Hannes Vogel

Publications

• Activated iron-containing microglia in the human hippocampus identified by magnetic resonance imaging in Alzheimer disease
  Zeineh, M. M., Chen, Y., Kitzler, H. H., Hammond, R., Vogel, H., & Rutt, B. K. (2015). Activated iron-containing microglia in the human hippocampus identified by magnetic resonance imaging in Alzheimer disease. NEUROBIOLOGY OF AGING, 36(9), 2483-2500.
• Pilomyxoid Astrocytoma (PMA) Shows Significant Differences in Gene Expression vs. Pilocytic Astrocytoma (PA) and Variable Tendency Toward Maturation to PA
  Kleinschmidt-DeMasters, B. K., Donson, A. M., Vogel, H., & Foreman, N. K. (2015). Pilomyxoid Astrocytoma (PMA) Shows Significant Differences in Gene Expression vs. Pilocytic Astrocytoma (PA) and Variable Tendency Toward Maturation to PA. BRAIN PATHOLOGY, 25(4), 429-440.
• Neuronal Activity Promotes Glioma Growth through Neuroligin-3 Secretion
  Venkatesh, H. S., Johung, T. B., Caretti, V., Noll, A., Tang, Y., & Monje, M. (2015). Neuronal Activity Promotes Glioma Growth through Neuroligin-3 Secretion. CELL, 161(4), 803-816.
• Inappropriate p53 activation during development induces features of CHARGE syndrome Van Nostrand, J. L., Brady, C. A., Jung, H., Fuentes, D. R., Kozak, M. M., & Attardi, L. D. (2014). Inappropriate p53 activation during development induces features of CHARGE syndrome. NATURE, 514(7521), 228-?.
  
• Evidence that Meningeal Mast Cells Can Worsen Stroke Pathology in Mice Arac, A., Grimbaldeston, M. A., Nepomuceno, A. Rb., Olayiwola, O., Pereira, M. P., & Steinbergtt, G. K. (2014). Evidence that Meningeal Mast Cells Can Worsen Stroke Pathology in Mice. AMERICAN JOURNAL OF PATHOLOGY, 184(9), 2493-2504.
  
• Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations Raphael, A. R., Couthouis, J., Sakamuri, S., Siskind, C., Vogel, H., & Gitler, A. D. (2014). Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations. BRAIN RESEARCH, 1575, 66-71.
  
• Lineage-specific splicing of a brain-enriched alternative exon promotes glioblastoma progression Ferrarese, R., Harsh, G. R., Yadav, A. K., Bug, E., Maticzka, D., & Bredel, M. (2014). Lineage-specific splicing of a brain-enriched alternative exon promotes glioblastoma progression. JOURNAL OF CLINICAL INVESTIGATION, 124(7), 2861-2876.
  
• Human pontine glioma cells can induce murine tumors Caretti, V., Sewing, A. C. P., Lagerweij, T., Schellen, P., Bugiani, M., & Wurdinger, T. (2014). Human pontine glioma cells can induce murine tumors. ACTA NEUROPATHOLOGICA, 127(6), 897-909.
  
• Neuronal Activity Promotes Oligodendrogenesis and Adaptive Myelination in the Mammalian Brain Gibson, E. M., Purger, D., Mount, C. W., Goldstein, A. K., Lin, G. L., & Monje, M. (2014). Neuronal Activity Promotes Oligodendrogenesis and Adaptive Myelination in the Mammalian Brain. SCIENCE, 344(6183), 487-?.
  
• Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain. Gibson, E. M., Purger, D., Mount, C. W., Goldstein, A. K., Lin, G. L., & Monje, M. (2014). Neuronal activity promotes oligodendrogenesis and adaptive myelination in the mammalian brain. Science , 344(6183), 1252304-?.
  
• Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy Couthouis, J., Raphael, A. R., Siskind, C., Findlay, A. R., Buenrostro, J. D., & Gitler, A. D. (2014). Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy. NEUROMUSCULAR DISORDERS, 24(5), 431-435.
  
• Composite pleomorphic xanthoastrocytoma-epithelioid glioneuronal tumor with BRAF V600E mutation - report of three cases Aisner, D. L., Newell, K. L., Pollack, A. G., Kleinschmidt-Demasters, B. K., Steinberg, G. K., & Vogel, H. (2014). Composite pleomorphic xanthoastrocytoma-epithelioid glioneuronal tumor with BRAF V600E mutation - report of three cases. CLINICAL NEUROPATHOLOGY, 33(2), 112-121.
  
• A positive feedback between p53 and miR-34 miRNAs mediates tumor suppression Okada, N., Lin, C.-P., Ribeiro, M. C., Biton, A., Lai, G., & He, L. (2014). A positive feedback between p53 and miR-34 miRNAs mediates tumor suppression. GENES & DEVELOPMENT, 28(5), 438-450.
  
• Targeting a Glioblastoma Cancer Stem-Cell Population Defined by EGF Receptor Variant III Emlet, D. R., Gupta, P., Holgado-Madruga, M., Del Vecchio, C. A., Mitra, S. S., & Wong, A. J. (2014). Targeting a Glioblastoma Cancer Stem-Cell Population Defined by EGF Receptor Variant III. CANCER RESEARCH, 74(4), 1238-1249.
  
• Relapse patterns in pediatric embryonal central nervous system tumors Perreault, S., Lober, R. M., Carret, A.-S., Zhang, G., Hershon, L., & Partap, S. (2013). Relapse patterns in pediatric embryonal central nervous system tumors. JOURNAL OF NEURO-ONCOLOGY, 115(2), 209-215.
  
