Stanley M. Gartler
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Genetics
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Biology
Why Is Stanley M. Gartler Influential?
(Suggest an Edit or Addition)Stanley M. Gartler's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome. (1999) (731)
- Sequencing newly replicated DNA reveals widespread plasticity in human replication timing (2009) (511)
- Clonal origin of chronic myelocytic leukemia in man. (1967) (510)
- Mammalian X chromosome inactivation. (1992) (453)
- Glucose-6-Phosphate Dehydrogenase Mosaicism: Utilization as a Cell Marker in the Study of Leiomyomas (1965) (377)
- Polymerase chain reaction-aided genomic sequencing of an X chromosome-linked CpG island: methylation patterns suggest clonal inheritance, CpG site autonomy, and an explanation of activity state stability. (1990) (271)
- Association of fragile X syndrome with delayed replication of the FMR1 gene (1993) (229)
- Apparent HeLa Cell Contamination of Human Heteroploid Cell Lines (1968) (196)
- Methylation analysis of CGG sites in the CpG island of the human FMR1 gene. (1992) (175)
- Histone deacetylase inhibition elicits an evolutionarily conserved self-renewal program in embryonic stem cells. (2009) (162)
- Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant. (2000) (153)
- Lesch-Nyhan Syndrome: Rapid Detection of Heterozygotes by Use of Hair Follicles (1971) (141)
- Analysis of CpG suppression in methylated and nonmethylated species. (1992) (140)
- Mammalian X-chromosome inactivation. (2003) (138)
- X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele (1985) (133)
- Transformation with DNA from 5-azacytidine-reactivated X chromosomes. (1982) (127)
- An XX/XY human hermaphrodite resulting from double fertilization. (1962) (124)
- Clonal origin for individual Burkitt tumours. (1970) (112)
- Role of late replication timing in the silencing of X-linked genes. (1996) (106)
- The occurrence of new mutants in the X-linked recessive Lesch-Nyhan disease. (1976) (104)
- Multiple cell origin of hereditary neurofibromas. (1971) (100)
- A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication. (1997) (98)
- High rate of recombination and double crossovers in the mouse pseudoautosomal region during male meiosis. (1987) (91)
- Genetic markers as tracers in cell culture. (1967) (87)
- Demethylation of specific sites in the 5' region of the inactive X-linked human phosphoglycerate kinase gene correlates with the appearance of nuclease sensitivity and gene expression (1988) (86)
- Ontogeny of X-chromosome inactivation in the female germ line. (1975) (78)
- Evidence for two functional X chromosomes in human oocytes. (1972) (76)
- 5-Azacytidine-induced reactivation of the human X chromosome-linked PGK1 gene is associated with a large region of cytosine demethylation in the 5' CpG island. (1990) (75)
- Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci. (1995) (70)
- SELECTION IN MAMMALIAN MOSAIC CELL POPULATIONS. (1964) (69)
- Comparison of transformation efficiency of human active and inactive X-chromosomal DNA (1983) (68)
- Reactivation of inactive X-linked genes. (1994) (63)
- Isolation of a cDNA clone for human X-linked 3-phosphoglycerate kinase by use of a mixture of synthetic oligodeoxyribonucleotides as a detection probe. (1983) (61)
- DISTRIBUTION OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ELECTROPHORETIC VARIANTS IN DIFFERENT TISSUES OF HETEROZYGOTES. (1965) (61)
- Molecular cytological differentiation of active from inactive X domains in interphase: implications for X chromosome inactivation. (1989) (57)
- Half chromatid mutations: transmission in humans? (1975) (57)
- The applications of genetic mosaicism to developmental problems. (1971) (56)
- Hemimethylation and Non-CpG Methylation Levels in a Promoter Region of Human LINE-1 (L1) Repeated Elements* (2005) (55)
- Glucose-6-phosphate dehydrogenase mosaicism as a tracer in the study of hereditary multiple trichoepithelioma. (1966) (54)
- Cystathionine synthase activity in human lymphocytes: induction by phytohemagglutinin. (1972) (54)
- THE LYON-BEUTLER HYPOTHESIS AND ISOCHROMOSOME X PATIENTS WITH TURNER SYNDROME. (1963) (53)
- Increased Incidence of Nontasters of Phenylthiocarbamide among Congenital Athyreotic Cretins (1960) (51)
