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 | 3080 | 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 | 1600 | 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 | 920 | 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 | 863 | 2010 |
The genetic architecture of the human cerebral cortex KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ... Science 367 (6484), eaay6690, 2020 | 744 | 2020 |
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 | 699 | 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 | 602 | 2007 |
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 | 589 | 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 | 508 | 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 | 420 | 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 | 411 | 2013 |
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 | 369 | 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 | 369 | 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 | 366 | 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 | 362 | 1995 |
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 | 359 | 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 | 316 | 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 | 306 | 2003 |
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 | 298 | 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 | 297 | 2012 |