Publications: Barbara Migeon

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  • Affiliation: Professor, Institute of Genetic Medicine, Johns Hopkins University
  • Google Scholar ID: srQShKwAAAAJ
  • Total Publications: 170

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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
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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
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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
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1981 337 92.5%
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: heterozygote has two clonal populations
Science 160 (3826), 425-427, 1968
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1968 232 92.0%
Mechanism of origin of complete hydatidiform moles
Nature 286 (5774), 714-716, 1980
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1980 300 91.8%
X-linked diseases: susceptible females
Genetics in Medicine 22 (7), 1156-1174, 2020
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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
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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
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1985 288 90.1%
Genetic inactivation of the α-galactosidase locus in carriers of Fabry's disease
Science 170 (3954), 180-181, 1970
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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
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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
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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
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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
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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
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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
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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
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2006 209 84.5%
Differential expression of steroid sulphatase locus on active and inactive human X chromosome
Nature 299 (5886), 838-840, 1982
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1982 163 84.5%
Studies of X chromosome DNA methylation in normal human cells
Nature 295 (5851), 667-671, 1982
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1982 159 84.0%
Complex chromosome rearrangements: report of a new case and literature review
Clinical genetics 18 (6), 436-444, 1980
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1980 156 83.8%
Clusters of CpG dinucleotides implicated by nuclease hypersensitivity as control elements of housekeeping genes
Nature 314 (6010), 467-469, 1985
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1985 158 83.0%
X-chromosome inactivation: molecular mechanisms and genetic consequences
Trends in Genetics 10 (7), 230-235, 1994
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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
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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
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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
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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
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1979 118 80.0%
Stability of X chromosomal inactivation in human somatic cells.
Nature 239 (5367), 1972
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1972 94 79.7%
Why females are mosaics, X-chromosome inactivation, and sex differences in disease
Gender medicine 4 (2), 97-105, 2007
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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
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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
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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
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1994 134 78.1%
X-linked hypoxanthine-guanine phosphoribosyl transferase deficiency: detection of heterozygotes by selective medium
Biochemical genetics 4 (3), 377-383, 1970
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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
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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
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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
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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
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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
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1982 99 75.9%
Genetic complementation after fusion of Tay-Sachs and Sandhoff cells
Nature 250 (5467), 580-582, 1974
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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
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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
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1968 63 74.8%
Non-random X chromosome inactivation in mammalian cells
Cytogenetic and Genome Research 80 (1-4), 142-148, 1998
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1998 117 73.8%
FAMILIAL VARIANT AUTOSOMES: NEW HUMAN CYTOGENETIC MARKERS.
Bulletin of the Johns Hopkins Hospital 116, 396-402, 1965
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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
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1990 96 73.2%
Human and mouse hypoxanthine-guanine phosphoribosyltransferase: dimers and tetramers
Science 203 (4376), 174-176, 1979
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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
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1997 108 72.6%
Selection against lethal alleles in females heterozygous for incontinentia pigmenti.
American journal of human genetics 44 (1), 100, 1989
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1989 87 71.9%
The nature of thymidine kinase in the human-mouse hybrid cell
Biochemical Genetics 3, 583-590, 1969
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1969 53 71.8%
Effect of ageing on reactivation of the human X-linked HPRT locus
Nature 335 (6185), 93-96, 1988
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1988 90 71.7%
Adrenoleukodystrophy: studies of the phenotype, genetics and biochemistry
Johns Hopkins Medical Journal 147 (6), 217-224, 1980
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1980 70 70.9%
Females are mosaics: X inactivation and sex differences in disease
Oxford university press, 2007
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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
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1986 73 70.0%
Isolation and characterization of cloned DNA sequences that hybridize to the human X chromosome
Cell 21 (1), 95-102, 1980
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1980 68 70.0%
Non–random loss of human markers from man–mouse somatic cell hybrids
Nature 251 (5470), 72-74, 1974
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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
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2008 92 69.6%
Evidence for two active X chromosomes in germ cells of female before meiotic entry
Nature 269 (5625), 242-243, 1977
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1977 65 69.6%
X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
American journal of human genetics 29 (5), 448, 1977
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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
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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
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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
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1984 63 68.1%
Interferon production and action in mouse, hamster, and somatic hybrid mouse-hamster cells
Science 160 (3827), 558-559, 1968
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1968 43 67.9%
Androgen receptors and metabolism in cultured human fetal fibroblasts
Pediatric research 14 (1), 67-69, 1980
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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
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1977 59 67.4%
Renal enzymes in kidney cells selected by D‐valine medium
Journal of Cellular Physiology 92 (2), 161-167, 1977
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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
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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
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1971 42 66.5%
Haptoglobin: a locus on the D1 chromosome?
