David C. Page, M.D. - Publications

Affiliations: 
Whitehead Institute (MIT), Cambridge, MA, United States 

217 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 San Roman AK, Skaletsky H, Godfrey AK, Bokil NV, Teitz L, Singh I, Blanton LV, Bellott DW, Pyntikova T, Lange J, Koutseva N, Hughes JF, Brown L, Phou S, Buscetta A, ... ... Page DC, et al. The human Y and inactive X chromosomes similarly modulate autosomal gene expression. Cell Genomics. 100462. PMID 38190107 DOI: 10.1016/j.xgen.2023.100462  0.403
2023 San Roman AK, Skaletsky H, Godfrey AK, Bokil NV, Teitz L, Singh I, Blanton LV, Bellott DW, Pyntikova T, Lange J, Koutseva N, Hughes JF, Brown L, Phou S, Buscetta A, ... ... Page DC, et al. The human Y and inactive X chromosomes similarly modulate autosomal gene expression. Biorxiv : the Preprint Server For Biology. PMID 37333288 DOI: 10.1101/2023.06.05.543763  0.403
2023 San Roman AK, Godfrey AK, Skaletsky H, Bellott DW, Groff AF, Harris HL, Blanton LV, Hughes JF, Brown L, Phou S, Buscetta A, Kruszka P, Banks N, Dutra A, Pak E, ... ... Page DC, et al. The human inactive X chromosome modulates expression of the active X chromosome. Cell Genomics. 3: 100259. PMID 36819663 DOI: 10.1016/j.xgen.2023.100259  0.366
2022 Hughes JF, Skaletsky H, Nicholls PK, Drake A, Pyntikova T, Cho TJ, Bellott DW, Page DC. A gene deriving from the ancestral sex chromosomes was lost from the X and retained on the Y chromosome in eutherian mammals. Bmc Biology. 20: 133. PMID 35676717 DOI: 10.1186/s12915-022-01338-8  0.37
2021 Jackson EK, Bellott DW, Skaletsky H, Page DC. GC-biased gene conversion in X-chromosome palindromes conserved in human, chimpanzee, and rhesus macaque. G3 (Bethesda, Md.). 11. PMID 34849781 DOI: 10.1093/g3journal/jkab224  0.344
2021 Jackson EK, Bellott DW, Cho TJ, Skaletsky H, Hughes JF, Pyntikova T, Page DC. Large palindromes on the primate X Chromosome are preserved by natural selection. Genome Research. PMID 34290043 DOI: 10.1101/gr.275188.120  0.362
2021 Bellott DW, Page DC. Dosage-sensitive functions in embryonic development drove the survival of genes on sex-specific chromosomes in snakes, birds, and mammals. Genome Research. PMID 33479023 DOI: 10.1101/gr.268516.120  0.361
2020 Hughes JF, Skaletsky H, Pyntikova T, Koutseva N, Raudsepp T, Brown LG, Bellott DW, Cho TJ, Dugan-Rocha S, Khan Z, Kremitzki C, Fronick C, Graves-Lindsay TA, Fulton L, Warren WC, ... ... Page DC, et al. Sequence analysis in reveals pervasiveness of X-Y arms races in mammalian lineages. Genome Research. PMID 33208454 DOI: 10.1101/gr.269902.120  0.372
2020 Mikedis MM, Fan Y, Nicholls PK, Endo T, Jackson EK, Cobb SA, de Rooij DG, Page DC. DAZL mediates a broad translational program regulating expansion and differentiation of spermatogonial progenitors. Elife. 9. PMID 32686646 DOI: 10.7554/Elife.56523  0.313
2020 Godfrey AK, Naqvi S, Chmatal L, Chick JM, Mitchell RN, Gygi SP, Skaletsky H, Page DC. Quantitative analysis of Y-Chromosome gene expression across 36 human tissues. Genome Research. PMID 32461223 DOI: 10.1101/Gr.261248.120  0.475
2020 Gura MA, Mikedis MM, Seymour KA, de Rooij DG, Page DC, Freiman RN. Dynamic and regulated TAF gene expression during mouse embryonic germ cell development. Plos Genetics. 16: e1008515. PMID 31914128 DOI: 10.1371/Journal.Pgen.1008515  0.373
2019 Dokshin GA, Davis GM, Sawle AD, Eldridge MD, Nicholls PK, Gourley TE, Romer KA, Molesworth LW, Tatnell HR, Ozturk AR, de Rooij DG, Hannon GJ, Page DC, Mello CC, Carmell MA. GCNA Interacts with Spartan and Topoisomerase II to Regulate Genome Stability. Developmental Cell. PMID 31839538 DOI: 10.1016/J.Devcel.2019.11.006  0.781
2019 Nicholls PK, Schorle H, Naqvi S, Hu YC, Fan Y, Carmell MA, Dobrinski I, Watson AL, Carlson DF, Fahrenkrug SC, Page DC. Mammalian germ cells are determined after PGC colonization of the nascent gonad. Proceedings of the National Academy of Sciences of the United States of America. PMID 31754036 DOI: 10.1073/Pnas.1910733116  0.403
2019 Naqvi S, Godfrey AK, Hughes JF, Goodheart ML, Mitchell RN, Page DC. Conservation, acquisition, and functional impact of sex-biased gene expression in mammals. Science (New York, N.Y.). 365. PMID 31320509 DOI: 10.1126/Science.Aaw7317  0.37
2019 Lesch BJ, Tothova Z, Morgan EA, Liao Z, Bronson RT, Ebert BL, Page DC. Intergenerational epigenetic inheritance of cancer susceptibility in mammals. Elife. 8. PMID 30963999 DOI: 10.7554/Elife.39380  0.318
2019 Nicholls PK, Bellott DW, Cho TJ, Pyntikova T, Page DC. Locating and Characterizing a Transgene Integration Site by Nanopore Sequencing. G3 (Bethesda, Md.). PMID 30837263 DOI: 10.1534/G3.119.300582  0.344
2019 Ly P, Brunner SF, Shoshani O, Kim DH, Lan W, Pyntikova T, Flanagan AM, Behjati S, Page DC, Campbell PJ, Cleveland DW. Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements. Nature Genetics. PMID 30833795 DOI: 10.1038/S41588-019-0360-8  0.446
2019 Kojima ML, de Rooij DG, Page DC. Amplification of a broad transcriptional program by a common factor triggers the meiotic cell cycle in mice. Elife. 8. PMID 30810530 DOI: 10.7554/Elife.43738  0.39
2019 San Roman AK, Page DC. A strategic research alliance: Turner syndrome and sex differences. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 30790449 DOI: 10.1002/Ajmg.C.31677  0.457
2019 Nicholls P, Schorle H, Naqvi S, Hu Y, Yuting F, Carmell M, Dobrinski I, Watson A, Carlson D, Fahrenkrug S, Page D. Germ cell commitment occurs after PGC colonization of the gonad in mammals European Urology Supplements. 18: 11-12. DOI: 10.1016/S1569-9056(19)32485-6  0.325
2018 Romer KA, de Rooij DG, Kojima ML, Page DC. Corrigendum to "Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting" [Dev. Biol. 443 (2018) 19-34]. Developmental Biology. PMID 30416000 DOI: 10.1016/J.Ydbio.2018.10.021  0.328
2018 Romer KA, de Rooij DG, Kojima ML, Page DC. Isolating mitotic and meiotic germ cells from male mice by developmental synchronization, staging, and sorting. Developmental Biology. PMID 30149006 DOI: 10.1016/J.Ydbio.2018.08.009  0.349
2018 Teitz LS, Pyntikova T, Skaletsky H, Page DC. Selection Has Countered High Mutability to Preserve the Ancestral Copy Number of Y Chromosome Amplicons in Diverse Human Lineages. American Journal of Human Genetics. 103: 261-275. PMID 30075113 DOI: 10.1016/J.Ajhg.2018.07.007  0.44
2018 Bellott DW, Cho TJ, Hughes JF, Skaletsky H, Page DC. Cost-effective high-throughput single-haplotype iterative mapping and sequencing for complex genomic structures. Nature Protocols. 13: 787-809. PMID 29565902 DOI: 10.1038/Nprot.2018.019  0.308
