Michael Hauser
Michael Hauser
Verified email at duke.edu
Title
Cited by
Cited by
Year
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
27472005
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
8732016
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
7092010
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
6882010
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
6052002
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
5212007
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
3892006
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
3432000
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
3361995
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
3341998
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
2992018
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
2982013
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
2772012
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
2722013
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
2682003
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
2342003
Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6
JL Haines, N Schnetz-Boutaud, S Schmidt, WK Scott, A Agarwal, ...
Investigative ophthalmology & visual science 47 (1), 329-335, 2006
2302006
Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease
ER Martin, WK Scott, MA Nance, RL Watts, JP Hubble, WC Koller, ...
Jama 286 (18), 2245-2250, 2001
2272001
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
2202012
Protective effect of complement factor B and complement component 2 variants in age-related macular degeneration
KL Spencer, MA Hauser, LM Olson, S Schmidt, WK Scott, P Gallins, ...
Human molecular genetics 16 (16), 1986-1992, 2007
2152007
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