David C Page

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David C Page is affiliated with the following schools: University of California, Berkeley, Stanford University, Massachusetts Institute of Technology, University of Washington, University of Turku

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David C Page

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David C Page'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

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes (2003) (2000)
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene (1995) (1255)
A Gene Map of the Human Genome (1996) (1080)
Four evolutionary strata on the human X chromosome. (1999) (903)
Retinoic acid regulates sex-specific timing of meiotic initiation in mice. (2006) (874)
Functional coherence of the human Y chromosome. (1997) (824)
The sex-determining region of the human Y chromosome encodes a finger protein (1987) (816)
An abundance of X-linked genes expressed in spermatogonia (2001) (760)
A comprehensive genetic map of the mouse genome (1996) (615)
Abundant gene conversion between arms of palindromes in human and ape Y chromosomes (2003) (574)
A genetic map of the mouse with 4,006 simple sequence length polymorphisms (1994) (571)
Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome (1996) (532)
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men (2001) (520)
Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice (2008) (514)
A comprehensive genetic map of the mouse genome (1996) (497)
Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators (2014) (491)
The human Y chromosome: a 43-interval map based on naturally occurring deletions. (1992) (475)
Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development. (2011) (472)
In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication (2006) (467)
The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned (1996) (460)
Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei (2003) (455)
Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure. (2002) (429)
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection (2003) (428)
Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome (1990) (395)
The human Y chromosome: overlapping DNA clones spanning the euchromatic region. (1992) (387)
Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content (2010) (371)
An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y (1999) (371)
A deletion map of the human Y chromosome based on DNA hybridization. (1986) (360)
A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. (1999) (356)
Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis (2004) (351)
Sexual differentiation of germ cells in XX mouse gonads occurs in an anterior-to-posterior wave. (2003) (328)
ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation (1989) (276)
Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the Y chromosome, and of 18 children conceived via ICSI. (2002) (268)
Hypothesis: a Y-chromosomal gene causes gonadoblastoma in dysgenetic gonads. (1987) (257)
Germ Cell-Intrinsic and -Extrinsic Factors Govern Meiotic Initiation in Mouse Embryos (2008) (255)
High mutation rates have driven extensive structural polymorphism among human Y chromosomes (2006) (255)
Sequencing the Mouse Y Chromosome Reveals Convergent Gene Acquisition and Amplification on Both Sex Chromosomes (2014) (248)
A physical map of the human Y chromosome (2001) (244)
Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. (2000) (244)
Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome. (2000) (238)
Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome. (1994) (233)
Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes (2012) (231)
Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution (1984) (225)
A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. (2004) (207)
A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated (1998) (204)
Isodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination that Maintains Palindromes (2009) (199)
Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis (2002) (198)
Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome (1999) (198)
Convergent Evolution of Chicken Z and Human X Chromosomes by Expansion and Gene Acquisition (2010) (197)
The Human UTY Gene Encodes a Novel HLA-B8-Restricted H-Y Antigen1 (2000) (187)
Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee (2005) (181)
Sexually dimorphic gene expression in the developing mouse gonad. (2002) (181)
Sequences homologous to ZFY, a candidate human sex-determining gene, are autosomal in marsupials (1988) (177)
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. (1991) (174)
Zfx mutation results in small animal size and reduced germ cell number in male and female mice. (1997) (172)
Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining (2016) (172)
