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Barbara Trask

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Rudd M Katharine; Endicott Raelynn M; Friedman Cynthia; Walker Megan; Young Janet M; Osoegawa Kazutoyo; de Jong Pieter J; Green Eric D; Trask Barbara J
Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event.
De Bustos Cecilia; Ramos Edward; Young Janet M; Tran Robert K; Menzel Uwe; Langford Cordelia F; Eichler Evan E; Hsu Li; Henikoff Steve; Dumanski Jan P; Trask Barbara J
Tissue-specific variation in DNA methylation levels along human chromosome 1.
Young Janet M; Endicott Raelynn M; Parghi Sean S; Walker Megan; Kidd Jeffrey M; Trask Barbara J
Extensive copy-number variation of the human olfactory receptor gene family.

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All Publications

2009: Rudd M Katharine; Endicott Raelynn M; Friedman Cynthia; Walker Megan; Young Janet M; Osoegawa Kazutoyo; de Jong Pieter J; Green Eric D; Trask Barbara J
Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event.
Genome research 2009;19(1):33-41.
2009: De Bustos Cecilia; Ramos Edward; Young Janet M; Tran Robert K; Menzel Uwe; Langford Cordelia F; Eichler Evan E; Hsu Li; Henikoff Steve; Dumanski Jan P; Trask Barbara J
Tissue-specific variation in DNA methylation levels along human chromosome 1.
Epigenetics & chromatin 2009;2(1):7.
2008: Young Janet M; Endicott Raelynn M; Parghi Sean S; Walker Megan; Kidd Jeffrey M; Trask Barbara J
Extensive copy-number variation of the human olfactory receptor gene family.
American journal of human genetics 2008;83(2):228-42.
2008: Holcomb Ilona N; Grove Douglas I; Kinnunen Martin; Friedman Cynthia L; Gallaher Ian S; Morgan Todd M; Sather Cassandra L; Delrow Jeffrey J; Nelson Peter S; Lange Paul H; Ellis William J; True Lawrence D; Young Janet M; Hsu Li; Trask Barbara J; Vessella Robert L
Genomic alterations indicate tumor origin and varied metastatic potential of disseminated cells from prostate cancer patients.
Cancer research 2008;68(14):5599-608.
2008: Raphael Benjamin J; Volik Stanislav; Yu Peng; Wu Chunxiao; Huang Guiqing; Linardopoulou Elena V; Trask Barbara J; Waldman Frederic; Costello Joseph; Pienta Kenneth J; Mills Gordon B; Bajsarowicz Krystyna; Kobayashi Yasuko; Sridharan Shivaranjani; Paris Pamela L; Tao Quanzhou; Aerni Sarah J; Brown Raymond P; Bashir Ali; Gray Joe W; Cheng Jan-Fang; de Jong Pieter; Nefedov Mikhail; Ried Thomas; Padilla-Nash Hesed M; Collins Colin C
A sequence-based survey of the complex structural organization of tumor genomes.
Genome biology 2008;9(3):R59.
2007: Linardopoulou Elena V; Parghi Sean S; Friedman Cynthia; Osborn Gregory E; Parkhurst Susan M; Trask Barbara J
Human subtelomeric WASH genes encode a new subclass of the WASP family.
PLoS genetics 2007;3(12):e237.
2007: Young Janet M; Trask Barbara J
V2R gene families degenerated in primates, dog and cow, but expanded in opossum.
Trends in genetics : TIG 2007;23(5):212-5.
2007: Rudd M Katharine; Friedman Cynthia; Parghi Sean S; Linardopoulou Elena V; Hsu Li; Trask Barbara J
Elevated rates of sister chromatid exchange at chromosome ends.
PLoS genetics 2007;3(2):e32.
2005: Linardopoulou Elena V; Williams Eleanor M; Fan Yuxin; Friedman Cynthia; Young Janet M; Trask Barbara J
Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication.
Nature 2005;437(7055):94-100.
2005: Rowen Lee; Williams Eleanor; Glusman Gustavo; Linardopoulou Elena; Friedman Cynthia; Ahearn Mary Ellen; Seto Jason; Boysen Cecilie; Qin Shizhen; Wang Kai; Kaur Amardeep; Bloom Scott; Hood Leroy; Trask Barbara J
Interchromosomal segmental duplications explain the unusual structure of PRSS3, the gene for an inhibitor-resistant trypsinogen.
Molecular biology and evolution 2005;22(8):1712-20.
