Publications: Barbara Migeon
Download CSV for Barbara Migeon
| Title | Year | Citations | Score |
|---|---|---|---|
|
D-valine as a selective agent for normal human and rodent epithelial cells in culture
Cell 5 (1), 11-17, 1975 View Details |
1975 | 458 | 95.8% |
|
Methylation of the hypoxanthine phosphoribosyltransferase locus on the human X chromosome: implications for X-chromosome inactivation.
Proceedings of the National Academy of Sciences 81 (9), 2806-2810, 1984 View Details |
1984 | 374 | 93.3% |
|
Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.
Proceedings of the National Academy of Sciences 78 (8), 5066-5070, 1981 View Details |
1981 | 337 | 92.5% |
|
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations
Science 160 (3826), 425-427, 1968 View Details |
1968 | 232 | 92.0% |
|
Mechanism of origin of complete hydatidiform moles
Nature 286 (5774), 714-716, 1980 View Details |
1980 | 300 | 91.8% |
|
X-linked diseases: susceptible females
Genetics in Medicine 22 (7), 1156-1174, 2020 View Details |
2020 | 131 | 91.6% |
|
Locus on human X chromosome for dihydrotestosterone receptor and androgen insensitivity.
Proceedings of the National Academy of Sciences 72 (4), 1469-1472, 1975 View Details |
1975 | 238 | 91.2% |
|
Three related centromere proteins are absent from the inactive centromere of a stable isodicentric chromosome
Chromosoma 92 (4), 290-296, 1985 View Details |
1985 | 288 | 90.1% |
|
Genetic inactivation of the α-galactosidase locus in carriers of Fabry's disease
Science 170 (3954), 180-181, 1970 View Details |
1970 | 163 | 88.9% |
|
Human-mouse somatic cell hybrids with single human chromosome (group E): link with thymidine kinase activity
Science 162 (3857), 1005-1006, 1968 View Details |
1968 | 145 | 88.6% |
|
DNA methylation stabilizes X chromosome inactivation in eutherians but not in marsupials: evidence for multistep maintenance of mammalian X dosage compensation.
Proceedings of the National Academy of Sciences 84 (17), 6210-6214, 1987 View Details |
1987 | 211 | 87.2% |
|
Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.
Proceedings of the National Academy of Sciences 77 (5), 2810-2813, 1980 View Details |
1980 | 186 | 86.6% |
|
Human thymidine kinase gene locus: assignment to chromosome 17 in a hybrid of man and mouse cells
Science 173 (3993), 244-245, 1971 View Details |
1971 | 137 | 86.5% |
|
Studies of the locus for androgen receptor: localization on the human X chromosome and evidence for homology with the Tfm locus in the mouse.
Proceedings of the National Academy of Sciences 78 (10), 6339-6343, 1981 View Details |
1981 | 179 | 85.6% |
|
Sex difference in methylation of single-copy genes in human meiotic germ cells: implications for X chromosome inactivation, parental imprinting, and origin of CpG mutations
Somatic cell and molecular genetics 16 (3), 267-282, 1990 View Details |
1990 | 193 | 85.0% |
|
The role of X inactivation and cellular mosaicism in women's health and sex-specific diseases
Jama 295 (12), 1428-1433, 2006 View Details |
2006 | 209 | 84.5% |
|
Differential expression of steroid sulphatase locus on active and inactive human X chromosome
Nature 299 (5886), 838-840, 1982 View Details |
1982 | 163 | 84.5% |
|
Studies of X chromosome DNA methylation in normal human cells
Nature 295 (5851), 667-671, 1982 View Details |
1982 | 159 | 84.0% |
|
Complex chromosome rearrangements: report of a new case and literature review
Clinical genetics 18 (6), 436-444, 1980 View Details |
1980 | 156 | 83.8% |
|
Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes
Nature 314 (6010), 467-469, 1985 View Details |
1985 | 158 | 83.0% |
|
X-chromosome inactivation: molecular mechanisms and genetic consequences
Trends in Genetics 10 (7), 230-235, 1994 View Details |
1994 | 178 | 82.8% |
|
The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease.
