Science 2 October 1992: Vol. 258. no. 5079, pp. 52 - 59 DOI: 10.1126/science.1439769

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Articles

DDX3Y encodes a class I MHC-restricted H-Y antigen that is expressed in leukemic stem cells.

K. V. Rosinski, N. Fujii, J. K. Mito, K. K. W. Koo, S. M. Xuereb, O. Sala-Torra, J. S. Gibbs, J. P. Radich, Y. Akatsuka, B. J. Van den Eynde, et al. (2008)
Blood 111, 4817-4826
 |  Abstract »  |  Full Text »  |  PDF »

Identification of new breakpoints in AZFb and AZFc.

P. Costa, R. Goncalves, C. Ferras, S. Fernandes, A. T. Fernandes, M. Sousa, and A. Barros (2008)
Mol. Hum. Reprod. 14, 251-258
 |  Abstract »  |  Full Text »  |  PDF »

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

J. Lange, H. Skaletsky, G. W. Bell, and D. C. Page (2008)
Nucleic Acids Res. 36, D809-D814
 |  Abstract »  |  Full Text »  |  PDF »

Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y.

M. A. Jobling, I. C. C. Lo, D. J. Turner, G. R. Bowden, A. C. Lee, Y. Xue, D. Carvalho-Silva, M. E. Hurles, S. M. Adams, Y. M. Chang, et al. (2007)
Hum. Mol. Genet. 16, 307-316
 |  Abstract »  |  Full Text »  |  PDF »

Profile of David C. Page.

B. Trivedi (2006)
PNAS 103, 2471-2473
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Genomic Instability of the DYZ1 Repeat in Patients with Y Chromosome Anomalies and Males Exposed to Natural Background Radiation.

D. Pathak, S. Premi, J. Srivastava, S. P. Chandy, and S. Ali (2006)
DNA Res 13, 103-109
 |  Abstract »  |  Full Text »  |  PDF »

Rearranging the centromere of the human Y chromosome with {varphi}C31 integrase.

S. Malla, F. Dafhnis-Calas, J. F. Y. Brookfield, M. C. M. Smith, and W. R. A. Brown (2005)
Nucleic Acids Res. 33, 6101-6113
 |  Abstract »  |  Full Text »  |  PDF »

The Y chromosome gr/gr subdeletion is associated with male infertility.

M. Lynch, D.S. Cram, A. Reilly, M.K. O'Bryan, H.W.G. Baker, D.M. de Kretser, and R.I. McLachlan (2005)
Mol. Hum. Reprod. 11, 507-512
 |  Abstract »  |  Full Text »  |  PDF »

High frequency of gr/gr chromosome Y deletions in consecutive oligospermic ICSI candidates.

M. de Llanos, J. L. Ballesca, C. Gazquez, E. Margarit, and R. Oliva (2005)
Hum. Reprod. 20, 216-220
 |  Abstract »  |  Full Text »  |  PDF »

A Novel HLA-A*3303-Restricted Minor Histocompatibility Antigen Encoded by an Unconventional Open Reading Frame of Human TMSB4Y Gene.

H. Torikai, Y. Akatsuka, M. Miyazaki, E. H. Warren III, T. Oba, K. Tsujimura, K. Motoyoshi, Y. Morishima, Y. Kodera, K. Kuzushima, et al. (2004)
J. Immunol. 173, 7046-7054
 |  Abstract »  |  Full Text »  |  PDF »

Androgen receptor gene GGN and CAG polymorphisms among severely oligozoospermic and azoospermic Swedish men.

Y. Ruhayel, K. Lundin, Y. Giwercman, C. Hallden, M. Willen, and A. Giwercman (2004)
Hum. Reprod. 19, 2076-2083
 |  Abstract »  |  Full Text »  |  PDF »

Y chromosome microdeletion screening in infertile men in France:a survey of French practice based on 88 IVF centres.

I. E. Aknin-Seifer, H. Lejeune, R. L. Touraine, R. Levy, and Under the aegis of the SALF (Societe d'Andrologie (2004)
Hum. Reprod. 19, 788-793
 |  Abstract »  |  Full Text »  |  PDF »

A simple, low cost and non-invasive method for screening Y-chromosome microdeletions in infertile men.

