D. Page

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ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

A. Schneider-Gädicke, P. Beer-Romero, L. Brown, 1989, Cell.

Inactivation of the Zfx gene on the mouse X chromosome.

V. Chapman, D. Page, D. Adler, 1991, Proceedings of the National Academy of Sciences of the United States of America.

CpG islands in human ZFX and ZFY and mouse Zfx genes: sequence similarities and methylation differences.

D. Page, S. Luoh, K. Jegalian, 1995, Genomics.

Inactivation of the Rps4 gene on the mouse X chromosome.

V. Chapman, P. Beer-Romero, D. Page, 1991, Genomics.

Sequences homologous to ZFY, a candidate human sex-determining gene, are autosomal in marsupials

D. Page, A. Sinclair, J. W. Foster, 1988, Nature.

Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family.

D. Page, C. Mahaffey, J. Bayleran, 1997, Genomics.

Homologous ribosomal protein genes on the human X and Y chromosomes: Escape from X inactivation and possible implications for turner syndrome

P. Beer-Romero, L. Brown, D. Page, 1990, Cell.

The sex-determining region of the human Y chromosome encodes a finger protein

L. Brown, D. Page, E. Simpson, 1987, Cell.

A Gene Map of the Human Genome

P. Deloukas, E. Lander, M. Adams, 1996, Science.

Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators

Nancy F. Chen, Daniel W Bellott, Ting-Jan Cho, 2017, Nature Genetics.

The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes

T. Graves, R. Wilson, S. Rock, 2003, Nature.

Sequencing the Mouse Y Chromosome Reveals Convergent Gene Acquisition and Amplification on Both Sex Chromosomes

Jennifer F. Hughes, T. Graves, R. Wilson, 2014, Cell.

The human Y chromosome: overlapping DNA clones spanning the euchromatic region.

D. Page, D. Vollrath, S. Foote, 1992, Science.

Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome

D. Page, B. Lahn, 1999, Nature Genetics.

Four evolutionary strata on the human X chromosome.

D. Page, B. Lahn, D. Page, 1999, Science.

A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes

D. Page, C. Mello, M. Carmell, 2016, eLife.

Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice

D. Page, D. D. de Rooij, Mina L. Kojima, 2019, eLife.

GCNA interacts with Spartan and Topoisomerase II to regulate genome stability

D. Page, C. Mello, G. Hannon, 2019, bioRxiv.

Gata4 Is Required for Formation of the Genital Ridge in Mice

D. Page, Yueh-Chiang Hu, L. M. Okumura, 2013, PLoS genetics.

Conservation, acquisition, and functional impact of sex-biased gene expression in mammals

Jennifer F. Hughes, D. Page, R. Mitchell, 2019, Science.

Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells

D. Page, Yueh-Chiang Hu, M. Gill, 2011, Proceedings of the National Academy of Sciences.

Functional coherence of the human Y chromosome.

D. Page, B. Lahn, D C Page, 1997, Science.

In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication

Anne E Carpenter, David C Page, Yueh-Chiang Hu, 2006, Nature Genetics.

Convergent Evolution of Chicken Z and Human X Chromosomes by Expansion and Gene Acquisition

Steve Rozen, Elaine R. Mardis, Helen Skaletsky, 2010, Nature.

Familial Premature Ovarian Failure Due to an Interstitial Deletion of the Long Arm of the X Chromosome

L. Brown, D. Page, Krauss Cm, 1987 .

A comprehensive genetic map of the mouse genome

Eric S. Lander, Nathan Goodman, Leonid Kruglyak, 1996, Nature.

A comprehensive genetic map of the mouse genome

Eric S. Lander, Nathan Goodman, Leonid Kruglyak, 1996, Nature.

Quantitative analysis of Y-Chromosome gene expression across 36 human tissues

D. Page, S. Gygi, R. Mitchell, 2020, Genome research.

An STS-Based Map of the Human Genome

L Kruglyak, M P Reeve-Daly, E S Lander, 1995, Science.

