| Year |
Citation |
Score |
| 2023 |
LaSalle JM. Epigenomic signatures reveal mechanistic clues and predictive markers for autism spectrum disorder. Molecular Psychiatry. PMID 36650278 DOI: 10.1038/s41380-022-01917-9 |
0.406 |
|
| 2022 |
Maggio AG, Shu HT, Laufer BI, Bi C, Lai Y, LaSalle JM, Hu VW. Elevated exposures to persistent endocrine disrupting compounds impact the sperm methylome in regions associated with autism spectrum disorder. Frontiers in Genetics. 13: 929471. PMID 36035158 DOI: 10.3389/fgene.2022.929471 |
0.339 |
|
| 2022 |
Williams LA, LaSalle JM. Future Prospects for Epigenetics in Autism Spectrum Disorder. Molecular Diagnosis & Therapy. PMID 35962910 DOI: 10.1007/s40291-022-00608-z |
0.323 |
|
| 2022 |
LaSalle JM. X Chromosome Inactivation Timing is Not e: Implications for Autism Spectrum Disorders. Frontiers in Genetics. 13: 864848. PMID 35356429 DOI: 10.3389/fgene.2022.864848 |
0.329 |
|
| 2022 |
Mouat JS, LaSalle JM. The Promise of DNA Methylation in Understanding Multigenerational Factors in Autism Spectrum Disorders. Frontiers in Genetics. 13: 831221. PMID 35242170 DOI: 10.3389/fgene.2022.831221 |
0.319 |
|
| 2022 |
Laufer BI, Neier K, Valenzuela AE, Yasui DH, Schmidt RJ, Lein PJ, LaSalle JM. Placenta and fetal brain share a neurodevelopmental disorder DNA methylation profile in a mouse model of prenatal PCB exposure. Cell Reports. 38: 110442. PMID 35235788 DOI: 10.1016/j.celrep.2022.110442 |
0.347 |
|
| 2022 |
Zhu Y, Gomez JA, Laufer BI, Mordaunt CE, Mouat JS, Soto DC, Dennis MY, Benke KS, Bakulski KM, Dou J, Marathe R, Jianu JM, Williams LA, Gutierrez Fugón OJ, Walker CK, ... ... LaSalle JM, et al. Placental methylome reveals a 22q13.33 brain regulatory gene locus associated with autism. Genome Biology. 23: 46. PMID 35168652 DOI: 10.1186/s13059-022-02613-1 |
0.37 |
|
| 2021 |
Sarode GV, Neier K, Shibata NM, Shen Y, Goncharov DA, Goncharova EA, Mazi TA, Joshi N, Settles ML, LaSalle JM, Medici V. Wilson disease: intersecting DNA methylation and histone acetylation regulation of gene expression in a mouse model of hepatic copper accumulation. Cellular and Molecular Gastroenterology and Hepatology. PMID 34098115 DOI: 10.1016/j.jcmgh.2021.05.020 |
0.301 |
|
| 2021 |
Laufer BI, Gomez JA, Jianu JM, LaSalle JM. Stable DNMT3L overexpression in SH-SY5Y neurons recreates a facet of the genome-wide Down syndrome DNA methylation signature. Epigenetics & Chromatin. 14: 13. PMID 33750431 DOI: 10.1186/s13072-021-00387-7 |
0.347 |
|
| 2021 |
Mendiola AJP, LaSalle JM. Epigenetics in Prader-Willi Syndrome. Frontiers in Genetics. 12: 624581. PMID 33659026 DOI: 10.3389/fgene.2021.624581 |
0.323 |
|
| 2020 |
Zhu Y, Mordaunt CE, Durbin-Johnson BP, Caudill MA, Malysheva OV, Miller JW, Green R, James SJ, Melnyk SB, Fallin MD, Hertz-Picciotto I, Schmidt RJ, LaSalle JM. Expression Changes in Epigenetic Gene Pathways Associated With One-Carbon Nutritional Metabolites in Maternal Blood From Pregnancies Resulting in Autism and Non-Typical Neurodevelopment. Autism Research : Official Journal of the International Society For Autism Research. PMID 33159718 DOI: 10.1002/aur.2428 |
0.326 |
|
| 2020 |
