David Nelson, Ph.D. - Publications

Baylor College of Medicine Baylor College of Medicine, Houston, TX 
Human genome and disease gene analysis

106 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Sparks ME, Bansal R, Benoit JB, Blackburn MB, Chao H, Chen M, Cheng S, Childers C, Dinh H, Doddapaneni HV, Dugan S, Elpidina EN, Farrow DW, Friedrich M, Gibbs RA, ... ... Nelson DR, et al. Brown marmorated stink bug, Halyomorpha halys (Stål), genome: putative underpinnings of polyphagy, insecticide resistance potential and biology of a top worldwide pest. Bmc Genomics. 21: 227. PMID 32171258 DOI: 10.1186/s12864-020-6510-7  0.4
2019 Katzner TE, Nelson DM, Diffendorfer JE, Duerr AE, Campbell CJ, Leslie D, Vander Zanden HB, Yee JL, Sur M, Huso MMP, Braham MA, Morrison ML, Loss SR, Poessel SA, Conkling TJ, et al. Wind energy: An ecological challenge. Science (New York, N.Y.). 366: 1206-1207. PMID 31806806 DOI: 10.1126/science.aaz9989  0.44
2019 Saha S, Hosmani PS, Villalobos-Ayala K, Miller S, Shippy T, Flores M, Rosendale A, Cordola C, Bell T, Mann H, DeAvila G, DeAvila D, Moore Z, Buller K, Ciolkevich K, ... ... Nelson D, et al. Improved annotation of the insect vector of citrus greening disease: biocuration by a diverse genomics community. Database : the Journal of Biological Databases and Curation. 2019. PMID 30820572 DOI: 10.1093/database/baz035  0.32
2018 Kong HE, Lim J, Zhang F, Huang L, Gu Y, Nelson DL, Allen EG, Jin P. Metabolic pathways modulate the neuronal toxicity associated with Fragile X-Associated Tremor/Ataxia Syndrome. Human Molecular Genetics. PMID 30476102 DOI: 10.1093/hmg/ddy410  0.44
2017 Saha S, Hosmani PS, Villalobos-Ayala K, Miller S, Shippy T, Flores M, Rosendale A, Cordola C, Bell T, Mann H, DeAvila G, DeAvila D, Moore Z, Buller K, Ciolkevich K, ... ... Nelson D, et al. Improved annotation of the insect vector of citrus greening disease: biocuration by a diverse genomics community. Database : the Journal of Biological Databases and Curation. 2017. PMID 29220441 DOI: 10.1093/database/bax032  0.32
2017 Campbell CJ, Nelson DM, Ogawa NO, Chikaraishi Y, Ohkouchi N. Trophic position and dietary breadth of bats revealed by nitrogen isotopic composition of amino acids. Scientific Reports. 7: 15932. PMID 29162842 DOI: 10.1038/s41598-017-15440-3  0.44
2017 Sakai S, Matsuda S, Hikida T, Shimono A, McManus BJ, Zahniser MS, Nelson DD, Dettman D, Yang D, Ohkouchi N. High-precision simultaneous (18)O/(16)O, (13)C/(12)C and (17)O/(16)O analyses for µg-quantities of CaCO3 by tunable infrared laser absorption spectroscopy. Analytical Chemistry. PMID 28937751 DOI: 10.1021/acs.analchem.7b03582  0.44
2016 McKenna DD, Scully ED, Pauchet Y, Hoover K, Kirsch R, Geib SM, Mitchell RF, Waterhouse RM, Ahn SJ, Arsala D, Benoit JB, Blackmon H, Bledsoe T, Bowsher JH, Busch A, ... ... Nelson DR, et al. Genome of the Asian longhorned beetle (Anoplophora glabripennis), a globally significant invasive species, reveals key functional and evolutionary innovations at the beetle-plant interface. Genome Biology. 17: 227. PMID 27832824 DOI: 10.1186/s13059-016-1088-8  0.4