2018 Naqvi S, Bellott DW, Lin KS, Page DC. Conserved microRNA targeting reveals preexisting gene dosage sensitivities that shaped amniote sex chromosome evolution. Genome Research. PMID 29449410 DOI: 10.1101/Gr.230433.117  0.453
2017 Soh YQ, Mikedis MM, Kojima M, Godfrey AK, de Rooij DG, Page DC. Meioc maintains an extended meiotic prophase I in mice. Plos Genetics. 13: e1006704. PMID 28380054 DOI: 10.1371/Journal.Pgen.1006704  0.464
2017 Bellott DW, Skaletsky H, Cho TJ, Brown L, Locke D, Chen N, Galkina S, Pyntikova T, Koutseva N, Graves T, Kremitzki C, Warren WC, Clark AG, Gaginskaya E, Wilson RK, ... Page DC, et al. Avian W and mammalian Y chromosomes convergently retained dosage-sensitive regulators. Nature Genetics. PMID 28135246 DOI: 10.1038/Ng.3778  0.497
2016 Ly P, Teitz LS, Kim DH, Shoshani O, Skaletsky H, Fachinetti D, Page DC, Cleveland DW. Selective Y centromere inactivation triggers chromosome shattering in micronuclei and repair by non-homologous end joining. Nature Cell Biology. PMID 27918550 DOI: 10.1038/ncb3450  0.47
2016 Carmell MA, Dokshin GA, Skaletsky H, Hu YC, von Wolfswinkel JC, Igarashi KJ, Bellott DW, Nefedov M, Reddien PW, Enders GC, Uversky VN, Mello CC, Page DC. A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes. Elife. 5. PMID 27718356 DOI: 10.7554/Elife.19993  0.787
2016 Lesch BJ, Silber SJ, McCarrey JR, Page DC. Parallel evolution of male germline epigenetic poising and somatic development in animals. Nature Genetics. PMID 27294618 DOI: 10.1038/Ng.3591  0.371
2016 Hughes JF, Page DC. The history of the Y chromosome in man. Nature Genetics. 48: 588-9. PMID 27230683 DOI: 10.1038/Ng.3580  0.403
2016 Kern DM, Nicholls PK, Page DC, Cheeseman IM. A mitotic SKAP isoform regulates spindle positioning at astral microtubule plus ends. The Journal of Cell Biology. PMID 27138257 DOI: 10.1083/Jcb.201510117  0.375
2016 Carmell MA, Dokshin GA, Skaletsky H, Hu Y, Wolfswinkel JCv, Igarashi KJ, Bellott DW, Nefedov M, Reddien PW, Enders GC, Uversky VN, Mello CC, Page DC. Author response: A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes Elife. DOI: 10.7554/Elife.19993.029  0.76
2015 Hughes JF, Page DC. The Biology and Evolution of Mammalian Y Chromosomes. Annual Review of Genetics. PMID 26442847 DOI: 10.1146/Annurev-Genet-112414-055311  0.47
2015 Soh YQ, Junker JP, Gill ME, Mueller JL, van Oudenaarden A, Page DC. A Gene Regulatory Program for Meiotic Prophase in the Fetal Ovary. Plos Genetics. 11: e1005531. PMID 26378784 DOI: 10.1371/Journal.Pgen.1005531  0.415
2015 Yang F, Silber S, Leu NA, Oates RD, Marszalek JD, Skaletsky H, Brown LG, Rozen S, Page DC, Wang PJ. TEX11 is mutated in infertile men with azoospermia and regulates genome-wide recombination rates in mouse. Embo Molecular Medicine. PMID 26136358 DOI: 10.15252/Emmm.201404967  0.365
2015 Hughes JF, Skaletsky H, Koutseva N, Pyntikova T, Page DC. Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals. Genome Biology. 16: 104. PMID 26017895 DOI: 10.1186/S13059-015-0667-4  0.48
2015 Endo T, Romer KA, Anderson EL, Baltus AE, de Rooij DG, Page DC. Periodic retinoic acid-STRA8 signaling intersects with periodic germ-cell competencies to regulate spermatogenesis. Proceedings of the National Academy of Sciences of the United States of America. 112: E2347-56. PMID 25902548 DOI: 10.1073/Pnas.1505683112  0.318
2015 Hu YC, Nicholls PK, Soh YQ, Daniele JR, Junker JP, van Oudenaarden A, Page DC. Licensing of primordial germ cells for gametogenesis depends on genital ridge signaling. Plos Genetics. 11: e1005019. PMID 25739037 DOI: 10.1371/Journal.Pgen.1005019  0.368
2014 Soh YQ, Alföldi J, Pyntikova T, Brown LG, Graves T, Minx PJ, Fulton RS, Kremitzki C, Koutseva N, Mueller JL, Rozen S, Hughes JF, Owens E, Womack JE, Murphy WJ, ... ... Page DC, et al. Sequencing the mouse Y chromosome reveals convergent gene acquisition and amplification on both sex chromosomes. Cell. 159: 800-13. PMID 25417157 DOI: 10.1016/J.Cell.2014.09.052  0.501
2014 Yesilaltay A, Dokshin GA, Busso D, Wang L, Galiani D, Chavarria T, Vasile E, Quilaqueo L, Orellana JA, Walzer D, Shalgi R, Dekel N, Albertini DF, Rigotti A, Page DC, et al. Excess cholesterol induces mouse egg activation and may cause female infertility. Proceedings of the National Academy of Sciences of the United States of America. 111: E4972-80. PMID 25368174 DOI: 10.1073/Pnas.1418954111  0.761
2014 Lesch BJ, Page DC. Poised chromatin in the mammalian germ line. Development (Cambridge, England). 141: 3619-26. PMID 25249456 DOI: 10.1242/Dev.113027  0.362
2014 Koubova J, Hu YC, Bhattacharyya T, Soh YQ, Gill ME, Goodheart ML, Hogarth CA, Griswold MD, Page DC. Retinoic acid activates two pathways required for meiosis in mice. Plos Genetics. 10: e1004541. PMID 25102060 DOI: 10.1371/Journal.Pgen.1004541  0.335
2014 Alpatov R, Lesch BJ, Nakamoto-Kinoshita M, Blanco A, Chen S, Stützer A, Armache KJ, Simon MD, Xu C, Ali M, Murn J, Prisic S, Kutateladze TG, Vakoc CR, Min J, ... ... Page DC, et al. A chromatin-dependent role of the fragile X mental retardation protein FMRP in the DNA damage response. Cell. 157: 869-81. PMID 24813610 DOI: 10.1016/J.Cell.2014.03.040  0.373
2014 Bellott DW, Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Cho TJ, Koutseva N, Zaghlul S, Graves T, Rock S, Kremitzki C, Fulton RS, Dugan S, Ding Y, Morton D, ... ... Page DC, et al. Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators. Nature. 508: 494-9. PMID 24759411 DOI: 10.1038/Nature13206  0.495
2014 Bellott DW, Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Cho T, Koutseva N, Zaghlul S, Graves T, Rock S, Kremitzki C, Fulton RS, Dugan S, Ding Y, Morton D, ... ... Page DC, et al. Erratum: Corrigendum: Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators Nature. 514: 126-126. DOI: 10.1038/Nature13719  0.334
2013 Hughes JF, Skaletsky H, Bellott DW, Chowdhary BP, Warren WC, Worley KC, Wilson RK, Gibbs RA, Page DC. No bull: upholding community standards in public sharing of biological datasets. Proceedings of the National Academy of Sciences of the United States of America. 110: E4277. PMID 24173037 DOI: 10.1073/Pnas.1315122110  0.332
2013 Lesch BJ, Dokshin GA, Young RA, McCarrey JR, Page DC. A set of genes critical to development is epigenetically poised in mouse germ cells from fetal stages through completion of meiosis. Proceedings of the National Academy of Sciences of the United States of America. 110: 16061-6. PMID 24043772 DOI: 10.1073/Pnas.1315204110  0.793
