P. Warburton

发表

Analysis of the largest tandemly repeated DNA families in the human genome

P. Warburton, Dan Hasson, Flavia Guillem, 2008, BMC Genomics.

Interhomologue sequence variation of alpha satellite DNA from human chromosome 17: Evidence for concerted evolution along haplotypic lineages

Huntington F. Willard, Peter E. Warburton, H. Willard, 1995, Journal of Molecular Evolution.

Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin

H. Willard, P. Warburton, J. Waye, 1993 .

PCR amplification of tandemly repeated DNA: analysis of intra- and interchromosomal sequence variation and homologous unequal crossing-over in human alpha satellite DNA.

H. Willard, P. Warburton, 1992, Nucleic acids research.

Pulsed-field and two-dimensional gel electrophoresis of long arrays of tandemly repeated DNA : analysis of human centromeric alpha satellite.

H. Willard, P. Warburton, R. Wevrick, 1992, Methods in molecular biology.

Integration of human α-satellite DNA into simian chromosomes: Centromere protein binding and disruption of normal chromosome segregation

H. Willard, P. Warburton, T. Haaf, 1992, Cell.

Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin

H. Willard, P. Warburton, J. Waye, 1993, Molecular and cellular biology.

Chromosomal dynamics of human neocentromere formation

P. Warburton, 2004, Chromosome Research.

Analysis of Transposon Interruptions Suggests Selection for L1 Elements on the X Chromosome

P. Warburton, György Abrusán, J. Giordano, 2008, PLoS genetics.

Centromeres, CENP-B and Tigger too.

P. Warburton, D. Kipling, Peter E. Warburton, 1997, Trends in genetics : TIG.

Tetrasomy 15q26: a distinct syndrome or Shprintzen-Goldberg syndrome phenocopy?

K. Hirschhorn, L. Ala‐Kokko, P. Warburton, 2012, Genetics in Medicine.

Chromosome engineering: prospects for gene therapy

P. Warburton, B. Grimes, C. Farr, 2002, Gene Therapy.

Biased Distributions and Decay of Long Interspersed Nuclear Elements in the Chicken Genome

H. Krambeck, P. Warburton, György Abrusán, 2008, Genetics.

Transmission of a fully functional human neocentromere through three generations.

C. Tyler-Smith, G. Gimelli, W. Earnshaw, 1999, American journal of human genetics.

Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.

P. Warburton, M. I. Melaragno, W. Berkofsky-Fessler, 2002, American journal of medical genetics.

A neocentromere in the DAZ region of the human Y chromosome

C. Tyler-Smith, G. Gimelli, W. Earnshaw, 2000, Chromosoma.

Neocentric X-chromosome in a girl with Turner-like syndrome

P. Warburton, M. Hemmat, Boris T Wang, 2012, Molecular Cytogenetics.

Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.

P. Warburton, M. Velinov, S. Brooks, 2004, Annales de genetique.

Providing a little stability

P. Warburton, D. Kipling, 1997, Nature.

Human centromere structure: organization and potential role of alpha satellite DNA.

H. Willard, P. Warburton, R. Wevrick, 1989, Progress in clinical and biological research.

Characterization of a neocentric supernumerary marker chromosome originating from the Xp distal region by FISH, CENP-C staining, and array CGH

P. Warburton, S. Yu, D. Barbouth, 2007, Cytogenetic and Genome Research.

CP248, a derivative of exisulind, causes growth inhibition, mitotic arrest, and abnormalities in microtubule polymerization in glioma cells.

J. Bruce, P. Warburton, I. Weinstein, 2002, Molecular cancer therapeutics.

CP 248 , a Derivative of Exisulind , Causes Growth Inhibition , Mitotic Arrest , and Abnormalities in Microtubule Polymerization in Glioma Cells 1

J. Bruce, P. Warburton, I. Weinstein, 2002 .

Recombineering linear DNA that replicate stably in E. coli.

P. Warburton, N. Ravin, Y. Ooi, 2008, Plasmid.

Untangling the role of DNA topoisomerase II in mitotic chromosome structure and function.

W. Earnshaw, P. Warburton, Peter E. Warburton, 1997, BioEssays : news and reviews in molecular, cellular and developmental biology.

PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.

H. Willard, P. Warburton, T. Haaf, 1991, Genomics.

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

Oligonucleotide probes for alpha satellite DNA variants can distinguish homologous chromosomes by FISH.

C. O'keefe, P. Warburton, A. Matera, 1996, Human molecular genetics.

Organization and evolution of an alpha satellite DNA subset shared by human chromosomes 13 and 21

H. Willard, P. Warburton, G. M. Greig, 1993, Journal of Molecular Evolution.

Evolutionary History of Mammalian Transposons Determined by Genome-Wide Defragmentation

Gary Benson, Yevgeniy Gelfand, György Abrusán, 2007, PLoS Comput. Biol..

Inverted repeat structure of the human genome: the X-chromosome contains a preponderance of large, highly homologous inverted repeats that contain testes genes.

Gary Benson, Joti Giordano, G. Benson, 2004, Genome research.

Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome

K. Hirschhorn, P. Warburton, P. Papenhausen, 2001, Cytogenetic and Genome Research.

Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere.

S. Schwartz, N. Spinner, J. Crolla, 2000, American journal of human genetics.

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

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

Mitotic phosphorylation of SUV39H1, a novel component of active centromeres, coincides with transient accumulation at mammalian centromeres.