2016 Benoit JB, Adelman ZN, Reinhardt K, Dolan A, Poelchau M, Jennings EC, Szuter EM, Hagan RW, Gujar H, Shukla JN, Zhu F, Mohan M, Nelson DR, Rosendale AJ, Derst C, et al. Unique features of a global human ectoparasite identified through sequencing of the bed bug genome. Nature Communications. 7: 10165. PMID 26836814 DOI: 10.1038/ncomms10165  0.4
2015 Lumaban JG, Nelson DL. The Fragile X proteins Fmrp and Fxr2p cooperate to regulate glucose metabolism in mice. Human Molecular Genetics. 24: 2175-84. PMID 25552647 DOI: 10.1093/hmg/ddu737  0.56
2014 Cook D, Nuro E, Jones EV, Altimimi HF, Farmer WT, Gandin V, Hanna E, Zong R, Barbon A, Nelson DL, Topisirovic I, Rochford J, Stellwagen D, Béïque JC, Murai KK. FXR1P limits long-term memory, long-lasting synaptic potentiation, and de novo GluA2 translation. Cell Reports. 9: 1402-16. PMID 25456134 DOI: 10.1016/j.celrep.2014.10.028  0.56
2014 Galloway JN, Shaw C, Yu P, Parghi D, Poidevin M, Jin P, Nelson DL. CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome. Human Molecular Genetics. 23: 5906-15. PMID 24986919 DOI: 10.1093/hmg/ddu314  0.56
2014 Yao B, Lin L, Street RC, Zalewski ZA, Galloway JN, Wu H, Nelson DL, Jin P. Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome. Human Molecular Genetics. 23: 1095-107. PMID 24108107 DOI: 10.1093/hmg/ddt504  0.56
2013 Vislay RL, Martin BS, Olmos-Serrano JL, Kratovac S, Nelson DL, Corbin JG, Huntsman MM. Homeostatic responses fail to correct defective amygdala inhibitory circuit maturation in fragile X syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 7548-58. PMID 23616559 DOI: 10.1523/JNEUROSCI.2764-12.2013  0.56
2013 Xu Z, Poidevin M, Li X, Li Y, Shu L, Nelson DL, Li H, Hales CM, Gearing M, Wingo TS, Jin P. Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration. Proceedings of the National Academy of Sciences of the United States of America. 110: 7778-83. PMID 23553836 DOI: 10.1073/pnas.1219643110  0.56
2013 Nelson DL, Orr HT, Warren ST. The unstable repeats--three evolving faces of neurological disease. Neuron. 77: 825-43. PMID 23473314 DOI: 10.1016/j.neuron.2013.02.022  0.56
2012 Yrigollen CM, Durbin-Johnson B, Gane L, Nelson DL, Hagerman R, Hagerman PJ, Tassone F. AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 14: 729-36. PMID 22498846 DOI: 10.1038/gim.2012.34  0.56
2012 Qurashi A, Liu H, Ray L, Nelson DL, Duan R, Jin P. Chemical screen reveals small molecules suppressing fragile X premutation rCGG repeat-mediated neurodegeneration in Drosophila. Human Molecular Genetics. 21: 2068-75. PMID 22298836 DOI: 10.1093/hmg/dds024  0.56
2012 Tan H, Qurashi A, Poidevin M, Nelson DL, Li H, Jin P. Retrotransposon activation contributes to fragile X premutation rCGG-mediated neurodegeneration. Human Molecular Genetics. 21: 57-65. PMID 21940752 DOI: 10.1093/hmg/ddr437  0.56
2011 Xu XL, Zong R, Li Z, Biswas MH, Fang Z, Nelson DL, Gao FB. FXR1P but not FMRP regulates the levels of mammalian brain-specific microRNA-9 and microRNA-124. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 13705-9. PMID 21957233 DOI: 10.1523/JNEUROSCI.2827-11.2011  0.56
2009 Nelson DL, Gibbs RA. X-cess of variants in XLMR. Nature Genetics. 41: 510-2. PMID 19399033 DOI: 10.1038/ng0509-510  0.56
2009 Hashem V, Galloway JN, Mori M, Willemsen R, Oostra BA, Paylor R, Nelson DL. Ectopic expression of CGG containing mRNA is neurotoxic in mammals. Human Molecular Genetics. 18: 2443-51. PMID 19377084 DOI: 10.1093/hmg/ddp182  0.56