2013 Hu YC, Okumura LM, Page DC. Gata4 is required for formation of the genital ridge in mice. Plos Genetics. 9: e1003629. PMID 23874227 DOI: 10.1371/Journal.Pgen.1003629  0.355
2013 Mueller JL, Skaletsky H, Brown LG, Zaghlul S, Rock S, Graves T, Auger K, Warren WC, Wilson RK, Page DC. Independent specialization of the human and mouse X chromosomes for the male germ line. Nature Genetics. 45: 1083-7. PMID 23872635 DOI: 10.1038/Ng.2705  0.47
2013 Hu YC, de Rooij DG, Page DC. Tumor suppressor gene Rb is required for self-renewal of spermatogonial stem cells in mice. Proceedings of the National Academy of Sciences of the United States of America. 110: 12685-90. PMID 23858447 DOI: 10.1073/Pnas.1311548110  0.356
2013 Dokshin GA, Baltus AE, Eppig JJ, Page DC. Oocyte differentiation is genetically dissociable from meiosis in mice. Nature Genetics. 45: 877-83. PMID 23770609 DOI: 10.1038/Ng.2672  0.804
2013 Okumura LM, Lesch BJ, Page DC. The ligand binding domain of GCNF is not required for repression of pluripotency genes in mouse fetal ovarian germ cells. Plos One. 8: e66062. PMID 23762465 DOI: 10.1371/Journal.Pone.0066062  0.375
2013 Wang H, Hu YC, Markoulaki S, Welstead GG, Cheng AW, Shivalila CS, Pyntikova T, Dadon DB, Voytas DF, Bogdanove AJ, Page DC, Jaenisch R. TALEN-mediated editing of the mouse Y chromosome. Nature Biotechnology. 31: 530-2. PMID 23666012 DOI: 10.1038/Nbt.2595  0.478
2013 Lange J, Noordam MJ, van Daalen SK, Skaletsky H, Clark BA, Macville MV, Page DC, Repping S. Intrachromosomal homologous recombination between inverted amplicons on opposing Y-chromosome arms. Genomics. 102: 257-64. PMID 23643616 DOI: 10.1016/J.Ygeno.2013.04.018  0.452
2013 Lesch BJ, Page DC. Sex-specific chromatin states in mammalian fetal germ cells Epigenetics & Chromatin. 6. DOI: 10.1186/1756-8935-6-S1-P45  0.369
2013 Banks N, Brown L, Hughes J, Solomon B, Muenke M, Page D. Phenotypic diversity amongst patients with an isodicentric y chromosome Fertility and Sterility. 100: S445. DOI: 10.1016/J.Fertnstert.2013.07.575  0.413
2012 Rozen SG, Marszalek JD, Irenze K, Skaletsky H, Brown LG, Oates RD, Silber SJ, Ardlie K, Page DC. AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes. American Journal of Human Genetics. 91: 890-6. PMID 23103232 DOI: 10.1016/J.Ajhg.2012.09.003  0.302
2012 Hughes JF, Skaletsky H, Page DC. Sequencing of rhesus macaque Y chromosome clarifies origins and evolution of the DAZ (Deleted in AZoospermia) genes. Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology. 34: 1035-44. PMID 23055411 DOI: 10.1002/Bies.201200066  0.479
2012 Lesch BJ, Page DC. Genetics of germ cell development. Nature Reviews. Genetics. 13: 781-94. PMID 23044825 DOI: 10.1038/Nrg3294  0.343
2012 Buganim Y, Itskovich E, Hu YC, Cheng AW, Ganz K, Sarkar S, Fu D, Welstead GG, Page DC, Jaenisch R. Direct reprogramming of fibroblasts into embryonic Sertoli-like cells by defined factors. Cell Stem Cell. 11: 373-86. PMID 22958931 DOI: 10.1016/J.Stem.2012.07.019  0.35
2012 Chen N, Bellott DW, Page DC, Clark AG. Identification of avian W-linked contigs by short-read sequencing. Bmc Genomics. 13: 183. PMID 22583744 DOI: 10.1186/1471-2164-13-183  0.421
2012 Heaney JD, Anderson EL, Michelson MV, Zechel JL, Conrad PA, Page DC, Nadeau JH. Germ cell pluripotency, premature differentiation and susceptibility to testicular teratomas in mice. Development (Cambridge, England). 139: 1577-86. PMID 22438569 DOI: 10.1242/Dev.076851  0.383
2012 Hughes JF, Skaletsky H, Brown LG, Pyntikova T, Graves T, Fulton RS, Dugan S, Ding Y, Buhay CJ, Kremitzki C, Wang Q, Shen H, Holder M, Villasana D, Nazareth LV, ... Page DC, et al. Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes. Nature. 483: 82-6. PMID 22367542 DOI: 10.1038/Nature10843  0.428
2011 Dawlaty MM, Ganz K, Powell BE, Hu YC, Markoulaki S, Cheng AW, Gao Q, Kim J, Choi SW, Page DC, Jaenisch R. Tet1 is dispensable for maintaining pluripotency and its loss is compatible with embryonic and postnatal development. Cell Stem Cell. 9: 166-75. PMID 21816367 DOI: 10.1016/J.Stem.2011.07.010  0.326
2011 Gill ME, Hu YC, Lin Y, Page DC. Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells. Proceedings of the National Academy of Sciences of the United States of America. 108: 7443-8. PMID 21504946 DOI: 10.1073/Pnas.1104501108  0.387
2010 Bellott DW, Skaletsky H, Pyntikova T, Mardis ER, Graves T, Kremitzki C, Brown LG, Rozen S, Warren WC, Wilson RK, Page DC. Convergent evolution of chicken Z and human X chromosomes by expansion and gene acquisition. Nature. 466: 612-6. PMID 20622855 DOI: 10.1038/Nature09172  0.496
2010 Hughes JF, Skaletsky H, Pyntikova T, Graves TA, van Daalen SK, Minx PJ, Fulton RS, McGrath SD, Locke DP, Friedman C, Trask BJ, Mardis ER, Warren WC, Repping S, Rozen S, ... Page DC, et al. Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content. Nature. 463: 536-9. PMID 20072128 DOI: 10.1038/Nature08700  0.492
2010 Page DC, Hughes JF, Bellott DW, Mueller JL, Gill ME, Larracuente A, Graves T, Muzny D, Warren WC, Gibbs RA, Wilson RK, Skaletsky H. Reconstructing sex chromosome evolution Genome Biology. 11. DOI: 10.1186/Gb-2010-11-S1-I21  0.48
2009 Bellott DW, Page DC. Reconstructing the evolution of vertebrate sex chromosomes. Cold Spring Harbor Symposia On Quantitative Biology. 74: 345-53. PMID 20508063 DOI: 10.1101/Sqb.2009.74.048  0.479
2009 Rozen S, Marszalek JD, Alagappan RK, Skaletsky H, Page DC. Remarkably little variation in proteins encoded by the Y chromosome's single-copy genes, implying effective purifying selection. American Journal of Human Genetics. 85: 923-8. PMID 20004767 DOI: 10.1016/J.Ajhg.2009.11.011  0.467
2009 Lange J, Skaletsky H, van Daalen SK, Embry SL, Korver CM, Brown LG, Oates RD, Silber S, Repping S, Page DC. Isodicentric Y chromosomes and sex disorders as byproducts of homologous recombination that maintains palindromes. Cell. 138: 855-69. PMID 19737515 DOI: 10.1016/J.Cell.2009.07.042  0.474
2008 Lin Y, Gill ME, Koubova J, Page DC. Germ cell-intrinsic and -extrinsic factors govern meiotic initiation in mouse embryos. Science (New York, N.Y.). 322: 1685-7. PMID 19074348 DOI: 10.1126/Science.1166340  0.339
2008 Anderson EL, Baltus AE, Roepers-Gajadien HL, Hassold TJ, de Rooij DG, van Pelt AM, Page DC. Stra8 and its inducer, retinoic acid, regulate meiotic initiation in both spermatogenesis and oogenesis in mice. Proceedings of the National Academy of Sciences of the United States of America. 105: 14976-80. PMID 18799751 DOI: 10.1073/Pnas.0807297105  0.449