I.E. Aknin-Seifer, R.L. Touraine, H. Lejeune, J.L. Laurent, B. Lauras, and R. Levy (2003)
Hum. Reprod. 18, 257-261
 |  Abstract »  |  Full Text »  |  PDF »

A comparative study between infertile males and patients with Turner syndrome to determine the influence of sex chromosome mosaicism and the breakpoints of structurally abnormal Y chromosomes on phenotypic sex.

C R Quilter, N Nathwani, G S Conway, R Stanhope, D Ralph, G Bahadur, P Serhal, K Taylor, and J D A Delhanty (2002)
J. Med. Genet. 39, e80-80
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Transmission of an unbalanced (Y;1) translocation in Brittany, France.

F Morel, I Dugueperoux, K McElreavey, M-J Le Bris, A Herry, P Parent, M-T Le Martelot, M Fellous, and M De Braekeleer (2002)
J. Med. Genet. 39, e52-52
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Localisation of the Y chromosome stature gene to a 700 kb interval in close proximity to the centromere.

S Kirsch, B Weiss, S Kleiman, K Roberts, J Pryor, A Milunsky, A Ferlin, C Foresta, G Matthijs, and G A Rappold (2002)
J. Med. Genet. 39, 507-513
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The Evaluation and Management of the Azoospermic Patient.

P. N. Kolettis (2002)
J Androl 23, 293-305
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Screening for Y chromosome microdeletions in 226 Slovenian subfertile men.

B. Peterlin, T. Kunej, J. Sinkovec, N. Gligorievska, and B. Zorn (2002)
Hum. Reprod. 17, 17-24
 |  Abstract »  |  Full Text »  |  PDF »

High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome.

C. Kamp, K. Huellen, S. Fernandes, M. Sousa, P.N. Schlegel, A. Mielnik, S. Kleiman, H. Yavetz, W. Krause, W. Kupker, et al. (2001)
Mol. Hum. Reprod. 7, 987-994
 |  Abstract »  |  Full Text »  |  PDF »

Triplication of several PAR1 genes and part of the Homo sapiens specific Yp11.2/Xq21.3 region of homology in a 46,X,t(X;Y)(p22.33;p11.2) male with schizophrenia.

N. L J Ross, J. Yang, C. A Sargent, C. A Boucher, S. Nanko, R. Wadekar, N. A Williams, N. A Affara, and T. J Crow (2001)
J. Med. Genet. 38, 710-719
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Breakpoint analysis of Turner patients with partial Xp deletions: implications for the lymphoedema gene location.

C. A Boucher, C. A Sargent, T. Ogata, and N. A Affara (2001)
J. Med. Genet. 38, 591-598
 |  Abstract »  |  Full Text »  |  PDF »

Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4).

K. Stouffs, W. Lissens, L. Van Landuyt, H. Tournaye, A. Van Steirteghem, and I. Liebaers (2001)
Mol. Hum. Reprod. 7, 603-610
 |  Abstract »  |  Full Text »  |  PDF »

Hierarchical Patterns of Global Human Y-Chromosome Diversity.

M. F. Hammer, T. M. Karafet, A. J. Redd, H. Jarjanazi, S. Santachiara-Benerecetti, H. Soodyall, and S. L. Zegura (2001)
Mol. Biol. Evol. 18, 1189-1203
 |  Abstract »  |  Full Text »  |  PDF »

Sertoli Cell Function in Infertile Patients with and without Microdeletions of the Azoospermia Factors on the Y Chromosome Long Arm.

C. Foresta, A. Bettella, E. Moro, A. Roverato, M. Merico, and A. Ferlin (2001)
J. Clin. Endocrinol. Metab. 86, 2414-2419
 |  Abstract »  |  Full Text »  |  PDF »

TTY2: A Multicopy Y-Linked Gene Family.

E. Makrinou, M. Fox, M. Lovett, K. Haworth, J. M. Cameron, K. Taylor, and Y. H. Edwards (2001)
Genome Res. 11, 935-945
 |  Abstract »  |  Full Text »  |  PDF »

Y Chromosome Microdeletions and Alterations of Spermatogenesis.

C. Foresta, E. Moro, and A. Ferlin (2001)
Endocr. Rev. 22, 226-239
 |  Abstract »  |  Full Text »

Prognostic value of Y deletion analysis: How reliable is the outcome of Y deletion analysis in providing a sound prognosis?.

S. L. Liow, E. L. Yong, and S. C. Ng (2001)
Hum. Reprod. 16, 9-12
 |  Abstract »  |  Full Text »  |  PDF »

Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events.

