Molnár, Mária Judit Semmelweis University affiliated publications (2019-2024)
Number of publications: 73
1.
Wallace, EL;Goker-Alpan, O;Wilcox, WR;Holida, M;Bernat, J;Longo, N;Linhart, A;Hughes, DA;Hopkin, RJ;Tondel, C;Langeveld, M;Giraldo, P;Pisani, A;Germain, DP;Mehta, A;Deegan, PB;Molnar, MJ;Ortiz, D;Jovanovic, A;Muriello, M;Barshop, BA;Kimonis, V;Vujkovac, B;Nowak, A;Geberhiwot, T;Kantola, I;Knoll, J;Waldek, S;Nedd, K;Karaa, A;Brill-Almon, E;Alon, S;Chertkoff, R;Rocco, R;Sakov, A;Warnock, DG
Q1
JOURNAL OF MEDICAL GENETICS
2024.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
2.
Koehler, W;Engelen, M;Eichler, F;Lachmann, R;Fatemi, A;Sampson, J;Salsano, E;Gamez, J;Molnar, MJ;Pascual, S;Rovira, M;Vila, A;Pina, G;Martin-Ugarte, I;Mantilla, A;Pizcueta, P;Rodriguez-Pascau, L;Traver, E;Vilalta, A;Pascual, M;Martinell, M;Meya, U;Mochel, F
D1
LANCET NEUROLOGY
2023.
Semmelweis University authors: Molnár, Mária Judit, Grosz, Zoltán,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
3.
Karaa, A;Bertini, E;Carelli, V;Cohen, BH;Enns, GM;Falk, MJ;Goldstein, A;Gorman, GS;Haas, R;Hirano, M;Klopstock, T;Koenig, MK;Kornblum, C;Lamperti, C;Lehman, A;Longo, N;Molnar, MJ;Parikh, S;Phan, H;Pitceathly, RDS;Saneto, R;Scaglia, F;Servidei, S;Tarnopolsky, M;Toscano, A;Van Hove, JLK;Vissing, J;Vockley, J;Finman, JS;Brown, DA;Shiffer, JA;Mancuso, M
D1
NEUROLOGY
2023.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
4.
Szabó, L;Gergely, A;Jakus, R;Fogarasi, A;Grosz, Z;Molnár, MJ;Andor, I;Schulcz, O;Goschler, A;Medveczky, E;Czövek, D;Herczegfalvi, A
Q1
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
2020.
Semmelweis University authors: Szabó, Léna, Fogarasi, András, Grosz, Zoltán, Molnár, Mária Judit, Andor, Ildikó, Goschler, Ádám, Czövek, Dorottya,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics, II. Department of Pediatrics, I. Department of Pediatrics,
5.
Zurek, Birte; Ellwanger, Kornelia; Vissers, Lisenka E. L. M.; Schuele, Rebecca; Synofzik, Matthis; Topf, Ana; de, Voer Richarda M.; Laurie, Steven; Matalonga, Leslie; Gilissen, Christian; Ossowski, Stephan; 't, Hoen Peter A. C.; Vitobello, Antonio; Schulze-Hentrich, Julia M.; Riess, Olaf; Brunner, Han G.; Brookes, Anthony J.; Rath, Ana; Bonne, Gisele; Gumus, Gulcin; Verloes, Alain; Hoogerbrugge, Nicoline; Evangelista, Teresinha; Harmuth, Tina; Swertz, Morris; Spalding, Dylan; Hoischen, Alexander...
Q1
EUROPEAN JOURNAL OF HUMAN GENETICS 1018-4813 1476-5438
2021.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
6.
Matalonga, Leslie; Hernandez-Ferrer, Carles; Piscia, Davide; Schuele, Rebecca; Synofzik, Matthis; Topf, Ana; Vissers, Lisenka E. L. M.; de, Voer Richarda; Tonda, Raul; Laurie, Steven; Fernandez-Callejo, Marcos; Pico, Daniel; Garcia-Linares, Carles; Papakonstantinou, Anastasios; Corvo, Alberto; Joshi, Ricky; Diez, Hector; Gut, Ivo; Hoischen, Alexander; Graessner, Holm; Beltran, Sergi; , ; Balicza, P; Molnár, MJ;
Q1
EUROPEAN JOURNAL OF HUMAN GENETICS 1018-4813 1476-5438
2021.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
7.
Molnar, MJ;Molnar, V;Fedor, M;Csehi, R;Acsai, K;Borsos, B;Grosz, Z
Q1
FRONTIERS IN PSYCHIATRY
2022.
Semmelweis University authors: Molnár, Mária Judit, Molnár, Viktor, Fedor, Mariann, Csehi, Réka, Borsos, Beáta, Grosz, Zoltán,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
8.