American journal of human genetics 28 (2), 123, 1976 View Details |
1976 | 140 | 82.6% |
|
Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation.
Proceedings of the National Academy of Sciences 81 (15), 4884-4888, 1984 View Details |
1984 | 129 | 81.1% |
|
Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNA.
The EMBO journal 7 (2), 401-406, 1988 View Details |
1988 | 149 | 80.6% |
|
DNA restriction endonuclease analysis for localization of human beta-and delta-globin genes on chromosome 11.
Proceedings of the National Academy of Sciences 76 (9), 4563-4565, 1979 View Details |
1979 | 118 | 80.0% |
|
Stability of X chromosomal inactivation in human somatic cells.
Nature 239 (5367), 1972 View Details |
1972 | 94 | 79.7% |
|
Why females are mosaics, X-chromosome inactivation, and sex differences in disease
Gender medicine 4 (2), 97-105, 2007 View Details |
2007 | 151 | 79.3% |
|
Incomplete X chromosome dosage compensation in chorionic villi of human placenta.
Proceedings of the National Academy of Sciences 82 (10), 3390-3394, 1985 View Details |
1985 | 121 | 78.7% |
|
Identification of TSIX, encoding an RNA antisense to human XIST, reveals differences from its murine counterpart: implications for X inactivation
The American Journal of Human Genetics 69 (5), 951-960, 2001 View Details |
2001 | 162 | 78.2% |
|
The severe phenotype of females with tiny ring X chromosomes is associated with inability of these chromosomes to undergo X inactivation.
American journal of human genetics 55 (3), 497, 1994 View Details |
1994 | 134 | 78.1% |
|
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: detection of heterozygotes by selective medium
Biochemical genetics 4 (3), 377-383, 1970 View Details |
1970 | 65 | 77.9% |
|
Species differences in TSIX/Tsix reveal the roles of these genes in X-chromosome inactivation
The American Journal of Human Genetics 71 (2), 286-293, 2002 View Details |
2002 | 158 | 77.8% |
|
Complete concordance between glucose-6-phosphate dehydrogenase activity and hypomethylation of 3′ CpG clusters: implications for X chromosome dosage compensation
Nucleic acids research 12 (24), 9333-9348, 1984 View Details |
1984 | 103 | 77.3% |
|
Comparison of contact-mediated communication in normal and transformed human cells in culture.
Proceedings of the National Academy of Sciences 74 (10), 4476-4480, 1977 View Details |
1977 | 92 | 76.6% |
|
Deficient transcription of XIST from tiny ring X chromosomes in females with severe phenotypes.
Proceedings of the National Academy of Sciences 90 (24), 12025-12029, 1993 View Details |
1993 | 114 | 76.4% |
|
The prenatal diagnosis of adrenoleukodystrophy. Demonstration of increased hexacosanoic acid levels in cultured amniocytes and fetal adrenal gland
Pediatric research 16 (3), 172-175, 1982 View Details |
1982 | 99 | 75.9% |
|
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells
Nature 250 (5467), 580-582, 1974 View Details |
1974 | 80 | 75.7% |
|
The Barr body is a looped X chromosome formed by telomere association.
Proceedings of the National Academy of Sciences 88 (14), 6191-6195, 1991 View Details |
1991 | 106 | 75.4% |
|
Hybridization of somatic cells derived from mouse and Syrian hamster: Evolution of karyotype and enzyme studies
Biochemical Genetics 1 (4), 305-322, 1968 View Details |
1968 | 63 | 74.8% |
|
Non-random X chromosome inactivation in mammalian cells
Cytogenetic and Genome Research 80 (1-4), 142-148, 1998 View Details |
1998 | 117 | 73.8% |
|
FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
Bulletin of the Johns Hopkins Hospital 116, 396-402, 1965 View Details |
1965 | 45 | 73.2% |
|
Asynchronous replication of homologous loci on human active and inactive X chromosomes.
