Evan M. Eicher

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Evan M. Eicher is affiliated with the following schools: Duke University, University of Maine

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Evan M. Eicher

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#2111

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Biology

Evan M. Eicher's Degrees

Bachelors Biology University of California, Berkeley

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Evan M. Eicher's Published Works

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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

Purkinje cell degeneration, a new neurological mutation in the mouse. (1976) (552)
Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets. (1976) (399)
Genetic analysis of MRL-lpr mice: relationship of the Fas apoptosis gene to disease manifestations and renal disease-modifying loci (1992) (356)
Evidence that Sry is expressed in pre-Sertoli cells and Sertoli and granulosa cells have a common precursor. (2001) (355)
Gonadal differentiation, sex determination and normal Sry expression in mice require direct interaction between transcription partners GATA4 and FOG2. (2002) (351)
Sry induces cell proliferation in the mouse gonad. (2000) (339)
A new mutation, gld, that produces lymphoproliferation and autoimmunity in C3H/HeJ mice (1984) (302)
Mus poschiavinus Y chromosome in the C57BL/6J murine genome causes sex reversal. (1982) (293)
Fat (fat) and tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse. (1990) (273)
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness. (1999) (263)
Genetic control of primary sex determination in mice. (1986) (250)
Inherited ateliotic dwarfism in mice. Characteristics of the mutation, little, on chromosome 6. (1976) (238)
Hereditary leucodystrophy in the mouse: the new mutant twitcher. (1980) (223)
Migration of mesonephric cells into the mammalian gonad depends on Sry (1999) (214)
ABRUPT CLINE FOR SEX CHROMOSOMES IN A HYBRID ZONE BETWEEN TWO SPECIES OF MICE (1992) (200)
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6 (2003) (180)
Inherited primary hypothyroidism in mice. (1981) (162)
Ank3 (epithelial ankyrin), a widely distributed new member of the ankyrin gene family and the major ankyrin in kidney, is expressed in alternatively spliced forms, including forms that lack the repeat domain (1995) (152)
Ovarian teratomas in mice are derived from oocytes that have completed the first meiotic division (1977) (152)
A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis (2001) (148)
Three new allelic mouse mutations that cause skeletal overgrowth involve the natriuretic peptide receptor C gene (Npr3). (1999) (138)
Assignment of genes to regions of mouse chromosomes. (1978) (132)
The mouse Y* chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region. (1991) (125)
H-Y antigen, serologically detectable male antigen and sex determination (1982) (125)
Sex–determining genes on mouse autosomes identified by linkage analysis of C57BL/6J–YPOS sex reversal (1996) (116)
Direct molecular identification of the mouse pink-eyed unstable mutation by genome scanning. (1991) (116)
X-autosome translocations in the mouse: total inactivation versus partial inactivation of the X chromosome. (1970) (112)
Sex reversal in XY mice caused by dominant mutation on chromosome 17 (1983) (110)
Stimulation of growth in the little mouse. (1976) (107)
Related function of mouse SOX3, SOX9, and SRY HMG domains assayed by male sex determination (2000) (101)
Gonadal sex reversal in mutant Dax1 XY mice: a failure to upregulate Sox9 in pre-Sertoli cells (2005) (100)
Correct dosage of Fog2 and Gata4 transcription factors is critical for fetal testis development in mice (2007) (99)
Antagonism of the testis- and ovary-determining pathways during ovotestis development in mice (2009) (97)
Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. (1992) (95)
Inherited sex reversal in mice: identification of a new primary sex-determining gene. (1983) (93)
New mouse dw allele: genetic location and effects on lifespan and growth hormone levels. (1980) (87)
Sry expression level and protein isoform differences play a role in abnormal testis development in C57BL/6J mice carrying certain Sry alleles. (2003) (84)
Distribution of ribosomal gene length variants among mouse chromosomes. (1982) (76)
Sex reversal in C57BL/6J-YPOS mice corrected by a Sry transgene. (1995) (73)
Deletion mapping by immunoselection against the H-Y histocompatibility antigen further resolves the Sxra region of the mouse Y chromosome and reveals complexity of the Hya locus. (1994) (72)
A cytogenetic investigation of inherited true hermaphroditism in BALB/cWt mice. (1980) (66)
Using real time RT-PCR analysis to determine multiple gene expression patterns during XX and XY mouse fetal gonad development. (2004) (66)
A repeated segment on the mouse Y chromosome is composed of retroviral-related, Y-enriched and Y-specific sequences. (1989) (64)
Late replication in an X-autosome translocation in the mouse: correlation with genetic inactivation and evidence for selective effects during embryogenesis. (1979) (62)
Segregation patterns of endogenous mouse mammary tumor viruses in five recombinant inbred strain sets (1990) (62)
Transcriptional profile of mouse pre-granulosa and Sertoli cells isolated from early-differentiated fetal gonads. (2007) (62)
The NXSM recombinant inbred strains of mice: genetic profile for 58 loci including the Mtv proviral loci. (1990) (60)
Mapping of the X-linked immune deficiency mutation (xid) of CBA/N mice. (1980) (58)
The chromosomal location of ribosomal DNA in the mouse (2004) (58)
Meiotic abnormalities in hybrid mice of the C57BL/6J x Mus spretus cross suggest a cytogenetic basis for Haldane's rule of hybrid sterility. (1993) (57)
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice (2004) (56)
Geographic origin of the Y Chromosomes in “old” inbred strains of mice (2004) (55)
Inherited congenital goiter in mice. (1987) (54)
DNA sequence analysis of Sry alleles (subgenus Mus) implicates misregulation as the cause of C57BL/6J-Y(POS) sex reversal and defines the SRY functional unit. (1997) (53)
New Candidate Genes Identified for Controlling Mouse Gonadal Sex Determination and the Early Stages of Granulosa and Sertoli Cell Differentiation1 (2010) (52)
Variation in ribosomal RNA gene number in mouse chromosomes. (1976) (51)
Male and female mouse DNAs can be discriminated using retroviral probes (1982) (51)
Y chromosome evolution in the subgenus Mus (genus Mus). (1989) (48)
Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2 (1993) (44)
Normal testis determination in the mouse depends on genetic interaction of a locus on chromosome 17 and the Y chromosome. (1989) (44)
Use of chimeras to transmit lethal genes in the mouse and to demonstrate allelism of the two X-linked male lethal genes jp and msd. (1973) (43)
C57BL/6J-T-associated sex reversal in mice is caused by reduced expression of a Mus domesticus Sry allele. (2001) (43)
Autosomal genes involved in mammalian primary sex determination. (1988) (42)
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism. (2000) (42)
Defective mesonephric cell migration is associated with abnormal testis cord development in C57BL/6J XY(Mus domesticus) mice. (2000) (42)
Myotonia, a new inherited muscle disease in mice (1982) (39)
Primary sex determining genes in mice. (1982) (38)
Mapping anti-müllerian hormone (Amh) and related sequences in the mouse: identification of a new region of homology between MMU10 and HSA19p. (1991) (38)
