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Heinz-Ulrich Weier

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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Co-Publications
Name
15
Fung, Jingly
9
Lersch, Robert
9
Gray, Joe
8
Weier, Jingly
8
Zitzelsberger, Horst
8
Munné, Santiago
7
Pedersen, Roger
6
Chu, Lisa
4
Clark, Orlo
4
Baumgartner, Adolf
4
Hsieh, HB
4
Pinkel, Daniel
4
Duh, Quan-Yang
4
Kim, UJ
4
Duell, Thomas

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Publications

TOP 3
Lu Chun-Mei; Kwan Johnson; Baumgartner Adolf; Weier Jingly F; Wang Mei; Escudero Tomas; Munné Santiago; Zitzelsberger Horst F; Weier Heinz-Ulrich G
DNA probe pooling for rapid delineation of chromosomal breakpoints.
Baumgartner Adolf; Weier Jingly Fung; Weier Heinz-Ulrich G
Chromosome-specific DNA repeat probes.
Weier J F; Ferlatte C; Baumgartner A; Jung C J; Nguyen H-N; Chu L W; Pedersen R A; Fisher S J; Weier H-U G
Molecular cytogenetic studies towards the full karyotype analysis of human blastocysts and cytotrophoblasts.

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All Publications

2009: Lu Chun-Mei; Kwan Johnson; Baumgartner Adolf; Weier Jingly F; Wang Mei; Escudero Tomas; Munné Santiago; Zitzelsberger Horst F; Weier Heinz-Ulrich G
DNA probe pooling for rapid delineation of chromosomal breakpoints.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2009;57(6):587-97.
2006: Baumgartner Adolf; Weier Jingly Fung; Weier Heinz-Ulrich G
Chromosome-specific DNA repeat probes.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2006;54(12):1363-70.
2006: Weier J F; Ferlatte C; Baumgartner A; Jung C J; Nguyen H-N; Chu L W; Pedersen R A; Fisher S J; Weier H-U G
Molecular cytogenetic studies towards the full karyotype analysis of human blastocysts and cytotrophoblasts.
Cytogenetic and genome research 2006;114(3-4):302-11.
2006: Weier H-U G; Tuton T B; Ito Y; Chu L W; Lu C-M; Baumgartner A; Zitzelsberger H F; Weier J F
Molecular cytogenetic characterization of chromosome 9-derived material in a human thyroid cancer cell line.
Cytogenetic and genome research 2006;114(3-4):284-91.
2006: Weier Heinz-Ulrich G; Chu Lisa W
Quantitative DNA fiber mapping in genome research and construction of physical maps.
Methods in molecular biology (Clifton, N.J.) 2006;338():31-57.
2005: Weier Jingly Fung; Weier Heinz-Ulrich G; Nureddin Aida; Pedersen Roger A; Racowsky Catherine
Aneuploidy involving chromosome 1 in failed-fertilized human oocytes is unrelated to maternal age.
Journal of assisted reproduction and genetics 2005;22(7-8):285-93.
2005: Weier Heinz-Ulli G; Weier Jingly F; Renom Maria Oter; Zheng Xuezhong; Colls Pere; Nureddin Aida; Pham Chau D; Chu Lisa W; Racowsky Catherine; Munné Santiago
Fluorescence in situ hybridization and spectral imaging analysis of human oocytes and first polar bodies.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):269-72.
2005: Liehr Thomas; Weier Heinz-Ulli G
14th workshop on fetal cells and fetal DNA.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):253-4.
2005: Breier Adam M; Weier Heinz-Ulrich G; Cozzarelli Nicholas R
Independence of replisomes in Escherichia coli chromosomal replication.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(11):3942-7.
2005: Weier Jingly F; Weier Heinz-Ulrich G; Jung Christine J; Gormley Matthew; Zhou Yan; Chu Lisa W; Genbacev Olga; Wright Alexi A; Fisher Susan J
Human cytotrophoblasts acquire aneuploidies as they differentiate to an invasive phenotype.
Developmental biology 2005;279(2):420-32.
2004: Weier Heinz-Ulli G; Chu Lisa W; Murnane John P; Weier Jingly F
Applications and technical challenges of fluorescence in situ hybridization in stem cell research.
Blood cells, molecules & diseases 2004;32(1):68-76.
2002: Weier Heinz-Ulrich G; Greulich-Bode Karin M; Ito Yuko; Lersch Robert A; Fung Jingly
FISH in cancer diagnosis and prognostication: from cause to course of disease.
Expert review of molecular diagnostics 2002;2(2):109-19.
2002: Liehr T; Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Weier H-U G; Claussen U
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
Cytogenetic and genome research 2002;97(1-2):43-50.
