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Thomas Haaf

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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Procedures

Anatomy

Living Beings

Mice

Concepts & Ideas

Chemicals & Drugs

Phenomena

Genes & Molecular Sequences

Genome

Physiology

DNA Methylation

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Co-Publications
Name
50
Schmid, Michael
18
Zechner, Ulrich
13
Ropers, Hans-Hilger
12
Steinlein, Claus
12
Nanda, Indrajit
10
Grossmann, Bärbel
10
Ward, David
9
Schartl, Manfred
9
Yue, Ying
9
Grützner, Frank
9
Galetzka, Danuta
7
Bartsch, Oliver
7
Shan, Zhihong
6
Wirth, J
6
Golub, Efim

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Publications

TOP 3
Haensel Jennifer; Kohlschmidt Nicolai; Pitz Susanne; Keilmann Annerose; Zenker Martin; Ullmann Reinhard; Haaf Thomas; Bartsch Oliver
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.
Zechner Ulrich; Kohlschmidt Nicolai; Kempf Olga; Gebauer Konstanze; Haug Karsten; Engels Hartmut; Haaf Thomas; Bartsch Oliver
Familial Sotos syndrome caused by a novel missense mutation, C2175S, in NSD1 and associated with normal intelligence, insulin dependent diabetes, bronchial asthma, and lipedema.
Zechner Ulrich; Nolte Jessica; Wolf Marieke; Shirneshan Katayoon; Hajj Nady El; Weise Daniela; Kaltwasser Britta; Zovoilis Athanasios; Haaf Thomas; Engel Wolfgang
Comparative methylation profiles and telomerase biology of mouse multipotent adult germline stem cells and embryonic stem cells.

