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Steven S. Scherer, MD PhD - Publications

Affiliations: 
Neurology University of Pennsylvania, Philadelphia, PA, United States 
Area:
Peripheral nerve
Website:
http://www.med.upenn.edu/ins/faculty/scherer.htm

127/337 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
2015 Scherer SS. Blocking bad. Brain : a Journal of Neurology. 138: 3132-3. PMID 26503937 DOI: 10.1093/brain/awv279  0.76
2015 Sanmaneechai O, Feely S, Scherer SS, Herrmann DN, Burns J, Muntoni F, Li J, Siskind CE, Day JW, Laura M, Sumner CJ, Lloyd TE, Ramchandren S, Shy RR, Grider T, et al. Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene. Brain : a Journal of Neurology. 138: 3180-92. PMID 26310628 DOI: 10.1093/Brain/Awv241  0.76
2015 Wasseff SK, Scherer SS. Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions. Neurobiology of Disease. 82: 86-98. PMID 26051537 DOI: 10.1016/J.Nbd.2015.05.018  0.76
2015 Motley WW, Griffin LB, Mademan I, Baets J, De Vriendt E, De Jonghe P, Antonellis A, Jordanova A, Scherer SS. A novel AARS mutation in a family with dominant myeloneuropathy. Neurology. 84: 2040-7. PMID 25904691 DOI: 10.1212/Wnl.0000000000001583  0.76
2015 Baets J, Duan X, Wu Y, Smith G, Seeley WW, Mademan I, McGrath NM, Beadell NC, Khoury J, Botuyan MV, Mer G, Worrell GA, Hojo K, DeLeon J, Laura M, ... ... Scherer SS, et al. Defects of mutant DNMT1 are linked to a spectrum of neurological disorders. Brain : a Journal of Neurology. 138: 845-61. PMID 25678562 DOI: 10.1093/Brain/Awv010  0.76
2015 Fridman V, Bundy B, Reilly MM, Pareyson D, Bacon C, Burns J, Day J, Feely S, Finkel RS, Grider T, Kirk CA, Herrmann DN, Laurá M, Li J, Lloyd T, ... ... Scherer SS, et al. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 873-8. PMID 25430934 DOI: 10.1136/Jnnp-2014-308826  0.76
2014 Abrams CK, Scherer SS, Flores-Obando R, Freidin MM, Wong S, Lamantea E, Farina L, Scaioli V, Pareyson D, Salsano E. A new mutation in GJC2 associated with subclinical leukodystrophy. Journal of Neurology. 261: 1929-38. PMID 25059390 DOI: 10.1007/S00415-014-7429-1  0.76
2014 Willison H, Scherer SS. Ranvier revisited: novel nodal antigens stimulate interest in GBS pathogenesis. Neurology. 83: 106-8. PMID 24920859 DOI: 10.1212/Wnl.0000000000000581  0.76
2014 King CH, Lancaster E, Salomon D, Peles E, Scherer SS. Kv7.2 regulates the function of peripheral sensory neurons. The Journal of Comparative Neurology. 522: 3262-80. PMID 24687876 DOI: 10.1002/Cne.23595  0.76
2014 Foley AR, Menezes MP, Pandraud A, Gonzalez MA, Al-Odaib A, Abrams AJ, Sugano K, Yonezawa A, Manzur AY, Burns J, Hughes I, McCullagh BG, Jungbluth H, Lim MJ, Lin JP, ... ... Scherer SS, et al. Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2. Brain : a Journal of Neurology. 137: 44-56. PMID 24253200 DOI: 10.1093/Brain/Awt315  0.76
2014 Scherer SS, Arroyo EJ. Myelin: Molecular Architecture of CNS and PNS Myelin Sheath Reference Module in Biomedical Research. DOI: 10.1016/B978-0-12-801238-3.04676-6  0.76
2014 Scherer SS, Kleopa KA, Benson MD. Peripheral Neuropathies Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease: Fifth Edition. 1051-1074. DOI: 10.1016/B978-0-12-410529-4.00088-7  0.76
2013 Niu J, Ding L, Li JJ, Kim H, Liu J, Li H, Moberly A, Badea TC, Duncan ID, Son YJ, Scherer SS, Luo W. Modality-based organization of ascending somatosensory axons in the direct dorsal column pathway. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 17691-709. PMID 24198362 DOI: 10.1523/Jneurosci.3429-13.2013  0.76
2013 Caramins M, Colebatch JG, Bainbridge MN, Scherer SS, Abrams CK, Hackett EL, Freidin MM, Jhangiani SN, Wang M, Wu Y, Muzny DM, Lindeman R, Gibbs RA. Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1). Human Molecular Genetics. 22: 4329-38. PMID 23773993 DOI: 10.1093/Hmg/Ddt282  0.76
2012 Kleopa KA, Abrams CK, Scherer SS. How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease? Brain Research. 1487: 198-205. PMID 22771394 DOI: 10.1016/J.Brainres.2012.03.068  0.76
2012 King CH, Scherer SS. Kv7.5 is the primary Kv7 subunit expressed in C-fibers. The Journal of Comparative Neurology. 520: 1940-50. PMID 22134895 DOI: 10.1002/Cne.23019  0.8
2012 Abrams CK, Scherer SS. Gap junctions in inherited human disorders of the central nervous system. Biochimica Et Biophysica Acta. 1818: 2030-47. PMID 21871435 DOI: 10.1016/J.Bbamem.2011.08.015  0.76
2011 Holzbaur EL, Scherer SS. Microtubules, axonal transport, and neuropathy. The New England Journal of Medicine. 365: 2330-2. PMID 22168648 DOI: 10.1056/Nejmcibr1112481  0.76
2011 Murphy SM, Herrmann DN, McDermott MP, Scherer SS, Shy ME, Reilly MM, Pareyson D. Reliability of the CMT neuropathy score (second version) in Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System : Jpns. 16: 191-8. PMID 22003934 DOI: 10.1111/J.1529-8027.2011.00350.X  0.76
2011 Zhai J, Zhou W, Li J, Hayworth CR, Zhang L, Misawa H, Klein R, Scherer SS, Balice-Gordon RJ, Kalb RG. The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease. Human Molecular Genetics. 20: 4116-31. PMID 21816949 DOI: 10.1093/Hmg/Ddr335  0.76
2011 Shroff S, Mierzwa A, Scherer SS, Peles E, Arevalo JC, Chao MV, Rosenbluth J. Paranodal permeability in "myelin mutants". Glia. 59: 1447-57. PMID 21618613 DOI: 10.1002/Glia.21188  0.76
2011 Potter KA, Kern MJ, Fullbright G, Bielawski J, Scherer SS, Yum SW, Li JJ, Cheng H, Han X, Venkata JK, Khan PA, Rohrer B, Hama H. Central nervous system dysfunction in a mouse model of FA2H deficiency. Glia. 59: 1009-21. PMID 21491498 DOI: 10.1002/Glia.21172  0.76
2011 Wasseff SK, Scherer SS. Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling. Neurobiology of Disease. 42: 506-13. PMID 21396451 DOI: 10.1016/J.Nbd.2011.03.003  0.01
2011 Lancaster E, Huijbers MG, Bar V, Boronat A, Wong A, Martinez-Hernandez E, Wilson C, Jacobs D, Lai M, Walker RW, Graus F, Bataller L, Illa I, Markx S, Strauss KA, ... ... Scherer SS, et al. Investigations of caspr2, an autoantigen of encephalitis and neuromyotonia. Annals of Neurology. 69: 303-11. PMID 21387375 DOI: 10.1002/Ana.22297  0.76
2011 Zhang J, Scherer SS, Yum SW. Dominant Cx26 mutants associated with hearing loss have dominant-negative effects on wild type Cx26. Molecular and Cellular Neurosciences. 47: 71-8. PMID 21040787 DOI: 10.1016/J.Mcn.2010.10.002  0.76
2010 Wasseff S, Abrams CK, Scherer SS. A dominant connexin43 mutant does not have dominant effects on gap junction coupling in astrocytes. Neuron Glia Biology. 6: 213-23. PMID 21375791 DOI: 10.1017/S1740925X11000019  0.76
2010 Kennerson ML, Nicholson GA, Kaler SG, Kowalski B, Mercer JF, Tang J, Llanos RM, Chu S, Takata RI, Speck-Martins CE, Baets J, Almeida-Souza L, Fischer D, Timmerman V, Taylor PE, ... Scherer SS, et al. Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. American Journal of Human Genetics. 86: 343-52. PMID 20170900 DOI: 10.1016/J.Ajhg.2010.01.027  0.76
2010 Yum SW, Zhang J, Scherer SS. Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30. Neurobiology of Disease. 38: 226-36. PMID 20096356 DOI: 10.1016/J.Nbd.2010.01.010  0.76
2009 Orthmann-Murphy JL, Salsano E, Abrams CK, Bizzi A, Uziel G, Freidin MM, Lamantea E, Zeviani M, Scherer SS, Pareyson D. Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. Brain : a Journal of Neurology. 132: 426-38. PMID 19056803 DOI: 10.1093/Brain/Awn328  0.76
2008 Scherer SS, Wrabetz L. Molecular mechanisms of inherited demyelinating neuropathies. Glia. 56: 1578-89. PMID 18803325 DOI: 10.1002/Glia.20751  1
2008 Sargiannidou I, Ahn M, Enriquez AD, Peinado A, Reynolds R, Abrams C, Scherer SS, Kleopa KA. Human oligodendrocytes express Cx31.3: function and interactions with Cx32 mutants. Neurobiology of Disease. 30: 221-33. PMID 18353664 DOI: 10.1016/J.Nbd.2008.01.009  0.76
2008 Feldman EL, Cornblath DR, Porter J, Dworkin R, Scherer S. National Institute of Neurological Disorders and Stroke (NINDS): Advances in understanding and treating neuropathy, 24-25 October 2006; Bethesda, Maryland Journal of the Peripheral Nervous System. 13: 1-6. PMID 18346227 DOI: 10.1111/J.1529-8027.2008.00154.X  0.76
2008 Orthmann-Murphy JL, Abrams CK, Scherer SS. Gap junctions couple astrocytes and oligodendrocytes. Journal of Molecular Neuroscience : Mn. 35: 101-16. PMID 18236012 DOI: 10.1007/S12031-007-9027-5  0.76
2008 Ahn M, Lee J, Gustafsson A, Enriquez A, Lancaster E, Sul JY, Haydon PG, Paul DL, Huang Y, Abrams CK, Scherer SS. Cx29 and Cx32, two connexins expressed by myelinating glia, do not interact and are functionally distinct. Journal of Neuroscience Research. 86: 992-1006. PMID 17972320 DOI: 10.1002/Jnr.21561  0.76
2007 Orthmann-Murphy JL, Freidin M, Fischer E, Scherer SS, Abrams CK. Two distinct heterotypic channels mediate gap junction coupling between astrocyte and oligodendrocyte connexins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 13949-57. PMID 18094232 DOI: 10.1523/Jneurosci.3395-07.2007  0.76
2007 Maurel P, Einheber S, Galinska J, Thaker P, Lam I, Rubin MB, Scherer SS, Murakami Y, Gutmann DH, Salzer JL. Nectin-like proteins mediate axon Schwann cell interactions along the internode and are essential for myelination. The Journal of Cell Biology. 178: 861-74. PMID 17724124 DOI: 10.1083/Jcb.200705132  0.76
2007 Yum SW, Zhang J, Valiunas V, Kanaporis G, Brink PR, White TW, Scherer SS. Human connexin26 and connexin30 form functional heteromeric and heterotypic channels. American Journal of Physiology. Cell Physiology. 293: C1032-48. PMID 17615163 DOI: 10.1152/Ajpcell.00011.2007  0.76
2007 Spiegel I, Adamsky K, Eshed Y, Milo R, Sabanay H, Sarig-Nadir O, Horresh I, Scherer SS, Rasband MN, Peles E. A central role for Necl4 (SynCAM4) in Schwann cell-axon interaction and myelination. Nature Neuroscience. 10: 861-9. PMID 17558405 DOI: 10.1038/Nn1915  0.76
2007 Shy ME, Siskind C, Swan ER, Krajewski KM, Doherty T, Fuerst DR, Ainsworth PJ, Lewis RA, Scherer SS, Hahn AF. CMT1X phenotypes represent loss of GJB1 gene function. Neurology. 68: 849-55. PMID 17353473 DOI: 10.1212/01.Wnl.0000256709.08271.4D  0.76
2007 Orthmann-Murphy JL, Enriquez AD, Abrams CK, Scherer SS. Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease. Molecular and Cellular Neurosciences. 34: 629-41. PMID 17344063 DOI: 10.1016/J.Mcn.2007.01.010  0.76
2007 Huang Y, Grinspan JB, Abrams CK, Scherer SS. Pannexin1 is expressed by neurons and glia but does not form functional gap junctions. Glia. 55: 46-56. PMID 17009242 DOI: 10.1002/Glia.20435  0.76
2006 Menichella DM, Majdan M, Awatramani R, Goodenough DA, Sirkowski E, Scherer SS, Paul DL. Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10984-91. PMID 17065440 DOI: 10.1523/Jneurosci.0304-06.2006  0.76
2006 Jeng LJ, Balice-Gordon RJ, Messing A, Fischbeck KH, Scherer SS. The effects of a dominant connexin32 mutant in myelinating Schwann cells. Molecular and Cellular Neurosciences. 32: 283-98. PMID 16790356 DOI: 10.1016/J.Mcn.2006.05.001  0.76
