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M Stephen Meyn
M Stephen Meyn
Director, Center for Human Genomics and Precision Medicine, University of Wisconsin (Madison)
在 wisc.edu 的电子邮件经过验证 - 首页
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引用次数
引用次数
年份
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway
I Garcia-Higuera, T Taniguchi, S Ganesan, MS Meyn, C Timmers, J Hejna, ...
Molecular cell 7 (2), 249-262, 2001
14442001
Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma.
Y Xu, T Ashley, EE Brainerd, RT Bronson, MS Meyn, D Baltimore
Genes & development 10 (19), 2411-2422, 1996
10061996
Comprehensive Analysis of Hypermutation in Human Cancer
BB Campbell, N Light, D Fabrizio, M Zatzman, F Fuligni, R de Borja, ...
Cell 171 (5), 1042-1056. e10, 2017
7112017
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ...
Genetics in Medicine 20 (4), 435-443, 2018
5292018
Ataxia-telangiectasia and cellular responses to DNA damage
MS Meyn
Cancer research 55 (24), 5991-6001, 1995
5201995
Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
A Shlien, BB Campbell, R de Borja, LB Alexandrov, D Merico, D Wedge, ...
Nat Genet 47 (3), 257-262, 2015
3862015
Whole genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine
DJ Stavropoulos, D Merico, R Jobling, S Bowdin, N Monfared, ...
npj Genomic Medicine 1 (1), doi:10.1038/npjgenmed.2015.12, 2016
3742016
The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes.
KS Keegan, DA Holtzman, AW Plug, ER Christenson, EE Brainerd, ...
Genes & development 10 (19), 2423-2437, 1996
3421996
The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors
E Kolomietz, MS Meyn, A Pandita, JA Squire
Genes, Chromosomes and Cancer 35 (2), 97-112, 2002
3322002
Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11. 2 in individuals ascertained for diagnosis of autism spectrum disorder
BA Fernandez, W Roberts, B Chung, R Weksberg, S Meyn, P Szatmari, ...
Journal of medical genetics 47 (3), 195-203, 2010
3272010
A distinctive DNA damage response in human hematopoietic stem cells reveals an apoptosis-independent role for p53 in self-renewal
M Milyavsky, OI Gan, M Trottier, M Komosa, O Tabach, F Notta, ...
Cell Stem Cell 7 (2), 186-197, 2010
3242010
Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice
S Houghtaling, C Timmers, M Noll, MJ Finegold, SN Jones, MS Meyn, ...
Genes & development 17 (16), 2021-2035, 2003
3202003
Human telomeric protein TRF2 associates with genomic double-strand breaks as an early response to DNA damage
PS Bradshaw, DJ Stavropoulos, MS Meyn
Nature genetics 37 (2), 193-197, 2005
2972005
Ataxia-Telangiectasia
MS Meyn
Chromosomal Instability and Aging: Basic Science and Clinical Implications …, 2003
284*2003
High spontaneous intrachromosomal recombination rates in ataxia-telangiectasia
MS Meyn
Science 260 (5112), 1327-1330, 1993
2841993
Ataxia‐telangiectasia, cancer and the pathobiology of the ATM gene
MS Meyn
Clinical genetics 55 (5), 289-304, 1999
2471999
PhenoTips: patient phenotyping software for clinical and research use
M Girdea, S Dumitriu, M Fiume, S Bowdin, KM Boycott, S Chénier, ...
Human mutation 34 (8), 1057-1065, 2013
2462013
The Bloom syndrome helicase BLM interacts with TRF2 in ALT cells and promotes telomeric DNA synthesis
DJ Stavropoulos, PS Bradshaw, X Li, I Pasic, K Truong, M Ikura, M Ungrin, ...
Human molecular genetics 11 (25), 3135-3144, 2002
2462002
The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists
K Boycott, T Hartley, S Adam, F Bernier, K Chong, BA Fernandez, ...
Journal of Medical Genetics, jmedgenet-2015-103144, 2015
2222015
Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell …
JCY Wong, N Alon, C Mckerlie, JR Huang, MS Meyn, M Buchwald
Human molecular genetics 12 (16), 2063-2076, 2003
1932003
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