Reinhard, C;Bachoud-Lévi, AC;Bäumer, T;Bertini, E;Brunelle, A;Buizer, AI;Federico, A;Gasser, T;Groeschel, S;Hermanns, S;Klockgether, T;Krägeloh-Mann, I;Landwehrmeyer, GB;Leber, I;Macaya, A;Mariotti, C;Meissner, WG;Molnar, MJ;Nonnekes, J;Escobar, JDO;Dueñas, BP;Linton, LR;Schöls, L;Schuele, R;Tijssen, MAJ;Vandenberghe, R;Volkmer, A;Wolf, NI;Graessner, H
Q1
FRONTIERS IN NEUROLOGY
2021.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
9.
Boros, FA;Szpisjak, L;Bozó, R;Kelemen, E;Zádori, D;Salamon, A;Danis, J;Kalmar, T;Maróti, Z;Molnár, MJ;Klivényi, P;Széll, M;Adám, É
D1
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
2023.
DOI:10.3390/ijms24032617 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
10.
Stengl, R;Bors, A;Agg, B;Pólos, M;Matyas, G;Molnár, MJ;Fekete, B;Csabán, D;Andrikovics, H;Merkely, B;Radovits, T;Szabolcs, Z;Benke, K
Q1
ORPHANET JOURNAL OF RARE DISEASES
2020.
Semmelweis University authors: Stengl, Roland, Bors, András, Ágg, Bence, Pólos, Miklós, Molnár, Mária Judit, Fekete, Bálint András, Csabán, Dóra, Andrikovics, Hajnalka, Merkely, Béla Péter, Radovits, Tamás, Szabolcs, Zoltán, Benke, Kálmán,
11.
Csehi, R;Molnar, V;Fedor, M;Zsumbera, V;Palasti, A;Acsai, K;Grosz, Z;Nemeth, G;Molnar, MJ
Q1
ORPHANET JOURNAL OF RARE DISEASES
2023.
Semmelweis University authors: Csehi, Réka, Molnár, Viktor, Fedor, Mariann, Palásti, Ágnes, Grosz, Zoltán, Németh, György, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
12.
Nagy, ZF;Pál, M;Engelhardt, JI;Molnár, MJ;Klivényi, P;Széll, M
Q2
BMC MEDICAL GENOMICS
2024.
Semmelweis University authors: Nagy, Zsófia Flóra, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
13.
Selvatici, R;Rossi, R;Fortunato, F;Trabanelli, C;Sifi, Y;Margutti, A;Neri, M;Gualandi, F;Szabò, L;Fekete, B;Angelova, L;Litvinenko, I;Ivanov, I;Vildan, Y;Iuhas, OA;Vintan, M;Burloiu, C;Lacramioara, B;Visa, G;Epure, D;Rusu, C;Vasile, D;Sandu, M;Vlodavets, D;Mager, M;Kyriakides, T;Delin, S;Lehman, I;Fures, JS;Bojinova, V;Militaru, M;Guergueltcheva, V;Burnyte, B;Molnar, MJ;Butoianu, N;Bensemmane, SD;Makri-Mokrane, S;Herczegfalvi, A;Panzaru, M;Emandi, AC;Lusakowska, A;Potulska-Chromik, A;Kostera-Pr...
Q1
NEUROLOGY-GENETICS
2021.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics, II. Department of Pediatrics,
14.
Csaban, D;Illes, A;Renata, TB;Balicza, P;Pentelenyi, K;Molnar, V;Gezsi, A;Grosz, Z;Gal, A;Kovacs, T;Klivenyi, P;Molnar, MJ
Q1
NEUROLOGICAL SCIENCES
2022.
Semmelweis University authors: Csabán, Dóra, Illés, Anett, Balicza, Péter, Pentelényi, Klára, Molnár, Viktor, Gézsi, András, Grosz, Zoltán, Gál, Anikó, Kovács, Tibor, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Neurology,
15.
Molnar, MJ;Jimoh, IJ;Zeke, H;Palásti, A;Fedor, M
Q1
FRONTIERS IN PHARMACOLOGY
2020.
Semmelweis University authors: Molnár, Mária Judit, Jimoh, Idris János, Zeke, Helga, Palásti, Ágnes, Fedor, Mariann,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
16.
Judit, MM;Judit, CS;Léna, S;Zoltán, G
Q4
ORVOSI HETILAP
2022.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics, II. Department of Pediatrics,
17.
Polymyositis and rhabdomyolysis caused by hepatocellular carcinoma-Case report and literature review
Bárdos, D;Molnár, MJ;Dudás, I;Tuza, S;Szijártó, A;Hahn, O
Q3
ANNALS OF MEDICINE AND SURGERY
2021.