Turner syndrome: the case of the missing sex chromosome. (1993) (168)
Familial Premature Ovarian Failure Due to an Interstitial Deletion of the Long Arm of the X Chromosome (1987) (168)
Dazl deficiency leads to embryonic arrest of germ cell development in XY C57BL/6 mice. (2005) (167)
Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. (1998) (167)
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. (1982) (165)
A map of 75 human ribosomal protein genes. (1998) (164)
Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells (2011) (161)
Gata4 Is Required for Formation of the Genital Ridge in Mice (2013) (157)
Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty. (1996) (154)
Direct reprogramming of fibroblasts into embryonic Sertoli-like cells by defined factors. (2012) (153)
Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse. (2005) (149)
Meiotic failure in male mice lacking an X-linked factor. (2008) (147)
The mouse X chromosome is enriched for multi-copy testis genes exhibiting post-meiotic expression (2008) (146)
Mir-290–295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects (2011) (146)
Independent specialization of the human and mouse X chromosomes for the male germline (2013) (146)
Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination. (1998) (144)
Periodic retinoic acid–STRA8 signaling intersects with periodic germ-cell competencies to regulate spermatogenesis (2015) (144)
Small deletions of the short arm of the Y chromosome in 46,XY females. (1986) (140)
The sex-determining region of the mouse Y chromosome encodes a protein with a highly acidic domain and 13 zinc fingers (1989) (140)
A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination (1987) (138)
TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse (2015) (135)
A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response (2014) (135)
Separation of the genetic loci for the H–Y antigen and for testis determination on human Y chromosome (1987) (134)
Dppa3 / Pgc7 / stella is a maternal factor and is not required for germ cell specification in mice (2004) (133)
Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility. (1999) (132)
A set of genes critical to development is epigenetically poised in mouse germ cells from fetal stages through completion of meiosis (2013) (129)
Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males (1986) (129)
Genetics of germ cell development (2012) (127)
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females. (1997) (124)
Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators (2017) (123)
Retinoic Acid Activates Two Pathways Required for Meiosis in Mice (2014) (122)
Functional equivalence of human X– and Y–encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome (1993) (122)
RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis (2005) (121)
Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. (1987) (119)
Linkage of an X-chromosome cleft palate gene (1987) (119)
Molecular mapping of the putative gonadoblastoma locus on the Y chromosome (1995) (118)
TALEN-mediated editing of the Mouse Y Chromosome (2013) (117)
Expression of DAZ, an azoospermia factor candidate, in human spermatogonia. (1997) (117)
Two closely related human nuclear export factors utilize entirely distinct export pathways. (2001) (116)
Sex–determining genes on mouse autosomes identified by linkage analysis of C57BL/6J–YPOS sex reversal (1996) (116)
Conservation, acquisition, and functional impact of sex-biased gene expression in mammals (2019) (111)
AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes. (2012) (111)
Abnormal Sperm in Mice Lacking the Taf7l Gene (2007) (111)
An X-to-autosome retrogene is required for spermatogenesis in mice (2004) (109)
Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility (1999) (106)
Chromosome Y-specific DNA in related human XX males (1985) (104)
The Biology and Evolution of Mammalian Y Chromosomes. (2015) (103)
Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome. (1989) (101)
Sex reversal: deletion mapping the male-determining function of the human Y chromosome. (1986) (99)
The Dazh gene is expressed in male and female embryonic gonads before germ cell sex differentiation. (1998) (96)
Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males (1987) (94)
A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins. (2000) (93)
Chromosome Segregation Errors Generate a Diverse Spectrum of Simple and Complex Genomic Rearrangements (2019) (92)
Unexpectedly similar rates of nucleotide substitution found in male and female hominids (2000) (91)
Oocyte differentiation is genetically dissociable from meiosis in mice (2013) (90)
Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis. (2002) (89)
Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female (1990) (88)
Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes. (1994) (84)
Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis (2017) (83)
Meioc maintains an extended meiotic prophase I in mice (2017) (82)
Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers (1990) (79)
A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary (2015) (78)
Parallel evolution of male germline epigenetic poising and somatic development in animals (2016) (77)
Putative transcription activator with alternative isoforms encoded by human ZFX gene (1989) (72)
Evidence that the SRY protein is encoded by a single exon on the human Y chromosome. (1993) (71)
Recommendations for Diagnosis, Treatment, and Management of Individuals with Turner Syndrome (1994) (68)
Poised chromatin in the mammalian germ line (2014) (67)
Germ cell pluripotency, premature differentiation and susceptibility to testicular teratomas in mice (2012) (61)
Mammalian germ cells are determined after PGC colonization of the nascent gonad (2019) (60)
Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals (2015) (60)
Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice (2019) (59)
Tet 1 Is Dispensable for Maintaining Pluripotency and Its Loss Is Compatible with Embryonic and Postnatal Development (2011) (58)
XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation. (1988) (57)
Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. (1988) (57)
An interstitial deletion in mouse Y chromosomal DNA created a transcribed Zfy fusion gene. (1991) (56)
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? (1994) (56)
Inactivation of the Zfx gene on the mouse X chromosome. (1991) (56)
The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome. (1999) (55)
Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. (1988) (54)
Tumor suppressor gene Rb is required for self-renewal of spermatogonial stem cells in mice (2013) (54)
Mapping the H-Y gene. (1987) (54)
Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection. (2009) (52)
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11 (1988) (52)
A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes (2016) (51)
Licensing of Primordial Germ Cells for Gametogenesis Depends on Genital Ridge Signaling (2015) (51)
An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome. (1989) (50)
The Mysteries of Sexual Identity: The Germ Cell's Perspective (2007) (49)
Expression of a mouse Zfy-1/lacZ transgene in the somatic cells of the embryonic gonad and germ cells of the adult testis. (1994) (49)
Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs. (1990) (48)
Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype (1994) (48)
Retinoic Acid and Germ Cell Development in the Ovary and Testis (2019) (46)
Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion (2001) (46)
The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms. (1984) (45)
Identification of avian W-linked contigs by short-read sequencing (2012) (44)
Y chromosome sequences in Turner's syndrome and risk of gonadoblastoma or virilisation (1994) (44)
A 45,X male with Y-specific DNA translocated onto chromosome 15. (1987) (43)
Is ZFY the sex-determining gene on the human Y chromosome? (1988) (43)
Inactivation of the Rps4 gene on the mouse X chromosome. (1991) (42)
Wt1 functions in the development of germ cells in addition to somatic cell lineages of the testis. (2004) (40)
Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12. (1995) (39)
Conserved microRNA targeting reveals preexisting gene dosage sensitivities that shaped amniote sex chromosome evolution (2017) (35)
Intergenerational epigenetic inheritance of cancer susceptibility in mammals (2019) (35)
Quantitative analysis of Y-Chromosome gene expression across 36 human tissues (2020) (33)
The origin of 45,X males. (1986) (33)
Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome (1999) (32)
GCNA interacts with Spartan and Topoisomerase II to regulate genome stability (2019) (32)
Excess cholesterol induces mouse egg activation and may cause female infertility (2014) (31)
Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated. (2000) (30)
A mitotic SKAP isoform regulates spindle positioning at astral microtubule plus ends (2016) (29)
CpG islands in human ZFX and ZFY and mouse Zfx genes: sequence similarities and methylation differences. (1995) (29)
MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome (2007) (27)
Selection Has Countered High Mutability to Preserve the Ancestral Copy Number of Y Chromosome Amplicons in Diverse Human Lineages. (2018) (27)
The E2 Ubiquitin-conjugating Enzyme UBE2J1 Is Required for Spermiogenesis in Mice* (2014) (26)
Are sequence family variants useful for identifying deletions in the human Y chromosome? (2004) (26)
Molecular detection of a translocation (Y;15) in a 45,X male (1986) (26)
Sequencing of rhesus macaque Y chromosome clarifies origins and evolution of the DAZ (Deleted in AZoospermia) genes (2012) (25)
Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome. (1989) (25)
Reconstructing the evolution of vertebrate sex chromosomes. (2009) (24)
Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia (1988) (24)
We're off to see the genome (1998) (24)
Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting (2018) (24)
DAZL mediates a broad translational program regulating expansion and differentiation of spermatogonial progenitors (2020) (23)
Dosage-sensitive functions in embryonic development drove the survival of genes on sex-specific chromosomes in snakes, birds, and mammals (2020) (23)
The pituitary–testicular axis in Klinefelter's syndrome and in oligo‐azoospermic patients with and without deletions of the Y chromosome long arm (2003) (23)
On Low Expectations Exceeded; or, The Genomic Salvation of the Y Chromosome * * Previously presented (2004) (22)
A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies. (1987) (22)
Locating and Characterizing a Transgene Integration Site by Nanopore Sequencing (2019) (21)
Optical mapping of BAC clones from the human Y chromosome DAZ locus. (2000) (20)
UvA-DARE ( Digital Academic Repository ) Recombination between palindromes P 5 and P 1 on the human Y chromosome causes massive deletions and spermatogenic failure (2002) (19)
2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome. (2004) (19)
Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms. (2013) (19)
Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages (2020) (19)
Deletion mapping of stature determinants on the long arm of the Y chromosome (1995) (19)
Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2,DCN, EPS8, andRPL6 (2000) (19)
Rps4 maps near the inactivation center on the mouse X chromosome. (1992) (17)
Dysgerminoma and gonadal dysgenesis in a 46,XX female with no evidence of Y chromosomal DNA. (1995) (17)
The structure of the Zfx gene on the mouse X chromosome. (1994) (16)
Proceedings from the Turner Resource Network symposium: The crossroads of health care research and health care delivery (2015) (15)
Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology. (1990) (15)
Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male (1988) (15)
Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family. (1997) (15)
Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. (1995) (15)
Regional assignments of three polymorphic DNA segments on human chromosome 15 (1986) (14)
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes (1992) (14)
Dynamic and regulated TAF gene expression during mouse embryonic germ cell development (2020) (13)
Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes. (1993) (12)
The history of the Y chromosome in man (2016) (11)
Steroid sulfatase gene in XX males. (1990) (11)
A strategic research alliance: Turner syndrome and sex differences (2019) (10)
Characterization of the murine Zfy1 and Zfy2 promoters. (1994) (9)
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction. (1987) (8)
A bird zinc-finger protein closely related to ZFY. (1990) (8)
Cost-effective high-throughput single-haplotype iterative mapping and sequencing for complex genomic structures (2017) (8)
Large palindromes on the primate X Chromosome are preserved by natural selection (2020) (7)
ICSI results with and without Y chromosomal deletions in men with severe oligospermia and azoospermia. (2001) (7)
The Ligand Binding Domain of GCNF Is Not Required for Repression of Pluripotency Genes in Mouse Fetal Ovarian Germ Cells (2013) (6)
Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe (1989) (6)
Has the chimpanzee Y chromosome been sequenced? (2006) (6)
Germ cell determination and the developmental origin of germ cell tumors. (2021) (6)
Haplotype and multipoint linkage analysis in Finnish choroideremia families (1989) (6)
Molecular evidence of Y-autosomal translocations in owl monkeys. (1989) (6)
Reconstructing sex chromosome evolution (2010) (5)
The parental origin and mechanism of formation of three dicentric X chromosomes (1988) (5)
Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice (2023) (5)
Dppa 3 / Pgc 7 / stellais a maternal factor and is not required for germ cell specification in mice Citation (2004) (4)
Velocardiofacial syndrome in an unexplained XX male (2003) (4)
Characterization of a (Y;4) translocation by DNA hybridization (1988) (4)
Erratum: Inactivation of the Rps4 gene on the mouse X chromosome (Genomics (1991) 11 (1097-1101)) (1992) (4)
Sequencing and Annotating New Mammalian Y Chromosomes A White Paper Proposal , July , 2006 (2006) (4)
Haplotyping finnish choroideremia patients (1987) (4)
Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators (2014) (4)
Correction: Corrigendum: Parallel evolution of male germline epigenetic poising and somatic development in animals (2016) (3)
