Necroptosis drives motor neuron death in models of both sporadic and familial ALS DB Re, V Le Verche, C Yu, MW Amoroso, KA Politi, S Phani, B Ikiz, ... Neuron 81 (5), 1001-1008, 2014 | 471 | 2014 |
A trithorax-group complex purified from Saccharomyces cerevisiae is required for methylation of histone H3 PL Nagy, J Griesenbeck, RD Kornberg, ML Cleary Proceedings of the national academy of sciences 99 (1), 90-94, 2002 | 386 | 2002 |
Axonally synthesized ATF4 transmits a neurodegenerative signal across brain regions J Baleriola, CA Walker, YY Jean, JF Crary, CM Troy, PL Nagy, U Hengst Cell 158 (5), 1159-1172, 2014 | 347 | 2014 |
Implementation of next generation sequencing into pediatric hematology-oncology practice: moving beyond actionable alterations JA Oberg, JL Glade Bender, ML Sulis, D Pendrick, AN Sireci, SJ Hsiao, ... Genome medicine 8, 1-19, 2016 | 180 | 2016 |
Analysis of the ABCA4 genomic locus in Stargardt disease J Zernant, Y Xie, C Ayuso, R Riveiro-Alvarez, MA Lopez-Martinez, ... Human molecular genetics 23 (25), 6797-6806, 2014 | 153 | 2014 |
Genomewide demarcation of RNA polymerase II transcription units revealed by physical fractionation of chromatin PL Nagy, ML Cleary, PO Brown, JD Lieb Proceedings of the National Academy of Sciences 100 (11), 6364-6369, 2003 | 151 | 2003 |
The Glc7 phosphatase subunit of the cleavage and polyadenylation factor is essential for transcription termination on snoRNA genes E Nedea, D Nalbant, D Xia, NT Theoharis, B Suter, CJ Richardson, ... Molecular cell 29 (5), 577-587, 2008 | 146 | 2008 |
Identification of the Bacillus subtilis pur operon repressor M Weng, PL Nagy, H Zalkin Proceedings of the National Academy of Sciences 92 (16), 7455-7459, 1995 | 141 | 1995 |
LMNA cardiomyopathy: cell biology and genetics meet clinical medicine JT Lu, A Muchir, PL Nagy, HJ Worman Disease models & mechanisms 4 (5), 562-568, 2011 | 116 | 2011 |
Cognitive-behavioral screening reveals prevalent impairment in a large multicenter ALS cohort J Murphy, P Factor-Litvak, R Goetz, C Lomen-Hoerth, PL Nagy, J Hupf, ... Neurology 86 (9), 813-820, 2016 | 100 | 2016 |
The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy CR Coughlin, MA Swanson, E Spector, NJL Meeks, KE Kronquist, ... Journal of inherited metabolic disease 42 (2), 353-361, 2019 | 79 | 2019 |
Formyltetrahydrofolate hydrolase, a regulatory enzyme that functions to balance pools of tetrahydrofolate and one-carbon tetrahydrofolate adducts in Escherichia coli PL Nagy, A Marolewski, SJ Benkovic, H Zalkin Journal of Bacteriology 177 (5), 1292-1298, 1995 | 79 | 1995 |
Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1 R Firestein, PL Nagy, M Daly, P Huie, M Conti, ML Cleary The Journal of clinical investigation 109 (9), 1165-1172, 2002 | 78 | 2002 |
Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72 JS Goldman, C Quinzii, J Dunning-Broadbent, C Waters, H Mitsumoto, ... JAMA neurology 71 (6), 771-774, 2014 | 70 | 2014 |
A mutation abolishing the ZMPSTE24 cleavage site in prelamin A causes a progeroid disorder Y Wang, U Lichter-Konecki, K Anyane-Yeboa, JE Shaw, JT Lu, C Östlund, ... Journal of cell science 129 (10), 1975-1980, 2016 | 67 | 2016 |
DNA-like class R inhibitory oligonucleotides (INH-ODNs) preferentially block autoantigen-induced B-cell and dendritic cell activation in vitro and autoantibody production in … P Lenert, K Yasuda, L Busconi, P Nelson, C Fleenor, RS Ratnabalasuriar, ... Arthritis research & therapy 11, 1-16, 2009 | 63 | 2009 |
Phenotypic and molecular analyses of primary lateral sclerosis H Mitsumoto, PL Nagy, C Gennings, J Murphy, H Andrews, R Goetz, ... Neurology: Genetics 1 (1), e3, 2015 | 60 | 2015 |
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations S Mercier, S Küry, E Salort-Campana, A Magot, U Agbim, T Besnard, ... Orphanet journal of rare diseases 10, 1-16, 2015 | 55 | 2015 |
purU, a source of formate for purT-dependent phosphoribosyl-N-formylglycinamide synthesis PL Nagy, GM McCorkle, H Zalkin Journal of Bacteriology 175 (21), 7066-7073, 1993 | 54 | 1993 |
LMNA variants cause cytoplasmic distribution of nuclear pore proteins in Drosophila and human muscle G Dialynas, KM Flannery, LN Zirbel, PL Nagy, KD Mathews, SA Moore, ... Human molecular genetics 21 (7), 1544-1556, 2012 | 52 | 2012 |