Proceedings of the National Academy of Sciences 87 (10), 3685-3689, 1990 View Details |
1990 | 96 | 73.2% |
|
Human and mouse hypoxanthine-guanine phosphoribosyltransferase: dimers and tetramers
Science 203 (4376), 174-176, 1979 View Details |
1979 | 80 | 73.0% |
|
The HumanNTTGene: identification of a novel 17-kb noncoding nuclear RNA expressed in activated CD4+ T cells
Genomics 39 (2), 171-184, 1997 View Details |
1997 | 108 | 72.6% |
|
Selection against lethal alleles in females heterozygous for incontinentia pigmenti.
American journal of human genetics 44 (1), 100, 1989 View Details |
1989 | 87 | 71.9% |
|
The nature of thymidine kinase in the human-mouse hybrid cell
Biochemical Genetics 3, 583-590, 1969 View Details |
1969 | 53 | 71.8% |
|
Effect of ageing on reactivation of the human X-linked HPRT locus
Nature 335 (6185), 93-96, 1988 View Details |
1988 | 90 | 71.7% |
|
Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistry
Johns Hopkins Medical Journal 147 (6), 217-224, 1980 View Details |
1980 | 70 | 70.9% |
|
Females are mosaics: X inactivation and sex differences in disease
Oxford university press, 2007 View Details |
2007 | 98 | 70.6% |
|
Complete reactivation of X chromosomes from human chorionic villi with a switch to early DNA replication.
Proceedings of the National Academy of Sciences 83 (7), 2182-2186, 1986 View Details |
1986 | 73 | 70.0% |
|
Isolation and characterization of cloned DNA sequences that hybridize to the human X chromosome
Cell 21 (1), 95-102, 1980 View Details |
1980 | 68 | 70.0% |
|
Non–random loss of human markers from man–mouse somatic cell hybrids
Nature 251 (5470), 72-74, 1974 View Details |
1974 | 58 | 69.9% |
|
X inactivation, female mosaicism, and sex differences in renal diseases
Journal of the American Society of Nephrology 19 (11), 2052-2059, 2008 View Details |
2008 | 92 | 69.6% |
|
Evidence for two active X chromosomes in germ cells of female before meiotic entry
Nature 269 (5625), 242-243, 1977 View Details |
1977 | 65 | 69.6% |
|
X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
American journal of human genetics 29 (5), 448, 1977 View Details |
1977 | 64 | 69.2% |
|
Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.
American journal of human genetics 56 (3), 647, 1995 View Details |
1995 | 80 | 68.3% |
|
DNA replication analysis of FMR1, XIST, and factor 8C loci by FISH shows nontranscribed X-linked genes replicate late.
American journal of human genetics 55 (1), 96, 1994 View Details |
1994 | 80 | 68.3% |
|
Assignment of the haemophilia B (Factor IX) locus to the q26‐qter region of the X chromosome
Annals of human genetics 48 (2), 145-152, 1984 View Details |
1984 | 63 | 68.1% |
|
Interferon production and action in mouse, hamster, and somatic hybrid mouse-hamster cells
Science 160 (3827), 558-559, 1968 View Details |
1968 | 43 | 67.9% |
|
Androgen receptors and metabolism in cultured human fetal fibroblasts
Pediatric research 14 (1), 67-69, 1980 View Details |
1980 | 60 | 67.5% |
|
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?
American journal of human genetics 29 (5), 455, 1977 View Details |
1977 | 59 | 67.4% |
|
Renal enzymes in kidney cells selected by D‐valine medium
Journal of Cellular Physiology 92 (2), 161-167, 1977 View Details |
1977 | 59 | 67.4% |
|
Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cells
Cell 29 (2), 595-600, 1982 View Details |
1982 | 61 | 66.8% |
|
Studies of skin fibroblasts from 10 families with HGPRT deficiency, with reference in X-chromosomal inactivation.
American journal of human genetics 23 (2), 199, 1971 View Details |
1971 | 42 | 66.5% |
|
Haptoglobin: a locus on the D1 chromosome?
American journal of human genetics 19 (3 Pt 2), 393, 1967 View Details |
1967 | 39 | 66.5% |
|
Isolation and analysis of somatic hybrids derived from two human diploid cells
Proceedings of the National Academy of Sciences 71 (3), 937-941, 1974 View Details |
1974 | 47 | 65.3% |
|
In search of non-random X inactivation: studies of fetal membranes heterozygous for glucose-6-phosphate dehydrogenase.