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All Publications

2009: Haensel Jennifer; Kohlschmidt Nicolai; Pitz Susanne; Keilmann Annerose; Zenker Martin; Ullmann Reinhard; Haaf Thomas; Bartsch Oliver
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.
American journal of medical genetics. Part A 2009;149A(10):2236-40.
2009: Zechner Ulrich; Kohlschmidt Nicolai; Kempf Olga; Gebauer Konstanze; Haug Karsten; Engels Hartmut; Haaf Thomas; Bartsch Oliver
Familial Sotos syndrome caused by a novel missense mutation, C2175S, in NSD1 and associated with normal intelligence, insulin dependent diabetes, bronchial asthma, and lipedema.
European journal of medical genetics 2009;52(5):306-10.
2009: Zechner Ulrich; Nolte Jessica; Wolf Marieke; Shirneshan Katayoon; Hajj Nady El; Weise Daniela; Kaltwasser Britta; Zovoilis Athanasios; Haaf Thomas; Engel Wolfgang
Comparative methylation profiles and telomerase biology of mouse multipotent adult germline stem cells and embryonic stem cells.
Molecular human reproduction 2009;15(6):345-53.
2009: Farcas Ruxandra; Schneider Eberhard; Frauenknecht Katrin; Kondova Ivanela; Bontrop Ronald; Bohl Jürgen; Navarro Bianca; Metzler Markus; Zischler Hans; Zechner Ulrich; Daser Angelika; Haaf Thomas
Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices.
Molecular biology and evolution 2009;26(6):1379-89.
2009: Zechner U; Kohlschmidt N; Rittner G; Damatova N; Beyer V; Haaf T; Bartsch O
Epimutation at human chromosome 14q32.2 in a boy with a upd(14)mat-like clinical phenotype.
Clinical genetics 2009;75(3):251-8.
2009: Haaf Thomas; Hahn Antje; Lambrecht Anne; Grossmann Bärbel; Schwaab Eva; Khanaga Omar; Hahn Thomas; Tresch Achim; Schorsch Martin
A high oocyte yield for intracytoplasmic sperm injection treatment is associated with an increased chromosome error rate.
Fertility and sterility 2009;91(3):733-8.
2009: Schneider Eberhard; Märker Tina; Daser Angelika; Frey-Mahn Gabriele; Beyer Vera; Farcas Ruxandra; Schneider-Rätzke Brigitte; Kohlschmidt Nicolai; Grossmann Bärbel; Bauss Katharina; Napiontek Ulrike; Keilmann Annerose; Bartsch Oliver; Zechner Ulrich; Wolfrum Uwe; Haaf Thomas
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.
Human molecular genetics 2009;18(4):655-66.
2009: May Andreas; Kirchner Roland; Müller Helena; Hartmann Petra; El Hajj Nady; Tresch Achim; Zechner Ulrich; Mann Wolfgang; Haaf Thomas
Multiplex rt-PCR expression analysis of developmentally important genes in individual mouse preimplantation embryos and blastomeres.
Biology of reproduction 2009;80(1):194-202.
2009: Damatova N; Beyer V; Galetzka D; Schneider E; Napiontek U; Keilmann A; Zechner U; Bartsch O; Haaf T
Haploinsufficiency of 16.4 Mb from chromosome 22pter-q11.21 in a girl with unilateral conductive hearing loss.
Cytogenetic and genome research 2009;125(3):241-7.
2009: Herlyn Holger; Zechner Ulrich; Oswald Franz; Pfeufer Arne; Zischler Hans; Haaf Thomas
Positive selection at codon 38 of the human KCNE1 (= minK) gene and sporadic absence of 38Ser-coding mRNAs in Gly38Ser heterozygotes.
BMC evolutionary biology 2009;9():188.
2008: May Andreas; Reifenberg Kurt; Zechner Ulrich; Haaf Thomas
Asynchronous replication dynamics of imprinted and non-imprinted chromosome regions in early mouse embryos.
Experimental cell research 2008;314(15):2788-95.
2008: Nanda I; Schlegelmilch K; Haaf T; Schartl M; Schmid M
Synteny conservation of the Z chromosome in 14 avian species (11 families) supports a role for Z dosage in avian sex determination.
Cytogenetic and genome research 2008;122(2):150-6.
2008: Weis E; Galetzka D; Herlyn H; Schneider E; Haaf T
Humans and chimpanzees differ in their cellular response to DNA damage and non-coding sequence elements of DNA repair-associated genes.
Cytogenetic and genome research 2008;122(2):92-102.
2008: Galetzka D; Weis E; Rittner G; Schindler D; Haaf T
Microarray mRNA expression analysis of Fanconi anemia fibroblasts.
Cytogenetic and genome research 2008;121(1):10-3.
2007: Ruf Nico; Bähring Sylvia; Galetzka Danuta; Pliushch Galyna; Luft Friedrich C; Nürnberg Peter; Haaf Thomas; Kelsey Gavin; Zechner Ulrich
