Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Stefan Kammerer"'
Autor:
Christopher I. Amos, John K. Field, Rainer Dierkesmann, Charles Cantor, Stefan Kammerer, Karl Haeussinger, Margaret R. Spitz, Stephen Duffy, Reiner Fischer, John D. Minna, Luc Girard, Adrian Cassidy, Melanie Barbara Boettger, Jonathan Myles, Triantafillos Liloglou, Peter Meyer, Ivan P. Gorlov
Supplementary Figure 1 from Seizure 6-Like (SEZ6L) Gene and Risk for Lung Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03f78afba770adb4a1380c45ec44e514
https://doi.org/10.1158/0008-5472.22367618
https://doi.org/10.1158/0008-5472.22367618
Autor:
Christopher I. Amos, John K. Field, Rainer Dierkesmann, Charles Cantor, Stefan Kammerer, Karl Haeussinger, Margaret R. Spitz, Stephen Duffy, Reiner Fischer, John D. Minna, Luc Girard, Adrian Cassidy, Melanie Barbara Boettger, Jonathan Myles, Triantafillos Liloglou, Peter Meyer, Ivan P. Gorlov
DNA pooling in combination with high-throughput sequencing was done as a part of the Sequenom-Genefinder project. In the pilot study, we tested 83,715 single nucleotide polymorphisms (SNP), located primarily in gene-based regions, to identify polymor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a1adbf590eff90bcd69a2697228f9af
https://doi.org/10.1158/0008-5472.c.6495623
https://doi.org/10.1158/0008-5472.c.6495623
Autor:
Christopher I. Amos, John K. Field, Rainer Dierkesmann, Charles Cantor, Stefan Kammerer, Karl Haeussinger, Margaret R. Spitz, Stephen Duffy, Reiner Fischer, John D. Minna, Luc Girard, Adrian Cassidy, Melanie Barbara Boettger, Jonathan Myles, Triantafillos Liloglou, Peter Meyer, Ivan P. Gorlov
Supplementary Table 1 from Seizure 6-Like (SEZ6L) Gene and Risk for Lung Cancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6ef3ef19d5bfbb8bdb754cc7ddd3781
https://doi.org/10.1158/0008-5472.22367615.v1
https://doi.org/10.1158/0008-5472.22367615.v1
Autor:
Peter Meyer, Ivan P. Gorlov, John D. Minna, Rainer Dierkesmann, Jonathan P. Myles, Reiner Fischer, Melanie Barbara Boettger, Adrian Cassidy, Christopher I. Amos, Stephen W. Duffy, Stefan Kammerer, Triantafillos Liloglou, Karl Haeussinger, John K. Field, Charles R. Cantor, Margaret R. Spitz, Luc Girard
Publikováno v:
Cancer Research. 67:8406-8411
DNA pooling in combination with high-throughput sequencing was done as a part of the Sequenom-Genefinder project. In the pilot study, we tested 83,715 single nucleotide polymorphisms (SNP), located primarily in gene-based regions, to identify polymor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79558f1474e73670b99ae4215a982568
https://doi.org/10.1158/0008-5472.can-06-4784
https://doi.org/10.1158/0008-5472.can-06-4784
Autor:
Matthew R. Nelson, Michael R. James, Stefan Kammerer, Nicholas K. Hayward, Lynn E. DeLisi, Bryan J. Mowry, Andreas Braun, Nathan J. Markward, Herlina Y. Handoko, Richard Reneland, Dale R. Nyholt, Steven Mah
Publikováno v:
Molecular Psychiatry. 11:471-478
The discovery of genetic factors that contribute to schizophrenia susceptibility is a key challenge in understanding the etiology of this disease. Here, we report the identification of a novel schizophrenia candidate gene on chromosome 1q32, plexin A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2cf5ce37fcf2b8a2f85e7f2a5c07a16
https://doi.org/10.1038/sj.mp.4001785
https://doi.org/10.1038/sj.mp.4001785
Autor:
Nicholas G. Martin, Richard B. Roth, Troy Dumenil, Stefan Kammerer, Grant W. Montgomery, Mitchell S. Stark, Nicholas K. Hayward, David L. Duffy, Andreas Braun, Michael M. Shi, Matthew R. Nelson, Michael R. James
Publikováno v:
Journal of Investigative Dermatology. 125(6):1252-1258
Somatic mutations of the BRAF gene are common in melanomas and nevi but the contribution of polymorphisms in this gene to melanoma or nevus susceptibility remains unclear. An Australian melanoma case-control sample was typed for 16 single nucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69ab3b4a9f4e528810074aad9cc72e16
Autor:
Richard Reneland, Richard B. Roth, Ulrike Schwarz-Boeger, Stefan Kammerer, Andreas Braun, Lyn R. Griffiths, Marion Kiechle, Carolyn R. Hoyal, Matthew R. Nelson, Florian Ebner, Charles R. Cantor, Joachim Rehbock, George Marnellos
Publikováno v:
Proceedings of the National Academy of Sciences. 102:2004-2009
The development of breast cancer is a complex process that involves multiple genes at many stages, from initial cell cycle dysregulation to disease progression. To identify genetic variations that influence this process, we conducted a large-scale as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7d40b09026b3a5024a36ec365334be5
https://doi.org/10.1073/pnas.0409806102
https://doi.org/10.1073/pnas.0409806102
Autor:
Charles R. Cantor, Michael M. Shi, George Marnellos, Carolyn R. Hoyal, Matthew R. Nelson, Stefan Kammerer, Andreas Braun
Publikováno v:
Genome Research. 14:1664-1668
Genome-wide association studies using large numbers of bi-allelic single nucleotide polymorphisms (SNPs) have been proposed as a potentially powerful method for identifying genes involved in common diseases. To assemble a SNP collection appropriate f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06a1da9f00c36c474835b2da6ae1d9d8
https://doi.org/10.1101/gr.2421604
https://doi.org/10.1101/gr.2421604
Autor:
Stefan Kammerer, Jonas Ekblom, Paul Oeth, Charles R. Cantor, Dirk van den Boom, Kai Tang, Mikhail F. Denissenko, and Andreas Braun, Christian Jurinke
Publikováno v:
Journal of Proteome Research. 3:218-227
To find genes that underlie disease susceptibilities, genome-wide single nucleotide polymorphisms (SNPs) have been analyzed using high-throughput matrix assisted laser desorption/ionization (MALDI) time-of-flight (TOF) mass spectrometry (MS). As a pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85326bad0d3fbd880a06c56bc63b0b84
https://doi.org/10.1021/pr034080s
https://doi.org/10.1021/pr034080s
Autor:
Matthew R. Nelson, Sara C. Hamon, Charles R. Cantor, Lora L. Burns-Hamuro, Stefan Kammerer, Susan S. Taylor, Yuliang Ma, Michael M. Shi, Andreas Braun, Jaume M. Canaves, Charles F. Sing
Publikováno v:
Proceedings of the National Academy of Sciences. 100:4066-4071
The focus of human genetics in recent years has shifted toward identifying genes that are involved in the development of common diseases such as cancer, diabetes, cardiovascular diseases, and Alzheimer's disease. Because many complex diseases are lat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8784907e815f936d25303675b1fa52ea
https://doi.org/10.1073/pnas.2628028100
https://doi.org/10.1073/pnas.2628028100