A Chromatin-Dependent Role of the Fragile X Mental Retardation Protein FMRP in the DNA Damage Response

D. Page, R. Kingston, S. Warren, 2014, Cell.

Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

U. Surti, D. Page, B. Lahn, 1994, Nature Genetics.

Dosage-sensitive functions in embryonic development drove the survival of genes on sex-specific chromosomes in snakes, birds, and mammals

D. Page, D. W. Bellott, 2020, bioRxiv.

Abnormal Sperm in Mice Lacking the Taf7l Gene

D. Page, Yong Cheng, M. Buffone, 2007, Molecular and Cellular Biology.

Development and Stem Cells Research Article 1577

D. Page, J. Nadeau, J. Heaney, 2022 .

Azoospermic men with deletion of the DAZ gene cluster are capable of completing spermatogenesis: fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection.

L. Brown, D. Page, J. Mulhall, 1997 .

Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis

D. Page, D. Menke, M. Matzuk, 2004, Developmental dynamics : an official publication of the American Association of Anatomists.

Cost-effective, high-throughput, single-haplotype iterative mapping and sequencing for complex genomic structures

Jennifer F. Hughes, D. Page, H. Skaletsky, 2017, bioRxiv.

Intergenerational epigenetic inheritance of cancer susceptibility in mammals

D. Page, B. Ebert, R. Bronson, 2019, eLife.

Sequence analysis in Bos taurus reveals pervasiveness of X–Y arms races in mammalian lineages

Jennifer F. Hughes, R. Wilson, Colin L. Kremitzki, 2020, Genome research.

Expression of DAZ, an azoospermia factor candidate, in human spermatogonia.

D. Page, D. Menke, G. Mutter, 1997, American journal of human genetics.

Locus DAZMapping of BAC Clones from the Human Y Chromosome

L. Brown, D. Page, T. Anantharaman, 2007 .

Parallel evolution of male germline epigenetic poising and somatic development in animals

D. Page, Bluma J. Lesch, J. McCarrey, 2016, Nature Genetics.

Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers

L. Brown, D. Page, S. Luoh, 1990, Molecular and cellular biology.

Periodic production of retinoic acid by meiotic and somatic cells coordinates four transitions in mouse spermatogenesis

D. Page, D. D. de Rooij, Elizaveta Freinkman, 2017, Proceedings of the National Academy of Sciences.

Function of the Human Y Chromosome Sex Reversal: Deletion Mapping the Male-determining

D. Page, 2008 .

The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms.

D. Page, A. de la Chapelle, 1984, American journal of human genetics.

Oocyte differentiation is genetically dissociable from meiosis in mice

D. Page, Gregoriy A Dokshin, J. Eppig, 2013, Nature Genetics.

The origin of 45,X males.

L. Brown, D. Page, A. de la Chapelle, 1986, American journal of human genetics.

Mapping the H-Y gene.

D. Page, C. Disteche, E. Simpson, 1987, Development.

A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies.

D. Page, M. Ramsay, M. Pinto, 1987, American journal of human genetics.

Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery.

Yonit A. Addissie, M. Luby, D. Page, 2019, Birth defects research.

Tumor suppressor gene Rb is required for self-renewal of spermatogonial stem cells in mice

D. Page, D. D. de Rooij, Yueh-Chiang Hu, 2013, Proceedings of the National Academy of Sciences.

Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11

D. Page, A. Chapelle, C. Turleau, 1988, Human Genetics.

Has the chimpanzee Y chromosome been sequenced?

Jennifer F. Hughes, R. Wilson, S. Rozen, 2006, Nature Genetics.