2005: Young Janet M; Kambere Marijo; Trask Barbara J; Lane Robert P
Divergent V1R repertoires in five species: Amplification in rodents, decimation in primates, and a surprisingly small repertoire in dogs.
Genome research 2005;15(2):231-40.
2004: Loo Lenora W M; Grove Douglas I; Williams Eleanor M; Neal Cassandra L; Cousens Laura A; Schubert Elizabeth L; Holcomb Ilona N; Massa Hillary F; Glogovac Jeri; Li Christopher I; Malone Kathleen E; Daling Janet R; Delrow Jeffrey J; Trask Barbara J; Hsu Li; Porter Peggy L
Array comparative genomic hybridization analysis of genomic alterations in breast cancer subtypes.
Cancer research 2004;64(23):8541-9.
2004: Sebat Jonathan; Lakshmi B; Troge Jennifer; Alexander Joan; Young Janet; Lundin Pär; Månér Susanne; Massa Hillary; Walker Megan; Chi Maoyen; Navin Nicholas; Lucito Robert; Healy John; Hicks James; Ye Kenny; Reiner Andrew; Gilliam T Conrad; Trask Barbara; Patterson Nick; Zetterberg Anders; Wigler Michael
Large-scale copy number polymorphism in the human genome.
Science (New York, N.Y.) 2004;305(5683):525-8.
2004: Lane Robert P; Young Janet; Newman Tera; Trask Barbara J
Species specificity in rodent pheromone receptor repertoires.
Genome research 2004;14(4):603-8.
2003: Newman Tera; Trask Barbara J
Complex evolution of 7E olfactory receptor genes in segmental duplications.
Genome research 2003;13(5):781-93.
2003: Young Janet M; Shykind Benjamin M; Lane Robert P; Tonnes-Priddy Lori; Ross Joseph A; Walker Megan; Williams Eleanor M; Trask Barbara J
Odorant receptor expressed sequence tags demonstrate olfactory expression of over 400 genes, extensive alternate splicing and unequal expression levels.
Genome biology 2003;4(11):R71.
2002: Fan Yuxin; Newman Tera; Linardopoulou Elena; Trask Barbara J
Gene content and function of the ancestral chromosome fusion site in human chromosome 2q13-2q14.1 and paralogous regions.
Genome research 2002;12(11):1663-72.
2002: Fan Yuxin; Linardopoulou Elena; Friedman Cynthia; Williams Eleanor; Trask Barbara J
Genomic structure and evolution of the ancestral chromosome fusion site in 2q13-2q14.1 and paralogous regions on other human chromosomes.
Genome research 2002;12(11):1651-62.
2002: Trask Barbara J
Human cytogenetics: 46 chromosomes, 46 years and counting.
Nature reviews. Genetics 2002;3(10):769-78.
2002: Sultana Razia; Yu Chang-En; Yu Jun; Munson Jeffery; Chen Donghui; Hua Wenhui; Estes Annette; Cortes Fanny; de la Barra Flora; Yu Dongmei; Haider Syed T; Trask Barbara J; Green Eric D; Raskind Wendy H; Disteche Christine M; Wijsman Ellen; Dawson Geraldine; Storm Daniel R; Schellenberg Gerard D; Villacres Enrique C
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Genomics 2002;80(2):129-34.
2002: Gygi Melanie P; Ferguson Mark D; Mefford Heather C; Lund Kevin P; O'Day Christine; Zhou Peiwen; Friedman Cynthia; van den Engh Ger; Stolowitz Mark L; Trask Barbara J
Use of fluorescent sequence-specific polyamides to discriminate human chromosomes by microscopy and flow cytometry.
Nucleic acids research 2002;30(13):2790-9.
2002: Tanaka Hisashi; Tapscott Stephen J; Trask Barbara J; Yao Meng-Chao
Short inverted repeats initiate gene amplification through the formation of a large DNA palindrome in mammalian cells.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(13):8772-7.
2002: Young Janet M; Trask Barbara J
The sense of smell: genomics of vertebrate odorant receptors.
Human molecular genetics 2002;11(10):1153-60.
2002: Young Janet M; Friedman Cynthia; Williams Eleanor M; Ross Joseph A; Tonnes-Priddy Lori; Trask Barbara J
Different evolutionary processes shaped the mouse and human olfactory receptor gene families.
Human molecular genetics 2002;11(5):535-46.
2002: Mefford Heather C; Trask Barbara J
The complex structure and dynamic evolution of human subtelomeres.
Nature reviews. Genetics 2002;3(2):91-102.