Characterization of the endogenous nonecotropic murine leukemia viruses of NZB/BINJ and SM/J inbred strains (2004) (37)
Application of the ovarian teratoma mapping method in the mouse. (1983) (37)
The mouse mutation claw paw: forelimb deformity and delayed myelination throughout the peripheral nervous system. (1991) (36)
Genetic organization of the agouti region of the mouse. (1987) (35)
Sex Reversal in C57BL/6J XY Mice Caused by Increased Expression of Ovarian Genes and Insufficient Activation of the Testis Determining Pathway (2012) (35)
Lack of effect of vitamin D and its metabolites on intestinal phosphate transport in familial hypophosphatemia of mice. (1977) (33)
Assignment of LH XVI to chromosome 3 in the mouse. (1980) (33)
The T6 translocation in the mouse: its use in trisomy mapping, centromere localization, and cytological identification of linkage group 3. (1972) (30)
Multigenic and imprinting control of ovarian granulosa cell tumorigenesis in mice. (1998) (30)
Demonstration in mouse of X-ray induced deletions for a known enzyme structural locus (1974) (30)
International Standing Committee on Human Cytogenetic Nomenclature (1976) (29)
Synapsis and obligate recombination between the sex chromosomes of male laboratory mice carrying the Y* rearrangement. (1991) (29)
Inheritance of T-associated sex reversal in mice. (1990) (29)
Influence of gene duplication and X-inactivation on mouse mitochondrial malic enzyme activity and electrophoretic patterns. (1977) (28)
Evolution of mammalian carbonic anhydrase loci by tandem duplication: Close linkage of Car-1 and Car-2 to the centromere region of chromosome 3 of the mouse (1976) (28)
Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14 (1977) (28)
Autosomal phosphoglycerate kinase linked to mouse major histocompatibility complex (1978) (28)
Conserved linkage of soluble aconitase and galactose-1-phosphate uridyl transferase in mouse and man: assignment of these genes to mouse chromosome 4. (1982) (27)
Fertile male mice with three sex chromosomes: Evidence that infertility in XYY male mice is an effect of two Y chromosomes (1991) (26)
The exon-intron structure and chromosomal localization of the mouse macrophage mannose receptor gene Mrc1: identification of a Ricin-like domain at the N-terminus of the receptor. (1994) (25)
Sex and trinucleotide repeats (1994) (24)
The use of molecular probes and chromosomal rearrangements to partition the mouse Y chromosome into functional regions. (1983) (23)
Chromosomal location and isoform analysis of mouse Fcϵ RII/CD23 (1993) (23)
Telomere-related markers for the pseudoautosomal region of the mouse genome. (1992) (22)
Gene order in linkage group XVI of the house mouse. (1979) (22)
Localization of insulin-2 (Ins-2) and the obesity mutant tubby (tub) to distinct regions of mouse chromosome 7. (1992) (21)
Late replication patterns in adult and embryonic mice carrying Searle's X-autosome translocation. (1981) (21)
Does one gene determine whether a C57BL/6J-Y(POS) mouse will develop as a female or as an hermaphrodite? (2001) (20)
Polymorphism of kidney pyruvate kinase in the mouse is determined by a gene, Pk-3, on chromosome 9 (1981) (20)
The original pink-eyed dilution mutation (p) arose in Asiatic mice: implications for the H4 minor histocompatibility antigen, Myod1 regulation and the origin of inbred strains. (1994) (20)
Spontaneous sex mosaicism in BALB/cWt mice. (1978) (19)
Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects. (1994) (19)
Murine tyrosine hydroxylase maps to the distal end of chromosome 7 within a region conserved in mouse and man. (1987) (18)
Cytological identification of the chromosomes involved in Searle's translocation and the location of the centromere in the X chromosome of the mouse. (1972) (18)
Chromosome 18 of the house mouse. (1981) (17)