- Glucose‐6‐phosphate dehydrogenase mosaicism: utilization in the study of hair follicle variegation (1971) (51)
- DNA methylation in transcriptional repression of two differentially expressed X-linked genes, GPC3 and SYBL1. (1999) (51)
- Cellular Uptake of Deoxyribonucleic Acid by Human Tissue Culture Cells (1959) (48)
- Two functional X chromosomes in human fetal oocytes. (1973) (48)
- Reactivation of XIST in normal fibroblasts and a somatic cell hybrid: abnormal localization of XIST RNA in hybrid cells. (1998) (48)
- Demonstration of cellular uptake of polymerized DNA in mammalian cell cultures (1960) (47)
- The chromosome number in humans: a brief history (2006) (46)
- Reverse replication timing for the XIST gene in human fibroblasts. (1995) (46)
- Glucose-6-Phosphate Dehydrogenase Deficient Mutant in Human Cell Culture (1962) (45)
- A chicken transferrin gene in transgenic mice escapes X-chromosome inactivation. (1987) (43)
- Developmental implications of multiple tissue studies in glucose-6-phosphate dehydrogenase-deficient heterozygotes. (1968) (43)
- Abnormal sexual development associated with sex chromosome mosaicism. Report of three cases. (1962) (42)
- Very late DNA replication in the human cell cycle. (1998) (42)
- REPLICATION PATTERNS OF BOVINE SEX CHROMOSOMES IN CELL CULTURE. (1964) (39)
- Analysis of replication timing at the FRA10B and FRA16B fragile site loci (2004) (37)
- Hemimethylation and hypersensitivity are early events in transcriptional reactivation of human inactive X-linked genes in a hamster x human somatic cell hybrid (1992) (36)
- Linkage of the steroid sulfatase gene to the sex-reversed mutation in the mouse. (1987) (35)
- Expression of two X-linked genes in human hair follicles of double heterozygotes. (1971) (34)
- Blood group studies on the family of an XX/XY hermaphrodite with generalized tissue mosaicism. (1963) (34)
- Effect of chronologic age on induction of cystathionine synthase, uroporphyrinogen I synthase, and glucose-6-phosphate dehydrogenase activities in lymphocytes. (1981) (34)
- Cytological evidence for an inactive X chromosome in murine oogonia. (1980) (34)
- The timing of XIST replication: dominance of the domain. (1999) (33)
- A two step model for mammalian X-chromosome inactivation. (1985) (33)
- A potentially critical Hpa II site of the X chromosome-linked PGK1 gene is unmethylated prior to the onset of meiosis of human oogenic cells. (1992) (32)
- Development of a nonselective technique for studying 2, 6, diaminopurine resistance in an established murine cell line. (1968) (31)
- Replication of the mouse sex chromosomes early in the S period. (1970) (30)
- Evidence for X-linkage of steroid sulfatase in the mouse: steroid sulfatase levels in oocytes of XX and XO mice. (1983) (29)
- A metabolic investigation of urinary β-aminoisobutyric acid excretion in man. (1959) (28)
- An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization (1998) (28)
- Biology of the X chromosome (2001) (27)
- X chromosome inactivation in cells from an individual heterozygous for two X-linked genes. (1972) (27)
- Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication (2001) (26)
- Evidence for two active X chromosomes in a human XXY triploid (1975) (25)
- Apparent masculinization of the female fetus diagnosed as true hermaphrodism by chromosomal studies. (1962) (25)
- A study of metabolic cooperation utilizing human mutant fibroblasts. (1971) (24)
- Homocystinuria: heterozygote detection using phytohemagglutinin-stimulated lymphocytes. (1973) (24)
- Evidence for a dosage effect at the X-linked steroid sulfatase locus in human tissues. (1983) (23)
- 5-Azadeoxycytidine-induced Chromatin Remodeling of the Inactive X-linked HPRT Gene Promoter Occurs prior to Transcription Factor Binding and Gene Reactivation* (1997) (23)
- Chromatin structure of active and inactive human X chromosomes. (1984) (23)
- Constitutive phosphorylation of ATM in lymphoblastoid cell lines from patients with ICF syndrome without downstream kinase activity. (2006) (23)
- Normal histone modifications on the inactive X chromosome in ICF and Rett syndrome cells: implications for methyl-CpG binding proteins (2004) (23)