Laufer BI, Hwang H, Jianu JM, Mordaunt CE, Korf IF, Hertz-Picciotto I, LaSalle JM. Low-Pass Whole Genome Bisulfite Sequencing of Neonatal Dried Blood Spots Identifies a Role for RUNX1 in Down Syndrome DNA Methylation Profiles. Human Molecular Genetics. PMID 33001180 DOI: 10.1093/hmg/ddaa218 |
0.365 |
|
| 2019 |
Lopez SJ, Laufer BI, Beitnere U, Berg EL, Silverman JL, O'Geen H, Segal DJ, LaSalle JM. Imprinting effects of UBE3A loss on synaptic gene networks and Wnt signaling pathways. Human Molecular Genetics. PMID 31625566 DOI: 10.1093/hmg/ddz221 |
0.375 |
|
| 2019 |
Vogel Ciernia A, Laufer BI, Hwang H, Dunaway KW, Mordaunt CE, Coulson RL, Yasui DH, LaSalle JM. Epigenomic Convergence of Neural-Immune Risk Factors in Neurodevelopmental Disorder Cortex. Cerebral Cortex (New York, N.Y. : 1991). PMID 31240313 DOI: 10.1093/cercor/bhz115 |
0.457 |
|
| 2019 |
Medici V, LaSalle JM. Genetics and epigenetic factors of Wilson disease. Annals of Translational Medicine. 7: S58. PMID 31179295 DOI: 10.21037/atm.2019.01.67 |
0.33 |
|
| 2019 |
Laufer BI, Hwang H, Vogel Ciernia A, Mordaunt CE, LaSalle JM. Whole genome bisulfite sequencing of Down syndrome brain reveals regional DNA hypermethylation and novel disorder insights. Epigenetics. PMID 31010359 DOI: 10.1080/15592294.2019.1609867 |
0.336 |
|
| 2019 |
Zhu Y, Mordaunt CE, Yasui DH, Marathe R, Coulson RL, Dunaway KW, Jianu JM, Walker CK, Ozonoff S, Hertz-Picciotto I, Schmidt RJ, LaSalle JM. Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study. Human Molecular Genetics. PMID 31009952 DOI: 10.1093/Hmg/Ddz084 |
0.346 |
|
| 2019 |
Sarode GV, Mordaunt C, Shibata N, Bowlus C, Czlonkowska A, Litwin T, Weiss KH, LaSalle J, Medici V. FRI-438-Histone deacetylase 5 methylation changes in mice and patients with Wilson disease Journal of Hepatology. 70: e587. DOI: 10.1016/S0618-8278(19)31175-2 |
0.322 |
|
| 2018 |
Lopez SJ, Segal DJ, LaSalle JM. UBE3A: An E3 Ubiquitin Ligase With Genome-Wide Impact in Neurodevelopmental Disease. Frontiers in Molecular Neuroscience. 11: 476. PMID 30686997 DOI: 10.3389/fnmol.2018.00476 |
0.324 |
|
| 2018 |
Coulson RL, Powell WT, Yasui DH, Dileep G, Resnick J, LaSalle JM. Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN. Human Molecular Genetics. PMID 30124848 DOI: 10.1093/Hmg/Ddy296 |
0.302 |
|
| 2018 |
Coulson RL, LaSalle JM. Epigenetics of Circadian Rhythms in Imprinted Neurodevelopmental Disorders. Progress in Molecular Biology and Translational Science. 157: 67-92. PMID 29933957 DOI: 10.1016/bs.pmbts.2017.11.023 |
0.377 |
|
| 2018 |
Coulson RL, Yasui DH, Dunaway KW, Laufer BI, Vogel Ciernia A, Zhu Y, Mordaunt CE, Totah TS, LaSalle JM. Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex. Nature Communications. 9: 1616. PMID 29691382 DOI: 10.1038/s41467-018-03676-0 |
0.389 |
|
| 2017 |
Vogel Ciernia A, Careaga M, LaSalle JM, Ashwood P. Microglia from offspring of dams with allergic asthma exhibit epigenomic alterations in genes dysregulated in autism. Glia. PMID 29134693 DOI: 10.1002/Glia.23261 |
0.364 |
|
| 2017 |
Copping NA, Christian SGB, Ritter DJ, Islam MS, Buscher N, Zolkowska D, Pride MC, Berg EL, LaSalle JM, Ellegood J, Lerch JP, Reiter LT, Silverman JL, Dindot SV. Neuronal overexpression of Ube3a isoform 2 causes behavioral impairments and neuroanatomical pathology relevant to 15q11.2-q13.3 duplication syndrome. Human Molecular Genetics. 26: 3995-4010. PMID 29016856 DOI: 10.1093/Hmg/Ddx289 |