2006 Spiegel I, Adamsky K, Eisenbach M, Eshed Y, Spiegel A, Mirsky R, Scherer SS, Peles E. Identification of novel cell-adhesion molecules in peripheral nerves using a signal-sequence trap. Neuron Glia Biology. 2: 27-38. PMID 16721426 DOI: 10.1017/S1740925X0600007X  0.76
2006 Kleopa KA, Elman LB, Lang B, Vincent A, Scherer SS. Neuromyotonia and limbic encephalitis sera target mature Shaker-type K+ channels: subunit specificity correlates with clinical manifestations. Brain : a Journal of Neurology. 129: 1570-84. PMID 16613892 DOI: 10.1093/Brain/Awl084  0.76
2006 Pan Z, Kao T, Horvath Z, Lemos J, Sul JY, Cranstoun SD, Bennett V, Scherer SS, Cooper EC. A common ankyrin-G-based mechanism retains KCNQ and NaV channels at electrically active domains of the axon. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 2599-613. PMID 16525039 DOI: 10.1523/Jneurosci.4314-05.2006  0.76
2006 Atanasoski S, Scherer SS, Sirkowski E, Leone D, Garratt AN, Birchmeier C, Suter U. ErbB2 signaling in Schwann cells is mostly dispensable for maintenance of myelinated peripheral nerves and proliferation of adult Schwann cells after injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 2124-31. PMID 16481445 DOI: 10.1523/Jneurosci.4594-05.2006  0.76
2006 Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Annals of Neurology. 59: 358-64. PMID 16437560 DOI: 10.1002/Ana.20777  0.76
2005 Occhi S, Zambroni D, Del Carro U, Amadio S, Sirkowski EE, Scherer SS, Campbell KP, Moore SA, Chen ZL, Strickland S, Di Muzio A, Uncini A, Wrabetz L, Feltri ML. Both laminin and Schwann cell dystroglycan are necessary for proper clustering of sodium channels at nodes of Ranvier. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 9418-27. PMID 16221851 DOI: 10.1523/Jneurosci.2068-05.2005  0.76
2005 Huang Y, Sirkowski EE, Stickney JT, Scherer SS. Prenylation-defective human connexin32 mutants are normally localized and function equivalently to wild-type connexin32 in myelinating Schwann cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 7111-20. PMID 16079393 DOI: 10.1523/Jneurosci.1319-05.2005  0.76
2005 Liang GS, de Miguel M, Gómez-Hernández JM, Glass JD, Scherer SS, Mintz M, Barrio LC, Fischbeck KH. Severe neuropathy with leaky connexin32 hemichannels. Annals of Neurology. 57: 749-54. PMID 15852376 DOI: 10.1002/Ana.20459  0.76
2005 Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ. Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 1550-9. PMID 15703409 DOI: 10.1523/Jneurosci.3082-04.2005  0.76
2004 Berger P, Sirkowski EE, Scherer SS, Suter U. Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom. Neurobiology of Disease. 17: 290-9. PMID 15474366 DOI: 10.1016/J.Nbd.2004.07.014  0.76
2004 Devaux JJ, Kleopa KA, Cooper EC, Scherer SS. KCNQ2 is a nodal K+ channel. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 1236-44. PMID 14762142 DOI: 10.1523/Jneurosci.4512-03.2004  0.76
2003 Taylor RA, Simon EM, Marks HG, Scherer SS. The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem. Neurology. 61: 1475-8. PMID 14663027 DOI: 10.1212/01.Wnl.0000095960.48964.25  0.76
2003 Scarlato M, Ara J, Bannerman P, Scherer S, Pleasure D. Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system. Experimental Neurology. 183: 489-98. PMID 14552889 DOI: 10.1016/S0014-4886(03)00046-3  0.76
2003 Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nature Reviews. Neuroscience. 4: 714-26. PMID 12951564 DOI: 10.1038/Nrn1196  0.76
2003 Menichella DM, Goodenough DA, Sirkowski E, Scherer SS, Paul DL. Connexins are critical for normal myelination in the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 5963-73. PMID 12843301 DOI: 10.1523/Jneurosci.23-13-05963.2003  0.76
2003 Devaux J, Alcaraz G, Grinspan J, Bennett V, Joho R, Crest M, Scherer SS. Kv3.1b is a novel component of CNS nodes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 4509-18. PMID 12805291 DOI: 10.1523/Jneurosci.23-11-04509.2003  0.76
2003 Street VA, Bennett CL, Goldy JD, Shirk AJ, Kleopa KA, Tempel BL, Lipe HP, Scherer SS, Bird TD, Chance PF. Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C. Neurology. 60: 22-6. PMID 12525712 DOI: 10.1212/Wnl.60.1.22  0.76
2003 Scherer SS, Arroyo EJ, Peles E. Functional Organization of the Nodes of Ranvier Myelin Biology and Disorders. 1: 89-116. DOI: 10.1016/B978-012439510-7/50057-7  0.76
2002 Yum SW, Kleopa KA, Shumas S, Scherer SS. Diverse trafficking abnormalities of connexin32 mutants causing CMTX. Neurobiology of Disease. 11: 43-52. PMID 12460545 DOI: 10.1006/Nbdi.2002.0545  0.76
2002 Bermingham JR, Shumas S, Whisenhunt T, Sirkowski EE, O'Connell S, Scherer SS, Rosenfeld MG. Identification of genes that are downregulated in the absence of the POU domain transcription factor pou3f1 (Oct-6, Tst-1, SCIP) in sciatic nerve. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 10217-31. PMID 12451123 DOI: 10.1523/Jneurosci.22-23-10217.2002  0.76
2002 Poliak S, Matlis S, Ullmer C, Scherer SS, Peles E. Distinct claudins and associated PDZ proteins form different autotypic tight junctions in myelinating Schwann cells. The Journal of Cell Biology. 159: 361-72. PMID 12403818 DOI: 10.1083/Jcb.200207050  0.76
2002 Genoud S, Lappe-Siefke C, Goebbels S, Radtke F, Aguet M, Scherer SS, Suter U, Nave KA, Mantei N. Notch1 control of oligodendrocyte differentiation in the spinal cord. The Journal of Cell Biology. 158: 709-18. PMID 12186854 DOI: 10.1083/Jcb.200202002  0.76
2002 Kleopa KA, Yum SW, Scherer SS. Cellular mechanisms of connexin32 mutations associated with CNS manifestations. Journal of Neuroscience Research. 68: 522-34. PMID 12111842 DOI: 10.1002/Jnr.10255  0.76
2002 Mikol DD, Scherer SS, Duckett SJ, Hong HL, Feldman EL. Schwann cell caveolin-1 expression increases during myelination and decreases after axotomy. Glia. 38: 191-9. PMID 11968057 DOI: 10.1002/Glia.10063  0.76
2002 Awatramani R, Shumas S, Kamholz J, Scherer SS. TGFbeta1 modulates the phenotype of Schwann cells at the transcriptional level. Molecular and Cellular Neurosciences. 19: 307-19. PMID 11906205 DOI: 10.1006/Mcne.2001.1094  0.76
2002 Arroyo EJ, Xu T, Grinspan J, Lambert S, Levinson SR, Brophy PJ, Peles E, Scherer SS. Genetic dysmyelination alters the molecular architecture of the nodal region. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 1726-37. PMID 11880502 DOI: 10.1523/Jneurosci.22-05-01726.2002  0.76
2002 Atanasoski S, Scherer SS, Nave KA, Suter U. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. Journal of Neuroscience Research. 67: 443-9. PMID 11835311 DOI: 10.1002/Jnr.10133  0.76
2001 Menichella DM, Arroyo EJ, Awatramani R, Xu T, Baron P, Vallat JM, Balsamo J, Lilien J, Scarlato G, Kamholz J, Scherer SS, Shy ME. Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells. Molecular and Cellular Neurosciences. 18: 606-18. PMID 11749037 DOI: 10.1006/Mcne.2001.1041  0.76
2001 Atanasoski S, Shumas S, Dickson C, Scherer SS, Suter U. Differential cyclin D1 requirements of proliferating Schwann cells during development and after injury. Molecular and Cellular Neurosciences. 18: 581-92. PMID 11749035 DOI: 10.1006/Mcne.2001.1055  0.76
2001 Scarlato M, Xu T, Bannerman P, Beesley J, Reddy UR, Rostami A, Scherer SS, Pleasure D. Axon-Schwann cell interactions regulate the expression of fibroblast growth factor-5 (FGF-5). Journal of Neuroscience Research. 66: 16-22. PMID 11598998 DOI: 10.1002/Jnr.1193  0.44
2001 Weiner JA, Fukushima N, Contos JJ, Scherer SS, Chun J. Regulation of Schwann cell morphology and adhesion by receptor-mediated lysophosphatidic acid signaling. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 7069-78. PMID 11549717  0.76
2001 Vogelezang MG, Liu Z, Relvas JB, Raivich G, Scherer SS, ffrench-Constant C. Alpha4 integrin is expressed during peripheral nerve regeneration and enhances neurite outgrowth. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 6732-44. PMID 11517262  0.76
2001 Arroyo EJ, Xu T, Poliak S, Watson M, Peles E, Scherer SS. Internodal specializations of myelinated axons in the central nervous system. Cell and Tissue Research. 305: 53-66. PMID 11512672 DOI: 10.1007/S004410100403  0.76
2001 Scherer SS, Xu T, Crino P, Arroyo EJ, Gutmann DH. Ezrin, radixin, and moesin are components of Schwann cell microvilli. Journal of Neuroscience Research. 65: 150-64. PMID 11438984 DOI: 10.1002/Jnr.1138  0.76
2001 Brown AA, Xu T, Arroyo EJ, Levinson SR, Brophy PJ, Peles E, Scherer SS. Molecular organization of the nodal region is not altered in spontaneously diabetic BB-Wistar rats. Journal of Neuroscience Research. 65: 139-49. PMID 11438983 DOI: 10.1002/Jnr.1137  0.76
2001 Sperber BR, Boyle-Walsh EA, Engleka MJ, Gadue P, Peterson AC, Stein PL, Scherer SS, McMorris FA. A unique role for Fyn in CNS myelination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 2039-47. PMID 11245687 DOI: 10.1523/Jneurosci.21-06-02039.2001  0.76
2001 Bermingham JR, Shumas S, Whisenhunt T, Rosenfeld MG, Scherer SS. Modification of representational difference analysis applied to the isolation of forskolin-regulated genes from Schwann cells. Journal of Neuroscience Research. 63: 516-24. PMID 11241587 DOI: 10.1002/Jnr.1046  0.76
2000 Jiang H, Duchala CS, Awatramani R, Shumas S, Carlock L, Kamholz J, Garbern J, Scherer SS, Shy ME, Macklin WB. Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system. Journal of Neurobiology. 44: 7-19. PMID 10880128 DOI: 10.1002/1097-4695(200007)44:1<7::Aid-Neu2>3.0.Co;2-A  0.76
2000 Kamholz J, Menichella D, Jani A, Garbern J, Lewis RA, Krajewski KM, Lilien J, Scherer SS, Shy ME. Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy. Brain : a Journal of Neurology. 123: 222-33. PMID 10648431 DOI: 10.1093/Brain/123.2.222  0.76
1999 Arroyo EJ, Xu YT, Zhou L, Messing A, Peles E, Chiu SY, Scherer SS. Myelinating Schwann cells determine the internodal localization of Kv1.1, Kv1.2, Kvbeta2, and Caspr. Journal of Neurocytology. 28: 333-47. PMID 10739575 DOI: 10.1023/A:1007009613484  0.76
1999 Lin GS, Glass JD, Shumas S, Scherer SS, Fischbeck KH. A unique mutation in connexin32 associated with severe, early onset CMTX in a heterozygous female. Annals of the New York Academy of Sciences. 883: 481-4. PMID 10586279  0.76
1999 Fischbeck KH, Abel A, Lin GS, Scherer SS. X-linked Charcot-Marie-Tooth disease and connexin32. Annals of the New York Academy of Sciences. 883: 36-41. PMID 10586227  0.76
1999 Abel A, Bone LJ, Messing A, Scherer SS, Fischbeck KH. Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease. Journal of Neuropathology and Experimental Neurology. 58: 702-10. PMID 10411340 DOI: 10.1097/00005072-199907000-00004  0.76
1999 Vogelezang MG, Scherer SS, Fawcett JW, ffrench-Constant C. Regulation of fibronectin alternative splicing during peripheral nerve repair. Journal of Neuroscience Research. 56: 323-33. PMID 10340741 DOI: 10.1002/(Sici)1097-4547(19990515)56:4<323::Aid-Jnr1>3.0.Co;2-6  0.76
