Salome Gluecksohn-Waelsch

Salome Gluecksohn-Waelsch's AcademicInfluence.com Rankings

Biology

#3963

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#5984

Historical Rank

Developmental Biology

#187

World Rank

#195

Historical Rank

Genetics

#715

World Rank

#807

Historical Rank

biology Degrees

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Biology

Why Is Salome Gluecksohn-Waelsch Influential?

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According to Wikipedia, Salome Gluecksohn-Waelsch was a German-born U.S. geneticist and co-founder of the field of developmental genetics, which investigates the genetic mechanisms of development. Biography Gluecksohn-Waelsch was born in Danzig, Germany to Nadia and Ilya Gluecksohn. She grew up in Germany between World War I and II, where her family faced hardships including her father's death in the 1918 influenza epidemic, severe post-war inflation, and intense anti-Semitic sentiment.

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Salome Gluecksohn-Waelsch'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

Is CCAAT/enhancer-binding protein a central regulator of energy metabolism? (1989) (244)
Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent. (1979) (157)
Expression of the zinc-finger gene PLZF at rhombomere boundaries in the vertebrate hindbrain. (1995) (120)
Lethal Genes and Analysis of Differentiation (1963) (105)
The T-locus of the mouse: implications for mechanisms of development. (1970) (97)
Genetic control of morphogenetic and biochemical differentiation: Lethal albino deletions in the mouse (1979) (72)
Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse. (1968) (61)
The role of inner hair cells in hearing (1979) (53)
Deletions near the albino locus on chromosome 7 of the mouse affect the level of tyrosine aminotransferase mRNA. (1985) (52)
ULTRASTRUCTURAL BASIS OF BIOCHEMICAL EFFECTS IN A SERIES OF LETHAL ALLELES IN THE MOUSE (1973) (51)
Fine structure of mutant (muscular dysgenesis) embryonic mouse muscle. (1972) (49)
Genetic Analysis of Seven Newly Discovered Mutant Alleles at Locus T in the House Mouse. (1953) (48)
Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase. (1974) (48)
Further studies of the effect of the T locus in the house mouse on male fertility. (1958) (45)
FILTER‐PAPER ELECTROPHORESIS OF MOUSE HAEMOGLOBIN: PRELIMINARY NOTE (1955) (45)
The morphological effects and the development of the fused mutation in the mouse (1956) (45)
Genetic variations of an oxidase in mammals. (1967) (41)
Trans regulation of the phosphoenolpyruvate carboxykinase (GTP) gene, identified by deletions in chromosome 7 of the mouse. (1986) (39)
Development in organ tissue culture of kidney rudiments from mutant mouse embryos. (1963) (36)
Regulatory genes in development (1987) (36)
The hereditary transmission of hemoglobin differences in mice. (1957) (35)
The developmental analysis of an embryonic lethal (C6H) in the mouse. (1976) (33)
The Effect of Maternal Immunization against Organ Tissues on Embryonic Differentiation in the Mouse (1957) (32)
Demonstration in mouse of X-ray induced deletions for a known enzyme structural locus (1974) (30)
Cytological detection of the c-25H deletion involving the albino (c) locus on chromosome 7 in the mouse. (1974) (26)
Lethal Factors in Development (1953) (24)
Metallothionein mRNA expression in mice homozygous for chromosomal deletions around the albino locus. (1988) (23)
Some genetic aspects of development. (1954) (23)
Genetics and morphology of a recessive mutation in the house mouse affecting head and limb skeleton (1956) (21)
Developmental genetics of arecessive allele at the complex T-locus in the mouse. (1967) (21)
The effects of a t-allele (tAE5) in the mouse on the lymphoid system and reproduction. (1976) (19)
Physiological genetics of the mouse. (1951) (19)
Hæmoglobin Differences in Inbred Strains of Mice (1960) (17)
A lethal deletion on mouse chromosome 7 affects regulation of liver-cell-specific functions: posttranscriptional control of serum protein and transcriptional control of aldolase B synthesis. (1985) (17)
The inheritance of hemoglobin types and other biochemical traits in mammals. (1960) (16)
Correction of a genetically caused enzyme defect by somatic cell hybridization. (1983) (15)
Deficiency in plasma protein synthesis caused by x-ray-incuded lethal albino alleles in mouse. (1976) (15)
Recessive lethal deletion on mouse chromosome 7 affects glucocorticoid receptor binding activities. (1983) (14)
Complementation of gene deletions by cell hybridization. (1981) (14)
A developmental study of the mutation “phocomelia” in the mouse (1959) (13)