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and human.
Human molecular genetics 2007;16(21):2591-9.
2007: Korenkov M; Kohlschmidt N; Zechner U; Haaf T; Junginger T
[Obesity surgery in patients suffering from monogenetic adipositas]
Zentralblatt für Chirurgie 2007;132(3):256-9.
2007: Yue Ying; Farcas Ruxandra; Thiel Gundula; Bommer Christiane; Grossmann Bärbel; Galetzka Danuta; Kelbova Christina; Küpferling Peter; Daser Angelika; Zechner Ulrich; Haaf Thomas
De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5' end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations.
European journal of human genetics : EJHG 2007;15(5):570-7.
2007: Galetzka Danuta; Weis Eva; Kohlschmidt Nicolai; Bitz Oliver; Stein Raimund; Haaf Thomas
Expression of somatic DNA repair genes in human testes.
Journal of cellular biochemistry 2007;100(5):1232-9.
2007: Galetzka Danuta; Weis Eva; Tralau Tim; Seidmann Larissa; Haaf Thomas
Sex-specific windows for high mRNA expression of DNA methyltransferases 1 and 3A and methyl-CpG-binding domain proteins 2 and 4 in human fetal gonads.
Molecular reproduction and development 2007;74(2):233-41.
2007: Bartsch O; Vlcková Z; Erdogan F; Ullmann R; Novotná D; Spiegel M; Beyer V; Haaf T; Zechner U; Seemanová E
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.
Cytogenetic and genome research 2007;119(1-2):158-64.
2007: Dünzinger U; Haaf T; Zechner U
Conserved synteny of mammalian imprinted genes in chicken, frog, and fish genomes.
Cytogenetic and genome research 2007;117(1-4):78-85.
2006: Yue Ying; Grossmann Bärbel; Galetzka Danuta; Zechner Ulrich; Haaf Thomas
Isolation and differential expression of two isoforms of the ROBO2/Robo2 axon guidance receptor gene in humans and mice.
Genomics 2006;88(6):772-8.
2006: Bartsch Oliver; Rasi Sasan; Delicado Alicia; Dyack Sarah; Neumann Luitgard M; Seemanová Eva; Volleth Marianne; Haaf Thomas; Kalscheuer Vera M
Evidence for a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias severe Rubinstein-Taybi syndrome.
Human genetics 2006;120(2):179-86.
2006: Galetzka Danuta; Tralau Tim; Stein Raimund; Haaf Thomas
Expression of DNMT3A transcripts and nucleolar localization of DNMT3A protein in human testicular and fibroblast cells suggest a role for de novo DNA methylation in nucleolar inactivation.
Journal of cellular biochemistry 2006;98(4):885-94.
2006: Ruf Nico; Dünzinger Ulrich; Brinckmann Anja; Haaf Thomas; Nürnberg Peter; Zechner Ulrich
Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes.
Genomics 2006;87(4):509-19.
2006: Yue Y; Stout K; Grossmann B; Zechner U; Brinckmann A; White C; Pilz D T; Haaf T
Disruption of TCBA1 associated with a de novo t(1;6)(q32.2;q22.3) presenting in a child with developmental delay and recurrent infections.
Journal of medical genetics 2006;43(2):143-7.
2006: Yue Y; Tsend-Ayush E; Grützner F; Grossmann B; Haaf T
Segmental duplication associated with evolutionary instability of human chromosome 3p25.1.
Cytogenetic and genome research 2006;112(3-4):202-7.
2006: Yue Y; Haaf T
7E olfactory receptor gene clusters and evolutionary chromosome rearrangements.
Cytogenetic and genome research 2006;112(1-2):6-10.
2005: Dünzinger Ulrich; Nanda Indrajit; Schmid Michael; Haaf Thomas; Zechner Ulrich
Chicken orthologues of mammalian imprinted genes are clustered on macrochromosomes and replicate asynchronously.
Trends in genetics : TIG 2005;21(9):488-92.
2005: Yue Ying; Grossmann Baerbel; Holder Susan E; Haaf Thomas
De novo t(7;10)(q33;q23) translocation and closely juxtaposed microdeletion in a patient with macrocephaly and developmental delay.
Human genetics 2005;117(1):1-8.
2005: Yue Ying; Grossmann Bärbel; Ferguson-Smith Malcolm; Yang Fengtang; Haaf Thomas
Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution.
Genomics 2005;85(1):36-47.
2005: Yue Y; Grossmann B; Tsend-Ayush E; Grützner F; Ferguson-Smith M A; Yang F; Haaf T
Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2.
Cytogenetic and genome research 2005;108(1-3):98-105.
2004: Tsend-Ayush Enkhjargal; Grützner Frank; Yue Ying; Grossmann Bärbel; Hänsel Ulrike; Sudbrak Ralf; Haaf Thomas