2009 Zhang J, Hou L, Klann E, Nelson DL. Altered hippocampal synaptic plasticity in the FMR1 gene family knockout mouse models. Journal of Neurophysiology. 101: 2572-80. PMID 19244359 DOI: 10.1152/jn.90558.2008  0.56
2008 Paylor R, Yuva-Paylor LA, Nelson DL, Spencer CM. Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene. Behavioral Neuroscience. 122: 1371-7. PMID 19045956 DOI: 10.1037/a0013047  0.56
2008 Sofola O, Sundram V, Ng F, Kleyner Y, Morales J, Botas J, Jackson FR, Nelson DL. The Drosophila FMRP and LARK RNA-binding proteins function together to regulate eye development and circadian behavior. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 10200-5. PMID 18842880 DOI: 10.1523/JNEUROSCI.2786-08.2008  0.56
2008 Zhang J, Fang Z, Jud C, Vansteensel MJ, Kaasik K, Lee CC, Albrecht U, Tamanini F, Meijer JH, Oostra BA, Nelson DL. Fragile X-related proteins regulate mammalian circadian behavioral rhythms. American Journal of Human Genetics. 83: 43-52. PMID 18589395 DOI: 10.1016/j.ajhg.2008.06.003  0.56
2008 Spencer CM, Graham DF, Yuva-Paylor LA, Nelson DL, Paylor R. Social behavior in Fmr1 knockout mice carrying a human FMR1 transgene. Behavioral Neuroscience. 122: 710-5. PMID 18513141 DOI: 10.1037/0735-7044.122.3.710  0.56
2007 Sofola OA, Jin P, Qin Y, Duan R, Liu H, de Haro M, Nelson DL, Botas J. RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS. Neuron. 55: 565-71. PMID 17698010 DOI: 10.1016/j.neuron.2007.07.021  0.56
2007 Sofola OA, Jin P, Botas J, Nelson DL. Argonaute-2-dependent rescue of a Drosophila model of FXTAS by FRAXE premutation repeat. Human Molecular Genetics. 16: 2326-32. PMID 17635840 DOI: 10.1093/hmg/ddm186  0.56
2007 Gibbs RA, Rogers J, Katze MG, Bumgarner R, Weinstock GM, Mardis ER, Remington KA, Strausberg RL, Venter JC, Wilson RK, Batzer MA, Bustamante CD, Eichler EE, Hahn MW, ... ... Nelson DL, et al. Evolutionary and biomedical insights from the rhesus macaque genome. Science (New York, N.Y.). 316: 222-34. PMID 17431167 DOI: 10.1126/science.1139247  0.44
2007 Sekine H, Ferreira RC, Pan-Hammarström Q, Graham RR, Ziemba B, de Vries SS, Liu J, Hippen K, Koeuth T, Ortmann W, Iwahori A, Elliott MK, Offer S, Skon C, Du L, ... ... Nelson DL, et al. Role for Msh5 in the regulation of Ig class switch recombination. Proceedings of the National Academy of Sciences of the United States of America. 104: 7193-8. PMID 17409188 DOI: 10.1073/pnas.0700815104  0.56
2007 Pan-Hammarström Q, Salzer U, Du L, Björkander J, Cunningham-Rundles C, Nelson DL, Bacchelli C, Gaspar HB, Offer S, Behrens TW, Grimbacher B, Hammarström L. Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency. Nature Genetics. 39: 429-30. PMID 17392797 DOI: 10.1038/ng0407-429  0.56
2007 Brouwer JR, Mientjes EJ, Bakker CE, Nieuwenhuizen IM, Severijnen LA, Van der Linde HC, Nelson DL, Oostra BA, Willemsen R. Elevated Fmr1 mRNA levels and reduced protein expression in a mouse model with an unmethylated Fragile X full mutation. Experimental Cell Research. 313: 244-53. PMID 17150213 DOI: 10.1016/j.yexcr.2006.10.002  0.44
