Published in Am J Hum Genet on August 01, 1987
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Molecular genetic analysis of tumors in von Recklinghausen neurofibromatosis: loss of heterozygosity for chromosome 17. Genes Chromosomes Cancer (1989) 1.13
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Induction of -globin synthesis in the -thalassaemia of Ferrara. Nat New Biol (1972) 1.08
Inducers of erythroid differentiation in K562 human leukemia cells. Exp Hematol (1981) 1.07
Erythroid colony formation from human fetal liver. Proc Natl Acad Sci U S A (1978) 1.06
Cystic fibrosis carrier population screening in the primary care setting. Am J Hum Genet (1996) 1.02
Prenatal hemoglobinopathy screening. IV. Follow-up of women at risk for a child with a clinically significant hemoglobinopathy. Am J Hum Genet (1991) 1.01
Newborn sickle cell screening. Benefits and burdens realized. Am J Dis Child (1983) 0.96
Hemoglobin synthesis in cultures of hepatic erythroid cells from the human fetus. Proc Natl Acad Sci U S A (1979) 0.94
Genetic counseling of asymptomatic carriers in a primary care setting. The effectiveness of screening and counseling for beta-thalassemia trait. Ann Intern Med (1986) 0.94
Family issues in a psychoeducation group for women with a BRCA mutation. Clin Genet (2002) 0.91
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Separation of malarial parasites according to age by density gradient centrifugation. J Lab Clin Med (1967) 0.89
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Multipotent human hematopoietic cell line K562: lineage-specific constitutive and inducible antigens. Leuk Res (1987) 0.88
The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin. Am J Hum Genet (1991) 0.86
Newborn screening for sicle-cell disease. Benefits and burdens. N Y State J Med (1978) 0.86
Protein synthesis in reticulocytes maturing in vivo. Nature (1965) 0.86
Carrier screening for cystic fibrosis: test acceptance and one year follow-up. Am J Med Genet (1997) 0.86
Erythroleukemia manifesting delta beta-thalassemia. Hemoglobin (1983) 0.85
An adult homozygous for persistent fetal hemoglobin. Ann Intern Med (1970) 0.85
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Regulation of K562 cell transferrin receptors by exogenous iron. J Cell Physiol (1985) 0.84
Linkage between the MN- and Hb beta-loci? Hum Hered (1972) 0.84
Sickle hemoglobin: a specific radioimmunoassay. Blood (1974) 0.84
Toward providing parents the option of avoiding the birth of the first child with Cooley's anemia: response to hemoglobinopathy screening and counseling during pregnancy. Ann N Y Acad Sci (1985) 0.84
A Lepore hemoglobin in a Rumanian family. Hum Hered (1969) 0.84
The diagnosis of beta-thalassemia trait: a review. Am J Hematol (1976) 0.84
Incorporation of screening and genetic counseling for beta-thalassemia trait into primary health care: effects on knowledge and attitudes. Birth Defects Orig Artic Ser (1982) 0.83
Hemoglobin S-C disease presenting as acute cor pulmonale. Am Rev Respir Dis (1968) 0.83
Acquired hemoglobin H disease in idiopathic myelofibrosis. Am J Hematol (1979) 0.82
K562 human erythroleukemia cells demonstrate commitment. Blood (1985) 0.81
K562 human leukemia cell passages differ in embryonic globin gene expression. Leuk Res (1984) 0.81
Solubilization of a reticulocyte ribosomal fraction responsible for the decline in ribosomal activity with cell maturation. Arch Biochem Biophys (1971) 0.81
The linkage relationships of the haemoglobin beta, delta and alpha loci with 34 genetic marker systems. Ann Hum Genet (1977) 0.80
Predicting immediate outcome of genetic counseling following screening. Soc Biol (1979) 0.80
Oncogene expression in neurofibromatosis. Ann N Y Acad Sci (1986) 0.80
Induction of megakaryocytic characteristics in human leukemic cell line K562: polyploidy, inducers, and secretion of mitogenic activity. J Biol Regul Homeost Agents (1988) 0.80
Human lymphocyte telomerase is genetically regulated. Genes Chromosomes Cancer (1998) 0.79
Telomere-related components are coordinately synthesized during human T-lymphocyte activation. Leuk Res (1999) 0.79