American journal of human genetics 31 (5), 581, 1979 View Details |
1979 | 56 | 65.1% |
|
Contact-mediated communication of ouabain resistance in mammalian cells in culture
Nature 268 (5622), 737-739, 1977 View Details |
1977 | 52 | 64.6% |
|
Stability of the “two active X” phenotype in triploid somatic cells
Cell 18 (3), 637-641, 1979 View Details |
1979 | 53 | 64.0% |
|
Short arm deletions in group E and chromosomal “deletion” syndromes
The Journal of pediatrics 69 (3), 432-438, 1966 View Details |
1966 | 32 | 64.0% |
|
Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa
Genetics Research 56 (2-3), 91-98, 1990 View Details |
1990 | 59 | 63.6% |
|
Evidence for the inactivation of an X chromosome early in the development of the human female.
American journal of human genetics 27 (2), 233, 1975 View Details |
1975 | 43 | 63.2% |
|
Choosing the active X: the human version of X inactivation
Trends in Genetics 33 (12), 899-909, 2017 View Details |
2017 | 44 | 62.3% |
|
Human X inactivation center induces random X chromosome inactivation in male transgenic mice
Genomics 59 (2), 113-121, 1999 View Details |
1999 | 68 | 62.3% |
|
Comparison of factor IX methylation on human active and inactive X chromosomes: implications for X inactivation and transcription of tissue‐specific genes.
The EMBO Journal 5 (9), 2223-2229, 1986 View Details |
1986 | 49 | 61.9% |
|
Frequent derepression of G6PD and HPRT on the marsupial inactive X chromosome associated with cell proliferation in vitro
Experimental cell research 182 (2), 597-609, 1989 View Details |
1989 | 52 | 61.8% |
|
Dosage compensation in the regulation of erythrocyte glucose-6-phosphate dehydrogenase activity.
Bulletin of the Johns Hopkins Hospital 112, 318-322, 1963 View Details |
1963 | 21 | 61.6% |
|
Hybridization of mammalian somatic cells
Progress in medical genetics 7, 1-28, 1970 View Details |
1970 | 28 | 61.1% |
|
Signal sequence and DNA‐mediated expression of human lysosomal α‐galactosidase A
European journal of biochemistry 165 (2), 275-280, 1987 View Details |
1987 | 49 | 60.8% |
|
DNA methylation of the fragile X locus in somatic and germ cells during fetal development: relevance to the fragile X syndrome and X inactivation
Somatic cell and molecular genetics 19, 393-404, 1993 View Details |
1993 | 51 | 60.3% |
|
Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A
European journal of human genetics 13 (5), 635-640, 2005 View Details |
2005 | 62 | 60.0% |
|
Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation.
American journal of human genetics 26 (3), 360, 1974 View Details |
1974 | 33 | 59.7% |
|
Lack of X inactivation associated with maternal X isodisomy: evidence for a counting mechanism prior to X inactivation during human embryogenesis.
American journal of human genetics 58 (1), 161, 1996 View Details |
1996 | 53 | 59.2% |
|
Quantitation of contact-feeding between somatic cells in culture
Experimental cell research 95 (1), 39-46, 1975 View Details |
1975 | 36 | 59.1% |
|
Genetic heterogeneity of α‐galactosidase in fabry's disease
Febs Letters 27 (1), 161-166, 1972 View Details |
1972 | 33 | 58.8% |
|
A chromosome abnormality with fragment in a paramongol child.
Bulletin of the Johns Hopkins Hospital 111, 221-229, 1962 View Details |
1962 | 17 | 58.4% |
|
Selection and cell communication as determinants of female phenotype
Genetic mosaics and chimeras in mammals, 417-432, 1978 View Details |
1978 | 35 | 57.6% |
|
Molecular characterization of tiny ring X chromosomes from females with functional X chromosome disomy and lack of cis X inactivation
Genomics 27 (1), 182-188, 1995 View Details |
1995 | 47 | 57.2% |
|
Centromeric inactivation in a dicentric human Y; 21 translocation chromosome
Chromosoma 106, 199-206, 1997 View Details |
1997 | 51 | 57.0% |
|
Gene expression in euploid human hybrid cells: ouabain resistance is codominant
Somatic cell genetics 4, 531-540, 1978 View Details |
1978 | 33 | 56.2% |
|
Familial occurrence of the somatic phenotype of Turner's syndrome.