T. Jenuwein, P. Warburton, L. Aagaard, 2000, Journal of cell science.

Genomic analysis of sequence variation in tandemly repeated DNA. Evidence for localized homogeneous sequence domains within arrays of alpha-satellite DNA.

H. Willard, P. Warburton, P E Warburton, 1990, Journal of molecular biology.

Digital Genotyping of Macrosatellites and Multicopy Genes Reveals Novel Biological Functions Associated with Copy Number Variation of Large Tandem Repeats

A. Sharp, P. Warburton, Dan Hasson, 2014, PLoS genetics.

Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres

C. Tyler-Smith, D. Warburton, K. Sullivan, 1997, Current Biology.

Analysis of Genome Organization and Rearrangements by Pulsed Field Gradient Gel Electrophoresis

Charles R. Cantor, Peter E. Warburton, C. Cantor, 1986 .

Interstitial Deletion of Proximal 8q Including Part of the Centromere from Unbalanced Segregation of a Paternal Deletion/Marker Karyotype with Neocentromere Formation at 8p22

S. Schwartz, P. Warburton, P. Papenhausen, 2011, Cytogenetic and Genome Research.

Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2

Andrew J Sharp, Edward J Hollox, A. Sharp, 2013, European Journal of Human Genetics.

An unstable dicentric Robertsonian translocation in a markedly discordant twin

P. Warburton, J. Milunsky, JM Milunsky, 2002, Clinical genetics.

DNA modification and functional delivery into human cells using Escherichia coli DH10B.

P. Warburton, K. Narayanan, 2003, Nucleic acids research.

Hamster chromosomes containing amplified human α-satellite DNA show delayed sister chromatid separation in the absence of de novo kinetochore formation

P. Warburton, H. Cooke, 1997, Chromosoma.

Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome.

S. Scott, P. Warburton, L. Edelmann, 2010, Human molecular genetics.

Surprising deficiency of CENP-B binding sites in African green monkey alpha-satellite DNA: implications for CENP-B function at centromeres

W. Earnshaw, P. Warburton, I. Goldberg, 1996, Molecular and cellular biology.

Independent centromere formation in a capricious, gene-free domain of chromosome 13q21 in Old World monkeys and pigs

E. Eichler, N. Archidiacono, M. Cardone, 2006, Genome Biology.

Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere--kinetochore complexes.

H. Masumoto, W. Earnshaw, P. Warburton, 2000, Human molecular genetics.

The octamer is the major form of CENP-A nucleosomes at human centromeres

Kevan J. Salimian, P. Warburton, Dan Hasson, 2013, Nature Structural &Molecular Biology.

Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres

P. Warburton, Dan Hasson, György Abrusán, 2007, Genome Biology.

Characterization of a chromosome-specific chimpanzee alpha satellite subset: evolutionary relationship to subsets on human chromosomes.

J Gosden, H. Willard, P. Warburton, 1996, Genomics.

Molecular Dissection of Heteromorphic Regions

P. Warburton, B. Levy, 2004 .

Formation of novel CENP-A domains on tandem repetitive DNA and across chromosome breakpoints on human chromosome 8q21 neocentromeres

P. Warburton, Dan Hasson, P. Papenhausen, 2011, Chromosoma.

Prenatal diagnosis of a karyotypically normal pregnancy in a mother with a supernumerary neocentric 13q21 → 13q22 chromosome and balancing reciprocal deletion

P. Warburton, J. Engelen, A. C. Knegt, 2003, Prenatal diagnosis.

Making CENs of mammalian artificial chromosomes.

P. Warburton, 1999, Molecular genetics and metabolism.

Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.

P. Warburton, K. Yoda, R. Mahmood, 2003, Human molecular genetics.

Epigenetic analysis of kinetochore assembly on variant human centromeres.

P. Warburton, 2001, Trends in genetics : TIG.

A paucity of heterochromatin at functional human neocentromeres

P. Warburton, Dan Hasson, A. Alonso, 2010, Epigenetics & Chromatin.

A neocentromere derived from a supernumerary marker deleted from the long arm of chromosome 6

P. Warburton, J. Bartley, N. Qin, 2007, Cytogenetic and Genome Research.

Chromosome 13q neocentromeres: molecular cytogenetic characterization of three additional cases and clinical spectrum.

K. Hirschhorn, P. Warburton, R. Mahmood, 2002, American journal of medical genetics.

Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant

H. Willard, K. Oegema, K. Sullivan, 2013, Chromosome Research.

Duplication of the ZIC2 gene is not associated with holoprosencephaly

V. Jobanputra, P. Warburton, B. Levy, 2012, American journal of medical genetics. Part A.

Journey Across the Western Interior of Australia

P. Warburton, H. Bates, C. Eden, 1875 .

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

K. Hirschhorn, V. Tonk, P. Warburton, 2002, American journal of medical genetics.

Centromeric heterochromatin comes clean with DNA methylation

P. Warburton, 2004, Nature Methods.

Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis

Stephen C. J. Parker, James T. Elder, L. Vissers, 2023, Nature Genetics.

Long-Read DNA Sequencing: Recent Advances and Remaining Challenges.

R. Sebra, P. Warburton, 2023, Annual review of genomics and human genetics.

Duplication of the ZIC2 gene is not associated with holoprosencephaly

V. Jobanputra, P. Warburton, B. Levy, 2012, American journal of medical genetics. Part A.

Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant

H. Willard, K. Oegema, K. Sullivan, 2013, Chromosome Research.