Clinical characterization of 42 oligospermic or azoospermic men with microdeletion of the AZFc region of the y chromosome, and of 18 children conceived via intracytoplasmic sperm injection (2002) (3)
Human Genome: What's Been Most Surprising? (2011) (3)
Author response: Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice (2019) (2)
Sex-specific chromatin states in mammalian fetal germ cells (2013) (2)
Genetic characterization of a missense mutation in the X-linked TAF7L gene identified in an oligozoospermic man (2022) (2)
Sex-specific chromatin states in mammalian fetal germ cells (2013) (1)
SHIMS 3.0: Highly efficient single-haplotype iterative mapping and sequencing using ultra-long nanopore reads (2020) (1)
Phenotypic diversity amongst patients with an isodicentric y chromosome (2013) (1)
Corrigendum to "Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting" [Dev. Biol. 443 (2018) 19-34]. (2019) (1)
A gene deriving from the ancestral sex chromosomes was lost from the X and retained on the Y chromosome in eutherian mammals (2022) (1)
O-014 Y chromosomal deletions in azoospermic and oligospermic men undergoing ICSI (1997) (1)
A gene-by-gene mosaic of dosage compensation strategies on the human X chromosome (2021) (1)
Author response: Intergenerational epigenetic inheritance of cancer susceptibility in mammals (2019) (1)
The human inactive X chromosome modulates expression of the active X chromosome (2022) (1)
Identification of avian W-linked contigs by short-read sequencing (2012) (1)
Locating a transgene integration site by nanopore sequencing (2019) (0)
Function of the Human Y Chromosome Sex Reversal: Deletion Mapping the Male-determining (2008) (0)
Clinical Report Velocardiofacial Syndrome in an Unexplained XX Male (2003) (0)
Turner syndrome: of the missing sex chromosome the case (1993) (0)
Aproposedpathbywhich genescommon tomammalian XandYchromosomesevolveto becomeX inactivated (0)
Genes specifiques de la reproduction (2001) (0)
Corrigendum: Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee (2006) (0)
P-064. Testicular histology of men with non-obstructive azoospermia or severe oligospermia caused by Y chromosomal deletions (1999) (0)
Structure andFunction ofRibosomal Protein S4Geneson the HumanandMouseSexChromosomes (1994) (0)
Whole exome sequencing in monozygotic twins discordant for premature ovarian insufficiency (2015) (0)
ICSI Offspring of Y-Deleted Men (2000) (0)
Identification of a novel, ancient family of germ cell enriched proteins (2014) (0)
Separation of the Genetic Loci for the H-Y Antigen and for Testis Determination on Human Y Chromosome (1988) (0)
Molecular analysis of patients with XY-gonadal dysgenesis (1989) (0)
Retinoic Acid Controls the Timinig of Spermatogonial Differentiation and Meiotic Initiation in Adult Male Mice. (2012) (0)
Cell type-specific role of CBX2-cPRC1 at the onset of spermatogonial differentiation (2022) (0)
Locus DAZMapping of BAC Clones from the Human Y Chromosome (2007) (0)
O-015. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing testicular sperm extraction and ICSI (1997) (0)
Sex reversal associated with a de novo point mutation in the SRY gene (1992) (0)
No bull: Upholding community standards in public sharing of biological datasets (2013) (0)
Has the chimpanzee Y chromosome been sequenced? Authors' reply (2006) (0)
A gene deriving from the ancestral sex chromosomes was lost from the X and retained on the Y chromosome in eutherian mammals (2022) (0)
REFINING CELLULAR IDENTITY IN THE HUMAN BLASTOCYST THROUGH SELECTIVE INNER CELL MASS AND TROPHECTODERM BIOPSY (2022) (0)
A “Four Core Genotypes” rat model to distinguish mechanisms underlying sex-biased phenotypes and diseases (2023) (0)
Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery. (2019) (0)
P–154 The role of the X Chromosome in early human embryo metabolism (2021) (0)
Preexisting heterogeneities in gene dosage sensitivity shaped sex chromosome evolution in mammals and birds (2017) (0)
Ribosomal protein gene mapping and human chromosomal disorders (1994) (0)
Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements (2019) (0)
Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals (2015) (0)
R-054. Y Chromosome deletions and the feasibility of ICSI (1999) (0)
O-058. Transmission of Y deletion to male offspring by ICSI (1999) (0)
Microsurgical distribution of spermatogenesis in the testes of azoospermic and severely oligospermic men with Y chromosomal deletions. (2001) (0)
Germ cell commitment occurs after PGC colonization of the gonad in mammals (2019) (0)
Male germ cells produce and secrete retinoic acid in a paracrine manner to regulate spermatogenesis in mouse testes (2016) (0)
Reproductive fitness of the human Y chromosome (2007) (0)
GC-biased gene conversion in X-chromosome palindromes conserved in human, chimpanzee, and rhesus macaque (2021) (0)

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