2002: Lane Robert P; Roach Jared C; Lee Inyoul Y; Boysen Cecilie; Smit Arian; Trask Barbara J; Hood Leroy
Genomic analysis of the olfactory receptor region of the mouse and human T-cell receptor alpha/delta loci.
Genome research 2002;12(1):81-7.
2002: Lane Robert P; Cutforth Tyler; Axel Richard; Hood Leroy; Trask Barbara J
Sequence analysis of mouse vomeronasal receptor gene clusters reveals common promoter motifs and a history of recent expansion.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(1):291-6.
2001: Kouros-Mehr H; Pintchovski S; Melnyk J; Chen Y J; Friedman C; Trask B; Shizuya H
Identification of non-functional human VNO receptor genes provides evidence for vestigiality of the human VNO.
Chemical senses 2001;26(9):1167-74.
2001: Linardopoulou E; Mefford H C; Nguyen O; Friedman C; van den Engh G; Farwell D G; Coltrera M; Trask B J
Transcriptional activity of multiple copies of a subtelomerically located olfactory receptor gene that is polymorphic in number and location.
Human molecular genetics 2001;10(21):2373-83.
2001: Mefford H C; Linardopoulou E; Coil D; van den Engh G; Trask B J
Comparative sequencing of a multicopy subtelomeric region containing olfactory receptor genes reveals multiple interactions between non-homologous chromosomes.
Human molecular genetics 2001;10(21):2363-72.
2001: Lane R P; Cutforth T; Young J; Athanasiou M; Friedman C; Rowen L; Evans G; Axel R; Hood L; Trask B J
Genomic analysis of orthologous mouse and human olfactory receptor loci.
Proceedings of the National Academy of Sciences of the United States of America 2001;98(13):7390-5.
2001: Bailey J A; Yavor A M; Massa H F; Trask B J; Eichler E E
Segmental duplications: organization and impact within the current human genome project assembly.
Genome research 2001;11(6):1005-17.
2000: Giorgi D; Friedman C; Trask B J; Rouquier S
Characterization of nonfunctional V1R-like pheromone receptor sequences in human.
Genome research 2000;10(12):1979-85.
2000: Siegel A F; van den Engh G; Hood L; Trask B; Roach J C
Modeling the feasibility of whole genome shotgun sequencing using a pairwise end strategy.
Genomics 2000;68(3):237-46.
2000: Singer M J; Mesner L D; Friedman C L; Trask B J; Hamlin J L
Amplification of the human dihydrofolate reductase gene via double minutes is initiated by chromosome breaks.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(14):7921-6.
2000: Lin B; White J T; Ferguson C; Bumgarner R; Friedman C; Trask B; Ellis W; Lange P; Hood L; Nelson P S
PART-1: a novel human prostate-specific, androgen-regulated gene that maps to chromosome 5q12.
Cancer research 2000;60(4):858-63.
2000: Deng Y; Madan A; Banta A B; Friedman C; Trask B J; Hood L; Li L
Characterization, chromosomal localization, and the complete 30-kb DNA sequence of the human Jagged2 (JAG2) gene.
Genomics 2000;63(1):133-8.
1999: Roach J C; Siegel A F; van den Engh G; Trask B; Hood L
Gaps in the Human Genome Project.
Nature 1999;401(6756):843-5.
1999: Yokota H; Fung K; Trask B J; van den Engh G; Sarikaya M; Aebersold R
Sharp DNA bends as landmarks of protein-binding sites on straightened DNA.
Analytical chemistry 1999;71(9):1663-7.
1999: DeSilva U; Massa H; Trask B J; Green E D
Comparative mapping of the region of human chromosome 7 deleted in williams syndrome.
Genome research 1999;9(5):428-36.
1999: Siegel A F; Trask B; Roach J C; Mahairas G G; Hood L; van den Engh G
Analysis of sequence-tagged-connector strategies for DNA sequencing.
Genome research 1999;9(3):297-307.
1999: Brand-Arpon V; Rouquier S; Massa H; de Jong P J; Ferraz C; Ioannou P A; Demaille J G; Trask B J; Giorgi D
A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13.
Genomics 1999;56(1):98-110.
1999: Katz S G; Schneider S S; Bartuski A; Trask B J; Massa H; Overhauser J; Lalande M; Lansdorp P M; Silverman G A
An 18q- syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA.
Human molecular genetics 1999;8(1):87-92.
1999: Vissinga C S; Yeo T C; Woessner J; Massa H F; Wilson R K; Trask B J; Concannon P
Identification, characterization, and mapping of a mouse homolog of the gene mutated in Nijmegen breakage syndrome.