The E2 Ubiquitin-conjugating Enzyme UBE2J1 Is Required for Spermiogenesis in Mice*

D. Page, M. Hagiwara, P. Koenig, 2014, The Journal of Biological Chemistry.

Locating and Characterizing a Transgene Integration Site by Nanopore Sequencing

D. Page, D. W. Bellott, Ting-Jan Cho, 2019, G3: Genes, Genomes, Genetics.

Locating a transgene integration site by nanopore sequencing

D. Page, D. W. Bellott, Ting-Jan Cho, 2019, bioRxiv.

Characterization of a (Y;4) translocation by DNA hybridization

L. Brown, D. Page, A. Chapelle, 1988, Human Genetics.

Retinoic Acid and Germ Cell Development in the Ovary and Testis

D. Page, D. D. de Rooij, P. Nicholls, 2019, Biomolecules.

Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes.

D. Page, E. Fisher, K. Schmitt, 1993, Human molecular genetics.

The sex-determining region of the mouse Y chromosome encodes a protein with a highly acidic domain and 13 zinc fingers

D. Page, G. Mardon, 1989, Cell.

Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse.

David C Page, John R McCarrey, D. Page, 2005, Human molecular genetics.

An abundance of X-linked genes expressed in spermatogonia

Fang Yang, David C. Page, D. Page, 2001, Nature Genetics.

Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis

D. Page, C. Allis, Jianxin Zhou, 2002, Proceedings of the National Academy of Sciences of the United States of America.

The Biology and Evolution of Mammalian Y Chromosomes.

Jennifer F. Hughes, D. Page, 2015, Annual review of genetics.

Sequencing and Annotating New Mammalian Y Chromosomes A White Paper Proposal , July , 2006

R. Wilson, G. Weinstock, R. Gibbs, 2006 .

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA–binding protein gene

S. Rozen, L. Brown, D. Page, 1995, Nature Genetics.

Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice

David C Page, D. Page, T. Hassold, 2008, Proceedings of the National Academy of Sciences.

Retinoic acid regulates sex-specific timing of meiotic initiation in mice.

David C Page, D. Page, D. Menke, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

Jennifer F. Hughes, T. Graves, R. Wilson, 2014, Nature.

GCNA interacts with Spartan and Topoisomerase II to regulate genome stability

D. Page, C. Mello, G. Hannon, 2019, bioRxiv.

Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated.

D. Page, E. Nieschlag, G. Weinbauer, 2000, International journal of andrology.

Germ cell determination and the developmental origin of germ cell tumors.

D. Page, P. Nicholls, 2021, Development.

The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned

S. Rozen, L. Brown, D. Page, 1996, Nature Genetics.

Functional coherence of the human Y chromosome.

D. Page, B. Lahn, D. Page, 1997, Science.

Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome

D. Page, P. Patrizio, R. Reijo, 1996, The Lancet.

Hypothesis: a Y-chromosomal gene causes gonadoblastoma in dysgenetic gonads.

D. Page, David L. Page, 1987, Development.

The Dazh gene is expressed in male and female embryonic gonads before germ cell sex differentiation.

D. Page, J. Seligman, D. Page, 1998, Biochemical and biophysical research communications.

Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty.

L. Brown, D. Page, C. Disteche, 1996, Genomics.

Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome.

D. Page, C. Disteche, K. Tsuchiya, 1995, American journal of human genetics.

Y chromosome sequences in Turner's syndrome and risk of gonadoblastoma or virilisation

D. Page, 1994, The Lancet.

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.

D. Page, C. Petit, D. Weil, 1997, Human molecular genetics.

XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation.

D. Page, M. Ramsay, T. Jenkins, 1988, American journal of human genetics.

DAZL mediates a broad translational program regulating expansion and differentiation of spermatogonial progenitors

Emily K. Jackson, D. Page, D. D. de Rooij, 2020, bioRxiv.

Dazl deficiency leads to embryonic arrest of germ cell development in XY C57BL/6 mice.

D. Page, Yanfeng Lin, 2005, Developmental biology.

Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome.

H Skaletsky, L. Brown, D. Page, 2000, Genomics.

The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome.

D. Page, H. Skaletsky, E. Nieschlag, 1999, Human molecular genetics.

Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion

D. Page, J. Bierła, L. Pawelczyk, 2001, Journal of medical genetics.

Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses.