1999 Scherer SS, Bone LJ, Deschênes SM, Abel A, Balice-Gordon RJ, Fischbeck KH. The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease. Novartis Foundation Symposium. 219: 175-85; discussion 1. PMID 10207904 DOI: 10.1002/9780470515587.Ch11  0.76
1999 Scherer SS, Fischbeck KH. Is CMTX an axonopathy? Neurology. 52: 432-3. PMID 9932989 DOI: 10.1212/Wnl.52.2.432-A  0.76
1998 Arroyo EJ, Bermingham JR, Rosenfeld MG, Scherer SS. Promyelinating Schwann cells express Tst-1/SCIP/Oct-6. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 7891-902. PMID 9742157 DOI: 10.1523/Jneurosci.18-19-07891.1998  0.76
1998 Balice-Gordon RJ, Bone LJ, Scherer SS. Functional gap junctions in the schwann cell myelin sheath. The Journal of Cell Biology. 142: 1095-104. PMID 9722620 DOI: 10.1083/Jcb.142.4.1095  0.76
1998 Wrabetz L, Taveggia C, Feltri ML, Quattrini A, Awatramani R, Scherer SS, Messing A, Kamholz J. A minimal human MBP promoter-lacZ transgene is appropriately regulated in developing brain and after optic enucleation, but not in shiverer mutant mice. Journal of Neurobiology. 34: 10-26. PMID 9469615 DOI: 10.1002/(Sici)1097-4695(199801)34:1<10::Aid-Neu2>3.0.Co;2-F  0.76
1997 Einheber S, Zanazzi G, Ching W, Scherer S, Milner TA, Peles E, Salzer JL. The axonal membrane protein Caspr, a homologue of neurexin IV, is a component of the septate-like paranodal junctions that assemble during myelination. The Journal of Cell Biology. 139: 1495-506. PMID 9396755 DOI: 10.1083/Jcb.139.6.1495  0.76
1997 Marchionni MA, Grinspan JB, Canoll PD, Mahanthappa NK, Salzer JL, Scherer SS. Neuregulins as potential neuroprotective agents. Annals of the New York Academy of Sciences. 825: 348-65. PMID 9370000 DOI: 10.1111/J.1749-6632.1997.Tb48446.X  0.76
1997 Deschênes SM, Walcott JL, Wexler TL, Scherer SS, Fischbeck KH. Altered trafficking of mutant connexin32. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 9077-84. PMID 9364054 DOI: 10.1523/Jneurosci.17-23-09077.1997  0.76
1997 Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS. Connexin32 and X-linked Charcot-Marie-Tooth disease. Neurobiology of Disease. 4: 221-30. PMID 9361298 DOI: 10.1006/Nbdi.1997.0152  0.76
1997 Lynch DR, Hara H, Yum SW, Chance PF, Scherer SS, Bird SJ, Fischbeck KH. Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III). Neurology. 49: 601-3. PMID 9270606 DOI: 10.1212/Wnl.49.2.601  0.76
1997 Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP). Journal of Neuropathology and Experimental Neurology. 56: 811-21. PMID 9210878 DOI: 10.1097/00005072-199756070-00008  0.76
1997 Feltri ML, Arona M, Scherer SS, Wrabetz L. Cloning and sequence of the cDNA encoding the beta 4 integrin subunit in rat peripheral nerve. Gene. 186: 299-304. PMID 9074510 DOI: 10.1016/S0378-1119(96)00725-1  1
1996 Fischbeck KH, Deschênes SM, Bone LJ, Scherer SS. Connexin32 and X-linked Charcot-Marie-Tooth disease. Cold Spring Harbor Symposia On Quantitative Biology. 61: 673-7. PMID 9246493  0.76
1996 Scherer SS, Gutmann DH. Expression of the neurofibromatosis 2 tumor suppressor gene product, merlin, in Schwann cells. Journal of Neuroscience Research. 46: 595-605. PMID 8951671 DOI: 10.1002/(Sici)1097-4547(19961201)46:5<595::Aid-Jnr8>3.0.Co;2-E  0.76
1996 Shy ME, Shi Y, Wrabetz L, Kamholz J, Scherer SS. Axon-Schwann cell interactions regulate the expression of c-jun in Schwann cells. Journal of Neuroscience Research. 43: 511-25. PMID 8833086 DOI: 10.1002/(Sici)1097-4547(19960301)43:5<511::Aid-Jnr1>3.0.Co;2-L  0.76
1996 Bermingham JR, Scherer SS, O'Connell S, Arroyo E, Kalla KA, Powell FL, Rosenfeld MG. Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration. Genes & Development. 10: 1751-62. PMID 8698235 DOI: 10.1101/Gad.10.14.1751  0.76
1995 Wrabetz L, Feltri ML, Kim H, Daston M, Kamholz J, Scherer SS, Ratner N. Regulation of neurofibromin expression in rat sciatic nerve and cultured Schwann cells. Glia. 15: 22-32. PMID 8847098 DOI: 10.1002/Glia.440150104  0.76
1995 Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL. Connexin32 is a myelin-related protein in the PNS and CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 15: 8281-94. PMID 8613761 DOI: 10.1523/Jneurosci.15-12-08281.1995  0.76
1995 Shy ME, Tani M, Shi YJ, Whyatt SA, Chbihi T, Scherer SS, Kamholz J. An adenoviral vector can transfer lacZ expression into Schwann cells in culture and in sciatic nerve. Annals of Neurology. 38: 429-36. PMID 7668829 DOI: 10.1002/Ana.410380313  0.76
1994 Scherer SS, Wang DY, Kuhn R, Lemke G, Wrabetz L, Kamholz J. Axons regulate Schwann cell expression of the POU transcription factor SCIP. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 14: 1930-42. PMID 8158248 DOI: 10.1523/Jneurosci.14-04-01930.1994  0.76
1994 Kamholz J, Shy M, Scherer S, Yoshikawa H, Nishimura T, Sakoda S, Yanagihara T. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A [5] Annals of Neurology. 36: 451-452. PMID 8080259 DOI: 10.1002/ana.410360326  0.76
1994 Feltri ML, Scherer SS, Nemni R, Kamholz J, Vogelbacker H, Scott MO, Canal N, Quaranta V, Wrabetz L. Beta 4 integrin expression in myelinating Schwann cells is polarized, developmentally regulated and axonally dependent. Development (Cambridge, England). 120: 1287-301. PMID 8026337  0.76
1994 Scherer SS, Braun PE, Grinspan J, Collarini E, Wang DY, Kamholz J. Differential regulation of the 2',3'-cyclic nucleotide 3'-phosphodiesterase gene during oligodendrocyte development. Neuron. 12: 1363-75. PMID 8011341 DOI: 10.1016/0896-6273(94)90451-0  0.76
1994 Bruzzone R, White TW, Scherer SS, Fischbeck KH, Paul DL. Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease. Neuron. 13: 1253-60. PMID 7946361 DOI: 10.1016/0896-6273(94)90063-9  0.76
1994 Chiu SY, Scherer SS, Blonski M, Kang SS, Messing A. Axons regulate the expression of Shaker-like potassium channel genes in Schwann cells in peripheral nerve. Glia. 12: 1-11. PMID 7843783 DOI: 10.1002/Glia.440120102  0.76
1994 Scherer SS, Xu YT, Roling D, Wrabetz L, Feltri ML, Kamholz J. Expression of growth-associated protein-43 kD in Schwann cells is regulated by axon-Schwann cell interactions and cAMP. Journal of Neuroscience Research. 38: 575-89. PMID 7815473 DOI: 10.1002/Jnr.490380510  0.76
1994 Curtis R, Scherer SS, Somogyi R, Adryan KM, Ip NY, Zhu Y, Lindsay RM, DiStefano PS. Retrograde axonal transport of LIF is increased by peripheral nerve injury: correlation with increased LIF expression in distal nerve. Neuron. 12: 191-204. PMID 7507340 DOI: 10.1016/0896-6273(94)90163-5  0.76
1993 Griot C, Pekosz A, Lukac D, Scherer SS, Stillmock K, Schmeidler D, Endres MJ, Gonzalez-Scarano F, Nathanson N. Polygenic control of neuroinvasiveness in California serogroup bunyaviruses. Journal of Virology. 67: 3861-7. PMID 8510208 DOI: 10.1128/Jvi.67.7.3861-3867.1993  0.76
1993 Scherer SS, Kamholz J, Jakowlew SB. Axons modulate the expression of transforming growth factor-betas in Schwann cells. Glia. 8: 265-76. PMID 8406683 DOI: 10.1002/Glia.440080407  0.76
1993 Bergoffen J, Scherer SS, Wang S, Scott MO, Bone LJ, Paul DL, Chen K, Lensch MW, Chance PF, Fischbeck KH. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science (New York, N.Y.). 262: 2039-42. PMID 8266101 DOI: 10.1126/Science.8266101  0.76
1993 Baron P, Kamholz J, Scherer S, Honda H, Shy M, Scarpini E, Scarlato G, Pleasure D. Appearance of PLP mRNA in Specific Regions of the Developing Rat Lumbosacral Spinal Cord as Revealed by in Situ Hybridization Experimental Neurology. 121: 139-147. PMID 7684334 DOI: 10.1006/Exnr.1993.1080  0.76
1993 Davis S, Aldrich TH, Ip NY, Stahl N, Scherer S, Farruggella T, DiStefano PS, Curtis R, Panayotatos N, Gascan H. Released form of CNTF receptor alpha component as a soluble mediator of CNTF responses. Science (New York, N.Y.). 259: 1736-9. PMID 7681218 DOI: 10.1126/Science.7681218  0.76
1992 Friedman B, Scherer SS, Rudge JS, Helgren M, Morrisey D, McClain J, Wang DY, Wiegand SJ, Furth ME, Lindsay RM. Regulation of ciliary neurotrophic factor expression in myelin-related Schwann cells in vivo. Neuron. 9: 295-305. PMID 1497895 DOI: 10.1016/0896-6273(92)90168-D  0.76
1992 Scherer SS, Vogelbacker HH, Kamholz J. Axons modulate the expression of proteolipid protein in the CNS. Journal of Neuroscience Research. 32: 138-48. PMID 1383558 DOI: 10.1002/Jnr.490320203  0.76
1992 Cohen JA, Yachnis AT, Arai M, Davis JG, Scherer SS. Expression of the neu proto-oncogene by Schwann cells during peripheral nerve development and Wallerian degeneration. Journal of Neuroscience Research. 31: 622-34. PMID 1374476 DOI: 10.1002/Jnr.490310406  0.76
1992 Kamholz J, Sessa M, Scherer S, Vogelbacker H, Mokuno K, Baron P, Wrabetz L, Shy M, Pleasure D. Structure and expression of proteolipid protein in the peripheral nervous system Journal of Neuroscience Research. 31: 231-244. PMID 1374129 DOI: 10.1002/Jnr.490310204  0.76
1992 Feltri ML, Scherer SS, Wrabetz L, Kamholz J, Shy ME. Mitogen-expanded Schwann cells retain the capacity to myelinate regenerating axons after transplantation into rat sciatic nerve. Proceedings of the National Academy of Sciences of the United States of America. 89: 8827-31. PMID 1326765 DOI: 10.1073/Pnas.89.18.8827  0.76
1989 Gutmann DH, Scherer S. Magnetic resonance imaging of ataxic hemiparesis localized to the corona radiata Stroke. 20: 1571-1573. PMID 2815193 DOI: 10.1161/01.Str.20.11.1571  0.76
1984 Scherer SS, Easter SS. Degenerative and regenerative changes in the trochlear nerve of goldfish. Journal of Neurocytology. 13: 519-65. PMID 6481411 DOI: 10.1007/BF01148079  0.76
1984 Easter SS, Bratton B, Scherer SS. Growth-related order of the retinal fiber layer in goldfish. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 4: 2173-90. PMID 6470771  0.76
Low-probability matches
1996 Bird SJ, Brown MJ, Shy ME, Scherer SS. Chronic inflammatory demyelinating polyneuropathy associated with malignant melanoma. Neurology. 46: 822-4. PMID 8618691 DOI: 10.1212/Wnl.46.3.822  0.24
2018 Saghira C, Bis DM, Stanek D, Strickland A, Herrmann DN, Reilly MM, Scherer SS, Shy ME, Züchner S. Variantpathogenicity evaluationin the community-driven Inherited Neuropathy Variant Browser. Human Mutation. PMID 29473246 DOI: 10.1002/Humu.23412  0.2
2017 Rossor AM, Carr AS, Devine H, Chandrashekar H, Pelayo-Negro AL, Pareyson D, Shy ME, Scherer SS, Reilly MM. Peripheral neuropathy in complex inherited diseases: an approach to diagnosis. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28794150 DOI: 10.1136/Jnnp-2016-313960  0.2
2020 Bray P, Cornett KMD, Estilow T, Pareyson D, Zuccarino R, Skorupinska M, Pipis M, Sowden JE, Scherer S, Reilly MM, Shy ME, Herrmann DN, Burns J, Eichinger KJ. Reliability of the Charcot-Marie-Tooth functional outcome measure. Journal of the Peripheral Nervous System : Jpns. 25: 288-291. PMID 32844461 DOI: 10.1111/Jns.12406  0.16