C. Kamp, P. Hirschmann, H. Voss, K. Huellen, and P. H. Vogt (2000)
Hum. Mol. Genet. 9, 2563-2572
 |  Abstract »  |  Full Text »  |  PDF »

Xp;Yp translocation inherited from the father in an SRY, RBM, and TSPY positive true hermaphrodite with oligozoospermia.

L. JAKUBOWSKI, A. JEZIOROWSKA, M. CONSTANTINOU, Z. HELSZER, A. BAUMSTARK, and W. VOGEL (2000)
J. Med. Genet. 37, 28e-28
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Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses.

C. Sun, H. Skaletsky, S. Rozen, J. Gromoll, E. Nieschlag, R. Oates, and D. C. Page (2000)
Hum. Mol. Genet. 9, 2291-2296
 |  Abstract »  |  Full Text »  |  PDF »

Occurrence of Gonadoblastoma in Females with Turner Syndrome and Y Chromosome Material: A Population Study.

C. H. Gravholt, J. Fedder, R. W. Naeraa, and J. Müller (2000)
J. Clin. Endocrinol. Metab. 85, 3199-3202
 |  Abstract »  |  Full Text »

The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility.

N. Saut, P. Terriou, A. Navarro, N. Levy, and M. J. Mitchell (2000)
Mol. Hum. Reprod. 6, 789-793
 |  Abstract »  |  Full Text »  |  PDF »

Y chromosome microdeletions and germinal mosaicism in infertile males.

C. Le Bourhis, J. P. Siffroi, K. McElreavey, and J. P. Dadoune (2000)
Mol. Hum. Reprod. 6, 688-693
 |  Abstract »  |  Full Text »  |  PDF »

FISH deletion mapping defines a single location for the Y chromosome stature gene, GCY.

S. Kirsch, B Weiss, M De Rosa, T Ogata, G Lombardi, and G A Rappold (2000)
J. Med. Genet. 37, 593-599
 |  Abstract »  |  Full Text »

Human mini-chromosomes with minimal centromeres.

J.W. Yang, C. Pendon, J. Yang, N. Haywood, A. Chand, and W.R.A. Brown (2000)
Hum. Mol. Genet. 9, 1891-1902
 |  Abstract »  |  Full Text »  |  PDF »

Population genetic implications from sequence variation in four Y chromosome genes.

P. Shen, F. Wang, P. A. Underhill, C. Franco, W.-H. Yang, A. Roxas, R. Sung, A. A. Lin, R. W. Hyman, D. Vollrath, et al. (2000)
PNAS 97, 7354-7359
 |  Abstract »  |  Full Text »  |  PDF »

Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility.

C. Foresta, A. Ferlin, and E. Moro (2000)
Hum. Mol. Genet. 9, 1161-1169
 |  Abstract »  |  Full Text »  |  PDF »

Validation of a simple Yq deletion screening programme in an ICSI candidate population.

L. Van Landuyt, W. Lissens, K. Stouffs, H. Tournaye, I. Liebaers, and A. Van Steirteghem (2000)
Mol. Hum. Reprod. 6, 291-297
 |  Abstract »  |  Full Text »  |  PDF »

The Human UTY Gene Encodes a Novel HLA-B8-Restricted H-Y Antigen.

E. H. Warren, M. A. Gavin, E. Simpson, P. Chandler, D. C. Page, C. Disteche, K. A. Stankey, P. D. Greenberg, and S. R. Riddell (2000)
J. Immunol. 164, 2807-2814
 |  Abstract »  |  Full Text »  |  PDF »

Y chromosome microdeletion in a father and his four infertile sons.

P. L. Chang, M. V. Sauer, and S. Brown (1999)
Hum. Reprod. 14, 2689-2694
 |  Abstract »  |  Full Text »  |  PDF »

Four Evolutionary Strata on the Human X Chromosome.

B. T. Lahn and D. C. Page (1999)
Science 286, 964-967
 |  Abstract »  |  Full Text »

A High Frequency of Y Chromosome Deletions in Males with Nonidiopathic Infertility.

C. Krausz, L. Quintana-Murci, S. Barbaux, J.-P. Siffroi, H. Rouba, D. Delafontaine, N. Souleyreau-Therville, G. Arvis, J. M. Antoine, E. Erdei, et al. (1999)
J. Clin. Endocrinol. Metab. 84, 3606-3612
 |  Abstract »  |  Full Text »  |  PDF »

Y Chromosome Microdeletions in Cryptorchidism and Idiopathic Infertility.