S. Rozen, D. Page, H. Skaletsky, 2000, Human molecular genetics.

An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y

B. Birren, D. Page, K. Devon, 1999, Nature Genetics.

Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility

L. Brown, D. Page, S. Silber, 1999 .

Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility.

L. Brown, D. Page, S. Silber, 1999, Human reproduction.

Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction.

L. Brown, D. Page, S. Silber, 1998, Human reproduction.

A deletion map of the human Y chromosome based on DNA hybridization.

D. Botstein, J. Weissenbach, L. Brown, 1986, American journal of human genetics.

Wt1 functions in the development of germ cells in addition to somatic cell lineages of the testis.

D. Page, R. Jaenisch, D. Housman, 2004, Developmental biology.

Molecular mapping of the putative gonadoblastoma locus on the Y chromosome

D. Page, A. de la Chapelle, P. Peltomäki, 1995, Genes, chromosomes & cancer.

The human Y chromosome: a 43-interval map based on naturally occurring deletions.

P. Beer-Romero, L. Brown, D. Page, 1992, Science.

Turner syndrome: the case of the missing sex chromosome.

D. Page, A. Zinn, E. Fisher, 1993, Trends in genetics : TIG.

Evidence that the SRY protein is encoded by a single exon on the human Y chromosome.

P. Beer-Romero, D. Page, M. Behlke, 1993, Genomics.

Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males

D. Page, A. de la Chapelle, M. Andersson, 1986, Science.

Small deletions of the short arm of the Y chromosome in 46,XY females.

D. Page, C. Disteche, J. Graham, 1986, Proceedings of the National Academy of Sciences of the United States of America.

Sex reversal: deletion mapping the male-determining function of the human Y chromosome.

D. Page, 1986, Cold Spring Harbor symposia on quantitative biology.

Dysgerminoma and gonadal dysgenesis in a 46,XX female with no evidence of Y chromosomal DNA.

D. Page, G. Letterie, 1995, Gynecologic oncology.

Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males

L. Brown, D. Page, A. Chapelle, 1987, Nature.

A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators.

C. S. Raymond, L. Brown, D. Page, 1999, Human molecular genetics.

Chromosome Y-specific DNA in related human XX males

J. Weissenbach, D. Page, A. Chapelle, 1985, Nature.

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes.

D. Botstein, D. Page, U. Francke, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Functional equivalence of human X– and Y–encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome

D. Page, A. Zinn, Minoru Watanabe, 1993, Nature Genetics.

Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei

D. Page, R. Jaenisch, K. Eggan, 2003, Development.

Germ Cell-Intrinsic and -Extrinsic Factors Govern Meiotic Initiation in Mouse Embryos

D. Page, M. Gill, Yanfeng Lin, 2008, Science.

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection

S. Rozen, D. Page, H. Skaletsky, 2003, Nature Genetics.

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.

L. Brown, D. Page, S. Silber, 2002, Human reproduction.

Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.

Julian Lange, S. Rozen, D. Page, 2002, American journal of human genetics.

AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.

S. Rozen, L. Brown, D. Page, 2012, American journal of human genetics.

A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region.

S. Rozen, L. Brown, D. Page, 2004, Genomics.

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men

R. Wilson, S. Rozen, R. Waterston, 2001, Nature Genetics.

Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome

D. Page, B. Lahn, 1999, Nature Genetics.

Mammalian germ cells are determined after PGC colonization of the nascent gonad

D. Page, M. Carmell, D. F. Carlson, 2019, Proceedings of the National Academy of Sciences.

Reproductive fitness of the human Y chromosome

S. Rozen, L. Brown, D. Page, 2007 .

Genetics of germ cell development

David C. Page, D. Page, Bluma J. Lesch, 2012, Nature Reviews Genetics.

UvA-DARE ( Digital Academic Repository ) Recombination between palindromes P 5 and P 1 on the human Y chromosome causes massive deletions and spermatogenic failure

Julian Lange, S. Rozen, D. Page, 2002 .

TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse

S. Rozen, L. Brown, D. Page, 2015, EMBO molecular medicine.

Direct reprogramming of fibroblasts into embryonic Sertoli-like cells by defined factors.

David C Page, Rudolf Jaenisch, Yueh-Chiang Hu, 2012, Cell stem cell.

Expression of a mouse Zfy-1/lacZ transgene in the somatic cells of the embryonic gonad and germ cells of the adult testis.

R. Palmiter, D. Page, E. Simpson, 1994, Development.

Deletion mapping of stature determinants on the long arm of the Y chromosome

D. Page, A. Chapelle, H. Kääriäinen, 1995, Human Genetics.

An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction.

L. Brown, D. Page, A. de la Chapelle, 1987, American journal of human genetics.

Sexual differentiation of germ cells in XX mouse gonads occurs in an anterior-to-posterior wave.

D. Page, D. Menke, J. Koubová, 2003, Developmental biology.

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region.

D. Page, P. Jacobs, T. Hassold, 1991, American journal of human genetics.

Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes.

M. Leppert, L. Brown, D. Page, 1987, Genomics.

An X-to-autosome retrogene is required for spermatogenesis in mice

Helen Skaletsky, David C Page, Ken Dewar, 2004, Nature Genetics.

A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins.

D. Page, B. Lahn, D. Page, 2000, Human molecular genetics.

Abundant gene conversion between arms of palindromes in human and ape Y chromosomes

Steve Rozen, Helen Skaletsky, David C. Page, 2003, Nature.

A genetic map of the mouse with 4,006 simple sequence length polymorphisms

Eric S. Lander, Nathan Goodman, Robert G. Steen, 1994, Nature Genetics.

Conserved microRNA targeting reveals preexisting gene dosage sensitivities that shaped amniote sex chromosome evolution

D. Page, D. W. Bellott, S. Naqvi, 2017, bioRxiv.

Preexisting heterogeneities in gene dosage sensitivity shaped sex chromosome evolution in mammals and birds

D. Page, D. W. Bellott, S. Naqvi, 2017, bioRxiv.

Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee

Steve Rozen, Helen Skaletsky, Jennifer F. Hughes, 2005, Nature.

A physical map of the human Y chromosome

S. Rozen, R. Waterston, J. McPherson, 2001, Nature.

Large palindromes on the primate X Chromosome are preserved by natural selection

Emily K. Jackson, Jennifer F. Hughes, D. Page, 2020, bioRxiv.

A strategic research alliance: Turner syndrome and sex differences

D. Page, A. S. San Roman, 2019, American journal of medical genetics. Part C, Seminars in medical genetics.

Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes

Steve Rozen, Christian J. Buhay, Donna M. Muzny, 2012, Nature.

Reconstructing sex chromosome evolution

Jennifer F. Hughes, T. Graves, R. Wilson, 2010, Genome Biology.

Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content

Steve Rozen, Elaine R. Mardis, Helen Skaletsky, 2010, Nature.

Isodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination that Maintains Palindromes

Helen Skaletsky, Julian Lange, David C. Page, 2009, Cell.

Reconstructing the evolution of vertebrate sex chromosomes.

D. Page, D. W. Bellott, David L. Page, 2009, Cold Spring Harbor symposia on quantitative biology.

On Low Expectations Exceeded; or, The Genomic Salvation of the Y Chromosome * * Previously presented

D. Page, 2004 .

2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome.

D. Page, 2004, American journal of human genetics.

A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated

D. Page, K. Jegalian, 1998, Nature.

Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution

D. Botstein, D. Page, M. Harper, 1984, Nature.

High mutation rates have driven extensive structural polymorphism among human Y chromosomes

Julian Lange, S. Rozen, L. Brown, 2006, Nature Genetics.

Independent specialization of the human and mouse X chromosomes for the male germline

T. Graves, R. Wilson, Katherine Auger, 2013, Nature Genetics.

Zfx mutation results in small animal size and reduced germ cell number in male and female mice.

D. Page, S. Luoh, R. Jaenisch, 1997, Development.

Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis?

