Science 30 September 1994: Vol. 265. no. 5181, pp. 2049 - 2054 DOI: 10.1126/science.8091227

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Articles

Colorectal Cancer Risk Is Not Associated with Increased Levels of Homozygosity in a Population from the United Kingdom.

S. L. Spain, J.-B. Cazier, The CORGI Consortium,, R. Houlston, L. Carvajal-Carmona, and I. Tomlinson (2009)
Cancer Res. 69, 7422-7429
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The human Major Histocompatibility Complex as a paradigm in genomics research.

C. Vandiedonck and J. C. Knight (2009)
Brief Funct Genomic Proteomic 8, 379-394
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Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis.

R. M. Spaapen, H. M. Lokhorst, K. van den Oudenalder, B. E. Otterud, H. Dolstra, M. F. Leppert, M. C. Minnema, A. C. Bloem, and T. Mutis (2008)
J. Exp. Med. 205, 2863-2872
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DNA sequencing: bench to bedside and beyond.

C. A. Hutchison III (2007)
Nucleic Acids Res. 35, 6227-6237
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A Microsatellite Linkage Map of Barramundi, Lates calcarifer.

C. M. Wang, Z. Y. Zhu, L. C. Lo, F. Feng, G. Lin, W. T. Yang, J. Li, and G. H. Yue (2007)
Genetics 175, 907-915
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A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3..

D J Verlaan, M-P Dube, J St-Onge, A Noreau, J Roussel, N Satge, M C Wallace, and G A Rouleau (2006)
J. Med. Genet. 43, e31
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Construction of a 10,000-Marker Ultradense Genetic Recombination Map of Potato: Providing a Framework for Accelerated Gene Isolation and a Genomewide Physical Map.

H. van Os, S. Andrzejewski, E. Bakker, I. Barrena, G. J. Bryan, B. Caromel, B. Ghareeb, E. Isidore, W. de Jong, P. van Koert, et al. (2006)
Genetics 173, 1075-1087
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Structural variants: changing the landscape of chromosomes and design of disease studies..

L. Feuk, C. R. Marshall, R. F. Wintle, and S. W. Scherer (2006)
Hum. Mol. Genet. 15, R57-R66
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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

G. Tamiya, M. Shinya, T. Imanishi, T. Ikuta, S. Makino, K. Okamoto, K. Furugaki, T. Matsumoto, S. Mano, S. Ando, et al. (2005)
Hum. Mol. Genet. 14, 2305-2321
 |  Abstract »  |  Full Text »  |  PDF »

Cyberinfrastructure: Empowering a "Third Way" in Biomedical Research.

K. H. Buetow (2005)
Science 308, 821-824
 |  Abstract »  |  Full Text »  |  PDF »

ALOHOMORA: a tool for linkage analysis using 10K SNP array data.

F. Ruschendorf and P. Nurnberg (2005)
Bioinformatics 21, 2123-2125
 |  Abstract »  |  Full Text »  |  PDF »

MAP-O-MAT: internet-based linkage mapping.

X. Kong and T. C. Matise (2005)
Bioinformatics 21, 557-559
 |  Abstract »  |  Full Text »  |  PDF »

Toward a Marker-Dense Meiotic Map of the Potato Genome: Lessons From Linkage Group I.

E. Isidore, H. van Os, S. Andrzejewski, J. Bakker, I. Barrena, G. J. Bryan, B. Caromel, H. van Eck, B. Ghareeb, W. de Jong, et al. (2003)
Genetics 165, 2107-2116
 |  Abstract »  |  Full Text »  |  PDF »

A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure.

J. Lespinasse, M.O. North, C. Paravy, M.J. Brunel, P. Malzac, and J.L. Blouin (2003)
Hum. Reprod. 18, 2058-2066
 |  Abstract »  |  Full Text »  |  PDF »

Identification of a Polymorphic Gene, BCL2A1, Encoding Two Novel Hematopoietic Lineage-specific Minor Histocompatibility Antigens.

Y. Akatsuka, T. Nishida, E. Kondo, M. Miyazaki, H. Taji, H. Iida, K. Tsujimura, M. Yazaki, T. Naoe, Y. Morishima, et al. (2003)
J. Exp. Med. 197, 1489-1500
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DMBT1 Polymorphisms: Relationship to Malignant Glioma Tumorigenesis.

