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Maria J. Molnar - Publications

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

Year Citation  Score
2020 Jimoh IJ, Sebe B, Balicza P, Fedor M, Pataky I, Rudas G, Gal A, Inczedy-Farkas G, Nemeth G, Molnar MJ. Wernicke-Korsakoff syndrome associated with mtDNA disease. Therapeutic Advances in Neurological Disorders. 13: 1756286420938972. PMID 32821290 DOI: 10.1177/1756286420938972  0.309
2020 Molnár MJ, Borsos B, Várdi KV, Grosz Z, Sebők Á, Dézsi L, Almássy Z, Kerényi L, Jobbágy Z, Jávor L, Bidló J. [The long-term follow-up of enzyme replacement treatment in late onset Pompe disease]. Ideggyogyaszati Szemle. 73: 151-159. PMID 32579304 DOI: 10.18071/Isz.73.0151  0.373
2020 Illés A, Balicza P, Gál A, Pentelényi K, Csabán D, Gézsi A, Molnár V, Molnár MJ. Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene Orvosi Hetilap. 161: 821-828. PMID 32364361 DOI: 10.1556/650.2020.31724  0.384
2019 Illés A, Csabán D, Grosz Z, Balicza P, Gézsi A, Molnár V, Bencsik R, Gál A, Klivényi P, Molnar MJ. The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials. Frontiers in Genetics. 10: 1061. PMID 31737044 DOI: 10.3389/Fgene.2019.01061  0.361
2018 Balicza P, Grosz Z, Molnár V, Illés A, Csabán D, Gézsi A, Dézsi L, Zádori D, Vécsei L, Molnár MJ. NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement Frontiers in Genetics. 9: 335. PMID 30186310 DOI: 10.3389/Fgene.2018.00335  0.348
2018 Kecskeméti N, Szönyi M, Gáborján A, Küstel M, Milley GM, Süveges A, Illés A, Kékesi A, Tamás L, Molnár MJ, Szirmai Á, Gál A. Analysis of GJB2 mutations and the clinical manifestation in a large Hungarian cohort. European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (Eufos) : Affiliated With the German Society For Oto-Rhino-Laryngology - Head and Neck Surgery. PMID 30094485 DOI: 10.1007/S00405-018-5083-4  0.357
2018 Beke A, Piko H, Haltrich I, Karcagi V, Rigo J, Molnar MJ, Fekete G. Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations. Bmc Medical Genetics. 19: 113. PMID 29986653 DOI: 10.1186/S12881-018-0634-5  0.318
2018 Márki S, Göblös A, Szlávicz E, Török N, Balicza P, Bereznai B, Takáts A, Engelhardt J, Klivényi P, Vécsei L, Molnár MJ, Nagy N, Széll M. The rs13388259 Intergenic Polymorphism in the Genomic Context of the Gene Is Associated with Parkinson's Disease in the Hungarian Population. Parkinson's Disease. 2018: 9351598. PMID 29850016 DOI: 10.1155/2018/9351598  0.392
2018 Varga NÁ, Pentelényi K, Balicza P, Gézsi A, Reményi V, Hársfalvi V, Bencsik R, Illés A, Prekop C, Molnár MJ. Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion Behavioral and Brain Functions. 14: 1-14. PMID 29458409 DOI: 10.1186/S12993-018-0135-X  0.372
2018 Milley GM, Varga ET, Grosz Z, Nemes C, Arányi Z, Boczán J, Diószeghy P, Molnár MJ, Gál A. Genotypic and phenotypic spectrum of the most common causative genes of Charcot-Marie-Tooth disease in Hungarian patients. Neuromuscular Disorders : Nmd. 28: 38-43. PMID 29174527 DOI: 10.1016/J.Nmd.2017.08.007  0.39
2017 Molnar MJ, Kovacs GG. Mitochondrial diseases. Handbook of Clinical Neurology. 145: 147-155. PMID 28987165 DOI: 10.1016/B978-0-12-802395-2.00010-9  0.335
2017 Zádori D, Füvesi J, Timár E, Horváth E, Bencsik R, Szépfalusi N, Must A, Vécsei L, Molnár MJ, Klivényi P. The Report of p.Val717Phe Mutation in the APP Gene in a Hungarian Family With Alzheimer Disease: A Phenomenological Study. Alzheimer Disease and Associated Disorders. PMID 28796010 DOI: 10.1097/Wad.0000000000000206  0.338