- Isoenzyme stability in human heteroploid cell lines. (1970) (22)
- Glucose-6-phosphate Dehydrogenase Mosaicism for studying the Development of Blood Cell Precursors (1969) (21)
- Analysis of a paracentric inversion in human oocytes: nonhomologous pairing in pachytene (1999) (20)
- Chromosome painting analysis of early oogenesis in human trisomy 18. (1995) (20)
- Chromatographic studies on urinary excretion patterns in monozygotic and dizygotic twins. II. Heritability of the excretion rates of certain substances. (1955) (20)
- Regional localization of the human factor IX gene by molecular hybridization (2004) (19)
- Glucose-6-phosphate dehydrogenase deficiency in an XO individual. (1962) (19)
- Answer to criticism of Morton and Lalouel. (1977) (17)
- Dosage Regulation of the Active X Chromosome in Human Triploid Cells (2009) (17)
- CHROMOSOME COMPLEMENT IN A TRUE HERMAPHRODITE (1962) (17)
- Dosage of the Sts gene in the mouse. (1986) (17)
- Urinary Excretion of β-Amino-isobutyric Acid in Eskimo and Indian Populations of Alaska (1959) (17)
- Chromosomal aberrations in 2 embryos from the same mother. An embryo with B trisomy and another with triploidy and associated cleft lip. (1968) (15)
- Analysis of inactive X chromosome structure by in situ nick translation (2004) (15)
- Abnormal X : autosome ratio, but normal X chromosome inactivation in human triploid cultures (2006) (15)
- A brief history of dosage compensation (2014) (15)
- A family study of urinary beta-aminoisobutyric acid excretion. (1956) (14)
- An investigation into the biochemical genetics of beta-aminoisobutyric aciduria. (1959) (14)
- Hypoxanthine guanine phosphoribosyl transferase expression in early mouse development. (1978) (13)
- Inactivation and reactivation of sex-linked steroid sulfatase gene in murine cell culture (1988) (13)
- High Prevalence of High-Level β-Amino-isobutyric Acid Excretors in Micronesians (1959) (13)
- Hyperploidy Effect of Lymphocyte Extract on Fibroblasts In Vitro (1966) (11)
- Transformation ofHprt gene with sperm DNA (1983) (11)
- Chromatographic studies on urinary excretion patterns in monozygotic and dizygotic twins. I. Methods and analysis. (1955) (11)
- CHROMATIN-POSITIVE GONADAL DYSGENESIS AND MOSAICISM (1961) (11)
- Problem of Single Cell Versus Multicell Origin of a Tumor (1967) (10)
- Nucleotide sequence of the 3' nuclease-sensitive region of the human phosphoglycerate kinase 1 (PGK1) gene. (1991) (10)
- Chromosomal fragile sites: molecular test of the delayed-replication model. (1993) (9)
- X-chromosome inactivation: Switching off blocks of genes (1983) (9)
- Xrep, a plasmid-stimulating X chromosomal sequence bearing similarities to the BK virus replication origin and viral enhancers. (1986) (8)
- Mammalian X-chromosome inactivation. (1983) (8)
- Excretion in Human Urine of an Unknown Amino-acid derived from Dates (1954) (8)
- A Yeast Mitogenic Factor Active on Human Peripheral Leucocytes in Culture (1964) (8)
- A chromatographic investigation of urinary amino-acids in the great apes. (1956) (7)
- ICF syndrome cells as a model system for studying X chromosome inactivation (2003) (7)
- CHROMOSOME REPLICATION PATTERN IN AN ESTABLISHED BOVINE CELL LINE. (1965) (7)
- Absence of methylation at HpaII sites in three human genomic tRNA sequences. (1990) (6)
- X-Chromosome Inactivation (2005) (6)
- General principles of medical genetics (1962) (6)
- Sex Chromosome Markers as Indicators in Embryonic Development (1971) (6)
- Identification of HeLa cell glucose 6-phosphate dehydrogenase (1971) (5)
- Some genetical and anthropological considerations of urinary beta-aminoisobutyric acid excretion. (1956) (5)
- Biochemical Identification of Cells in Culture: A. Human Cell Lines by Enzyme Polymorphism (1973) (5)
- Transformation of the Hprt gene with DNA from spermatogenic cells (2004) (5)
- An investigation into the genetics and racial variation of BAIB excretion. (1957) (4)
- Differential excretion of D-phenylalanine in man. (1957) (4)
- Genetics of mammalian cell cultures (1966) (4)
- Patterns of protein synthesis at the onset of oogenesis in the mouse. (1982) (3)
- X-chromosome inactivation and selection in somatic cells. (1976) (3)
- Distribution of Chromatin Bodies in an XX/XY True Hermaphrodite.∗ (1962) (3)