Plasticity of human chromosome 3 during primate evolution.
Genomics 2004;83(2):193-202.
2004: Schmid M; Steinlein C; Haaf T
Chromosome banding in Amphibia. XXX. Karyotype aberrations in cultured fibroblast cells.
Cytogenetic and genome research 2004;104(1-4):277-82.
2003: Schmid M; Steinlein C; Haaf T
Chromosome banding in Amphibia. XXVII. DNA replication banding patterns in three anuran species with greatly differing genome sizes.
Cytogenetic and genome research 2003;101(1):54-61.
2002: Nanda Indrajit; Schrama David; Feichtinger Wolfgang; Haaf Thomas; Schartl Manfred; Schmid Michael
Distribution of telomeric (TTAGGG)(n) sequences in avian chromosomes.
Chromosoma 2002;111(4):215-27.
2002: Shi W; Haaf T
Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure.
Molecular reproduction and development 2002;63(3):329-34.
2002: Grützner Frank; Roest Crollius Hugues; Lütjens Götz; Jaillon Olivier; Weissenbach Jean; Ropers Hans-Hilger; Haaf Thomas
Four-hundred million years of conserved synteny of human Xp and Xq genes on three Tetraodon chromosomes.
Genome research 2002;12(9):1316-22.
2002: Nanda Indrajit; Kondo Mariko; Hornung Ute; Asakawa Shuichi; Winkler Christoph; Shimizu Atsushi; Shan Zhihong; Haaf Thomas; Shimizu Nobuyoshi; Shima Akihiro; Schmid Michael; Schartl Manfred
A duplicated copy of DMRT1 in the sex-determining region of the Y chromosome of the medaka, Oryzias latipes.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(18):11778-83.
2002: Zend-Ajusch Enchshargal; Hornung Ute; Burgtorf Carola; Lütjens Götz; Shan Zhihong; Schartl Manfred; Haaf Thomas
Isolation and characterization of cold-shock domain protein genes, Oryzias latipes Y-box protein 2 (OlaYP2) and Fugu rubripes Y-box protein 1 (FruYP1), in medakafish and pufferfish.
Gene 2002;296(1-2):111-9.
2002: Felbor Ute; Rutschow Désirée; Haaf Thomas; Schmid Michael
Centromeric association of chromosome 16- and 18-derived microchromosomes.
Human genetics 2002;111(1):16-25.
2002: Raderschall Elke; Bazarov Alex; Cao Jiangping; Lurz Rudi; Smith Avril; Mann Wolfgang; Ropers Hans-Hilger; Sedivy John M; Golub Efim I; Fritz Eberhard; Haaf Thomas
Formation of higher-order nuclear Rad51 structures is functionally linked to p21 expression and protection from DNA damage-induced apoptosis.
Journal of cell science 2002;115(Pt 1):153-64.
2002: Raderschall Elke; Stout Karen; Freier Susanne; Suckow Vanessa; Schweiger Susann; Haaf Thomas
Elevated levels of Rad51 recombination protein in tumor cells.
Cancer research 2002;62(1):219-25.
2002: Schmid M; Feichtinger W; Steinlein C; Haaf T; Schartl M; Visbal García R; Manzanilla Pupo J; Fernández Badillo A
Chromosome banding in Amphibia. XXVI. Coexistence of homomorphic XY sex chromosomes and a derived Y-autosome translocation in Eleutherodactylus maussi (Anura, Leptodactylidae).
Cytogenetic and genome research 2002;99(1-4):330-43.
2002: Schmid M; Feichtinger W; Steinlein C; Haaf T; Visbal García R; Fernández Badillo A
X chromosomes of American marsupials contain minimal amounts of euchromatin.
Cytogenetic and genome research 2002;99(1-4):315-22.
2002: Grandy I; Hardt T; Schmid M; Haaf T
Effects of higher-order nuclear structure and Rad51 overexpression on radiation-induced chromosome rearrangements.
Cytogenetic and genome research 2002;98(4):265-9.
2002: Schmid M; Feichtinger W; Steinlein C; Nanda I; Mais C; Haaf T; Visbal García R; Fernández Badillo A
Chromosome banding in Amphibia. XXII. Atypical y chromosomes in Gastrotheca walkeri and Gastrotheca ovifera (Anura, Hylidae).
Cytogenetic and genome research 2002;96(1-4):228-38.
2002: Schmid M; Feichtinger W; Steinlein C; Rupprecht A; Haaf T; Kaiser H
Chromosome banding in amphibia. XXIII. Giant W sex chromosomes and extremely small genomes in Eleutherodactylus euphronides and Eleutherodactylus shrevei (Anura, Leptodactylidae).
Cytogenetic and genome research 2002;97(1-2):81-94.
2002: Schmid M; Haaf T; Steinlein C; Nanda I; Mahony M
Chromosome banding in Amphibia. XXV. Karyotype evolution and heterochromatin characterization in Australian Mixophyes (Anura, Myobatrachidae).
Cytogenetic and genome research 2002;97(3-4):239-53.