Semmelweis University authors: Bárdos, Dávid, Molnár, Mária Judit, Dudás, Ibolyka, Tuza, Sebestyén, Szijártó, Attila, Hahn, Oszkár,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Patológiai, Igazságügyi és Biztosítási Orvostani Intézet, Orvosi Képalkotó Klinika, Sebészeti, Transzplantációs és Gasztroenterológiai Klinika, 1st. Department of Surgery and Interventional Gastroenterology, II. Department of Pathology,
18.
Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability
Balicza, P;Bencsik, R;Lengyel, A;Gal, A;Grosz, Z;Csaban, D;Rudas, G;Danics, K;Kovacs, GG;Molnar, MJ
Q1
NEUROLOGY-GENETICS
2020.
Semmelweis University authors: Balicza, Péter, Gál, Anikó, Grosz, Zoltán, Csabán, Dóra, Rudas, Gábor, Danics, Krisztina, Molnár, Mária Judit,
19.
Hathy, E;Szabó, E;Varga, N;Erdei, Z;Tordai, C;Czehlár, B;Baradits, M;Jezsó, B;Koller, J;Nagy, L;Molnár, MJ;Homolya, L;Nemoda, Z;Apáti, A;Réthelyi, JM
D1
STEM CELL RESEARCH & THERAPY
2020.
Semmelweis University authors: Hathy, Edit Margit, Tordai, Csongor, Baradits, Máté, Koller, Júlia, Molnár, Mária Judit, Nemoda, Zsófia, Apáti, Ágota, Réthelyi, János,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Biokémiai és Molekuláris Biológiai Intézet, Molekuláris Biológiai Tanszék, Genomic Medicine and the Institute of Rare Diseases, Pszichiátriai és Pszichoterápiás Klinika, Department of Medical Chemistry, Molecular Biology and Pathobiochemistry,
20.
Mancuso, M;Houlden, H;Molnar, MJ;Filla, A;Breza, M;Graessner, H;Bassetti, CLA;Boesch, S
Q1
EUROPEAN JOURNAL OF NEUROLOGY
2022.
DOI:10.1111/ene.15320 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
21.
Kecskeméti, N;Gáborján, A;Szonyi, M;Küstel, M;Baranyi, I;Judit, MM;Tamás, L;Gál, A;Szirmai, A
Q3
ORVOSI HETILAP
2019.
Semmelweis University authors: Kecskeméti, Nóra, Gáborján, Anita, Szőnyi, Magdolna, Küstel, Marianna, Molnár, Mária Judit, Tamás, László, Gál, Anikó, Szirmai, Ágnes,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Otorhinolaryngology, Head and Neck Surgery,
22.
Viti, F;De Giorgio, R;Ceccherini, I;Ahluwalia, A;Alves, MM;Baldo, C;Baldussi, G;Bonora, E;Borrelli, O;Dall'Oglio, L;De Coppi, P;De Filippo, C;Barbara, PD;Diamanti, A;Di Lorenzo, C;Di Maulo, R;Galeone, A;Gandullia, P;Hashmi, SK;Lacaille, F;Lancon, L;Leone, S;Mahe, MM;Molnar, MJ;Palmitelli, A;Perin, S;Prato, AP;Thapar, N;Vassalli, M;Heuckeroth, RO
Q1
DIGESTIVE DISEASES AND SCIENCES
2023.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
23.
Balicza, P;Varga, NA;Bolgár, B;Pentelényi, K;Bencsik, R;Gál, A;Gézsi, A;Prekop, C;Molnár, V;Molnár, MJ
Q1
FRONTIERS IN GENETICS
2019.
Semmelweis University authors: Balicza, Péter, Varga, Noémi-Ágnes, Pentelényi, Klára, Gál, Anikó, Gézsi, András, Molnár, Viktor, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
24.
Nanetti, L;Kearney, M;Boesch, S;Stovickova, L;Ortigoza-Escobar, JD;Macaya, A;Gomez-Andres, D;Roze, E;Molnar, MJ;Wolf, NI;Darling, A;Vasco, G;Bertini, E;Indelicato, E;Neubauer, D;Haack, TB;Sagi, JC;Danti, FR;Sival, D;Zanni, G;Kolk, A;Boespflug-Tanguy, O;Schols, L;van de Warrenburg, B;Vidailhet, M;Willemsen, MA;Buizer, AI;Orzes, E;Ripp, S;Reinhard, C;Moroni, I;Mariotti, C
Q1
NEUROLOGICAL SCIENCES
2024.
Semmelweis University authors: Molnár, Mária Judit, C. Sági, Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Department of Genetics, Cell- and Immunology, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics,
25.