Electrophoretic patterns of lens proteins from genetically caused cataract in the mouse. (1967) (13)
Developmental regulation of constitutive and inducible expression of hepatocyte-specific genes in the mouse. (1988) (13)
Glutamine synthetase in newborn mice homozygous for lethal albino alleles. (1975) (12)
The glucocorticoid hormone signal transduction pathway in mice homozygous for chromosomal deletions causing failure of cell type-specific inducible gene expression. (1991) (12)
Does the T-locus in the mouse include ribosomal DNA? (1976) (12)
Selective loss of a DNase I hypersensitive site upstream of the tyrosine aminotransferase gene in mice homozygous for lethal albino deletions. (1992) (10)
The Failure of a T-Allele (t) to Suppress Crossing over in the Mouse. (1953) (10)
Evidence for regulatory genes on mouse chromosome 7 that affect the quantitative expression of proteins in the fetal and newborn liver. (1992) (10)
On the origin and genetic behavior of new mutation (t3) at a mutable locus in the mouse. (1951) (10)
Multiple biochemical effects of a series of X-ray induced mutations at the albino locus in the mouse (2004) (9)
Genetic control of insulin receptors. (1981) (9)
Absence of mitochondrial malic enzyme in mice carrying two complementing lethal albino alleles. (1978) (9)
Lethal chromosomal deletions in the mouse, a model system for the study of development and regulation of postnatal gene expression (1991) (8)
Developmental Genetics of Hepatic Gluconeogenic Enzymes a (1986) (7)
Metabolic studies in a mouse model of hepatorenal tyrosinemia: absence of perinatal abnormalities. (1992) (7)
Physiological Investigations of a Mutation in Mice with Pleiotropic Effects (1955) (7)
The Genetics of the spermatozoon : proceedings of an international symposium held at the University of Edinburgh, Scotland, on August 16-20, 1971 (1972) (6)
Genetic control of embryonic growth and differentiation. (1954) (5)
Epidermal growth factor and glucagon receptors in mice homozygous for a lethal chromosomal deletion. (1983) (5)
Trends in mammalian teratology. (1957) (5)
Lipid deficiencies, leukocytosis, brittle skin--a lethal syndrome caused by a recessive mutation, edematous (oed), in the mouse. (1975) (5)
Abnormalities of the nervous system in the mouse. (1959) (5)
Glucose 6-phosphatase deficiency: Mechanisms of genetic control and biochemistry (2004) (4)
Ultrastructural studies of lethal c 2SH lc 25H mouse embryos (1979) (4)
Gene regulation in Mammalian cells. (1970) (3)
Cytological observations of deletions in pachytene stages of oogenesis and spermatogenesis in the mouse (1976) (3)
Genetic rescue of lethal genotypes in the mouse. (1979) (3)
Haemoglobin differences in inbred strains of mice. (1960) (3)
An overview of developmental genetics in mammals. (1992) (2)
Ultrastructural studies of lethal c25H/C25H mouse embryos. (1979) (2)
Chemical and immunological studies of liver microsomes from mouse mutants with ultrastructurally abnormal hepatic endoplasmic reticulum (1974) (2)
Fifty Years of Developmental Geneticsa,b (1983) (1)
Regulatory genes linked to the albino locus in the mouse confer competence for inducible expression on the structural gene encoding serine dehydratase. (1992) (1)
An overview of the developmental genetics in mammals (1992) (1)
A genetical study of the mutation ‘fused’ in the house mouse, with evidence concerning its allelism with a similar mutation ‘kink’ (1954) (1)
Developmental genetics of mammals. (1961) (1)
Interaction oft alleles at theT locus in the house mouse (1961) (1)
HEMOGLOBIN POLYMORPHISM AND SUSCEPTIBILITY TO PLASMODIUM INFECTION IN MICE. (1964) (1)
Developmental Genetics 2 (1977) (1)
Recessive lethal deletion on mouse I glucocorticoid receptor binding act: (gene regulation/hormone induction/enzyme deficiencies) (2016) (0)
Fifty years of developmental genetics. (1983) (0)
Complementation Studies of Lethal Allele' Deficiencies of Glucose-6-Phosphatase, Ty and Serine Dehydratase (microsomal membrane abnormalities/enzyme differenti (2016) (0)
Genetic control of insulin receptors (mouse/gene regulation/cell differentiation/hormone receptors) (0)
DEVELOPMENTAL GENETICS OF SPECIFIC LOCUS MUTATIONS (1983) (0)
Tyrosine aminotransferase induced in cells genetically and epigenetically deficient for this enzyme. (1982) (0)
Erratum: The glucocorticoid hormone signal transduction pathway in mice homozygous for chromosomal deletions causing failure of cell type-specific inducible gene expression (Proc. Natl. Acad. Sci. USA (July 1991) 88 (5607-5610)) (1991) (0)

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Salome Gluecksohn-Waelsch's Published Works

Published Works

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