Ralf Krahe

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Fred A WrightNorth Carolina State UniversityZweryfikowany adres z ncsu.edu
Stefano ColellaResearch Scientist, Institut National de la Recherche Agronomique (INRA)Zweryfikowany adres z lyon.inra.fr
Bo Yuan (苑波)Professor of Computer Science, Shanghai Jiao Tong UniversityZweryfikowany adres z sjtu.edu.cn
Christopher AmosDirector of Clinical and Translational Research, Baylor College of MedicineZweryfikowany adres z bcm.edu
Christoph PlassProfessor für Epigenetik, DKFZ, HeidelbergZweryfikowany adres z dkfz.de
Dominic J SmiragliaAssociate Professor of Oncology, Department of Cancer Genetics, Roswell Park Cancer InstituteZweryfikowany adres z roswellpark.org
Mark D. Shriver, Ph.D.Professor of Anthropology, Penn State UniversityZweryfikowany adres z psu.edu
Natalia PellegataAACRZweryfikowany adres z helmholtz-muenchen.de
Mark E. S. BaileyUniversity of GlasgowZweryfikowany adres z glasgow.ac.uk
Richard M. MyersHudsonAlpha Institute for BiotechnologyZweryfikowany adres z hudsonalpha.com
Len A. PennacchioSenior Staff Scientist, Lawrence Berkeley National LaboratoryZweryfikowany adres z lbl.gov
Mark ScreenCharles River LaboratoriesZweryfikowany adres z crl.com
Berl OakleyDepartment of Molecular Biosciences, University of KansasZweryfikowany adres z ku.edu
Khandan KeyomarsiUniversity of Texas, MD Anderson Cancer CenterZweryfikowany adres z mdanderson.org
Morgan SammonsUniversity at Albany, SUNYZweryfikowany adres z albany.edu
Louis PtacekDepartment of Neurology; University of California, San FranciscoZweryfikowany adres z ucsf.edu
Barkardottir R BLaboratory of Cell Biology, Department of Pathology, Landspitali University Hospital, ReykjavikZweryfikowany adres z landspitali.is
Bahri KARAÇAYUniversity of Iowa, Stead Family Department of Pediatrics and Iowa Neuroscience InstituteZweryfikowany adres z uiowa.edu
Karl KornackerEmeritus Professor of Sensory Biophysics, The Ohio State UniversityZweryfikowany adres z midohio.twcbc.com
Krzysztof MrózekResearch Scientist, The Ohio State UniversityZweryfikowany adres z osumc.edu

Obserwuj

Ralf Krahe

University of Texas MD Anderson Cancer Center

Zweryfikowany adres z mdanderson.org - Strona główna

human & molecular genetics cancer genetics neurogenetics genomics mouse models


Tytuł Sortuj wg cytatów Sortuj wg roku Sortuj wg tytułu	Cytowane przez Cytowane przez	Rok
Sensitive and quantitative universal Pyrosequencing™ methylation analysis of CpG sites S Colella, L Shen, KA Baggerly, JPJ Issa, R Krahe Biotechniques 35 (1), 146-150, 2003	598	2003
The myotonic dystrophies: molecular, clinical, and therapeutic challenges B Udd, R Krahe The Lancet Neurology 11 (10), 891-905, 2012	590	2012
Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics K Virtaneva, FA Wright, SM Tanner, B Yuan, WJ Lemon, MA Caligiuri, ... Proceedings of the National Academy of Sciences 98 (3), 1124-1129, 2001	382	2001
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1 M Aminoff, JE Carter, RB Chadwick, C Johnson, R Gräsbeck, ... Nature genetics 21 (3), 309-313, 1999	322	1999
The intrinsic factor–vitamin B12 receptor, cubilin, is a high-affinity apolipoprotein AI receptor facilitating endocytosis of high-density lipoprotein R Kozyraki, J Fyfe, M Kristiansen, C Gerdes, C Jacobsen, S Cui, ... Nature medicine 5 (6), 656-661, 1999	312	1999
Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: Evidence for its fusion with MLL in acute myeloid leukemia PJ Kourlas, MP Strout, B Becknell, ML Veronese, CM Croce, KS Theil, ... Proceedings of the National Academy of Sciences 97 (5), 2145-2150, 2000	306	2000
Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2) G Meola, V Sansone, D Perani, S Scarone, S Cappa, C Dragoni, ... Neuromuscular Disorders 13 (10), 813-821, 2003	289	2003
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement G Van Goethem, P Luoma, M Rantamaki, A Al Memar, S Kaakkola, ... Neurology 63 (7), 1251-1257, 2004	288	2004
A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)_n repeat CA Boucher, SK King, N Carey, R Krahe, CL Winchester, S Rahman, ... Human molecular genetics 4 (10), 1919-1925, 1995	238	1995
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 K Virtaneva, E D'Amato, J Miao, M Koskiniemi, R Norio, G Avanzini, ... Nature genetics 15 (4), 393-396, 1997	230	1997
Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2 A Vihola, G Bassez, G Meola, S Zhang, H Haapasalo, A Paetau, ... Neurology 60 (11), 1854-1857, 2003	222	2003
Mutations in KERA, encoding keratocan, cause cornea plana NS Pellegata, JL Dieguez-Lucena, T Joensuu, S Lau, KT Montgomery, ... Nature genetics 25 (1), 91-95, 2000	194	2000
Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes JS Müller, A Herczegfalvi, JJ Vilchez, J Colomer, LL Bachinski, ... Brain 130 (6), 1497-1506, 2007	189	2007
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland T Suominen, LL Bachinski, S Auvinen, P Hackman, KA Baggerly, ... European journal of human genetics 19 (7), 776-782, 2011	180	2011
Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing R Krahe, T Ashizawa, C Abbruzzese, E Roeder, P Carango, M Giacanelli, ... Genomics 28 (1), 1-14, 1995	178	1995
Splicing factors PTBP1 and PTBP2 promote proliferation and migration of glioma cell lines HC Cheung, T Hai, W Zhu, KA Baggerly, S Tsavachidis, R Krahe, GJ Cote Brain 132 (8), 2277-2288, 2009	175	2009
Confirmation of the type 2 myotonic dystrophy (CCTG) n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins … LL Bachinski, B Udd, G Meola, V Sansone, G Bassez, B Eymard, ... The American Journal of Human Genetics 73 (4), 835-848, 2003	173	2003
Proximal myotonic dystrophy—a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? B Udd, R Krahe, C Wallgren-Pettersson, B Falck, H Kalimo Neuromuscular Disorders 7 (4), 217-228, 1997	159	1997
Genome-wide hypomethylation in head and neck cancer is more pronounced in HPV-negative tumors and is associated with genomic instability KL Richards, B Zhang, KA Baggerly, S Colella, JC Lang, DE Schuller, ... PloS one 4 (3), e4941, 2009	158	2009
New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1) International Myotonic Dystrophy Consortium (IDMC) Neurology 54 (6), 1218-1221, 2000	155	2000

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