Pozsonyi, Z;Peskó, G;Takács, H;Csuka, D;Nagy, V;Szilágyi, A;Hategan, L;Muk, B;Csányi, B;Nyolczas, N;Dézsi, L;Molnár, JM;Csillik, A;Révész, K;Iványi, B;Szabó, F;Birtalan, K;Masszi, T;Arányi, Z;Sepp, R
Q2
GENES
2021.
Semmelweis University authors: Pozsonyi, Zoltán, Peskó, Gergely, Csuka, Dorottya, Szilágyi, Ágnes, Molnár, Mária Judit, Csillik, Anita, Révész, Katalin, Szabó, Fruzsina, Masszi, Tamás, Arányi, Zsuzsanna,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Belgyógyászati és Hematológiai Klinika, Department of Neurology,
26.
Fekete, B;Pentelényi, K;Rudas, G;Gál, A;Grosz, Z;Illés, A;Idris, J;Csukly, G;Domonkos, A;Molnar, MJ
Q3
BMC MEDICAL GENETICS
2019.
Semmelweis University authors: Fekete, Bálint András, Pentelényi, Klára, Rudas, Gábor, Gál, Anikó, Grosz, Zoltán, Illés, Anett, Jimoh, Idris János, Csukly, Gábor, Domonkos, Andor, Molnár, Mária Judit,
27.
Angelini, C;Marozzo, R;Pinzan, E;Pegoraro, V;Molnar, MJ;Torella, A;Nigro, V
Q1
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS
2019.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
28.
Carvalho, V;Colonna, I;Curia, G;Ferretti, MT;Arabia, G;Molnar, MJ;Lebedeva, ER;Moro, E;de Visser, M;Bui, E
Q1
EUROPEAN JOURNAL OF NEUROLOGY
2023.
DOI:10.1111/ene.15916 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
29.
Balicza, P;Gezsi, A;Fedor, M;Sagi, JC;Gal, A;Varga, NA;Molnar, MJ
Q1
FRONTIERS IN PSYCHIATRY
2023.
Semmelweis University authors: Balicza, Péter, Gézsi, András, Fedor, Mariann, C. Sági, Judit, Gál, Anikó, Varga, Noémi-Ágnes, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
30.
Csehi, R;Dombi, ZB;Sebe, B;Molnár, MJ
Q1
FRONTIERS IN PSYCHIATRY
2022.
Semmelweis University authors: Csehi, Réka, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
31.
El-Hassar, L;Amara, A;Sanson, B;Lacatus, O;Belhouchet, AA;Kroneman, M;Claeys, K;Plançon, JP;Rodolico, C;Primiano, G;Trojsi, F;Filosto, M;Mongini, TE;Bortolani, S;Monforte, M;Carraro, E;Maggi, L;Ricci, F;Silani, V;Orsucci, D;Créange, A;Péréon, Y;Stojkovic, T;van der Beek, NAME;Toscano, A;Pareyson, D;Attarian, S;Van den Bergh, PYK;Remiche, G;Hoeijmakers, JGJ;Badrising, U;Voermans, NC;Kaindl, AM;Schara-Schmidt, U;Schoser, B;Gazzerro, E;Haberlová, J;Vohánka, S;Pál, E;Molnar, MJ;Leonardis, L;T...
Q2
JOURNAL OF NEUROMUSCULAR DISEASES
2023.
DOI:10.3233/JND-221525 (Copy DOI)
Semmelweis University authors: Pál, Endre, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
32.
Csaban, D;Pentelenyi, K;Toth-Bencsik, R;Illes, A;Grosz, Z;Gezsi, A;Molnar, MJ
Q2
LIFE-BASEL
2021.
DOI:10.3390/life11040321 (Copy DOI)
Semmelweis University authors: Csabán, Dóra, Pentelényi, Klára, Illés, Anett, Grosz, Zoltán, Gézsi, András, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
33.
Jimoh, IJ;Sebe, B;Balicza, P;Fedor, M;Pataky, I;Rudas, G;Gal, A;Inczedy-Farkas, G;Nemeth, G;Molnar, MJ
Q1
THERAPEUTIC ADVANCES IN NEUROLOGICAL DISORDERS
2020.
Semmelweis University authors: Jimoh, Idris János, Balicza, Péter, Fedor, Mariann, Rudas, Gábor, Gál, Anikó, Inczédy-Farkas, Gabriella, Németh, György, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Orvosi Képalkotó Klinika,
34.
Kárteszi, J;Ziegler, A;Tihanyi, M;Elmont, B;Zhang, YB;Patócs, B;Molnár, MJ;Méhes, G;Wells, K;Jakus, R;Bessenyei, B;Ranatunga, W;Morava, E
Q2
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
2023.
DOI:10.1002/ajmg.a.63340 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
35.