2020 Fridman V, Sillau S, Acsadi G, Bacon C, Dooley K, Burns J, Day J, Feely S, Finkel RS, Grider T, Gutmann L, Herrmann DN, Kirk CA, Knause SA, Laurá M, ... ... Scherer SS, et al. A longitudinal study of CMT1A using Rasch analysis based CMT neuropathy and examination scores. Neurology. PMID 32047073 DOI: 10.1212/Wnl.0000000000009035  0.16
2017 Panosyan FB, Laura M, Rossor AM, Pisciotta C, Piscosquito G, Burns J, Li J, Yum SW, Lewis RA, Day J, Horvath R, Herrmann DN, Shy ME, Pareyson D, Reilly MM, ... Scherer SS, et al. Cross-sectional analysis of a large cohort with X-linked Charcot-Marie-Tooth disease (CMTX1). Neurology. PMID 28768847 DOI: 10.1212/Wnl.0000000000004296  0.16
2017 Panosyan FB, Kirk CA, Marking D, Reilly MM, Scherer SS, Shy ME, Herrmann DN. Carpal Tunnel Syndrome in Inherited Neuropathies: A Retrospective Survey. Muscle & Nerve. PMID 28692128 DOI: 10.1002/Mus.25742  0.16
2010 Chin MS, Ogawa R, Lancerotto L, Pietramaggiori G, Schomacker KT, Mathews JC, Scherer SS, Van Duyn P, Prsa MJ, Ottensmeyer MP, Veves A, Orgill DP. In vivo acceleration of skin growth using a servo-controlled stretching device. Tissue Engineering. Part C, Methods. 16: 397-405. PMID 19601702 DOI: 10.1089/Ten.Tec.2009.0185  0.01
2019 Lee DC, Meyer-Schuman R, Bacon C, Shy ME, Antonellis A, Scherer SS. A recurrent GARS mutation causes distal hereditary motor neuropathy. Journal of the Peripheral Nervous System : Jpns. PMID 31628756 DOI: 10.1111/Jns.12353  0.12
2006 Kleopa KA, Scherer SS. Molecular genetics of X-linked Charcot-Marie-Tooth disease. Neuromolecular Medicine. 8: 107-22. PMID 16775370 DOI: 10.1385/Nmm:8:1-2:107  0.01
2005 Devaux JJ, Scherer SS. Altered ion channels in an animal model of Charcot-Marie-Tooth disease type IA. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 1470-80. PMID 15703401 DOI: 10.1523/Jneurosci.3328-04.2005  0.01
2000 Arroyo EJ, Scherer SS. On the molecular architecture of myelinated fibers. Histochemistry and Cell Biology. 113: 1-18. PMID 10664064 DOI: 10.1007/S004180050001  0.01
1999 Lin GS, Glass JD, Shumas S, Scherer SS, Fischbeck KH. A Unique Mutation in Connexin32 Associated with Severe, Early Onset CMTX in a Heterozygous Female. Annals of the New York Academy of Sciences. 883: 481-484. PMID 29086962 DOI: 10.1111/J.1749-6632.1999.Tb08616.X  0.12
2021 Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, ... ... Scherer SS, et al. Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study. Brain : a Journal of Neurology. PMID 33415332 DOI: 10.1093/brain/awaa323  0.08
2020 Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, ... ... Scherer SS, et al. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32367058 DOI: 10.1038/S41588-020-0615-4  0.08
2019 Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Morrow JM, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, ... ... Scherer SS, et al. Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A. Annals of Neurology. PMID 30706531 DOI: 10.1002/Ana.25426  0.08
2016 Wang W, Wang C, Dawson DB, Thorland EC, Lundquist PA, Eckloff BW, Wu Y, Baheti S, Evans JM, Scherer SS, Dyck PJ, Klein CJ. Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy. Neurology. 86: 1762-71. PMID 27164712 DOI: 10.1212/Wnl.0000000000002659  0.08
2016 Cornett KM, Menezes MP, Bray P, Halaki M, Shy RR, Yum SW, Estilow T, Moroni I, Foscan M, Pagliano E, Pareyson D, Laurá M, Bhandari T, Muntoni F, Reilly MM, et al. Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease. Jama Neurology. PMID 27043305 DOI: 10.1001/Jamaneurol.2016.0171  0.08
2016 Thomas FP, Guergueltcheva V, Gondim FA, Tournev I, Rao CV, Ishpekova B, Kinsella LJ, Pan Y, Geller TJ, Litvinenko I, De Jonghe P, Scherer SS, Jordanova A. Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy. Journal of Neurology. PMID 26725087 DOI: 10.1007/S00415-015-7989-8  0.08
2011 Dastouri P, Helm DL, Scherer SS, Pietramaggiori G, Younan G, Orgill DP. Waveform modulation of negative-pressure wound therapy in the murine model. Plastic and Reconstructive Surgery. 127: 1460-6. PMID 21460654 DOI: 10.1097/Prs.0B013E31820A63Cb  0.01
2010 Curinga G, Pietramaggiori G, Scherer SS, Masellis A, Gherardini G, Brancato R, Conte F, Bistoni G. Electrical injuries due to theft of copper. Journal of Burn Care & Research : Official Publication of the American Burn Association. 31: 341-6. PMID 20182374 DOI: 10.1097/BCR.0b013e3181d0f50d  0.01
2010 Pietramaggiori G, Scherer SS, Mathews JC, Gennaoui T, Lancerotto L, Ragno G, Valeri CR, Orgill DP. Quiescent platelets stimulate angiogenesis and diabetic wound repair. The Journal of Surgical Research. 160: 169-77. PMID 19482315 DOI: 10.1016/J.Jss.2008.09.010  0.01
2009 Pietramaggiori G, Scherer SS, Alperovich M, Chen B, Orgill DP, Wagers AJ. Improved cutaneous healing in diabetic mice exposed to healthy peripheral circulation. The Journal of Investigative Dermatology. 129: 2265-74. PMID 19295612 DOI: 10.1038/Jid.2009.60  0.01
2008 Scherer SS, Pietramaggiori G, Mathews JC, Prsa MJ, Huang S, Orgill DP. The mechanism of action of the vacuum-assisted closure device. Plastic and Reconstructive Surgery. 122: 786-97. PMID 18766042 DOI: 10.1097/Prs.0B013E31818237Ac  0.01
2004 Arroyo EJ, Sirkowski EE, Chitale R, Scherer SS. Acute demyelination disrupts the molecular organization of peripheral nervous system nodes. The Journal of Comparative Neurology. 479: 424-34. PMID 15514980 DOI: 10.1002/Cne.20321  0.04
2002 Kleopa KA, Scherer SS. Inherited neuropathies. Neurologic Clinics. 20: 679-709. PMID 12432826 DOI: 10.1016/S0733-8619(01)00016-0  0.01
2002 Scherer SS, Arroyo EJ. Recent progress on the molecular organization of myelinated axons. Journal of the Peripheral Nervous System : Jpns. 7: 1-12. PMID 11939347 DOI: 10.1046/J.1529-8027.2002.02001.X  0.01
2019 Pareyson D, Stojkovic T, Reilly MM, Leonard-Louis S, Laurà M, Blake J, Parman Y, Battaloglu E, Tazir M, Bellatache M, Bonello-Palot N, Lévy N, Sacconi S, Guimarães-Costa R, Attarian S, ... ... Scherer SS, et al. A multicentre retrospective study of Charcot-Marie-Tooth disease type 4B (CMT4B) due to mutations in Myotubularin-related proteins (MTMRs). Annals of Neurology. PMID 31070812 DOI: 10.1002/Ana.25500  0.04
2019 Tao F, Beecham GW, Rebelo AP, Blanton SH, Moran JJ, Lopez-Anido C, Svaren J, Abreu L, Rizzo D, Kirk CA, Wu X, Feely S, Verhamme C, Saporta MA, Herrmann DN, ... ... Scherer SS, et al. Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Journal of Neuromuscular Diseases. PMID 30958311 DOI: 10.3233/Jnd-190377  0.04
2018 Lancaster E, Li J, Hanania T, Liem R, Scheideler MA, Scherer SS. Myelinated axons fail to develop properly in a genetically authentic mouse model of Charcot-Marie-Tooth disease type 2E. Experimental Neurology. PMID 29940160 DOI: 10.1016/J.Expneurol.2018.06.010  0.04
2018 Lassuthova P, Rebelo AP, Ravenscroft G, Lamont PJ, Davis MR, Manganelli F, Feely SM, Bacon C, Brožková DŠ, Haberlova J, Mazanec R, Tao F, Saghira C, Abreu L, Courel S, ... ... Scherer SS, et al. Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2. American Journal of Human Genetics. 102: 505-514. PMID 29499166 DOI: 10.1016/J.Ajhg.2018.01.023  0.04
2017 Zhao HT, Damle S, Ikeda-Lee K, Kuntz S, Li J, Mohan A, Kim A, Hung G, Scheideler MA, Scherer SS, Svaren J, Swayze EE, Kordasiewicz HB. PMP22 antisense oligonucleotides reverse Charcot-Marie-Tooth disease type 1A features in rodent models. The Journal of Clinical Investigation. PMID 29202483 DOI: 10.1172/Jci96499  0.04
2015 Lancaster E, Scherer SS. Subtype-specific therapy for autoimmune neuropathies? Neurology® Neuroimmunology & Neuroinflammation. 2: e152. PMID 26756037 DOI: 10.1212/Nxi.0000000000000152  0.04
2015 Arora S, Choudhury S, Althoff D, Scherer S. Emergency maneuver library - Ensuring safe navigation in partially known environments Proceedings - Ieee International Conference On Robotics and Automation. 2015: 6431-6438. DOI: 10.1109/ICRA.2015.7140102  0.04
2015 Fang Z, Scherer S. Real-time onboard 6DoF localization of an indoor MAV in degraded visual environments using a RGB-D camera Proceedings - Ieee International Conference On Robotics and Automation. 2015: 5253-5259. DOI: 10.1109/ICRA.2015.7139931  0.04
2015 Arora S, Scherer S. PASP: Policy based approach for sensor planning Proceedings - Ieee International Conference On Robotics and Automation. 2015: 3479-3486. DOI: 10.1109/ICRA.2015.7139680  0.04
2015 Maturana D, Scherer S. 3D Convolutional Neural Networks for landing zone detection from LiDAR Proceedings - Ieee International Conference On Robotics and Automation. 2015: 3471-3478. DOI: 10.1109/ICRA.2015.7139679  0.04
2015 Althoff D, Scherer S. Connected invariant sets for high-speed motion planning in partially-known environments Proceedings - Ieee International Conference On Robotics and Automation. 2015: 3279-3285. DOI: 10.1109/ICRA.2015.7139651  0.04
2015 Choudhury S, Arora S, Scherer S. The planner ensemble: Motion planning by executing diverse algorithms Proceedings - Ieee International Conference On Robotics and Automation. 2015: 2389-2395. DOI: 10.1109/ICRA.2015.7139517  0.04
2015 Choudhury S, Scherer S. The Dynamics Projection Filter (DPF) - Real-time nonlinear trajectory optimization using projection operators Proceedings - Ieee International Conference On Robotics and Automation. 2015: 644-649. DOI: 10.1109/ICRA.2015.7139247  0.04
2015 Ünal Y, Küçükarslan A, Scherer S. Interaction of the vector-meson octet with the baryon octet in effective field theory Physical Review C - Nuclear Physics. 92. DOI: 10.1103/PhysRevC.92.055208  0.04
2015 Djukanovic D, Gegelia J, Keller A, Scherer S, Tiator L. Vector form factor of the pion in chiral effective field theory Physics Letters, Section B: Nuclear, Elementary Particle and High-Energy Physics. 742: 55-60. DOI: 10.1016/j.physletb.2015.01.007  0.04
2015 Ju J, Yang C, Scherer S, Ko H. Recognition of human group activity for video analytics Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 9315: 161-169. DOI: 10.1007/978-3-319-24078-7_16  0.04
2015 Jain S, Nuske S, Chambers A, Yoder L, Cover H, Chamberlain L, Scherer S, Singh S. Autonomous river exploration Springer Tracts in Advanced Robotics. 105: 93-106. DOI: 10.1007/978-3-319-07488-7_7  0.04
2015 Nuske S, Choudhury S, Jain S, Chambers A, Yoder L, Scherer S, Chamberlain L, Cover H, Singh S. Autonomous exploration and motion planning for an unmanned aerial vehicle navigating rivers Journal of Field Robotics. 32: 1141-1162. DOI: 10.1002/Rob.21596  0.04
2015 Paduano J, Wissler J, Drozeski G, Piedmonte M, Dadkhah N, Francis J, Shortlidge C, Bold J, Langford F, Chaoui M, Liu CJ, Foster E, Singh S, Chamberlain L, Hamner B, ... Scherer S, et al. TALOS: An unmanned cargo delivery system for rotorcraft landing to unprepared sites Annual Forum Proceedings - Ahs International. 4: 2840-2856.  0.04