2006 Nishijima I, Yamagata T, Spencer CM, Weeber EJ, Alekseyenko O, Sweatt JD, Momoi MY, Ito M, Armstrong DL, Nelson DL, Paylor R, Bradley A. Secretin receptor-deficient mice exhibit impaired synaptic plasticity and social behavior. Human Molecular Genetics. 15: 3241-50. PMID 17008357 DOI: 10.1093/hmg/ddl402  0.56
2006 Spencer CM, Serysheva E, Yuva-Paylor LA, Oostra BA, Nelson DL, Paylor R. Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins. Human Molecular Genetics. 15: 1984-94. PMID 16675531 DOI: 10.1093/hmg/ddl121  0.44
2005 Yu F, Sabeti PC, Hardenbol P, Fu Q, Fry B, Lu X, Ghose S, Vega R, Perez A, Pasternak S, Leal SM, Willis TD, Nelson DL, Belmont J, Gibbs RA. Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. Plos Genetics. 1: e41. PMID 16205789 DOI: 10.1371/journal.pgen.0010041  0.56
2005 Koekkoek SK, Yamaguchi K, Milojkovic BA, Dortland BR, Ruigrok TJ, Maex R, De Graaf W, Smit AE, VanderWerf F, Bakker CE, Willemsen R, Ikeda T, Kakizawa S, Onodera K, Nelson DL, et al. Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome. Neuron. 47: 339-52. PMID 16055059 DOI: 10.1016/j.neuron.2005.07.005  0.56
2004 Nelson DL, Gibbs RA. Genetics. The critical region in trisomy 21. Science (New York, N.Y.). 306: 619-21. PMID 15499000 DOI: 10.1126/science.1105226  0.4
2004 Mientjes EJ, Willemsen R, Kirkpatrick LL, Nieuwenhuizen IM, Hoogeveen-Westerveld M, Verweij M, Reis S, Bardoni B, Hoogeveen AT, Oostra BA, Nelson DL. Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivo. Human Molecular Genetics. 13: 1291-302. PMID 15128702 DOI: 10.1093/hmg/ddh150  0.44
2004 Matsuura T, Fang P, Lin X, Khajavi M, Tsuji K, Rasmussen A, Grewal RP, Achari M, Alonso ME, Pulst SM, Zoghbi HY, Nelson DL, Roa BB, Ashizawa T. Somatic and germline instability of the ATTCT repeat in spinocerebellar ataxia type 10. American Journal of Human Genetics. 74: 1216-24. PMID 15127363 DOI: 10.1086/421526  0.56
2004 Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, Nelson DL, Moses K, Warren ST. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nature Neuroscience. 7: 113-7. PMID 14703574 DOI: 10.1038/nn1174  0.56
2003 Gibbs RA, Nelson DL. Human genetics. Primate shadow play. Science (New York, N.Y.). 299: 1331-3. PMID 12610290 DOI: 10.1126/science.1082931  0.4
2002 Peier AM, Nelson DL. Instability of a premutation-sized CGG repeat in FMR1 YAC transgenic mice. Genomics. 80: 423-32. PMID 12376097 DOI: 10.1006/geno.2002.6849  0.56
2002 Morales J, Hiesinger PR, Schroeder AJ, Kume K, Verstreken P, Jackson FR, Nelson DL, Hassan BA. Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain. Neuron. 34: 961-72. PMID 12086643 DOI: 10.1016/S0896-6273(02)00731-6  0.56
2002 Sterioff S, Nelson DL. A teacher of surgical thought. Surgery. 131: 117-8. PMID 11812974 DOI: 10.1067/msy.2002.114147  0.56
2001 Stewart DM, Lian L, Nelson DL. The clinical spectrum of Bruton's agammaglobulinemia. Current Allergy and Asthma Reports. 1: 558-65. PMID 11892085 DOI: 10.1007/s11882-001-0065-8  0.56
2001 Kenwrick S, Woffendin H, Jakins T, Shuttleworth SG, Mayer E, Greenhalgh L, Whittaker J, Rugolotto S, Bardaro T, Esposito T, D'Urso M, Soli F, Turco A, Smahi A, Hamel-Teillac D, ... ... Nelson DL, et al. Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndrome. American Journal of Human Genetics. 69: 1210-7. PMID 11673821 DOI: 10.1086/324591  0.56
