Dr. Molnár Mária Judit

Citata da

	Tutte	Dal 2019
Citazioni	3608	1978
Indice H	32	24
i10-index	91	54

500

250

125

375

200020012002200320042005200620072008200920102011201220132014201520162017201820192020202120222023202418 21 28 36 27 38 46 38 40 68 130 112 142 128 127 107 118 150 168 182 233 293 361 398 500

Accesso pubblico

Visualizza tutto

45 articoli

4 articoli

Disponibili

Non disponibili

In base ai mandati di finanziamento

Coautori

Balicza PéterSemmelweis University, Institute of Genomic Medicine and Rare DisordersEmail verificata su med.semmelweis-univ.hu
Gál AnikóSemmelweis UniversityEmail verificata su semmelweis-univ.hu
András GézsiAssociate professor, Budapest University of Technology and EconomicsEmail verificata su mit.bme.hu
Klivenyi PeterUniversity of SzegedEmail verificata su med.u-szeged.hu
Noemi Agnes VargaClinical geneticist fellow, PhD student in neuroscienceEmail verificata su med.semmelweis-univ.hu
J. Michael SchröderUniversity Hospital, RWTH Aachen, GermanyEmail verificata su netcologne.de
András Falus, Professor, PhD, DSc, m...Professor of Immunology and Genomics, Semmelweis UniversityEmail verificata su dgci.sote.hu
Stephan ZuchnerProfessor, Department of Human Genetics, University of Miami Miller School of MedicineEmail verificata su med.miami.edu
György NémethGedeon RichterEmail verificata su richter.hu
Edit BuzasSemmelweis University, HCEMM SU, HUN-REN-SUEmail verificata su semmelweis.hu
Herbert BudkaProfessor of Neuropathol., ret., Med. Univ. Vienna, AustriaEmail verificata su meduniwien.ac.at
Basil Petrofmcgill universityEmail verificata su mcgill.ca
Laszlo NagyProfessor and Co-Director, Johns Hopkins University School of Medicine and University of DebrecenEmail verificata su jhmi.edu
Dóra CsabánSemmelweis UniveristyEmail verificata su med.semmelweis-univ.hu
Christos ChinopoulosAssociate Professor, Department of Medical Biochemistry Semmelweis UniversityEmail verificata su semmelweis.hu
Judit BoczanAssistant Professor, Department of Neurology, University of DebrecenEmail verificata su med.unideb.hu
János M. RethelyiSemmelweis UniversityEmail verificata su med.semmelweis-univ.hu
Peter AntalAssociate professor, Budapest University of Technology and EconomicsEmail verificata su mit.bme.hu
Júlia KollerSemmelweis EgyetemEmail verificata su med.semmelweis-univ.hu
Léna SzabóAssistant professor of Pediatric Neurology, Semmelweis UniversityEmail verificata su gyerekklinika.com