0.456 |
|
| 2017 |
Lopez SJ, Dunaway K, Islam MS, Mordaunt C, Ciernia AV, Meguro-Horike M, Horike SI, Segal DJ, LaSalle J. UBE3A-mediated regulation of imprinted genes and epigenome-wide marks in human neurons. Epigenetics. 0. PMID 28925810 DOI: 10.1080/15592294.2017.1376151 |
0.462 |
|
| 2016 |
Dunaway K, Goorha S, Matelski L, Urraca N, Lein PJ, Korf I, Reiter LT, LaSalle JM. Dental Pulp Stem Cells Model Early Life and Imprinted DNA Methylation Patterns. Stem Cells (Dayton, Ohio). PMID 28032673 DOI: 10.1002/Stem.2563 |
0.313 |
|
| 2016 |
Dunaway KW, Islam MS, Coulson RL, Lopez SJ, Vogel Ciernia A, Chu RG, Yasui DH, Pessah IN, Lott P, Mordaunt C, Meguro-Horike M, Horike SI, Korf I, LaSalle JM. Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes. Cell Reports. 17: 3035-3048. PMID 27974215 DOI: 10.1016/J.Celrep.2016.11.058 |
0.441 |
|
| 2016 |
Veeraragavan S, Wan YW, Connolly DR, Hamilton SM, Ward CS, Soriano S, Pitcher MR, McGraw CM, Huang SG, Green JR, Yuva LA, Liang AJ, Neul JL, Yasui DH, LaSalle JM, et al. Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome. Human Molecular Genetics. PMID 27365498 DOI: 10.1093/Hmg/Ddw178 |
0.704 |
|
| 2016 |
Ciernia AV, LaSalle J. The landscape of DNA methylation amid a perfect storm of autism aetiologies. Nature Reviews. Neuroscience. PMID 27150399 DOI: 10.1038/nrn.2016.41 |
0.364 |
|
| 2016 |
Rube HT, Lee W, Hejna M, Chen H, Yasui DH, Hess JF, LaSalle JM, Song JS, Gong Q. Sequence features accurately predict genome-wide MeCP2 binding in vivo. Nature Communications. 7: 11025. PMID 27008915 DOI: 10.1038/Ncomms11025 |
0.317 |
|
| 2015 |
LaSalle JM, Reiter LT, Chamberlain SJ. Epigenetic regulation of UBE3A and roles in human neurodevelopmental disorders. Epigenomics. PMID 26585570 DOI: 10.2217/Epi.15.70 |
0.398 |
|
| 2015 |
Schroeder DI, Jayashankar K, Douglas KC, Thirkill TL, York D, Dickinson PJ, Williams LE, Samollow PB, Ross PJ, Bannasch DL, Douglas GC, LaSalle JM. Early Developmental and Evolutionary Origins of Gene Body DNA Methylation Patterns in Mammalian Placentas. Plos Genetics. 11: e1005442. PMID 26241857 DOI: 10.1371/Journal.Pgen.1005442 |
0.323 |
|
| 2014 |
Lee W, Yun JM, Woods R, Dunaway K, Yasui DH, Lasalle JM, Gong Q. MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons. Human Molecular Genetics. 23: 6366-74. PMID 25008110 DOI: 10.1093/Hmg/Ddu358 |
0.647 |
|
| 2014 |
Selmi C, Cavaciocchi F, Lleo A, Cheroni C, De Francesco R, Lombardi SA, De Santis M, Meda F, Raimondo MG, Crotti C, Folci M, Zammataro L, Mayo MJ, Bach N, Shimoda S, ... ... Lasalle JM, et al. Genome-wide analysis of DNA methylation, copy number variation, and gene expression in monozygotic twins discordant for primary biliary cirrhosis. Frontiers in Immunology. 5: 128. PMID 24734033 DOI: 10.3389/Fimmu.2014.00128 |
0.354 |
|
| 2014 |
Medici V, Schroeder DI, Woods R, LaSalle JM, Geng Y, Shibata NM, Peerson J, Hodzic E, Dayal S, Tsukamoto H, Kharbanda KK, Tillman B, French SW, Halsted CH. Methylation and gene expression responses to ethanol feeding and betaine supplementation in the cystathionine beta synthase-deficient mouse. Alcoholism, Clinical and Experimental Research. 38: 1540-9. PMID 24730561 DOI: 10.1111/Acer.12405 |
0.567 |
|
| 2014 |