2001 Richter BW, Mir SS, Eiben LJ, Lewis J, Reffey SB, Frattini A, Tian L, Frank S, Youle RJ, Nelson DL, Notarangelo LD, Vezzoni P, Fearnhead HO, Duckett CS. Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein family. Molecular and Cellular Biology. 21: 4292-301. PMID 11390657 DOI: 10.1128/MCB.21.13.4292-4301.2001  0.56
2000 Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nature Genetics. 26: 191-4. PMID 11017075 DOI: 10.1038/79911  0.56
2000 Tamanini F, Kirkpatrick LL, Schonkeren J, van Unen L, Bontekoe C, Bakker C, Nelson DL, Galjaard H, Oostra BA, Hoogeveen AT. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins. Human Molecular Genetics. 9: 1487-93. PMID 10888599 DOI: 10.1093/hmg/9.10.1487  0.56
2000 Peier AM, McIlwain KL, Kenneson A, Warren ST, Paylor R, Nelson DL. (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features. Human Molecular Genetics. 9: 1145-59. PMID 10767339 DOI: 10.1093/hmg/9.8.1145  0.56
1999 Zhong N, Ju W, Nelson D, Dobkin C, Brown WT. Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation American Journal of Medical Genetics. 84: 268-271. PMID 10331605 DOI: 10.1002/(SICI)1096-8628(19990528)84:3<268::AID-AJMG20>3.0.CO;2-#  0.56
1998 Gunter C, Paradee W, Crawford DC, Meadows KA, Newman J, Kunst CB, Nelson DL, Schwartz C, Murray A, Macpherson JN, Sherman SL, Warren ST. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. Human Molecular Genetics. 7: 1935-46. PMID 9811938 DOI: 10.1093/hmg/7.12.1935  0.56
1998 Nickerson E, Nelson DL. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics. 50: 368-72. PMID 9676431 DOI: 10.1006/geno.1998.5332  0.56
1998 Pearson CE, Eichler EE, Lorenzetti D, Kramer SF, Zoghbi HY, Nelson DL, Sinden RR. Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation. Biochemistry. 37: 2701-8. PMID 9485421 DOI: 10.1021/bi972546c  0.56
1997 Eichler EE, Budarf ML, Rocchi M, Deaven LL, Doggett NA, Baldini A, Nelson DL, Mohrenweiser HW. Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity. Human Molecular Genetics. 6: 991-1002. PMID 9215666 DOI: 10.1093/hmg/6.7.991  0.56
1997 Timms KM, Bondeson ML, Ansari-Lari MA, Lagerstedt K, Muzny DM, Dugan-Rocha SP, Nelson DL, Pettersson U, Gibbs RA. Molecular and phenotypic variation in patients with severe Hunter syndrome. Human Molecular Genetics. 6: 479-86. PMID 9147653 DOI: 10.1093/hmg/6.3.479  0.4
1997 Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, et al. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus. Genomics. 39: 55-65. PMID 9027486 DOI: 10.1006/geno.1996.4466  0.56
1997 Falik-Zaccai TC, Shachak E, Yalon M, Lis Z, Borochowitz Z, Macpherson JN, Nelson DL, Eichler EE. Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype. American Journal of Human Genetics. 60: 103-12. PMID 8981953  0.56
1996 Eichler EE, Macpherson JN, Murray A, Jacobs PA, Chakravarti A, Nelson DL. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. Human Molecular Genetics. 5: 319-30. PMID 8852655  0.56
1996 Eichler EE, Nelson DL. Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations. American Journal of Medical Genetics. 64: 220-5. PMID 8826480 DOI: 10.1002/(SICI)1096-8628(19960712)64:1<220::AID-AJMG40>3.0.CO;2-M  0.56
