Published in Nature on August 25, 1972
Comparable rates of gene loss and functional divergence after genome duplications early in vertebrate evolution. Genetics (1997) 2.55
Identification of a cDNA encoding a parathyroid hormone-like peptide from a human tumor associated with humoral hypercalcemia of malignancy. Proc Natl Acad Sci U S A (1988) 2.20
Homologous genes for enolase, phosphogluconate dehydrogenase, phosphoglucomutase, and adenylate kinase are syntenic on mouse chromosome 4 and human chromosome 1p. Proc Natl Acad Sci U S A (1978) 1.48
Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man. Am J Hum Genet (1973) 1.39
Isolation and characterization of the human parathyroid hormone-like peptide gene. Proc Natl Acad Sci U S A (1989) 1.31
Molecular and functional characterization of amylin, a peptide associated with type 2 diabetes mellitus. Proc Natl Acad Sci U S A (1989) 1.04
Estimation of allele frequencies at isoloci. Genetics (1988) 0.96
Evolutionary implications of the human aldolase-A, -B, -C, and -pseudogene chromosome locations. Am J Hum Genet (1987) 0.87
PTHrP gene expression in cancer: do all paths lead to Ets? Crit Rev Eukaryot Gene Expr (2005) 0.86
Two loci affecting B cell responses to B cell maturation factors. J Exp Med (1986) 0.85
Mouse map of paralogous genes. Mamm Genome (1991) 0.78
Familial multifocal fibrosclerosis. Findings suggesting that retroperitoneal fibrosis, mediastinal fibrosis, sclerosing cholangitis, Riedel's thyroiditis, and pseudotumor of the orbit may be different manifestations of a single disease. Ann Intern Med (1967) 4.00
Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene. Lancet (1993) 2.91
Reward deficiency syndrome: a biogenetic model for the diagnosis and treatment of impulsive, addictive, and compulsive behaviors. J Psychoactive Drugs (2000) 2.82
A general theory of carcinogenesis. Proc Natl Acad Sci U S A (1973) 2.28
The D2 dopamine receptor gene as a determinant of reward deficiency syndrome. J R Soc Med (1996) 1.98
The rationale for an ordered arrangement of chromatin in the interphase nucleus. Am J Hum Genet (1968) 1.95
Association of the dopamine transporter gene (DAT1) with poor methylphenidate response. J Am Acad Child Adolesc Psychiatry (1999) 1.88
Arrangement of chromatin in the nucleus. Hum Genet (1980) 1.82
Nuclear proteins. III. The fibrillar nature of the nuclear matrix. Exp Cell Res (1976) 1.77
The structure and function of chromatin. Adv Hum Genet (1972) 1.74
Holocentric chromosomes in Oncopeltus: kinetochore plates are present in mitosis but absent in meiosis. Chromosoma (1972) 1.70
Initiation of deoxyribonucleic acid replication at the nuclear membrane in human cells. J Mol Biol (1968) 1.63
Pc 1 Duarte, a common polymorphism of a human brain protein, and its relationship to depressive disease and multiple sclerosis. Nature (1979) 1.61
Mechanisms of chromosome banding and implications for chromosome structure. Annu Rev Genet (1978) 1.57
Detection of major gene for Gilles de la Tourette syndrome. Am J Hum Genet (1984) 1.54
Association of chromatin fibers with the annuli of the nuclear membrane. Exp Cell Res (1970) 1.49
Partial albinism. JAMA (1966) 1.42
Electron microscopy of human fibroblasts in tissue culture during logarithmic and confluent stages of growth. Exp Cell Res (1970) 1.41
Mechanisms of chromosome banding. VIII. Hoechst 33258-DNA interaction. Chromosoma (1975) 1.40
The mechanism of C- and G-banding of chromosomes. Exp Cell Res (1973) 1.38
Dopamine D2 receptor gene variants: association and linkage studies in impulsive-addictive-compulsive behaviour. Pharmacogenetics (1995) 1.35
A search for protein cores in chromosomes: is the scaffold an artifact? Am J Hum Genet (1980) 1.24
Partial deletion of chromosome 6p: delineation of the syndrome. Am J Med Genet (1991) 1.22
Fine structure of kinetochore in Indian muntjac. Exp Cell Res (1971) 1.22
Optical Studies of the interaction of 4'-6'-diamidino-2-phenylindole with DNA and metaphase chromosomes. Chromosoma (1977) 1.16
Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3. Am J Hum Genet (1996) 1.16
Dopamine receptor genes are associated with age at first sexual intercourse. J Biosoc Sci (1999) 1.14