2008 Mueller JL, Mahadevaiah SK, Park PJ, Warburton PE, Page DC, Turner JM. The mouse X chromosome is enriched for multicopy testis genes showing postmeiotic expression. Nature Genetics. 40: 794-9. PMID 18454149 DOI: 10.1038/Ng.126  0.465
2008 Yang F, Gell K, van der Heijden GW, Eckardt S, Leu NA, Page DC, Benavente R, Her C, Höög C, McLaughlin KJ, Wang PJ. Meiotic failure in male mice lacking an X-linked factor. Genes & Development. 22: 682-91. PMID 18316482 DOI: 10.1101/Gad.1613608  0.484
2008 Lange J, Skaletsky H, Bell GW, Page DC. MSY Breakpoint Mapper, a database of sequence-tagged sites useful in defining naturally occurring deletions in the human Y chromosome. Nucleic Acids Research. 36: D809-14. PMID 17965095 DOI: 10.1093/Nar/Gkm849  0.477
2007 Kimble J, Page DC. The mysteries of sexual identity. The germ cell's perspective. Science (New York, N.Y.). 316: 400-1. PMID 17446389 DOI: 10.1126/Science.1142109  0.34
2007 Cheng Y, Buffone MG, Kouadio M, Goodheart M, Page DC, Gerton GL, Davidson I, Wang PJ. Abnormal sperm in mice lacking the Taf7l gene. Molecular and Cellular Biology. 27: 2582-9. PMID 17242199 DOI: 10.1128/Mcb.01722-06  0.433
2006 Baltus AE, Menke DB, Hu YC, Goodheart ML, Carpenter AE, de Rooij DG, Page DC. In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication. Nature Genetics. 38: 1430-4. PMID 17115059 DOI: 10.1038/Ng1919  0.731
2006 Hughes JF, Skaletsky H, Rozen S, Wilson RK, Page DC. Has the chimpanzee Y chromosome been sequenced? Nature Genetics. 38: 853-4; author reply . PMID 16874316 DOI: 10.1038/Ng0806-853B  0.417
2006 Repping S, van Daalen SK, Brown LG, Korver CM, Lange J, Marszalek JD, Pyntikova T, van der Veen F, Skaletsky H, Page DC, Rozen S. High mutation rates have driven extensive structural polymorphism among human Y chromosomes. Nature Genetics. 38: 463-7. PMID 16501575 DOI: 10.1038/Ng1754  0.405
2006 Koubova J, Menke DB, Zhou Q, Capel B, Griswold MD, Page DC. Retinoic acid regulates sex-specific timing of meiotic initiation in mice. Proceedings of the National Academy of Sciences of the United States of America. 103: 2474-9. PMID 16461896 DOI: 10.1073/Pnas.0510813103  0.694
2006 Hughes JF, Skaletsky H, Pyntikova T, Minx PJ, Graves T, Rozen S, Wilson RK, Page DC. Erratum: Corrigendum: Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee Nature. 441: 248-248. DOI: 10.1038/Nature04776  0.348
2005 Lin Y, Page DC. Dazl deficiency leads to embryonic arrest of germ cell development in XY C57BL/6 mice. Developmental Biology. 288: 309-16. PMID 16310179 DOI: 10.1016/J.Ydbio.2005.06.032  0.353
2005 Hughes JF, Skaletsky H, Pyntikova T, Minx PJ, Graves T, Rozen S, Wilson RK, Page DC. Conservation of Y-linked genes during human evolution revealed by comparative sequencing in chimpanzee. Nature. 437: 100-3. PMID 16136134 DOI: 10.1038/Nature04101  0.444
2005 Wang PJ, Page DC, McCarrey JR. Differential expression of sex-linked and autosomal germ-cell-specific genes during spermatogenesis in the mouse. Human Molecular Genetics. 14: 2911-8. PMID 16118233 DOI: 10.1093/Hmg/Ddi322  0.455
2005 Pan J, Goodheart M, Chuma S, Nakatsuji N, Page DC, Wang PJ. RNF17, a component of the mammalian germ cell nuage, is essential for spermiogenesis. Development (Cambridge, England). 132: 4029-39. PMID 16093322 DOI: 10.1242/Dev.02003  0.383
2004 Repping S, Korver CM, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Are sequence family variants useful for identifying deletions in the human Y chromosome? American Journal of Human Genetics. 75: 514-7; author reply . PMID 15284951 DOI: 10.1086/423394  0.363
2004 Bradley J, Baltus A, Skaletsky H, Royce-Tolland M, Dewar K, Page DC. An X-to-autosome retrogene is required for spermatogenesis in mice. Nature Genetics. 36: 872-6. PMID 15258580 DOI: 10.1038/Ng1390  0.465
2004 Repping S, van Daalen SK, Korver CM, Brown LG, Marszalek JD, Gianotten J, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. A family of human Y chromosomes has dispersed throughout northern Eurasia despite a 1.8-Mb deletion in the azoospermia factor c region. Genomics. 83: 1046-52. PMID 15177557 DOI: 10.1016/J.Ygeno.2003.12.018  0.425
2004 Yao HH, Matzuk MM, Jorgez CJ, Menke DB, Page DC, Swain A, Capel B. Follistatin operates downstream of Wnt4 in mammalian ovary organogenesis. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 230: 210-5. PMID 15162500 DOI: 10.1002/Dvdy.20042  0.687
2004 Natoli TA, Alberta JA, Bortvin A, Taglienti ME, Menke DB, Loring J, Jaenisch R, Page DC, Housman DE, Kreidberg JA. Wt1 functions in the development of germ cells in addition to somatic cell lineages of the testis. Developmental Biology. 268: 429-40. PMID 15063178 DOI: 10.1016/J.Ydbio.2003.12.033  0.704
2004 Page DC. 2003 Curt Stern Award address. On low expectation exceeded; or, the genomic salvation of the Y chromosome. American Journal of Human Genetics. 74: 399-402. PMID 15053010 DOI: 10.1086/382659  0.408
2004 Bortvin A, Goodheart M, Liao M, Page DC. Dppa3 / Pgc7 / stella is a maternal factor and is not required for germ cell specification in mice. Bmc Developmental Biology. 4: 2. PMID 15018652 DOI: 10.1186/1471-213X-4-2  0.362
2003 Menke DB, Koubova J, Page DC. Sexual differentiation of germ cells in XX mouse gonads occurs in an anterior-to-posterior wave. Developmental Biology. 262: 303-12. PMID 14550793 DOI: 10.1016/S0012-1606(03)00391-9  0.721
2003 Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nature Genetics. 35: 247-51. PMID 14528305 DOI: 10.1038/Ng1250  0.455
2003 Tomasi PA, Oates R, Brown L, Delitala G, Page DC. The pituitary-testicular axis in Klinefelter's syndrome and in oligo-azoospermic patients with and without deletions of the Y chromosome long arm. Clinical Endocrinology. 59: 214-22. PMID 12864799 DOI: 10.1046/J.1365-2265.2003.01828.X  0.396
2003 Rozen S, Skaletsky H, Marszalek JD, Minx PJ, Cordum HS, Waterston RH, Wilson RK, Page DC. Abundant gene conversion between arms of palindromes in human and ape Y chromosomes. Nature. 423: 873-6. PMID 12815433 DOI: 10.1038/Nature01723  0.462
2003 Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, Cordum HS, Hillier L, Brown LG, Repping S, Pyntikova T, Ali J, Bieri T, Chinwalla A, Delehaunty A, Delehaunty K, Du H, Fewell G, ... ... Page DC, et al. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature. 423: 825-37. PMID 12815422 DOI: 10.1038/Nature01722  0.462