Genetic and physical mapping of the dreher locus on mouse chromosome 1. (1999) (17)
Murine ovarian teratomas and parthenotes as cytogenetic tools. (1978) (16)
A serum protein polymorphism determinant on chromosome 9 of Mus musculus (2004) (16)
Liver-specific lysosomal acid phosphatase deficiency (Apl) on mouse chromosome 17 (1977) (15)
Genes on chromosome 3 of the mouse. (1976) (15)
Colinearity in the mouse genome: a study of chromosome 2. (1979) (15)
Analysis of recombination in the centromere region of mouse chromosome 7 using ovarian teratoma and backcross methods. (1988) (15)
X linkage of phosphoglycerate kinase in the mouse (2004) (15)
The genetic extent of the insertion involved in the flecked translocation in the mouse. (1967) (15)
Translocation Trisomic Mice: Production by Female but Not Male Translocation Carriers (1973) (14)
Mapping of the MouseLy-6, Xp-14, andGdc-1 loci to chromosome 15 (2004) (14)
XY female mice express H-Y antigen. (1982) (13)
Mouse microcytic anaemia caused by a defect in the gene encoding the globin enhancer-binding protein NF-E2 (1994) (13)
The Mos proto-oncogene maps near the centromere on mouse chromosome 4. (1989) (13)
Foundation for the future: formal genetics of the mouse. (1981) (12)
The Position of ru-2 and qv with Respect to the FLECKED Translocation in the Mouse. (1970) (12)
Male sterility caused by p6H and qk mutations is not corrected in chimeric mice. (1987) (12)
The Chromosome 11 Region From Strain 129 Provides Protection From Sex Reversal in XYPOS Mice (2008) (12)
Overlapping deletions spanning the proximal two-thirds of the mouse t complex. (2003) (11)
Genetic Analysis of MRL.Ipr Mice: Relationship of the Fas Apoptosis Gene to Disease Manifestations and Renal Disease-modifying Loci By Mark L. Watson,*~ Jaya K. gao,* Gary S. Gilkeson,*$ (1992) (11)
An air-drying procedure for mammalian male meiotic chromosomes, following softening in gluconic acid and cell separation by an ethanol-acetic mixture. (1966) (11)
The identification of the chromosome bearing linkage group XII in the mouse. (1971) (11)
Genetic localization of Cd63, a member of the transmembrane 4 superfamily, reveals two distinct loci in the mouse genome. (1996) (11)
Chromosomal location of soluble glutamic-pyruvic transaminase-1 (Gpt-1) in the mouse (1977) (10)
High-resolution genetic map of X-linked juvenile-type granulosa cell tumor susceptibility genes in mouse. (2003) (10)
Localization of the growth hormone gene to the distal half of mouse chromosome 11. (1990) (10)
On the feasibility of mapping low-multiplicity genes by in situ hybridization. (1975) (10)
Chromosome 19 of the house mouse. (1974) (10)
Absence of mitochondrial malic enzyme in mice carrying two complementing lethal albino alleles. (1978) (9)
Growth hormone receptor (Ghr) and hemoglobin α-chain pseudogene 3 (Hba-ps3) map proximal to the myelocytomatosis oncogene (Myc) on mouse chromosome 15 (2004) (9)
Immunopathology of streaker mice. A remutation to nude in the akr/j strain, p. 211-222. In m. Eric gershwin and e. L. Cooper [eds.] Animal models of comparative and developmental aspects of immunity and disease. (1978) (9)
An amplified endogenous retroviral sequence on the murine Y chromosome related to murine leukemia viruses and viruslike 30S sequences (1989) (9)
Molecular markers that define the distal ends of mouse autosomes 4, 13, and 19 and the sex chromosomes (2004) (9)
Location of plucked (pk) on chromosome 18 of the mouse. (1985) (8)
A globoid cell type of leucodystrophy in the mouse: the mutant twitcher. (1980) (7)
H-Y typing of karyotypically abnormal mice. (1983) (7)
Mapping of the Sca1 and pcd genes on mouse chromosome 13 provides evidence that they are different genes. (1995) (7)
Mapping the "x-linked immune deficiency gene" of cba/n mice. Abstr. (1978) (6)
Stumbler, a new mutant mouse with cerebellar disease (1981) (6)