K. Lange, D. Page, E. Fisher, 1994, American journal of human genetics.

Optical mapping of BAC clones from the human Y chromosome DAZ locus.

L. Brown, D. Page, T. Anantharaman, 2000, Genome research.

Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection.

S. Rozen, D. Page, H. Skaletsky, 2009, American journal of human genetics.

An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome.

D. Page, H. Donis-Keller, V. Brown, 1989, Nucleic acids research.

Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining

Helen Skaletsky, David C Page, Peter Ly, 2016, Nature Cell Biology.

Meiotic failure in male mice lacking an X-linked factor.

D. Page, K. Mclaughlin, Fang Yang, 2008, Genes & development.

Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis.

D. Page, P. Wang, P. Wang, 2002, Human molecular genetics.

Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals

Jennifer F Hughes, Helen Skaletsky, David C Page, 2015, Genome Biology.

Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development.

D. Page, R. Jaenisch, A. Cheng, 2011, Cell stem cell.

Selection Has Countered High Mutability to Preserve the Ancestral Copy Number of Y Chromosome Amplicons in Diverse Human Lineages.

D. Page, H. Skaletsky, Tatyana Pyntikova, 2018, American journal of human genetics.

GC-biased gene conversion in X-chromosome palindromes conserved in human, chimpanzee, and rhesus macaque

Emily K. Jackson, D. Page, H. Skaletsky, 2021, bioRxiv.

Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome.

D. Page, M. Mennuti, D. Huff, 1989, American journal of medical genetics.

Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2,DCN, EPS8, andRPL6

D. Page, E. Mariman, R. Kucherlapati, 2000, Journal of medical genetics.

A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary

A. Oudenaarden, D. Page, A. van Oudenaarden, 2015, PLoS genetics.

The mouse X chromosome is enriched for multi-copy testis genes exhibiting post-meiotic expression

D. Page, P. Park, P. Warburton, 2008, Nature Genetics.

An interstitial deletion in mouse Y chromosomal DNA created a transcribed Zfy fusion gene.

D. Page, E. Simpson, D. Page, 1991, Genomics.

Licensing of Primordial Germ Cells for Gametogenesis Depends on Genital Ridge Signaling

A. Oudenaarden, D. Page, A. van Oudenaarden, 2015, PLoS genetics.

Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology.

D. Page, S. Luoh, E. Fisher, 1990, Genomics.

Haplotype and multipoint linkage analysis in Finnish choroideremia families

D. Page, A. Chapelle, J. Ott, 1989, Human Genetics.

Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs.

L. Brown, D. Page, C. Disteche, 1990, Genomics.

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.

D. Page, J. Ott, L. Kunkel, 1988, Genomics.

Helen Skaletsky, David C. Page, D. Page, 2000, Nature.

Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms.

Julian Lange, D. Page, H. Skaletsky, 2013, Genomics.

MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome

Helen Skaletsky, Julian Lange, George W. Bell, 2007, Nucleic Acids Res..

Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination.

L. Brown, D. Page, C. Disteche, 1998, Human molecular genetics.

Chromosome Segregation Errors Generate a Diverse Spectrum of Simple and Complex Genomic Rearrangements

D. Page, P. Campbell, S. Behjati, 2019, Nature Genetics.

Sex–determining genes on mouse autosomes identified by linkage analysis of C57BL/6J–YPOS sex reversal

D. Page, N. Schork, R. Dredge, 1996, Nature Genetics.

TALEN-mediated editing of the Mouse Y Chromosome

A. Bogdanove, D. Voytas, D. Page, 2013, Nature Biotechnology.

A map of 75 human ribosomal protein genes.

N Goodman, S. Rozen, T. Hudson, 1998, Genome research.

Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.