- The irreversibility of subunit associations in glucose-6-phosphate dehydrogenase and a suggestion regarding an early step in cellular morphogenesis. (1979) (3)
- Glucose-6-phosphate dehydrogenase mosaicism: ito;ozatopm om tje study of hair follicle variegation. (1971) (3)
- Neuraminic Acid Investigations of Human Cell Strains derived from Explants of Skin in Cell Culture (1964) (3)
- Urinary excretion of beta-aminoisobutyric acid in Eskimo and Indian populations of Alaska. (1959) (2)
- The absence of inactivation at two autosomal loci (2004) (2)
- Physiologic variation of renal function in twins: diuresis after water intake. (1958) (2)
- On a case of arteriovenous fistulas of the hand (1959) (1)
- A Family Study of Urinary o-aminoisobutyric Acid Excretion (2006) (1)
- Elimination of recessive lethals from the population when the heterozygote can be detected. (1953) (1)
- The urinary excretion of beta-amino-isobutyric acid in Pacific populations. (1961) (1)
- The evolutionary problem of genetic disease (1955) (1)
- Switching off blocks of genes. (1983) (1)
- Demonstration of celluar uptake of polymerized DNA in mammalian cell cultures. (1960) (1)
- Patterns of cellular proliferation in normal and tumor cell populations. (1977) (1)
- High prevalence of high-level beta-amino-isobutyric acid excretors in Micronesians. (1959) (1)
- The biochemistry of semen. (1955) (0)
- Mutations, Second Conference on Genetics, Josiah Macy Jr. Foundation. (1963) (0)
- Cell biology: A current summary. (1966) (0)
- The utilization of the human phosphoglycerate kinase gene in the investigation of X-chromosome inactivation. (1986) (0)
- Increased Factor IX (2009) (0)
- Identification of imprinted genes using a novel screening method based on asynchronous DNA replication (1994) (0)
- Steroid Sulphatase Inactivation Patterns and X-chromosome Inactivation (1990) (0)
- 5-Azacytidine-induced reactivation of the human X chromosome-linked PGKJ gene is associated with a large region of cytosine demethylation in the 5 ' CpG island ( X chromosome inactivation / hamster-human cell hybrid / de novo methylation ) (0)
- Desulfuration of Thiourea by Saliva.∗ (1963) (0)
- Demethylation ofSpecific Sites inthe5'RegionoftheInactive X-Linked HumanPhosphoglycerate Kinase GeneCorrelates with theAppearance ofNuclease Sensitivity andGeneExpression (1988) (0)
- Inducible Costimulator Deficiency (2009) (0)
- Selected bibliography of Susumu Ohno (1998) (0)
- Genetic implications of certain physiological processes affecting the metabolism of L-phenylalanine in man. (1957) (0)
- Thoughts on the action committees of the American society of human genetics. (1988) (0)
- The Evolution of Man: a Brief Introduction to Physical Anthropology. (1961) (0)
- Contents Vol. 99, 2002 (2003) (0)
- New Editors, Features and Procedures (1989) (0)
- Cystathionine synthase activity in human leukocyte cultures. (1973) (0)
- The Xist Locus (2019) (0)
- Consanguinity and marriage. (1959) (0)
- Editorial help (2004) (0)
- Mary Lyon’s X-inactivation studies in the mouse laid the foundation for the field of mammalian dosage compensation (2015) (0)
- Studies of tumor cell origins in mosaics. (1982) (0)
- Mary Lyon’s X-inactivation studies in the mouse laid the foundation for the field of mammalian dosage compensation (2015) (0)
- Subject Index, Vol. 70, 1995 (1995) (0)
- 2016 Victor A. McKusick Leadership Award. (2017) (0)
- Genetics and disease. (1967) (0)
- DISTRIBUTION OF CHROMATIN BODIES IN AN XX/XY TRUE HERMAPHRODITE. (27630) (1963) (0)
- Subject Index Vol. 99, 2002 (2003) (0)
- X-linkage of steroid sulphatase in the mouse is evidence for a functional Y-linked allele (1985) (0)
- PROGRESS IN THE UTILIZATION OF CELL CULTURE TECHNIQUES FOR STUDIES IN MAMMALIAN AND HUMAN SOMATIC CELL GENETICS (1964) (0)
- Active alleles of the human XIST gene replicate late in S phase (1994) (0)
- Trisomy G/normal mosaicism. A cytological and clinical investigation (1973) (0)
- Fluorescent in situ hybridization analyses of human oocytes in trisomy 18 and 21 (1994) (0)
- A brief history of dosage compensation (2014) (0)
- Textbook of human genetics (1973) (0)
- A further note on some considerations of heterozygote detection. (1954) (0)
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