• A Mutation in TGFB3 Associated With a Syndrome of Low Muscle Mass, Growth Retardation, Distal Arthrogryposis and Clinical Features Overlapping With Marfan and Loeys-Dietz Syndrome Rienhoff, H. Y., Yeo, C.-Y., Morissette, R., Khrebtukova, I., Melnick, J., & Whitman, M. (2013). A Mutation in TGFB3 Associated With a Syndrome of Low Muscle Mass, Growth Retardation, Distal Arthrogryposis and Clinical Features Overlapping With Marfan and Loeys-Dietz Syndrome. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 161(8), 2040-2046.
  
• AG10 inhibits amyloidogenesis and cellular toxicity of the familial amyloid cardiomyopathy-associated V122I transthyretin Penchala, S. C., Connelly, S., Wang, Y., Park, M. S., Zhao, L., & Alhamadsheh, M. M. (2013). AG10 inhibits amyloidogenesis and cellular toxicity of the familial amyloid cardiomyopathy-associated V122I transthyretin. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 110(24), 9992-9997.
  
• Central nervous system stem cell transplantation for children with neuronal ceroid lipofuscinosis Selden, N. R., Al-Uzri, A., Huhn, S. L., Koch, T. K., Sikora, D. M., & Steiner, R. D. (2013). Central nervous system stem cell transplantation for children with neuronal ceroid lipofuscinosis. JOURNAL OF NEUROSURGERY-PEDIATRICS, 11(6), 643-652.
  
• EGFRvIII gene rearrangement is an early event in glioblastoma tumorigenesis and expression defines a hierarchy modulated by epigenetic mechanisms Del Vecchio, C. A., Giacomini, C. P., Vogel, H., Jensen, K. C., Florio, T., & Wong, A. J. (2013). EGFRvIII gene rearrangement is an early event in glioblastoma tumorigenesis and expression defines a hierarchy modulated by epigenetic mechanisms. ONCOGENE, 32(21), 2670-2681.
  
• Diffusion-weighted MRI: distinction of skull base chordoma from chondrosarcoma. Yeom, K. W., Lober, R. M., Mobley, B. C., Harsh, G., Vogel, H., & Fischbein, N. J. (2013). Diffusion-weighted MRI: distinction of skull base chordoma from chondrosarcoma. AJNR. American journal of neuroradiology, 34(5), 1056-?.
  
• Chd5 Requires PHD-Mediated Histone 3 Binding for Tumor Suppression Paul, S., Kuo, A., Schalch, T., Vogel, H., Joshua-Tor, L., & Mills, A. A. (2013). Chd5 Requires PHD-Mediated Histone 3 Binding for Tumor Suppression. CELL REPORTS, 3(1), 92-102.
  
• Isocitrate dehydrogenase 1 R132H mutation is not detected in angiocentric glioma Raghunathan, A., Olar, A., Vogel, H., Parker, J. R., Coventry, S. C., & Fuller, G. N. (2012). Isocitrate dehydrogenase 1 R132H mutation is not detected in angiocentric glioma. ANNALS OF DIAGNOSTIC PATHOLOGY, 16(4), 255-259.
  
• Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism Horev, G., Ellegood, J., Lerch, J. P., Son, Y.-E. E., Muthuswamy, L., & Mills, A. A. (2011). Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 108(41), 17076-17081.
  
• Hedgehog-responsive candidate cell of origin for diffuse intrinsic pontine glioma Monje, M., Mitra, S. S., Freret, M. E., Raveh, T. B., Kim, J., & Beachy, P. A. (2011). Hedgehog-responsive candidate cell of origin for diffuse intrinsic pontine glioma. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 108(11), 4453-4458.
  
• NFKBIA Deletion in Glioblastomas. Bredel, M., Scholtens, D. M., Yadav, A. K., Alvarez, A. A., Renfrow, J. J., & Harsh, G. R. (2011). NFKBIA Deletion in Glioblastomas. NEW ENGLAND JOURNAL OF MEDICINE, 364(7), 627-637.
  
• Loss of SMARCB1/INI1 expression in poorly differentiated chordomas Mobley, B. C., McKenney, J. K., Bangs, C. D., Callahan, K., Yeom, K. W., & Vogel, H. (2010). Loss of SMARCB1/INI1 expression in poorly differentiated chordomas. ACTA NEUROPATHOLOGICA, 120(6), 745-753.
  
• G1 arrest and differentiation can occur independently of Rb family function Wirt, S. E., Adler, A. S., Gebala, V., Weimann, J. M., Schaffer, B. E., & Sage, J. (2010). G1 arrest and differentiation can occur independently of Rb family function. JOURNAL OF CELL BIOLOGY, 191(4), 809-825.
  
• End-Stage Cardiac Disease as an Initial Presentation of Systemic Myopathies: Case Series and Literature Review Katzberg, H., Karamchandani, J., So, Y. T., Vogel, H., & Wang, C. H. (2010). End-Stage Cardiac Disease as an Initial Presentation of Systemic Myopathies: Case Series and Literature Review. JOURNAL OF CHILD NEUROLOGY, 25(11), 1382-1388.
  
• TAp63 induces senescence and suppresses tumorigenesis in vivo Guo, X., Keyes, W. M., Papazoglu, C., Zuber, J., Li, W., & Mills, A. A. (2009). TAp63 induces senescence and suppresses tumorigenesis in vivo. NATURE CELL BIOLOGY, 11(12), 1451-U150.
  
• Monosomy of Chromosome 10 Associated With Dysregulation of Epidermal Growth Factor Signaling in Glioblastomas Yadav, A. K., Renfrow, J. J., Scholtens, D. M., Xie, H., Duran, G. E., & Bredel, M. (2009). Monosomy of Chromosome 10 Associated With Dysregulation of Epidermal Growth Factor Signaling in Glioblastomas. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 302(3), 276-289.
  
• A Network Model of a Cooperative Genetic Landscape in Brain Tumors Bredel, M., Scholtens, D. M., Harsh, G. R., Bredel, C., Chandler, J. P., & Sikic, B. I. (2009). A Network Model of a Cooperative Genetic Landscape in Brain Tumors. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 302(3), 261-275.
  
