P. Bray-Ward

发表

Mutation detection and single-molecule counting using isothermal rolling-circle amplification

P. Lizardi, Xiaohua Huang, Zhengrong Zhu, 1998, Nature Genetics.

Improvements in cytogenetic slide preparation: controlled chromosome spreading, chemical aging and gradual denaturing.

P. Bray-Ward, D. Ward, N. Heerema, 2001, Cytometry.

Comprehensive human genome amplification using multiple displacement amplification

S. Kingsmore, M. Egholm, P. Bray-Ward, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Human metalloprotease-disintegrin Kuzbanian regulates sympathoadrenal cell fate in development and neoplasia.

P. Bray-Ward, M. Brines, C. Adida, 1998, Human molecular genetics.

Serum protein markers for early detection of ovarian cancer.

Hongyu Zhao, Gil Mor, Yinglei Lai, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Serum proteins marker for early detection of ovarian cancer

Hongyu Zhao, P. Bray-Ward, D. Ward, 2005 .

Assignment1 of SYNJ1 to human chromosome 21q22.2 and Synj12 to the murine homologous region on chromosome 16C3–4 by in situ hybridization

P. De Camilli, P. Bray-Ward, D. Ward, 2000, Cytogenetic and Genome Research.

Efficacy of the swim-up method in eliminating sperm with diminished maturity and aneuploidy.

P. Bray-Ward, D. Ward, G. Huszar, 2003, Human Reproduction.

FISH assessment of aneuploidy frequencies in mature and immature human spermatozoa classified by the absence or presence of cytoplasmic retention.

P. Bray-Ward, D. Ward, E. Moretti, 2001, Human reproduction.

Sperm selection for ICSI: shape properties do not predict the absence or presence of numerical chromosomal aberrations.

P. Bray-Ward, D. Ward, R. Demir, 2004, Human reproduction.

Generation of an inbred miniature pig model of retinitis pigmentosa.

B. Jones, R. Marc, P. Bray-Ward, 2012, Investigative ophthalmology & visual science.

A transcription map of the major histocompatibility complex (MHC) class I region.

S. Weissman, P. Bray-Ward, J. Pan, 1996, Genomics.

Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones.

P. Bray-Ward, D. Ward, J. Menninger, 1996, Genomics.

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

D C Ward, T. Golub, S. Raimondi, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Human Sperm Maintain Their Shape Following Decondensation and Denaturation for Fluorescent In Situ Hybridization: Shape Analysis and Objective Morphometry1

P. Bray-Ward, D. Ward, R. Demir, 2003, Biology of reproduction.

Genomic structure, chromosomal mapping, and promoter region analysis of murine uridine phosphorylase gene.

P. Bray-Ward, F. Wang, D. Cao, 1999, Cancer research.

Region Analysis of Murine Uridine Phosphorylase Gene Genomic Structure , Chromosomal Mapping , and Promoter Updated

P. Bray-Ward, D. Cao, R. Handschumacher, 1999 .

Amplification de signal par sondes i lollipop /i

P. Bray-Ward, D. Ward, M. J. Lane, 2001 .

Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010, American journal of medical genetics. Part C, Seminars in medical genetics.

Common Genetic Variants Found in HLA and KIR Immune Genes in Autism Spectrum Disorder

P. Bray-Ward, D. Ward, L. Croen, 2016, Front. Neurosci..

Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood.

C. Reynolds, J. Sklar, P. Bray-Ward, 1995, Blood.

Small Marker Chromosome Identification in Metaphase and Interphase Using Centromeric Multiplex FISH (CM-FISH)

P. Bray-Ward, D. Ward, S. Artan, 2001, Laboratory Investigation.

Region-specific YAC banding and painting probes for comparative genome mapping: implications for the evolution of human chromosome 2

P. Bray-Ward, T. Haaf, 1996, Chromosoma.

Genome Rearrangements Detected by SNP Microarrays in Individuals with Intellectual Disability Referred with Possible Williams Syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010, PloS one.

A novel nucleic acid-binding protein that interacts with human rad51 recombinase.