American journal of human genetics 19 (3 Pt 2), 393, 1967
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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
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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
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1979 56 65.1%
Contact-mediated communication of ouabain resistance in mammalian cells in culture
Nature 268 (5622), 737-739, 1977
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1977 52 64.6%
Stability of the “two active X” phenotype in triploid somatic cells
Cell 18 (3), 637-641, 1979
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1979 53 64.0%
Short arm deletions in group E and chromosomal “deletion” syndromes
The Journal of pediatrics 69 (3), 432-438, 1966
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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
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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
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1975 43 63.2%
Choosing the active X: the human version of X inactivation
Trends in Genetics 33 (12), 899-909, 2017
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2017 44 62.3%
Human X inactivation center induces random X chromosome inactivation in male transgenic mice
Genomics 59 (2), 113-121, 1999
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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
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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
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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
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1963 21 61.6%
Hybridization of mammalian somatic cells
Progress in medical genetics 7, 1-28, 1970
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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
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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
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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
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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
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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
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1996 53 59.2%
Quantitation of contact-feeding between somatic cells in culture
Experimental cell research 95 (1), 39-46, 1975
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1975 36 59.1%
Genetic heterogeneity of α‐galactosidase in fabry's disease
Febs Letters 27 (1), 161-166, 1972
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1972 33 58.8%
A chromosome abnormality with fragment in a paramongol child.
Bulletin of the Johns Hopkins Hospital 111, 221-229, 1962
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1962 17 58.4%
Selection and cell communication as determinants of female phenotype
Genetic mosaics and chimeras in mammals, 417-432, 1978
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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
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1995 47 57.2%
Centromeric inactivation in a dicentric human Y; 21 translocation chromosome
Chromosoma 106, 199-206, 1997
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1997 51 57.0%
Gene expression in euploid human hybrid cells: ouabain resistance is codominant
Somatic cell genetics 4, 531-540, 1978
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1978 33 56.2%
Familial occurrence of the somatic phenotype of Turner's syndrome.
The Johns Hopkins medical journal 120 (2), 78-80, 1967
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1967 22 56.2%
Females are mosaics: X inactivation and sex differences in disease
OUP USA, 2014
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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
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1985 37 55.3%
Clonal evolution in human lymphoblast cultures.
American journal of human genetics 42 (5), 742, 1988
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1988 39 55.1%
Reciprocal (D; E) translocation: Euploid transmission in three generations
The Journal of pediatrics 65 (6 PART 2), 1098, 1964
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1964 20 54.7%
Artefactual chromatid aberrations in untreated and X-ray-treated human lymphocytes
Nature 203 (4952), 1395-1396, 1964
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1964 19 53.4%
X chromosome inactivation: theme and variations
Cytogenetic and genome research 99 (1-4), 8-16, 2002
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2002 44 52.4%
Is Tsix repression of Xist specific to mouse?