H. Sasaki, R. A. Betensky, J. G. Cairncross, and D. N. Louis (2002)
Cancer Res. 62, 1790-1796
 |  Abstract »  |  Full Text »  |  PDF »

Overrepresentation of the EBAG9 Gene at 8q23 Associated with Early-Stage Breast Cancers.

M. Tsuneizumi, M. Emi, H. Nagai, H. Harada, G. Sakamoto, F. Kasumi, S. Inoue, T. Kazui, and Y. Nakamura (2001)
Clin. Cancer Res. 7, 3526-3532
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Identification of a new mutation in the {alpha}4(IV) collagen gene in a family with autosomal dominant Alport syndrome and hypercholesterolaemia.

M. Ciccarese, D. Casu, F. K. Wong, R. Faedda, S. Arvidsson, G. Tonolo, H. Luthman, and A. Satta (2001)
Nephrol. Dial. Transplant. 16, 2008-2012
 |  Abstract »  |  Full Text »  |  PDF »

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.

B. Cormand, H. Pihko, M. Bayes, L. Valanne, P. Santavuori, B. Talim, R. Gershoni-Baruch, A. Ahmad, H. van Bokhoven, H.G. Brunner, et al. (2001)
Neurology 56, 1059-1069
 |  Abstract »  |  Full Text »  |  PDF »

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q.

International Molecular Genetic Study of Autism Co (2001)
Hum. Mol. Genet. 10, 973-982
 |  Abstract »  |  Full Text »  |  PDF »

Sporadic and Familial Pheochromocytomas Are Associated with Loss of at Least Two Discrete Intervals on Chromosome 1p.

D. E. Benn, T. Dwight, A. L. Richardson, L. Delbridge, C. P. Bambach, M. Stowasser, R. D. Gordon, D. J. Marsh, and B. G. Robinson (2000)
Cancer Res. 60, 7048-7051
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Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

D. WIECZOREK, M. KRAUSE, F. MAJEWSKI, B. ALBRECHT, P. MEINECKE, O. RIESS, and G. GILLESSEN-KAESBACH (2000)
J. Med. Genet. 37, 798-804
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Expression-based Genetic/Physical Maps of Single-Nucleotide Polymorphisms Identified by the Cancer Genome Anatomy Project.

R. Clifford, M. Edmonson, Y. Hu, C. Nguyen, T. Scherpbier, and K. H. Buetow (2000)
Genome Res. 10, 1259-1265
 |  Abstract »  |  Full Text »

Hereditary Motor and Sensory Neuropathy Type 2C Is Genetically Distinct From Types 2B and 2D.

M. Nagamatsu, R. B. Jenkins, D. J. Schaid, D. M. Klein, and P. J. Dyck (2000)
Arch Neurol 57, 669-672
 |  Abstract »  |  Full Text »  |  PDF »

Genetic Heterogeneity of the Coppock-like Cataract: A Mutation in CRYBB2 on Chromosome 22q11.2.

D. Gill, R. Klose, F. L. Munier, M. McFadden, M. Priston, G. Billingsley, N. Ducrey, D. F. Schorderet, and E. Héon (2000)
Invest. Ophthalmol. Vis. Sci. 41, 159-165
 |  Abstract »  |  Full Text »

An Integrated Physical Map for the Short Arm of Human Chromosome 5.

E. T. Peterson, R. Sutherland, D. L. Robinson, L. Chasteen, M. Gersh, J. Overhauser, L. L. Deaven, R. K. Moyzis, and D. L. Grady (1999)
Genome Res. 9, 1250-1267
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The human genome project: a false dawn?.

R L Zimmern (1999)
BMJ 319, 1282
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High-Resolution Landmark Framework for the Sequence-Ready Mapping of Xq23-q26.1.

H. E. Steingruber, A. Dunham, A. J. Coffey, S. M. Clegg, G. R. Howell, G. L. Maslen, C. E. Scott, R. Gwilliam, P. J. Hunt, E. C. Sotheran, et al. (1999)
Genome Res. 9, 751-762
 |  Abstract »  |  Full Text »

A paradigm for finding genes for a complex human trait: Polycystic ovary syndrome and follistatin.