2001: Weier H; Munné S; Lersch R A; Hsieh H; Smida J; Chen X; Korenberg J R; Pedersen R A; Fung J
Towards a full karyotype screening of interphase cells: 'FISH and chip' technology.
Molecular and cellular endocrinology 2001;183 Suppl 1():S41-5.
2001: Hsieh H B; Lersch R A; Callahan D E; Hayward S; Wong M; Clark O H; Weier H U
Monitoring signal transduction in cancer: cDNA microarray for semiquantitative analysis.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(8):1057-8.
2001: Weier H U
DNA fiber mapping techniques for the assembly of high-resolution physical maps.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(8):939-48.
2001: Lersch R A; Fung J; Hsieh H B; Smida J; Weier H U
Monitoring signal transduction in cancer: from chips to fish.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(7):925-6.
2001: Fung J; Weier H U; Pedersen R A
Detection of structural and numerical chromosome abnormalities in interphase cells using spectral imaging.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(6):797-8.
2001: Weier H U; Zitzelsberger H F; Hsieh H B; Sun M V; Wong M; Lersch R A; Yaswen P; Smida J; Kuschnick C; Clark O H
Monitoring signal transduction in cancer: tyrosine kinase gene expression profiling.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2001;49(5):673-4.
2001: Fung J; Munné S; Weier H U
Detection of chromosome translocation products in single interphase cell nuclei.
Methods in cell biology 2001;64():97-114.
2000: Fung J; Weier H U; Goldberg J D; Pedersen R A
Multilocus genetic analysis of single interphase cells by spectral imaging.
Human genetics 2000;107(6):615-22.
2000: Lin S D; Cooper P; Fung J; Weier H U; Rubin E M
Genome scan identifies a locus affecting gamma-globin level in human beta-cluster YAC transgenic mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(11):1024-9.
2000: Hsieh H B; Wang M; Lersch R A; Kim U J; Weier H U
Rational design of landmark probes for quantitative DNA fiber mapping (QDFM).
Nucleic acids research 2000;28(8):E30.
2000: Lersch R A; Fung J; Munné S; Pedersen R A; Weier H U
Case-specific, breakpoint-spanning DNA probes for analysis of single interphase cells.
Genetic testing 2000;4(3):273-8.
2000: Weier H U; George C X; Lersch R A; Breitweser S; Cheng J F; Samuel C E
Assignment of the RNA-specific adenosine deaminase gene (Adar) to mouse chromosome 3F2 by in situ hybridization.
Cytogenetics and cell genetics 2000;89(3-4):214-5.
1999: Gerling M C; Jossart G; Duh Q Y; Weier H U; Clark O H; Young D M
Invasion of human follicular thyroid carcinoma cells in an in vivo invasion model.
Thyroid : official journal of the American Thyroid Association 1999;9(12):1221-6.
1999: Cao Y; Kang H L; Xu X; Wang M; Dho S H; Huh J R; Lee B J; Kalush F; Bocskai D; Ding Y; Tesmer J G; Lee J; Moon E; Jurecic V; Baldini A; Weier H U; Doggett N A; Simon M I; Adams M D; Kim U J
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2.
Genome research 1999;9(8):763-74.
1999: Weier H U; Munné S; Fung J
Patient-specific probes for preimplantation genetic diagnosis of structural and numerical aberrations in interphase cells.
Journal of assisted reproduction and genetics 1999;16(4):182-91.
1999: Fung J; Munné S; Garcia J; Kim U J; Weier H U
Molecular cloning of translocation breakpoints in a case of constitutional translocation t(11;22)(q23;q11) and preparation of probes for preimplantation genetic diagnosis.
Reproduction, fertility, and development 1999;11(1):17-23.
1999: Weier H U; Fung J; Lersch R A
Assignment of protooncogene MERTK (a.k.a. c-mer) to human chromosome 2q14.1 by in situ hybridization.
Cytogenetics and cell genetics 1999;84(1-2):91-2.
1998: Fung J; Moronne M M; Weier H U
Simple blocking system for use with maleimide-labeled nucleic acid probes.
BioTechniques 1998;25(3):390-2, 394.
1998: Nielsen L B; Kahn D; Duell T; Weier H U; Taylor S; Young S G
Apolipoprotein B gene expression in a series of human apolipoprotein B transgenic mice generated with recA-assisted restriction endonuclease cleavage-modified bacterial artificial chromosomes. An intestine-specific enhancer element is located between 54 and 62 kilobases 5' to the structural gene.
The Journal of biological chemistry 1998;273(34):21800-7.
1998: Munné S; Fung J; Cassel M J; Márquez C; Weier H U
Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis.
Human genetics 1998;102(6):663-74.
