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MERED PARNES

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
Address6701 FANNIN
Houston, TX 77030
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Rinaldi B, Bayat A, Zachariassen LG, Sun JH, Ge YH, Zhao D, Bonde K, Madsen LH, Awad IAA, Bagiran D, Sbeih A, Shah SM, El-Sayed S, Lyngby SM, Pedersen MG, Stenum-Berg C, Walker LC, Krey I, Delahaye-Duriez A, Emrick LT, Sully K, Murali CN, Burrage LC, Plaud Gonzalez JA, Parnes M, Friedman J, Isidor B, Lefranc J, Redon S, Heron D, Mignot C, Keren B, Fradin M, Dubourg C, Mercier S, Besnard T, Cogne B, Deb W, Rivier C, Milani D, Bedeschi MF, Di Napoli C, Grilli F, Marchisio P, Koudijs S, Veenma D, Argilli E, Lynch SA, Au PYB, Ayala Valenzuela FE, Brown C, Masser-Frye D, Jones M, Patron Romero L, Li WL, Thorpe E, Hecher L, Johannsen J, Denecke J, McNiven V, Szuto A, Wakeling E, Cruz V, Sency V, Wang H, Piard J, Kort?m F, Herget T, Bierhals T, Condell A, Zeev BB, Kaur S, Christodoulou J, Piton A, Zweier C, Kraus C, Micalizzi A, Trivisano M, Specchio N, Lesca G, M?ller RS, T?mer Z, Musgaard M, Gerard B, Lemke JR, Shi YS, Kristensen AS. Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes. Brain. 2023 Dec 01. PMID: 38038360.
      Citations:    Fields:    
    2. Parnes M. Reply to: "Susceptibility-Weighted Imaging Reveals Subcortical Iron Deposition in PLAN: The "Double Cortex Sign"". Mov Disord. 2023 10; 38(10):1973. PMID: 37885407.
      Citations:    Fields:    Translation:Humans
    3. Hentrich L, Parnes M, Lotze TE, Coorg R, de Koning TJ, Nguyen KM, Yip CK, Jungbluth H, Koy A, Dafsari HS. Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. Genes (Basel). 2023 09 25; 14(10). PMID: 37895210; PMCID: PMC10606070.
      Citations: 2     Fields:    Translation:Humans
    4. Hull M, Parnes M, Jankovic J. Botulinum Neurotoxin Injections in Children with Self-Injurious Behaviors. Toxins (Basel). 2023 03 23; 15(4). PMID: 37104174; PMCID: PMC10141007.
      Citations:    Fields:    Translation:Humans
    5. Saida K, Maroofian R, Sengoku T, Mitani T, Pagnamenta AT, Marafi D, Zaki MS, O'Brien TJ, Karimiani EG, Kaiyrzhanov R, Takizawa M, Ohori S, Leong HY, Akay G, Galehdari H, Zamani M, Romy R, Carroll CJ, Toosi MB, Ashrafzadeh F, Imannezhad S, Malek H, Ahangari N, Tomoum H, Gowda VK, Srinivasan VM, Murphy D, Dominik N, Elbendary HM, Rafat K, Yilmaz S, Kanmaz S, Serin M, Krishnakumar D, Gardham A, Maw A, Rao TS, Alsubhi S, Srour M, Buhas D, Jewett T, Goldberg RE, Shamseldin H, Frengen E, Misceo D, Str?mme P, Magliocco Ceroni JR, Kim CA, Yesil G, Sengenc E, Guler S, Hull M, Parnes M, Aktas D, Anlar B, Bayram Y, Pehlivan D, Posey JE, Alavi S, Madani Manshadi SA, Alzaidan H, Al-Owain M, Alabdi L, Abdulwahab F, Sekiguchi F, Hamanaka K, Fujita A, Uchiyama Y, Mizuguchi T, Miyatake S, Miyake N, Elshafie RM, Salayev K, Guliyeva U, Alkuraya FS, Gleeson JG, Monaghan KG, Langley KG, Yang H, Motavaf M, Safari S, Alipour M, Ogata K, Brown AEX, Lupski JR, Houlden H, Matsumoto N. Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42?affected individuals. Genet Med. 2023 01; 25(1):90-102. PMID: 36318270.
      Citations: 4     Fields:    Translation:HumansAnimals
    6. Kurian MA, Millan F, Telegrafi A, Marks W, Castro-Jimenez M, Joriot S, Blumkin L, Hull M, Parnes M, Nemeth AH, Smith M, Barnicoat A, Acosta F, Nowak C, Wilson WG, Steel D, Lin JP, Wirth T, Garone G, Piton A, Drouot N, Rudolf G, Chelly J, Burglen L, Demailly D, Coubes P, Ghoumid J, Belin J, Faucheux JM, Ravelli C, Poulen G, Calmels N, Ewenczyk C, M?neret A, Roze E, Keren B, Mignot C, Beroud C, Capuano A, Vidailhet M, Tranchant C, Cif L, Doummar D, Anheim M. Highlighting the Dystonic Phenotype Related to GNAO1. Mov Disord. 2022 07; 37(7):1547-1554. PMID: 35722775; PMCID: PMC9545634.