P. Bray-Ward, D. Ward, E. Golub, 1997, Nucleic acids research.

18 Immune Dysfunction in Autism Spectrum Disorder

P. Bray-Ward, J. Westover, A. Torres, 2018 .

Immune Dysfunction in Autism Spectrum Disorder

P. Bray-Ward, J. Westover, A. Torres, 2011 .

The human HNRPD locus maps to 4q21 and encodes a highly conserved protein.

P. Bray-Ward, A. DePace, N. Maizels, 1998, Genomics.

Custom fluorescent-nucleotide synthesis as an alternative method for nucleic acid labeling

P. Bray-Ward, D. Ward, O. Henegariu, 2000, Nature Biotechnology.

Simultaneous detection of microsatellite repeats and SNPs in the macrophage migration inhibitory factor (MIF) gene by thin-film biosensor chips and application to rural field studies

Sung-Hwan Park, Insoo Kang, Lin Leng, 2005, Nucleic acids research.

Characteristics of three homologous 202 genes (Ifi202a, Ifi202b, and Ifi202c) from the murine interferon-activatable gene 200 cluster.

P. Bray-Ward, P. Lengyel, C. Liu, 1999, Genomics.

Inversion Common Polymorphism of the Williams Found Syndrome More Region Frequently Is a in Parents of Children With Williams Syndrome

C. Mervis, P. Bray-Ward, C. Morris, 2010 .

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

P. Bray-Ward, D. Ward, J. Wienberg, 1996, Human molecular genetics.

Emergence of the ZNF91 Krüppel-associated box-containing zinc finger gene family in the last common ancestor of anthropoidea.

P. Bray-Ward, D. Ward, J. Martial, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Visualization of oligonucleotide probes and point mutations in interphase nuclei and DNA fibers using rolling circle DNA amplification

D C Ward, P. Lizardi, Xiaohua Huang, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Colour-changing karyotyping: an alternative to M-FISH/SKY

P. Bray-Ward, D. Ward, N. Heerema, 1999, Nature Genetics.

Cryptic Translocation Identification in Human and Mouse Using Several Telomeric Multiplex FISH (TM-FISH) Strategies

J. Korenberg, P. Bray-Ward, D. Ward, 2001, Laboratory Investigation.

A transcription map of the major histocompatibility complex (MHC) class I region.

S. Weissman, P. Bray-Ward, J. Pan, 1996, Genomics.

Cloning, Characterization, and Chromosomal Mapping of a Human Electroneutral Na+-driven Cl-HCO3Exchanger*

P. Bray-Ward, W. Boron, J. Russell, 2001, The Journal of Biological Chemistry.

Simple method for preparation of fluor/hapten-labeled dUTP.

P. Bray-Ward, D. Ward, O. Henegariu, 2000, BioTechniques.

Characterization of the human myeloid leukemia‐derived cell line GF‐D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization

S. Scherer, P. Bray-Ward, L. Kearney, 1999, Genes, chromosomes & cancer.

Rapid DNA fiber technique for size measurements of linear and circular DNA probes.

P. Bray-Ward, D. Ward, M. State, 2001, BioTechniques.

FISH-Mapped CEPH YACs spanning 0 to 46 cM on human chromosome 6.

J. Weissenbach, D. Paslier, P. Bray-Ward, 1996, Genomics.

UKCCCR guidelines for the use of cell lines in cancer research

T. Thangarajah, M. Hattori, N. Saitou, 1999, Cytogenetic and Genome Research.

Assignment1 of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1→p23.3 and murine 5B by in situ hybridization

P. Bray-Ward, P. Gallagher, N. Manjunath, 1999, Cytogenetic and Genome Research.

Molecular Cloning of a Zinc Finger Gene eZNF from a Human Inner Ear cDNA Library, and In Situ Expression Pattern of Its Mouse Homologue In Mouse Inner Ear

P. Bray-Ward, R. Kandpal, A. Jacob, 1998, Somatic cell and molecular genetics.

Genomic localization of the human gene for KCNA10, a cGMP-activated K channel.

P. Bray-Ward, G. Desir, M. Curran, 1997, Genomics.

CEPH viewer: a client-server database to browse and manipulate CEPH physical mapping and linkage data.

P. Bray-Ward, P. Nadkarni, 1995, Genomics.