2014 Schwartzentruber J, Buhas D, Majewski J, Sasarman F, Papillon-Cavanagh S, Thiffault I, Thiffaut I, Sheldon KM, Massicotte C, Patry L, Simon M, Zare AS, McKernan KJ, Michaud J, et al. Mutation in the nuclear-encoded mitochondrial isoleucyl-tRNA synthetase IARS2 in patients with cataracts, growth hormone deficiency with short stature, partial sensorineural deafness, and peripheral neuropathy or with Leigh syndrome. Human Mutation. 35: 1285-9. PMID 25130867 DOI: 10.1002/Humu.22629  0.04
2014 Fang Z, Scherer S. Experimental study of odometry estimation methods using RGB-D cameras Ieee International Conference On Intelligent Robots and Systems. 680-687. DOI: 10.1109/IROS.2014.6942632  0.04
2014 Bauer T, Scherer S, Tiator L. Electromagnetic transition form factors of the Roper resonance in a phenomenological field theory Physical Review C - Nuclear Physics. 90. DOI: 10.1103/PhysRevC.90.015201  0.04
2014 Medne L, Bönnemann C, Scherer S, Finkel RS, Ortiz-Gonzalez X, Glanzman A, Estilow T, Moll A, Leshner R, Wang Y, Winder T, Yum S. G.P.239 Neuromuscular Disorders. 24: 888-889. DOI: 10.1016/J.Nmd.2014.06.315  0.04
2014 Choudhury S, Arora S, Scherer S. The planner ensemble and trajectory executive: A high performance motion planning system with guaranteed safety Annual Forum Proceedings - Ahs International. 4: 2872-2891.  0.04
2014 Arora S, Choudhury S, Althoff D, Scherer S. A principled approach to enable safe and high performance maneuvers for autonomous rotorcraft Annual Forum Proceedings - Ahs International. 4: 3228-3236.  0.04
2012 Heit YI, Dastouri P, Helm DL, Pietramaggiori G, Younan G, Erba P, Münster S, Orgill DP, Scherer SS. Foam pore size is a critical interface parameter of suction-based wound healing devices. Plastic and Reconstructive Surgery. 129: 589-97. PMID 22090246 DOI: 10.1097/Prs.0B013E3182402C89  0.01
2011 Scherer SS, Pietramaggiori G, Matthews JC, Gennaoui A, Demcheva M, Fischer TH, Valeri CR, Orgill DP. Poly-N-acetyl glucosamine fibers induce angiogenesis in ADP inhibitor-treated diabetic mice. The Journal of Trauma. 71: S183-6. PMID 21814116 DOI: 10.1097/Ta.0B013E318225585B  0.01
2010 Mathews JC, Chin MS, Fernandez-Esparrach G, Shaikh SN, Pietramaggiori G, Scherer SS, Ryan MB, Ferrigno M, Orgill DP, Thompson CC. Early healing of transcolonic and transgastric natural orifice transluminal endoscopic surgery access sites. Journal of the American College of Surgeons. 210: 480-90. PMID 20347741 DOI: 10.1016/J.Jamcollsurg.2010.01.005  0.01
2010 Curinga G, Scherer SS, Rusciani A, Gherardini G, Pietramaggiori G. Comments on "Platelet-rich plasma in burns". Burns : Journal of the International Society For Burn Injuries. 36: 944-5; author reply . PMID 20022705 DOI: 10.1016/j.burns.2009.08.018  0.01
2009 Yum SW, Zhang J, Mo K, Li J, Scherer SS. A novel recessive Nefl mutation causes a severe, early-onset axonal neuropathy. Annals of Neurology. 66: 759-70. PMID 20039262 DOI: 10.1002/Ana.21728  0.01
2009 Scherer SS, Pietramaggiori G, Mathews JC, Orgill DP. Short periodic applications of the vacuum-assisted closure device cause an extended tissue response in the diabetic mouse model. Plastic and Reconstructive Surgery. 124: 1458-65. PMID 20009831 DOI: 10.1097/Prs.0B013E3181Bbc829  0.01
2008 Pietramaggiori G, Scherer SS, Cervi D, Klement G, Orgill DP. Tumors stimulate platelet delivery of angiogenic factors in vivo: an unexpected benefit. The American Journal of Pathology. 173: 1609-16. PMID 18988799 DOI: 10.2353/Ajpath.2008.080474  0.01
2008 Pietramaggiori G, Scherer SS, Mathews JC, Alperovich M, Yang HJ, Neuwalder J, Czeczuga JM, Chan RK, Wagner CT, Orgill DP. Healing modulation induced by freeze-dried platelet-rich plasma and micronized allogenic dermis in a diabetic wound model. Wound Repair and Regeneration : Official Publication of the Wound Healing Society [and] the European Tissue Repair Society. 16: 218-25. PMID 18318807 DOI: 10.1111/J.1524-475X.2008.00362.X  0.01
2008 Pedrola L, Espert A, Valdés-Sánchez T, Sánchez-Piris M, Sirkowski EE, Scherer SS, Fariñas I, Palau F. Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease. Journal of Cellular and Molecular Medicine. 12: 679-89. PMID 18021315 DOI: 10.1111/J.1582-4934.2007.00158.X  0.04
2007 Pietramaggiori G, Liu P, Scherer SS, Kaipainen A, Prsa MJ, Mayer H, Newalder J, Alperovich M, Mentzer SJ, Konerding MA, Huang S, Ingber DE, Orgill DP. Tensile forces stimulate vascular remodeling and epidermal cell proliferation in living skin. Annals of Surgery. 246: 896-902. PMID 17968184 DOI: 10.1097/Sla.0B013E3180Caa47F  0.01
2002 Altevogt BM, Kleopa KA, Postma FR, Scherer SS, Paul DL. Connexin29 is uniquely distributed within myelinating glial cells of the central and peripheral nervous systems. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 6458-70. PMID 12151525 DOI: 10.1523/Jneurosci.22-15-06458.2002  0.01
2001 Vogelezang MG, Liu Z, Relvas JB, Raivich G, Scherer SS, ffrench-Constant C. α4 Integrin Is Expressed during Peripheral Nerve Regeneration and Enhances Neurite Outgrowth The Journal of Neuroscience. 21: 6732-6744. DOI: 10.1523/Jneurosci.21-17-06732.2001  0.04
1998 Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ. Connexin32-null mice develop demyelinating peripheral neuropathy. Glia. 24: 8-20. PMID 9700485 DOI: 10.1002/(Sici)1098-1136(199809)24:1<8::Aid-Glia2>3.0.Co;2-3  0.04
1996 Zorick TS, Syroid DE, Arroyo E, Scherer SS, Lemke G. The Transcription Factors SCIP and Krox-20 Mark Distinct Stages and Cell Fates in Schwann Cell Differentiation Molecular and Cellular Neurosciences. 8: 129-45. PMID 8954628 DOI: 10.1006/Mcne.1996.0052  0.01
1995 Scherer SS, Xu YT, Bannerman PG, Sherman DL, Brophy PJ. Periaxin expression in myelinating Schwann cells: modulation by axon-glial interactions and polarized localization during development. Development (Cambridge, England). 121: 4265-73. PMID 8575326  0.01
1995 Scherer SS, Chance PF. Myelin genes: getting the dosage right. Nature Genetics. 11: 226-8. PMID 7581438 DOI: 10.1038/Ng1195-226  0.04
2021 Guo MH, Bardakjian TM, Brzozowski MR, Scherer SS, Quinn C, Elman L, Orthmann-Murphy J, Tropea TF, Ellis CA, Gonzalez-Alegre P. Temporal trends and yield of clinical diagnostic genetic testing in adult neurology. American Journal of Medical Genetics. Part A. PMID 34075706 DOI: 10.1002/ajmg.a.62372  0.01
2021 Hain HS, Pandey R, Bakay M, Strenkowski BP, Harrington D, Romer M, Motley WW, Li J, Lancaster E, Roth L, Grinspan JB, Scherer SS, Hakonarson H. Inducible knockout of Clec16a in mice results in sensory neurodegeneration. Scientific Reports. 11: 9319. PMID 33927318 DOI: 10.1038/s41598-021-88895-0  0.01
2021 Vujovic D, Cornblath DR, Scherer SS. A recurrent MORC2 mutation causes Charcot-Marie-Tooth disease type 2Z. Journal of the Peripheral Nervous System : Jpns. PMID 33844363 DOI: 10.1111/jns.12443  0.01
2020 Motley WW, Züchner S, Scherer SS. Isoform-specific loss of dystonin causes hereditary motor and sensory neuropathy. Neurology. Genetics. 6: e496. PMID 32802955 DOI: 10.1212/Nxg.0000000000000496  0.01
2020 Sase S, Almad AA, Boecker CA, Guedes-Dias P, Li JJ, Takanohashi A, Patel A, McCaffrey T, Patel H, Sirdeshpande D, Curiel J, Shih-Hwa Liu J, Padiath Q, Holzbaur EL, Scherer SS, et al. mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model. Elife. 9. PMID 32463361 DOI: 10.7554/Elife.52986  0.01
2020 Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, ... ... Scherer SS, et al. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32457452 DOI: 10.1038/S41588-020-0649-7  0.01
2020 Hamedani AG, Wilson JA, Avery RA, Scherer SS. Optic Neuropathy in Charcot-Marie-Tooth Disease. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society. PMID 32441898 DOI: 10.1097/Wno.0000000000000965  0.01
2020 Roshandel D, Chen Z, Canty AJ, Bull SB, Natarajan R, Paterson AD. DNA methylation age calculators reveal association with diabetic neuropathy in type 1 diabetes. Clinical Epigenetics. 12: 52. PMID 32248841 DOI: 10.1186/S13148-020-00840-6  0.01
2020 Li JJ, Sarute N, Lancaster E, Otkiran-Clare G, Fagla BM, Ross SR, Scherer SS. A recessive Trim2 mutation causes an axonal neuropathy in mice. Neurobiology of Disease. 104845. PMID 32205255 DOI: 10.1016/J.Nbd.2020.104845  0.01
2020 Sase S, Almad AA, Boecker CA, Guedes-Dias P, Li JJ, Takanohashi A, Patel A, McCaffrey T, Patel H, Sirdeshpande D, Curiel J, Liu JS, Padiath Q, Holzbaur EL, Scherer SS, et al. Author response: TUBB4A mutations result in both glial and neuronal degeneration in an H-ABC leukodystrophy mouse model Elife. DOI: 10.7554/Elife.52986.Sa2  0.01
2019 Lee DC, Dankwa L, Edmundson C, Cornblath DR, Scherer SS. Yield of next-generation neuropathy gene panels in axonal neuropathies. Journal of the Peripheral Nervous System : Jpns. PMID 31701603 DOI: 10.1111/Jns.12356  0.01
2019 . Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network. American Journal of Human Genetics. PMID 31447099 DOI: 10.1016/J.Ajhg.2019.07.018  0.01
2019 Bardakjian T, Scherer SS. A MT-ATP6 Mutation Causes a Slowly Progressive Myeloneuropathy. Journal of Neuromuscular Diseases. PMID 31424416 DOI: 10.3233/Jnd-190400  0.01
2019 Horga A, Bugiardini E, Manole A, Bremner F, Jaunmuktane Z, Dankwa L, Rebelo AP, Woodward CE, Hargreaves IP, Cortese A, Pittman AM, Brandner S, Polke JM, Pitceathly RDS, Züchner S, ... ... Scherer SS, et al. Autosomal dominant optic atrophy and cataract "plus" phenotype including axonal neuropathy. Neurology. Genetics. 5: e322. PMID 31119193 DOI: 10.1212/Nxg.0000000000000322  0.01
2019 Phillips J, Courel S, Rebelo AP, Bis-Brewer DM, Bardakjian T, Dankwa L, Hamedani AG, Züchner S, Scherer SS. POLG mutations presenting as CMT. Journal of the Peripheral Nervous System : Jpns. PMID 30843307 DOI: 10.1111/Jns.12313  0.01
2018 Dankwa L, Richardson J, Motley WW, Scavina M, Courel S, Bardakjian T, Züchner S, Scherer SS. A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family. Neuromuscular Disorders : Nmd. PMID 30642740 DOI: 10.1016/J.Nmd.2018.12.008  0.01
2018 Meister-Broekema M, Freilich R, Jagadeesan C, Rauch JN, Bengoechea R, Motley WW, Kuiper EFE, Minoia M, Furtado GV, van Waarde MAWH, Bird SJ, Rebelo A, Zuchner S, Pytel P, Scherer SS, et al. Myopathy associated BAG3 mutations lead to protein aggregation by stalling Hsp70 networks. Nature Communications. 9: 5342. PMID 30559338 DOI: 10.1038/S41467-018-07718-5  0.01
2018 Allard DE, Wang Y, Li JJ, Conley B, Xu EW, Sailer D, Kimpston C, Notini R, Smith CJ, Koseoglu E, Starmer J, Zeng XL, Howard JF, Hoke A, Scherer SS, et al. Schwann cell-derived periostin promotes autoimmune peripheral polyneuropathy via macrophage recruitment. The Journal of Clinical Investigation. PMID 30222134 DOI: 10.1172/Jci99308  0.01
2018 Bardakjian TM, Helbig I, Quinn C, Elman LB, McCluskey LF, Scherer SS, Gonzalez-Alegre P. Genetic test utilization and diagnostic yield in adult patients with neurological disorders. Neurogenetics. PMID 29589152 DOI: 10.1007/S10048-018-0544-X  0.01