2002: Schmid M; Ziegler C G; Steinlein C; Nanda I; Haaf T
Chromosome banding in Amphibia. XXIV. The B chromosomes of Gastrotheca espeletia (Anura, Hylidae).
Cytogenetic and genome research 2002;97(3-4):205-18.
2001: Barton S C; Arney K L; Shi W; Niveleau A; Fundele R; Surani M A; Haaf T
Genome-wide methylation patterns in normal and uniparental early mouse embryos.
Human molecular genetics 2001;10(26):2983-7.
2001: Brunner B; Hornung U; Shan Z; Nanda I; Kondo M; Zend-Ajusch E; Haaf T; Ropers H H; Shima A; Schmid M; Kalscheuer V M; Schartl M
Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1.
Genomics 2001;77(1-2):8-17.
2001: Nothwang H G; Kim H G; Aoki J; Geisterfer M; Kübart S; Wegner R D; van Moers A; Ashworth L K; Haaf T; Bell J; Arai H; Tommerup N; Ropers H H; Wirth J
Functional hemizygosity of PAFAH1B3 due to a PAFAH1B3-CLK2 fusion gene in a female with mental retardation, ataxia and atrophy of the brain.
Human molecular genetics 2001;10(8):797-806.
2001: Borck G; Wirth J; Hardt T; Tönnies H; Brøndum-Nielsen K; Bugge M; Tommerup N; Nothwang H G; Ropers H H; Haaf T
Molecular cytogenetic characterisation of a complex 46,XY,t(7;8;11;13) chromosome rearrangement in a patient with Moebius syndrome.
Journal of medical genetics 2001;38(2):117-21.
2001: Grützner F; Zend-Ajusch E; Stout K; Munsche S; Niveleau A; Nanda I; Schmid M; Haaf T
Chicken microchromosomes are hypermethylated and can be identified by specific painting probes.
Cytogenetics and cell genetics 2001;93(3-4):265-9.
2001: Maurer B; Haaf T; Stout K; Reissmann N; Steinlein C; Schmid M
Two supernumerary marker chromosomes, originating from chromosomes 6 and 11, in a child with developmental delay and craniofacial dysmorphism.
Cytogenetics and cell genetics 2001;93(3-4):182-7.
2001: Haaf T
The battle of the sexes after fertilization: behaviour of paternal and maternal chromosomes in the early mammalian embryo.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2001;9(4):263-71.
2000: Shan Z; Zabel B; Trautmann U; Hillig U; Ottolenghi C; Wan Y; Haaf T
FISH mapping of the sex-reversal region on human chromosome 9p in two XY females and in primates.
European journal of human genetics : EJHG 2000;8(3):167-73.
2000: Mayer W; Smith A; Fundele R; Haaf T
Spatial separation of parental genomes in preimplantation mouse embryos.
The Journal of cell biology 2000;148(4):629-34.
2000: Mayer W; Niveleau A; Walter J; Fundele R; Haaf T
Demethylation of the zygotic paternal genome.
Nature 2000;403(6769):501-2.
2000: Haaf T; Schmid M
Experimental condensation inhibition in constitutive and facultative heterochromatin of mammalian chromosomes.
Cytogenetics and cell genetics 2000;91(1-4):113-23.
2000: Nothwang H G; Schröer A; van der Maarel S; Kübart S; Schneider S; Riesselmann L; Menzel C; Hinzmann B; Vogt D; Rosenthal A; Fryns J; Tommerup N; Haaf T; Ropers H H; Wirth J
Molecular cloning of Xp11 breakpoints in two unrelated mentally retarded females with X;autosome translocations.
Cytogenetics and cell genetics 2000;90(1-2):126-33.
2000: Mayer W; Fundele R; Haaf T
Spatial separation of parental genomes during mouse interspecific (Mus musculus x M. spretus) spermiogenesis.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2000;8(6):555-8.
2000: Shan Z; Nanda I; Wang Y; Schmid M; Vortkamp A; Haaf T
Sex-specific expression of an evolutionarily conserved male regulatory gene, DMRT1, in birds.
Cytogenetics and cell genetics 2000;89(3-4):252-7.
2000: Nanda I; Zend-Ajusch E; Shan Z; Grützner F; Schartl M; Burt D W; Koehler M; Fowler V M; Goodwin G; Schneider W J; Mizuno S; Dechant G; Haaf T; Schmid M
Conserved synteny between the chicken Z sex chromosome and human chromosome 9 includes the male regulatory gene DMRT1: a comparative (re)view on avian sex determination.
Cytogenetics and cell genetics 2000;89(1-2):67-78.
1999: Roemer I; Grützner F; Winking H; Haaf T; Orth A; Skidmore L; Antczak D; Fundele R
Genome evolution. Global methylation in eutherian hybrids.
Nature 1999;401(6749):131-2.
1999: Guttenbach M; Haaf T; Steinlein C; Caesar J; Schinzel A; Schmid M
Ectopic NORs on human chromosomes 4qter and 8q11: rare chromosomal variants detected in two families.