2003 Bortvin A, Eggan K, Skaletsky H, Akutsu H, Berry DL, Yanagimachi R, Page DC, Jaenisch R. Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei. Development (Cambridge, England). 130: 1673-80. PMID 12620990 DOI: 10.1242/Dev.00366  0.388
2003 Phelan MC, Rogers RC, Crawford EC, Brown LG, Page DC. Velocardiofacial syndrome in an unexplained XX male. American Journal of Medical Genetics. Part A. 116: 77-9. PMID 12476456 DOI: 10.1002/Ajmg.A.10833  0.424
2002 Menke DB, Page DC. Sexually dimorphic gene expression in the developing mouse gonad. Gene Expression Patterns : Gep. 2: 359-67. PMID 12617826 DOI: 10.1016/S1567-133X(02)00022-4  0.702
2002 Oates RD, Silber S, Brown LG, Page DC. 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. Human Reproduction (Oxford, England). 17: 2813-24. PMID 12407032 DOI: 10.1093/Humrep/17.11.2813  0.397
2002 Repping S, Skaletsky H, Lange J, Silber S, Van Der Veen F, Oates RD, Page DC, Rozen S. Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure. American Journal of Human Genetics. 71: 906-22. PMID 12297986 DOI: 10.1086/342928  0.429
2002 Wang PJ, Page DC. Functional substitution for TAF(II)250 by a retroposed homolog that is expressed in human spermatogenesis. Human Molecular Genetics. 11: 2341-6. PMID 12217962 DOI: 10.1093/Hmg/11.19.2341  0.443
2002 Lahn BT, Tang ZL, Zhou J, Barndt RJ, Parvinen M, Allis CD, Page DC. Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis. Proceedings of the National Academy of Sciences of the United States of America. 99: 8707-12. PMID 12072557 DOI: 10.1073/Pnas.082248899  0.652
2002 Oates RD, Silber S, Brown L, Page D. 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 Fertility and Sterility. 78: S30. DOI: 10.1016/S0015-0282(02)03460-X  0.361
2001 Jaruzelska J, Korcz A, Wojda A, Jedrzejczak P, Bierla J, Surmacz T, Pawelczyk L, Page DC, Kotecki M. Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion. Journal of Medical Genetics. 38: 798-802. PMID 11732492 DOI: 10.1136/Jmg.38.11.798  0.454
2001 Kuroda-Kawaguchi T, Skaletsky H, Brown LG, Minx PJ, Cordum HS, Waterston RH, Wilson RK, Silber S, Oates R, Rozen S, Page DC. The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nature Genetics. 29: 279-86. PMID 11687796 DOI: 10.1038/Ng757  0.411
2001 Wang PJ, McCarrey JR, Yang F, Page DC. An abundance of X-linked genes expressed in spermatogonia. Nature Genetics. 27: 422-6. PMID 11279525 DOI: 10.1038/86927  0.473
2001 Tilford CA, Kuroda-Kawaguchi T, Skaletsky H, Rozen S, Brown LG, Rosenberg M, McPherson JD, Wylie K, Sekhon M, Kucaba TA, Waterston RH, Page DC. A physical map of the human Y chromosome. Nature. 409: 943-5. PMID 11237016 DOI: 10.1038/35057170  0.441
2001 Silber S, Page D, Brown L, Oates R. Microsurgical distribution of spermatogenesis in the testes of azoospermic and severely oligospermic men with Y chromosomal deletions. Fertility and Sterility. 76: S141. DOI: 10.1016/S0015-0282(01)02414-1  0.383
2001 Silber S, Page D, Brown L, Oates R. ICSI results with and without Y chromosomal deletions in men with severe oligospermia and azoospermia. Fertility and Sterility. 76: S140. DOI: 10.1016/S0015-0282(01)02411-6  0.415
2000 Reijo RA, Dorfman DM, Slee R, Renshaw AA, Loughlin KR, Cooke H, Page DC. DAZ family proteins exist throughout male germ cell development and transit from nucleus to cytoplasm at meiosis in humans and mice. Biology of Reproduction. 63: 1490-6. PMID 11058556 DOI: 10.1095/Biolreprod63.5.1490  0.471
2000 Sun C, Skaletsky H, Rozen S, Gromoll J, Nieschlag E, Oates R, Page DC. Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. Human Molecular Genetics. 9: 2291-6. PMID 11001932 DOI: 10.1093/Oxfordjournals.Hmg.A018920  0.387
2000 Giacalone J, Delobette S, Gibaja V, Ni L, Skiadas Y, Qi R, Edington J, Lai Z, Gebauer D, Zhao H, Anantharaman T, Mishra B, Brown LG, Saxena R, Page DC, et al. Optical mapping of BAC clones from the human Y chromosome DAZ locus. Genome Research. 10: 1421-9. PMID 10984460 DOI: 10.1101/Gr.112100  0.398
2000 Bohossian HB, Skaletsky H, Page DC. Unexpectedly similar rates of nucleotide substitution found in male and female hominids. Nature. 406: 622-5. PMID 10949301 DOI: 10.1038/35020557  0.439
2000 Saxena R, de Vries JW, Repping S, Alagappan RK, Skaletsky H, Brown LG, Ma P, Chen E, Hoovers JM, Page DC. Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome. Genomics. 67: 256-67. PMID 10936047 DOI: 10.1006/Geno.2000.6260  0.448
2000 Warren EH, Gavin MA, Simpson E, Chandler P, Page DC, Disteche C, Stankey KA, Greenberg PD, Riddell SR. The human UTY gene encodes a novel HLA-B8-restricted H-Y antigen. Journal of Immunology (Baltimore, Md. : 1950). 164: 2807-14. PMID 10679124 DOI: 10.4049/Jimmunol.164.5.2807  0.354
2000 Rocchietti-March M, Weinbauer GF, Page DC, Nieschlag E, Gromoll J. Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated. International Journal of Andrology. 23: 51-6. PMID 10632763 DOI: 10.1046/J.1365-2605.2000.00207.X  0.414
2000 Lahn BT, Page DC. A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins. Human Molecular Genetics. 9: 311-9. PMID 10607842 DOI: 10.1093/Hmg/9.2.311  0.693
2000 Silber SJ, Brown L, Page DC. ICSI Offspring of Y-Deleted Men Fertility and Sterility. 74. DOI: 10.1016/S0015-0282(00)00842-6  0.324
1999 Sun C, Skaletsky H, Birren B, Devon K, Tang Z, Silber S, Oates R, Page DC. An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y. Nature Genetics. 23: 429-32. PMID 10581029 DOI: 10.1038/70539  0.415
1999 Lahn BT, Page DC. Four evolutionary strata on the human X chromosome. Science (New York, N.Y.). 286: 964-7. PMID 10542153 DOI: 10.1126/Science.286.5441.964  0.698
1999 Gromoll J, Weinbauer GF, Skaletsky H, Schlatt S, Rocchietti-March M, Page DC, Nieschlag E. The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome. Human Molecular Genetics. 8: 2017-24. PMID 10484770 DOI: 10.1093/Hmg/8.11.2017  0.426
1999 Page DC, Silber S, Brown LG. Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility. Human Reproduction (Oxford, England). 14: 1722-6. PMID 10402375 DOI: 10.1093/Humrep/14.7.1722  0.42
1999 Raymond CS, Parker ED, Kettlewell JR, Brown LG, Page DC, Kusz K, Jaruzelska J, Reinberg Y, Flejter WL, Bardwell VJ, Hirsch B, Zarkower D. A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. Human Molecular Genetics. 8: 989-96. PMID 10332030 DOI: 10.1093/Hmg/8.6.989  0.412
1999 Lahn BT, Page DC. Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome. Nature Genetics. 21: 429-33. PMID 10192397 DOI: 10.1038/7771  0.71
