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Herdit Schüler

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Oligonucleotide Array Sequence Analysis

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Anne Schellenberg; Herdit Schüler; Christoph V Suschek; Bernd Denecke; Sylvia Joussen; Carmen M Koch; Qiong Lin; Norbert Pallua; Gudrun Walenda; Martin Zenke; Wolfga Wagner
Replicative senescence of mesenchymal stem cells causes DNA-methylation changes which correlate with repressive histone marks.
Miriam Elbracht; Andreas Roos; Nadine Schönherr; Sabine Busse; Reinhild Damen; Klaus Zerres; Sabine Rudnik-Schöneborn; Herdit Schüler
Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype.
Andreas Roos; Miriam Elbracht; Baudis Michael; Jan Senderek; Nadine Schönherr; Thomas Eggermann; Herdit Schüler
A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant.

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All Publications

2011: Anne Schellenberg; Herdit Schüler; Christoph V Suschek; Bernd Denecke; Sylvia Joussen; Carmen M Koch; Qiong Lin; Norbert Pallua; Gudrun Walenda; Martin Zenke; Wolfga Wagner
Replicative senescence of mesenchymal stem cells causes DNA-methylation changes which correlate with repressive histone marks.
Aging 2011;3(9):873-88.
2009: Miriam Elbracht; Andreas Roos; Nadine Schönherr; Sabine Busse; Reinhild Damen; Klaus Zerres; Sabine Rudnik-Schöneborn; Herdit Schüler
Pure distal trisomy 2q: a rare chromosomal abnormality with recognizable phenotype.
American journal of medical genetics. Part A 2009;149A(11):2547-50.
2008: Andreas Roos; Miriam Elbracht; Baudis Michael; Jan Senderek; Nadine Schönherr; Thomas Eggermann; Herdit Schüler
A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant.
American journal of medical genetics. Part A 2008;146A(18):2417-20.
2008: Sabine Rudnik-Schöneborn; Klaus Zerres; Martin Häusler; Alexandra Lott; Timo Krings; Herdit Schüler
A new case of proximal monosomy 1p36, extending the phenotype.
American journal of medical genetics. Part A 2008;146A(15):2018-22.
2008: A Roos; Thomas Eggermann; Klaus Zerres; Herdit Schüler
Polymorphic subtelomeric deletion 1q demonstrates the need to reevaluate subtelomere screening methods: determination of the boundary between pathogenic deletion and benign variant for subtelomere 1q.
American journal of medical genetics. Part A 2008;146A(6):795-8.
2006: A Roos; Sabine Rudnik-Schöneborn; Katja Eggermann; Thomas Eggermann; Jan Senderek; Gesa Schwanitz; Klaus Zerres; Herdit Schüler
Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH.
European journal of medical genetics 2006;49(6):505-10.
2005: Thomas Eggermann; Esther Meyer; Caitriona Obermann; Ingeborg Heil; Herdit Schüler; Michael B Ranke; Katja Eggermann; Hartmut A Wollmann
Is maternal duplication of 11p15 associated with Silver-Russell syndrome?
Journal of medical genetics 2005;42(5):e26.
2005: Thomas Eggermann; D Meschede; Herdit Schüler; S Palm; D Gläser; B Horsthemke; Katja Eggermann; F Haverkamp; Klaus Zerres
Premature ovarian failure associated with a small terminal Xq deletion: narrowing the POF1 region down to Xq27.2/Xq27.3-qter.
Clinical genetics 2005;67(5):434-7.
2005: Thomas Eggermann; Ulrike Gamerdinger; Kristin Bosse; Christiane Heidrich-Kaul; Ruth Raff; Esther Meyer; Ingeborg Heil; Herdit Schüler; Eckhard Korsch; Gesa Schwanitz
Mosaic tetrasomy 14pter-q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q.
American journal of medical genetics. Part A 2005;134(3):305-8.
2005: Katja Eggermann; Carsten Bergmann; Ingeborg Heil; Thomas Eggermann; Klaus Zerres; Herdit Schüler
Rare proximal interstitial deletion of chromosome 4q, del(4)(q13.2q21.22): New case and comparison with the literature.
American journal of medical genetics. Part A 2005;134A(2):226-8.
2005: Martin Häusler; D Anhuf; Herdit Schüler; Vincent T Ramaekers; Armin Thron; Klaus Zerres; Walter Möller-Hartmann
White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelination.
Neuroradiology 2005;47(1):83-6.
2004: Wim Wuyts; Gerard Waeber; Peter Meinecke; Herdit Schüler; Timm Goecke; Wim Van Hul; Oliver Bartsch
Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects.
European journal of human genetics : EJHG 2004;12(5):400-6.