1996 Eichler EE, Lu F, Shen Y, Antonacci R, Jurecic V, Doggett NA, Moyzis RK, Baldini A, Gibbs RA, Nelson DL. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution. Human Molecular Genetics. 5: 899-912. PMID 8817324 DOI: 10.1093/hmg/5.7.899  0.56
1996 Gu Y, Shen Y, Gibbs RA, Nelson DL. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nature Genetics. 13: 109-13. PMID 8673086 DOI: 10.1038/ng0596-109  0.4
1996 Kunst CB, Zerylnick C, Karickhoff L, Eichler E, Bullard J, Chalifoux M, Holden JJ, Torroni A, Nelson DL, Warren ST. FMR1 in global populations. American Journal of Human Genetics. 58: 513-22. PMID 8644711  0.56
1995 Eichler EE, Hammond HA, Macpherson JN, Ward PA, Nelson DL. Population survey of the human FMR1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Human Molecular Genetics. 4: 2199-208. PMID 8634688  0.56
1995 Chastain PD, Eichler EE, Kang S, Nelson DL, Levene SD, Sinden RR. Anomalous rapid electrophoretic mobility of DNA containing triplet repeats associated with human disease genes. Biochemistry. 34: 16125-31. PMID 8519769 DOI: 10.1021/bi00049a027  0.56
1995 Wilson AC, Parrish JE, Massa HF, Nelson DL, Trask BJ, Herr W. The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 25: 462-8. PMID 7789979 DOI: 10.1016/0888-7543(95)80046-O  0.56
1995 Nelson DL. The fragile X syndromes Seminars in Cell Biology. 6: 5-11. PMID 7620122 DOI: 10.1016/1043-4682(95)90009-8  0.56
1995 Eichler EE, Kunst CB, Lugenbeel KA, Ryder OA, Davison D, Warren ST, Nelson DL. Evolution of the cryptic FMR1 CGG repeat. Nature Genetics. 11: 301-8. PMID 7581454 DOI: 10.1038/ng1195-301  0.56
1995 Nelson DL. Positional cloning reaches maturity Current Opinion in Genetics and Development. 5: 298-303. PMID 7549422 DOI: 10.1016/0959-437X(95)80042-5  0.56
1994 Eichler EE, Richards S, Gibbs RA, Nelson DL. Fine structure of the human FMR1 gene. Human Molecular Genetics. 3: 684-5. PMID 8069329  0.56
1994 Merenstein SA, Shyu V, Sobesky WE, Staley L, Berry-Kravis E, Nelson DL, Lugenbeel KA, Taylor AK, Pennington BF, Hagerman RJ. Fragile X syndrome in a normal IQ male with learning and emotional problems. Journal of the American Academy of Child and Adolescent Psychiatry. 33: 1316-21. PMID 7995799 DOI: 10.1097/00004583-199411000-00014  0.56
1994 Eichler EE, Holden JJ, Popovich BW, Reiss AL, Snow K, Thibodeau SN, Richards CS, Ward PA, Nelson DL. Length of uninterrupted CGG repeats determines instability in the FMR1 gene. Nature Genetics. 8: 88-94. PMID 7987398 DOI: 10.1038/ng0994-88  0.56
1994 Chong SS, Eichler EE, Nelson DL, Hughes MR. Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase. American Journal of Medical Genetics. 51: 522-6. PMID 7943034 DOI: 10.1002/ajmg.1320510447  0.56
1994 Ouweland AMwVD, Deelen WH, Kunst CB, Uzielli MLG, Nelson DL, Warren ST, Oostra BA, Halley DJJ. Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes Human Molecular Genetics. 3: 1823-1827. PMID 7849707 DOI: 10.1093/hmg/3.10.1823  0.56
1994 Gu Y, Lugenbeel KA, Vockley JG, Grody WW, Nelson DL. A de novo deletion in FMR1 in a patient with developmental delay Human Molecular Genetics. 3: 1705-1706. PMID 7530551 DOI: 10.1093/hmg/3.9.1705  0.56
1994 Warren ST, Nelson DL. Advances in Molecular Analysis of Fragile X Syndrome Jama: the Journal of the American Medical Association. 271: 536-542. DOI: 10.1001/jama.1994.03510310066040  0.44