Cytogenetics and cell genetics 1999;87(1-2):80-4.
1998: Bartuski A J; Kamachi Y; Schick C; Massa H; Trask B J; Silverman G A
A murine ortholog of the human serpin SCCA2 maps to chromosome 1 and inhibits chymotrypsin-like serine proteinases.
Genomics 1998;54(2):297-306.
1998: Trask B J; Massa H; Brand-Arpon V; Chan K; Friedman C; Nguyen O T; Eichler E; van den Engh G; Rouquier S; Shizuya H; Giorgi D
Large multi-chromosomal duplications encompass many members of the olfactory receptor gene family in the human genome.
Human molecular genetics 1998;7(13):2007-20.
1998: Yokota H; Nickerson D A; Trask B J; van den Engh G; Hirst M; Sadowski I; Aebersold R
Mapping a protein-binding site on straightened DNA by atomic force microscopy.
Analytical biochemistry 1998;264(2):158-64.
1998: Meng X; Lu X; Li Z; Green E D; Massa H; Trask B J; Morris C A; Keating M T
Complete physical map of the common deletion region in Williams syndrome and identification and characterization of three novel genes.
Human genetics 1998;103(5):590-9.
1998: Rouquier S; Friedman C; Delettre C; van den Engh G; Blancher A; Crouau-Roy B; Trask B J; Giorgi D
A gene recently inactivated in human defines a new olfactory receptor family in mammals.
Human molecular genetics 1998;7(9):1337-45.
1998: Li L; Huang G M; Banta A B; Deng Y; Smith T; Dong P; Friedman C; Chen L; Trask B J; Spies T; Rowen L; Hood L
Cloning, characterization, and the complete 56.8-kilobase DNA sequence of the human NOTCH4 gene.
Genomics 1998;51(1):45-58.
1998: Chaudhary P M; Ferguson C; Nguyen V; Nguyen O; Massa H F; Eby M; Jasmin A; Trask B J; Hood L; Nelson P S
Cloning and characterization of two Toll/Interleukin-1 receptor-like genes TIL3 and TIL4: evidence for a multi-gene receptor family in humans.
Blood 1998;91(11):4020-7.
1998: La Spada A R; Peterson K R; Meadows S A; McClain M E; Jeng G; Chmelar R S; Haugen H A; Chen K; Singer M J; Moore D; Trask B J; Fischbeck K H; Clegg C H; McKnight G S
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability.
Human molecular genetics 1998;7(6):959-67.
1998: Rouquier S; Taviaux S; Trask B J; Brand-Arpon V; van den Engh G; Demaille J; Giorgi D
Distribution of olfactory receptor genes in the human genome.
Nature genetics 1998;18(3):243-50.
1998: Thai T H; Du F; Tsan J T; Jin Y; Phung A; Spillman M A; Massa H F; Muller C Y; Ashfaq R; Mathis J M; Miller D S; Trask B J; Baer R; Bowcock A M
Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers.
Human molecular genetics 1998;7(2):195-202.
1998: Sharma V; Poorkaj P; Hisama F; Bonnycastle L; Yu C E; Massa H; Trask B; Clancy K P; Patterson D; Weissman S M; Schellenberg G D
An expression map from human chromosome 14q24.3.
Genomics 1998;47(2):314-8.
1998: Li L; Milner L A; Deng Y; Iwata M; Banta A; Graf L; Marcovina S; Friedman C; Trask B J; Hood L; Torok-Storb B
The human homolog of rat Jagged1 expressed by marrow stroma inhibits differentiation of 32D cells through interaction with Notch1.
Immunity 1998;8(1):43-55.
1998: Trask B J; Friedman C; Martin-Gallardo A; Rowen L; Akinbami C; Blankenship J; Collins C; Giorgi D; Iadonato S; Johnson F; Kuo W L; Massa H; Morrish T; Naylor S; Nguyen O T; Rouquier S; Smith T; Wong D J; Youngblom J; van den Engh G
Members of the olfactory receptor gene family are contained in large blocks of DNA duplicated polymorphically near the ends of human chromosomes.
Human molecular genetics 1998;7(1):13-26.
1997: Han D K; Chaudhary P M; Wright M E; Friedman C; Trask B J; Riedel R T; Baskin D G; Schwartz S M; Hood L
MRIT, a novel death-effector domain-containing protein, interacts with caspases and BclXL and initiates cell death.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(21):11333-8.