Journal of medical genetics 1999;36(4):339-42.
1999: Wirth J; Nothwang H G; van der Maarel S; Menzel C; Borck G; Lopez-Pajares I; Brøndum-Nielsen K; Tommerup N; Bugge M; Ropers H H; Haaf T
Systematic characterisation of disease associated balanced chromosome rearrangements by FISH: cytogenetically and genetically anchored YACs identify microdeletions and candidate regions for mental retardation genes.
Journal of medical genetics 1999;36(4):271-8.
1999: Nanda I; Shan Z; Schartl M; Burt D W; Koehler M; Nothwang H; Grützner F; Paton I R; Windsor D; Dunn I; Engel W; Staeheli P; Mizuno S; Haaf T; Schmid M
300 million years of conserved synteny between chicken Z and human chromosome 9.
Nature genetics 1999;21(3):258-9.
1999: Raderschall E; Golub E I; Haaf T
Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):1921-6.
1999: Grützner F; Himmelbauer H; Paulsen M; Ropers H H; Haaf T
Comparative mapping of mouse and rat chromosomes by fluorescence in situ hybridization.
Genomics 1999;55(3):306-13.
1999: Haaf T; Raderschall E; Reddy G; Ward D C; Radding C M; Golub E I
Sequestration of mammalian Rad51-recombination protein into micronuclei.
The Journal of cell biology 1999;144(1):11-20.
1999: Grützner F; Lütjens G; Rovira C; Barnes D W; Ropers H H; Haaf T
Classical and molecular cytogenetics of the pufferfish Tetraodon nigroviridis.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1999;7(8):655-62.
1999: Hardt T; Himmelbauer H; Mann W; Ropers H; Haaf T
Towards identification of individual homologous chromosomes: comparative genomic hybridization and spectral karyotyping discriminate between paternal and maternal euchromatin in Mus musculus x M. spretus interspecific hybrids.
Cytogenetics and cell genetics 1999;86(3-4):187-93.
1999: Riesselmann L; Haaf T
Preferential S-phase pairing of the imprinted region on distal mouse chromosome 7.
Cytogenetics and cell genetics 1999;86(1):39-42.
1999: Stout K; van der Maarel S; Frants R R; Padberg G W; Ropers H H; Haaf T
Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1999;7(5):323-9.
1998: Zechner U; Scheel S; Hemberger M; Hopp M; Haaf T; Fundele R; Wanker E E; Lehrach H; Wedemeyer N; Himmelbauer H
Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2.
Genomics 1998;54(3):505-10.
1998: Golub E I; Gupta R C; Haaf T; Wold M S; Radding C M
Interaction of human rad51 recombination protein with single-stranded DNA binding protein, RPA.
Nucleic acids research 1998;26(23):5388-93.
1998: Ott G; Haaf T; Schmid M
Inhibition of condensation in human chromosomes induced by the thymidine analogue 5-iododeoxyuridine.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1998;6(6):495-9.
1998: Haaf T; Willard H F
Orangutan alpha-satellite monomers are closely related to the human consensus sequence.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(6):440-7.
1998: Himmelbauer H; Wedemeyer N; Haaf T; Wanker E E; Schalkwyk L C; Lehrach H
IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(1):26-31.
1997: Haaf T; Willard H F
Chromosome-specific alpha-satellite DNA from the centromere of chimpanzee chromosome 4.
Chromosoma 1997;106(4):226-32.
1997: Koehler M R; Haaf T; Guttenbach M; Schartl M; Schmid M
Cytogenetics of the genus Leporinus (Pisces, Anostomidae). II. Molecular cytogenetics, organization and evolutionary conservation of a chromosome-specific satellite DNA from Leporinus obtusidens.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1997;5(5):325-31.
1997: Koehler M R; Dehm D; Guttenbach M; Nanda I; Haaf T; Molina W F; Galetti P M; Schmid M
Cytogenetics of the genus Leporinus (Pisces, Anostomidae). 1. Karyotype analysis, heterochromatin distribution and sex chromosomes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1997;5(1):12-22.
1997: Nothwang H G; Wirth J; Brandl B; Haaf T; Nielsen K B; Tommerup N; Ropers H H
Identification of positional candidates for neurological disorders on chromsome 13q14-->q22.
Cytogenetics and cell genetics 1997;79(3-4):293-7.
1997: Kingsley K; Wirth J; van der Maarel S; Freier S; Ropers H H; Haaf T