2018 Dankwa L, Richardson J, Motley WW, Züchner S, Scherer SS. A mutation in the heptad repeat 2 domain of MFN2 in a large CMT2A family. Journal of the Peripheral Nervous System : Jpns. PMID 29341354 DOI: 10.1111/Jns.12248  0.01
2017 Burnor E, Yang L, Zhou H, Patterson KR, Quinn C, Reilly MM, Rossor AM, Scherer SS, Lancaster E. Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathies. Neurology. PMID 29187518 DOI: 10.1212/Wnl.0000000000004773  0.01
2017 Fehmi J, Scherer SS, Willison HJ, Rinaldi S. Nodes, paranodes and neuropathies. Journal of Neurology, Neurosurgery, and Psychiatry. PMID 28819062 DOI: 10.1136/Jnnp-2016-315480  0.01
2017 Laurá M, Singh D, Ramdharry G, Morrow J, Skorupinska M, Pareyson D, Burns J, Lewis RA, Scherer S, Herrmann DN, Cullen N, Bradish C, Gaiani L, Martinelli N, Gibbons P, et al. Prevalence and orthopedic management of foot and ankle deformities in Charcot Marie Tooth disease. Muscle & Nerve. PMID 28632967 DOI: 10.1002/Mus.25724  0.01
2017 Abrams CK, Goman M, Wong S, Scherer SS, Kleopa KA, Peinado A, Freidin MM. Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations. Scientific Reports. 7: 40166. PMID 28071741 DOI: 10.1038/Srep40166  0.01
2017 Bengoechea R, Motley W, Bird S, Zuchner S, Scherer S, Weihl C. A novel BAG3 mutation associated with myofibrillar myopathy emphasizes HSP70 dependent activity Neuromuscular Disorders. 27: S120. DOI: 10.1016/J.Nmd.2017.06.105  0.01
2016 Auer-Grumbach M, Toegel S, Schabhüttl M, Weinmann D, Chiari C, Bennett DL, Beetz C, Klein D, Andersen PM, Böhme I, Fink-Puches R, Gonzalez M, Harms MB, Motley W, Reilly MM, ... ... Scherer SS, et al. Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies. American Journal of Human Genetics. 99: 607-623. PMID 27588448 DOI: 10.1016/J.Ajhg.2016.07.008  0.01
2016 Lenherr SM, Clemens JQ, Braffett BH, Cleary PA, Dunn RL, Hotaling JM, Jacobson AM, Kim C, Herman W, Brown JS, Wessells H, Sarma AV. Glycemic Control and Urinary Tract Infections in Women with Type 1 Diabetes: Results from the DCCT/EDIC. The Journal of Urology. PMID 27131462 DOI: 10.1016/J.Juro.2016.04.071  0.01
2016 Kagiava A, Sargiannidou I, Theophilidis G, Karaiskos C, Richter J, Bashiardes S, Schiza N, Nearchou M, Christodoulou C, Scherer SS, Kleopa KA. Intrathecal gene therapy rescues a model of demyelinating peripheral neuropathy. Proceedings of the National Academy of Sciences of the United States of America. PMID 27035961 DOI: 10.1073/Pnas.1522202113  0.01
2016 Motley WW, Palaima P, Yum SW, Gonzalez MA, Tao F, Wanschitz JV, Strickland AV, Löscher WN, De Vriendt E, Koppi S, Medne L, Janecke AR, Jordanova A, Zuchner S, Scherer SS. De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. PMID 27009151 DOI: 10.1093/Brain/Aww055  0.01
2016 Gordon AS, Fulton RS, Qin X, Mardis ER, Nickerson DA, Scherer S. PGRNseq: a targeted capture sequencing panel for pharmacogenetic research and implementation. Pharmacogenetics and Genomics. PMID 26736087 DOI: 10.1097/Fpc.0000000000000202  0.01
2016 Scherer S, Alder J, Gaab J, Berger T, Ihde K, Urech C. Patient satisfaction and psychological well-being after internet-based cognitive behavioral stress management (IB-CBSM) for women with preterm labor: A randomized controlled trial. Journal of Psychosomatic Research. 80: 37-43. PMID 26721546 DOI: 10.1016/j.jpsychores.2015.10.011  0.01
2016 Auer-Grumbach M, Bennett DLH, Andersen P, Harms MB, Reilly MM, Weishaupt J, Strom TM, Walther T, Scherer SS, Zuchner S, Martini R, Senderek J. Rare Coding Variants In The Mme Gene, Encoding The Metalloprotease Neprilysin, Are Linked To Late-Onset Axonal Neuropathies Journal of the Peripheral Nervous System. 21: 235-235. DOI: 10.1111/Jns.12181  0.01
2016 Krewinkel M, Baur C, Kranz B, von Neubeck M, Wenning M, Scherer S, Stoeckel M, Hinrichs J, Fischer L. A Sensitive and Robust Method for Direct Determination of Lipolytic Activity in Natural Milk Environment Food Analytical Methods. 9: 646-655. DOI: 10.1007/s12161-015-0233-4  0.01
2015 Fellner L, Simon S, Scherling C, Witting M, Schober S, Polte C, Schmitt-Kopplin P, Keim DA, Scherer S, Neuhaus K. Evidence for the recent origin of a bacterial protein-coding, overlapping orphan gene by evolutionary overprinting. Bmc Evolutionary Biology. 15: 283. PMID 26677845 DOI: 10.1186/s12862-015-0558-z  0.01
2015 Didier A, Jeßberger N, Krey V, Dietrich R, Scherer S, Märtlbauer E. The Mutation Glu151Asp in the B-Component of the Bacillus cereus Non-Hemolytic Enterotoxin (Nhe) Leads to a Diverging Reactivity in Antibody-Based Detection Systems. Toxins. 7: 4655-67. PMID 26569304 DOI: 10.3390/toxins7114655  0.01
2015 Daniel V, Sadeghi M, Suesal C, Scherer S, Tran H, Gombos P, Trojan K, Morath C, Opelz G. Clinical Relevance of Preformed IgG and IgM Antibodies Against Donor Endothelial Progenitor Cells in Recipients of Living Donor Kidney Grafts. Clinical Transplantation. PMID 26537026 DOI: 10.1111/ctr.12665  0.01
2015 Wollrab E, Scherer S, Aubriet F, Carré V, Carlomagno T, Codutti L, Ott A. Chemical Analysis of a "Miller-Type" Complex Prebiotic Broth : Part I: Chemical Diversity, Oxygen and Nitrogen Based Polymers. Origins of Life and Evolution of the Biosphere : the Journal of the International Society For the Study of the Origin of Life. PMID 26508401 DOI: 10.1007/S11084-015-9468-8  0.01
2015 Sborgi L, Ravotti F, Dandey VP, Dick MS, Mazur A, Reckel S, Chami M, Scherer S, Huber M, Böckmann A, Egelman EH, Stahlberg H, Broz P, Meier BH, Hiller S. Structure and assembly of the mouse ASC inflammasome by combined NMR spectroscopy and cryo-electron microscopy. Proceedings of the National Academy of Sciences of the United States of America. 112: 13237-42. PMID 26464513 DOI: 10.1073/Pnas.1507579112  0.01
2015 Nyunt MS, Shuvo FK, Eng JY, Yap KB, Scherer S, Hee LM, Chan SP, Ng TP. Objective and subjective measures of neighborhood environment (NE): relationships with transportation physical activity among older persons. The International Journal of Behavioral Nutrition and Physical Activity. 12: 108. PMID 26373320 DOI: 10.1186/s12966-015-0276-3  0.01
2015 Pietramaggiori G, Scherer SS, Peled ZM, Wassim R. Supraorbital Neuroma: A Rare and Unreported Complication Following Blepharoplasty. Journal of Reconstructive Microsurgery. 31: 614-6. PMID 26220427 DOI: 10.1055/s-0035-1555012  0.01
2015 Olsen AL, Lai Y, Dalmau J, Scherer SS, Lancaster E. Caspr2 autoantibodies target multiple epitopes. Neurology® Neuroimmunology & Neuroinflammation. 2: e127. PMID 26185774 DOI: 10.1212/Nxi.0000000000000127  0.01
2015 Sargiannidou I, Kagiava A, Bashiardes S, Richter J, Christodoulou C, Scherer SS, Kleopa KA. Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease. Annals of Neurology. 78: 303-16. PMID 26010264 DOI: 10.1002/Ana.24441  0.01
2015 Majd H, Scherer SS, Boo S, Ramondetti S, Cambridge E, Raffoul W, Friedrich M, Pittet B, Pioletti D, Hinz B, Pietramaggiori G. Novel micropatterns mechanically control fibrotic reactions at the surface of silicone implants. Biomaterials. 54: 136-47. PMID 25907047 DOI: 10.1016/j.biomaterials.2015.03.027  0.01
2015 Liu H, Sawyer SL, Gos M, Grynspan D, Issa K, Ramphal R, Rotaru C, Consortium FC, Majewski J, Boycott KM, Graham G, Bromwich M. Atypical fibrodysplasia ossificans progressiva diagnosed by whole-exome sequencing. American Journal of Medical Genetics. Part A. 167: 1337-41. PMID 25899773 DOI: 10.1002/Ajmg.A.36969  0.01
2015 Süsal C, Wettstein D, Döhler B, Morath C, Ruhenstroth A, Scherer S, Tran TH, Gombos P, Schemmer P, Wagner E, Fehr T, Živ?i?-?osi? S, Balen S, Weimer R, Slavcev A, et al. Association of Kidney Graft Loss With De Novo Produced Donor-Specific and Non-Donor-Specific HLA Antibodies Detected by Single Antigen Testing. Transplantation. PMID 25769065 DOI: 10.1097/TP.0000000000000672  0.01
2015 Kudryashev M, Wang RY, Brackmann M, Scherer S, Maier T, Baker D, DiMaio F, Stahlberg H, Egelman EH, Basler M. Structure of the type VI secretion system contractile sheath. Cell. 160: 952-62. PMID 25723169 DOI: 10.1016/J.Cell.2015.01.037  0.01
2015 Rousseau-Nepton I, Okubo M, Grabs R, Mitchell J, Polychronakos C, Rodd C. A founder AGL mutation causing glycogen storage disease type IIIa in Inuit identified through whole-exome sequencing: a case series. Cmaj : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne. 187: E68-73. PMID 25602008 DOI: 10.1503/cmaj.140840  0.01
2015 Chardon JW, Smith AC, Woulfe J, Pena E, Rakhra K, Dennie C, Beaulieu C, Huang L, Schwartzentruber J, Hawkins C, Harms MB, Dojeiji S, Zhang M, Majewski J, et al. LIMS2 mutations are associated with a novel muscular dystrophy, severe cardiomyopathy and triangular tongues. Clinical Genetics. PMID 25589244 DOI: 10.1111/Cge.12561  0.01
2015 Adamek M, Klages C, Bauer M, Kudlek E, Drechsler A, Leuser B, Scherer S, Opelz G, Tran TH. Seven novel HLA alleles reflect different mechanisms involved in the evolution of HLA diversity: description of the new alleles and review of the literature. Human Immunology. 76: 30-5. PMID 25500251 DOI: 10.1016/j.humimm.2014.12.007  0.01
2015 Sawyer SL, Tian L, Kähkönen M, Schwartzentruber J, Kircher M, Majewski J, Dyment DA, Innes AM, Boycott KM, Moreau LA, Moilanen JS, Greenberg RA. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype. Cancer Discovery. 5: 135-42. PMID 25472942 DOI: 10.1158/2159-8290.CD-14-1156  0.01
2015 Lücking G, Frenzel E, Rütschle A, Marxen S, Stark TD, Hofmann T, Scherer S, Ehling-Schulz M. Ces locus embedded proteins control the non-ribosomal synthesis of the cereulide toxin in emetic Bacillus cereus on multiple levels Frontiers in Microbiology. 6. DOI: 10.3389/fmicb.2015.01101  0.01
2015 Jeßberger N, Krey VM, Rademacher C, Böhm ME, Mohr AK, Ehling-Schulz M, Scherer S, Märtlbauer E. From genome to toxicity: A combinatory approach highlights the complexity of enterotoxin production in Bacillus cereus Frontiers in Microbiology. 6. DOI: 10.3389/fmicb.2015.00560  0.01
2015 Frosk P, Chodirker B, Simard L, El-Matary W, Hanlon-Dearman A, Schwartzentruber J, Majewski J, Boycott K, Friedman J, Michaud J, Bernier F, Brudno M, Fernandez B, Knoppers B, Samuels M, Scherer S, et al. A novel CCBE1 mutation leading to a mild form of hennekam syndrome: Case report and review of the literature Bmc Medical Genetics. 16. DOI: 10.1186/s12881-015-0175-0  0.01
2015 Böhm ME, Huptas C, Krey VM, Scherer S. Massive horizontal gene transfer, strictly vertical inheritance and ancient duplications differentially shape the evolution of Bacillus cereus enterotoxin operons hbl, cytK and nhe Bmc Evolutionary Biology. 15. DOI: 10.1186/s12862-015-0529-4  0.01
2015 Guetto R, Luijkx R, Scherer S. Religiosity, gender attitudes and women’s labour market participation and fertility decisions in Europe Acta Sociologica (United Kingdom). 58: 155-172. DOI: 10.1177/0001699315573335  0.01
2015 Scherer S, Wimmer MA, Strykowski S. Social government: A concept supporting communities in co-creation and co-production of public services Acm International Conference Proceeding Series. 27: 204-209. DOI: 10.1145/2757401.2757417  0.01