2017 Gal A, Balicza P, Weaver D, Naghdi S, Joseph SK, Várnai P, Gyuris T, Horváth A, Nagy L, Seifert EL, Molnar MJ, Hajnóczky G. MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans. Embo Molecular Medicine. PMID 28554942 DOI: 10.15252/Emmm.201607058  0.312
2016 Bock I, Németh K, Pentelényi K, Balicza P, Balázs A, Molnár MJ, Román V, Nagy J, Lévay G, Kobolák J, Dinnyés A. Targeted next generation sequencing of a panel of autism-related genes identifies an EHMT1 mutation in a Kleefstra syndrome patient with autism and normal intellectual performance. Gene. PMID 27651234 DOI: 10.1016/J.Gene.2016.09.027  0.355
2016 Milley GM, Varga ET, Grosz Z, Bereznai B, Aranyi Z, Boczan J, Dioszeghy P, Kálmán B, Gal A, Molnar MJ. Three novel mutations and genetic epidemiology analysis of the Gap Junction Beta 1 (GJB1) gene among Hungarian Charcot-Marie-Tooth disease patients. Neuromuscular Disorders : Nmd. PMID 27544631 DOI: 10.1016/J.Nmd.2016.07.012  0.317
2016 Ács P, Molnár MJ, Klivényi P, Kálmán B. [GENETICALLY DETERMINED DISEASES ASSOCIATED WITH PATHOLOGICAL BRAIN IRON ACCUMULATION AND NEURODEGENERATION]. IdeggyóGyáSzati Szemle. 69: 157-66. PMID 27468605 DOI: 10.18071/Isz.69.0157  0.304
2015 Gal A, Inczedy-Farkas G, Pal E, Remenyi V, Bereznai B, Geller L, Szelid Z, Merkely B, Molnar MJ. The coexistence of dynamin 2 mutation and multiple mitochondrial DNA (mtDNA) deletions in the background of severe cardiomyopathy and centronuclear myopathy. Clinical Neuropathology. 34: 89-95. PMID 25492887 DOI: 10.5414/Np300789  0.362
2014 Reményi V, Inczédy-Farkas G, Gál A, Bereznai B, Pál Z, Karcagi V, Mechler F, Molnár MJ. The modifying effect a PMP22 deletion in a family with Charcot-Marie-Tooth type 1 neuropathy due to an EGR2 mutation. Ideggyã³Gyã¡Szati Szemle. 67: 420-5. PMID 25720245  0.716
2014 Pentelenyi K, Remenyi V, Gal A, Milley GM, Csosz A, Mende BG, Molnar MJ. Asian-specific mitochondrial genome polymorphism (9-bp deletion) in Hungarian patients with mitochondrial disease. Mitochondrial Dna. 1-4. PMID 25242187 DOI: 10.3109/19401736.2014.961128  0.361
2014 Pal Z, Tóthfalusi L, Lörincz Z, György B, Molnar MJ, Falus A, Buzás EI. Immunosuppressants increase the levels of natural autoantibodies reactive with glycosaminoglycans in myasthenia gravis. Journal of Neuroimmunology. 276: 224-8. PMID 25139014 DOI: 10.1016/J.Jneuroim.2014.08.002  0.706
2014 Varga VE, Katkó M, Harangi J, Balogh I, Kapás I, Madar L, Seres I, Molnár MJ, Paragh G, Kovács GG, Harangi M. [Laboratory diagnosis of a rare congenital neurodegenerative disease: cerebrotendinous xanthomatosis]. Orvosi Hetilap. 155: 811-6. PMID 24836315 DOI: 10.1556/Oh.2014.29887  0.308
2014 Kapás I, Katkó M, Harangi M, Paragh G, Balogh I, Kóczi Z, Regelsberger G, Molnár MJ, Kovacs GG. Cerebrotendinous xanthomatosis with the c.379C>T (p.R127W) mutation in the CYP27A1 gene associated with premature age-associated limbic tauopathy. Neuropathology and Applied Neurobiology. 40: 345-50. PMID 23659550 DOI: 10.1111/Nan.12058  0.317
2014 Remenyi V, Kekesi A, Pentelenyi K, Gal A, Hársfalvi V, Molnar MJ. Predictiting valproate toxicity in patients with mitochondrial disorders The Epma Journal. 5: 1-1. DOI: 10.1186/1878-5085-5-S1-A140  0.371
2013 Schulte EC, Stahl I, Czamara D, Ellwanger DC, Eck S, Graf E, Mollenhauer B, Zimprich A, Lichtner P, Haubenberger D, Pirker W, Brücke T, Bereznai B, Molnar MJ, Peters A, et al. Rare variants in PLXNA4 and Parkinson's disease. Plos One. 8: e79145. PMID 24244438 DOI: 10.1371/Journal.Pone.0079145  0.3