Illés, A;Csabán, D;Grosz, Z;Balicza, P;Gézsi, A;Molnár, V;Bencsik, R;Gál, A;Klivényi, P;Molnar, MJ
Q1
FRONTIERS IN GENETICS
2019.
Semmelweis University authors: Illés, Anett, Csabán, Dóra, Grosz, Zoltán, Balicza, Péter, Gézsi, András, Molnár, Viktor, Gál, Anikó, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
36.
Illés, A;Balicza, P;Gál, A;Pentelényi, K;Csabán, D;Gézsi, A;Molnár, V;Mária, JM
Q4
ORVOSI HETILAP
2020.
Semmelweis University authors: Illés, Anett, Balicza, Péter, Gál, Anikó, Pentelényi, Klára, Csabán, Dóra, Gézsi, András, Molnár, Viktor, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
37.
Molnár, MJ;Borsos, B;Várdi, VK;Grosz, Z;Sebok, A;Dézsi, L;Almássy, Z;Kerényi, L;Jobbágy, Z;Jávor, L;Bidló, J
Q4
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
2020.
DOI:10.18071/isz.73.0151 (Copy DOI)
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
38.
Melicher, D;Illés, A;Littvay, L;Tárnoki, AD;Tárnoki, DL;Bikov, A;Kunos, L;Csabán, D;Buzás, EI;Molnár, MJ;Falus, A
Q2
ARCHIVES OF MEDICAL SCIENCE
2021.
Semmelweis University authors: Melicher, Dóra, Illés, Anett, Tárnoki, Ádám Domonkos, Tárnoki, Dávid László, Kunos, László, Csabán, Dóra, Buzás, Edit Irén, Molnár, Mária Judit, Falus, András,
39.
Toth-Bencsik, R;Balicza, P;Varga, ET;Lengyel, A;Rudas, G;Gal, A;Molnar, MJ
Q2
FRONTIERS IN GENETICS
2021.
40.
Várhegyi, V;Molnár, V;Gérsi, A;Sárközy, P;Antal, P;Mária, JM
Q4
ORVOSI HETILAP
2021.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
41.
Illés, A;Balicza, P;Molnár, V;Bencsik, R;Szilvási, I;Molnar, MJ
Q1
BMC NEUROLOGY
2019.
Semmelweis University authors: Illés, Anett, Balicza, Péter, Molnár, Viktor, Szilvási, István, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
42.
Szatmari, B;Balicza, P;Nemeth, G;Molnar, MJ
Q1
CURRENT MEDICINAL CHEMISTRY
2019.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
43.
Boczán, J;Klivényi, P;Kálmán, B;Széll, M;Karcagi, V;Zádori, D;Molnár, MJ
Q4
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
2021.
DOI:10.18071/isz.74.0079 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
44.
Gal, A;Grosz, Z;Borsos, B;Szatmari, I;Sebok, A;Jávor, L;Harmath, V;Szakszon, K;Dezsi, L;Balku, E;Jobbagy, Z;Herczegfalvi, A;Almássy, Z;Kerényi, L;Molnar, MJ
Q2
LIFE-BASEL
2021.
DOI:10.3390/life11060507 (Copy DOI)
Semmelweis University authors: Gál, Anikó, Grosz, Zoltán, Borsos, Beáta, Szatmári, Ildikó, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics, I. Department of Pediatrics, II. Department of Pediatrics,
45.
Molnar, V;Cs Sagi, J;Molnar, MJ
Q4
ORVOSI HETILAP
2023.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
46.
Molnár, MJ;Molnár, V;László, I;Szegedi, M;Varhegyi, V;Grosz, Z
Q4
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
2021.
DOI:10.18071/isz.74.0105 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit, Molnár, Viktor, László, Izabella, Szegedi, Márta, Várhegyi, Vera, Grosz, Zoltán,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
47.
Szabó-Taylor, K;Molnár, MJ
Q4
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
2023.
DOI:10.18071/isz.76.0077 (Copy DOI)
Semmelweis University authors: Szabó-Taylor, Katalin, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Department of Genetics, Cell- and Immunology, Genomic Medicine and the Institute of Rare Diseases,
48.
Grosz, Z;Várdi, VK;Molnár, MJ
Q4
IDEGGYOGYASZATI SZEMLE-CLINICAL NEUROSCIENCE
2020.
DOI:10.18071/isz.73.0339 (Copy DOI)
Semmelweis University authors: Grosz, Zoltán, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
49.
Szlepák, T;Kossev, AP;Csabán, D;Illés, A;Udvari, S;Balicza, P;Borsos, B;Takáts, A;Klivényi, P;Molnár, MJ
Q1
NEUROLOGICAL SCIENCES
2024.