• Impaired human hippocampal neurogenesis after treatment for central nervous system Monje, M. L., Vogel, H., Masek, M., Ligon, K. L., Fisher, P. G., & Palmer, T. D. (2007). Impaired human hippocampal neurogenesis after treatment for central nervous system. ANNALS OF NEUROLOGY, 62(5), 515-520.
  
• Atypical and Rare Variants of Central Neurocytomas Choudhri, O., Razavi, S.-M., Vogel, H., & Li, G. (2015). Atypical and Rare Variants of Central Neurocytomas. NEUROSURGERY CLINICS OF NORTH AMERICA, 26(1), 91-?.
  
• Endoscopic resection of a giant intradural retroclival ecchordosis physaliphora: surgical technique and literature review. Choudhri, O., Feroze, A., Hwang, P., Vogel, H., Ajlan, A., & Harsh, G. (2014). Endoscopic resection of a giant intradural retroclival ecchordosis physaliphora: surgical technique and literature review. World neurosurgery, 82(5), 912 e21-6.
  
• Endoscopic Resection of a Giant Intradural Retroclival Ecchordosis Physaliphora: Surgical Technique and Literature Review Choudhri, O., Feroze, A., Hwang, P., Vogel, H., Ajlan, A., & Harsh, G. (2014). Endoscopic Resection of a Giant Intradural Retroclival Ecchordosis Physaliphora: Surgical Technique and Literature Review. WORLD NEUROSURGERY, 82(5).
  
• Abnormal Hepatocellular Mitochondria in Methylmalonic Acidemia Wilnai, Y., Enns, G. M., Niemi, A.-K., Higgins, J., & Vogel, H. (2014). Abnormal Hepatocellular Mitochondria in Methylmalonic Acidemia. ULTRASTRUCTURAL PATHOLOGY, 38(5), 309-314.
  
• MRI Surrogates for Molecular Subgroups of Medulloblastoma Perreault, S., Ramaswamy, V., Achrol, A. S., Chao, K., Liu, T. T., & Yeom, K. W. (2014). MRI Surrogates for Molecular Subgroups of Medulloblastoma. AMERICAN JOURNAL OF NEURORADIOLOGY, 35(7), 1263-1269.
  
• Diffusion-weighted MRI derived apparent diffusion coefficient identifies prognostically distinct subgroups of pediatric diffuse intrinsic pontine glioma Lober, R. M., Cho, Y.-J., Tang, Y., Barnes, P. D., Edwards, M. S., & Yeom, K. W. (2014). Diffusion-weighted MRI derived apparent diffusion coefficient identifies prognostically distinct subgroups of pediatric diffuse intrinsic pontine glioma. JOURNAL OF NEURO-ONCOLOGY, 117(1), 175-182.
  
• Tectal pineal cyst in a 1-year-old girl Plowey, E. D., Vogel, H., Yeom, K. W., Jung, H., Chao, K., & Edwards, M. Sb. (2014). Tectal pineal cyst in a 1-year-old girl. HUMAN PATHOLOGY, 45(3), 653-656.
  
• A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome. Rienhoff, H. Y., Yeo, C.-Y., Morissette, R., Khrebtukova, I., Melnick, J., & Whitman, M. (2013). A mutation in TGFB3 associated with a syndrome of low muscle mass, growth retardation, distal arthrogryposis and clinical features overlapping with Marfan and Loeys-Dietz syndrome. American journal of medical genetics. Part A, 161A(8), 2040-2046.
  
• Pituitary stalk Langerhans cell histiocytosis treated with CyberKnife radiosurgery Hong, W.-C., Murovic, J. A., Gibbs, I., Vogel, H., & Chang, S. D. (2013). Pituitary stalk Langerhans cell histiocytosis treated with CyberKnife radiosurgery. CLINICAL NEUROLOGY AND NEUROSURGERY, 115(5), 573-577.
  
• Spinal Pilocytic Astrocytoma in an Elderly Patient Harraher, C. D., Vogel, H., & Steinberg, G. K. (2013). Spinal Pilocytic Astrocytoma in an Elderly Patient. WORLD NEUROSURGERY, 79(5-6).
  
• Spinal pilocytic astrocytoma in an elderly patient. Harraher, C. D., Vogel, H., & Steinberg, G. K. (2013). Spinal pilocytic astrocytoma in an elderly patient. World neurosurgery, 79(5-6), 799 E7-9.
  
• Diffusion-Weighted MRI: Distinction of Skull Base Chordoma from Chondrosarcoma Yeom, K. W., Lober, R. M., Mobley, B. C., Harsh, G., Vogel, H., & Fischbein, N. J. (2013). Diffusion-Weighted MRI: Distinction of Skull Base Chordoma from Chondrosarcoma. AMERICAN JOURNAL OF NEURORADIOLOGY, 34(5), 1056-1061.
  
• Distinctive MRI Features of Pediatric Medulloblastoma Subtypes Yeom, K. W., Mobley, B. C., Lober, R. M., Andre, J. B., Partap, S., & Barnes, P. D. (2013). Distinctive MRI Features of Pediatric Medulloblastoma Subtypes. AMERICAN JOURNAL OF ROENTGENOLOGY, 200(4), 895-903.
  
• Late profound muscle weakness following heart transplantation due to danon disease van der Starre, P., Deuse, T., Pritts, C., Brun, C., Vogel, H., & Oyer, P. (2013). Late profound muscle weakness following heart transplantation due to danon disease. MUSCLE & NERVE, 47(1), 135-137.
  
• Unimpaired Skin Carcinogenesis in Desmoglein 3 Knockout Mice Baron, S., Anabel Hoang, A., Vogel, H., & Attardi, L. D. (2012). Unimpaired Skin Carcinogenesis in Desmoglein 3 Knockout Mice. PLOS ONE, 7(11).
  