1999 Silber S, Alagappan R, Brown L, Page D. R-054. Y Chromosome deletions and the feasibility of ICSI Human Reproduction. 14: 303-303. DOI: 10.1093/Humrep/14.Suppl_3.303  0.376
1999 Silber S, Alagappan R, Brown L, Page D. P-064. Testicular histology of men with non-obstructive azoospermia or severe oligospermia caused by Y chromosomal deletions Human Reproduction. 14: 173-173. DOI: 10.1093/Humrep/14.Suppl_3.173  0.381
1998 Silber SJ, Alagappan R, Brown LG, Page DC. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Human Reproduction (Oxford, England). 13: 3332-7. PMID 9886509 DOI: 10.1093/Humrep/13.12.3332  0.438
1998 Jegalian K, Page DC. A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated Nature. 394: 776-780. PMID 9723615 DOI: 10.1038/29522  0.427
1998 Seligman J, Page DC. The Dazh gene is expressed in male and female embryonic gonads before germ cell sex differentiation Biochemical and Biophysical Research Communications. 245: 878-882. PMID 9588208 DOI: 10.1006/Bbrc.1998.8530  0.434
1998 Kenmochi N, Kawaguchi T, Rozen S, Davis E, Goodman N, Hudson TJ, Tanaka T, Page DC. A map of 75 human ribosomal protein genes Genome Research. 8: 509-523. PMID 9582194 DOI: 10.1101/Gr.8.5.509  0.439
1998 Schwartz A, Chan DC, Brown LG, Alagappan R, Pettay D, Disteche C, McGillivray B, De La Chapelle A, Page DC. Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination Human Molecular Genetics. 7: 1-11. PMID 9384598 DOI: 10.1093/Hmg/7.1.1  0.455
1998 Mulhall JP, Reijo R, Alagappan R, Brown L, Page D, Carson R, Oates RD. 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 The Journal of Urology. 159: 609-609. DOI: 10.1016/S0022-5347(01)63891-6  0.317
1997 Lahn BT, Page DC. Functional coherence of the human Y chromosome. Science (New York, N.Y.). 278: 675-80. PMID 9381176 DOI: 10.1126/SCIENCE.278.5338.675  0.702
1997 Schiebel K, Winkelmann M, Mertz A, Xu X, Page DC, Weil D, Petit C, Rappold GA. 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 Human Molecular Genetics. 6: 1985-1989. PMID 9302280 DOI: 10.1093/Hmg/6.11.1985  0.464
1997 Mulhall JP, Reijo R, Alagappan R, Brown L, Page D, Carson R, Oates RD. 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. Human Reproduction (Oxford, England). 12: 503-8. PMID 9130751 DOI: 10.1093/Humrep/12.3.503  0.375
1997 Mahaffey CL, Bayleran JK, Yeh GY, Lee TC, Page DC, Simpson EM. Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family Genomics. 41: 123-127. PMID 9126493 DOI: 10.1006/Geno.1997.4611  0.366
1997 Silber S, Alagappan R, Brown L, Page D. O-015. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing testicular sperm extraction and ICSI Human Reproduction. 12: 7-7. DOI: 10.1093/Humrep/12.Suppl_2.7  0.369
1997 Silber S, Alagappan R, Brown L, Page D. O-014 Y chromosomal deletions in azoospermic and oligospermic men undergoing ICSI Fertility and Sterility. 68: S8. DOI: 10.1016/S0015-0282(97)90647-6  0.375
1996 Saxena R, Brown LG, Hawkins T, Alagappan RK, Skaletsky H, Reeve MP, Reijo R, Rozen S, Dinulos MB, Disteche CM, Page DC. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned Nature Genetics. 14: 292-299. PMID 8896558 DOI: 10.1038/Ng1196-292  0.482
1996 Schuler GD, Boguski MS, Stewart EA, Stein LD, Gyapay G, Rice K, White RE, Rodriguez-Tomé P, Aggarwal A, Bajorek E, Bentolila S, Birren BB, Butler A, Castle AB, Chiannilkulchai N, ... ... Page DC, et al. A gene map of the human genome. Science (New York, N.Y.). 274: 540-6. PMID 8849440 DOI: 10.1126/Science.274.5287.540  0.372
1996 Eicher EM, Washburn LL, Schork NJ, Lee BK, Shown EP, Xu X, Dredge RD, Pringle MJ, Page DC. Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal. Nature Genetics. 14: 206-9. PMID 8841197 DOI: 10.1038/Ng1096-206  0.477
1996 Reijo R, Seligman J, Dinulos MB, Jaffe T, Brown LG, Disteche CM, Page DC. Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty Genomics. 35: 346-352. PMID 8661148 DOI: 10.1006/Geno.1996.0366  0.479
1996 Reijo R, Alagappan RK, Patrizio P, Page DC. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome Lancet. 347: 1290-1293. PMID 8622504 DOI: 10.1016/S0140-6736(96)90938-1  0.44
1996 Dietrich WF, Miller J, Steen R, Merchant MA, Damron-Boles D, Husain Z, Dredge R, Daly MJ, Ingalls KA, O'Connor TJ, Evans CA, DeAngelis MM, Levinson DM, Kruglyak L, Goodman N, ... ... Page DC, et al. A comprehensive genetic map of the mouse genome Nature. 380: 149-152. PMID 8600386 DOI: 10.1038/380149A0  0.304
1996 Ried K, Mertz A, Nagaraja R, Trusgnich M, Riley JH, Anand R, Lehrach H, Page D, Ellison JW, Rappold G. Characterization of a YAC contig spanning the pseudoautosomal region. Genomics. 29: 787-92. PMID 8575778 DOI: 10.1006/Geno.1995.9933  0.375
1996 Reijo R, Lee TY, Salo P, Alagappan R, Brown LG, Rosenberg M, Rozen S, Jaffe T, Straus D, Hovatta O, De la Chapelle A, Silber S, Page DC, Edwards, Simpson. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene Human Reproduction. 11: 27-54. DOI: 10.1093/Humrep/11.Suppl_4.27  0.461
1995 Callen DF, Lane SA, Kozman H, Kremmidiotis G, Whitmore SA, Lowenstein M, Doggett NA, Kenmochi N, Page DC, Maglott DR, Nierman WC, Murakawa K, Berry R, Sikela JM, Houlgatte R, et al. Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: Demonstration of a 'hot spot' for recombination at 16p12 Genomics. 29: 503-511. PMID 8666401 DOI: 10.1006/Geno.1995.9005  0.415
1995 LUOH SW, JEGALIAN K, LEE A, CHEN EY, RIDLEY A, PAGE DC. CpG Islands in HumanZFXandZFYand MouseZfxGenes: Sequence Similarities and Methylation Differences Genomics. 29: 353-363. PMID 8666382 DOI: 10.1006/Geno.1995.9994  0.408
1995 Salo P, Kaariainen H, Petrovic V, Peltomaki P, Page DC, De la Chapelle A. Molecular mapping of the putative gonadoblastoma locus on the Y chromosome Genes Chromosomes and Cancer. 14: 210-214. PMID 8589038 DOI: 10.1002/Gcc.2870140309  0.453
1995 Tsuchiya K, Reijo R, Page DC, Disteche CM. Gonadoblastoma: Molecular definition of the susceptibility region on the Y chromosome American Journal of Human Genetics. 57: 1400-1407. PMID 8533770  0.374
1995 Hudson TJ, Stein LD, Gerety SS, Ma J, Castle AB, Silva J, Slonim DK, Baptista R, Kruglyak L, Xu SH, Hu X, Colbert AM, Rosenberg C, Reeve-Daly MP, Rozen S, ... ... Page DC, et al. An STS-based map of the human genome. Science (New York, N.Y.). 270: 1945-54. PMID 8533086 DOI: 10.1126/Science.270.5244.1945  0.324
1995 Salo P, Kääriäinen H, Page DC, de la Chapelle A. Deletion mapping of stature determinants on the long arm of the Y chromosome Human Genetics. 95: 283-286. PMID 7868119 DOI: 10.1007/Bf00225194  0.444