Semmelweis University authors: Szlepák, Tamás, Csabán, Dóra, Illés, Anett, Udvari, Szabolcs, Balicza, Péter, Borsos, Beáta, Takáts, Annamária, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Internal Medicine and Oncology, Department of Neurology,
50.
Molnar, MJ;Szlepak, T;Csürke, I;Loth, S;Káposzta, R;Erdos, M;Dezsofi, A
Q2
FRONTIERS IN GENETICS
2023.
Semmelweis University authors: Molnár, Mária Judit, Szlepák, Tamás, Lóth, Szendile, Erdős, Melinda, Dezsőfi-Gottl, Antal,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Dermatology, Dermatooncology and Venerology, Department of Pediatrics,
51.
Molnar, MJ;Szabó, L;Vladacenco, OA;Cobzaru, AM;Dor, T;Dori, A;Papadimas, G;Juríková, L;Litvinenko, I;Tournev, I;Dixon, C
Q1
ORPHANET JOURNAL OF RARE DISEASES
2024.
Semmelweis University authors: Molnár, Mária Judit, Szabó, Léna,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics,
52.
Pizzamiglio, C;Pitceathly, RDS;Lunn, MP;Brady, S;De Marchi, F;Galan, L;Heckmann, JM;Horga, A;Molnar, MJ;Oliveira, ASB;Pinto, WBVR;Primiano, G;Santos, E;Schoser, B;Servidei, S;Souza, PVS;Venugopalan, V;Hanna, MG;Dimachkie, MM;Machado, PM
Q1
EUROPEAN JOURNAL OF NEUROLOGY
2023.
DOI:10.1111/ene.15613 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
53.
Lavorgna, L;Maida, E;Reinhard, C;Cras, P;Reetz, K;Molnar, MJ;Nonnekes, J;Medijainen, K;Summa, S;Diserens, K;Petrarca, M;Albanese, A;Leocani, L;Delussi, M;Vinciguerra, C;Pagliano, E;Kubica, J;Lallemant, P;Wenning, G;Sival, D;Srsen, KG;Bertini, ES;Lopane, G;Boesch, S;Bonavita, S;Crosiers, D;Muresanu, D;Timmann, D;Federico, A
Q1
TELEMEDICINE AND E-HEALTH
2024.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
54.
Tordai, Csongor; Hathy, Edit; Gyergyák, Hella; Vincze, Katalin; Baradits, Máté; Koller, Júlia; Póti, Ádám; Jezsó, Bálint; Homolya, László; Molnár, Mária Judit; Nagy, László; Szüts, Dávid; Apáti, Ágota; Réthelyi, János M.;
Q1
SCHIZOPHRENIA RESEARCH 0920-9964 1573-2509
2024.
Semmelweis University authors: Tordai, Csongor, Hathy, Edit Margit, Vincze, Katalin, Baradits, Máté, Koller, Júlia, Molnár, Mária Judit, Apáti, Ágota, Réthelyi, János,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Pszichiátriai és Pszichoterápiás Klinika,
55.
Erdei, Zs; Maneschg, Otto Alexander; Szabó, Viktória; Gál, Anikó; Molnár, Mária Judit; Nagy, Zoltán Zsolt; Knézy, Krisztina;
SZEMÉSZET 0039-8101
2019.
Semmelweis University authors: Maneschg, Otto, Szabó, Viktória, Gál, Anikó, Molnár, Mária Judit, Nagy, Zoltán Zsolt, Knézy, Krisztina,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Ophthalmology,
56.
Diaz-Manera, Jordi; S Kishnani, Priya; Kushlaf, Hani; Ladha, Shafeeq; Mozaffar, Tahseen; Straub, Volker; Toscano, Antonio; T van der Ploeg, Ans; I Berger, Kenneth; R Clemens, Paula; Chien, Yin-Hsiu; W Day, John; Illarioshkin, Sergey; Roberts, Mark; Attarian, Shahram; Lindolfo Borges, Joao; Bouhour, Francoise; Chul Choi, Young; Erdem-Ozdamar, Sevim; Goker-Alpan, Ozlem; Kostera-Pruszczyk, Anna; An Haack, Kristina; Hug, Christopher; Huynh-Ba, Olivier; Johnson, Judith; Thibault, Nathan; Zhou, Tianyu...
D1
LANCET NEUROLOGY 1474-4422 1474-4465
2021.
Semmelweis University authors: Molnár, Mária Judit, Grosz, Zoltán,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
57.
Schoser, Benedikt; Roberts, Mark; Byrne, Barry J; Sitaraman, Sheela; Jiang, Hai; Laforêt, Pascal; Toscano, Antonio; Castelli, Jeff; Díaz-Manera, Jordi; Goldman, Mitchell; der Ploeg, Ans Tvan; Bratkovic, Drago; Kuchipudi, Srilakshmi; Mozaffar, Tahseen; Kishnani, Priya S; Sebok, Agnes; Pestronk, Alan; , ; Dominovic-Kovacevic, Aleksandra; Khan, Aneal; Koritnik, Blaž; Tard, Celine; Lindberg, Christopher; Quinn, Colin; Eldridge, Crystal; Bodkin, Cynthia; Reyes-Leiva, David; Hughes, Derralynn; Stef...