C. Foresta, E. Moro, A. Garolla, M. Onisto, and A. Ferlin (1999)
J. Clin. Endocrinol. Metab. 84, 3660-3665
 |  Abstract »  |  Full Text »  |  PDF »

Absence of testicular DAZ gene expression in idiopathic severe testiculopathies.

A. Ferlin, E. Moro, M. Onisto, E. Toscano, A. Bettella, and C. Foresta (1999)
Hum. Reprod. 14, 2286-2292
 |  Abstract »  |  Full Text »  |  PDF »

The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.

C. A Sargent, C. A Boucher, S. Kirsch, G. Brown, B. Weiss, A. Trundley, P. Burgoyne, N. Saut, C. Durand, N. Levy, et al. (1999)
J. Med. Genet. 36, 670-677
 |  Abstract »  |  Full Text »

A human DAZ transgene confers partial rescue of the mouse Dazl null phenotype.

R. Slee, B. Grimes, R. M. Speed, M. Taggart, S. M. Maguire, A. Ross, N. I. McGill, P. T. K. Saunders, and H. J. Cooke (1999)
PNAS 96, 8040-8045
 |  Abstract »  |  Full Text »  |  PDF »

Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY.

A. Ferlin, E. Moro, A. Garolla, and C. Foresta (1999)
Hum. Reprod. 14, 1710-1716
 |  Abstract »  |  Full Text »  |  PDF »

Screening for microdeletions of Y chromosome genes in patients undergoing intracytoplasmic sperm injection.

C. Krausz, C. Bussani-Mastellone, S. Granchi, K. McElreavey, G. Scarselli, and G. Forti (1999)
Hum. Reprod. 14, 1717-1721
 |  Abstract »  |  Full Text »  |  PDF »

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

D. C. Page, S. Silber, and L. G. Brown (1999)
Hum. Reprod. 14, 1722-1726
 |  Abstract »  |  Full Text »  |  PDF »

Two male patients with ring Y: definition of an interval in Yq contributing to Turner syndrome.

M. Tzancheva, R. Kaneva, P. Kumanov, G. Williams, and C. Tyler-Smith (1999)
J. Med. Genet. 36, 549-553
 |  Abstract »  |  Full Text »

Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosome.

K. Kusz, M. Kotecki, A. Wojda, M. Szarras-Czapnik, A. Latos-Bielenska, A. Warenik-Szymankiewicz, A. Ruszczynska-Wolska, and J. Jaruzelska (1999)
J. Med. Genet. 36, 452-456
 |  Abstract »  |  Full Text »

A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome.

D O Robinson, P Dalton, P A Jacobs, K Mosse, M M Power, D H Skuse, and J A Crolla (1999)
J. Med. Genet. 36, 279-284
 |  Abstract »  |  Full Text »

Genetic evaluation of infertile men.

S.E. Kleiman, L. Yogev, R. Gamzu, R. Hauser, A. Botchan, J.B. Lessing, G. Paz, and H. Yavetz (1999)
Hum. Reprod. 14, 33-38
 |  Abstract »  |  Full Text »  |  PDF »

A Map of 75 Human Ribosomal Protein Genes.

N. Kenmochi, T. Kawaguchi, S. Rozen, E. Davis, N. Goodman, T. J. Hudson, T. Tanaka, and D. C. Page (1998)
Genome Res. 8, 509-523
 |  Abstract »  |  Full Text »

Regulation of Sexual Dimorphism in Mammals.

C. M. HAQQ and P. K. DONAHOE (1998)
Physiol Rev 78, 1-33
 |  Abstract »  |  Full Text »  |  PDF »

Functional Coherence of the Human Y Chromosome.

B. T. Lahn and D. C. Page (1997)
Science 278, 675-680
 |  Abstract »  |  Full Text »

Detection of Numerous Y Chromosome Biallelic Polymorphisms by Denaturing High-Performance Liquid Chromatography.

P. A. Underhill, L. Jin, A. A. Lin, S. Q. Mehdi, T. Jenkins, D. Vollrath, R. W. Davis, L. L. Cavalli-Sforza, and P. J. Oefner (1997)
Genome Res. 7, 996-1005
 |  Abstract »  |  Full Text »  |  PDF »

A Physical Map of Human Chromosome 7: An Integrated YAC Contig Map with Average STS Spacing of 79 kb.