The Johns Hopkins medical journal 120 (2), 78-80, 1967 View Details |
1967 | 22 | 56.2% |
|
Females are mosaics: X inactivation and sex differences in disease
OUP USA, 2014 View Details |
2014 | 42 | 55.3% |
|
Evidence for a relationship between DNA methylation and DNA replication from studies of the 5-azacytidine-reactivated allocyclic X chromosome
Experimental cell research 158 (2), 301-310, 1985 View Details |
1985 | 37 | 55.3% |
|
Clonal evolution in human lymphoblast cultures.
American journal of human genetics 42 (5), 742, 1988 View Details |
1988 | 39 | 55.1% |
|
Reciprocal (D; E) translocation: Euploid transmission in three generations
The Journal of pediatrics 65 (6 PART 2), 1098, 1964 View Details |
1964 | 20 | 54.7% |
|
Artefactual chromatid aberrations in untreated and X-ray-treated human lymphocytes
Nature 203 (4952), 1395-1396, 1964 View Details |
1964 | 19 | 53.4% |
|
X chromosome inactivation: theme and variations
Cytogenetic and genome research 99 (1-4), 8-16, 2002 View Details |
2002 | 44 | 52.4% |
|
Is Tsix repression of Xist specific to mouse?
Nature genetics 33 (3), 337-337, 2003 View Details |
2003 | 43 | 51.9% |
|
Differential X reactivation in human placental cells: implications for reversal of X inactivation
The American Journal of Human Genetics 77 (3), 355-364, 2005 View Details |
2005 | 42 | 51.8% |
|
Stability of X chromosomal inactivation in human somatic cells transformed by SV-40
Humangenetik 29, 165-170, 1975 View Details |
1975 | 24 | 51.2% |
|
Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome
Annales de genetique 44 (4), 179-182, 2001 View Details |
2001 | 40 | 51.2% |
|
Effect of intercellular communication on the selection of intraspecific human hybrids in HAT and ouabain
Somatic Cell Genetics 4, 541-551, 1978 View Details |
1978 | 25 | 51.0% |
|
Severe hemophilia A in a female by cryptic translocation: order and orientation of factor VIII within Xq28
Genomics 16 (1), 20-25, 1993 View Details |
1993 | 31 | 50.6% |
|
Programmed demethylation in CpG islands during human fetal development
Somatic cell and molecular genetics 17, 159-168, 1991 View Details |
1991 | 31 | 50.5% |
|
Thyroxin, satellite association and trisomy
Nature 209 (5029), 1198-1200, 1966 View Details |
1966 | 16 | 49.9% |
|
Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters
Molecular and cellular biology, 1989 View Details |
1989 | 27 | 48.4% |
|
Severe phenotypes associated with inactive ring X chromosomes
American journal of medical genetics 93 (1), 52-57, 2000 View Details |
2000 | 35 | 48.0% |
|
Studies of X-chromosome inactivation in trisomies
Cytogenetic and Genome Research 50 (2-3), 75-77, 1989 View Details |
1989 | 26 | 47.7% |
|
Familial skewed X inactivation and X-linked mutations: unbalanced X inactivation is a powerful means to ascertain X-linked genes that affect cell proliferation
The American Journal of Human Genetics 62 (6), 1555-1557, 1998 View Details |
1998 | 30 | 46.7% |
|
Molecular studies of marsupial X chromosomes reveal limited sequence homology of mammalian X-linked genes
Genomics 1 (1), 19-28, 1987 View Details |
1987 | 23 | 46.0% |
|
Genetic disorders of male sexual differentiation
Advances in Human Genetics 10, 333-377, 1980 View Details |
1980 | 19 | 45.9% |
|
A chromosome abnormality with centric fragment in a paramongoloid child
Amer. J. Dis. Child. 104, 533, 1962 View Details |
1962 | 8 | 45.2% |
|
Unusual (CGG) n expansion and recombination in a family with fragile X and DiGeorge syndrome.