D1
LANCET NEUROLOGY 1474-4422 1474-4465
2021.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
58.
Zeke, H; Fekete, BA; Molnár, MJ;
ORVOSKÉPZÉS 0030-6037
2021.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
59.
Balicza, Péter; Balicza-Ripka, Eszter; Molnár, Mária Judit;
ORVOSTOVÁBBKÉPZŐ SZEMLE 1218-2583
2022.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
60.
Borsos, B; Molnár, MJ;
ORVOSTOVÁBBKÉPZŐ SZEMLE 1218-2583
2022.
Semmelweis University authors: Borsos, Beáta, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
61.
Hentzen, Nina B; Ferretti, Maria Teresa; Santuccione, Antonella; Jaarsma, Joke; de Visser, Marianne; Moro, Elena; Hege Aamodt, Anne; , ; Arabia, Gennarina; Aybeck, Selma; Carvalho, Vanessa; de Visser, Marianne; Teresa Ferretti, Maria; Goudier, Riadh; Grisold, Wolfgang; Lebedeva, Elena R; Jaarsma, Joke; Matczack, Magda; Magyari, Melinda; Maria Judit, Molnar; Moro, Elena; Rakusa, Martin; Pajediene, Evelina; Tracy, Irene; Vonck, Kristl;
Q1
EUROPEAN JOURNAL OF NEUROLOGY 1351-5101 1468-1331
2022.
DOI:10.1111/ene.15439 (Copy DOI)
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
62.
István, Lilla; Benyó, Fruzsina; Csorba, Anita; Jimoh, Idris János; Gál, Anikó; Molnár, Mária Judit; Nagy, Zoltán Zsolt; Szabó, Viktória;
SZEMÉSZET 0039-8101
2022.
Semmelweis University authors: István, Lilla, Benyó, Fruzsina, Csorba, Anita, Jimoh, Idris János, Gál, Anikó, Molnár, Mária Judit, Nagy, Zoltán Zsolt, Szabó, Viktória,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Ophthalmology,
63.
Jimoh, IJ; Molnár, MJ;
ORVOSTOVÁBBKÉPZŐ SZEMLE 1218-2583
2022.
Semmelweis University authors: Jimoh, Idris János, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
64.
Oomen, Loes; Leijte, Erik; Shilhan, Darren E.; Battye, Michelle; Waltregny, David; Van, der Aa Frank; Spinoit, Anne-Françoise; Rösch, Wolfgang H.; Schmiedeke, Eberhard; Fisch, Margit; Märzheuser, Stefanie; Gosemann, Jan-Hendrik; Hubertus, Jochen; Rawashdeh, Yazan; Thorup, Jorgen; Heloury, Yves; Leva, Ernesto; Mancini, Mariangela; Bagolan, Pietro; Sacco, Emilio; Verkauskas, Gilvydas; Feitz, Wout; Sloots, Cornelius; Czauderna, Piotr; Mauricio, Maria; Holmdahl, Gundela; Abrahamsson, Kate; Thomas...
D1
EUROPEAN UROLOGY 0302-2838 1873-7560 1421-993X
2022.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
65.
Denommé-Pichon, Anne-Sophie; Matalonga, Leslie; de Boer, Elke; Jackson, Adam; Benetti, Elisa; Banka, Siddharth; Bruel, Ange-Line; Ciolfi, Andrea; Clayton-Smith, Jill; Dallapiccola, Bruno; Duffourd, Yannis; Ellwanger, Kornelia; Fallerini, Chiara; Gilissen, Christian; Graessner, Holm; B Haack, Tobias; Havlovicova, Marketa; Hoischen, Alexander; Jean-Marçais, Nolwenn; Kleefstra, Tjitske; López-Martín, Estrella; Macek, Milan; Antonietta Mencarelli, Maria; Moutton, Sébastien; Pfundt, Rolph; Pizzi...
D1
GENETICS IN MEDICINE 1098-3600 1530-0366
2023.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
66.
Jackson, Adam; Lin, Sheng-Jia; Jones, Elizabeth A; Chandler, Kate E; Orr, David; Moss, Celia; Haider, Zahra; Ryan, Gavin; Holden, Simon; Harrison, Mike; Burrows, Nigel; Jones, Wendy D; Loveless, Mary; Petree, Cassidy; Stewart, Helen; Low, Karen; Donnelly, Deirdre; Lovell, Simon; Drosou, Konstantina; Varshney, Gaurav K; , ; Banka, Siddharth; Ambrose, J C; Arumugam, P; Bevers, R; Bleda, M; , ; Boardman-Pretty, F; Boustred, C R; Brittain, H; Brown, M A; Caulfield, M J; Chan, G C; Giess, A; Griffin,...