1998: Fung J; Hyun W; Dandekar P; Pedersen R A; Weier H U
Spectral imaging in preconception/preimplantation genetic diagnosis of aneuploidy: multicolor, multichromosome screening of single cells.
Journal of assisted reproduction and genetics 1998;15(5):323-30.
1997: Duell T; Wang M; Wu J; Kim U J; Weier H U
High-resolution physical map of the immunoglobulin lambda variant gene cluster assembled by quantitative DNA fiber mapping.
Genomics 1997;45(3):479-86.
1997: Cassel M J; Munné S; Fung J; Weier H U
Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells.
Human reproduction (Oxford, England) 1997;12(9):2019-27.
1997: Sawicki M; Arnold E; Ebrahimi S; Duell T; Jin S; Wood T; Chakrabarti R; Peters J; Wan Y; Samara G; Weier H U; Udar N; Passaro E; Srivatsan E S
A transcript map encompassing the multiple endocrine neoplasia type-1 (MEN1) locus on chromosome 11q13.
Genomics 1997;42(3):405-12.
1997: Robbins W A; Meistrich M L; Moore D; Hagemeister F B; Weier H U; Cassel M J; Wilson G; Eskenazi B; Wyrobek A J
Chemotherapy induces transient sex chromosomal and autosomal aneuploidy in human sperm.
Nature genetics 1997;16(1):74-8.
1997: Smith D J; Stevens M E; Sudanagunta S P; Bronson R T; Makhinson M; Watabe A M; O'Dell T J; Fung J; Weier H U; Cheng J F; Rubin E M
Functional screening of 2 Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down syndrome.
Nature genetics 1997;16(1):28-36.
1997: Duell T; Nielsen L B; Jones A; Young S G; Weier H U
Construction of two near-kilobase resolution restriction maps of the 5' regulatory region of the human apolipoprotein B gene by quantitative DNA fiber mapping (QDFM).
Cytogenetics and cell genetics 1997;79(1-2):64-70.
1996: Hessel H; Mittermüller J; Zitzelsberger H; Weier H U; Bauchinger M
Combined immunophenotyping and FISH with sex chromosome-specific DNA probes for the detection of chimerism in epidermal Langerhans cells after sex-mismatched bone marrow transplantation.
Histochemistry and cell biology 1996;106(5):481-5.
1996: Jossart G H; Epstein H D; Shaver J K; Weier H U; Greulich K M; Tezelman S; Grossman R F; Siperstein A E; Duh Q Y; Clark O H
Immunocytochemical detection of p53 in human thyroid carcinomas is associated with mutation and immortalization of cell lines.
The Journal of clinical endocrinology and metabolism 1996;81(10):3498-504.
1996: Zitzelsberger H; Szücs S; Robens E; Weier H U; Höfler H; Bauchinger M
Combined cytogenetic and molecular genetic analyses of fifty-nine untreated human prostate carcinomas.
Cancer genetics and cytogenetics 1996;90(1):37-44.
1996: Munné S; Weier H U
Simultaneous enumeration of chromosomes 13, 18, 21, X, and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy.
Cytogenetics and cell genetics 1996;75(4):263-70.
1996: Jossart G H; O'Brien B; Cheng J F; Tong Q; Jhiang S M; Duh Q; Clark O H; Weier H U
A novel multicolor hybridization scheme applied to localization of a transcribed sequence (D10S170/H4) and deletion mapping in the thyroid cancer cell line TPC-1.
Cytogenetics and cell genetics 1996;75(4):254-7.
1995: Jossart G H; Greulich K M; Siperstein A E; Duh Q; Clark O H; Weier H U
Molecular and cytogenetic characterization of a t(1;10;21) translocation in the human papillary thyroid cancer cell line TPC-1 expressing the ret/H4 chimeric transcript.
Surgery 1995;118(6):1018-23.
1995: Weier H U; George C X; Greulich K M; Samuel C E
The interferon-inducible, double-stranded RNA-specific adenosine deaminase gene (DSRAD) maps to human chromosome 1q21.1-21.2.
Genomics 1995;30(2):372-5.
1995: Weier H U; Wang M; Mullikin J C; Zhu Y; Cheng J F; Greulich K M; Bensimon A; Gray J W
Quantitative DNA fiber mapping.
Human molecular genetics 1995;4(10):1903-10.
1995: Weier H U; Greulich K M; Young D M
Dual temperature in situ hybridization.
BioTechniques 1995;19(3):364-6.
1995: Weier H U; Rhein A P; Shadravan F; Collins C; Polikoff D
Rapid physical mapping of the human trk protooncogene (NTRK1) to human chromosome 1q21-q22 by P1 clone selection, fluorescence in situ hybridization (FISH), and computer-assisted microscopy.
Genomics 1995;26(2):390-3.