Nature genetics 33 (3), 337-337, 2003
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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
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2005 42 51.8%
Stability of X chromosomal inactivation in human somatic cells transformed by SV-40
Humangenetik 29, 165-170, 1975
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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
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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
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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
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1993 31 50.6%
Programmed demethylation in CpG islands during human fetal development
Somatic cell and molecular genetics 17, 159-168, 1991
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1991 31 50.5%
Thyroxin, satellite association and trisomy
Nature 209 (5029), 1198-1200, 1966
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1966 16 49.9%
Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters
Molecular and cellular biology, 1989
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1989 27 48.4%
Severe phenotypes associated with inactive ring X chromosomes
American journal of medical genetics 93 (1), 52-57, 2000
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2000 35 48.0%
Studies of X-chromosome inactivation in trisomies
Cytogenetic and Genome Research 50 (2-3), 75-77, 1989
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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
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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
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1987 23 46.0%
Genetic disorders of male sexual differentiation
Advances in Human Genetics 10, 333-377, 1980
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1980 19 45.9%
A chromosome abnormality with centric fragment in a paramongoloid child
Amer. J. Dis. Child. 104, 533, 1962
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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
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1995 25 45.1%
X-11 TRANSLOCATION-REPLICATION AND MAPPING STUDIES
CYTOGENETICS AND CELL GENETICS 25 (1-4), 199-200, 1979
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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
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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
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2008 29 44.3%
Effect of ouabain resistance on human diploid fibroblasts carrying other genetic variants
Experimental cell research 95 (1), 47-53, 1975
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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1981 14 38.3%
Translocation of the nucleolus organizer region to the human X chromosome.
American journal of human genetics 39 (2), 245, 1986
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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
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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
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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
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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
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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
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1993 15 37.2%
An overview of X inactivation based on species differences
Seminars in Cell & Developmental Biology 56, 111-116, 2016
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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
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1983 12 36.2%
Biochemical and genetic aspects of mental retardation
Annual review of medicine 17 (1), 407-430, 1966
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1966 8 35.9%
The single active X in human cells: evolutionary tinkering personified
Human genetics 130, 281-293, 2011
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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
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1983 11 34.6%
Adrenoleukodystrophy variant in a heterozygous female
Neurology 32, A81, 1982
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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
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1979 9 30.4%
X-chromosome inactivation as a determinant of female phenotype
Genetic mechanisms of sexual development. Academic, New York, 293-303, 1979
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1979 9 30.4%
Fetal mortality and sex ratio
Science 206 (4425), 1428-1428, 1979
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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
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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
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2022 4 27.9%
Linkage between loci for adrenoleukodystrophy (ALD) and G6PD
CYTOGENETICS AND CELL GENETICS 32 (1-4), 298-299, 1982
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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
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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
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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
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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
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1995 5 18.3%
Some insights into X chromosome inactivation from studies of human cells.
Annales D'endocrinologie 41 (4), 275-280, 1980
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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
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1960 3 17.5%
LOCALIZATION OF THE FACTOR-IX LOCUS TO XQ26-] QTER
CYTOGENETICS AND CELL GENETICS 37 (1-4), 425-426, 1984
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1984 4 16.8%
Phenotypic heterogeneity within clones of fetal human cells.
American journal of human genetics 33 (6), 950, 1981
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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
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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
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1988 4 15.2%
Selection of epithelial cells in culture by D-valine medium
Birth defects original article series 16 (2), 239-247, 1980
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1980 3 13.9%
Titles and abstracts of scientific reports ignore variation among species
ELife 3, e05075, 2014
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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
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1978 3 13.7%
Fabryl's disease: Evidence for structural mutation of α-galactosidase
Pediatric Research 5 (8), 420-421, 1971
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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
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1993 3 11.7%
Hybridization of Mammalian Cells
Annals of the New York Academy of Sciences 171 (2), 396-405, 1970
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1970 2 8.9%
STUDIES OF HUMAN PLACENTAE IN SEARCH OF NONRANDOM X-INACTIVATION
AMERICAN JOURNAL OF HUMAN GENETICS 30 (6), A132-A132, 1978
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1978 2 7.5%
Somatic cell hybrids: Applications relevant to genetic disease
The Journal of pediatrics 79 (6), 887-897, 1971
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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
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1991 2 6.2%
X-LINKED HYPOXANTHINE GUANINE PHOSPHORIBOSYL TRANSFERASE DEFICIENCY-HETEROZYGOTE HAS 2 CLONAL POPULATIONS
PEDIATRIC RESEARCH 2 (5), 414-&, 1968
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1968 1 0.0%
The role of the locus coeruleus
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