1997: Mefford H; van den Engh G; Friedman C; Trask B J
Analysis of the variation in chromosome size among diverse human populations by bivariate flow karyotyping.
Human genetics 1997;100(1):138-44.
1997: Li L; Krantz I D; Deng Y; Genin A; Banta A B; Collins C C; Qi M; Trask B J; Kuo W L; Cochran J; Costa T; Pierpont M E; Rand E B; Piccoli D A; Hood L; Spinner N B
Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1.
Nature genetics 1997;16(3):243-51.
1997: Yokota H; Singer M J; van den Engh G J; Trask B J
Regional differences in the compaction of chromatin in human G0/G1 interphase nuclei.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1997;5(3):157-66.
1997: Geier S J; Algate P A; Carlberg K; Flowers D; Friedman C; Trask B; Rohrschneider L R
The human SHIP gene is differentially expressed in cell lineages of the bone marrow and blood.
Blood 1997;89(6):1876-85.
1997: Yokota H; Johnson F; Lu H; Robinson R M; Belu A M; Garrison M D; Ratner B D; Trask B J; Miller D L
A new method for straightening DNA molecules for optical restriction mapping.
Nucleic acids research 1997;25(5):1064-70.
1997: Wise C A; Clines G A; Massa H; Trask B J; Lovett M
Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.
Genome research 1997;7(1):10-6.
1997: Lanyi A; Li B; Li S; Talmadge C B; Brichacek B; Davis J R; Kozel B A; Trask B; van den Engh G; Uzvolgyi E; Stanbridge E J; Nelson D L; Chinault C; Heslop H; Gross T G; Seemayer T A; Klein G; Purtilo D T; Sumegi J
A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
Genomics 1997;39(1):55-65.
1996: Trask B J; Mefford H; van den Engh G; Massa H F; Juyal R C; Potocki L; Finucane B; Abuelo D N; Witt D R; Magenis E; Baldini A; Greenberg F; Lupski J R; Patel P I
Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients.
Human genetics 1996;98(6):710-8.
1996: Yu C E; Oshima J; Hisama F M; Matthews S; Trask B J; Schellenberg G D
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Genomics 1996;35(3):431-40.
1996: Gorski J L; Bialecki M D; McDonald M T; Massa H F; Trask B J; Burright E N
Cosmids map two incontinentia pigmenti type 1 (IP1) translocation breakpoints to a 180-kb region within a 1.2-Mb YAC contig.
Genomics 1996;35(2):338-45.
1995: Bryson G L; Massa H; Trask B J; Van Etten R L
Gene structure, sequence, and chromosomal localization of the human red cell-type low-molecular-weight acid phosphotyrosyl phosphatase gene, ACP1.
Genomics 1995;30(2):133-40.
1995: Rouquier S; Trask B J; Taviaux S; van den Engh G; Diriong S; Lennon G G; Giorgi D
Direct selection of cDNAs using whole chromosomes.
Nucleic acids research 1995;23(21):4415-20.
1995: Juyal R C; Greenberg F; Mengden G A; Lupski J R; Trask B J; van den Engh G; Lindsay E A; Christy H; Chen K S; Baldini A
Smith-Magenis syndrome deletion: a case with equivocal cytogenetic findings resolved by fluorescence in situ hybridization.
American journal of medical genetics 1995;58(3):286-91.
1995: Yokota H; van den Engh G; Hearst J E; Sachs R K; Trask B J
Evidence for the organization of chromatin in megabase pair-sized loops arranged along a random walk path in the human G0/G1 interphase nucleus.
The Journal of cell biology 1995;130(6):1239-49.
1995: Silverman G A; Schneider S S; Massa H F; Flint A; Lalande M; Leonard J C; Overhauser J; van den Engh G; Trask B J
The 18q- syndrome: analysis of chromosomes by bivariate flow karyotyping and the PCR reveals a successive set of deletion breakpoints within 18q21.2-q22.2.
American journal of human genetics 1995;56(4):926-37.
1995: Sachs R K; van den Engh G; Trask B; Yokota H; Hearst J E
A random-walk/giant-loop model for interphase chromosomes.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(7):2710-4.
1995: Hui S M; Trask B; van den Engh G; Bartuski A J; Smith A; Flint A; Lalande M; Silverman G A
Analysis of randomly amplified flow-sorted chromosomes using the polymerase chain reaction.
Genomics 1995;26(2):364-71.
1995: Yokota H; van den Engh G; Mostert M; Trask B J
Treatment of cells with alkaline borate buffer extends the capability of interphase FISH mapping.