1995 Polakiewicz RD, Munroe DJ, Sait SN, Tycowski KT, Nowak NJ, Shows TB, Housman DE, Page DC. Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. Genomics. 25: 577-80. PMID 7789996 DOI: 10.1016/0888-7543(95)80063-R  0.434
1995 Letterie GS, Page DC. Dysgerminoma and gonadal dysgenesis in a 46,XX female with no evidence of Y chromosomal DNA Gynecologic Oncology. 57: 423-425. PMID 7774849 DOI: 10.1006/Gyno.1995.1166  0.41
1994 Luoh SW, Page DC. The Structure of the Zfx Gene on the Mouse X Chromosome Genomics. 19: 310-319. PMID 8188262 DOI: 10.1006/Geno.1994.1063  0.443
1994 Zinn AR, Alagappan RK, Brown LG, Wool I, Page DC. Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes. Molecular and Cellular Biology. 14: 2485-92. PMID 8139551 DOI: 10.1128/Mcb.14.4.2485  0.444
1994 Bogan JS, Page DC. Ovary? Testis?-A mammalian dilemma Cell. 76: 603-607. PMID 8124705 DOI: 10.1016/0092-8674(94)90501-0  0.683
1994 Page DC. Y chromosome sequences in Turner's syndrome and risk of gonadoblastoma or virilisation The Lancet. 343: 240. PMID 7904699 DOI: 10.1016/S0140-6736(94)91028-6  0.367
1994 Lahn BT, Ma N, Breg WR, Stratton R, Surti U, Page DC. Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Nature Genetics. 8: 243-50. PMID 7874166 DOI: 10.1038/Ng1194-243  0.692
1993 Zinn AR, Page DC, Fisher EM. Turner syndrome: the case of the missing sex chromosome. Trends in Genetics : Tig. 9: 90-3. PMID 8488568 DOI: 10.1016/0168-9525(93)90230-F  0.64
1993 Watanabe M, Zinn AR, Page DC, Nishimoto T. Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome. Nature Genetics. 4: 268-71. PMID 8358435 DOI: 10.1038/Ng0793-268  0.437
1993 Schmitt K, Vollralh D, Foote S, Fisher EMC, Page DC, Arnheim N. Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes Human Molecular Genetics. 2: 1978. PMID 8281166 DOI: 10.1093/Hmg/2.11.1978  0.408
1993 Behlke MA, Bogan JS, Beer-Romero P, Page DC. Evidence That the SRY Protein Is Encoded by a Single Exon on the Human Y Chromosome Genomics. 17: 736-739. PMID 8244390 DOI: 10.1006/Geno.1993.1395  0.729
1992 Hamvas RMJ, Zinn A, Keer JT, Fisher EMC, Beer-Romero P, Brown SDM, Page DC. Rps4 maps near the inactivation center on the mouse X chromosome Genomics. 12: 363-367. PMID 1740345 DOI: 10.1016/0888-7543(92)90386-7  0.466
1992 Lindgren V, Chen Cp, Bryke CR, Lichter P, Page DC, Yang-Feng TL. Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes Human Genetics. 88: 393-398. PMID 1740316 DOI: 10.1007/Bf00215672  0.447
1992 Vollrath D, Foote S, Hilton A, Brown LG, Beer-Romero P, Bogan JS, Page DC. The human Y chromosome: A 43-interval map based on naturally occurring deletions Science. 258: 52-59. PMID 1439769 DOI: 10.1126/Science.1439769  0.736
1992 Foote S, Vollrath D, Hilton A, Page DC. The human Y chromosome: Overlapping DNA clones spanning the euchromatic region Science. 258: 60-66. PMID 1359640 DOI: 10.1126/Science.1359640  0.455
1992 Zinn AR, Bressler SL, Beer-Romero P, Adler DA, Chapman VM, Page DC, Disteche CM. Erratum: Inactivation of the Rps4 gene on the mouse X chromosome (Genomics (1991) 11 (1097-1101)) Genomics. 13. DOI: 10.1016/0888-7543(92)90192-U  0.453
1991 Fisher EM, Beer-Romero P, Brown LG, Ridley A, McNeil JA, Lawrence JB, Willard HF, Bieber FR, Page DC. Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome. Cell. 63: 1205-18. PMID 2124517 DOI: 10.1016/0092-8674(90)90416-C  0.646
1991 Adler DA, Bressler SL, Chapman VM, Page DC, Disteche CM. Inactivation of the Zfx gene on the mouse X chromosome. Proceedings of the National Academy of Sciences of the United States of America. 88: 4592-5. PMID 2052543 DOI: 10.1073/Pnas.88.11.4592  0.461
1991 Hassold TJ, Sherman SL, Pettay D, Page DC, Jacobs PA. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region American Journal of Human Genetics. 49: 253-260. PMID 1867189  0.316
1991 Zinn AR, Bressler SL, Beer-Romero P, Adler DA, Chapman VM, Page DC, Disteche CM. Inactivation of the Rps4 gene on the mouse X chromosome. Genomics. 11: 1097-101. PMID 1783379 DOI: 10.1016/0888-7543(91)90037-F  0.467
1991 Simpson EM, Page DC. An interstitial deletion in mouse Y chromosomal DNA created a transcribed Zfy fusion gene Genomics. 11: 601-608. PMID 1774064 DOI: 10.1016/0888-7543(91)90067-O  0.451
1990 Sankila EM, Lehner T, Eriksson AW, Forsius H, Kärnä J, Page D, Ott J, de la Chapelle A. Haplotype and multipoint linkage analysis in Finnish choroideremia families. Human Genetics. 84: 66-70. PMID 2575071 DOI: 10.1007/Bf00210674  0.424
1990 Fisher EM, Alitalo T, Luoh SW, de la Chapelle A, Page DC. Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology. Genomics. 7: 625-8. PMID 2387589 DOI: 10.1016/0888-7543(90)90209-D  0.621
1990 Mardon G, Luoh SW, Simpson EM, Gill G, Brown LG, Page DC. Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers. Molecular and Cellular Biology. 10: 681-8. PMID 2105457 DOI: 10.1128/Mcb.10.2.681  0.433
1990 Keer JT, Hamvas RM, Brockdorff N, Page D, Rastan S, Brown SD. Genetic mapping in the region of the mouse X-inactivation center. Genomics. 7: 566-72. PMID 1974879 DOI: 10.1016/0888-7543(90)90200-E  0.577
1990 Page DC, Fisher EM, McGillivray B, Brown LG. Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female. Nature. 346: 279-81. PMID 1973823 DOI: 10.1038/346279A0  0.612
1990 Page DC, Disteche CM, Simpson EM, de la Chapelle A, Andersson M, Alitalo T, Brown LG, Green P, Akots G. Chromosomal localization of ZFX--a human gene that escapes X inactivation--and its murine homologs. Genomics. 7: 37-46. PMID 1970799 DOI: 10.1016/0888-7543(90)90516-W  0.477
1989 Sinclair AH, Foster JW, Spencer JA, Page DC, Palmer M, Goodfellow PN, Graves JA. Sequences homologous to ZFY, a candidate human sex-determining gene, are autosomal in marsupials. Nature. 336: 780-3. PMID 3144651 DOI: 10.1038/336780A0  0.493
1989 Knowlton RG, Nelson CA, Brown VA, Page DC, Donis-Keller H. An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome Nucleic Acids Research. 17: 423-437. PMID 2911472 DOI: 10.1093/Nar/17.1.423  0.458
1989 Page DC. Is ZFY the sex-determining gene on the human Y chromosome? Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 322: 155-7. PMID 2907799 DOI: 10.1098/Rstb.1988.0123  0.49
1989 Kwan SP, Sandkuyl LA, Blaese M, Kunkel LM, Bruns G, Parmley R, Skarshaug S, Page DC, Ott J, Rosen FS. Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. Genomics. 3: 39-43. PMID 2906042 DOI: 10.1016/0888-7543(88)90156-5  0.367
