Published in Prog Med Genet on January 01, 1980
Human disease genes. Nature (2001) 5.31
Human genetics teaching in U.S. medical schools. Am J Hum Genet (1981) 5.30
Genetic counseling: a consumers' view. N Engl J Med (1972) 3.90
Hereditary prostate cancer: epidemiologic and clinical features. J Urol (1993) 3.86
Preliminary evidence for genetic anticipation in Crohn's disease. Lancet (1996) 3.32
Mendelian inheritance of familial prostate cancer. Proc Natl Acad Sci U S A (1992) 3.28
Family history and the risk of prostate cancer. Prostate (1990) 3.27
Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet (1998) 3.00
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations. Science (1968) 2.69
Crohn's disease: influence of age at diagnosis on site and clinical type of disease. Gastroenterology (1996) 2.50
Genetics in the medical curriculum. Am J Med Genet (1982) 2.31
The effect of Mendelian disease on human health: a measurement. Am J Med Genet (1985) 2.18
Risk factors in schizophrenia. Season of birth, gender, and familial risk. Br J Psychiatry (1992) 1.81
Clinical and genetic heterogeneity in idiopathic Addison's disease and hypoparathyroidism. J Clin Endocrinol Metab (1968) 1.78
Tay-Sachs screening: motives for participating and knowledge of genetics and probability. Am J Hum Genet (1976) 1.74
Genetic susceptibility of benign prostatic hyperplasia. J Urol (1994) 1.66
Report of the Task Force on Teaching Human Genetics in North American Medical Schools. Am J Hum Genet (1989) 1.65
I. Feature article: Genetics for medical students. Am J Hum Genet (1987) 1.59
Perspectives in the teaching of human genetics. Adv Hum Genet (1987) 1.57
Ifosfamide, carboplatin, and etoposide: a highly effective cytoreduction and peripheral-blood progenitor-cell mobilization regimen for transplant-eligible patients with non-Hodgkin's lymphoma. J Clin Oncol (1999) 1.54
Photo quiz. Clin Infect Dis (1995) 1.52
X-linked 6-phosphogluconate dehydrogenase in drosophila: subunit associations. Science (1965) 1.52
Physiologic jaundice: the enterohepatic circulation of bilirubin. N Engl J Med (1971) 1.51
Genetic regulation of glucose 6-phosphate dehydrogenase activity in Drosophila melanogaster. Biochem Genet (1969) 1.32
Crystalline fibril structure of type II collagen in lamprey notochord sheath. J Mol Biol (1984) 1.31
Glucose 6-phosphate dehydrogenase in Drosophila malanogaster: starch gel electrophoretic variation due to molecular instability. Biochem Genet (1968) 1.30
Comparison of effectiveness of pancreatic enzyme preparations in cystic fibrosis. Am J Dis Child (1982) 1.22
The genetics of specific reading disability. Ann Hum Genet (1976) 1.19
Season of birth of siblings of schizophrenic patients. Br J Psychiatry (1992) 1.13
Familial nonhemolytic jaundice with late onset of neurological damage. Pediatrics (1968) 1.13
Genetic heterogeneity. N Engl J Med (1968) 1.13
The William Allan Memorial Award Lecture. A place for genetics in health education, and vice versa. Am J Hum Genet (1974) 1.12
Tay-Sachs screening: social and psychological impact. Am J Hum Genet (1976) 1.11
Age at onset and causes of disease. Perspect Biol Med (1986) 1.09
The personal impact of Tay-Sachs carrier screening. Prog Clin Biol Res (1977) 1.08
Persistent echoes of the nature-nurture argument. Am J Hum Genet (1977) 1.05
Sir Archibald Garrod's conception of chemical individuality: a modern appreciation. N Engl J Med (1970) 1.05
Influence of binding on the toxicity of bilirubin. Ann N Y Acad Sci (1973) 1.03
Mortality risk of exchange transfusion. Pediatrics (1968) 1.03
Hemin: levels in experimental subarachnoid hematoma and effects on dissociated vascular smooth-muscle cells. J Neurosurg (1993) 1.02
Bilirubin nephropathy in the Gunn strain of rat. Am J Physiol (1967) 1.02
Studies in kernicterus. 3. The saturation of serum proteins with bilirubin during neonatal life and its relationship to brain damage at five years. J Pediatr (1970) 1.00
"Physiologic" hyperbilirubinemia in the neonatal period. N Engl J Med (1967) 0.98
The effect of Mendelian disease on human health. II: Response to treatment. Am J Med Genet (1985) 0.94
Genetic screening. Annu Rev Genet (1975) 0.92
Studies in kernicterus. II. The determination of the saturation of serum albumin with bilirubin. J Pediatr (1969) 0.92
Familial risk factors for prostate cancer. Cancer Surv (1991) 0.91
Prevalence of hypertension in patients with type II diabetes in referral versus primary care clinics. J Diabetes Complications (1999) 0.88
The influence of bicarbonate administration on blood pH in a "closed system": clinical implications. J Pediatr (1972) 0.88
Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison. Am J Hum Genet (1995) 0.88