2013 Pál Z, Antal P, Srivastava S, Gál J, André S, Gordeeva E, Nagy G, Kaltner H, Bovin N, Molnár M, Falus A, Gabius H, Buzás E. A7.4 Association of Galectin Single Nucleotide Polymorphisms with Autoimmune Diseases Annals of the Rheumatic Diseases. 72: A49.1-A49. DOI: 10.1136/Annrheumdis-2013-203221.4  0.753
2012 Pál Z, Antal P, Srivastava SK, Hullám G, Semsei AF, Gál J, Svébis M, Soós G, Szalai C, André S, Gordeeva E, Nagy G, Kaltner H, Bovin NV, Molnár MJ, et al. Non-synonymous single nucleotide polymorphisms in genes for immunoregulatory galectins: association of galectin-8 (F19Y) occurrence with autoimmune diseases in a Caucasian population. Biochimica Et Biophysica Acta. 1820: 1512-8. PMID 22683700 DOI: 10.1016/J.Bbagen.2012.05.015  0.744
2012 Inczedy-Farkas G, Remenyi V, Gal A, Varga Z, Balla P, Udvardy-Meszaros A, Bereznai B, Molnar MJ. Psychiatric symptoms of patients with primary mitochondrial DNA disorders. Behavioral and Brain Functions : Bbf. 8: 9. PMID 22329956 DOI: 10.1186/1744-9081-8-9  0.314
2012 Pál Z, Varga Z, Semsei Á, Reményi V, Rózsa C, Falus A, Illes Z, Buzás EI, Molnar MJ. Interleukin-4 receptor alpha polymorphisms in autoimmune myasthenia gravis in a Caucasian population. Human Immunology. 73: 193-5. PMID 22119518 DOI: 10.1016/J.Humimm.2011.11.001  0.744
2012 Molnar MJ, Nemeth G. Gene therapy in neurology: review of ongoing clinical trials Clinical Investigation. 2: 639-652. DOI: 10.4155/Cli.12.47  0.336
2012 Kovacs T, Remenyi V, Molnar MJ, Tegze N, Miltenberger-Miltenyi G. Rare finding in early-onset dementia: Description of a patient with a novel PSEN2 mutation harbouring pathogenic huntingtin allele Alzheimers & Dementia. 8: 681. DOI: 10.1016/J.Jalz.2012.05.1842  0.362
2011 Pál Z, Boczán J, Bereznai B, Lovas G, Molnár MJ. [Therapy for anti-MuSK antibody positive myasthenia gravis]. Orvosi Hetilap. 152: 1586-9. PMID 21920845 DOI: 10.1556/Oh.2011.29177  0.687
2010 Pál Z, Antal P, Millinghoffer A, Hullám G, Pálóczi K, Tóth S, Gabius HJ, Molnár MJ, Falus A, Buzás EI. A novel galectin-1 and interleukin 2 receptor β haplotype is associated with autoimmune myasthenia gravis. Journal of Neuroimmunology. 229: 107-11. PMID 20728947 DOI: 10.1016/J.Jneuroim.2010.07.015  0.729
2010 Bereznai B, Lovas G, Pentelenyi K, Rudas G, Molnar MJ. Coexisting huntingtin and SCA8 repeat expansion: case report of a severe complex neurodegenerative syndrome. Journal of the Neurological Sciences. 293: 116-8. PMID 20403608 DOI: 10.1016/J.Jns.2010.03.006  0.311
2010 Gal A, Pentelenyi K, Remenyi V, Pal Z, Csanyi B, Tomory G, Rasko I, Molnar MJ. Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNA(Lys) associated with dystonia and stroke-like episodes. Acta Neurologica Scandinavica. 122: 252-6. PMID 19930207 DOI: 10.1111/J.1600-0404.2009.01297.X  0.724
2010 Kovacs GG, Sanchez-Juan P, Ströbel T, Schuur M, Poleggi A, Nocentini S, Giannattasio C, Belay G, Bishop M, Capellari S, Parchi P, Gelpi E, Gal A, Bakos A, Molnar MJ, et al. Cathepsin D (C224T) polymorphism in sporadic and genetic Creutzfeldt-Jakob disease. Alzheimer Disease and Associated Disorders. 24: 104-7. PMID 19571726 DOI: 10.1097/Wad.0B013E3181Ad378C  0.385
2010 Gal A, Komlosi K, Maasz A, Pentelenyi K, Remenyi V, Ovary C, Valikovics A, Dioszeghy P, Bereczki D, Melegh B, Molnár MJ. Analysis of mtDNA A3243G mutation frequency in Hungary Central European Journal of Medicine. 5: 322-328. DOI: 10.2478/S11536-009-0118-2  0.341
2009 Pal Z, Gal A, Remenyi V, Tordai A, Molnar MJ. Oestrogen receptor alpha gene intronic polymorphisms and autoimmune myasthenia gravis in Caucasian women. Neuromuscular Disorders : Nmd. 19: 822-4. PMID 19793653 DOI: 10.1016/J.Nmd.2009.09.002  0.737
