Michael Hauser
Michael Hauser
Adresă de e-mail confirmată pe duke.edu
Citat de
Citat de
Complement factor H variant increases the risk of age-related macular degeneration
JL Haines, MA Hauser, S Schmidt, WK Scott, LM Olson, P Gallins, ...
Science 308 (5720), 419-421, 2005
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
LG Fritsche, W Igl, JNC Bailey, F Grassmann, S Sengupta, ...
Nature genetics 48 (2), 134-143, 2016
PGC-1α, A Potential Therapeutic Target for Early Intervention in Parkinson’s Disease
B Zheng, Z Liao, JJ Locascio, KA Lesniak, SS Roderick, ML Watt, ...
Science translational medicine 2 (52), 52ra73-52ra73, 2010
The pivotal role of the complement system in aging and age-related macular degeneration: hypothesis re-visited
DH Anderson, MJ Radeke, NB Gallo, EA Chapin, PT Johnson, CR Curletti, ...
Progress in retinal and eye research 29 (2), 95-112, 2010
Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy
SQ Harper, MA Hauser, C DelloRusso, D Duan, RW Crawford, SF Phelps, ...
Nature medicine 8 (3), 253-261, 2002
Molecular markers of early Parkinson's disease based on gene expression in blood
CR Scherzer, AC Eklund, LJ Morse, Z Liao, JJ Locascio, D Fefer, ...
Proceedings of the National Academy of Sciences 104 (3), 955-960, 2007
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
International meta-analysis of PTSD genome-wide association studies identifies sex-and ancestry-specific genetic risk loci
CM Nievergelt, AX Maihofer, T Klengel, EG Atkinson, CY Chen, KW Choi, ...
Nature communications 10 (1), 4558, 2019
Largest GWAS of PTSD (N= 20 070) yields genetic overlap with schizophrenia and sex differences in heritability
LE Duncan, A Ratanatharathorn, AE Aiello, LM Almli, AB Amstadter, ...
Molecular psychiatry 23 (3), 666-673, 2018
Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration
S Schmidt, MA Hauser, WK Scott, EA Postel, A Agarwal, P Gallins, ...
The American Journal of Human Genetics 78 (5), 852-864, 2006
Relationship between methylome and transcriptome in patients with nonalcoholic fatty liver disease
SK Murphy, H Yang, CA Moylan, H Pang, A Dellinger, MF Abdelmalek, ...
Gastroenterology 145 (5), 1076-1087, 2013
Myotilin is mutated in limb girdle muscular dystrophy 1A
MA Hauser, SK Horrigan, P Salmikangas, UM Torian, KD Viles, R Dancel, ...
Human molecular genetics 9 (14), 2141-2147, 2000
Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted
A Amalfitano, MA Hauser, H Hu, D Serra, CR Begy, JS Chamberlain
Journal of virology 72 (2), 926-933, 1998
Expression of full-length and truncated dystrophin mini-genes in transgenic mdx mice
SF Phelps, MA Hauser, NM Cole, JA Rafael, RT Hinkle, JA Faulkner, ...
Human molecular genetics 4 (8), 1251-1258, 1995
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155-163, 2013
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
JL Wiggs, BL Yaspan, MA Hauser, JH Kang, RR Allingham, LM Olson, ...
PLoS genetics 8 (4), e1002654, 2012
Hepatic gene expression profiles differentiate presymptomatic patients with mild versus severe nonalcoholic fatty liver disease
CA Moylan, H Pang, A Dellinger, A Suzuki, ME Garrett, CD Guy, ...
Hepatology 59 (2), 471-482, 2014
Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease
YJ Li, SA Oliveira, P Xu, ER Martin, JE Stenger, CR Scherzer, MA Hauser, ...
Human molecular genetics 12 (24), 3259-3267, 2003
Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy
J Sarparanta, PH Jonson, C Golzio, S Sandell, H Luque, M Screen, ...
Nature genetics 44 (4), 450-455, 2012
Chiari type I malformation with or without syringomyelia: prevalence and genetics
MC Speer, DS Enterline, L Mehltretter, P Hammock, J Joseph, ...
Journal of genetic counseling 12 (4), 297-311, 2003
Sistemul nu poate realiza operația în acest moment. Încercați din nou mai târziu.
Articole 1–20