Journal of medical genetics 32 (3), 236-239, 1995 View Details |
1995 | 25 | 45.1% |
|
X-11 TRANSLOCATION-REPLICATION AND MAPPING STUDIES
CYTOGENETICS AND CELL GENETICS 25 (1-4), 199-200, 1979 View Details |
1979 | 20 | 45.1% |
|
In search of nonrandom X inactivation: studies of the placenta from newborns heterozygous for glucose-6-phosphate dehydrogenase
Genetic mosaics and chimeras in mammals, 379-391, 1978 View Details |
1978 | 18 | 44.9% |
|
X inactivation in triploidy and trisomy: the search for autosomal transfactors that choose the active X
European journal of human genetics 16 (2), 153-162, 2008 View Details |
2008 | 29 | 44.3% |
|
Effect of ouabain resistance on human diploid fibroblasts carrying other genetic variants
Experimental cell research 95 (1), 47-53, 1975 View Details |
1975 | 17 | 44.3% |
|
The syndrome of androgen insensitivity in man: its relation to our understanding of male sex differentiation
Genetic mechanisms of sexual differentiation, 93-103, 1979 View Details |
1979 | 19 | 44.1% |
|
Localization of glucose-6-phosphate dehydrogenase in mouse and man by in situ hybridization: evidence for a single locus and transposition of homologous X-linked genes
Cytogenetic and Genome Research 39 (2), 87-92, 1985 View Details |
1985 | 21 | 43.9% |
|
Sex differences in activity of glucose 6-phosphate dehydrogenase from cultured human fetal lung cells despite X-inactivation
Biochemical Genetics 9 (2), 163-168, 1973 View Details |
1973 | 16 | 43.3% |
|
Low-copy-number human transgene is recognized as an X inactivation center in mouse ES cells, but fails to induce cis-inactivation in chimeric mice
Genomics 71 (2), 156-162, 2001 View Details |
2001 | 25 | 42.7% |
|
Concerning the role of X‐inactivation and DNA methylation in fragile X syndrome
American journal of medical genetics 43 (1‐2), 291-298, 1992 View Details |
1992 | 20 | 41.7% |
|
Embryonic loss of human females with partial trisomy 19 identifies region critical for the single active X
PLoS One 12 (4), e0170403, 2017 View Details |
2017 | 19 | 40.6% |
|
Studies of human-mouse cell hybrids with respect to X-chromosome inactivation
Genetic mosaics and chimeras in mammals, 329-337, 1978 View Details |
1978 | 14 | 40.1% |
|
Assignment of human thymidine kinase gene locus to chromosome 17 by identification of its distinctive quinacrine-fluorescence in man/mouse somatic hybrid cells
Pediatric Research 5 (8), 424-424, 1971 View Details |
1971 | 11 | 39.6% |
|
Characterization of reiterated human DNA with respect to mammalian X chromosome homology
Somatic Cell and Molecular Genetics 10, 93-103, 1984 View Details |
1984 | 15 | 39.6% |
|
Reactivation of X-linked genes in human fibroblasts transformed by origin-defective SV40
Somatic cell and molecular genetics 12, 585-594, 1986 View Details |
1986 | 15 | 39.3% |
|
Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase.
American journal of human genetics 33 (5), 752, 1981 View Details |
1981 | 14 | 38.3% |
|
Translocation of the nucleolus organizer region to the human X chromosome.
American journal of human genetics 39 (2), 245, 1986 View Details |
1986 | 14 | 38.1% |
|
Methylation status of genes flanking the fragile site in males with the fragile-X syndrome: a test of the imprinting hypothesis.
