Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis
Kwiatkowski, T.J. Jr, Bosco, D.A, LeClerc, A.L, Tamrazian, E, Vanderburg, C.R, Russ, C, Davis, A, Gilchrist, J, Kasarskis, E.J, Munsat, T, Valdmanis, P, Rouleau, G.A, Hosler, B.A, Cortelli, P, de Jong, P.J, Yoshinaga, Y, Haines, J.L, Pericak-Vance, M.A, Yan, J, Ticozzi, N, Siddique, T, McKenna-Yasek, D, Sapp, P.C, Horvitz, H.R, Landers, J.E, Brown, R.H. Jr
Published in Science (American Association for the Advancement of Science) (27.02.2009)
Published in Science (American Association for the Advancement of Science) (27.02.2009)
Get full text
Journal Article
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
Morita, M, Al-Chalabi, A, Andersen, P M, Hosler, B, Sapp, P, Englund, E, Mitchell, J E, Habgood, J J, de Belleroche, J, Xi, J, Jongjaroenprasert, W, Horvitz, H R, Gunnarsson, L-G, Brown, Jr, R H
Published in Neurology (28.03.2006)
Published in Neurology (28.03.2006)
Get more information
Journal Article
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis
Cudkowicz, M E, McKenna-Yasek, D, Sapp, P E, Chin, W, Geller, B, Hayden, D L, Schoenfeld, D A, Hosler, B A, Horvitz, H R, Brown, R H
Published in Annals of neurology (01.02.1997)
Published in Annals of neurology (01.02.1997)
Get more information
Journal Article
A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
Showguchi-Miyata, Junko, Hosler, Betsy A, Devon, Rebecca S, Skaug, Jennifer, Scherer, Stephen W, Okada, Yoshinori, Hayden, Michael R, Kwiatkowski, Thomas, Hadano, Shinji, Otomo, Asako, Nasir, Jamal, Singaraja, Roshni, Rouleau, Guy A, Brown, Robert H, Ikeda, Joh-E, Sagie, Tally, Yanagisawa, Yoshiko, Miyamoto, Natsuki, Osuga, Hitoshi, Figlewicz, Denise A, Hand, Collette K
Published in Nature genetics (01.10.2001)
Published in Nature genetics (01.10.2001)
Get full text
Journal Article
Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele
Niemann, S, Landers, J E, Churchill, M J, Hosler, B, Sapp, P, Speed, W C, Lahn, B T, Kidd, K K, Brown, Jr, R H, Hayashi, Y
Published in Neurology (26.02.2008)
Published in Neurology (26.02.2008)
Get more information
Journal Article
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Liu, J, Aoki, M, Illa, I, Wu, C, Fardeau, M, Angelini, C, Serrano, C, Urtizberea, J A, Hentati, F, Hamida, M B, Bohlega, S, Culper, E J, Amato, A A, Bossie, K, Oeltjen, J, Bejaoui, K, McKenna-Yasek, D, Hosler, B A, Schurr, E, Arahata, K, de Jong, P J, Brown, Jr, R H
Published in Nature genetics (01.09.1998)
Published in Nature genetics (01.09.1998)
Get full text
Journal Article
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis
Aoki, M, Lin, C L, Rothstein, J D, Geller, B A, Hosler, B A, Munsat, T L, Horvitz, H R, Brown, Jr, R H
Published in Annals of neurology (01.05.1998)
Published in Annals of neurology (01.05.1998)
Get more information
Journal Article
Linkage of Familial Amyotrophic Lateral Sclerosis With Frontotemporal Dementia to Chromosome 9q21-q22
Hosler, Betsy A, Siddique, Teepu, Sapp, Peter C, Sailor, Wen, Huang, Michael C, Hossain, Anwar, Daube, Jasper R, Nance, Martha, Fan, Chaohong, Kaplan, Jocelyn, Hung, Wu-Yen, McKenna-Yasek, Diane, Haines, Jonathan L, Pericak-Vance, Margaret A, Horvitz, H. Robert, Brown, Jr, Robert H
Published in JAMA : the journal of the American Medical Association (04.10.2000)
Published in JAMA : the journal of the American Medical Association (04.10.2000)
Get full text
Journal Article
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Brown, Robert H, Liu, Jing, Aoki, Masashi, Illa, Isabel, Wu, Chenyan, Fardeau, Michel, Angelini, Corrado, Serrano, Carmen, Urtizberea, J. Andoni, Hentati, Faycal, Hamida, Mongi Ben, Bohlega, Saeed, Culper, Edward J, Amato, Anthony A, Bossie, Karen, Oeltjen, Joshua, Bejaoui, Khemissa, McKenna-Yasek, Diane, Hosler, Betsy A, Schurr, Erwin, Arahata, Kiichi, de Jong, Pieter J
Published in Nature genetics (01.09.1998)
Published in Nature genetics (01.09.1998)
Get full text
Journal Article
Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22
Bejaoui, K, McKenna-Yasek, D, Hosler, B A, Burns-Deater, E, Deater, L M, O'Neill, G, Haines, J L, Brown, Jr, R H
Published in Neurology (01.02.1999)
Published in Neurology (01.02.1999)
Get more information
Journal Article
A Video Camera Model Identification System Using Deep Learning and Fusion
Hosler, B., Mayer, O., Bayar, B., Zhao, X., Chen, C., Shackleford, J. A., Stamm, M. C.
Published in ICASSP 2019 - 2019 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP) (01.05.2019)
Published in ICASSP 2019 - 2019 IEEE International Conference on Acoustics, Speech and Signal Processing (ICASSP) (01.05.2019)
Get full text
Conference Proceeding
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosis
Hosler, Betsy A., Nicholson, Garth A., Sapp, Peter C., Chin, Wendy, Orrell, Richard W., De Belleroche, Jackie S., Esteban, Jesus, Hayward, Lawrence J., McKenna-Yasek, Diane, Yeung, Leone, Cherryson, Annia K., Dench, Joanne E., Wilton, Steve D., Laing, Nigel G., Horvitz, H.Robert, Brown, Robert H.
Published in Neuromuscular disorders : NMD (01.10.1996)
Published in Neuromuscular disorders : NMD (01.10.1996)
Get full text
Journal Article