• Extravascular Papillary Endothelial Hyperplasia Mimicking Neoplasm After Radiosurgery: Case Report Karamchandani, J., Vogel, H., Fischbein, N., Gibbs, I., Edwards, M. Sb., & Harsh, G. (2012). Extravascular Papillary Endothelial Hyperplasia Mimicking Neoplasm After Radiosurgery: Case Report. NEUROSURGERY, 70(4), E1043-E1048.
  
• Notch signaling inhibits hepatocellular carcinoma following inactivation of the RB pathway Viatour, P., Ehmer, U., Saddic, L. A., Dorrell, C., Andersen, J. B., & Sage, J. (2011). Notch signaling inhibits hepatocellular carcinoma following inactivation of the RB pathway. JOURNAL OF EXPERIMENTAL MEDICINE, 208(10), 1963-1976.
  
• Gene-protein correlation in single cells Renfrow, J. J., Scheck, A. C., Dhawan, N. S., Lukac, P. J., Vogel, H., & Bredel, M. (2011). Gene-protein correlation in single cells. NEURO-ONCOLOGY, 13(8), 880-885.
  
• Mosaic Analysis with Double Markers Reveals Tumor Cell of Origin in Glioma Liu, C., Sage, J. C., Miller, M. R., Verhaak, R. Gw., Hippenmeyer, S., & Zong, H. (2011). Mosaic Analysis with Double Markers Reveals Tumor Cell of Origin in Glioma. CELL, 146(2), 209-221.
  
• Liposomal cytarabine for central nervous system embryonal tumors in children and young adults Partap, S., Murphy, P. A., Vogel, H., Barnes, P. D., Edwards, M. Sb., & Fisher, P. G. (2011). Liposomal cytarabine for central nervous system embryonal tumors in children and young adults. JOURNAL OF NEURO-ONCOLOGY, 103(3), 561-566.
  
• The pro-longevity gene FoxO3 is a direct target of the p53 tumor suppressor Renault, V. M., Thekkat, P. U., Hoang, K. L., WHITE, J. L., Brady, C. A., & Brunet, A. (2011). The pro-longevity gene FoxO3 is a direct target of the p53 tumor suppressor. ONCOGENE, 30(29), 3207-3221.
  
• Functional Interactions between Retinoblastoma and c-MYC in a Mouse Model of Hepatocellular Carcinoma Saddic, L. A., Wirt, S., Vogel, H., Felsher, D. W., & Sage, J. (2011). Functional Interactions between Retinoblastoma and c-MYC in a Mouse Model of Hepatocellular Carcinoma. PLOS ONE, 6(5).
  
• Endocervical Fibroblastic Malignant Peripheral Nerve Sheath Tumor (Neurofibrosarcoma): Report of a Novel Entity Possibly Related to Endocervical CD34 Fibrocytes Mills, A. M., Karamchandani, J. R., Vogel, H., & Longacre, T. A. (2011). Endocervical Fibroblastic Malignant Peripheral Nerve Sheath Tumor (Neurofibrosarcoma): Report of a Novel Entity Possibly Related to Endocervical CD34 Fibrocytes. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 35(3), 404-412.
  
• Brain Abscess Caused by Phaeoacremonium parasiticum in an Immunocompromised Patient McNeil, C. J., Luo, R. F., Vogel, H., Banaei, N., & Ho, D. Y. (2011). Brain Abscess Caused by Phaeoacremonium parasiticum in an Immunocompromised Patient. JOURNAL OF CLINICAL MICROBIOLOGY, 49(3), 1171-1174.
  
• Delta Np630 alpha Is an Oncogene that Targets Chromatin Remodeler Lsh to Drive Skin Stem Cell Proliferation and Tumorigenesis Keyes, W. M., Pecoraro, M., Aranda, V., Vernersson-Lindahl, E., Li, W., & Mills, A. A. (2011). Delta Np630 alpha Is an Oncogene that Targets Chromatin Remodeler Lsh to Drive Skin Stem Cell Proliferation and Tumorigenesis. CELL STEM CELL, 8(2), 164-176.
  
• Isocitrate Dehydrogenase 1 (IDH1)R132H Mutation Is Not Detected in Angiocentric Glioma Raghunathan, A., Olar, A., Vogel, H., Parker, J. R., Coventry, S. C., & Fuller, G. N. (2011). Isocitrate Dehydrogenase 1 (IDH1)R132H Mutation Is Not Detected in Angiocentric Glioma. MODERN PATHOLOGY, 24, 384A-384A.
  
• Isocitrate Dehydrogenase 1 (IDH1) R132H Mutation Is Not Detected in Angiocentric Glioma Raghunathan, A., Olar, A., Vogel, H., Parker, J. R., Coventry, S. C., & Fuller, G. N. (2011). Isocitrate Dehydrogenase 1 (IDH1) R132H Mutation Is Not Detected in Angiocentric Glioma. LABORATORY INVESTIGATION, 91, 384A-384A.
  
• Extravascular Papillary Endothelial Hyperplasia Mimicking Neoplasm Following Radiosurgery. Karamchandani, J., Vogel, H., Fischbein, N., Gibbs, I., Edwards, M. S., & Harsh, G. (2011). Extravascular Papillary Endothelial Hyperplasia Mimicking Neoplasm Following Radiosurgery. Neurosurgery.
  
• ECTOPIC ACROMEGALY DUE TO A PANCREATIC NEUROENDOCRINE TUMOR PRODUCING GROWTH HORMONE-RELEASING HORMONE Weiss, D. E., Vogel, H., Lopes, M. B. S., Chang, S. D., & Katznelson, L. (2011). ECTOPIC ACROMEGALY DUE TO A PANCREATIC NEUROENDOCRINE TUMOR PRODUCING GROWTH HORMONE-RELEASING HORMONE. ENDOCRINE PRACTICE, 17(1), 79-84.
  