      Citations:    Fields:    Translation:Humans
    7. Manor J, Calame DG, Gijavanekar C, Tran A, Fatih JM, Lalani SR, Mizerik E, Parnes M, Mehta VP, Adesina AM, Lupski JR, Scaglia F, Elsea SH. Niacin therapy improves outcome and normalizes metabolic abnormalities in an NAXD-deficient patient. Brain. 2022 06 03; 145(5):e36-e40. PMID: 35231119.
      Citations:    Fields:    Translation:Humans
    8. Hull M, Emrick L, Sadat R, Parnes M. A case of treatable encephalopathy, developmental regression, and proximal tremor. Parkinsonism Relat Disord. 2021 12; 93:111-113. PMID: 34920839.
      Citations:    Fields:    Translation:Humans
    9. Hull M, Parnes M, Jankovic J. Increased Incidence of Functional (Psychogenic) Movement Disorders in Children and Adults Amid the COVID-19 Pandemic: A Cross-sectional Study. Neurol Clin Pract. 2021 Oct; 11(5):e686-e690. PMID: 34840884; PMCID: PMC8610548.
      Citations: 14     
    10. Hull M, Parnes M. Tics and TikTok: Functional Tics Spread Through Social Media. Mov Disord Clin Pract. 2021 Nov; 8(8):1248-1252. PMID: 34765689; PMCID: PMC8564820.
      Citations: 8     
    11. Hull M, PARNES M. Tics and TikTok: functional tics spread through social media. Movement Disorders Clinical Practice. 2021. View Publication.
    12. Hull M, PARNES M, Jankovic J. Increased Incidence of Functional (Psychogenic) Movement Disorders in Children and Adults Amidst the COVID-19 Pandemic: A Cross-Sectional Study. Neurology Clinical Practice. 2021. View Publication.
    13. Blackburn J, Parnes M. Tics, tremors and other movement disorders in childhood. Curr Probl Pediatr Adolesc Health Care. 2021 03; 51(3):100983. PMID: 33832853.
      Citations:    Fields:    Translation:Humans
    14. Hull M, Parnes M, Jankovic J. Botulinum Neurotoxin Injections in Childhood Opisthotonus. Toxins (Basel). 2021 02 12; 13(2). PMID: 33673369; PMCID: PMC7918608.
      Citations:    Fields:    Translation:Humans
    15. Calame DG, Houck K, Lotze T, Emrick L, Parnes M. A novel ATP1A2 variant associated with severe stepwise regression, hemiplegia, epilepsy and movement disorders in two unrelated patients. Eur J Paediatr Neurol. 2021 Mar; 31:21-26. PMID: 33578253.
      Citations:    Fields:    Translation:Humans
    16. Hull M, PARNES M. Cervical myelopathy as a complication of untreated motor tics: a cautionary tale. Journal of Pediatric Neurology. 2020. View Publication.
    17. Parnes M, Srinivasan C, Wangler MF, Martinez-Moreno R, Selga E, Riur? H, Carreras D, P?rez GJ, Scornik FS, Brugada R. An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders. Front Cell Dev Biol. 2020; 8:528742. PMID: 33134290; PMCID: PMC7550680.
      Citations: 1     
    18. Hull M, Parnes M. Effective Treatment of Geniospasm: Case Series and Review of the Literature. Tremor Other Hyperkinet Mov (N Y). 2020 08 17; 10:31. PMID: 32874771; PMCID: PMC7442170.
      Citations: 1     Fields:    Translation:Humans
    19. Raskin JS, PARNES M, Lam S. Progressive chorea and dystonia associated with a large arteriovenous malformation. Journal of the International Child Neurology Society. 2019; 148(19).
    20. Herring R, Desai N, Parnes M, Jarjour I. Pediatric West Nile Virus-Associated Neuroinvasive Disease: A Review of the Literature. Pediatr Neurol. 2019 03; 92:16-25. PMID: 30611518.
      Citations:    Fields:    Translation:HumansCells
    21. Parnes M, Bashir H, Jankovic J. Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by NKX2-1 Mutations. Mov Disord Clin Pract. 2019 Jan; 6(1):34-39. PMID: 30746413; PMCID: PMC6335533.
      Citations: 4     
    22. Pillai NR, Marafi D, Monteiro SA, Parnes M, Chandy BM, Patel A, Bacino CA, Breman AM, Burrage LC. Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly. Eur J Med Genet. 2019 Jun; 62(6):103531. PMID: 30142436.
      Citations:    Fields:    Translation:HumansCells
    23. Hemb M, Velasco TR, Parnes MS, Wu JY, Lerner JT, Matsumoto JH, Yudovin S, Shields WD, Sankar R, Salamon N, Vinters HV, Mathern GW. Improved outcomes in pediatric epilepsy surgery: the UCLA experience, 1986-2008. Neurology. 2010 Jun 01; 74(22):1768-75. PMID: 20427752; PMCID: PMC2882215.
      Citations: 37     Fields:    Translation:Humans
    24. Hull M, Emrick L, Sadat R, PARNES M. A case of treatable encephalopathy, developmental regression, and proximal tremor. Parkinsonism & Related Disorders. In Press.
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