Woods R, Lasalle JM. Epigenetic epidemiology of autism and other neurodevelopmental disorders Epigenetic Epidemiology. 2147483647: 321-342. DOI: 10.1007/978-94-007-2495-2_17 |
0.612 |
|
| 2013 |
Powell WT, Coulson RL, Gonzales ML, Crary FK, Wong SS, Adams S, Ach RA, Tsang P, Yamada NA, Yasui DH, Chédin F, LaSalle JM. R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation. Proceedings of the National Academy of Sciences of the United States of America. 110: 13938-43. PMID 23918391 DOI: 10.1073/Pnas.1305426110 |
0.428 |
|
| 2013 |
Powell WT, Coulson RL, Crary FK, Wong SS, Ach RA, Tsang P, Alice Yamada N, Yasui DH, Lasalle JM. A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure. Human Molecular Genetics. 22: 4318-28. PMID 23771028 DOI: 10.1093/hmg/ddt281 |
0.302 |
|
| 2013 |
Schroeder DI, Blair JD, Lott P, Yu HO, Hong D, Crary F, Ashwood P, Walker C, Korf I, Robinson WP, LaSalle JM. The human placenta methylome. Proceedings of the National Academy of Sciences of the United States of America. 110: 6037-42. PMID 23530188 DOI: 10.1073/Pnas.1215145110 |
0.311 |
|
| 2013 |
Yasui DH, Xu H, Dunaway KW, Lasalle JM, Jin LW, Maezawa I. MeCP2 modulates gene expression pathways in astrocytes. Molecular Autism. 4: 3. PMID 23351786 DOI: 10.1186/2040-2392-4-3 |
0.432 |
|
| 2013 |
Medici V, Shibata NM, Kharbanda KK, LaSalle JM, Woods R, Liu S, Engelberg JA, Devaraj S, Török NJ, Jiang JX, Havel PJ, Lönnerdal B, Kim K, Halsted CH. Wilson's disease: changes in methionine metabolism and inflammation affect global DNA methylation in early liver disease. Hepatology (Baltimore, Md.). 57: 555-65. PMID 22945834 DOI: 10.1002/Hep.26047 |
0.589 |
|
| 2013 |
Medici V, Schroeder DI, Woods R, LaSalle JM, Dayal S, Tsukamoto H, Kharbanda KK, French SW, Halsted CH. 615 Epigenetic Regulation of iNOS, PPAR-Alpha, and Dnmt1 in the Cystathionine Beta Synthase Deficient Mouse Model of Alcoholic Steatohepatitis Gastroenterology. 144: S-953. DOI: 10.1016/S0016-5085(13)63543-X |
0.538 |
|
| 2012 |
Mitchell MM, Woods R, Chi LH, Schmidt RJ, Pessah IN, Kostyniak PJ, LaSalle JM. Levels of select PCB and PBDE congeners in human postmortem brain reveal possible environmental involvement in 15q11-q13 duplication autism spectrum disorder. Environmental and Molecular Mutagenesis. 53: 589-98. PMID 22930557 DOI: 10.1002/Em.21722 |
0.684 |
|
| 2012 |
Selmi C, Feghali-Bostwick CA, Lleo A, Lombardi SA, De Santis M, Cavaciocchi F, Zammataro L, Mitchell MM, Lasalle JM, Medsger T, Gershwin ME. X chromosome gene methylation in peripheral lymphocytes from monozygotic twins discordant for scleroderma. Clinical and Experimental Immunology. 169: 253-62. PMID 22861365 DOI: 10.1111/j.1365-2249.2012.04621.x |
0.35 |
|
| 2012 |
Gonzales ML, Adams S, Dunaway KW, LaSalle JM. Phosphorylation of distinct sites in MeCP2 modifies cofactor associations and the dynamics of transcriptional regulation. Molecular and Cellular Biology. 32: 2894-903. PMID 22615490 DOI: 10.1128/MCB.06728-11 |
0.384 |
|
| 2012 |
Woods R, Vallero RO, Golub MS, Suarez JK, Ta TA, Yasui DH, Chi LH, Kostyniak PJ, Pessah IN, Berman RF, LaSalle JM. Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation. Human Molecular Genetics. 21: 2399-411. PMID 22343140 DOI: 10.1093/Hmg/Dds046 |
0.621 |
|
| 2012 |