1995: Robbins W A; Baulch J E; Moore D; Weier H U; Blakey D; Wyrobek A J
Three-probe fluorescence in situ hybridization to assess chromosome X, Y, and 8 aneuploidy in sperm of 14 men from two healthy groups: evidence for a paternal age effect on sperm aneuploidy.
Reproduction, fertility, and development 1995;7(4):799-809.
1994: Wyrobek A J; Robbins W A; Mehraein Y; Pinkel D; Weier H U
Detection of sex chromosomal aneuploidies X-X, Y-Y, and X-Y in human sperm using two-chromosome fluorescence in situ hybridization.
American journal of medical genetics 1994;53(1):1-7.
1994: Weier H U; Polikoff D; Fawcett J J; Greulich K M; Lee K H; Cram S; Chapman V M; Gray J W
Generation of five high-complexity painting probe libraries from flow-sorted mouse chromosomes.
Genomics 1994;21(3):641-4.
1994: Zitzelsberger H; Szücs S; Weier H U; Lehmann L; Braselmann H; Enders S; Schilling A; Breul J; Höfler H; Bauchinger M
Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific DNA probes.
The Journal of pathology 1994;172(4):325-35.
1993: Yu L C; Williams J; Wang B B; Vooijs M; Weier H U; Sakamoto M; Ying K L
Characterization of i(18p) in prenatal diagnosis by fluorescence in situ hybridization.
Prenatal diagnosis 1993;13(5):355-61.
1993: Weier H U; Miller B M; Yu L C; Fuscoe J C
PCR cloning of a repeated DNA fragment from Chinese hamster ovary (CHO) cell X chromosomes and mapping by fluorescence in situ hybridization.
DNA sequence : the journal of DNA sequencing and mapping 1993;4(1):47-51.
1992: Miller B M; Werner T; Weier H U; Nüsse M
Analysis of radiation-induced micronuclei by fluorescence in situ hybridization (FISH) simultaneously using telomeric and centromeric DNA probes.
Radiation research 1992;131(2):177-85.
1992: Lucas J N; Awa A; Straume T; Poggensee M; Kodama Y; Nakano M; Ohtaki K; Weier H U; Pinkel D; Gray J
Rapid translocation frequency analysis in humans decades after exposure to ionizing radiation.
International journal of radiation biology 1992;62(1):53-63.
1992: Weier H U; Gray J W
A degenerate alpha satellite probe, detecting a centromeric deletion on chromosome 21 in an apparently normal human male, shows limitations of the use of satellite DNA probes for interphase ploidy analysis.
Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology 1992;4(2):81-6.
1992: Weier H U; Zitzelsberger H F; Gray J W
Differential staining of human and murine chromatin in situ by hybridization with species-specific satellite DNA probes.
Biochemical and biophysical research communications 1992;182(3):1313-9.
1991: Weier H U; Kleine H D; Gray J W
Labeling of the centromeric region on human chromosome 8 by in situ hybridization.
Human genetics 1991;87(4):489-94.
1991: Weier H U; Lucas J N; Poggensee M; Segraves R; Pinkel D; Gray J W
Two-color hybridization with high complexity chromosome-specific probes and a degenerate alpha satellite probe DNA allows unambiguous discrimination between symmetrical and asymmetrical translocations.
Chromosoma 1991;100(6):371-6.
1991: Miller B M; Zitzelsberger H F; Weier H U; Adler I D
Classification of micronuclei in murine erythrocytes: immunofluorescent staining using CREST antibodies compared to in situ hybridization with biotinylated gamma satellite DNA.
Mutagenesis 1991;6(4):297-302.
1991: Weier H U; Zitzelsberger H F; Gray J W
Non-isotopical labeling of murine heterochromatin in situ by hybridization with in vitro-synthesized biotinylated gamma (major) satellite DNA.
BioTechniques 1991;10(4):498-502, 504-5.
1991: Gray J W; Lucas J; Kallioniemi O; Kallioniemi A; Kuo W L; Straume T; Tkachuk D; Tenjin T; Weier H U; Pinkel D
Applications of fluorescence in situ hybridization in biological dosimetry and detection of disease-specific chromosome aberrations.
Progress in clinical and biological research 1991;372():399-411.
1990: Weier H U; Segraves R; Pinkel D; Gray J W
Synthesis of Y chromosome-specific labeled DNA probes by in vitro DNA amplification.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1990;38(3):421-6.
1990: Weier H U; Rosette C
Generation of clonal DNA templates for in vitro transcription without plasmid purification.
BioTechniques 1990;8(3):252-7.
1988: Weier H U; Rosette C
Generation of labeled RNA probes from enzymatically amplified DNA templates.
Nucleic acids research 1988;16(24):11836.

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