Complex FISH probes for the subtelomeric regions of all human chromosomes: comparative hybridization of CEPH YACs to chromosomes of the Old World monkey Presbytis cristata and great apes.
Cytogenetics and cell genetics 1997;78(1):12-9.
1996: Haaf T; Bray-Ward P
Region-specific YAC banding and painting probes for comparative genome mapping: implications for the evolution of human chromosome 2.
Chromosoma 1996;104(8):537-44.
1996: Haaf T; Ward D C
Inhibition of RNA polymerase II transcription causes chromatin decondensation, loss of nucleolar structure, and dispersion of chromosomal domains.
Experimental cell research 1996;224(1):163-73.
1996: Kovalenko O V; Plug A W; Haaf T; Gonda D K; Ashley T; Ward D C; Radding C M; Golub E I
Mammalian ubiquitin-conjugating enzyme Ubc9 interacts with Rad51 recombination protein and localizes in synaptonemal complexes.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(7):2958-63.
1996: Haaf T; Sirugo G; Kidd K K; Ward D C
Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization.
Nature genetics 1996;12(2):183-5.
1995: Haaf T; Mater A G; Wienberg J; Ward D C
Presence and abundance of CENP-B box sequences in great ape subsets of primate-specific alpha-satellite DNA.
Journal of molecular evolution 1995;41(4):487-91.
1995: Haaf T; Ward D C
Higher order nuclear structure in mammalian sperm revealed by in situ hybridization and extended chromatin fibers.
Experimental cell research 1995;219(2):604-11.
1995: Haaf T; Golub E I; Reddy G; Radding C M; Ward D C
Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(6):2298-302.
1995: Haaf T
The effects of 5-azacytidine and 5-azadeoxycytidine on chromosome structure and function: implications for methylation-associated cellular processes.
Pharmacology & therapeutics 1995;65(1):19-46.
1995: Haaf T; Ward D C
Rabl orientation of CENP-B box sequences in Tupaia belangeri fibroblasts.
Cytogenetics and cell genetics 1995;70(3-4):258-62.
1994: Haaf T; Ward D C
Structural analysis of alpha-satellite DNA and centromere proteins using extended chromatin and chromosomes.
Human molecular genetics 1994;3(5):697-709.
1994: Haaf T; Ward D C
High resolution ordering of YAC contigs using extended chromatin and chromosomes.
Human molecular genetics 1994;3(4):629-33.
1993: Haaf T; Schmid M; Steinlein C; Galetti P M; Willard H F
Organization and molecular cytogenetics of a satellite DNA family from Hoplias malabaricus (Pisces, Erythrinidae).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1993;1(1):77-86.
1993: Haaf T; Werner P; Schmid M
5-Azadeoxycytidine distinguishes between active and inactive X chromosome condensation.
Cytogenetics and cell genetics 1993;63(3):160-8.
1992: Haaf T; Warburton P E; Willard H F
Integration of human alpha-satellite DNA into simian chromosomes: centromere protein binding and disruption of normal chromosome segregation.
Cell 1992;70(4):681-96.
1992: Haaf T; Schmid M
Translocation (6;8)(q22;q12) in Ph+ chronic myelocytic leukemia.
Cancer genetics and cytogenetics 1992;61(1):104-5.
1992: Haaf T; Willard H F
Organization, polymorphism, and molecular cytogenetics of chromosome-specific alpha-satellite DNA from the centromere of chromosome 2.
Genomics 1992;13(1):122-8.
1992: Haaf T; Sumner A T; Köhler J; Willard H F; Schmid M;
A microchromosome derived from chromosome 11 in a patient with the CREST syndrome of scleroderma.
Cytogenetics and cell genetics 1992;60(1):12-7.
1991: Warburton P E; Greig G M; Haaf T; Willard H F
PCR amplification of chromosome-specific alpha satellite DNA: definition of centromeric STS markers and polymorphic analysis.
Genomics 1991;11(2):324-33.
1991: Haaf T; Hofmann R; Schmid M
Opitz trigonocephaly syndrome.
American journal of medical genetics 1991;40(4):444-6.
1991: Haaf T; Hayman D L; Schmid M
Quantitative determination of rDNA transcription units in vertebrate cells.
Experimental cell research 1991;193(1):78-86.
1991: Haaf T; Schmid M
Chromosome topology in mammalian interphase nuclei.
Experimental cell research 1991;192(2):325-32.
1990: Haaf T; Steinlein C; Schmid M
Nucleolar transcriptional activity in mouse Sertoli cells is dependent on centromere arrangement.