G. G. Bouffard, J. R. Idol, V. V. Braden, L. M. Iyer, A. F. Cunningham, L. A. Weintraub, J. W. Touchman, R. M. Mohr-Tidwell, D. C. Peluso, R. S. Fulton, et al. (1997)
Genome Res. 7, 673-692
 |  Abstract »  |  Full Text »  |  PDF »

Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm.

D. J. Elliott, M. R. Millar, K. Oghene, A. Ross, F. Kiesewetter, J. Pryor, M. McIntyre, T. B. Hargreave, P. T. K. Saunders, P. H. Vogt, et al. (1997)
PNAS 94, 3848-3853
 |  Abstract »  |  Full Text »  |  PDF »

Evolutionary Features of the 4-Mb Xq21.3 XY Homology Region Revealed by a Map at 60-kb Resolution.

S. Mumm, B. Molini, J. Terrell, A. Srivastava, and D. Schlessinger (1997)
Genome Res. 7, 307-314
 |  Abstract »  |  Full Text »  |  PDF »

Y-Chromosome Deletions in Idiopathic Severe Testiculopathies.

C. Foresta, A. Ferlin, A. Garolla, M. Rossato, S. Barbaux, and A. De Bortoli (1997)
J. Clin. Endocrinol. Metab. 82, 1075-1080
 |  Abstract »  |  Full Text »  |  PDF »

Microdeletions in the Y Chromosome of Infertile Men.

J. L. Pryor, M. Kent-First, A. Muallem, A. H. Van Bergen, W. E. Nolten, L. Meisner, and K. P. Roberts (1997)
N. Engl. J. Med. 336, 534-540
 |  Abstract »  |  Full Text »  |  PDF »

A collection of 1814 human chromosome 7-specific STSs..

G G Bouffard, L M Iyer, J R Idol, V V Braden, A F Cunningham, L A Weintraub, R M Mohr-Tidwell, D C Peluso, R S Fulton, M P Leckie, et al. (1997)
Genome Res. 7, 59-64
 |  Abstract »  |  PDF »

Mapping the human Y chromosome by fingerprinting cosmid clones..

K Taylor, N Hornigold, D Conway, D Williams, Z Ulinowski, M Agochiya, P Fattorini, P de Jong, P F Little, and J Wolfe (1996)
Genome Res. 6, 235-248
 |  Abstract »  |  PDF »

A Combined Cytogenetic and Molecular Approach for Diagnosing Delayed Puberty.

Hon Fong Louie Mark, J. K. Bayleran, D. B. Seifer, and C. H. Meyers-Seifer (1996)
Clinical Pediatrics 35, 62-66
 |  Abstract »  |  PDF »

Detection of Y-Chromosome Sequences in Gonadal Tissue of Patients with Turner's Syndrome (45,X).

M. Kocova, S. F. Siegel, M. Nalesnick, and M. Trucco (1994)
N. Engl. J. Med. 331, 682-683
 |  Full Text »

Analysis of DNA sequences.

B. Weir (1993)
Statistical Methods in Medical Research 2, 225-239
 |  Abstract »  |  PDF »

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

S Foote, D Vollrath, A Hilton, and D. Page (1992)
Science 258, 60-66
 |  Abstract »  |  PDF »

A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group.

(1992)
Science 258, 67-86
 |  Abstract »  |  PDF »

Genome analysis and the human X chromosome.

J. Mandel, A. Monaco, D. Nelson, D Schlessinger, and H Willard (1992)
Science 258, 103-109
 |  Abstract »  |  PDF »

High levels of Y-chromosome nucleotide diversity in the genus Pan.

A. C. Stone, R. C. Griffiths, S. L. Zegura, and M. F. Hammer (2002)
PNAS 99, 43-48
 |  Abstract »  |  Full Text »  |  PDF »

Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypes.

M. F. Hammer, A. J. Redd, E. T. Wood, M. R. Bonner, H. Jarjanazi, T. Karafet, S. Santachiara-Benerecetti, A. Oppenheim, M. A. Jobling, T. Jenkins, et al. (2000)
PNAS 97, 6769-6774
 |  Abstract »  |  Full Text »  |  PDF »

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