K. Odunsi and K. K. Kidd (1999)
PNAS 96, 8315-8317
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A study of loss of heterozygosity at 70 loci in anaplastic astrocytoma and glioblastoma multiforme with implications for tumor evolution.

E. C. Wooten, D. Fults, R. Duggirala, K. Williams, A. P. Kyritsis, M. L. Bondy, V. A. Levin, and P. O'Connell (1999)
Neuro-oncol 1, 169-176
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Medical and Societal Consequences of the Human Genome Project.

F. S. Collins (1999)
N. Engl. J. Med. 341, 28-37
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"KARIBIN," an Information Resource for Obtaining Genomic Information in a Cytogenetic Band.

J. Zhang, G. Shen-Ong, and J. Ostell (1999)
Genome Res. 9, 91-98
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Toward a Complete Human Genome Sequence.

T. S. Centre and T. W. U. G. S. Center (1998)
Genome Res. 8, 1097-1108
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Homogeneous Multiplex Genotyping of Hemochromatosis Mutations with Fluorescent Hybridization Probes.

P. S. Bernard, R. S. Ajioka, J. P. Kushner, and C. T. Wittwer (1998)
Am. J. Pathol. 153, 1055-1061
 |  Abstract »  |  Full Text »  |  PDF »

A Simple Method for Automated Allele Binning in Microsatellite Markers.

R. M. Idury and L. R. Cardon (1997)
Genome Res. 7, 1104-1109
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Characterization of Short Tandem Repeats from Thirty-One Human Telomeres.

M. Rosenberg, L. Hui, J. Ma, H. C. Nusbaum, K. Clark, L. Robinson, L. Dziadzio, P. M. Swain, T. Keith, T. J. Hudson, et al. (1997)
Genome Res. 7, 917-923
 |  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 »

Characterization of Alu Repeats That Are Associated with Trinucleotide and Tetranucleotide Repeat Microsatellites.

C. N. Yandava, J. M. Gastier, J. C. Pulido, T. Brody, V. Sheffield, J. Murray, K. Buetow, and G. M. Duyk (1997)
Genome Res. 7, 716-724
 |  Abstract »  |  Full Text »  |  PDF »

An STS-Based Radiation Hybrid Map of the Human Genome.

E. A. Stewart, K. B. McKusick, A. Aggarwal, E. Bajorek, S. Brady, A. Chu, N. Fang, D. Hadley, M. Harris, S. Hussain, et al. (1997)
Genome Res. 7, 422-433
 |  Abstract »  |  Full Text »  |  PDF »

Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group..

S Ghosh, Z E Karanjawala, E R Hauser, D Ally, J I Knapp, J B Rayman, A Musick, J Tannenbaum, C Te, S Shapiro, et al. (1997)
Genome Res. 7, 165-178
 |  Abstract »  |  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 »

Linkage Analysis Using Platelet-Activating Factor Ca2+ Response in Transformed Lymphoblasts.

L. M. Brzustowicz, J. P. Gardner, L. Hopp, E. Jeanclos, J. Ott, X. Y. Yang, Z. Fekete, and A. Aviv (1997)
Hypertension 29, 158-164
 |  Abstract »  |  Full Text »  |  PDF »

A complete genome screen for genes predisposing to severe bipolar disorder in two Costa Rican pedigrees.

L. A. McInnes, M. A. Escamilla, S. K. Service, V. I. Reus, P. Leon, S. Silva, E. Rojas, M. Spesny, S. Baharloo, K. Blankenship, et al. (1996)
PNAS 93, 13060-13065
 |  Abstract »  |  Full Text »  |  PDF »

Current Concepts Review - Update on the Genetic Bases of Disorders with Orthopaedic Manifestations.

F. R. DIETZ and K. D. MATHEWS (1996)
J. Bone Joint Surg. Am. 78, 1583-98
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An approach to high-throughput genotyping..

J M Hall, C A LeDuc, A R Watson, and A H Roter (1996)
Genome Res. 6, 781-790
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Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes..

S L Sunden, W L Alward, B E Nichols, T R Rokhlina, A Nystuen, E M Stone, and V C Sheffield (1996)
Genome Res. 6, 862-869
 |  Abstract »  |  PDF »

Mapping of the OB receptor to 1p in a region of nonconserved gene order from mouse and rat to human..