Segui

Dr. Molnár Mária Judit

Semmelweis University

Email verificata su med.semmelweis-univ.hu

neurology psychiatry personalized medicine genetics


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea GG Kovacs, JR Murrell, S Horvath, L Haraszti, K Majtenyi, MJ Molnar, ... Movement Disorders 24 (12), 1842-1847, 2009	244	2009
Factors influencing the efficacy, longevity, and safety of electroporation-assisted plasmid-based gene transfer into mouse muscles MJ Molnar, R Gilbert, Y Lu, AB Liu, A Guo, N Larochelle, K Orlopp, ... Molecular Therapy 10 (3), 447-455, 2004	185	2004
A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions H Tyynismaa, E Ylikallio, M Patel, MJ Molnar, RG Haller, A Suomalainen The American Journal of Human Genetics 85 (2), 290-295, 2009	147	2009
Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trial J Diaz-Manera, PS Kishnani, H Kushlaf, S Ladha, T Mozaffar, V Straub, ... The Lancet Neurology 20 (12), 1012-1026, 2021	119	2021
Cerebral blood flow and glucose metabolism in mitochondrial disorders MJ Molnár, A Valikovics, S Molnár, L Trón, P Diószeghy, F Mechler, ... Neurology 55 (4), 544-548, 2000	95	2000
Safety and efficacy of cipaglucosidase alfa plus miglustat versus alglucosidase alfa plus placebo in late-onset Pompe disease (PROPEL): an international, randomised, double … B Schoser, M Roberts, BJ Byrne, S Sitaraman, H Jiang, P Laforêt, ... The Lancet Neurology 20 (12), 1027-1037, 2021	91	2021
Mitochondrial diseases MJ Molnar, GG Kovacs Handbook of clinical neurology 145, 147-155, 2018	88	2018
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ... European Journal of Human Genetics 29 (9), 1325-1331, 2021	83	2021
Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries T Zelei, MJ Molnár, M Szegedi, Z Kaló Orphanet journal of rare diseases 11, 1-11, 2016	78	2016
Psychiatric symptoms of patients with primary mitochondrial DNA disorders G Inczedy-Farkas, V Remenyi, A Gal, Z Varga, P Balla, ... Behavioral and Brain Functions 8, 1-9, 2012	73	2012
MAPT S305I mutation: implications for argyrophilic grain disease GG Kovacs, A Pittman, T Revesz, C Luk, A Lees, E Kiss, P Tariska, ... Acta neuropathologica 116, 103-118, 2008	71	2008
MSTO 1 is a cytoplasmic pro‐mitochondrial fusion protein A Gal, P Balicza, D Weaver, S Naghdi, SK Joseph, P Várnai, T Gyuris, ... EMBO molecular medicine 9 (7), 967-984, 2017	62	2017
Efficacy of nusinersen in type 1, 2 and 3 spinal muscular atrophy: real world data from Hungarian patients L Szabó, A Gergely, R Jakus, A Fogarasi, Z Grosz, MJ Molnár, I Andor, ... European Journal of Paediatric Neurology 27, 37-42, 2020	58	2020
Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion NÁ Varga, K Pentelényi, P Balicza, A Gézsi, V Reményi, V Hársfalvi, ... Behavioral and Brain Functions 14, 1-14, 2018	58	2018
Rare variants in β-Amyloid precursor protein (APP) and Parkinson’s disease EC Schulte, A Fukumori, B Mollenhauer, H Hor, T Arzberger, R Perneczky, ... European Journal of Human Genetics 23 (10), 1328-1333, 2015	54	2015
Peripheral nerve and skeletal muscle involvement in CADASIL JM Schröder, S Züchner, M Dichgans, Z Nagy, MJ Molnar Acta neuropathologica 110, 587-599, 2005	54	2005
How bioinformatics influences health informatics: usage of biomolecular sequences, expression profiles and automated microscopic image analyses for clinical needs and public health V Kuznetsov, HK Lee, S Maurer-Stroh, MJ Molnár, S Pongor, ... Health Information Science and Systems 1, 1-18, 2013	50	2013
Structural and molecular basis of skeletal muscle diseases G Karpati, M Molnar ISN Neuropath Press, 2002	49	2002
Two transgenic mouse models for β-subunit components of succinate-CoA ligase yielding pleiotropic metabolic alterations G Kacso, D Ravasz, J Doczi, B Németh, O Madgar, A Saada, P Ilin, ... Biochemical Journal 473 (20), 3463-3485, 2016	44	2016
The European reference network for rare neurological diseases C Reinhard, AC Bachoud-Lévi, T Bäumer, E Bertini, A Brunelle, AI Buizer, ... Frontiers in neurology 11, 616569, 2021	43	2021

Il sistema al momento non può eseguire l'operazione. Riprova più tardi.

Articoli 1–20

Citazioni per anno

Citazioni duplicate

Citazioni unite

Aggiungi coautoriCoautori

Segui

Citata da

Coautori