D. Page, D. Maglott, N. Kenmochi, 1995, Genomics.

RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis

D. Page, Jieyan Pan, N. Nakatsuji, 2005, Development.

Separation of the genetic loci for the H–Y antigen and for testis determination on human Y chromosome

D. Page, C. Disteche, M. Ferguson-Smith, 1987, Nature.

A set of genes critical to development is epigenetically poised in mouse germ cells from fetal stages through completion of meiosis

R. Young, D. Page, Bluma J. Lesch, 2013, Proceedings of the National Academy of Sciences.

Dynamic and regulated TAF gene expression during mouse embryonic germ cell development

D. Page, D. D. de Rooij, M. Mikedis, 2020, PLoS genetics.

The majority of cloned animals derived by nuclear transfer from somatic cell nuclei develop to the blastocyst stage

D. Page, R. Jaenisch, K. Eggan, 2003 .

Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome.

D. Page, C. Disteche, R. Mosher, 1989, Science.

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female

L. Brown, D. Page, E. Fisher, 1990, Nature.

Periodic retinoic acid–STRA8 signaling intersects with periodic germ-cell competencies to regulate spermatogenesis

D. Page, Katherine A. Romer, D. D. de Rooij, 2015, Proceedings of the National Academy of Sciences.

Retinoic Acid Activates Two Pathways Required for Meiosis in Mice

D. Page, M. Griswold, Y. Q. S. Soh, 2014, PLoS genetics.

Excess cholesterol induces mouse egg activation and may cause female infertility

D. Page, A. Rigotti, M. Krieger, 2014, Proceedings of the National Academy of Sciences.

Mir-290–295 deficiency in mice results in partially penetrant embryonic lethality and germ cell defects

P. Sharp, D. Page, R. Jaenisch, 2011, Proceedings of the National Academy of Sciences.

SHIMS 3.0: Highly efficient single-haplotype iterative mapping and sequencing using ultra-long nanopore reads

Emily K. Jackson, Jennifer F. Hughes, D. Page, 2020, bioRxiv.

Cost-effective high-throughput single-haplotype iterative mapping and sequencing for complex genomic structures

Daniel W Bellott, Ting-Jan Cho, Jennifer F Hughes, 2017, Nature Protocols.

Sexually dimorphic gene expression in the developing mouse gonad.

D. Page, D. Menke, 2002, Gene expression patterns : GEP.

Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.

L. Brown, D. Page, A. Zinn, 1994, Molecular and cellular biology.

Structure andFunction ofRibosomal Protein S4Geneson the HumanandMouseSexChromosomes

D. Page, I. Wool, 1994 .

A sex chromosome rearrangement in a human XX male caused by Alu—Alu recombination

J. Weissenbach, D. Page, F. Rouyer, 1987, Cell.

Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome.

L. Brown, D. Page, L. Atkins, 1988, The New England journal of medicine.

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

D. Page, E. Niebuhr, M. Schwartz, 1988, Human Genetics.

Rps4 maps near the inactivation center on the mouse X chromosome.

P. Beer-Romero, D. Page, A. Zinn, 1992, Genomics.

The history of the Y chromosome in man

Jennifer F. Hughes, D. Page, 2016, Nature Genetics.

Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome

D. Page, B. Lahn, 1999, Nature Genetics.

Aproposedpathbywhich genescommon tomammalian XandYchromosomesevolveto becomeX inactivated

D. Page, K. Jegalian, 2022 .

Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting

D. Page, Katherine A. Romer, D. D. de Rooij, 2018, bioRxiv.

Identification of avian W-linked contigs by short-read sequencing

Nancy F. Chen, A. Clark, D. Page, 2012, BMC Genomics.

Dppa3 / Pgc7 / stella is a maternal factor and is not required for germ cell specification in mice

D. Page, M. Goodheart, A. Bortvin, 2004, BMC Developmental Biology.

Tet 1 Is Dispensable for Maintaining Pluripotency and Its Loss Is Compatible with Embryonic and Postnatal Development

D. Page, R. Jaenisch, A. Cheng, 2011 .

Molecular detection of a translocation (Y;15) in a 45,X male

L. Brown, D. Page, C. Disteche, 1986, Human Genetics.

Independent specialization of the human and mouse X chromosomes for the male germline

T. Graves, R. Wilson, Katherine Auger, 2013, Nature Genetics.

Regional assignments of three polymorphic DNA segments on human chromosome 15

D. Botstein, D. Page, J. Trowsdale, 1986, Genetic epidemiology.

Poised chromatin in the mammalian germ line

D. Page, Bluma J. Lesch, 2014, Development.

Are sequence family variants useful for identifying deletions in the human Y chromosome?