2015 Park S, Scherer S, Gratch J, Carnevale PJ, Morency LP. I can already guess your answer: Predicting respondent reactions during dyadic negotiation Ieee Transactions On Affective Computing. 6: 86-96. DOI: 10.1109/Taffc.2015.2396079  0.01
2015 Scherer S, Morency LP, Gratch J, Pestian J. Reduced vowel space is a robust indicator of psychological distress: A cross-corpus analysis Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 2015: 4789-4793. DOI: 10.1109/ICASSP.2015.7178880  0.01
2015 Shim HS, Park S, Chatterjee M, Scherer S, Sagae K, Morency LP. Acoustic and para-verbal indicators of persuasiveness in social multimedia Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 2015: 2239-2243. DOI: 10.1109/ICASSP.2015.7178369  0.01
2015 Kearns KP, Livingston J, Scherer S, McShane L. Leadership skills as construed by nonprofit chief executives Leadership and Organization Development Journal. 36: 712-727. DOI: 10.1108/LODJ-11-2013-0143  0.01
2015 Barbieri P, Bozzon R, Scherer S, Grotti R, Lugo M. The Rise of a Latin Model? Family and fertility consequences of employment instability in Italy and Spain European Societies. 17: 423-446. DOI: 10.1080/14616696.2015.1064147  0.01
2015 Marxen S, Stark TD, Rütschle A, Lücking G, Frenzel E, Scherer S, Ehling-Schulz M, Hofmann T. Depsipeptide intermediates interrogate proposed biosynthesis of cereulide, the emetic toxin of Bacillus cereus Scientific Reports. 5. DOI: 10.1038/srep10637  0.01
2015 Marxen S, Stark TD, Rütschle A, Lücking G, Frenzel E, Scherer S, Ehling-Schulz M, Hofmann T. Multiparametric Quantitation of the Bacillus cereus Toxins Cereulide and Isocereulides A-G in Foods Journal of Agricultural and Food Chemistry. 63: 8307-8313. DOI: 10.1021/acs.jafc.5b03705  0.01
2015 Cummins N, Scherer S, Krajewski J, Schnieder S, Epps J, Quatieri TF. A review of depression and suicide risk assessment using speech analysis Speech Communication. 71: 10-49. DOI: 10.1016/J.Specom.2015.03.004  0.01
2015 Schwenker F, Scherer S, Morency LP. Preface of pattern recognition in human computer interaction Pattern Recognition Letters. 66: 1-3. DOI: 10.1016/J.Patrec.2015.07.029  0.01
2015 Trentin E, Scherer S, Schwenker F. Emotion recognition from speech signals via a probabilistic echo-state network Pattern Recognition Letters. 66: 4-12. DOI: 10.1016/j.patrec.2014.10.015  0.01
2015 von Neubeck M, Baur C, Krewinkel M, Stoeckel M, Kranz B, Stressler T, Fischer L, Hinrichs J, Scherer S, Wenning M. Biodiversity of refrigerated raw milk microbiota and their enzymatic spoilage potential International Journal of Food Microbiology. 211: 57-65. DOI: 10.1016/j.ijfoodmicro.2015.07.001  0.01
2015 Baur C, Krewinkel M, Kutzli I, Kranz B, von Neubeck M, Huptas C, Wenning M, Scherer S, Stoeckel M, Hinrichs J, Stressler T, Fischer L. Isolation and characterisation of a heat-resistant peptidase from Pseudomonas panacis withstanding general UHT processes International Dairy Journal. 49: 46-55. DOI: 10.1016/j.idairyj.2015.04.009  0.01
2015 Baur C, Krewinkel M, Kranz B, von Neubeck M, Wenning M, Scherer S, Stoeckel M, Hinrichs J, Stressler T, Fischer L. Quantification of the proteolytic and lipolytic activity of microorganisms isolated from raw milk International Dairy Journal. 49: 23-29. DOI: 10.1016/j.idairyj.2015.04.005  0.01
2015 Stratou G, Scherer S, Gratch J, Morency LP. Automatic nonverbal behavior indicators of depression and PTSD: the effect of gender Journal On Multimodal User Interfaces. 9: 17-29. DOI: 10.1007/S12193-014-0161-4  0.01
2015 Marxen S, Stark TD, Frenzel E, Rütschle A, Lücking G, Pürstinger G, Pohl EE, Scherer S, Ehling-Schulz M, Hofmann T. Chemodiversity of cereulide, the emetic toxin of Bacillus cereus Analytical and Bioanalytical Chemistry. 407: 2439-2453. DOI: 10.1007/s00216-015-8511-y  0.01
2015 Scherer S, Wimmer M, Lotzmann U, Moss S, Pinotti D. Evidence based and conceptual model driven approach for agent-based policy modelling Jasss. 18.  0.01
2014 Cogan TM, Goerges S, Gelsomino R, Larpin S, Hohenegger M, Bora N, Jamet E, Rea MC, Mounier J, Vancanneyt M, Guéguen M, Desmasures N, Swings J, Goodfellow M, Ward AC, ... ... Scherer S, et al. Biodiversity of the Surface Microbial Consortia from Limburger, Reblochon, Livarot, Tilsit, and Gubbeen Cheeses. Microbiology Spectrum. 2: CM-0010-2012. PMID 26082119 DOI: 10.1128/microbiolspec.CM-0010-2012  0.01
2014 Vincent A, Forster N, Maynes JT, Paton TA, Billingsley G, Roslin NM, Ali A, Sutherland J, Wright T, Westall CA, Paterson AD, Marshall CR, Héon E. OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium. Journal of Medical Genetics. 51: 797-805. PMID 25293953 DOI: 10.1136/Jmedgenet-2014-102620  0.01
2014 Scherer S, Urech C, Hösli I, Tschudin S, Gaab J, Berger T, Alder J. Internet-based stress management for women with preterm labour--a case-based experience report. Archives of Women's Mental Health. 17: 593-600. PMID 25123471 DOI: 10.1007/s00737-014-0454-3  0.01
2014 Mühlig A, Behr J, Scherer S, Müller-Herbst S. Stress response of Salmonella enterica serovar typhimurium to acidified nitrite. Applied and Environmental Microbiology. 80: 6373-82. PMID 25107963 DOI: 10.1128/AEM.01696-14  0.01
2014 Mühlig A, Kabisch J, Pichner R, Scherer S, Müller-Herbst S. Contribution of the NO-detoxifying enzymes HmpA, NorV and NrfA tonitrosative stress protection of Salmonella Typhimurium in raw sausages Food Microbiology. 42: 26-33. PMID 24929713 DOI: 10.1016/j.fm.2014.02.006  0.01
2014 Landstorfer R, Simon S, Schober S, Keim D, Scherer S, Neuhaus K. Comparison of strand-specific transcriptomes of enterohemorrhagic Escherichia coli O157:H7 EDL933 (EHEC) under eleven different environmental conditions including radish sprouts and cattle feces. Bmc Genomics. 15: 353. PMID 24885796 DOI: 10.1186/1471-2164-15-353  0.01
2014 Wenning M, Breitenwieser F, Konrad R, Huber I, Busch U, Scherer S. Identification and differentiation of food-related bacteria: A comparison of FTIR spectroscopy and MALDI-TOF mass spectrometry Journal of Microbiological Methods. 103: 44-52. PMID 24878140 DOI: 10.1016/j.mimet.2014.05.011  0.01
2014 Kaspar D, Auer F, Schardt J, Schindele F, Ospina A, Held C, Ehrenreich A, Scherer S, Müller-Herbst S. Temperature- and nitrogen source-dependent regulation of GlnR target genes in Listeria monocytogenes Fems Microbiology Letters. 355: 131-141. PMID 24801548 DOI: 10.1111/1574-6968.12458  0.01
2014 Wasseff SK, Scherer SS. Activated microglia do not form functional gap junctions in vivo. Journal of Neuroimmunology. 269: 90-3. PMID 24582000 DOI: 10.1016/J.Jneuroim.2014.02.005  0.01
2014 Scherer S, Hansen SH, Lynnerup N. Sexually assaulted victims are getting younger. Danish Medical Journal. 61: A4780. PMID 24495887  0.01
2014 Greenway SC, McLeod R, Hume S, Roslin NM, Alvarez N, Giuffre M, Zhan SH, Shen Y, Preuss C, Andelfinger G, Jones SJ, Gerull B. Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect. The Canadian Journal of Cardiology. 30: 181-7. PMID 24461919 DOI: 10.1016/J.Cjca.2013.12.003  0.01
2014 Scherer S, Arheit M, Kowal J, Zeng X, Stahlberg H. Single particle 3D reconstruction for 2D crystal images of membrane proteins. Journal of Structural Biology. 185: 267-77. PMID 24382495 DOI: 10.1016/J.Jsb.2013.12.011  0.01
2014 Au PY, Racher HE, Graham JM, Kramer N, Lowry RB, Parboosingh JS, Innes AM. De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical review. American Journal of Medical Genetics. Part A. 164: 676-84. PMID 24357594 DOI: 10.1002/ajmg.a.36340  0.01
2014 Scherer S, Hammal Z, Yang Y, Morency LP, Cohn JF. Dyadic behavior analysis in depression severity assessment interviews Icmi 2014 - Proceedings of the 2014 International Conference On Multimodal Interaction. 112-119. DOI: 10.1145/2663204.2663238  0.01
2014 Venek V, Scherer S, Morency LP, Rizzo AS, Pestian J. Adolescent suicidal risk assessment in clinician-patient interaction: A study of verbal and acoustic behaviors 2014 Ieee Workshop On Spoken Language Technology, Slt 2014 - Proceedings. 277-282. DOI: 10.1109/SLT.2014.7078587  0.01
2014 Chatterjee M, Stratou G, Scherer S, Morency LP. Context-based signal descriptors of heart-rate variability for anxiety assessment Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 3631-3635. DOI: 10.1109/ICASSP.2014.6854278  0.01
2014 Degottex G, Kane J, Drugman T, Raitio T, Scherer S. COVAREP - A collaborative voice analysis repository for speech technologies Icassp, Ieee International Conference On Acoustics, Speech and Signal Processing - Proceedings. 960-964. DOI: 10.1109/ICASSP.2014.6853739  0.01
2014 Müller-Herbst S, Wüstner S, Mühlig A, Eder D, Fuchs TM, Held C, Ehrenreich A, Scherer S. Identification of genes essential for anaerobic growth of Listeria monocytogenes Microbiology (United Kingdom). 160: 752-765. DOI: 10.1099/mic.0.075242-0  0.01
2014 Grotti R, Scherer S. Accumulation of employment instability among partners-evidence from six EU countries European Sociological Review. 30: 627-639. DOI: 10.1093/esr/jcu063  0.01
2014 De Looze C, Scherer S, Vaughan B, Campbell N. Investigating automatic measurements of prosodic accommodation and its dynamics in social interaction Speech Communication. 58: 11-34. DOI: 10.1016/j.specom.2013.10.002  0.01
2014 Scherer S, Stratou G, Lucas G, Mahmoud M, Boberg J, Gratch J, Rizzo A, Morency LP. Automatic audiovisual behavior descriptors for psychological disorder analysis Image and Vision Computing. 32: 648-658. DOI: 10.1016/J.Imavis.2014.06.001  0.01
2014 DeVault D, Artstein R, Benn G, Dey T, Fast E, Gainer A, Georgila K, Gratch J, Hartholt A, Lhommet M, Lucas G, Marsella S, Morbini F, Nazarian A, Scherer S, et al. SimSensei kiosk: A virtual human interviewer for healthcare decision support 13th International Conference On Autonomous Agents and Multiagent Systems, Aamas 2014. 2: 1061-1068.  0.01
2014 Chollet M, Sratou G, Shapiro A, Morency LP, Scherer S. An interactive virtual audience platform for public speaking training 13th International Conference On Autonomous Agents and Multiagent Systems, Aamas 2014. 2: 1657-1658.  0.01
2014 Ledur GR, Matesco VC, da Costa FVA, Bianchi SP, Scherer S, Gerardi DG, Juffo GD, Driemeier D. Cholangiocellular carcinoma in a cat | Carcinoma colangiocelular em gato Acta Scientiae Veterinariae. 42.  0.01
2013 Fleisher J, Richie M, Price R, Scherer S, Dalmau J, Lancaster E. Acquired neuromyotonia heralding recurrent thymoma in myasthenia gravis. Jama Neurology. 70: 1311-4. PMID 23978943 DOI: 10.1001/Jamaneurol.2013.2863  0.01
2012 Scherer SS, Kleopa KA. X-linked Charcot-Marie-Tooth disease. Journal of the Peripheral Nervous System : Jpns. 17: 9-13. PMID 23279425 DOI: 10.1111/J.1529-8027.2012.00424.X  0.01
2012 Ferguson TA, Scherer SS. Neuronal cadherin (NCAD) increases sensory neurite formation and outgrowth on astrocytes. Neuroscience Letters. 522: 108-12. PMID 22698587 DOI: 10.1016/J.Neulet.2012.06.013  0.01