Genomics 1995;25(2):485-91.
1995: Wilson A C; Parrish J E; Massa H F; Nelson D L; Trask B J; Herr W
The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney.
Genomics 1995;25(2):462-8.
1995: Martin-Gallardo A; Lamerdin J; Sopapan P; Friedman C; Fertitta A L; Garcia E; Carrano A; Negorev D; Macina R A; Trask B J
Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution.
Cytogenetics and cell genetics 1995;71(3):289-95.
1994: Bonnycastle L L; Yu C E; Hunt C R; Trask B J; Clancy K P; Weber J L; Patterson D; Schellenberg G D
Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).
Genomics 1994;23(1):85-93.
1993: Malo D; Gros P; Bergmann A; Trask B; Mohrenweiser H W; Canfield V A; Levenson R
Genes encoding the H,K-ATPase alpha and Na,K-ATPase alpha 3 subunits are linked on mouse chromosome 7 and human chromosome 19.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(11):644-9.
1993: Roa B B; Garcia C A; Pentao L; Killian J M; Trask B J; Suter U; Snipes G J; Ortiz-Lopez R; Shooter E M; Patel P I; Lupski J R
Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A.
Nature genetics 1993;5(2):189-94.
1993: Rouquier S; Giorgi D; Trask B; Bergmann A; Phillips M S; MacLennan D H; de Jong P
A cosmid and yeast artificial chromosome contig containing the complete ryanodine receptor (RYR1) gene.
Genomics 1993;17(2):330-40.
1993: Pasteris N G; Trask B J; Sheldon S; Gorski J L
Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35.
Human molecular genetics 1993;2(7):953-9.
1993: Trask B; Fertitta A; Christensen M; Youngblom J; Bergmann A; Copeland A; de Jong P; Mohrenweiser H; Olsen A; Carrano A
Fluorescence in situ hybridization mapping of human chromosome 19: cytogenetic band location of 540 cosmids and 70 genes or DNA markers.
Genomics 1993;15(1):133-45.
1993: Trask B J; Allen S; Massa H; Fertitta A; Sachs R; van den Engh G; Wu M
Studies of metaphase and interphase chromosomes using fluorescence in situ hybridization.
Cold Spring Harbor symposia on quantitative biology 1993;58():767-75.
1992: McCabe E R; Towbin J A; van den Engh G; Trask B J
Xp21 contiguous gene syndromes: deletion quantitation with bivariate flow karyotyping allows mapping of patient breakpoints.
American journal of human genetics 1992;51(6):1277-85.
1992: Hendricks-Taylor L R; Bachinski L L; Siciliano M J; Fertitta A; Trask B; de Jong P J; Ledbetter D H; Darlington G J
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1.
Genomics 1992;14(1):12-7.
1992: van den Engh G; Sachs R; Trask B J
Estimating genomic distance from DNA sequence location in cell nuclei by a random walk model.
Science (New York, N.Y.) 1992;257(5075):1410-2.
1992: Trask B; Christensen M; Fertitta A; Bergmann A; Ashworth L; Branscomb E; Carrano A; Van Den Engh G
Fluorescence in situ hybridization mapping of human chromosome 19: mapping and verification of cosmid contigs formed by random restriction enzyme fingerprinting.
Genomics 1992;14(1):162-7.
1992: Guzzetta V; Franco B; Trask B J; Zhang H; Saucedo-Cardenas O; Montes de Oca-Luna R; Greenberg F; Chinault A C; Lupski J R; Patel P I
Somatic cell hybrids, sequence-tagged sites, simple repeat polymorphisms, and yeast artificial chromosomes for physical and genetic mapping of proximal 17p.
Genomics 1992;13(3):551-9.
1992: Trask B J; Massa H F; Burmeister M
Fluorescence in situ hybridization establishes the order cen-DXS28(C7)-DXS67(B24)-DXS68(L1)-tel in human chromosome Xp21.3.
Genomics 1992;13(2):455-7.
1992: Patel P I; Roa B B; Welcher A A; Schoener-Scott R; Trask B J; Pentao L; Snipes G J; Garcia C A; Francke U; Shooter E M; Lupski J R; Suter U
The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A.
Nature genetics 1992;1(3):159-65.
1992: Yen R W; Vertino P M; Nelkin B D; Yu J J; el-Deiry W; Cumaraswamy A; Lennon G G; Trask B J; Celano P; Baylin S B
Isolation and characterization of the cDNA encoding human DNA methyltransferase.