Martins-Taylor K, Schroeder DI, LaSalle JM, Lalande M, Xu RH. Role of DNMT3B in the regulation of early neural and neural crest specifiers. Epigenetics : Official Journal of the Dna Methylation Society. 7: 71-82. PMID 22207353 DOI: 10.4161/Epi.7.1.18750 |
0.622 |
|
| 2011 |
Scoles HA, Urraca N, Chadwick SW, Reiter LT, Lasalle JM. Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples. Molecular Autism. 2: 19. PMID 22152151 DOI: 10.1186/2040-2392-2-19 |
0.445 |
|
| 2011 |
Yasui DH, Scoles HA, Horike S, Meguro-Horike M, Dunaway KW, Schroeder DI, Lasalle JM. 15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain. Human Molecular Genetics. 20: 4311-23. PMID 21840925 DOI: 10.1093/Hmg/Ddr357 |
0.405 |
|
| 2011 |
Schroeder DI, Lott P, Korf I, LaSalle JM. Large-scale methylation domains mark a functional subset of neuronally expressed genes. Genome Research. 21: 1583-91. PMID 21784875 DOI: 10.1101/Gr.119131.110 |
0.364 |
|
| 2011 |
Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S. Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome. Human Molecular Genetics. 20: 3798-810. PMID 21725066 DOI: 10.1093/Hmg/Ddr298 |
0.372 |
|
| 2011 |
Artuso R, Papa FT, Grillo E, Mucciolo M, Yasui DH, Dunaway KW, Disciglio V, Mencarelli MA, Pollazzon M, Zappella M, Hayek G, Mari F, Renieri A, Lasalle JM, Ariani F. Investigation of modifier genes within copy number variations in Rett syndrome. Journal of Human Genetics. 56: 508-15. PMID 21593744 DOI: 10.1038/jhg.2011.50 |
0.364 |
|
| 2011 |
Singleton MK, Gonzales ML, Leung KN, Yasui DH, Schroeder DI, Dunaway K, LaSalle JM. MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation. Neurobiology of Disease. 43: 190-200. PMID 21420494 DOI: 10.1016/J.Nbd.2011.03.011 |
0.655 |
|
| 2011 |
Leung KN, Chamberlain SJ, Lalande M, LaSalle JM. Neuronal chromatin dynamics of imprinting in development and disease. Journal of Cellular Biochemistry. 112: 365-73. PMID 21268055 DOI: 10.1002/Jcb.22958 |
0.743 |
|
| 2011 |
Mitchell MM, Lleo A, Zammataro L, Mayo MJ, Invernizzi P, Bach N, Shimoda S, Gordon S, Podda M, Gershwin ME, Selmi C, LaSalle JM. Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis. Epigenetics : Official Journal of the Dna Methylation Society. 6: 95-102. PMID 20864813 DOI: 10.4161/epi.6.1.13405 |
0.367 |
|
| 2010 |
Gonzales ML, LaSalle JM. The role of MeCP2 in brain development and neurodevelopmental disorders. Current Psychiatry Reports. 12: 127-34. PMID 20425298 DOI: 10.1007/s11920-010-0097-7 |
0.407 |
|
| 2010 |
Hogart A, Wu D, LaSalle JM, Schanen NC. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease. 38: 181-91. PMID 18840528 DOI: 10.1016/J.Nbd.2008.08.011 |
0.803 |
|
| 2009 |
LaSalle JM, Yasui DH. Evolving role of MeCP2 in Rett syndrome and autism. Epigenomics. 1: 119-30. PMID 20473347 DOI: 10.2217/epi.09.13 |
0.462 |
|
| 2009 |
Leung KN, Vallero RO, DuBose AJ, Resnick JL, LaSalle JM. Imprinting regulates mammalian snoRNA-encoding chromatin decondensation and neuronal nucleolar size. Human Molecular Genetics. 18: 4227-38. PMID 19656775 DOI: 10.1093/Hmg/Ddp373 |
0.712 |
|
| 2009 |
Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW. Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 5051-61. PMID 19386901 DOI: 10.1523/Jneurosci.0324-09.2009 |
0.435 |
|
| 2009 |
Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism. Human Molecular Genetics. 18: 525-34. PMID 19000991 DOI: 10.1093/Hmg/Ddn380 |
0.758 |
|
| 2009 |
Adegbola AA, Gonzales ML, Chess A, LaSalle JM, Cox GF. A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype. Human Genetics. 124: 615-23. PMID 18989701 DOI: 10.1007/s00439-008-0585-6 |
0.318 |
|
| 2009 |
Hogart A, Leung KN, Wang NJ, Wu DJ, Driscoll J, Vallero RO, Schanen NC, LaSalle JM. Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46: 86-93. PMID 18835857 DOI: 10.1136/Jmg.2008.061580 |
0.823 |
|
| 2008 |
Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM. MECP2 promoter methylation and X chromosome inactivation in autism. Autism Research : Official Journal of the International Society For Autism Research. 1: 169-78. PMID 19132145 DOI: 10.1002/Aur.24 |
0.574 |
|
| 2008 |
Hogart A, Patzel KA, LaSalle JM. Gender influences monoallelic expression of ATP10A in human brain. Human Genetics. 124: 235-42. PMID 18726118 DOI: 10.1007/S00439-008-0546-0 |
0.831 |
|
| 2008 |
Kumar A, Kamboj S, Malone BM, Kudo S, Twiss JL, Czymmek KJ, LaSalle JM, Schanen NC. Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo. Journal of Cell Science. 121: 1128-37. PMID 18334558 DOI: 10.1242/Jcs.016865 |
0.313 |
|
| 2008 |
Wang NJ, Parokonny AS, Thatcher KN, Driscoll J, Malone BM, Dorrani N, Sigman M, LaSalle JM, Schanen NC. Multiple forms of atypical rearrangements generating supernumerary derivative chromosome 15. Bmc Genetics. 9: 2. PMID 18177502 DOI: 10.1186/1471-2156-9-2 |
0.7 |
|
| 2007 |
Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM. Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences of the United States of America. 104: 19416-21. PMID 18042715 DOI: 10.1073/Pnas.0707442104 |
0.785 |
|
| 2007 |
LaSalle JM. The odyssey of MeCP2 and parental imprinting. Epigenetics : Official Journal of the Dna Methylation Society. 2: 5-10. PMID 17486180 |
0.359 |
|
| 2007 |
Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM. 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Human Molecular Genetics. 16: 691-703. PMID 17339270 DOI: 10.1093/Hmg/Ddm014 |
0.844 |
|
| 2006 |
Nagarajan RP, Hogart AR, Gwye Y, Martin MR, LaSalle JM. Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation. Epigenetics : Official Journal of the Dna Methylation Society. 1: e1-11. PMID 17486179 DOI: 10.4161/epi.1.4.3514 |
0.826 |
|
| 2006 |
Thatcher KN, LaSalle JM. Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. Epigenetics : Official Journal of the Dna Methylation Society. 1: 24-31. PMID 17464364 DOI: 10.4161/epi.1.1.2339 |
0.757 |
|
| 2006 |
Delgado IJ, Kim DS, Thatcher KN, LaSalle JM, Van den Veyver IB. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. Bmc Medical Genetics. 7: 61. PMID 16859563 DOI: 10.1186/1471-2350-7-61 |
0.747 |
|
| 2006 |
Peddada S, Yasui DH, LaSalle JM. Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome. Human Molecular Genetics. 15: 2003-14. PMID 16682435 DOI: 10.1093/Hmg/Ddl124 |
0.686 |
|
| 2005 |
LaSalle JM, Hogart A, Thatcher KN. Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism. International Review of Neurobiology. 71: 131-65. PMID 16512349 DOI: 10.1016/S0074-7742(05)71006-0 |
0.812 |
|
| 2005 |