S. Rozen, D. Page, S. Repping, 2004, American journal of human genetics.

Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe

D. C. Walker, D. Page, C. Disteche, 1989, Human Genetics.

Meioc maintains an extended meiotic prophase I in mice

D. Page, D. G. Rooij, D. D. de Rooij, 2017, PLoS genetics.

Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes

D. Page, P. Lichter, Chih-ping Chen, 1992, Human Genetics.

Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5.

D. Page, N. Nowak, D. Housman, 1995, Genomics.

A 45,X male with Y-specific DNA translocated onto chromosome 15.

D. Page, G. Neri, W. Schempp, 1987, American journal of human genetics.

D. Page, B. Cullen, H. Bogerd, 2001, Molecular cell.

Is ZFY the sex-determining gene on the human Y chromosome?

D. Page, 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The structure of the Zfx gene on the mouse X chromosome.

D. Page, S. Luoh, 1994, Genomics.

Putative transcription activator with alternative isoforms encoded by human ZFX gene

A. Schneider-Gädicke, P. Beer-Romero, L. Brown, 1989, Nature.

A mitotic SKAP isoform regulates spindle positioning at astral microtubule plus ends

D. Page, I. Cheeseman, P. Nicholls, 2016, The Journal of cell biology.

Molecular evidence of Y-autosomal translocations in owl monkeys.

D. Page, N. Ma, T. S. Harris, 1989, The Journal of heredity.

Steroid sulfatase gene in XX males.

P. Yen, T. Mohandas, L. Shapiro, 1990, American journal of human genetics.

The Ligand Binding Domain of GCNF Is Not Required for Repression of Pluripotency Genes in Mouse Fetal Ovarian Germ Cells

D. Page, Bluma J. Lesch, L. M. Okumura, 2013, PloS one.

The parental origin and mechanism of formation of three dicentric X chromosomes

D. Page, R. Stevenson, C. Schwartz, 1988, Human Genetics.

Clinical Report Velocardiofacial Syndrome in an Unexplained XX Male

L. Brown, D. Page, R. C. Rogers, 2003 .

Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

Jennifer F. Hughes, T. Graves, R. Wilson, 2014, Nature.

Dppa 3 / Pgc 7 / stellais a maternal factor and is not required for germ cell specification in mice Citation

D. Page, M. Goodheart, A. Bortvin, 2004 .

Intergenerational epigenetic inheritance of cancer susceptibility in mammals

D. Page, B. Ebert, R. Bronson, 2019, eLife.

Erratum: Inactivation of the Rps4 gene on the mouse X chromosome (Genomics (1991) 11 (1097-1101))

V. Chapman, P. Beer-Romero, D. Page, 1992 .

The Mysteries of Sexual Identity: The Germ Cell's Perspective

David C Page, D. Page, J. Kimble, 2007, Science.

Turner syndrome: of the missing sex chromosome the case

D. Page, R. Andrew, 1993 .

Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining

D. Page, H. Skaletsky, D. Cleveland, 2016, Nature Cell Biology.

RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis

D. Page, Jieyan Pan, N. Nakatsuji, 2005, Development.

Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection.

S. Rozen, D. Page, H. Skaletsky, 2009, American journal of human genetics.

Isodicentric Y Chromosomes and Sex Disorders as Byproducts of Homologous Recombination that Maintains Palindromes

Julian Lange, L. Brown, D. Page, 2009, Cell.

The Biology and Evolution of Mammalian Y Chromosomes.

Jennifer F. Hughes, D. Page, 2015, Annual review of genetics.

We're off to see the genome

D. Page, P. Reilly, 1998, Nature Genetics.