• Primary Pediatric Skull Tumors Gephart, M. Gh., Colglazier, E., Paulk, K. L., Vogel, H., Guzman, R., & Edwards, M. Sb. (2011). Primary Pediatric Skull Tumors. PEDIATRIC NEUROSURGERY, 47(3), 198-203.
  
• AN RNAI SCREEN IDENTIFIES TRRAP AS A REGULATOR OF BRAIN TUMOR-INITIATING CELL DIFFERENTIATION Skirboll, S. L., Wurdak, H., Zhu, S., Romero, A., Lorger, M., & Schultz, P. G. (2010). AN RNAI SCREEN IDENTIFIES TRRAP AS A REGULATOR OF BRAIN TUMOR-INITIATING CELL DIFFERENTIATION. NEURO-ONCOLOGY, 12, 122-122.
  
• Langerhans cell histiocytosis in a 5-month-old presenting with biparietal masses Case report Pricola, K. L., Karamchandani, J., Vogel, H., Dahl, G. V., Yeom, K. W., & Guzman, R. (2010). Langerhans cell histiocytosis in a 5-month-old presenting with biparietal masses Case report. JOURNAL OF NEUROSURGERY-PEDIATRICS, 6(4), 393-397.
  
• Loss of the p53/p63 Regulated Desmosomal Protein Perp Promotes Tumorigenesis Beaudry, V. G., Jiang, D., Dusek, R. L., Park, E. J., Knezevich, S., & Attardi, L. D. (2010). Loss of the p53/p63 Regulated Desmosomal Protein Perp Promotes Tumorigenesis. PLOS GENETICS, 6(10).
  
• Retrosellar intracranial extracerebral glioneuronal heterotopion: case report Karamchandani, J., Fischbein, N., Harsh, G., Katznelson, L., & Vogel, H. (2010). Retrosellar intracranial extracerebral glioneuronal heterotopion: case report. CLINICAL NEUROPATHOLOGY, 29(5), 297-300.
  
• Inhibition of vasculogenesis, but not angiogenesis, prevents the recurrence of glioblastoma after irradiation in mice Kioi, M., Vogel, H., Schultz, G., Hoffman, R. M., Harsh, G. R., & Brown, J. M. (2010). Inhibition of vasculogenesis, but not angiogenesis, prevents the recurrence of glioblastoma after irradiation in mice. JOURNAL OF CLINICAL INVESTIGATION, 120(3), 694-705.
  
• Breast cancer brain metastases express the sodium iodide symporter Renier, C., Vogel, H., Offor, O., Yao, C., & Wapnir, I. (2010). Breast cancer brain metastases express the sodium iodide symporter. JOURNAL OF NEURO-ONCOLOGY, 96(3), 331-336.
  
• Timing of Bone Marrow Cell Delivery Has Minimal Effects on Cell Viability and Cardiac Recovery After Myocardial Infarction Swijnenburg, R.-J., Govaert, J. A., van der Bogt, K. Ea., Pearl, J. I., Huang, M., & Wu, J. C. (2010). Timing of Bone Marrow Cell Delivery Has Minimal Effects on Cell Viability and Cardiac Recovery After Myocardial Infarction. CIRCULATION-CARDIOVASCULAR IMAGING, 3(1), 77-U109.
  
• The Lysosomal Sialic Acid Transporter Sialin Is Required for Normal CNS Myelination Prolo, L. M., Vogel, H., & Reimer, R. J. (2009). The Lysosomal Sialic Acid Transporter Sialin Is Required for Normal CNS Myelination. JOURNAL OF NEUROSCIENCE, 29(49), 15355-15365.
  
• Intraventricular metaplastic meningioma in a child: case report and review of the literature Dulai, M. S., Khan, A.-M., Edwards, M. Sb., & Vogel, H. (2009). Intraventricular metaplastic meningioma in a child: case report and review of the literature. NEUROPATHOLOGY, 29(6), 708-712.
  
• Papillary Tumor of the Spinal Cord Report of 2 Cases Mobley, B., Kalani, M.-Y. S., Harsh, G. R., Edwards, M. Sb., & Vogel, H. (2009). Papillary Tumor of the Spinal Cord Report of 2 Cases. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 33(8), 1191-1197.
  
• Distinguishing Chordoid Meningiomas From Their Histologic Mimics An Immunohistochemical Evaluation Sangoi, A. R., Dulai, M. S., Beck, A. H., Brat, D. J., & Vogel, H. (2009). Distinguishing Chordoid Meningiomas From Their Histologic Mimics An Immunohistochemical Evaluation. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 33(5), 669-681.
  
• A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy Mobley, B. C., Enns, G. M., Wong, L.-J., & Vogel, H. (2009). A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy. CLINICAL NEUROPATHOLOGY, 28(2), 143-149.
  
• The Transcription Factor LMO2 Is a Robust Marker of Vascular Endothelium and Vascular Neoplasms and Selected Other Entities Gratzinger, D., Zhao, S., West, R., Rouse, R. V., Vogel, H., & Natkunam, Y. (2009). The Transcription Factor LMO2 Is a Robust Marker of Vascular Endothelium and Vascular Neoplasms and Selected Other Entities. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 131(2), 264-278.
  
• Drosophila Models of Neurodegenerative Diseases Lu, B., & Vogel, H. (2009). Drosophila Models of Neurodegenerative Diseases. ANNUAL REVIEW OF PATHOLOGY-MECHANISMS OF DISEASE, 4, 315-342.
  
• Wnt-mediated self-renewal of neural stem/progenitor cells Kalani, M. Y. S., Cheshier, S. H., Cord, B. J., Bababeygy, S. R., Vogel, H., & Nusse, R. (2008). Wnt-mediated self-renewal of neural stem/progenitor cells. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 105(44), 16970-16975.
  