2012 Scherer SS, Tobalem M, Vigato E, Heit Y, Modarressi A, Hinz B, Pittet B, Pietramaggiori G. Nonactivated versus thrombin-activated platelets on wound healing and fibroblast-to-myofibroblast differentiation in vivo and in vitro. Plastic and Reconstructive Surgery. 129: 46e-54e. PMID 22186584 DOI: 10.1097/PRS.0b013e3182362010  0.01
2012 Zuchner S, Gonzalez M, Schuele R, Siskind C, Powell E, Montenegro G, Shengru G, Blanton S, Beecham G, Speziani F, Deconinck T, Young P, Kennerson M, Nicholson G, De Jonghe P, ... ... Scherer S, et al. Gene Identification in Axonopathies by Applying Massive Whole Exome Sequencing (S27.005) Neurology. 78: S27.005-S27.005. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S27.005  0.01
2012 Siskind C, Feely S, Burns J, Zuchner S, Pareyson D, Herrmann D, Scherer S, Bird T, Lloyd T, Sumner C, Croker S, Krischer J, Muntoni F, Finkel R, Neal S, et al. Update - Inherited Neuropathies Consortium (P05.144) Neurology. 78: P05.144-P05.144. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.144  0.01
2011 Scherer SS. The debut of a rational treatment for an inherited neuropathy? The Journal of Clinical Investigation. 121: 4624-7. PMID 22045569 DOI: 10.1172/Jci60511  0.01
2011 Scherer SS. CMT2A: the name doesn't tell the whole story. Neurology. 76: 1686-7. PMID 21508332 DOI: 10.1212/Wnl.0B013E31821Bcc42  0.01
2011 Sarkar A, Tatlidede S, Scherer SS, Orgill DP, Berthiaume F. Combination of stromal cell-derived factor-1 and collagen-glycosaminoglycan scaffold delays contraction and accelerates reepithelialization of dermal wounds in wild-type mice. Wound Repair and Regeneration : Official Publication of the Wound Healing Society [and] the European Tissue Repair Society. 19: 71-9. PMID 21134036 DOI: 10.1111/J.1524-475X.2010.00646.X  0.01
2010 Fiorina P, Pietramaggiori G, Scherer SS, Jurewicz M, Mathews JC, Vergani A, Thomas G, Orsenigo E, Staudacher C, La Rosa S, Capella C, Carothers A, Zerwes HG, Luzi L, Abdi R, et al. The mobilization and effect of endogenous bone marrow progenitor cells in diabetic wound healing. Cell Transplantation. 19: 1369-81. PMID 20977829 DOI: 10.3727/096368910X514288  0.01
2010 Vavlitou N, Sargiannidou I, Markoullis K, Kyriacou K, Scherer SS, Kleopa KA. Axonal pathology precedes demyelination in a mouse model of X-linked demyelinating/type I Charcot-Marie Tooth neuropathy. Journal of Neuropathology and Experimental Neurology. 69: 945-58. PMID 20720503 DOI: 10.1097/Nen.0B013E3181Efa658  0.01
2010 Lancaster E, Elman LB, Scherer SS. A patient with neurofibromatosis type 1 and Charcot-Marie-Tooth disease type 1B. Muscle & Nerve. 41: 555-8. PMID 19918771 DOI: 10.1002/Mus.21546  0.01
2009 Scherer SS, Pietramaggiori G, Matthews J, Perry S, Assmann A, Carothers A, Demcheva M, Muise-Helmericks RC, Seth A, Vournakis JN, Valeri RC, Fischer TH, Hechtman HB, Orgill DP. Poly-N-acetyl glucosamine nanofibers: a new bioactive material to enhance diabetic wound healing by cell migration and angiogenesis. Annals of Surgery. 250: 322-30. PMID 19638916 DOI: 10.1097/Sla.0B013E3181Ae9D45  0.01
2009 Sargiannidou I, Vavlitou N, Aristodemou S, Hadjisavvas A, Kyriacou K, Scherer SS, Kleopa KA. Connexin32 mutations cause loss of function in Schwann cells and oligodendrocytes leading to PNS and CNS myelination defects. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 4736-49. PMID 19369543 DOI: 10.1523/Jneurosci.0325-09.2009  0.01
2008 Scherer SS, Pietramaggiori G, Mathews JC, Chan R, Fiorina P, Orgill DP. Wound healing kinetics of the genetically diabetic mouse. Wounds : a Compendium of Clinical Research and Practice. 20: 18-28. PMID 25942757  0.01
2008 Pietramaggiori G, Yang HJ, Scherer SS, Kaipainen A, Chan RK, Alperovich M, Newalder J, Demcheva M, Vournakis JN, Valeri CR, Hechtman HB, Orgill DP. Effects of poly-N-acetyl glucosamine (pGlcNAc) patch on wound healing in db/db mouse. The Journal of Trauma. 64: 803-8. PMID 18332827 DOI: 10.1097/01.Ta.0000244382.13937.A8  0.01
2006 Scherer SS. Inherited neuropathies: new genes don't fit old models. Neuron. 51: 672-4. PMID 16982409 DOI: 10.1016/J.Neuron.2006.09.008  0.01
2006 Scherer SS. Finding the causes of inherited neuropathies. Archives of Neurology. 63: 812-6. PMID 16769861 DOI: 10.1001/Archneur.63.6.812  0.01
2006 Scherer S. 2 PAIN AND HEREDITARY PERIPHERAL NEUROPATHIES European Journal of Pain. 10: S1a-S1. DOI: 10.1016/S1090-3801(06)60005-0  0.01
2004 Kleopa KA, Orthmann JL, Enriquez A, Paul DL, Scherer SS. Unique distributions of the gap junction proteins connexin29, connexin32, and connexin47 in oligodendrocytes. Glia. 47: 346-57. PMID 15293232 DOI: 10.1002/Glia.20043  0.01
2004 Scarlato M, Ara J, Bannerman P, Scherer S, Pleasure D. Erratum to “Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system” [Exp. Neurol. 183 (2003) 489–498] Experimental Neurology. 187: 539. DOI: 10.1016/J.Expneurol.2004.02.012  0.01
2002 Scherer SS. Myelination: some receptors required. The Journal of Cell Biology. 156: 13-5. PMID 11781330 DOI: 10.1083/Jcb.200112017  0.01
2001 Weiner JA, Fukushima N, Contos JJA, Scherer SS, Chun J. Regulation of Schwann Cell Morphology and Adhesion by Receptor-Mediated Lysophosphatidic Acid Signaling The Journal of Neuroscience. 21: 7069-7078. DOI: 10.1523/Jneurosci.21-18-07069.2001  0.01
2000 Kleopa KA, Teener JW, Scherer SS, Galetta SL, Bird SJ. Chronic multiple paraneoplastic syndromes. Muscle & Nerve. 23: 1767-72. PMID 11054759 DOI: 10.1002/1097-4598(200011)23:11<1767::Aid-Mus16>3.0.Co;2-A  0.01
1999 Fischbeck KH, Abel A, Lin GS, Scherer SS. X-linked Charcot-Marie-Tooth Disease and Connexin32. Annals of the New York Academy of Sciences. 883: 36-41. PMID 29086942 DOI: 10.1111/J.1749-6632.1999.Tb08564.X  0.01
1999 Scherer SS. Nodes, Paranodes, and Incisures: From Form to Function. Annals of the New York Academy of Sciences. 883: 131-142. PMID 29086913 DOI: 10.1111/J.1749-6632.1999.Tb08576.X  0.01
1999 Scherer SS. Nodes, paranodes, and incisures: from form to function. Annals of the New York Academy of Sciences. 883: 131-42. PMID 10586239  0.01
1999 Chernousov MA, Scherer SS, Stahl RC, Carey DJ. p200, a collagen secreted by Schwann cells, is expressed in developing nerves and in adult nerves following axotomy. Journal of Neuroscience Research. 56: 284-94. PMID 10336258 DOI: 10.1002/(Sici)1097-4547(19990501)56:3<284::Aid-Jnr8>3.0.Co;2-Q  0.01
1999 Scherer S. Axonal pathology in demyelinating diseases Annals of Neurology. 45: 6-7. PMID 9894870 DOI: 10.1002/1531-8249(199901)45:1<6::Aid-Art3>3.0.Co;2-3  0.01
1998 Grinspan JB, Coulalaglou M, Beesley JS, Carpio DF, Scherer SS. Maturation-dependent apoptotic cell death of oligodendrocytes in myelin-deficient rats. Journal of Neuroscience Research. 54: 623-34. PMID 9843153 DOI: 10.1002/(Sici)1097-4547(19981201)54:5<623::Aid-Jnr7>3.0.Co;2-R  0.01
1998 Burstyn-Cohen T, Frumkin A, Xu YT, Scherer SS, Klar A. Accumulation of F-spondin in injured peripheral nerve promotes the outgrowth of sensory axons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 8875-85. PMID 9786993 DOI: 10.1523/Jneurosci.18-21-08875.1998  0.01
1998 Burstyn-Cohen T, Frumkin A, Xu Y, Scherer SS, Klar A. Accumulation ofF-Spondinin Injured Peripheral Nerve Promotes the Outgrowth of Sensory Axons The Journal of Neuroscience. 18: 8875-8885. DOI: 10.1523/JNEUROSCI.18-21-08875.1998  0.01
1997 Bermingham-McDonogh O, Xu YT, Marchionni MA, Scherer SS. Neuregulin expression in PNS neurons: isoforms and regulation by target interactions. Molecular and Cellular Neurosciences. 10: 184-95. PMID 9532580 DOI: 10.1006/Mcne.1997.0654  0.01
1997 Fabrizi C, Kelly BM, Gillespie CS, Schlaepfer WW, Scherer SS, Brophy PJ. Transient expression of the neurofilament proteins NF-L and NF-M by Schwann cells is regulated by axonal contact. Journal of Neuroscience Research. 50: 291-9. PMID 9373038 DOI: 10.1002/(Sici)1097-4547(19971015)50:2<291::Aid-Jnr17>3.0.Co;2-B  0.01
1997 Scherer SS. The biology and pathobiology of Schwann cells. Current Opinion in Neurology. 10: 386-97. PMID 9330884 DOI: 10.1097/00019052-199710000-00006  0.01
1997 Scherer SS. Molecular genetics of demyelination: new wrinkles on an old membrane. Neuron. 18: 13-6. PMID 9010201 DOI: 10.1016/S0896-6273(01)80042-8  0.01
1997 Awatramani R, Scherer S, Grinspan J, Collarini E, Skoff R, O’Hagan D, Garbern J, Kamholz J. Evidence That the Homeodomain Protein Gtx Is Involved in the Regulation of Oligodendrocyte Myelination The Journal of Neuroscience. 17: 6657-6668. DOI: 10.1523/Jneurosci.17-17-06657.1997  0.01
1997 Shy ME, Arroyo E, Sladky J, Menichella D, Jiang H, Xu W, Kamholz J, Scherer SS. Heterozygous P0 Knockout Mice Develop a Peripheral Neuropathy that Resembles Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) Journal of Neuropathology and Experimental Neurology. 56: 811-821. DOI: 10.1097/00005072-199756070-00008  0.01
1996 Zorick TS, Syroid DE, Arroyo E, Scherer SS, Lemke G. The transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation. Molecular and Cellular Neurosciences. 8: 129-45. PMID 8918830 DOI: 10.1006/mcne.1996.0052  0.01
1996 Scherer SS. Molecular specializations at nodes and paranodes in peripheral nerve. Microscopy Research and Technique. 34: 452-61. PMID 8837021 DOI: 10.1002/(Sici)1097-0029(19960801)34:5<452::Aid-Jemt5>3.0.Co;2-O  0.01
1996 Grinspan JB, Marchionni MA, Reeves M, Coulaloglou M, Scherer SS. Axonal interactions regulate Schwann cell apoptosis in developing peripheral nerve: neuregulin receptors and the role of neuregulins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 6107-18. PMID 8815893 DOI: 10.1523/Jneurosci.16-19-06107.1996  0.01
1995 Khella SL, Frost S, Hermann GA, Leventhal L, Whyatt S, Sajid MA, Scherer SS. Hepatitis C infection, cryoglobulinemia, and vasculitic neuropathy. Treatment with interferon alfa: case report and literature review. Neurology. 45: 407-11. PMID 7898685 DOI: 10.1212/WNL.45.3.407  0.01
1995 Scherer S, Deschenes S, Xu Y, Grinspan J, Fischbeck K, Paul D. Connexin32 is a myelin-related protein in the PNS and CNS The Journal of Neuroscience. 15: 8281-8294. DOI: 10.1523/JNEUROSCI.15-12-08281.1995  0.01
1994 Chen MS, Bermingham-McDonogh O, Danehy FT, Nolan C, Scherer SS, Lucas J, Gwynne D, Marchionni MA. Expression of multiple neuregulin transcripts in postnatal rat brains. The Journal of Comparative Neurology. 349: 389-400. PMID 7852632 DOI: 10.1002/Cne.903490306  0.01
1986 Scherer SS. Reinnervation of the extraocular muscles in goldfish is nonselective. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 6: 764-73. PMID 3958794  0.01
1984 Easter S, Bratton B, Scherer S. Growth-related order of the retinal fiber layer in goldfish The Journal of Neuroscience. 4: 2173-2190. DOI: 10.1523/JNEUROSCI.04-08-02173.1984  0.01
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