W K Chung, L Power-Kehoe, M Chua, and R L Leibel (1996)
Genome Res. 6, 431-438
 |  Abstract »  |  PDF »

A Founder Mutation as a Cause of Cerebral Cavernous Malformation in Hispanic Americans.

M. Gunel, I. A. Awad, K. Finberg, J. A. Anson, G. K. Steinberg, H. H. Batjer, T. A. Kopitnik, L. Morrison, S. L. Giannotta, C. Nelson-Williams, et al. (1996)
N. Engl. J. Med. 334, 946-951
 |  Abstract »  |  Full Text »  |  PDF »

Toward the construction of integrated physical and genetic maps of the mouse genome using interspersed repetitive sequence PCR (IRS-PCR) genomics..

K W Hunter, L Riba, L Schalkwyk, M Clark, S Resenchuk, A Beeghly, J Su, F Tinkov, P Lee, E Ramu, et al. (1996)
Genome Res. 6, 290-299
 |  Abstract »  |  PDF »

Periodic Vestibulocerebellar Ataxia, an Autosomal Dominant Ataxia With Defective Smooth Pursuit, Is Genetically Distinct From Other Autosomal Dominant Ataxias.

K. F. Damji, R. R. Allingham, S. C. Pollock, K. Small, K. E. Lewis, J. M. Stajich, L. H. Yamaoka, J. M. Vance, and M. A. Pericak-Vance (1996)
Arch Neurol 53, 338-344
 |  Abstract »  |  PDF »

Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31..

P Hoglund, S Haila, S W Scherer, L C Tsui, E D Green, J Weissenbach, C Holmberg, A de la Chapelle, and J Kere (1996)
Genome Res. 6, 202-210
 |  Abstract »  |  PDF »

An STS-Based Map of the Human Genome.

T. J. Hudson, L. D. Stein, S. S. Gerety, J. Ma, A. B. Castle, J. Silva, D. K. Slonim, R. Baptista, L. Kruglyak, S.-H. Xu, et al. (1995)
Science 270, 1945-1954
 |  Abstract »

Molecular Analysis of Nondisjunction in Down Syndrome Patients With and Without Atrioventricular Septal Defects.

M. M. Zittergruen, J. C. Murray, R. M. Lauer, T. L. Burns, and V. C. Sheffield (1995)
Circulation 92, 2803-2810
 |  Abstract »  |  Full Text »

Refined localization of the cerebral cavernous malformation gene (CCM1) to a 4-cM interval of chromosome 7q contained in a well-defined YAC contig..

E W Johnson, L M Iyer, S S Rich, H T Orr, A Gil-Nagel, J H Kurth, J M Zabramski, D A Marchuk, J Weissenbach, and C L Clericuzio (1995)
Genome Res. 5, 368-380
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Recent Advances in the Molecular Genetics of Hypertrophic Cardiomyopathy.

A.J. Marian and R. Roberts (1995)
Circulation 92, 1336-1347
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Regional assignment of 68 new human gene transcripts on chromosome 11..

M F Rosier, I Reguigne-Arnould, P Couillin, M D Devignes, and C Auffray (1995)
Genome Res. 5, 60-70
 |  Abstract »  |  PDF »

Medical Genetics.

J. R. Korenberg and D. L. Rimoin (1995)
JAMA 273, 1692-1693
 |  Abstract »  |  PDF »

Batched analysis of genotypes..

C LeDuc, P Miller, J Lichter, and P Parry (1995)
Genome Res. 4, 331-336
 |  Abstract »  |  PDF »

Genetic Linkage of Wagner Disease and Erosive Vitreoretinopathy to Chromosome 5q13-14.

D. M. Brown, R. A. Graemiger, M. Hergersberg, A. Schinzel, E. P. Messmer, G. Niemeyer, S. A. Schneeberger, L. M. Streb, C. M. Taylor, A. E. Kimura, et al. (1995)
Arch Ophthalmol 113, 671-675
 |  Abstract »  |  PDF »

A genome survey indicates a possible susceptibility locus for bipolar disorder on chromosome 22.

J. R. Kelsoe, M. A. Spence, E. Loetscher, M. Foguet, A. D. Sadovnick, R. A. Remick, P. Flodman, J. Khristich, Z. Mroczkowski-Parker, J. L. Brown, et al. (2001)
PNAS 98, 585-590
 |  Abstract »  |  Full Text »  |  PDF »

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