Published in Blood on February 01, 1954
An Rh blood factor, rh1 (Ce), and its relationship to hr (ce). Am J Hum Genet (1958) 0.91
Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. Pediatrics (1954) 5.36
The destruction of red cells by antibodies in man. I. Observations of the sequestration and lysis of red cells altered by immune mechanisms. J Clin Invest (1957) 4.37
THE SYNDROME OF PANCREATIC INSUFFICIENCY AND BONE MARROW DYSFUNCTION. J Pediatr (1964) 4.12
Autoerythrocyte sensitization; a form of purpura producing painful bruising following autosensitization to red blood cells in certain women. Blood (1955) 3.69
A genetic and statistical study of psoriasis. Am J Hum Genet (1951) 3.69
HEREDITARY PROGRESSIVE ARTHRO-OPHTHALMOPATHY. Mayo Clin Proc (1965) 3.51
A reconsideration of the phenomenon of anticipation in diabetes mellitus. Proc Staff Meet Mayo Clin (1950) 3.09
Nine blood-group antibodies in a single serum after multiple transfusions. Br Med J (1950) 3.04
Anaphylactoid purpura in children (Schonlein-Henoch syndrome): review with a follow-up of the renal complications. AMA J Dis Child (1960) 3.04
A study of the genetics of diabetes mellitus. Am J Hum Genet (1952) 3.02
Temporary remissions in acute leukemia in children produced by folic acid antagonist, 4-aminopteroyl-glutamic acid. N Engl J Med (1948) 2.81
Sequential test for linkage between cystic fibrosis of the pancreas and the MNS locus. Am J Hum Genet (1956) 2.65
Congenital (erythroid) hypoplastic anemia. A 25-year study. Am J Dis Child (1961) 2.61
Pedigree of a family with hereditary chronic relapsing pancreatitis. Gastroenterology (1952) 2.41
Erythroblastosis fetalis. Pediatrics (1952) 2.36
Abnormalities observed during the first six days of life in 8,716 live-born infants. Pediatrics (1954) 2.31
The inheritance of serum haptoglobin types in American Negroes: evidence for a third allele Hp-2m. Am J Hum Genet (1960) 2.28
Erythroblastosis fetalis. VIII. Studies of serum bilirubin in relation to Kernicterus. N Engl J Med (1952) 2.23
A GENETIC STUDY OF THE ANTIGENS ASSOCIATED WITH THE GM(B) FACTOR OF HUMAN GAMMA GLOBULIN. Am J Hum Genet (1965) 2.07
John Haddy James. J Bone Joint Surg Br (1953) 2.06
Blood grouping, blood banking and blood transfusion. N Engl J Med (1951) 2.06
An analysis of the phenomenon of "anticipation" in diabetes mellitus. Ann Intern Med (1952) 2.05
Linkage studies with cystic fibrosis of the pancreas. Am J Hum Genet (1956) 2.04
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
Transfusion reactions in the absence of demonstrable incompatibility. N Engl J Med (1957) 1.81
The hematocrit of capillary blood. N Engl J Med (1955) 1.76
The genetics of diabetes: a review. Ann N Y Acad Sci (1959) 1.70
Maternal afibrinogenemia associated with long-standing intrauterine fetal death. Am J Obstet Gynecol (1953) 1.68
Suspected correlation between blood-group frequency and pituitary adenomas. Science (1956) 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 detection of minor erythrocyte populations by mixed agglutinates. Blood (1958) 1.58
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
A review of Rh serology and presentation of a new terminology. Transfusion (1962) 1.53
Frequency of genetic transmission of sporadic retinoblastoma. AMA Arch Ophthalmol (1957) 1.52
Serum bilirubin levels in the newborn infant. J Pediatr (1953) 1.51
STUDIES ON THE GM, INV, HP AND TF SERUM FACTORS OF JAPANESE POPULATIONS AND FAMILIES. Hum Biol (1964) 1.49
Methodology in human genetics. J Med Educ (1959) 1.42
Prolonged obstructive jaundice in infancy. I. General survey of 156 cases. Pediatrics (1952) 1.42
A new Rh blood type which reveals the Rh antigen G. Vox Sang (1958) 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
Age, sex, serum lipids, and coronary atherosclerosis. J Am Med Assoc (1956) 1.39
Testosterone-induced remission in aplastic anemia of both acquired and congenital types. Further observations in 24 cases. N Engl J Med (1961) 1.39
Heredity and diabetes. Diabetes (1958) 1.39
Hereditary globulin factors and immune tolerance in man. Science (1963) 1.38
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
A Gm-like factor present in Negroes and rare or absent in whites: its relation to Gma and Gmx. Am J Hum Genet (1960) 1.32
ACID PHOSPHATASES OF HUMAN RED CELLS: PREDICTED PHENOTYPE CONFORMS TO A GENETIC HYPOTHESIS. Science (1964) 1.30
Heredity, environment, and serum cholesterol; a study of 201 healthy families. Circulation (1958) 1.28
A new phenotype (McLeod) in the Kell blood-group system. Vox Sang (1961) 1.27
Kpa, (Penney), a new antigen in the Kell blood group system. Vox Sang (1957) 1.27
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
A new human gamma globulin factor determined by an allele at the Inv locus. Vox Sang (1962) 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
Erythroblastosis fetalis. VI. Prevention of kernicterus. AMA Am J Dis Child (1950) 1.22
On the inheritance of the antigen f of the Rh complex. Am J Hum Genet (1954) 1.22
Studies on linkage between phenylketonuria and the blood groups. Am J Hum Genet (1960) 1.20
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
Studies of anti-Kpb, a new antibody in the Kell blood group system. Vox Sang (1958) 1.16
THE GASTROINTESTINAL EFFECTS OF IRON-DEFICIENCY ANEMIA. Pediatrics (1964) 1.14
DEPENDENCE OF A GM(B) ANTIGEN ON THE QUATERNARY STRUCTURE OF HUMAN GAMMA GLOBULIN. Science (1964) 1.12
The effect of adrenocorticotrophic hormone (ACTH) in idiopathic acquired hemolytic anemia as related to the hemolytic mechanisms. J Lab Clin Med (1951) 1.11
THE MN GENE MU, WHICH PRODUCES M AND U BUT NO N, S, OR S. Vox Sang (1964) 1.10
Genetic and population studies of the blood types and serum factors among Indians and Chinese from Malaya. Am J Hum Genet (1961) 1.10
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
The distribution of the gamma globulin types Gm(a), Gm(x) and Gm-like in South and Southeast Asia and Australia. Am J Hum Genet (1963) 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