• Suprasellar giant cell ependymoma: a rare neoplasm in a unique location Sangoi, A. R., Lim, M., Dulai, M. S., Vogel, H., & Chang, S. D. (2008). Suprasellar giant cell ependymoma: a rare neoplasm in a unique location. HUMAN PATHOLOGY, 39(9), 1396-1401.
  
• Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure Schule, B., Armstrong, D. D., Vogel, H., Oviedo, A., & Francke, U. (2008). Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure. CLINICAL GENETICS, 74(2), 116-126.
  
• Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy Mast, J. D., Tomalty, K. Mh., Vogel, H., & Clandinin, T. R. (2008). Reactive oxygen species act remotely to cause synapse loss in a Drosophila model of developmental mitochondrial encephalopathy. DEVELOPMENT, 135(15), 2669-2679.
  
• Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery Yang, Y., Ouyang, Y., Yang, L., Beal, M. F., McQuibban, A., & Lu, B. (2008). Pink1 regulates mitochondrial dynamics through interaction with the fission/fusion machinery. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 105(19), 7070-7075.
  
• Intracerebral hemorrhage caused by cerebral amyloid angiopathy in a 53-year-old man Campbell, D. M., Bruins, S., Vogel, H., Shuer, L. M., & Wijman, C. Ac. (2008). Intracerebral hemorrhage caused by cerebral amyloid angiopathy in a 53-year-old man. JOURNAL OF NEUROLOGY, 255(4), 597-598.
  
• CNS T-cell lymphoma: an under-recognized entity? Dulai, M. S., Park, C. Y., Howell, W. D., Smyth, L. T., Desai, M., & Vogel, H. (2008). CNS T-cell lymphoma: an under-recognized entity?. ACTA NEUROPATHOLOGICA, 115(3), 345-356.
  
• Progressive cerebral vascular degeneration with mitochondrial encephalopathy Longo, N., Schrijver, I., Vogel, H., Pique, L. M., Cowan, T. M., & Enns, G. M. (2008). Progressive cerebral vascular degeneration with mitochondrial encephalopathy. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 146A(3), 361-367.
  
• Congenital glioblastoma multiforme: Case report and review of the literature Hou, L. C., Bababeygy, S. R., Sarkissian, V., Fisher, P. G., Vogel, H., & Huhn, S. L. (2008). Congenital glioblastoma multiforme: Case report and review of the literature. PEDIATRIC NEUROSURGERY, 44(4), 304-312.
  
• Muscle lymphocytic infiltrates in thymoma-associated myasthenia gravis are phenotypically different from those in polymyositis Zamecnik, J., Vesely, D., Jakubicka, B., Simkova, L., Pitha, J., & Vogel, H. (2007). Muscle lymphocytic infiltrates in thymoma-associated myasthenia gravis are phenotypically different from those in polymyositis. NEUROMUSCULAR DISORDERS, 17(11-12), 935-942.
  
• Intraventricular myxoid meningioma in a 7-year-old female Dulai, M. S., Khan, A.-M., Edwards, M. Sb., & Vogel, H. (2007). Intraventricular myxoid meningioma in a 7-year-old female. NEURO-ONCOLOGY, 9(4), 550-551.
  
• A 35-year-old woman with a dural-based mass. Haddix, T., Chang, S., & Vogel, H. (2007). A 35-year-old woman with a dural-based mass. Brain pathology , 17(3), 331-332.
  
• Multimodality molecular imaging of glioblastoma growth inhibition with vasculature-targeting fusion toxin VEGF(121)/rGel Hsu, A. R., Cai, W., Veeravagu, A., Mohamedali, K. A., Chen, K., & Chen, X. (2007). Multimodality molecular imaging of glioblastoma growth inhibition with vasculature-targeting fusion toxin VEGF(121)/rGel. JOURNAL OF NUCLEAR MEDICINE, 48(3), 445-454.
  
• CHD5 is a tumor suppressor at human 1p36 Bagchi, A., Papazoglu, C., Wu, Y., Capurso, D., Brodt, M., & Mills, A. A. (2007). CHD5 is a tumor suppressor at human 1p36. CELL, 128(3), 459-475.
  
• In vivo near-infrared fluorescence imaging of integrin alpha(v)beta(3) in an orthotopic glioblastoma model Hsu, A. R., Hou, L. C., Veeravagu, A., Greve, J. M., Vogel, H., & Chen, X. (2006). In vivo near-infrared fluorescence imaging of integrin alpha(v)beta(3) in an orthotopic glioblastoma model. MOLECULAR IMAGING AND BIOLOGY, 8(6), 315-323.
  
• Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused inactivation of Drosophila Pink1 is rescued by by Parkin Yang, Y., Gehrke, S., Imai, Y., Huang, Z., Ouyang, Y., & Lu, B. (2006). Mitochondrial pathology and muscle and dopaminergic neuron degeneration caused inactivation of Drosophila Pink1 is rescued by by Parkin. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 103(28), 10793-10798.
  
• Transcriptional profiling of aging in human muscle reveals a common aging signature Zahn, J. M., Sonu, R., Vogel, H., Crane, E., Mazan-Mamczarz, K., & Kim, S. K. (2006). Transcriptional profiling of aging in human muscle reveals a common aging signature. PLOS GENETICS, 2(7), 1058-1069.
  
• p63 heterozygous mutant mice are not prone to spontaneous or chemically induced tumors Keyes, W. M., Vogel, H., Koster, M. I., Guo, X., Qi, Y., & Mills, A. A. (2006). p63 heterozygous mutant mice are not prone to spontaneous or chemically induced tumors. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 103(22), 8435-8440.
  