1989 Blagowidow N, Page DC, Huff D, Mennuti MT. Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome. American Journal of Medical Genetics. 34: 159-62. PMID 2816992 DOI: 10.1002/Ajmg.1320340204  0.458
1989 Ma NF, Page DC, Harris TS. Molecular evidence of y-autosomal translocations in owl monkeys Journal of Heredity. 80: 259-263. PMID 2754231 DOI: 10.1093/Oxfordjournals.Jhered.A110850  0.462
1989 Cantrell MA, Bicknell JN, Pagon RA, Page DC, Walker DC, Saal HM, Zinn AB, Disteche CM. Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe. Human Genetics. 83: 88-92. PMID 2570023 DOI: 10.1007/Bf00274156  0.451
1989 Mardon G, Mosher R, Disteche CM, Nishioka Y, McLaren A, Page DC. Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome. Science (New York, N.Y.). 243: 78-80. PMID 2563173 DOI: 10.1126/Science.2563173  0.483
1989 Schneider-Gädicke A, Beer-Romero P, Brown LG, Mardon G, Luoh SW, Page DC. Putative transcription activator with alternative isoforms encoded by human ZFX gene. Nature. 342: 708-11. PMID 2512506 DOI: 10.1038/342708A0  0.459
1989 Schneider-Gädicke A, Beer-Romero P, Brown LG, Nussbaum R, Page DC. ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation. Cell. 57: 1247-58. PMID 2500252 DOI: 10.1016/0092-8674(89)90061-5  0.483
1989 Mardon G, Page DC. The sex-determining region of the mouse Y chromosome encodes a protein with a highly acidic domain and 13 zinc fingers. Cell. 56: 765-70. PMID 2493989 DOI: 10.1016/0092-8674(89)90680-6  0.393
1988 Schwartz M, Yang HM, Niebuhr E, Rosenberg T, Page DC. Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia. Human Genetics. 78: 156-60. PMID 3422216 DOI: 10.1007/Bf00278188  0.421
1988 Phelan MC, Prouty LA, Stevenson RE, Howard-Peebles PN, Page DC, Schwartz CE. The parental origin and mechanism of formation of three dicentric X chromosomes. Human Genetics. 80: 81-4. PMID 3417308 DOI: 10.1007/Bf00451462  0.422
1988 Andersson M, Page DC, Brown LG, Elfving K, de la Chapelle A. Characterization of a (Y;4) translocation by DNA hybridization. Human Genetics. 78: 377-81. PMID 3360449 DOI: 10.1007/Bf00291741  0.419
1988 Münke M, Page DC, Brown LG, Armson BA, Zackai EH, Mennuti MT, Emanuel BS. Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male. Human Genetics. 80: 219-223. PMID 3192211 DOI: 10.1007/Bf01790089  0.455
1988 Andersson M, Page DC, Pettay D, Subrt I, Turleau C, de Grouchy J, de la Chapelle A. Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11. Human Genetics. 79: 2-7. PMID 3163319 DOI: 10.1007/Bf00291700  0.473
1988 Page DC, Bieker K, Brown LG, Hinton S, Leppert M, Lalouel JM, Lathrop M, Nystrom-Lahti M, de la Chapelle A, White R. Linkage, physical mapping, and DNA sequence analysis of pseudoautosomal loci on the human X and Y chromosomes. Genomics. 1: 243-56. PMID 2895727 DOI: 10.1016/0888-7543(87)90051-6  0.442
1987 Disteche CM, Brown L, Saal H, Friedman C, Thuline HC, Hoar DI, Pagon RA, Page DC. Molecular detection of a translocation (Y;15) in a 45,X male. Human Genetics. 74: 372-7. PMID 3793100 DOI: 10.1007/Bf00280488  0.448
1987 Page DC, Mosher R, Simpson EM, Fisher EM, Mardon G, Pollack J, McGillivray B, de la Chapelle A, Brown LG. The sex-determining region of the human Y chromosome encodes a finger protein. Cell. 51: 1091-104. PMID 3690661 DOI: 10.1016/0092-8674(87)90595-2  0.661
1987 Krauss CM, Turksoy RN, Atkins L, McLaughlin C, Brown LG, Page DC. Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. The New England Journal of Medicine. 317: 125-31. PMID 3600701 DOI: 10.1097/00006254-198802000-00015  0.408
1987 Simpson E, Chandler P, Goulmy E, Disteche CM, Ferguson-Smith MA, Page DC. Separation of the genetic loci for the H-Y antigen and for testis determination on human Y chromosome. Nature. 326: 876-8. PMID 3494951 DOI: 10.1097/00006254-198801000-00016  0.481
1987 Page DC. Sex reversal: deletion mapping the male-determining function of the human Y chromosome. Cold Spring Harbor Symposia On Quantitative Biology. 229-35. PMID 3472719 DOI: 10.1101/Sqb.1986.051.01.028  0.435
1987 Page DC, Brown LG, de la Chapelle A. Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males. Nature. 328: 437-40. PMID 2886915 DOI: 10.1038/328437A0  0.461
1987 Moore GE, Ivens A, Chambers J, Farrall M, Williamson R, Page DC, Bjornsson A, Arnason A, Jensson O. Linkage of an X-chromosome cleft palate gene. Nature. 326: 91-2. PMID 2881212 DOI: 10.1038/326091A0  0.381
1987 Rouyer F, Simmler MC, Page DC, Weissenbach J. A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination Cell. 51: 417-425. PMID 2822256 DOI: 10.1016/0092-8674(87)90637-4  0.474
1986 Andersson M, Page DC, de la Chapelle A. Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males. Science (New York, N.Y.). 233: 786-8. PMID 3738510 DOI: 10.1126/Science.3738510  0.458
1986 Disteche CM, Casanova M, Saal H, Friedman C, Sybert V, Graham J, Thuline H, Page DC, Fellous M. Small deletions of the short arm of the Y chromosome in 46,XY females. Proceedings of the National Academy of Sciences of the United States of America. 83: 7841-4. PMID 3464001 DOI: 10.1073/Pnas.83.20.7841  0.478
1986 Brissenden JE, Page DC, de Martinville B, Trowsdale J, Botstein D, Francke U. Regional assignments of three polymorphic DNA segments on human chromosome 15. Genetic Epidemiology. 3: 231-9. PMID 3017806 DOI: 10.1002/Gepi.1370030404  0.588
1986 Vergnaud G, Page DC, Simmler MC, Brown L, Rouyer F, Noel B, Botstein D, de la Chapelle A, Weissenbach J. A deletion map of the human Y chromosome based on DNA hybridization. American Journal of Human Genetics. 38: 109-24. PMID 3004206 DOI: 10.1097/00006254-198610000-00015  0.607
1985 Page DC, de la Chapelle A, Weissenbach J. Chromosome Y-specific DNA in related human XX males. Nature. 315: 224-6. PMID 2987697 DOI: 10.1038/315224A0  0.427
1984 Chapelle Adl, Tippett PA, Wetterstrand G, Page D. Genetic evidence of X–Y interchange in a human XX male Nature. 307: 170-171. PMID 6537827 DOI: 10.1038/307170A0  0.473
1984 Page DC, Harper ME, Love J, Botstein D. Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution. Nature. 311: 119-23. PMID 6088994 DOI: 10.1038/311119A0  0.595
1982 Page D, de Martinville B, Barker D, Wyman A, White R, Francke U, Botstein D. Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. Proceedings of the National Academy of Sciences of the United States of America. 79: 5352-6. PMID 6291041 DOI: 10.1073/Pnas.79.17.5352  0.605
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