Q1
Human Genetics and Genomics Advances 2666-2477 2666-2477
2023.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
67.
Efficacy and Safety of Avalglucosidase Alfa in Patients With Late-Onset Pompe Disease After 97 Weeks
Kishnani, Priya S; Diaz-Manera, Jordi; Toscano, Antonio; Clemens, Paula R; Ladha, Shafeeq; Berger, Kenneth I; Kushlaf, Hani; Straub, Volker; Carvalho, Gerson; Mozaffar, Tahseen; Roberts, Mark; Attarian, Shahram; Chien, Yin-Hsiu; Choi, Young-Chul; Day, John W; Erdem-Ozdamar, Sevim; Illarioshkin, Sergey; Goker-Alpan, Ozlem; Kostera-Pruszczyk, Anna; van der Ploeg, Ans T; An Haack, Kristina; Huynh-Ba, Olivier; Tammireddy, Swathi; Thibault, Nathan; Zhou, Tianyue; Dimachkie, Mazen M; Schoser, Benedikt...
D1
JAMA NEUROLOGY 2168-6149 2168-6157
2023.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
68.
Mikos, Borbála; Szatmári, Ildikó; Monostori, Péter; Molnár, Mária Judit; Bereczki, Csaba; Szabó, Attila; Csõsz, Katalin; Muzsik, Béla; Velkey, György János;
GYERMEKGYÓGYÁSZAT 0017-5900
2023.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics,
69.
Szalai, Klára Szilvia; Molnár, Mária Judit; Molnár, Viktor; Ács, Andrea;
NŐVÉR 0864-7003 1588-1423
2023.
Semmelweis University authors: Szalai, Klára Szilvia, Molnár, Mária Judit, Molnár, Viktor, Ács, Andrea,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Faculty of Health Sciences,
70.
Varga, Noémi Ágnes; Molnár, Mária Judit;
ORVOSTOVÁBBKÉPZŐ SZEMLE 1218-2583
2023.
Semmelweis University authors: Varga, Noémi-Ágnes, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
71.
Yaldiz, Burcu; Kucuk, Erdi; Hampstead, Juliet; Hofste, Tom; Pfundt, Rolph; Corominas Galbany, Jordi; Rinne, Tuula; Yntema, Helger G; Hoischen, Alexander; Nelen, Marcel; Gilissen, Christian; , ; Riess, Olaf; Haack, Tobias B; Graessner, Holm; Zurek, Birte; Ellwanger, Kornelia; Ossowski, Stephan; Demidov, German; Sturm, Marc; Schulze-Hentrich, Julia M; Schüle, Rebecca; Xu, Jishu; Kessler, Christoph; Wayand, Melanie; Synofzik, Matthis; Wilke, Carlo; Traschütz, Andreas; Schöls, Ludger; Hengel, Hol...
Q1
HUMAN GENOMICS 1473-9542 1479-7364
2023.
Semmelweis University authors: Balicza, Péter, Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
72.
Mikos, Borbála; Molnár, Mária Judit; Szatmári, Ildikó; Monostori, Péter; Bereczki, Csaba; Szabó, Attila József; Szabó, Léna; Csősz, Katalin; Muzsik, Béla; Velkey, György János;
Q4
ORVOSI HETILAP 0030-6002 1788-6120
2024.
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases, Department of Pediatrics,
73.
Schoser, Benedikt; Kishnani, Priya S; Bratkovic, Drago; Byrne, Barry J; Claeys, Kristl G; Díaz-Manera, Jordi; Laforêt, Pascal; Roberts, Mark; Toscano, Antonio; van der Ploeg, Ans T; Castelli, Jeff; Goldman, Mitchell; Holdbrook, Fred; Sitaraman Das, Sheela; Wasfi, Yasmine; Mozaffar, Tahseen; , ; Sebok, Agnes; Pestronk, Alan; Dominovic-Kovacevic, Aleksandra; Khan, Aneal; Koritnik, Blaž; Tard, Celine; Lindberg, Christopher; Quinn, Colin; Eldridge, Crystal; Bodkin, Cynthia; Reyes-Leiva, David; Hu...
Q1
JOURNAL OF NEUROLOGY 0340-5354 1432-1459
2024.
Semmelweis University authors: Molnár, Mária Judit,
Semmelweis University departments: Semmelweis University, Faculty of Medicine, Genomic Medicine and the Institute of Rare Diseases,
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