American journal of human genetics 46 (4), 744, 1990 View Details |
1990 | 15 | 37.5% |
|
Localization of loci for HPRT and glucose-6-phosphate dehydrogenase and biochemical evidence for non-random X-chromosome expression from studies of a human X-autosome translocation
Proc Natl Acad Sci USA 77, 2810-2813, 1980 View Details |
1980 | 12 | 37.3% |
|
The XIST locus replicates late on the active X, and earlier on the inactive X based on FISH DNA replication analysis of somatic cell hybrids
Somatic cell and molecular genetics 21 (5), 327-333, 1995 View Details |
1995 | 16 | 37.3% |
|
XIST expression is repressed when X inactivation is reversed in human placental cells: A model for study ofXIST regulation
Somatic cell and molecular genetics 21, 51-60, 1995 View Details |
1995 | 16 | 37.3% |
|
The postulated X-inactivation center at Xq27 is most reasonably explained by ascertainment bias: heterozygous expression of recessive mutations is a powerful means of detecting unbalanced X inactivation.
American journal of human genetics 52 (2), 431, 1993 View Details |
1993 | 15 | 37.2% |
|
An overview of X inactivation based on species differences
Seminars in Cell & Developmental Biology 56, 111-116, 2016 View Details |
2016 | 17 | 36.5% |
|
Glucose-6-phosphate dehydrogenase as a probe for the study of X-chromosome inactivation in hunan females.
Isozymes 9, 189-200, 1983 View Details |
1983 | 12 | 36.2% |
|
Biochemical and genetic aspects of mental retardation
Annual review of medicine 17 (1), 407-430, 1966 View Details |
1966 | 8 | 35.9% |
|
The single active X in human cells: evolutionary tinkering personified
Human genetics 130, 281-293, 2011 View Details |
2011 | 18 | 35.4% |
|
Implications for X-chromosome regulation from studies of human X-chromosome DNA
Cold Spring Harbor symposia on quantitative biology 47, 621-630, 1983 View Details |
1983 | 11 | 34.6% |
|
Adrenoleukodystrophy variant in a heterozygous female
Neurology 32, A81, 1982 View Details |
1982 | 10 | 31.7% |
|
Enrichment of human heterokaryons by ficoll gradient for complementation analysis of iduronate sulfatase deficiency
Somatic Cell Genetics 5, 1079-1089, 1979 View Details |
1979 | 9 | 30.4% |
|
X-chromosome inactivation as a determinant of female phenotype
Genetic mechanisms of sexual development. Academic, New York, 293-303, 1979 View Details |
1979 | 9 | 30.4% |
|
Fetal mortality and sex ratio
Science 206 (4425), 1428-1428, 1979 View Details |
1979 | 9 | 30.4% |
|
Hyperexpression of HPRT induced by 5-azacytidine in mouse-human hybrid reactivants.
American journal of human genetics 37 (3), 608, 1985 View Details |
1985 | 9 | 28.8% |
|
Silencing XIST on the future active X: Searching human and bovine preimplantation embryos for the repressor
European Journal of Human Genetics, 1-8, 2022 View Details |
2022 | 4 | 27.9% |
|
Linkage between loci for adrenoleukodystrophy (ALD) and G6PD
CYTOGENETICS AND CELL GENETICS 32 (1-4), 298-299, 1982 View Details |
1982 | 8 | 27.8% |
|
Unreliability of the microcomplement fixation method for Xga typing of cultured fibroblasts
Cytogenetics and cell genetics 16 (1-5), 382-386, 1976 View Details |
1976 | 7 | 27.3% |
|
Role of DNA methylation in X inactivation and the fragile X syndrome
American journal of medical genetics 46 (6), 685-686, 1993 View Details |
1993 | 8 | 26.3% |
|
Stochastic gene expression and chromosome interactions in protecting the human active X from silencing by XIST
Nucleus 12 (1), 1-5, 2021 View Details |
2021 | 4 | 19.1% |
|
Molecular characterization of a deleted X chromosome (Xq13. 3-Xq21. 31) exhibiting random X inactivation
Somatic cell and molecular genetics 21, 113-120, 1995 View Details |
1995 | 5 | 18.3% |
|
Some insights into X chromosome inactivation from studies of human cells.