1993 Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL. Alternative splicing in the fragile X gene FMR1. Human Molecular Genetics. 2: 399-404. PMID 8504300 DOI: 10.1093/hmg/2.4.399  0.56
1993 Hinds HL, Ashley CT, Sutcliffe JS, Nelson DL, Warren ST, Housman DE, Schalling M. Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genetics. 3: 36-43. PMID 8490651 DOI: 10.1038/ng0193-36  0.56
1993 Verkerk AJ, de Graaff E, De Boulle K, Eichler EE, Konecki DS, Reyniers E, Manca A, Poustka A, Willems PJ, Nelson DL. Alternative splicing in the fragile X gene FMR1. Human Molecular Genetics. 2: 1348. PMID 8401531  0.56
1993 Eichler EE, Richards S, Gibbs RA, Nelson DL. Fine structure of the human FMR1 gene. Human Molecular Genetics. 2: 1147-53. PMID 8401496  0.56
1993 Ashley CT, Sutcliffe JS, Kunst CB, Leiner HA, Eichler EE, Nelson DL, Warren ST. Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat. Nature Genetics. 4: 244-51. PMID 8358432 DOI: 10.1038/ng0793-244  0.56
1993 Nelson DL, Warren ST. Trinucleotide repeat instability: When and where? Nature Genetics. 4: 107-108. PMID 8348143 DOI: 10.1038/ng0693-107  0.56
1993 Hornstra LK, Nelson DL, Warren ST, Yang TP. High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome Human Molecular Genetics. 2: 1659-1665. PMID 8268919 DOI: 10.1093/hmg/2.10.1659  0.56
1993 Warren ST, Nelson DL. Trinucleotide repeat expansions in neurological disease Current Opinion in Neurobiology. 3: 752-759. PMID 8260825 DOI: 10.1016/0959-4388(93)90149-S  0.56
1993 Parrish JE, Nelson DL. Methods for finding genes a major rate-limiting step in positional cloning Genetic Analysis Techniques and Applications. 10: 29-41. PMID 8217302 DOI: 10.1016/1050-3862(93)90043-I  0.56
1993 Wang Q, Ishikawa-Brush Y, Monaco AP, Nelson DL, Caskey CT, Pauly SP, Lenoir GM, Sylla BS. Physical mapping of Xq24-25 around loci closely linked to the X-linked lymphoproliferative syndrome locus: an overlapping YAC map and linkage between DXS12, DXS42, and DXS37. European Journal of Human Genetics : Ejhg. 1: 64-71. PMID 8069652 DOI: 10.1159/000472388  0.56
1992 Riggins GJ, Sherman SL, Oostra BA, Sutcliffe JS, Feitell D, Nelson DL, Van Oost BA, Smits APT, Ramos FJ, Pfendner E, Kuhl DPA, Caskey CT, Warren ST. Characterization of a highly polymorphic dinucleotide repeat 150 kb proximal to the fragile X site American Journal of Medical Genetics. 43: 237-243. PMID 1605197 DOI: 10.1002/ajmg.1320430138  0.56
1992 Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Intragenic probe used for diagnostics in fragile X families. American Journal of Medical Genetics. 43: 192-6. PMID 1605192 DOI: 10.1002/ajmg.1320430132  0.56
1992 Macpherson JN, Nelson DL, Jacobs PA. Frequent small amplifications in the FMR-1 gene in fra(X) families: limits to the diagnosis of 'premutations'. Journal of Medical Genetics. 29: 802-6. PMID 1453431 DOI: 10.1136/jmg.29.11.802  0.48
1992 Mandel JL, Monaco AP, Nelson DL, Schlessinger D, Willard HF, Chipperfield M, Pearson P, Gilna P, Cinkosky M. Genome maps III. 1992. Wall Chart. Science (New York, N.Y.). 258: 87-102. PMID 1439771 DOI: 10.1126/science.1439771  0.56
1992 Sutcliffe JS, Zhang F, Caskey CT, Nelson DL, Warren ST. PCR amplification and analysis of yeast artificial chromosomes. Genomics. 13: 1303-6. PMID 1380485 DOI: 10.1016/0888-7543(92)90051-S  0.56