Nuclear proteins. I. Electrophoretic comparison of mouse nucleoli, heterochromatin, euchromatin and contractile proteins. Exp Cell Res (1975) 1.13
Tourette syndrome: clinical and psychological aspects of 250 cases. Am J Hum Genet (1985) 1.13
Role of the cholinergic muscarinic 2 receptor (CHRM2) gene in cognition. Mol Psychiatry (2003) 1.11
Higher order structure of chromosomes. Chromosoma (1979) 1.10
Nuclear proteins. IV. Deficiency of non-histone proteins in condensed chromatin of Drosophila virilis and mouse. Exp Cell Res (1977) 1.10
A common C-1018G polymorphism in the human 5-HT1A receptor gene. Psychiatr Genet (1999) 1.09
Non-histone proteins. The effect of nuclear washes and comparison of metaphase and interphase chromatin. Exp Cell Res (1973) 1.06
Nuclear proteins. II. Similarity of nonhistone proteins in nuclear sap and chromatin, and essential absence of contractile proteins from mouse liver nuclei. J Cell Biol (1976) 1.04
Determination of subfractions of amniotic fluid alpha-fetoprotein in diagnosing spina bifida and congenital nephrosis. Br Med J (1979) 1.04
Benign symmetric lipomatosis. JAMA (1968) 1.03
Stress as a mediating factor in the association between the DRD2 TaqI polymorphism and alcoholism. Alcohol (2001) 1.03
A controlled study of Tourette syndrome. V. Depression and mania. Am J Hum Genet (1987) 1.03
Whole mount electron microscopy of meiotic chromosomes and the synaptonmal complex. Chromosoma (1970) 1.01
Two-dimensional gel electrophoresis of human brain proteins. III. Genetic and non-genetic variations in 145 brains. Clin Chem (1982) 1.00
Mechanisms of chromosome banding. IX. Are variations in DNA base composition adequate to account for quinacrine, Hoechst 33258 and daunomycin banding? Chromosoma (1976) 1.00
Tourette's syndrome and attention deficit disorder with hyperactivity: are they genetically related? J Am Acad Child Psychiatry (1984) 0.99
Fibroblasts in Huntington's disease. N Engl J Med (1975) 0.98
Autosomal dominant insensitivity to pain with hyperplastic myelinopathy and autosomal dominant indifference to pain. Neurology (1974) 0.97
A case of familial exhibitionism in Tourette's syndrome successfully treated with haloperidol. Am J Psychiatry (1982) 0.94
The chromatoid body in mouse spermatogenesis: evidence that it may be formed by the extrusion of nucleolar components. J Ultrastruct Res (1972) 0.93
Heterochromatin of the Indian muntjac. Replication, condensation, DNA ultracentrifugation, fluorescent and heterochromatin staining. Exp Cell Res (1971) 0.93
Sister chromatid exchange and chromosome organization based on a bromodeoxyuridine Giemsa-C-banding technique (TC-banding). Chromosoma (1975) 0.91
Do the Giemsa-banding patterns of chromosomes change during embryonic development? Exp Cell Res (1972) 0.91
Whole-mount electron microscopy of the centromere region of metacentric and telocentric mammalian chromosomes. Cytogenetics (1970) 0.91
DNA loss during Robertsonian fusion in studies of the tobacco mouse. Nat New Biol (1972) 0.91
Triple-spot proteins in two-dimensional gel electrophoresis. Am J Hum Genet (1979) 0.91
Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse. Mol Psychiatry (1998) 0.91
Powerful new tools in genetics. Am J Hum Genet (1979) 0.90
The duration of replication of the inactive X chromosome in humans based on the persistence of the heterochromatic sex chromatin body during DNA synthesis. Cytogenetics (1967) 0.90
The genetics of Rett syndrome: the consequences of a disorder where every case is a new mutation. Am J Med Genet Suppl (1986) 0.89
Histones of genetically active and inactive chromatin. J Cell Biol (1967) 0.89
Fibronectin from human germ-cell tumors resembles amniotic fluid fibronectin. Int J Cancer (1981) 0.89
Huntington disease and Tourette syndrome. I. Electron spin resonance of bed ghosts. Am J Hum Genet (1981) 0.89
DNA-binding properties of nuclear matrix proteins. J Cell Sci (1978) 0.88
A storage form of ribosomes in mouse oocytes. Exp Cell Res (1971) 0.87
Absence of cis delta chain synthesis in (sigma beta) thalassemia (F-thalassemia). Blood (1966) 0.87