Annales D'endocrinologie 41 (4), 275-280, 1980 View Details |
1980 | 4 | 17.9% |
|
Some observations on the Staphylococcus in a pediatric out-patient population.
Bulletin of the Johns Hopkins Hospital 107, 262-270, 1960 View Details |
1960 | 3 | 17.5% |
|
LOCALIZATION OF THE FACTOR-IX LOCUS TO XQ26-] QTER
CYTOGENETICS AND CELL GENETICS 37 (1-4), 425-426, 1984 View Details |
1984 | 4 | 16.8% |
|
Phenotypic heterogeneity within clones of fetal human cells.
American journal of human genetics 33 (6), 950, 1981 View Details |
1981 | 4 | 16.4% |
|
The non-random location of autosomal genes that participate in X inactivation
Frontiers in Cell and Developmental Biology 7, 144, 2019 View Details |
2019 | 4 | 15.9% |
|
Localization of G6PD and HPRT to different arms of the X chromosome of the North American marsupial (Didelphis virginiana) by in situ hybridization and delection mapping: Evolutionary significance
Genomics 3 (4), 308-314, 1988 View Details |
1988 | 4 | 15.2% |
|
Selection of epithelial cells in culture by D-valine medium
Birth defects original article series 16 (2), 239-247, 1980 View Details |
1980 | 3 | 13.9% |
|
Titles and abstracts of scientific reports ignore variation among species
ELife 3, e05075, 2014 View Details |
2014 | 4 | 13.7% |
|
Clonal analysis of development: X-inactivation and cell communication as determinants of female phenotype
The Clonal Basis of Development, 205-205, 1978 View Details |
1978 | 3 | 13.7% |
|
Fabryl's disease: Evidence for structural mutation of α-galactosidase
Pediatric Research 5 (8), 420-421, 1971 View Details |
1971 | 3 | 12.8% |
|
DNA-REPLICATION ANALYSIS OF X-LINKED FMR-1, XIST AND FACTOR-8C LOCI USING FLUORESCENCE IN-SITU HYBRIDIZATION INDICATES NONTRANSCRIBED GENES ARE LATE REPLICATING
AMERICAN JOURNAL OF HUMAN GENETICS 53 (3), 224-224, 1993 View Details |
1993 | 3 | 11.7% |
|
Hybridization of Mammalian Cells
Annals of the New York Academy of Sciences 171 (2), 396-405, 1970 View Details |
1970 | 2 | 8.9% |
|
STUDIES OF HUMAN PLACENTAE IN SEARCH OF NONRANDOM X-INACTIVATION
AMERICAN JOURNAL OF HUMAN GENETICS 30 (6), A132-A132, 1978 View Details |
1978 | 2 | 7.5% |
|
Somatic cell hybrids: Applications relevant to genetic disease
The Journal of pediatrics 79 (6), 887-897, 1971 View Details |
1971 | 2 | 7.2% |
|
ISOLATION OF COSMID CLONES CONTAINING CPG ISLANDS AT XQ24-QTER REGION
CYTOGENETICS AND CELL GENETICS 58 (3-4), 2069-2070, 1991 View Details |
1991 | 2 | 6.2% |
|
X-LINKED HYPOXANTHINE GUANINE PHOSPHORIBOSYL TRANSFERASE DEFICIENCY-HETEROZYGOTE HAS 2 CLONAL POPULATIONS
PEDIATRIC RESEARCH 2 (5), 414-&, 1968 View Details |
1968 | 1 | 0.0% |
|
The role of the locus coeruleus
Trends in Neurosciences 2, 170, 1979 View Details |
1979 | 1 | 0.0% |
|
X Inactivation and Cellular Mosaicism—Reply
JAMA 296 (8), 930-931, 2006 View Details |
2006 | 1 | 0.0% |
|
Barton Childs 1916–2010
Nature Genetics 43 (1), 7-7, 2011 View Details |
2011 | 1 | 0.0% |
|
Reflections on the history of genetic medicine at Johns Hopkins University
American Journal of Medical Genetics Part A 185 (11), 3224-3229, 2021 View Details |
2021 | 1 | 0.0% |