Experimental cell research 1990;191(1):157-60.
1990: Haaf T; Schmid M
Y isochromosome associated with a mosaic karyotype and inactivation of the centromere.
Human genetics 1990;85(5):486-90.
1990: Poot M; Kausch K; Köhler J; Haaf T; Hoehn H
The minor-groove binding DNA-ligands netropsin, distamycin A and berenil cause polyploidisation via impairment of the G2 phase of the cell cycle.
Cell structure and function 1990;15(3):151-7.
1990: Haaf T; Schmid M
Kinetochore formation in experimentally undercondensed chromosomes.
Human genetics 1990;84(6):535-8.
1990: Haaf T; Grunenberg H; Schmid M
Paired arrangement of nonhomologous centromeres during vertebrate spermiogenesis.
Experimental cell research 1990;187(1):157-61.
1990: Haaf T; Groscurth A G; Machens A; Schmid M
Human autoantibodies to spermatogenic antigens and Sertoli cells.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1990;38(1):129-34.
1990: Haaf T; Dominguez-Steglich M; Schmid M
Immunocytogenetics. VI. A nonhistone antigen is cell type-specially associated with constitutive heterochromatin and reveals condensation centers in metaphase chromosomes.
Cytogenetics and cell genetics 1990;54(3-4):121-6.
1990: Haaf T; Dominguez-Steglich M; Schmid M
Immunocytogenetics. IV. Human autoantibodies to heterochromatin-associated proteins.
Cytogenetics and cell genetics 1990;53(1):40-51.
1990: Haaf T; Schmid M
Immunocytogenetics. V. A highly conserved NOR antigen (He) is facultatively associated with nucleolar or nucleoplasmic granules.
Cytogenetics and cell genetics 1990;54(3-4):112-20.
1989: Haaf T; Schmid M
5-Azadeoxycytidine induced undercondensation in the giant X chromosomes of Microtus agrestis.
Chromosoma 1989;98(2):93-8.
1989: Schmid M; Haaf T; Schindler D; Meurer M
Centromeric association of a microchromosome. A new category of non-random arrangement of metaphase chromosomes.
Human genetics 1989;81(2):127-36.
1989: Haaf T; Schmid M
Centromeric association and non-random distribution of centromeres in human tumour cells.
Human genetics 1989;81(2):137-43.
1989: Haaf T; Machens A; Schmid M
Immunocytogenetics. II. Human autoantibodies to synaptonemal complexes.
Cytogenetics and cell genetics 1989;50(1):6-13.
1989: Haaf T; Winking H; Schmid M
Immunocytogenetics. III. Analysis of trivalent and multivalent configurations in mouse pachytene spermatocytes by human autoantibodies to synaptonemal complexes and kinetochores.
Cytogenetics and cell genetics 1989;50(1):14-22.
1989: Haaf T; Feichtinger W; Guttenbach M; Sanchez L; Müller C R; Schmid M
Berenil-induced undercondensation in human heterochromatin.
Cytogenetics and cell genetics 1989;50(1):27-33.
1988: Kausch K; Haaf T; Schmid M
Duplication 8q24.2----qter and 15q14----pter resulting from a 3:1 meiotic segregation of a maternal reciprocal translocation.
American journal of medical genetics 1988;31(4):981-5.
1988: Kausch K; Haaf T; Köhler J; Schmid M
Complex chromosomal rearrangement in a woman with multiple miscarriages.
American journal of medical genetics 1988;31(2):415-20.
1988: Haaf T; Ott G; Schmid M
Inhibition of condensation in the late-replicating X chromosome induced by 5-azadeoxycytidine in human lymphocyte cultures.
Human genetics 1988;79(1):18-23.
1988: Haaf T; Schmid M
Analysis of double minutes and double minute-like chromatin in human and murine tumor cells using antikinetochore antibodies.
Cancer genetics and cytogenetics 1988;30(1):73-82.
1988: Haaf T; Reimer G; Schmid M
Immunocytogenetics: localization of transcriptionally active rRNA genes in nucleoli and nucleolus organizer regions by use of human autoantibodies to RNA polymerase I.
Cytogenetics and cell genetics 1988;48(1):35-42.
1987: Haaf T; Schmid M
Chromosome heteromorphisms in the gorilla karyotype. Analyses with distamycin A/DAPI, quinacrine and 5-azacytidine.
The Journal of heredity 1987;78(5):287-92.
1987: Schmid M; Johannisson R; Haaf T; Neitzel H
The chromosomes of Micromys minutus (Rodentia, Murinae). II. Pairing pattern of X and Y chromosomes in meiotic prophase.
Cytogenetics and cell genetics 1987;45(3-4):121-31.

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