Nucleic acids research 1992;20(9):2287-91.
1992: Wilkie T M; Gilbert D J; Olsen A S; Chen X N; Amatruda T T; Korenberg J R; Trask B J; de Jong P; Reed R R; Simon M I
Evolution of the mammalian G protein alpha subunit multigene family.
Nature genetics 1992;1(2):85-91.
1992: Tynan K; Olsen A; Trask B; de Jong P; Thompson J; Zimmermann W; Carrano A; Mohrenweiser H
Assembly and analysis of cosmid contigs in the CEA-gene family region of human chromosome 19.
Nucleic acids research 1992;20(7):1629-36.
1992: Brandriff B F; Gordon L A; Tynan K T; Olsen A S; Mohrenweiser H W; Fertitta A; Carrano A V; Trask B J
Order and genomic distances among members of the carcinoembryonic antigen (CEA) gene family determined by fluorescence in situ hybridization.
Genomics 1992;12(4):773-9.
1992: Schmitz A; Guilly M N; Trask B; van den Engh G
Immunofluorescent labeling of centromeres for flow cytometric analysis.
Cytometry 1992;13(5):478-84.
1991: Kwiatkowski T J; Beaudet A L; Trask B J; Zoghbi H Y
Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels.
Genomics 1991;10(4):921-6.
1991: Franco B; Lai L W; Patterson D; Ledbetter D H; Trask B J; van den Engh G; Iannaccone S; Frances S; Patel P I; Lupski J R
Molecular characterization of a patient with del(1)(q23-q25).
Human genetics 1991;87(3):269-77.
1991: Lupski J R; de Oca-Luna R M; Slaugenhaupt S; Pentao L; Guzzetta V; Trask B J; Saucedo-Cardenas O; Barker D F; Killian J M; Garcia C A; Chakravarti A; Patel P I
DNA duplication associated with Charcot-Marie-Tooth disease type 1A.
Cell 1991;66(2):219-32.
1991: Brandriff B; Gordon L; Trask B
A new system for high-resolution DNA sequence mapping interphase pronuclei.
Genomics 1991;10(1):75-82.
1991: Trask B J; van den Engh G; Christensen M; Massa H F; Gray J W; Van Dilla M
Characterization of somatic cell hybrids by bivariate flow karyotyping and fluorescence in situ hybridization.
Somatic cell and molecular genetics 1991;17(2):117-36.
1991: Trask B J; Massa H; Kenwrick S; Gitschier J
Mapping of human chromosome Xq28 by two-color fluorescence in situ hybridization of DNA sequences to interphase cell nuclei.
American journal of human genetics 1991;48(1):1-15.
1991: Trask B J
DNA sequence localization in metaphase and interphase cells by fluorescence in situ hybridization.
Methods in cell biology 1991;35():3-35.
1991: Brandriff B F; Gordon L A; Trask B J
DNA sequence mapping by fluorescence in situ hybridization.
Environmental and molecular mutagenesis 1991;18(4):259-62.
1990: Gray J W; Kuo W L; Liang J; Pinkel D; van den Engh G; Trask B; Tkachuk D; Waldman F; Westbrook C
Analytical approaches to detection and characterization of disease-linked chromosome aberrations.
Bone marrow transplantation 1990;6 Suppl 1():14-9.
1990: Trask B; van den Engh G; Nussbaum R; Schwartz C; Gray J
Quantification of the DNA content of structurally abnormal X chromosomes and X chromosome aneuploidy using high resolution bivariate flow karyotyping.
Cytometry 1990;11(1):184-95.
1990: van den Engh G; Hanson D; Trask B
A computer program for analyzing bivariate flow karyotypes.
Cytometry 1990;11(1):173-83.
1990: Trask B; Pinkel D
Fluorescence in situ hybridization with DNA probes.
Methods in cell biology 1990;33():383-400.
1990: Trask B; van den Engh G
Chromosome and nuclei isolation with the MgSO4 procedure.
Methods in cell biology 1990;33():363-7.
1989: Trask B; van den Engh G; Gray J W
Inheritance of chromosome heteromorphisms analyzed by high-resolution bivariate flow karyotyping.
American journal of human genetics 1989;45(5):753-60.
1989: Trask B; Pinkel D; van den Engh G
The proximity of DNA sequences in interphase cell nuclei is correlated to genomic distance and permits ordering of cosmids spanning 250 kilobase pairs.
Genomics 1989;5(4):710-7.