1992 Sutcliffe JS, Nelson DL, Zhang F, Pieretti M, Caskey CT, Saxe D, Warren ST. DNA methylation represses FMR-1 transcription in fragile X syndrome. Human Molecular Genetics. 1: 397-400. PMID 1301913 DOI: 10.1093/hmg/1.6.397  0.56
1991 Nelson DL, Ballabio A, Victoria MF, Pieretti M, Bies RD, Gibbs RA, Maley JA, Chinault AC, Webster TD, Caskey CT. Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus. Proceedings of the National Academy of Sciences of the United States of America. 88: 6157-61. PMID 2068096 DOI: 10.1073/pnas.88.14.6157  0.56
1991 Pieretti M, Zhang FP, Fu YH, Warren ST, Oostra BA, Caskey CT, Nelson DL. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell. 66: 817-22. PMID 1878973 DOI: 10.1016/0092-8674(91)90125-I  0.56
1991 Nelson DL. Applications of polymerase chain reaction methods in genome mapping Current Opinion in Genetics and Development. 1: 62-68. PMID 1688122 DOI: 10.1016/0959-437X(91)80043-L  0.56
1991 Nelson DL. Interspersed repetitive sequence polymerase chain reaction (IRS PCR) for generation of human DNA fragments from complex sources Methods. 2: 60-74. DOI: 10.1016/S1046-2023(05)80126-4  0.56
1990 Cook-Deegan RM, Guyer M, Rossiter BJ, Nelson DL, Caskey CT. The large DNA insert cloning workshop. Genomics. 7: 654-60. PMID 2387593 DOI: 10.1016/0888-7543(90)90215-G  0.56
1990 Cook-Deegan RM, Rossiter BJ, Engel L, Nelson DL, Caskey CT. Report of the X chromosome workshop. Genomics. 7: 647-54. PMID 2387592 DOI: 10.1016/0888-7543(90)90214-F  0.56
1990 Corbo L, Maley JA, Nelson DL, Caskey CT. Direct cloning of human transcripts with HnRNA from hybrid cell lines. Science (New York, N.Y.). 249: 652-5. PMID 2382140 DOI: 10.1126/science.2382140  0.56
1990 Ledbetter SA, Nelson DL, Warren ST, Ledbetter DH. Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reaction Genomics. 6: 475-481. PMID 2328990 DOI: 10.1016/0888-7543(90)90477-C  0.56
1990 Nelson DL. Current methods for YAC clone characterization Gene Analysis Techniques. 7: 100-106. PMID 2091691 DOI: 10.1016/0735-0651(90)90014-7  0.56
1989 Rapaport MH, Mcallister CG, Pickar D, Nelson DL, Paul SM. Elevated Levels of Soluble Interleukin 2 Receptors in Schizophrenia Archives of General Psychiatry. 46: 291-292. PMID 2784047 DOI: 10.1001/archpsyc.1989.01810030097017  0.56
1989 Nelson DL, Ledbetter SA, Corbo L, Victoria MF, Ramírez-Solis R, Webster TD, Ledbetter DH, Caskey CT. Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proceedings of the National Academy of Sciences of the United States of America. 86: 6686-90. PMID 2771952 DOI: 10.1073/pnas.86.17.6686  0.56
1987 Myers MW, Lazzarini RA, Lee VM, Schlaepfer WW, Nelson DL. The human mid-size neurofilament subunit: a repeated protein sequence and the relationship of its gene to the intermediate filament gene family. The Embo Journal. 6: 1617-26. PMID 3608989  0.56
1986 Nelson DL, Chang SM, Henkel-Tigges J, Wager-Smith K, Belmont JW, Caskey CT. Gene replacement therapy for inborn errors of purine metabolism. Cold Spring Harbor Symposia On Quantitative Biology. 51: 1065-71. PMID 3555977 DOI: 10.1101/SQB.1986.051.01.124  0.56
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