Chromosomal location and isoform analysis of mouse Fc epsilon RII/CD23. (1993) (6)
Mapping of the murine Ly-15(LFA-1) locus to chromosome 7 (2004) (5)
The mouse linkage map. A computer program. (1983) (5)
X-linked hypophosphatemia in Hyp/Y mouse a model of the human disease. (1974) (5)
Ernst W. Caspari: geneticist, teacher, and mentor. (1987) (4)
The ubiquitous subunit of the globin enhancer-binding protein NF-E2 (Nfe2u) maps to mouse chromosome 5. (1994) (4)
Feasibility tests for mapping low-multiplicity genes by hybridization in situ. (1976) (4)
AnAmplified Endogenous Retroviral Sequence on theMurineY ChromosomeRelated toMurineLeukemia Viruses and Viruslike 30SSequencest (1989) (3)
Corrected centromere orientation for mouse Chromosome 19 MIT markers (2004) (3)
The gene encoding the erythrocyte membrane skeleton protein dematin (Epb4.9) maps to mouse chromosome 14. (1995) (2)
Brain β spectrin isoform 235 (Spnb-2) maps to mouse Chromosome 11 (2004) (2)
The mouse pink-eyed unstable mutation: a DNA duplication revealed by genome scanning. (2008) (2)
The mouse A/HeJ Y chromosome: Another good Y gone bad (2008) (2)
On the feasibility of mapping low-multiplicity genes by in situ by hybridization. (1975) (1)
Location of phosphorylase kinase (Phk) in the mouse X chromosome (1973) (1)
Expression of H-Y antigen unaltered in XY female mice (2004) (1)
Brain beta spectrin isoform 235 (Spnb-2) maps to mouse chromosome 11. (1992) (1)
The gongenitally athymic streaker mouse, p. 33-39. In norman reed, et al. [eds.] Proc. Third internat. Workshop on nude mice. New york. Gustav fischer new (1982) (1)
Feasibility tests for mapping low-multiplicity genes by hybridization in situ. (1976) (0)
Familial hypophosphatemia (familial hypophosphatemic rickets) p. 69-70. In e. J. Andrews, w. Ward and n. Altman [eds.], Spontaneous animal models of human diseases. Vol. II. N.y., Academic (1979) (0)
Subject Index Vol. 17, 1976 (1976) (0)
MAPPING , CENTROMERE LOCALIZATION , AND CYTOLOGICAL IDENTIFICATION OF LINKAGE GROUP (2003) (0)
References to the committee reports (1975) (0)
Chromosome 11 Region from Strain 129 Provides Protection from Sex Reversal in XY Mice AUTHORS AND AFFILIATIONS (2008) (0)
Mouse Sex-Reversed Rearrangement (2001) (0)
Contents, Vol. 34, 1982 (1982) (0)
MUTATIONS TO SEX-LINKED LETHALS IN THE MOUSE. [Progress Report], August 15, 1967-August 15, 1968. (1968) (0)
Human Genetic Mutant Cell Repository Index (1979) (0)
Subject Index Vol. 34, 1982 (1982) (0)
Subject Index Vol. 20, 1978 (1978) (0)
TRANSCRIPTION FACTOR DOSAGE AND GENETIC BACKGROUND IN MOUSE GONADAL SEX DETERMINATION: A CRITICAL ROLE FOR Fog2 AND Gata4 IN FETAL TESTIS DEVELOPMENT (2007) (0)
Carrying two complementing lethal albino alleles. (1978) (0)
Contents, Vol. 23, 1979 (1979) (0)
Mapping the position of the break-point of the T6 translocation in chromosome III. (1966) (0)
X-LINKED HYPOPHOSPHATEMIA IN Hyp/Y MOUSE. A MODEL OF THE HUMAN DISEASE (1974) (0)
(duplication-deficiency mapping/gene duplication/mouse trans (2016) (0)
Contents, Vol. 63, 1993 (1993) (0)
Sex Determination, Mouse (2001) (0)
Nonsense-associated alternative splicing as a putative reno-protective mechanism in Pkhd1cyli/Pkhd1cyli mutant mice (2021) (0)
Sex reversal and h-y typing. Abstr. (1983) (0)
Subject Index Vol. 57, 1991 (1991) (0)
Human cytogenetic nomenclature (1980) (0)
Chapter 181 – Familial Hypophosphatemia (Familial Hypophosphatemic Rickets) (1979) (0)
Genetics, Molecular Biology, Evolution, Endocrinology, Embryology and Pathology of Sex Determination and Diff erentiation (2008) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Subject Index Vol. 63, 1993 (1993) (0)

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What Schools Are Affiliated With Evan M. Eicher?

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