umbilical vein catheterization. Pediatrics (1963) 0.89
Studies on the origin of streptomycin resistant mutants in Chlamydomonas reinhardi. Genetics (1962) 0.88
Rh and other blood groups. N Engl J Med (1949) 0.88
EXTREME HEMOLYSIS AND RED-CELL DISTORTION IN ERYTHROCYTE PYRUVATE KINASE DEFICIENCY. II. MEASUREMENTS OF ERYTHROCYTE GLUCOSE CONSUMPTION, POTASSIUM FLUX AND ADENOSINE TRIPHOSPHATE STABILITY. N Engl J Med (1965) 0.88
Taxonomic categories in fossil hominids. Cold Spring Harb Symp Quant Biol (1950) 0.87
The species concept. Evolution (1949) 0.87
Turnover among hospital staff nurses. Nurs Outlook (1958) 0.86
Inheritance of the human blood group antigen JKa. Nature (1951) 0.86
Erythroblastosis fetalis: serum bilirubin. AMA Am J Dis Child (1952) 0.85
The inadequacies of routine bleeding and clotting times. N Engl J Med (1958) 0.84
Erythroblastosis fetalis. N Engl J Med (1957) 0.84
Prevention of kernicterus; management of erythroblastosis fetalis according to current knowledge. J Am Med Assoc (1954) 0.84
Erythrocyte glycolysis in erythroblastotic newborns. Erythrocyte glycolysis also in Rh-positive red cells coated with anti-D antibodies. AMA J Dis Child (1960) 0.83
Thalassemia intermedia due to interaction of Lepore trait with thalassemia trait; report of three cases. AMA J Dis Child (1959) 0.82
Skull changes in infants with chronic iron-deficiency anemia. N Engl J Med (1960) 0.82
The production and proper use of Rh typing reagents. Am J Public Health Nations Health (1948) 0.81
THE DETERMINANTS AND EVOLUTION OF LIFE. THE EVOLUTION OF LIVING SYSTEMS. Proc Natl Acad Sci U S A (1964) 0.80
Evolution in the family Dicruridae. Evolution (1948) 0.80
HEREDITARY EOSINOPHILIA: REPORT OF A FAMILY AND REVIEW OF THE LITERATURE. Am J Hum Genet (1964) 0.80
Replacement transfusion as a treatment for erythroblastosis fetalis. Pediatrics (1948) 0.79
Speciation and selection. Proc Am Philos Soc (1949) 0.78
IRON DEFICIENCY ANEMIA ASSOCIATED WITH AN ERROR OF IRON METABOLISM IN TWO SIBLINGS. J Clin Invest (1964) 0.78
Congenital hemolytic anemia in the newborn; relationship to kernicterus. AMA J Dis Child (1957) 0.77
The treatment of iron-deficiency anemia--palatable but ineffective iron medication. Pediatrics (1963) 0.77
The bearing of the new systematics on genetical problems; the nature of species. Adv Genet (1948) 0.76
FROM MOLECULES TO ORGANIC DIVERSITY. Fed Proc (1965) 0.76
HISTORY OF BLOOD BANKING IN THE UNITED STATES. JAMA (1965) 0.76
Variability in erythroblastosis fetalis: a study of multiple pregnancies and of twins. AMA Am J Dis Child (1952) 0.75
ELEVATION OF FACTOR VIII (ANTIHEMOPHILIC FACTOR) DURING PREGNANCY IN NORMAL PERSONS AND IN A PATIENT WITH VON WILLEBRAND'S DISEASE. N Engl J Med (1963) 0.75
HEMOPHILIA: MEDICAL AND ORTHOPEDIC MANAGEMENT. Postgrad Med (1963) 0.75
NUTRITIONAL ANEMIA IN INFANTS AND CHILDREN. Postgrad Med (1963) 0.75