1989: Trask B; van den Engh G; Mayall B; Gray J W
Chromosome heteromorphism quantified by high-resolution bivariate flow karyotyping.
American journal of human genetics 1989;45(5):739-52.
1989: van Dekken H; Pinkel D; Mullikin J; Trask B; van den Engh G; Gray J
Three-dimensional analysis of the organization of human chromosome domains in human and human-hamster hybrid interphase nuclei.
Journal of cell science 1989;94 ( Pt 2)():299-306.
1989: Merry D E; Lesko J G; Sosnoski D M; Lewis R A; Lubinsky M; Trask B; van den Engh G; Collins F S; Nussbaum R L
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
American journal of human genetics 1989;45(4):530-40.
1989: van Dekken H; Pinkel D; Mullikin J; Trask B; van den Engh G; Gray J
Three dimensional reconstruction of human chromosomes in hybrid and human cell line nuclei using fluorescence in situ hybridization.
Acta histochemica. Supplementband 1989;37():91-4.
1988: Martin A O; Northrup H; Ledbetter D H; Trask B; van den Engh G; Le Beau M M; Beaudet A L; Gray J W; Sekhon G; Krassikoff N
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysis.
American journal of medical genetics 1988;31(3):643-54.
1988: van den Engh G; Trask B; Lansdorp P; Gray J
Improved resolution of flow cytometric measurements of Hoechst- and chromomycin-A3-stained human chromosomes after addition of citrate and sulfite.
Cytometry 1988;9(3):266-70.
1988: Trask B; van den Engh G; Pinkel D; Mullikin J; Waldman F; van Dekken H; Gray J
Fluorescence in situ hybridization to interphase cell nuclei in suspension allows flow cytometric analysis of chromosome content and microscopic analysis of nuclear organization.
Human genetics 1988;78(3):251-9.
1988: Gray J W; Trask B; van den Engh G; Silva A; Lozes C; Grell S; Schonberg S; Yu L C; Golbus M S
Application of flow karyotyping in prenatal detection of chromosome aberrations.
American journal of human genetics 1988;42(1):49-59.
1987: Patterson M; Schwartz C; Bell M; Sauer S; Hofker M; Trask B; van den Engh G; Davies K E
Physical mapping studies on the human X chromosome in the region Xq27-Xqter.
Genomics 1987;1(4):297-306.
1987: Gray J W; Dean P N; Fuscoe J C; Peters D C; Trask B J; van den Engh G J; Van Dilla M A
High-speed chromosome sorting.
Science (New York, N.Y.) 1987;238(4825):323-9.
1986: Pinkel D; Gray J W; Trask B; van den Engh G; Fuscoe J; van Dekken H
Cytogenetic analysis by in situ hybridization with fluorescently labeled nucleic acid probes.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():151-7.
1986: Gray J W; Lucas J; Peters D; Pinkel D; Trask B; van den Engh G; Van Dilla M
Flow karyotyping and sorting of human chromosomes.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():141-9.
1986: van den Engh G J; Trask B J; Gray J W
The binding kinetics and interaction of DNA fluorochromes used in the analysis of nuclei and chromosomes by flow cytometry.
Histochemistry 1986;84(4-6):501-8.
1985: Trask B; van den Engh G; Landegent J; in de Wal N J; van der Ploeg M
Detection of DNA sequences in nuclei in suspension by in situ hybridization and dual beam flow cytometry.
Science (New York, N.Y.) 1985;230(4732):1401-3.
1985: van den Engh G J; Trask B J; Gray J W; Langlois R G; Yu L C
Preparation and bivariate analysis of suspensions of human chromosomes.
Cytometry 1985;6(2):92-100.
1984: van den Engh G; Trask B; Cram S; Bartholdi M
Preparation of chromosome suspensions for flow cytometry.
Cytometry 1984;5(2):108-17.
1984: Trask B; van den Engh G; Gray J; Vanderlaan M; Turner B
Immunofluorescent detection of histone 2B on metaphase chromosomes using flow cytometry.
Chromosoma 1984;90(4):295-302.
1982: Trask B J; van den Engh G J; Elgershuizen J H
Analysis of phytoplankton by flow cytometry.
Cytometry 1982;2(4):258-64.
1981: van den Engh G; Trask B; Visser J
Surface antigens of pluripotent and committed haemopoietic stem cells.
Haematology and blood transfusion 1981;26():305-8.
1980: van den Engh G; Visser J; Bol S; Trask B
Concentration of hemopoietic stem cells using a light-activated cell sorter.
Blood cells 1980;6(4):609-23.

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