Hybridization of mammalian somatic cells. Prog Med Genet (1970) 0.87
Bilirubin in the liver and kidney in jaundiced rats. Am J Dis Child (1966) 0.86
The "bronze" baby syndrome: a complication of phototherapy. J Pediatr (1972) 0.86
The effect of bilirubin on the function of hamster small intestine. Pediatr Res (1981) 0.86
Schizophrenia: age at onset, gender and familial risk. Acta Psychiatr Scand (1990) 0.85
A follow-up study of dyslexic boys. Ann Dyslexia (1985) 0.84
Genetic heterogeneity. N Engl J Med (1968) 0.82
The photodynamic action of bilirubin on erythrocytes. J Pediatr (1972) 0.82
Use of the hand refractometer in determining total serum proteins of infants and children. J Pediatr (1967) 0.82
The influence of fatty acids on the binding of bilirubin to albumin. J Lab Clin Med (1977) 0.82
Hypocalcemia associated with phototherapy in newborn rats: light source dependence. Photochem Photobiol (1983) 0.82
Comparison of juvenile diabetics with positive and negative organ specific antibody titers. Evidence for genetic heterogeneity. Diabetes (1973) 0.81
Cytomegalovirus infection and compromise. Exp Hematol (1993) 0.80
Identification of an N-acetylated microsomal glutathione S-transferase by mass spectrometry. Biochem Pharmacol (1995) 0.80
Garrod, Galton, and clinical medicine. Yale J Biol Med (1973) 0.80
Influence of pH on distribution of bilirubin between albumin and mitochondria. Proc Soc Exp Biol Med (1965) 0.80
The distribution and toxicity of bilirubin. E. Mead Johnson address 1969. Pediatrics (1970) 0.80
A phase II trial of recombinant tumor necrosis factor in patients with advanced colorectal carcinoma. Cancer (1990) 0.80
Electrophoretic study of human ribosomal core proteins: evidence for selection against variation. Johns Hopkins Med J (1975) 0.79
Alpha 1-antitrypsin deficiency and the PiMS phenotype: case report and literature review. J Pediatr Gastroenterol Nutr (1989) 0.79
Dye-sensitized photooxidation of albumin associated with a decreased capacity for protein-binding of bilirubin. Birth Defects Orig Artic Ser (1970) 0.79
Reaction of bilirubin glucuronides with serum albumin. J Chromatogr (1986) 0.78
Effects of anesthetic agents on bile pigment excretion in the rat. Hepatology (1985) 0.78
The response of jaundiced and non-jaundiced weanling rats to thirsting. Pediatr Res (1968) 0.78
An electrophoretic method for detecting hypoxanthine-guanine phosphoribosyl transferase variants. Biochem Genet (1969) 0.78
Acute cholestasis in patients with toxic- shock syndrome. Gastroenterology (1981) 0.78
Demonstration of giardia in duodenal fluid by scanning electron microscopy. N Engl J Med (1978) 0.78
Differential growth patterns in SCID mice of patient-derived chronic myelogenous leukemias. Bone Marrow Transplant (1998) 0.78
Patterns of alkaline phosphatase in developing Drosophila. Science (1966) 0.77
Bilirubin levels in subarachnoid clot and effects on canine arterial smooth muscle cells. Stroke (1993) 0.77
Causes of essential hypertension. Prog Med Genet (1983) 0.77
A multisite physician's office laboratory evaluation of an immunological method for the measurement of HbA1c. Diabetes Care (1992) 0.77
Recombinant DNA analysis of multifactorial disease. Prog Med Genet (1988) 0.77
Human behavior genetics. Adv Hum Genet (1976) 0.77
Kernicterus: revised concepts of pathogenesis and management. Pediatrics (1966) 0.77
Hepatic bilirubin UDP-glucuronyltransferase in patients with sickle cell anemia. Gastroenterology (1978) 0.77
Molecular genetics in medicine. Introduction. Prog Med Genet (1988) 0.76
Prospects for genetic screening. J Pediatr (1975) 0.76
Familial distributions of organ specific antibodies in the blood of patients with Addison's disease and hypoparathyroidism and their relatives. Clin Exp Immunol (1969) 0.76
The association between season of birth and the risk for schizophrenia. Am J Epidemiol (1981) 0.76
Effects of phototherapy on neonatal hyperbilirubinemia. J Pediatr (1970) 0.76
The presence of a microsomal UDP-glucuronyl transferase for bilirubin in homozygous jaundiced Gunn rats and in the Crigler-Najjar syndrome. Hepatology (1981) 0.76
Derivation and validation of a quantitative definition of specific reading disability for adults. Dev Med Child Neurol (1984) 0.76
Analytical methods for water disinfection byproducts in foods and beverages. J Expo Anal Environ Epidemiol (2001) 0.76
Frontiers of psychiatric genetics. Neurosci Res Program Bull (1976) 0.76
Empirical validation of reading and spelling quotients. Dev Med Child Neurol (1982) 0.75
Why do some individuals have more infections than others? JAMA (2001) 0.75
Obstetricians' attitudes toward genetic screening. Am J Public Health (1977) 0.75
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. Am J Hum Genet (1979) 0.75