Search Results - Heike Fiegler
- Showing 1 - 20 results of 21
- Go to Next Page
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
Radial chromatin positioning is shaped by local gene density, not by gene expression by Katrin Küpper, Alexandra C. Kölbl, Dorothee Biener, Sandra Dittrich, Johann von Hase, Tobias Thormeyer, Heike Fiegler, Nigel P. Carter, Michael R. Speicher, Thomas Cremer, Marion Cremer
Published 2007Artigo -
10
A Whole-Genome Mouse BAC Microarray With 1-Mb Resolution for Analysis of DNA Copy Number Changes by Array Comparative Genomic Hybridization by Yeun‐Jun Chung, Jos Jonkers, Hannah Kitson, Heike Fiegler, Sean Humphray, Carol Scott, Sarah Hunt, Yuejin Yu, Ichiko Nishijima, Arno Velds, Henne Holstege, Nigel Carter, Allan Bradley
Published 2004Artigo -
11
Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization by John C. Marioni, Natalie Thorne, Armand Valsesia, Tomas Fitzgerald, Richard Redon, Heike Fiegler, T. Daniel Andrews, Barbara E. Stranger, Andy G. Lynch, Emmanouil T. Dermitzakis, Nigel P. Carter, Simon Tavaré, Matthew E. Hurles
Published 2007Artigo -
12
Diet and the evolution of human amylase gene copy number variation by George H. Perry, Nathaniel J. Dominy, Katrina G. Claw, Arthur S. Lee, Heike Fiegler, Richard Redon, John C. Werner, Fernando A. Villanea, Joanna L. Mountain, Rajeev Misra, Nigel P. Carter, Charles Lee, Anne C. Stone
Published 2007Artigo -
13
Clinical implication of recurrent copy number alterations in hepatocellular carcinoma and putative oncogenes in recurrent gains on 1q by Tae‐Min Kim, Seon‐Hee Yim, Seung–Hun Shin, Haidong Xu, Yuchae Jung, C. K. Park, Jong‐Young Choi, Won‐Sang Park, Miseon Kwon, Heike Fiegler, Nigel P. Carter, Mun‐Gan Rhyu, Yeun‐Jun Chung
Published 2008Artigo -
14
Guidelines for molecular karyotyping in constitutional genetic diagnosis by Joris Vermeesch, Heike Fiegler, Nicole de Leeuw, Károly Szuhai, Jacqueline Schoumans, Roberto Ciccone, Frank Speleman, Anita Rauch, Jill Clayton‐Smith, Conny van Ravenswaaij, Damien Sanlaville, Philippos C. Patsalis, Helen V. Firth, Koenraad Devriendt, Orsetta Zuffardi
Published 2007Revisão -
15
Genomic Profiling Identifies Discrete Deletions Associated with Translocations in Glioblastoma Multiforme by Paul Mulholland, Heike Fiegler, Chiara Maria Mazzanti, P.A. Gorman, Peter Sasieni, Julian Adams, T. Alwyn Jones, J. W. Babbage, R Vatcheva, Kouichi Ichimura, Philip East, C. Poullikas, V. Peter Collins, N.P. Carter, Ian Tomlinson, Denise Sheer
Published 2006Artigo -
16
A comprehensive study of chromosome 16q in invasive ductal and lobular breast carcinoma using array CGH by Rebecca Roylance, Patricia Gorman, T Papior, Y. Louise Wan, Megan L. Ives, J. E. Vivienne Watson, Collin C. Collins, Noel C. Wortham, Cordelia Langford, Heike Fiegler, N Carter, Cheryl Gillett, Peter Sasieni, S Pinder, A M Hanby, Ian Tomlinson
Published 2006Artigo -
17
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents by Carla Rosenberg, Jeroen Knijnenburg, Egbert Bakker, Angela Maria Vianna‐Morgante, Willem C.R. Sloos, Paulo Alberto Otto, Marjolein Kriek, Kerstin Hansson, Ana Cristina Victorino Krepischi, Heike Fiegler, Nigel P. Carter, Emilia K. Bijlsma, Arie van Haeringen, Károly Szuhai, Hans J. Tanke
Published 2005Carta -
18
An integrated resource for genome-wide identification and analysis of human tissue-specific differentially methylated regions (tDMRs) by Vardhman K. Rakyan, Thomas A. Down, Natalie Thorne, Paul Flicek, Eugene Kulesha, Stefan Gräf, Eleni M. Tomazou, Liselotte Bäckdahl, Nathan Johnson, Marlis Herberth, Kevin Howe, David K. Jackson, Marcos Miretti, Heike Fiegler, John C. Marioni, Ewan Birney, Tim Hubbard, Nigel P. Carter, Simon Tavaré, Stephan Beck
Published 2008Artigo -
19
Accurate and reliable high-throughput detection of copy number variation in the human genome by Heike Fiegler, Richard Redon, Dan Andrews, Clare L. Scott, Robert Andrews, C. Carder, Richard Clark, Oliver M. Dovey, Peter J. I. Ellis, Lars Feuk, Lisa French, Paul Hunt, Dimitrios Rafail Kalaitzopoulos, James R. Larkin, Lyndal Montgomery, George H. Perry, Bob Plumb, Keith Porter, Rachel E. Rigby, Diane Rigler, Armand Valsesia, Cordelia Langford, Sean Humphray, Stephen W. Scherer, Charles Lee, Matthew E. Hurles, Nigel P. Carter
Published 2006Artigo -
20
Global variation in copy number in the human genome by Richard Redon, Shumpei Ishikawa, Karen Fitch, Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wei‐Wen Chen, Eun Kyung Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. González, Mónica Gratacòs, Jing Huang, Dimitrios Rafail Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, K. Okamura, Fan Shen, Martin J. Somerville, Joëlle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluı́s Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler‐Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith Jones, Stephen W. Scherer, Matthew E. Hurles
Published 2006Artigo
Search Tools:
Related Subjects
Biology
Genetics
Gene
Genome
Computational biology
Chromosome
Gene expression
Copy-number variation
Comparative genomic hybridization
DNA
Human genome
Cancer research
DNA microarray
Medicine
Molecular biology
Chromatin
Pathology
genomic DNA
Breakpoint
Cancer
Carcinoma
Cell biology
ChIA-PET
Chromatin remodeling
Chromosomal translocation
Copy number analysis
CpG site
DNA damage
DNA methylation
DNA replication