David C Page
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(Suggest an Edit or Addition)David C Page'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 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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