New frontiers in genetic medicine. Ann Intern Med (1986) 0.87
Similarities in the cytoplasmic proteins of different organs and species examined by SDS gel electrophoresis. Exp Cell Res (1972) 0.87
Whole mount electron microscopy of metaphase. I. Chromosomes and microtubules from mouse oocytes. Exp Cell Res (1972) 0.87
Association of polymorphisms of dopamine D2 receptor (DRD2), and dopamine transporter (DAT1) genes with schizoid/avoidant behaviors (SAB). Mol Psychiatry (1997) 0.86
Serotonin transporter gene polymorphisms in alcohol dependence. Alcohol (2000) 0.86
Chinese hamster nuclear proteins. An electrophoretic analysis of interphase, metaphase and nuclear matrix preparations. Eur J Biochem (1982) 0.86
Condensation of chromosomes onto the nuclear membrane during prophase. Exp Cell Res (1970) 0.86
Mechanism of chromosome pairing during meiosis. Nature (1970) 0.85
Fine structure of the synaptonemal complex. Regular and stereo electron microscopy of deoxyribonuclease-treated whole mount preparations. Exp Cell Res (1971) 0.85
Replicative heterogeneity of mammalian DNA. Exp Cell Res (1972) 0.85
Molecular heterosis as the explanation for the controversy about the effect of the DRD2 gene on dopamine D2 receptor density. Mol Psychiatry (1999) 0.85
Two-dimensional gel electrophoresis of human brain proteins. IV. Disorders of glial proliferation and a polymorphism of glial fibrillary acidic protein--GFAP Duarte. Clin Chem (1982) 0.84
Buoyant density and satellite composition of DNA of mouse heterochromatin. Nat New Biol (1971) 0.84
Methylation of euchromatic and heterochromatic DNA. Exp Cell Res (1972) 0.84
Association between the cannabinoid receptor gene (CNR1) and the P300 event-related potential. Mol Psychiatry (1997) 0.84
Molecular mechanisms of chromosome pairing, folding and function. Nature (1971) 0.83
Replication of repetitious DNA and the S period. Proc Natl Acad Sci U S A (1970) 0.83
Lymphocyte transformation in response to phytohemagglutinin during and following a pregnancy. Am J Obstet Gynecol (1967) 0.83
Conradi's disease. Chondrodystrophia calcificans congenita, congenital stippled epiphyses. J Pediatr (1968) 0.83
DNA of mammalian and avian heterochromatin. Exp Cell Res (1972) 0.83
DNA replication and the nuclear membrane. J Mol Biol (1973) 0.83
Mechanisms of chromosome banding. II. Evidence that histones are not involved. Exp Cell Res (1974) 0.82
Phenylethanolamine N-methyltransferase (PNMT) gene and early-onset Alzheimer disease. Am J Med Genet (2001) 0.82
Two-dimensional gel electrophoresis of human brain proteins. I. Technique and nomenclature of proteins. Clin Chem (1982) 0.82
Mechanisms of chromosome banding. III. Similarity between G-bands of mitotic chromosomes and chromomeres of meiotic chromosomes. Chromosoma (1974) 0.82
Huntington disease and Tourette syndrome. II. Uptake of glutamic acid and other amino acids by fibroblasts. Am J Hum Genet (1981) 0.81
Localization of indoleamine 2,3-dioxygenase gene (INDO) to chromosome 8p12-->p11 by fluorescent in situ hybridization. Cytogenet Cell Genet (1993) 0.80
Substitution of polybuffer for ampholytes in isoelectric focusing. Anal Biochem (1982) 0.80
Structure of mammalian chromosomes. Basic Life Sci (1974) 0.80
Incorporation of tritium of 3H-5-uridine into DNA. Exp Cell Res (1966) 0.80
The ups and downs of Huntington disease research. Am J Hum Genet (1981) 0.80
Specific interaction between mouse liver non-histone chromosomal proteins and mouse DNA demonstrated by a sequential DNA-protein binding procedure. Biochim Biophys Acta (1978) 0.80
Two-dimensional gel electrophoresis of human brain proteins. V. Non-equilibrium gel electrophoresis, with detection of a myelin basic protein mutation--MBL-Duarte. Clin Chem (1982) 0.80
Methods and mechanisms of chromosome banding. Methods Cell Biol (1978) 0.79
Mutation screening of the dopamine D1 receptor gene in Tourette's syndrome and alcohol dependent patients. Am J Med Genet (1998) 0.79
Sex chromatin, nuclear size and the cell cycle. Cytogenetics (1967) 0.79
Tourette's syndrome and attention-deficit hyperactivity disorder: evidence for a genetic relationship. J Clin Psychiatry (1993) 0.79