• Gene targeting of GAN in mouse causes a toxic accumulation of microtubule-associated protein 8 and impaired retrograde axonal transport Ding, J. Q., Allen, E., Wang, W., Valle, A., Wu, C. B., & Yang, Y. M. (2006). Gene targeting of GAN in mouse causes a toxic accumulation of microtubule-associated protein 8 and impaired retrograde axonal transport. HUMAN MOLECULAR GENETICS, 15(9), 1451-1463.
  
• Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea Jang, T. C., Savarese, T., Low, H. P., Kim, S., Vogel, H., & Recht, L. (2006). Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea. AMERICAN JOURNAL OF PATHOLOGY, 168(5), 1676-1685.
  
• Tumor necrosis factor-alpha-induced protein 3 as a putative regulator of nuclear factor-kappa B-mediated resistance to O-6-alkylating agents in human glioblastomas Bredel, M., Bredel, C., Juric, D., Duran, G. E., Yu, R. X., & Sikic, B. I. (2006). Tumor necrosis factor-alpha-induced protein 3 as a putative regulator of nuclear factor-kappa B-mediated resistance to O-6-alkylating agents in human glioblastomas. JOURNAL OF CLINICAL ONCOLOGY, 24(2), 274-287.
  
• Gigaxonin interacts with tubulin folding cofactor B and controls its degradation through the ubiquitin-proteasome pathway Wang, W., Ding, J. Q., Allen, E., Zhu, P., Zhang, L., & Yang, Y. M. (2005). Gigaxonin interacts with tubulin folding cofactor B and controls its degradation through the ubiquitin-proteasome pathway. CURRENT BIOLOGY, 15(22), 2050-2055.
  
• Identification of phenotypic neural stem cells in a pediatric astroblastoma Huhn, S. L., Yung, Y., Cheshier, S., Harsh, G., Ailles, L., & Tse, V. (2005). Identification of phenotypic neural stem cells in a pediatric astroblastoma. JOURNAL OF NEUROSURGERY, 103(5), 446-450.
  
• Functional network analysis reveals extended gliomagenesis pathway maps and three novel MYC-interacting genes in human gliomas Bredel, M., Bredel, C., Juric, D., Harsh, G. R., Vogel, H., & Sikic, B. I. (2005). Functional network analysis reveals extended gliomagenesis pathway maps and three novel MYC-interacting genes in human gliomas. CANCER RESEARCH, 65(19), 8679-8689.
  
• p63 deficiency activates a program of cellular senescence and leads to accelerated aging Keyes, W. M., Wu, Y., Vogel, H., Guo, X. C., Lowe, S. W., & Mills, A. A. (2005). p63 deficiency activates a program of cellular senescence and leads to accelerated aging. GENES & DEVELOPMENT, 19(17), 1986-1999.
  
• Embryonic stem cell immunogenicity increases upon differentiation after transplantation into ischemic myocardium Swijnenburg, R. J., Tanaka, M., Vogel, H., Baker, J., Kofidis, T., & Robbins, R. C. (2005). Embryonic stem cell immunogenicity increases upon differentiation after transplantation into ischemic myocardium. CIRCULATION, 112(9), I166-I172.
  
• alpha(v)beta(3) integrin in central nervous system tumors Lim, M., Guccione, S., Haddix, T., Sims, L., Cheshier, S., & Harsh, G. (2005). alpha(v)beta(3) integrin in central nervous system tumors. HUMAN PATHOLOGY, 36(6), 665-669.
  
• Hematopoietic cells maintain hematopoietic fates upon entering the brain Massengale, M., Wagers, A. J., Vogel, H., & Weissman, I. L. (2005). Hematopoietic cells maintain hematopoietic fates upon entering the brain. JOURNAL OF EXPERIMENTAL MEDICINE, 201(10), 1579-1589.
  
• High-resolution genome-wide mapping of genetic alterations in human glial brain tumors Bredel, M., Bredel, C., Juric, D., Harsh, G. R., Vogel, H., & Sikic, B. I. (2005). High-resolution genome-wide mapping of genetic alterations in human glial brain tumors. CANCER RESEARCH, 65(10), 4088-4096.
  
• NF90 regulates cell cycle exit and terminal myogenic differentiation by direct binding to the 3 '-untranslated region of MyoD and p21(WAF1/CIP1) mRNAs Shi, L. F., Zhao, G. H., Qiu, D. M., Godfrey, W. R., Vogel, H., & Kao, P. N. (2005). NF90 regulates cell cycle exit and terminal myogenic differentiation by direct binding to the 3 '-untranslated region of MyoD and p21(WAF1/CIP1) mRNAs. JOURNAL OF BIOLOGICAL CHEMISTRY, 280(19), 18981-18989.
  
• Myopathy with skeletal asymmetry and hemidiaphragm elevation is caused by myotubularin mutations Grogan, P. M., Tanner, S. M., Orstavik, K. H., Knudsen, G. Ps., Saperstein, D. S., & Katz, J. S. (2005). Myopathy with skeletal asymmetry and hemidiaphragm elevation is caused by myotubularin mutations. NEUROLOGY, 64(9), 1638-1640.
  
• Amplification of whole tumor genomes and geneby-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA Bredel, M., Bredel, C., Juric, D., Kim, Y., Vogel, H., & Sikic, B. I. (2005). Amplification of whole tumor genomes and geneby-gene mapping of genomic aberrations from limited sources of fresh-frozen and paraffin-embedded DNA. JOURNAL OF MOLECULAR DIAGNOSTICS, 7(2), 171-182.
  
• Overexpression of osteopontin (OPN) in glioblastoma multiforme (GBM). Haddix, T. L., Recht, L. D., Myles, T., Leung, L. Lk., & Vogel, H. (2005). Overexpression of osteopontin (OPN) in glioblastoma multiforme (GBM). JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 64(5), 456-456.
  
• Diagnostic immunohistology of muscle diseases Vogel, H., & Zamecnik, J. (2005). Diagnostic immunohistology of muscle diseases. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 64(3), 181-193.
  