2009 Tyynismaa H, Ylikallio E, Patel M, Molnar MJ, Haller RG, Suomalainen A. A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions. American Journal of Human Genetics. 85: 290-5. PMID 19664747 DOI: 10.1016/J.Ajhg.2009.07.009  0.361
2009 Kovacs GG, Murrell JR, Horvath S, Haraszti L, Majtenyi K, Molnar MJ, Budka H, Ghetti B, Spina S. TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1843-7. PMID 19609911 DOI: 10.1002/Mds.22697  0.303
2009 Pál Z, Kiss E, Gál A, Csépány T, Lengyel A, Molnar MJ. Genetically determined neuropathy (CMT 1A) accompanied by immune dysfunction: a case report. Inflammation Research : Official Journal of the European Histamine Research Society ... [Et Al.]. 58: 359-61. PMID 19274435 DOI: 10.1007/S00011-009-0025-7  0.717
2008 Kovacs GG, Pittman A, Revesz T, Luk C, Lees A, Kiss E, Tariska P, Laszlo L, Molnár K, Molnar MJ, Tolnay M, de Silva R. MAPT S305I mutation: implications for argyrophilic grain disease. Acta Neuropathologica. 116: 103-18. PMID 18066559 DOI: 10.1007/S00401-007-0322-6  0.331
2005 Schröder JM, Züchner S, Dichgans M, Nagy Z, Molnar MJ. Peripheral nerve and skeletal muscle involvement in CADASIL. Acta Neuropathologica. 110: 587-99. PMID 16328531 DOI: 10.1007/S00401-005-1082-9  0.328
2005 Szabo A, Züchner S, Siska E, Mechler F, Molnar MJ. Marked phenotypic variation in a family with a new myelin protein zero mutation. Neuromuscular Disorders : Nmd. 15: 760-3. PMID 16198109 DOI: 10.1016/J.Nmd.2005.07.006  0.376
2004 Kovács GG, Kalev O, Gelpi E, Haberler C, Wanschitz J, Strohschneider M, Molnár MJ, László L, Budka H. The prion protein in human neuromuscular diseases. The Journal of Pathology. 204: 241-7. PMID 15476279 DOI: 10.1002/Path.1633  0.317
2000 Molnár MJ, Valikovics A, Molnár S, Trón L, Diószeghy P, Mechler F, Gulyás B. Cerebral blood flow and glucose metabolism in mitochondrial disorders. Neurology. 55: 544-8. PMID 10953189 DOI: 10.1212/Wnl.55.4.544  0.306
2000 Zanssen S, Molnar M, Buse G, Schröder MJ. Novel Cluster of tRNA Leu (UUR) Mutations in a Sporadic Case of Infantile Myopathy Restricted to Muscle Tissue Neuropediatrics. 31: 93-96. PMID 10832584 DOI: 10.1055/S-2000-7480  0.313
1998 Molnar M, Schröder JM. Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions Acta Neuropathologica. 96: 41-51. PMID 9678512 DOI: 10.1007/S004010050858  0.316
1997 Schröder JM, Molnar M. Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy, especially inclusion body myositis. Molecular and Cellular Biochemistry. 174: 277-281. DOI: 10.1007/978-1-4615-6111-8_43  0.314
1997 Zanssen S, Molnar M, Schröder JM, Buse G. Multiple mitochondrial tRNA(Leu[UUR]) mutations associated with infantile myopathy. Molecular and Cellular Biochemistry. 174: 231-236. DOI: 10.1007/978-1-4615-6111-8_36  0.341
1996 Molnar M, Zanssen S, Buse G, Schröder JM. A large-scale deletion of mitochondrial DNA in a case with pure mitochondrial myopathy and neuropathy. Acta Neuropathologica. 91: 654-658. PMID 8781666 DOI: 10.1007/S004010050480  0.315
1995 Molnar M, Neudecker S, Schröder JM. Increase of mitochondria in vasa nervorum of cases with mitochondrial myopathy, Kearns-Sayre syndrome, progressive externaI ophthalmoplegia and MEWS* Neuropathology and Applied Neurobiology. 21: 432-439. PMID 8632838 DOI: 10.1111/J.1365-2990.1995.Tb01080.X  0.323
1991 Molnár M, Diószeghy P, Mechler F. Inflammatory changes in facioscapulohumeral muscular dystrophy. European Archives of Psychiatry and Clinical Neuroscience. 241: 105-8. PMID 1834179 DOI: 10.1007/Bf02191151  0.304
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