Thatcher KN, Peddada S, Yasui DH, Lasalle JM. Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples. Human Molecular Genetics. 14: 785-97. PMID 15689352 DOI: 10.1093/Hmg/Ddi073 |
0.821 |
|
| 2005 |
Samaco RC, Hogart A, LaSalle JM. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. 14: 483-92. PMID 15615769 DOI: 10.1093/Hmg/Ddi045 |
0.834 |
|
| 2004 |
Braunschweig D, Simcox T, Samaco RC, LaSalle JM. X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain. Human Molecular Genetics. 13: 1275-86. PMID 15115765 DOI: 10.1093/Hmg/Ddh142 |
0.794 |
|
| 2004 |
Samaco RC, Nagarajan RP, Braunschweig D, LaSalle JM. Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders. Human Molecular Genetics. 13: 629-39. PMID 14734626 DOI: 10.1093/Hmg/Ddh063 |
0.819 |
|
| 2003 |
Balmer D, Goldstine J, Rao YM, LaSalle JM. Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation. Journal of Molecular Medicine (Berlin, Germany). 81: 61-8. PMID 12545250 DOI: 10.1007/S00109-002-0396-5 |
0.691 |
|
| 2002 |
Balmer D, Arredondo J, Samaco RC, LaSalle JM. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. Human Genetics. 110: 545-52. PMID 12107440 DOI: 10.1007/S00439-002-0724-4 |
0.816 |
|
| 2001 |
LaSalle J, Lalande M. Flow cytometry and FISH to investigate allele-specific replication timing and homologous association of imprinted chromosomes. Methods in Molecular Biology (Clifton, N.J.). 181: 181-92. PMID 12843450 DOI: 10.1385/1-59259-211-2:181 |
0.609 |
|
| 2001 |
LaSalle JM, Goldstine J, Balmer D, Greco CM. Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry. Human Molecular Genetics. 10: 1729-40. PMID 11532982 DOI: 10.1093/Hmg/10.17.1729 |
0.695 |
|
| 2001 |
Balmer D, LaSalle JM. Clonal maintenance of imprinted expression of SNRPN and IPW in normal lymphocytes: correlation with allele-specific methylation of SNRPN intron 1 but not intron 7. Human Genetics. 108: 116-22. PMID 11281449 DOI: 10.1007/S004390000455 |
0.653 |
|
| 1998 |
LaSalle JM, Ritchie RJ, Glatt H, Lalande M. Clonal heterogeneity at allelic methylation sites diagnostic for Prader-Willi and Angelman syndromes. Proceedings of the National Academy of Sciences of the United States of America. 95: 1675-80. PMID 9465075 DOI: 10.1073/Pnas.95.4.1675 |
0.582 |
|
| 1997 |
Strehl S, LaSalle JM, Lalande M. High-resolution analysis of DNA replication domain organization across an R/G-band boundary. Molecular and Cellular Biology. 17: 6157-66. PMID 9315676 DOI: 10.1128/Mcb.17.10.6157 |
0.482 |
|
| 1997 |
Mizuta R, LaSalle JM, Cheng HL, Shinohara A, Ogawa H, Copeland N, Jenkins NA, Lalande M, Alt FW. RAB22 and RAB163/mouse BRCA2: proteins that specifically interact with the RAD51 protein. Proceedings of the National Academy of Sciences of the United States of America. 94: 6927-32. PMID 9192668 DOI: 10.1073/Pnas.94.13.6927 |
0.482 |
|
| 1996 |
LaSalle JM, Lalande M. Homologous association of oppositely imprinted chromosomal domains. Science (New York, N.Y.). 272: 725-8. PMID 8614834 DOI: 10.1126/Science.272.5262.725 |
0.557 |
|
| 1995 |
LaSalle JM, Lalande M. Domain organization of allele-specific replication within the GABRB3 gene cluster requires a biparental 15q11-13 contribution. Nature Genetics. 9: 386-94. PMID 7795644 DOI: 10.1038/Ng0495-386 |
0.548 |
|
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