• Capsaicin-sensitive sensory neurons contribute to the maintenance of trabecular bone integrity Offley, S. C., Guo, T. Z., Wei, T. P., Clark, J. D., Vogel, H., & Kingery, W. S. (2005). Capsaicin-sensitive sensory neurons contribute to the maintenance of trabecular bone integrity. JOURNAL OF BONE AND MINERAL RESEARCH, 20(2), 257-267.
  
• Characterization of the integrin alpha v beta 3 in arteriovenous malformations and cavernous malformations Lim, M., Haddix, T., Harsh, G. R., Vogel, H., Steinberg, G. K., & Guccione, S. (2005). Characterization of the integrin alpha v beta 3 in arteriovenous malformations and cavernous malformations. CEREBROVASCULAR DISEASES, 20(1), 23-27.
  
• Burden of proof in the postmortem diagnosis of mitochondrial disease: Leigh disease Vogel, H. (2004). Burden of proof in the postmortem diagnosis of mitochondrial disease: Leigh disease. PEDIATRIC AND DEVELOPMENTAL PATHOLOGY, 7(6), 615-619.
  
• Immunogenicity of embryonic stem cells increases upon differentiation in ischemic myocardium Swijnenburg, R. J., Tanaka, M., Baker, J., Vogel, H., Lebl, D. R., & Robbins, R. C. (2004). Immunogenicity of embryonic stem cells increases upon differentiation in ischemic myocardium. CIRCULATION, 110(17), 507-507.
  
• Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease Scaglia, F., Towbin, J. A., Craigen, W. J., Belmont, J. W., Smith, E. O., & Vogel, H. (2004). Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease. PEDIATRICS, 114(4), 925-931.
  
• Primitive neuroectodermal tumors, embryonal tumors, and other small cell and poorly differentiated malignant neoplasms of the central and peripheral nervous systems. Vogel, H., & Fuller, G. N. (2003). Primitive neuroectodermal tumors, embryonal tumors, and other small cell and poorly differentiated malignant neoplasms of the central and peripheral nervous systems. Annals of diagnostic pathology, 7(6), 387-398.
  
• Novel homoplasmic mutation in the mitochondrial tRNA(Tyr) gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomeruloselerosis Scaglia, F., Vogel, H., Hawkins, E. P., Vladutiu, G. D., Liu, L. L., & Wong, L. Jc. (2003). Novel homoplasmic mutation in the mitochondrial tRNA(Tyr) gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomeruloselerosis. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 123A(2), 172-178.
  
• COP9 signalosome subunit 3 (Csn3) is essential for maintenance of cell proliferation in the mouse embryonic epiblast. Yan, J., Walz, K., Nakamura, H., Carattini-Rivera, S., Zhao, Q., & Lupski, J. R. (2003). COP9 signalosome subunit 3 (Csn3) is essential for maintenance of cell proliferation in the mouse embryonic epiblast. AMERICAN JOURNAL OF HUMAN GENETICS, 73(5), 328-328.
  
• Cooperativity of p19(ARF), Mdm2, and p53 in murine tumorigenesis Moore, L., Venkatachalam, S., Vogel, H., Watt, J. C., Wu, C. L., & Donehower, L. A. (2003). Cooperativity of p19(ARF), Mdm2, and p53 in murine tumorigenesis. ONCOGENE, 22(49), 7831-7837.
  
• COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast Yan, J., Walz, K., Nakamura, H., Carattini-Rivera, S., Zhao, Q., & Lupski, J. R. (2003). COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast. MOLECULAR AND CELLULAR BIOLOGY, 23(19), 6798-6808.
  
• Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: Phenotypic consequences of gene dosage imbalance Walz, K., Caratini-Rivera, S., Bi, W. M., Fonseca, P., Mansouri, D. L., & Lupski, J. R. (2003). Modeling del(17)(p11.2p11.2) and dup(17)(p11.2p11.2) contiguous gene syndromes by chromosome engineering in mice: Phenotypic consequences of gene dosage imbalance. MOLECULAR AND CELLULAR BIOLOGY, 23(10), 3646-3655.
  
• Phenotypic consequences of gene dosage imbalance in chromosome engineered mouse models for del(17)p11.2 (Smith-Magenis syndrome) and it's reciprocal duplication. Walz, K., Carattini-Rivera, S., Bi, W., Mansouri, D., Vogel, H., & Lupski, J. L. (2002). Phenotypic consequences of gene dosage imbalance in chromosome engineered mouse models for del(17)p11.2 (Smith-Magenis syndrome) and it's reciprocal duplication. AMERICAN JOURNAL OF HUMAN GENETICS, 71(4), 195-195.
  
• Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria Scaglia, F., Sutton, V. R., Bodamer, O. Af., Vogel, H., Shapira, S. K., & Vladutiu, G. D. (2001). Mitochondrial DNA depletion associated with partial complex II and IV deficiencies and 3-methylglutaconic aciduria. JOURNAL OF CHILD NEUROLOGY, 16(2), 136-138.
  
• Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation Venkatachalam, S., Shi, Y. P., Jones, S. N., Vogel, H., Bradley, A., & Donehower, L. A. (1998). Retention of wild-type p53 in tumors from p53 heterozygous mice: reduction of p53 dosage can promote cancer formation. EMBO JOURNAL, 17(16), 4657-4667.
  
• EFFECTS OF GENETIC BACKGROUND ON TUMORIGENESIS IN P53-DEFICIENT MICE Donehower, L. A., Harvey, M., Vogel, H., McArthur, M. J., Montgomery, C. A., & Bradley, A. (1995). EFFECTS OF GENETIC BACKGROUND ON TUMORIGENESIS IN P53-DEFICIENT MICE. MOLECULAR CARCINOGENESIS, 14(1), 16-22.