Hemin preferentially stimulates synthesis of alpha-globin in K562 human erythroleukemia cells. Blood (1982) 0.79
High resolution analysis of hemoglobins: polyacrylamide isoelectric focusing. Biochem Med (1972) 0.79
Tumor suppressor genes and inherited predisposition to malignancy. Semin Oncol (1989) 0.78
Serm alpha-antitrypsin types: elastase inhibition versus trypsin inhibition. Hum Hered (1974) 0.78
Induction of HL60 cell differentiation by tiazofurin and its analogues: characterization and efficacy. Blood (1991) 0.77
Demonstration of commitment by K562 human erythroleukemia cells. Prog Clin Biol Res (1985) 0.77
Hereditary haemorrhagic telangiectasia: aggravation by oral contraceptives? Lancet (1970) 0.77
Serum antitrypsin synthesis by the isolated perfused rat liver. Proc Soc Exp Biol Med (1975) 0.77
Disappearance of ribosomes and polyribosomes during in vivo erythroid maturation. Nature (1967) 0.77
Regulation of the activity of heme degradative enzymes in K562 erythroleukemic cells: induction by thymidine. Exp Hematol (1987) 0.76
Sickle beta-thalassemia: identical twins differing in severity implicate nongenetic factors influencing course. Am J Hematol (1976) 0.76
Prenatal screening for hemoglobinopathies. Am J Hum Genet (1991) 0.75
K562 human erythroleukemia cell variants resistant to growth inhibition by butyrate have deficient histone acetylation. Am J Hum Genet (1984) 0.75
Characteristics of the antitrypsin activity of human serum. J Clin Pathol (1973) 0.75
Confusion about breast-cancer screening. N Engl J Med (1997) 0.75
Assessment of evaluation of hospitalized pediatric patients with genetic disorders. Clin Pediatr (Phila) (1981) 0.75
Erythroid differentiation of K562 cells: mixed colonies as an index of delayed expression of commitment. Exp Hematol (1987) 0.75
Genetic counseling in medical practice. Alaska Med (1969) 0.75
What you should know about chromosome analysis. Alaska Med (1969) 0.75
Erythroid induction of K562 human leukemia cells: enhancement by purines. Arch Biochem Biophys (1985) 0.75
Familial hearing loss associated with branchial fistulas. Pediatrics (1969) 0.75
Tetrahydrocannabinol inhibits adenyl cyclase in human leukemia cells. Life Sci (1990) 0.75
Genetic screening: whose responsibility? JAMA (1976) 0.75
Textural differences between AA and SS blood specimens as detected by image analysis. Cytometry (1994) 0.75
Trypsin enhances erythropoiesis in vitro. J Lab Clin Med (1980) 0.75
Deleterious mutations of both BRCA1 and BRCA2 in three siblings. Genet Test (1998) 0.75
K562 cell erythroid differentiation: requirement for a factor in fetal bovine serum. Exp Hematol (1985) 0.75
Induction of hemoglobin synthesis in K562 cells by carbon dioxide deficiency. Int J Cell Cloning (1987) 0.75
The contribution of red cell morphology to the diagnosis of beta-thalassemia trait. Blood Cells (1986) 0.75
Genetics for the cardiologist. Part II: Chromosomal and polygenic inheritance and genetic counseling. Mod Concepts Cardiovasc Dis (1978) 0.75
Genetics for the cardiologist. Part I: mendelian inheritance. Mod Concepts Cardiovasc Dis (1978) 0.75
Genetic testing for breast-ovarian cancer susceptibility: a regional trial. Genet Test (1998) 0.75
Single-cell analysis of the relationship among transferrin receptors, proliferation, and cell cycle phase in K562 cells. Cytometry (1985) 0.75
Long survival in sickle-cell disease. Lancet (1973) 0.75
Erythropoiesis in vitro: enhancement by neuraminidase. Blood (1981) 0.75
Genetic considerations in neuromuscular diseases. Adv Neurol (1977) 0.75
Sickle cell trait/hereditary persistence of fetal hemoglobin trait. Misdiagnosis as sickle cell anemia by newborn screening. Am J Dis Child (1979) 0.75
Enhanced polyribosome recovery from reticulocytes using heparin. Exp Cell Res (1967) 0.75
No limits to genetic inquiry. Hastings Cent Rep (1988) 0.75
Issues in implementing prenatal screening for cystic fibrosis: results of a working conference. Genet Med (2001) 0.75
Oncogene expression in myelopoiesis. Int J Cell Cloning (1987) 0.75
Letter: Family history-taking. J Med Educ (1976) 0.75
Drug-sensitive hemoglobinopathies. N Engl J Med (1973) 0.75
Hypersplenic thrombocytopenia in sickle cell-bata thalassemia. Am J Med Sci (1972) 0.75